N-6 substituted-5′-(N-substituted carboxamide)adenosines as cardiac vasodilator and antihypertensive agents

Abstract

Compounds of the formula are disclosed, wherein R1, represents secondary alkyl; aralkyl; cycloalkyl; heteroaryl substituted alkyl; norbornyl; and substituted secondary alkyl, aralkyl, cycloalkyl, heteroaryl substituted alkyl, norbornyl; and para-substituted phenyl groups; and R2 and R3 are hydrogen or pharmacologically acceptable acyl groups. The compounds of the invention are useful as cardiovascular vasodilator or anti-hypertensive agents. The therapeutically useful compounds of the invention as well as similar 5-N and N-6 substituted adenosine 5-uronamides are prepared, in accordance with a novel process, from isopropylidene (or otherwise suitably blocked) inosine-5′-uronic acid. Isopropylideneinosine-5′-uronic acid is reacted with a suitable inorganic acid halide, such as thionyl chloride, to yield 6-halogeno-9-[2′,3′-O-isopropylidene-&bgr;-D-ribofuranosyl-5-uronic acid halide]-9H-purine. This intermediate is reacted with an amine of the general formula R4R5NH to give a 6-halogeno substituted, substituted uronic acid amide of the formula wherein X is halogen. Reaction of the latter intermediate with an amine of the formula R1—NH2, and removal of the isopropylidene (or other) blocking groups yields the compounds of the invention.

Description

BACKGROUND OF THE INVENTION

1. Cross-reference to Related Application

The present application is a reissue of a U.S. Pat. No. 5,310,731, issued on May 10, 1994, which was a continuation-in-part of application Ser. No. 625,450 filed on Jun. 28, 1984, now abandoned by the same inventors, and assigned to the same assignee as the present application.

2. Field of the Invention

The present invention is directed to certain N-6 and 5′-N substituted carboxamidoadenosine derivatives which have beneficial cardiovascular and antihypertensive activity in mammals, including humans and domestic animals. The present invention is also directed to a process for making said compounds.

3. Brief Description of the Prior Art

Adenosine has been known for a long time to possess certain cardiovascular activity and particularly coronary dilatory activity. In an effort to obtain adenosine analogs of greater potency, or longer duration of activity, or both, many analogs of this naturally occurring nucleoside have been synthesized and tested.

Moreover, numerous studies have been conducted in order to elucidate the biochemical mechanism of action of adenosine and its analogs, and several theories and hypotheses have been proposed regarding biochemical pathways and receptor sites.

For discussion of current theories regarding the foregoing, reference is made to the following articles and publications: Adenosine Receptors: Targets for Future Drugs, by John W. Daly, Journal of Medicinal Chemistry, 25, 197 (1982); Cardiovascular Effects of Nucleoside Analogs, by Herman H. Stein and Pitambar Somani, Annals New York Academy of Sciences, 255, 380 (1979); Coronary Dilatory Action of Adenosine Analogs: a Comparative Study, by G. Reberger, W. Schutz and O. Kraupp, Archives internationales de Pharmacodynamie et de Therapie 230, 140-149 (1977); Chapter 6 of the book titled: Regulatory Function of Adenosine, (pages 77-96), R. M. Berne, T. W. Rall and R. Rubio editors, Martinus Nijhoff publishers, The Hague/Boston/London; Ethyl Adenosine-5′-carboxylate: A Potent Vasoactive Agent in the Dog, by Herman H. Stein, Journal of Medicinal Chemistry, 16, 1306 (1973); Modification of the 5′ Position of Purine Nucleosides: 2. Synthesis and Some Cardiovascular Properties of Adenosine-5′-(N-substituted)carboxamides, by Raj N. Prasad et al., Journal of Medicinal Chemistry, 23, 313 (1980); and Modification of the 5′ Position of Purine Nucleosides: 1. Synthesis and Biological Properties of Alkyl Adenosine-5′-carboxylates by Raj N. Prasad et al., Journal of Medicinal Chemistry, 19, 1180 (1976).

In addition to the foregoing publications, German Offenlegungschrift Nos. 2133273, 2426682, 1795761, 1913818, 2007273, 2238923, 2060189, 2244328, 1814711, 2136624, South African Patent Application No. 677630 (filed on Dec. 20, 1967) and British Patent Specification No. 1,123,245 describe adenosine derivatives which have cardiovascular, coronary dilator or antilipolytic activities. Still more adenosine derivatives having beneficial cardiovascular activity are described in another application for U.S. Letters Patent of the present inventors, Ser. No. 601,435, filed on Apr. 18, 1984.

Still further, Published Japanese Patent Application Nos. 58-167599 and 58-167600 disclose adenosine 5′-carboxamide derivatives which have fibrinolysis accelerating activity. U.S. Pat. No. 4,029,334 discloses anti-hypertensive and anti-anginal adenosine 5′-carboxamide derivatives where the N6 amino group is unsubstituted. U.S. Pat. No. 4,167,565 discloses adenosine 5′-carboxamide derivatives which have substituents both in the N6 and 5′-carboxamido position, and which are useful as poisons for certain noxious animals, such as rodents and coyotes.

In the cardiovascular and anti-hypertensive field, however, the therapeutic utility of the natural nucleoside adenosine and many of its analogs is limited because the desired beneficial effect is often of relatively short duration.

More particularly, the short duration of the beneficial cardiovascular effects of adenosine and those of its analogs which have an unsubstituted hydroxyl group at C-5 of the ribofuranose moiety is usually attributed to rapid penetration into cells followed by enzymatic conversion into less active or impermeant metabolites. For example, adenosine deaminase converts adenosine into inosine, which is a weak cardiovascular agonist. Alternatively, phosphorylation, catalyzed by adenosine kinase, forms adenylic acid (5′-AMP). Ionization of the phosphate group under physiological conditions prevents the escape of 5′-AMP from the cells in which it is formed. Thus trapped, 5′-AMP cannot exert its cardiovascular actions, which are mediated by cell surface receptors, as is discussed below.

Some known adenosine analogs, however, cannot be phosphorylated in the 5′ position because the 5′ position is effectively blocked. 5′-N-Ethylcarboxamidoadenosine [NECA] (Compound 1 in General Formula 1) is an example of such an adenosine analog incapable of phosphorylation by adenosine kinase. Nevertheless, this compound binds potently to certain adenosine receptor sites and exhibits substantial cardiovascular activity. Other examples of known derivatives of adenosine-5′-carboxamide, (Compound 2) and of adenosine-5′-carboxylic acid (Compound 9) are shown below in General Formulae 1 and 2. Generally speaking, in these compounds, the 5′-carboxylate or 5′-carboxamide group of the uronic acid moiety is substituted with lower alkyl or lower acyl groups. Some of the adenosine-5′-carboxamide derivatives shown in General Formula 1 are disclosed in Chemical Abstracts Volume 100, 68652c and 68653d (1984) and in the corresponding Published Japanese Patent Application Nos. 58-167599 and 58-167600.

The biological activity of adenosine-5′-carboxamide derivatives, such as NECA, is thought to be due to the activation of adenylate cyclase through cell surface “Ra” or “A2” receptors. Structure-activity studies show that the Ra receptor recognizes the alkyl uronamide moiety of NECA and its congeners. A second type of cell surface adenosine receptor designated “Ri” or “A1” inhibits the catalytic activity of adenylate cyclase. Adenosine analogs possessing certain N-6 alkyl or aralkyl substituents such as cyclohexyl or R-1-phenyl-2-propyl are selective agonists at Ri receptors. Many mammalian and human cells contain both Ra and Ri receptors; examples of exceptions are fat cells which contain Ri receptors only, and blood platelets and human placenta, in which Ra receptors predominate.

Currently available agonists are only selective, not absolutely specific, for Ra and Ri receptors. Because the two types of receptors coexist in many organs, including brain and heart, even a selective agonist will activate both to a certain degree. A goal of pharmaceutical chemistry is the development of agonists which are as nearly specific as possible because unselectivity can be a source of side effects.

The prior art makes no prediction about receptor selectivity of adenosine analogs which contain, in the same molecule, the recognition groups which confer specificity for Ra and Ri receptors.

Many of the known adenosine derivatives, including the above-noted N-6 substituted and the 5′-carboxamide derivatives are less than satisfactory as cardiovascular or antihypertensive drugs for animal and human use. This is either because of low activity, short duration of the desired activity, undue toxicity or undesirable side effects. Undesirable side effects of cardiovascularly active adenosine analogs often include cardiac depression.

In light of the foregoing, the pharmaceutical industry is still striving to obtain adenosine analogs having high cardiovascular and hypotensive potency coupled with other optimal physiological characteristics, such as relatively long duration of the desired activity, low toxicity and minimal side effects. The compounds of the present invention constitute a step in this direction.

SUMMARY OF THE INVENTION

It is an object of the present invention to provide adenosine analogs which have potent and prolonged cardiovascular activity in mammals and humans, coupled with relatively low toxicity and minimal side effects.

It is another object of the present invention to provide adenosine analogs which have potent or prolonged anti-hypertensive activity in mammals and humans, coupled with relatively low toxicity and minimal side effects.

It is still another object of the present invention to provide a relatively efficient synthetic process for the preparation of the adenosine derivatives which meet the above-noted objectives.

The foregoing and other objects and advantages are attained by compounds of the General Formula 3, wherein R1 represents secondary alkyl; hydroxy, lower alkoxy or halogen substituted secondary alkyl; aralkyl; aralkyl substituted in the aromatic nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups; cycloalkyl; hydroxy, lower alkoxy, lower alkyl or halogen substituted cycloalkyl; para-substituted phenyl; heteroaryl substituted alkyl; heteroaryl substituted alkyl substituted in the heteroaryl nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups; norbornyl, and hydroxy, alkyl or halogen substituted norbornyl groups.

The substituent R2 and R3 groups in the compounds of the present invention, as shown in General Formula 3, are hydrogen, or pharmacologically acceptable organic acyl groups, or inorganic acid radicals, such as NO2 groups, which esterify the hydroxyl groups of the ribofuranose moiety. The R2 and R3 groups are preferably of the type which are relatively readily hydrolyzed under physiological conditions. The R2 and R3 substituents need not be identical with one another.

Still further, in the compounds of General Formula 3, the substituent R4 is straight chain lower alkyl having 1-4 carbon atoms; hydroxy, lower alkoxy or halogen substituted straight chain lower alkyl having 1-4 carbon atoms; cyclopropyl; secondary alkyl having 3-6 carbon atoms; hydroxy, lower alkoxy or halogen substituted secondary alkyl having 3-6 carbon atoms; alkenyl having 3 to 6 carbon atoms; aralkyl having 1 to 4 carbons in the alkyl chain; aralkyl having 1 to 4 carbons in the alkyl chain and substituted in the aryl nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups; heteroarylalkyl having 1 to 4 carbons in the alkyl chain; and heteroarylalkyl having 1 to 4 carbons in the alkyl chain and substituted in the heteroaryl nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups. R5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons.

The compounds of the present invention are resistant to enzymatic phosphorylation and to deamination by adenosine deaminase. The compounds exhibit significant cardiovascular activity.

In accordance with a novel process of the invention, the compounds of General Formula 3 are obtained from 2′,3′-O-isopropylideneinosine-5′-uronic acid by treatment with a suitable inorganic acid halide, such as thionyl chloride, to yield the intermediate, 6-chloro-9-[2,3-O-isopropylidene-&bgr;-D-ribofuranosyl-5-uronic acid chloride]-9H-purine. The intermediate, 6-chloro-9-[2,3-O-isopropylidene-&bgr;-D-ribofuranosyl-5-uronic acid chloride]-9H-purine, (or the corresponding bromide, if, for example thionyl bromide is used instead of thionyl chloride) is usually not isolated in a pure state.

The acid chloride moiety of 6-chloro-9-[2,3-O-isopropylidene-&bgr;-D-ribofuranosyl-5-uronic acid chloride]-9H-purine (or the acid bromide of the corresponding bromo- analog) is significantly more readily displaced by nucleophilic reagents than the halide group in the 6 position of the purine moiety. Therefore, in accordance with the process of the present invention, 6-chloro-9-[2,3-O-isopropylidene-&bgr;-D-ribofuranosyl-5-uronic acid chloride]-9H purine is reacted with a first nucleophilic reagent having the formula R4,R5-NH (General Formula 4) to yield an intermediate substituted carboxamide shown in General Formula 5, wherein the halide is retained in the 6position of the purine moiety.

The intermediate of General Formula 5 is subsequently reacted with a nucleophile having the formula R1- NH2 (General Formula 6) and the isopropylidene blocking group is removed with acid to yield the compounds of the invention (General Formula 3), having free hydroxyl groups in the 2′ and 3′ positions of the ribofuranose moiety. Instead of the isopropylidene blocking group, other acid stable blocking groups can also be used to protect the 2′—OH and 3′—OH groups of the ribofuranose moiety during the step of treatment with the inorganic acid halide.

The groups R1, R4 and R5 in General Formulae 4-6 are defined the same as in General Formula 3.

DETAILED DESCRIPTION OF THE INVENTION

Certain derivatives of 5′-carboxamidoadenosine wherein both the amino nitrogen (N-6) of the purine moiety and the amino nitrogen of the 5′-carboxamido moiety are substituted, have been found, in accordance with the present invention, to possess significant cardiovascular and/or anti-hypertensive activity. The compounds of the invention have the composition characterized by General Formula 3. The substituent R1, R2, R3, R4 and R5 groups are defined above in the summary description of the present invention.

A preferred subclass of the compounds of the present invention consists of N-6 substituted derivatives of 5′-N-ethylcarboxamidoadenosine shown in General Formula 7, wherein the R1 substituents of the N-6 amino nitrogen comprise: secondary alkyl; hydroxy, lower alkoxy or halogen substituted secondary alkyl; aralkyl; aralkyl substituted in the aromatic nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups; cycloalkyl; hydroxy, lower alkoxy, lower alkyl or halogen substituted cycloalkyl; para-substituted phenyl; heteroaryl substituted alkyl; heteroaryl substituted alkyl substituted in the heteroaryl nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups.

The R2 and R3 substituent groups on the 2′ and 3′ positions of the ribofuranose moiety are hydrogen, or pharmaceutically acceptable acyl groups, such as acetyl, propionyl, butyryl and benzoyl groups. Especially preferred in this regard, are those acyl groups which are relatively readily split off the ribofuranose moiety under physiological conditions. The R2 and R3 substituent groups can also represent inorganic acid radicals, such as NO2 groups, which esterify the hydroxyl groups of the ribofuranose moiety.

The R4 substituent in the foregoing subclass of compounds shown in General Formula 7, is hydrogen, methyl or ethyl.

Another preferred subclass of the compounds of the present invention consists of derivatives of 5′-carboxamidoadenosine, compounds of General Formula 8, wherein both the N-6 and 5′-carboxamido nitrogens are monosubstituted with the substituents R1 and R4 respectively, and where the R2 and R3 substituents are defined the same as for the compounds of General Formula 7.

In this preferred subclass of compounds, shown in General Formula 8, the R1 substituents are: secondary alkyl; hydroxy, lower alkoxy or halogen substituted secondary alkyl; aralkyl; aralkyl substituted in the aromatic nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups; cycloalkyl; hydroxy, lower alkoxy, lower alkyl or halogen substituted cycloalkyl; para-substituted phenyl; heteroaryl substituted alkyl; heteroaryl substituted alkyl substituted in the heteroaryl nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups.

The substituents R4 of the preferred subclass shown in General Formula 8 are: straight chain lower alkyl having 1-4 carbon atoms; hydroxy, lower alkoxy or halogen substituted straight chain lower alkyl having 1-4 carbon atoms; cyclopropyl; secondary alkyl having 3-6 carbon atoms; hydroxy, lower alkoxy or halogen substituted secondary alkyl having 3-6 carbon atoms; alkenyl having 3 to 6 carbon atoms.

Specific examples of preferred compounds of this subclass (General Formula 8) are those where the R1 (N-6) and R4 (5′-carboxamido) substituents are as follows, with R2 and R3 being hydrogen:

Compound 17: R1 is 3-pentyl, R4 is ethyl;

Compound 18: R1 is cyclohexyl, R4 is ethyl;

Compound 19: R1 is (S)-1-phenyl-2-butyl, R4 is ethyl;

Compound 20: R1 is 4-methoxy-phenyl, R4 is ethyl;

Compound 21: R1 is 2-(3,4,5-trimethoxyphenyl)ethyl, R4 is ethyl;

Compound 22: R1 is 3-phenyl-propyl, R4 is ethyl;

Compound 23: R1 is (R)-1-phenylethyl, R4 is ethyl;

Compound 24: R1 is 2-(2-pyridyl)ethyl, R4 is ethyl;

Compound 25: R1 is (2-chlorophenyl)methyl, R4 is ethyl;

Compound 26: R1 is (2-thienyl)methyl, R4 is ethyl;

Compound 27: R1 is endo-2-norbornyl, R4 is 2-hydroxyethyl;

Compound 28: R1 is 3-pentyl, R4 is methyl;

Compound 29: R1 is 3-pentyl, R4 is isopropyl;

Compound 30: R1 is 3-pentyl, R4 is 3-pentyl;

Compound 31: R1 is 3-pentyl, R4 is allyl;

Compound 32: R1 is 3-pentyl, R4 is (2-methyl)propyl;

Compound 33: R1 is 3-pentyl, R4 is cyclopropyl;

Compound 34: R1 is (R)-1-phenyl-2-propyl, R4 is ethyl;

A preferred subgroup within the subclass shown by General Formula 8 comprise compounds in which the 5′-carboxamido group is ethyl substituted. With reference to General Formula 8, specific examples of compounds of this subgroup are:

Compound 17: R1 is 3-pentyl, R4 is ethyl;

Compound 18: R1 is cyclohexyl, R4 is ethyl;

Compound 19: R1 is (S)-1-phenyl-2-butyl, R4 is ethyl;

Compound 20: R1 is 4-methoxy-phenyl, R4 is ethyl;

Compound 21: R1 is 2-(3,4,5-trimethoxyphenyl)ethyl, R4 is ethyl;

Compound 22: R1 is 3-phenylpropyl, R4 is ethyl;

Compound 23: R1 is (R)-1-phenylethyl, R4 is ethyl;

Compound 24: R1 is 2-(2-pyridyl)ethyl, R4 is ethyl;

Compound 25: R1 is (2-chlorophenyl)methyl, R4 is ethyl;

Compound 26: R1 is (2-thienyl)methyl, R4 is ethyl;

Compound 34: R1 is (R)-1-phenyl-2-propyl, R4 is ethyl;

Another preferred subclass of the cardiovascularly active or anti-hypertensive compounds of the present invention is shown by General Formula 9, where the substituents R1, R2 and R3 signify the same groups as in the compounds of General Formula 8. The 5′-carboxamido substituents groups comprise, in this subclass of compounds, aralkyl having 1 to 4 carbons in the alkyl chain, unsubstituted or substituted in the aryl nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups; heteroarylalkyl having 1 to 4 carbons in the alkyl chain; and heteroarylalkyl having 1 to 4 carbons in the alkyl chain, unsubstituted or substituted in the heteroaryl nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups. Thus, in the structure symbolized by General Formula 9, n is an integer having the values of 1 to 4, and Q is an aromatic nucleus, or aromatic heterocycle, and Z is one or more H, hydroxy, halogen, lower alkoxy or lower alkyl.

Specific examples of compounds of the subclass of general formula 9 are:

Compound 35 R1 is 3-pentyl and the 5′-carboxamido substituent is phenylmethyl;

Compound 36 R1 is 3-pentyl and the 5′-carboxamido substituent is 2-methoxyphenylmethyl;

Compound 37 R1 is 3-pentyl and the 5′-carboxamido substituent is 2-thienylmethyl;

Compound 38 R1 is 3-pentyl and the 5′-carboxamido substituent is 2-phenylethyl.

Yet another subclass of the compounds of the present invention is shown in General Formula 10. In this subclass of compounds, the N-6 amino group of the purine moiety is substituted with a 3-pentyl group, and the R1 substituent of the 5′-carboxamido group is straight chain lower alkyl having 1-4 carbon atoms; hydroxy, lower alkoxy or halogen substituted straight chain lower alkyl having 1-4 carbon atoms; cyclopropyl; secondary alkyl having 3-6 carbon atoms; hydroxy, lower alkoxy or halogen substituted secondary alkyl having 3-6 carbon atoms; alkenyl having 3 to 6 carbon atoms; aralkyl having 1 to 4 carbons in the alkyl chain; aralkyl having 1 to 4 carbons in the alkyl chain and substituted in the aryl nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups; heteroarylalkyl having 1 to 4 carbons in the alkyl chain; and heteroarylalkyl having 1 to 4 carbons in the alkyl chain and substituted in the heteroaryl nucleus with hydroxy, halogen, lower alkoxy or lower alkyl groups. The second substituent on the 5′-carboxamido nitrogen, R4, is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. The R2 and R3 substituents on the hydroxyl groups of the ribofuranose moiety are the same as described above in connection with the compounds of General Formulae 7, 8, and 9.

Specific examples of compounds of the subclass of General Formula 10, where the R2 and R3 substituents are hydrogen, are:

Compound 17: R1 is ethyl, R4 is H;

Compound 28: R1 is methyl, R4 is H;

Compound 29: R1 is isopropy, R4 is H;

Compound 30: R1 is 3-pentyl, R4 is H;

Compound 31: R1 is allyl, R4 is H;

Compound 32: R1 is (2-methyl)propyl, R4 is H;

Compound 33: R1 is cyclopropyl, R4 is H;

Compound 35 R1 is phenylmethyl, R4 is H;

Compound 36 R1 is 2-methoxyphenylmethyl, R4 is H;

Compound 37 R1 is 2-thienylmethyl, R4 is H;

Compound 38 R1 is 2-phenylethyl, R4 is H;

Compound 39 R1 is methyl, R4 is methyl;

Compound 40 R1 is n-butyl, R4 is methyl;

Compound 41 R1 is ethyl, R4 is ethyl;

The physical characteristics and biological activity of specific examples of the compounds of the present invention are noted below together with certain biological activity data. The tests showing the biological activity of the compounds of the present invention are discussed after description of the specific examples.

SPECIFIC EXAMPLES

Ethyl N6-(3-pentyl)adenosine-5′-uronamide, (Compound 17) mp 176-177, uv &lgr;max(&egr;)=269 nm(18.1×103) at pH 7. Anal. Calculated for C17H26N6O4 (378.44): C, 53.96; H, 6.93; N, 22.21. Found: C, 53.82; H, 6.95; N, 22.17. Molar potency ratio (mpr) 3.3±0.25; anti-hypertensive activity at 0.05 mg/kg (22,20,22).

Ethyl N6-cyclohexyladenosine-5′-uronamide, (Compound 18) mp 133-135; uv&lgr;max(&egr;)=270(18.8×103) at pH 7. Anal. Calculated for C18H26N6O4 (382.38): C, 55.37; H, 6.71; N, 21.52. Found: C, 55.34; H, 6.86; N, 21.42. Molar potency ratio (mpr) 1.5±0.24; anti-hypertensive activity at 0.1 mg/kg (13,17,15).

Ethyl N6-(S)-1-phenyl-2-butyladenosine-5′-uronamide, (Compound 19) mp 177-179; uv &lgr;max(&egr;)270 nm(19.2×103) at pH 7; &agr;D25=+27 c=1 in 95% ETOH. Anal. Calculated for C22H28N6O4 (440.51): C, 59.99; H, 6.41; N, 19.08. Found: C, 59.89; H, 6.37; N, 19.06. Anti-hypertensive activity at 0.1 mg/kg (12,14,12).

Ethyl N6-4-methoxyphenyladenosine-5′-uronamide, (Compound 20) mp 189-190; uv &lgr;max(&egr;)287 nm(19.4×103) at pH 7; Anal. Calculated for C19H22N6O4 (414.42): C, 55.07; H, 5.35; N, 20.28. Found: C, 55.16; H, 5.45; N, 20.23. Anti-hypertensive activity at 10 mg/kg (40,47,52)+

Ethyl N6-2-(3,4,5-trimethoxyphenyl)ethyladenosine-5′-uronamide, (Compound 21) mp 154-155; uv&lgr;max(&egr;)270.5 nm(15.7×103) at pH 7; Anal. Calculated for C23H30N6O7 (502.53): C, 54.97; H, 6.02; N, 16.72. Found: C, 55.14; H, 6.13; N, 16.71. Anti-hypertensive activity at 10 mg/kg (18,0,8)+

Ethyl N6-3-phenylpropyladenosine-5′-uronamide, (Compound 22) mp 153-156; uv &lgr;max(&egr;)268 nm(17.6×103) at pH 7; Anal. Calculated for C21H26N6O4 (426.48): C, 59.14; H, 6.15; N, 19.71. Found: C, 59.24; H, 5.91; N, 19.85. Anti-hypertensive activity at 10 mg/kg (39,40,39).+

Ethyl N6-(R)-1-phenyl-ethyladenosine-5′-uronamide, (Compound 23) mp 144-147; uv &lgr;max(&egr;)270 nm(19.9×103) at pH 7; Anal. Calculated for C20H24N6O4 (412.45): C, 58.24; H, 5.87; N, 20.06. Found: C, 58.26; H, 6.00; N, 20.22. Anti-hypertensive activity at 1 mg/kg, rio detectable signal of blood pressure.

Ethyl N6-2-(2-pyridyl)ethyladenosine-5′-uronamide, (Compound 24) mp 126-127; uv &lgr;max(&egr;)268.5 nm(20.5×103) at pH 7; Anal. Calculated for C19H23N7O4 (413.44): C, 55.20; H, 5.61; N, 23.71. Found: C, 55.38; H, 5.82; N, 23.87. Anti-hypertensive activity at 10 mg/kg (31,16,21).+

Ethyl N6-(2-chlorophenyl)methyladenosine-5′-uronamide, (Compound 25) mp 134-136; uv &lgr;max(&egr;)267.5 nm(19.4×103) at pH 7; Anal. Calculated for C19H21C1N6O4.4.H2O (450.89): C, 50.61; H, 5.14; N, 18.64. Found: C, 50.85; H, 5.04; N, 18.49. Anti-hypertensive activity at 5 mg/kg, no detectable signal of blood pressure.

Ethyl N6-2-thienylmethyladenosine-5′-uronamide, (Compound 26) mp 164-165; uv &lgr;max(&egr;)268.5 nm(21.2×103) at pH 7. Anal. Calculated for C17H20N6O4S (404.45): C, 50.49; H, 4.98; N, 20.78. Found: C, 50.46; H, 5.21; N, 20.81. Anti-hypertensive activity at 5 mg/kg (22,32,29)+

2-Hydroxyethyl N6-endo-2-norbornyladenosine-5′-uronamide, (Compound 27) mp 132-134; uv&lgr;max(&egr;)270.5 nm(18.5×103) at pH 7; Anal. Calculated for C19H26N6O5.H2O (420.48): C, 54.27; H, 6.71; N, 19.99. Found: C, 54.22; H, 6.66; N, 19.90. Anti-hypertensive activity at 1 mg/kg (8,33,36)*

Methyl N6-3-pentyladenosine-5′-uronamide, (Compound 28) mp 126-128; uv &lgr;max(&egr;)269 nm(18.5×103) at pH 7; Anal. Calculated for C16H24N6O4 (364.41): C, 52.74; H, 6.64; N, 23.06. Found: C, 52.66; H, 6.70; N, 23.16. Anti-hypertensive activity at 0.5 mg/kg (14,17,17).

Isopropyl N6 -3-pentyladenosine-5′-uronamide, (Compound 29) mp 191-193; uv &lgr;max(&egr;)269 nm(18.3×103) at pH 7; Anal. Calculated for C18H28N6O4 (392..46): C, 55.09; H, 7.19; N, 21.41. Found: C, 55.03; H, 7.37; N, 21.27. Anti-hypertensive activity at 0.5 mg/kg (11,24,18).

3-Pentyl N6-3-pentyladenosine-5′-uronamide, (Compound 30) mp 211-212; uv &lgr;max(&egr;)270 nm(17.9×103) at pH 7; Anal. Calculated for C20H32N6O4 (420.52): C, 57.13; H, 7.67; N, 19.98. Found: C, 57.35; H, 7.76; N, 19.81. Anti-hypertensive activity at 20 mg/kg (6,21,17).

Allyl-N6-3-pentyladenosine-5′-uronamide, (Compound 31) mp 169-170; uv &lgr;max(&egr;)269 nm(19.2×103) at pH 7; Anal. Calculated for C18H26N6O4 (390.45): C, 55.37; H, 6.71; N, 21.52. Found: C, 55.24; H, 6.97; N, 21.31. Anti-hypertensive activity at 2.5 mg/kg (15,15,20).

(2-Methyl)-propyl N6-3-pentyladenosine-5′-uronamide, (Compound 32) mp 206-207; uv &lgr;max(&egr;)268.5 nm(16.9×103) at pH 7; Anal. Calculated for C19H30N6O4 (406.49): C, 56.14; H, 7.44; N, 20.67. Found: C, 56.22; H, 7.46; N, 20.76. Anti-hypertensive activity at 10 mg/kg (15,19,13).

Cyclopropyl N6-3-pentyladenosine-5′-uronamide, (Compound 33) mp 181-183; uv &lgr;max(&egr;)269 nm(20.0×103) at pH 7; Anal. Calculated for C18H26N6O4 (390.45): C, 55.37; H, 6.71; N, 21.52. Found: C, 55.11; H, 6.65; N, 21.66. Anti-hypertensive activity at 0.25 mg/kg (21,21,28), molar potency ratio (mpr) 2.3.

Ethyl N6-(R)-1-phenyl-2-propyladenosine-5′-uronamide, (Compound 34) mp 157-158; uv &lgr;max(&egr;)=270 nm(18.0×103) at pH 7. &agr;%hd D25=−104.5. Anal. Calculated for C21H26N6O4 (426.48): C, 59.14; H, 6.15; N, 19.71. Found: C, 58.91; H, 6.10; N, 19.64. Molar potency ratio (mpr) 4.3.±0.60;

Phenylmethyl N6-3-penthyladenosine-5′-uronamide, (Compound 35) mp 174-175; uv &lgr;max(&egr;)269 nm(17.4×103) at pH 7; Anal. Calculated for C22H28N6O4 (440.51): C, 59.99; H, 6.41; N, 19.08. Found: C, 59.76; H, 6.34; N, 19.07. Anti-hypertensive activity at 5 mg/kg (18,26,22).

2-Methoxyphenylmethyl N6-3-pentyladenosine-5′-uronamide, (Compound 36) mp 176-178; uv &lgr;max(&egr;)269.5 nm(18.9×103) at pH 7; Anal. Calculated for C23H30N6O5 (470.53): C, 58.71; H, 6.43; N, 17.86. Found: C, 58.53; H, 6.68; N, 17.65. Anti-hypertensive activity at 10 mg/kg (12,18,18).

2-Thienylmethyl N6-3-pentyladenosine-5′-uronamide, (Compound 37) mp 160-161; uv &lgr;max(&egr;)237 nm(10.1×103), 269.0 nm(17.4×103) at pH 7; Anal. Calculated for C20H26N6O4 S (446.53): C, 53.80; H, 5.87; N, 18.82. Found: C, 53.62; H, 6.00; N, 19.00. Anti-hypertensive activity at 5 mg/kg (16,16,14).

2-Phenylethyl N6 -3-pentyladenosine-5′-uronamide, (Compound 38) mp 203-204; uv &lgr;max(&egr;)268.5 nm(18.8×103) at pH 7; Anal. Calculated for C23H30N6O4 (453.53): C, 60.78; H, 6.65; N, 18.49. Found: C, 60.88; H, 6.67; N, 18.50. Anti-hypertensive activity at 40 mg/kg (17,13,15).

Dimethyl N6-3-pentyladenosine-5′-uronamide, (Compound 39) mp 168-169; uv &lgr;max(&egr;)269 nm(18.7×103) at pH 7; Anal. Calculated for C17H26N6O4 (378.44): C, 53.96; H, 6.93; N, 22.21. Found: C, 53.71; H, 7.11; N, 22.34. Anti-hypertensive activity at 2.5 mg/kg (25,23,17).

Methyl,n-butyl N6-3-pentyladenosine-5′-uronamide, (Compound 40) mp 139-141; uv &lgr;max(&egr;)270 nm(19.2×103) at pH 7; Anal. Calculated for C20H32N6O4 (420.52): C, 57.13; H, 7.67; N, 19.98. Found: C, 57.26; H, 7.50; N, 19.92. Anti-hypertensive activity at 1 mg/kg (31,21,27).

Diethyl N6-3-pentyladenosine-5′-uronamide, (Compound 41) mp 148-150; uv &lgr;max(&egr;)269 nm(19.0×103) at pH 7; Anal. Calculated for C17H30N6O4 (406.49): C, 56.14; H, 7.44; N, 20.67. Found: C, 56.42; H, 7.29; N, 20.67. Anti-hypertensive activity at 1 mg/kg (10,13,11).

Dimethyl N6-2-(2-chlorophenyl)-ethyladenosine-5′-uronamide, (Compound 42) mp 129-131; uv &lgr;max(&egr;)268.5 nm(20.2×103) at pH 7; Anal. Calculated for C20H23C1N6O4 (446.90): C, 53.75; H, 5.19; N, 18.81. Found: C, 53.91; H, 5.37; N, 18.59. Anti-hypertensive activity at 5 mg/kg (20,19,13)+.

PROCESS FOR MAKING THE COMPOUNDS OF THE INVENTION

The compounds of the present invention are prepared in accordance with a novel process of the invention from a suitably blocked derivative of inosine-5′-uronic acid, such as 2′,3′-O-isopropylideneinosine-5′-uronic acid (Compound 43). 2′,3′-O-isopropylideneinosine-5′-uronic acid (Compound 43) is readily obtained from inosine by treatment with acetone to block the 2′- and 3′- hydroxy groups of the ribofuranose moiety, followed by oxidation with chromic acid, in accordance with the published procedure of R. R. Schmidt and H. J. Fritz, Chemische Berichte., 103, 1867 (1970).

2′,3′-O-isopropylideneinosine-5′-uronic acid (Compound 43) is treated in accordance with the process of the present invention, with a suitable inorganic acid halide, such as thionyl chloride, to convert, in the same reaction step, the uronic acid moiety into a uronic acid halide and to introduce a halogen substitutent into the 6 position of the purine moiety. In this regard it is noted that the blocking groups of the 2′ and 3′ hydroxyl groups must be capable of withstanding the conditions of this reaction, which is advantageously conducted in neutral solvents, such as chloroform, in the presence of dimethylformamide or other dialkylamides. The isopropylidene blocking group serves well for this purpose. Nevertheless, other ketal, acetal or even acyl blocking groups are also suitable. Instead of thionyl chloride other inorganic acid halides, such as thionyl bromide, may also be used. The product of the just described first step of the novel reaction sequence is 6-chloro-9-[2,3-O-isopropylidene-&bgr;-D-ribofuranosyl 5-uronic acid chloride]-9H-purine (Compound 44).

The reaction sequence leading to the compounds of the present invention, using the example of 6-chloro-9-[2,3-O-isopropylidene-&bgr;-D-ribofuranosyl 5-uronic acid chloride)-9H-purine (Compound 44) as the important intermediate, is shown in Reaction Scheme 1.

6-chloro-9-[2,3-O-isopropylidene-&bgr;-D-ribofuranosyl-5-uronic acid chloride]-9H-purine (Compound 44) is preferably not isolated in a pure state. Rather, it is reacted with an amine of the General Formula 4 to displace the halide of the uronic acid moiety and to provide compounds of the General Formula 5, wherein the halogen in the 6 position of the purine nucleus is retained. This selective displacement of the “acid chloride” group is readily conducted in neutral solvents, such as chloroform, preferably at low temperature.

The intermediates of General Formula 5, may be isolated in a purified state. They are subsequently reacted with a nucleophilic amine of General Formula 6 in a suitable solvent such as ethyl alcohol, to displace the halogen substituent in the 6 position of the purine nucleus. The displacement reaction is preferably conducted in the presence of an acid acceptor, such as triethyl amine. The blocking groups of the 2′ and 3′ hydroxyls of the ribofuranose moiety are thereafter removed to provide the compounds of the invention (General Formula 3). Removal of the isopropylidene blocking groups is affected, for example, by heating with aqueous hydrochloric acid. These steps are illustrated in the continuation of Reaction Scheme 1. In the formulae shown in Reaction Scheme 1, the definition of the substituent R groups is the same as was given above in connection with the respective general formulae.

Specific examples of the steps of the novel process of the present invention for the preparation of ethyl N6-(3-pentyl)adenosine-5′-uronamide (Compound 17) and of N,N-dimethyl N6-(3-pentyl)adenosine-5′-uronamide (Compound 39) are given below.

Actually, the invention of the herein disclosed novel process is broader than the preparation of the herein disclosed compounds having beneficial cardiovascular or anti-hypertensive properties. In a broad sense, a multitude of N-6 and 5′-N substituted adenosine 5′-uronamides can be synthesized in accordance with the process of the present invention. The compounds which are obtainable by the process of the present invention include, in addition to the compounds described above, those compounds wherein the carboxamido nitrogen is mono or di substituted with alkyl, alkenyl, cycloalkyl, aralkyl, and heterocyclyl groups. The carboxamido nitrogen (5′-N) can also be a member of a saturated heterocyclic ring such as a piperidine or morpholine ring.

An alternative process for the preparation of at least some of the compounds of the present invention comprises the steps of oxidizing N-6 substituted adenosine derivatives which are suitably protected (for example by isopropylidene or benzyl groups) on the 2′ and 3′ hydroxyl groups. The step of oxidation is conducted in analogy to the procedure published by R. R. Schmidt and H. J. Fritz in Chemische Berichte, 103, 1867 (1970). The N-6 substituted adenosine derivatives can be obtained by reaction of 6-chloro-&bgr;-D-ribofuranosyl-9H-purine with the suitable amine.

The resulting uronic acid is then converted to the corresponding acid halide by treatment, for example, with thionyl chloride, in analogy to the process which was described above. The resulting uronic acid halide is thereafter reacted with a primary amine bearing the desired R4 and R5 substituents. After removal of the protecting groups from the ribofuranosyl moiety, the compounds of the present invention are obtained.

6-Chloro-9-[2,3-O-isopropylidene-5-ethylcarboxamido-&bgr;-D-ribofuranosyl]-9H-purine (Compound 45).

A mixture of 2′,3′-O-isopropylideneinosine-5′-uronic acid (6.5 g, 20 mmols), thionyl chloride (4 ml, 53.3 mmols), dry dimethylformamide (1.5 ml, 40 mmols) and dry chloroform (250 ml) was refluxed for 4 to 5 hours. The chloroform was removed in vacuo to give a syrup. The syrup was dissolved in dry chloroform (80 ml), and the resulting solution was added to a mixture of ethylamine (14 mi) and dry chloroform (150 ml) at 10° C. The mixture was stirred for one hour at 10° C., and then poured into cold water (300 ml). The resulting organic layer was separated and washed in succession with aqueous hydrochloric acid (10%, 2×200 ml), aqueous sodium bicarbonate solution (saturated, 1×200 ml) and water (1×100 ml), and dried over magnesium sulfate. The chloroform solvent was removed in vacuo to give 6.3 g (85% yield) of a slightly yellow solid. The product is usable in the subsequent reaction steps without further purification.

Ethyl N6-(3-pentyl)adenosine-5′-uronamide, (Compound 17)

A mixture of 6-Chloro-9-[2,3-O-isopropylidene-5-ethylcarboxamido-&bgr;-D-ribofuranosyl]-9H-purine (Compound 45) (6.3 g, 17.1 mmols), 3-pentylamine (1.6 g, 18.4 mmols), triethylamine (4.7 ml, 34 mmols) and absolute ethanol (200 ml) was refluxed for about 48 hours, or until thin layer chromatography indicated complete reaction. The ethanol was removed in vacuo and the product purified by chromatography on a silica gel column eluted with chloroform/acetone 16:1. Evaporation of fractions containing product yielded a syrup which was heated for 1.5 hours with aqueous hydrochloric acid (1.0 N, 100 ml) at 70° C. Upon cooling it yielded Compound 17 as white crystals. Recrystallization from ethanol yielded white needles, (4.5 g, 70% yield). The physical characteristics and analytical data of Compound 17 were described above.

Dimethyl N6-(3-pentyl)adenosine-5′-uronamide (Compound 39) from 2′,3′-O-isopropylideneinosine-5′-uronic acid (Compound 43)

A mixture of 2′,3′-O-isopropylideneinosine-5′-uronic acid (5.0 g; 15.5 mmols) thionyl chloride (2.5 ml; 33.3 mmols) dry dimethylformamide (1.25 ml; 18.1 mmols) and dry chloroform (170 ml) was refluxed for 5 hours. The solvents were removed in vacuo to give a syrup. The syrup was dissolved in dry chloroform (50 ml) and the resulting solution was added to a mixture of dimethylamine (20 ml, 302 mmols) and dry chloroform (150 ml) at 10° C. The mixture was stirred for 15 minutes after the addition was complete, and thereafter poured into cold water (300 ml). The organic phase was separated and washed successively with water (1×100 ml), 10% aqueous hydrochloric acid solution (2×100 ml), saturated aqueous sodium bicarbonate solution, and was thereafter dried with anhydrous magnesium sulfate. The chloroform solvent was removed in vacuo to give a syrup. The syrup was refluxed for 48 hours (or until thin layer chromatography indicated complete reaction) with 3-pentylamine (2.3 ml; 20 mmols), triethylamine (2.8 ml, 20 mmols) and anhydrous ethanol (100 ml). The solvent and volatile reagents were removed in vacuo to give a syrup (blocked nucleoside). The blocked (isopropylidine) nucleoside was purified by C-18 high performance low pressure liquid chromatography (HPLPLC), methanol-water (70%) being used as the eluent. The solvent was removed in vacuo from the appropriate fractions, to yield a light yellow solid which was thereafter heated at 70° C. for 1.5 hours in 2N aqueous hydrochloric acid (100 ml). Cooling and neutralization with solid sodium bicarbonate yielded Compound 39 as a white syrup, which was crystallized from methanol/water to give 4.0 g (68%) of colorless needles. The physical characteristics and analytical data of Compound 39 were described above.

BIOLOGICAL ACTIVITY AND PHARMACOLOGICAL PROPERTIES

The cardiovascular and anti-hypertensive activities of the compounds of the present invention were determined in bioassays conducted on dogs and spontaneously hypertensive rats.

More particularly, in one type of assay in which the activity of the compounds of the present invention was determined, the compounds to be tested are infused intracoronarily into either open-chest anesthetized or conscious dogs. Adenosine has a demonstrable coronary dilator effect under these conditions. The concentration of the test compound in coronary plasma which causes half-maximal vasodilation is designated ED-50.

More specifically, ED-50 is determined in the following manner. Late diastolic coronary conductance (LDCC) of the experimental dog is monitored through suitable instrumentation. Late diastolic coronary conductance is measured at maximum coronary vasodilation (peak reactive hyperemid), and is designated LDCCmax. Late diastolic coronary conductance is also measured at basal coronary vasodilation, and is designated LDCC0.

The difference between instantaneously measured late diastolic coronary conductance (LDCC) and basal late diastolic coronary conductance (LDCC0) is expressed as a fraction of the difference between maximum late diastolic coronary conductance (LDCCmax) and basal late diastolic coronary conductance (LDCC0). Thus, LDCC is defined by Equation I. LDCC = LDCC - LDCC 0 LDCC max - LDCC 0 EQUATION ⁢   ⁢ I

As the concentration of the test compound is varied, and the corresponding LDCC is obtained through measurements and the above-summarized calculations, data of an “LDCC versus concentration” function or plot are obtained.

ED-50 is derived from these data by log-logit transformation of the “LDCC versus concentration” plot; namely by solving the linear regression of logit (LDCC) on log (concentration) for LDCC=0.5.

When ED-50 of a tested compound is compared to ED-50 of adenosine in the same dog, as is set forth in EQUATION II, then the resulting molar potency ratio (mpr) provides good comparison of the cardiovascular activity of the tested compound with cardivascular activity of other compounds in the same or other experimental dogs. Thus, molar potency ratio (mpr) is a useful measure of the cardiovascular vasodilatory effect, and hence of the utility of the tested compounds. The greater the vasodilatory effect of a tested compound, the larger the corresponding molar potency ratio (mpr). MPR = ED - 50 ⁢ ( adenosine ) ED 50 ⁡ ( tested ⁢   ⁢ compound ) EQUATION ⁢   ⁢ II

For a more detailed description of the bioassay used for determining molar potency ratios, reference is made to an article written by Olsson et al., and titled “Coronary Vasoactivity of Adenosine in the Conscious Dog”, Circulation Research, 45, 468 (1979).

Molar potency ratios of the specific examples of the compounds of the present invention are listed above next to the detailed description of the specific compounds. These data demonstrate that the compounds are cardiovascularly active.

In another assay for the anti-hypertensive activity of the compounds of the invention, blood pressure of unanesthetized, unheated spontaneously hypertensive rats (SHR) is measured indirectly (through a tail cuff) usually at 2, 4, and 6 hours after oral administration of a single dose of the compounds of the invention. Reduction in mean blood pressure by more than ten per cent (10%) indicates anti-hypertensive activity. The test itself, is well established in the art and need not described here in further detail.

The data obtained in the hypertensive rat (SHR) assay are indicated next to the description of the compounds. In the data, the percentage reduction of blood pressure in 2, 4 and 6 hours after the single oral dose is indicated in parentheses. A * sign after the data shows that the measured reduction of blood pressure occurred 1, 2, and 3 hours after the oral dose; a + sign indicates that the measured reduction occurred in 1, 2 and 2.5 hours after the oral dose. The data demonstrate the anti-hypertensive activity of the compounds of the invention.

An assay for the affinity of some of the compounds of the present invention for Ra receptors employs a modification of the radioligand displacement method described by Fox and Kurpis in The Journal of Biological Chemistry, Volume 258 pages 6952-55 (1983). Briefly, this method comprises the steps of incubating [3H]NECA and the analogs to be tested, with human placenta membrane particles, a source of Ra receptors. The particles are then filtered, washed with a buffer to remove unbound ligand and then the amount of bound radioligand is measured. By varying the concentration of the competing analog one may estimate an index of binding affinity, IC-50, the concentration of which causes half-maximum displacement of [3H]NECA. Using [3H]NECA in this assay instead of [3H]-2-chloroadenosine is a modification of the original method.

The compounds of the present invention were found to compete weakly, or not at all, with [3H]ethyladenosine-5′-uronamide at Ra receptor sites of human placenta.

The foregoing indicates that the compounds of the present invention are selective to Ra receptors of the cardiovascular system. Such selectivity would not be expected on the basis of prevailing prior art theory.

Further advantages of the compounds of the present invention include their inability to undergo phosphorylation in the 5′-position, and their stability to acid. Therefore, the therapeutic effect of the compounds of the present invention is unlikely to be eliminated by the action of phosphorylating enzymes, and the compounds are unlikely to be incorporated into DNA or RNA. As is known, incorporation into RNA or DNA is likely to cause teratogenic, mutagenic or carcinogenic effects.

Moreover, because the compounds of the present invention are stable to acid (they survive heating with 1N aqueous HCl for 1.5 hour at 70° C.) they are capable of surviving the acidic conditions prevailing in the stomach. Therefore, they are suitable as drugs for oral administration to humans and animals.

Various modifications of the herein disclosed invention, in terms of structural modifications of the invented compounds and also in terms of making or using the same, may become readily apparent to those skilled in the art in light of the above disclosure. For example the compounds of the present invention may be administered as pharmaceutically acceptable salts.

Inasmuch as the compounds of the present invention are useful as cardiac vasodilators, cardivascular, and particularly as anti-hypertensive agents in mammals, domestic animals and humans, various modes of administering the compounds will be apparent to a person having average skill in the art. Such modes of administering the compounds include oral and topical administration, and intravenous infusion. One having average skill in the art may readily prepare suitable formulations for the above-mentioned and other modes of administering the compounds of the invention.

In light of the foregoing, the scope of the present invention should be interpreted solely from the following claims, as such claims are read in light of the disclosure.

Claims

1. Compounds A compound of the formula: wherein: R 1 represents secondary alkyl having from 3 to 10 carbons, phenylalkyl, having from 1 to 7 carbons in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 2. Compounds The compound of claim 1 wherein R 4 is methyl or ethyl. 3. Compounds The compound of claim 1 wherein R 1 is endo-2-norbornyl, R 4 is 2-hydroxyethyl and R 5 is hydrogen. 4. Compounds The compound of claim 1 wherein R 4 is ethyl and R 5 is hydrogen. 5. Compounds The compound of claim 4 wherein R 1 is cyclohexyl. 6. Compounds The compound of claim 4 wherein R 1 is (S)-1-phenyl-2-butyl. 7. Compounds The compound of claim 4 wherein R 1 is 4-methoxyphenyl. 8. Compounds The compound of claim 4 wherein R 1 is 2-(3,4,5-trimethoxyphenyl)-ethyl. 9. Compounds The compound of claim 4 wherein R 1 is 3-phenylpropyl. 10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

2. Compounds The compound of claim 1 wherein R 4 is methyl or ethyl. 3. Compounds The compound of claim 1 wherein R 1 is endo-2-norbornyl, R 4 is 2-hydroxyethyl and R 5 is hydrogen. 4. Compounds The compound of claim 1 wherein R 4 is ethyl and R 5 is hydrogen. 5. Compounds The compound of claim 4 wherein R 1 is cyclohexyl. 6. Compounds The compound of claim 4 wherein R 1 is (S)-1-phenyl-2-butyl. 7. Compounds The compound of claim 4 wherein R 1 is 4-methoxyphenyl. 8. Compounds The compound of claim 4 wherein R 1 is 2-(3,4,5-trimethoxyphenyl)-ethyl. 9. Compounds The compound of claim 4 wherein R 1 is 3-phenylpropyl. 10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

3. Compounds The compound of claim 1 wherein R 1 is endo-2-norbornyl, R 4 is 2-hydroxyethyl and R 5 is hydrogen. 4. Compounds The compound of claim 1 wherein R 4 is ethyl and R 5 is hydrogen. 5. Compounds The compound of claim 4 wherein R 1 is cyclohexyl. 6. Compounds The compound of claim 4 wherein R 1 is (S)-1-phenyl-2-butyl. 7. Compounds The compound of claim 4 wherein R 1 is 4-methoxyphenyl. 8. Compounds The compound of claim 4 wherein R 1 is 2-(3,4,5-trimethoxyphenyl)-ethyl. 9. Compounds The compound of claim 4 wherein R 1 is 3-phenylpropyl. 10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

4. Compounds The compound of claim 1 wherein R 4 is ethyl and R 5 is hydrogen. 5. Compounds The compound of claim 4 wherein R 1 is cyclohexyl. 6. Compounds The compound of claim 4 wherein R 1 is (S)-1-phenyl-2-butyl. 7. Compounds The compound of claim 4 wherein R 1 is 4-methoxyphenyl. 8. Compounds The compound of claim 4 wherein R 1 is 2-(3,4,5-trimethoxyphenyl)-ethyl. 9. Compounds The compound of claim 4 wherein R 1 is 3-phenylpropyl. 10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

5. Compounds The compound of claim 4 wherein R 1 is cyclohexyl. 6. Compounds The compound of claim 4 wherein R 1 is (S)-1-phenyl-2-butyl. 7. Compounds The compound of claim 4 wherein R 1 is 4-methoxyphenyl. 8. Compounds The compound of claim 4 wherein R 1 is 2-(3,4,5-trimethoxyphenyl)-ethyl. 9. Compounds The compound of claim 4 wherein R 1 is 3-phenylpropyl. 10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

6. Compounds The compound of claim 4 wherein R 1 is (S)-1-phenyl-2-butyl. 7. Compounds The compound of claim 4 wherein R 1 is 4-methoxyphenyl. 8. Compounds The compound of claim 4 wherein R 1 is 2-(3,4,5-trimethoxyphenyl)-ethyl. 9. Compounds The compound of claim 4 wherein R 1 is 3-phenylpropyl. 10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

7. Compounds The compound of claim 4 wherein R 1 is 4-methoxyphenyl. 8. Compounds The compound of claim 4 wherein R 1 is 2-(3,4,5-trimethoxyphenyl)-ethyl. 9. Compounds The compound of claim 4 wherein R 1 is 3-phenylpropyl. 10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

8. Compounds The compound of claim 4 wherein R 1 is 2-(3,4,5-trimethoxyphenyl)-ethyl. 9. Compounds The compound of claim 4 wherein R 1 is 3-phenylpropyl. 10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

9. Compounds The compound of claim 4 wherein R 1 is 3-phenylpropyl. 10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

10. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-ethyl. 11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

11. Compounds The compound of claim 4 wherein R 1 is 2-(2-pyridyl)ethyl. 12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

12. Compounds The compound of claim 4 wherein R 1 is (2-chloro-phenyl)-methyl. 13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

13. Compounds The compound of claim 4 wherein R 1 is (2-thienyl)methyl. 14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

14. Compounds The compound of claim 4 wherein R 1 is (R)-1-phenyl-2-propyl. 15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

15. The compounds compound of claim 1 wherein R 4 is Z—Q—(CH 2 ) n wherein n is an integer having the values of 1 to 4; Q is selected from the group consisting of phenyl, and thienyl, or pyridyl, and Z is one or more H, hydroxy, halogen, alkoxy having from 1 to 4 carbon atoms, or alkyl having from 1 to 7 carbon atoms. 16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

16. Compounds The compound of claim 1 wherein R 1 is cycloalkyl or bicycloalkyl. 17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

17. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is H. 18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

18. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is H. 19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

19. Compounds The compound of claim 16 wherein R 4 is isopropyl, and R 5 is H. 20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

20. Compounds The compound of claim 16 wherein R 4 is 3-pentyl, and R 5 is H. 21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

21. Compounds The compound of claim 16 wherein R 4 is allyl, and R 5 is H. 22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

22. Compounds The compound of claim 16 wherein R 4 is (2-methyl) propyl, and R 5 is H. 23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

23. Compounds The compound of claim 16 wherein R 4 is cyclopropyl, and R 5 is H. 24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

24. Compounds The compound of claim 16 wherein R 4 is phenylmethyl, and R 5 is H. 25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

25. Compounds The compound of claim 16 wherein R 4 is 2-methoxyphenylmethyl, and R 5 is H. 26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

26. Compounds The compound of claim 16 wherein R 4 is 2-thienylmethyl, and R 5 is H. 27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

27. Compounds The compound of claim 16 wherein R 4 is 2-phenylmethyl, and R 5 is H. 28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

28. Compounds The compound of claim 16 wherein R 4 is methyl, and R 5 is methyl. 29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

29. Compounds The compound of claim 16 wherein R 4 is n-butyl, and R 5 is methyl. 30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

30. Compounds The compound of claim 16 wherein R 4 is ethyl, and R 5 is ethyl. 31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

31. Compounds The compound of claim 1 wherein R 1 is and R 4 and R 5 are methyl. 32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers. 33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

32. A pharmaceutical composition comprising a compound of claim 1 in admixture with one or more pharmaceutically acceptable carriers.

33. A method of administering to humans or animals of the mammalian species a vasodilator or anti-hypertensive compound in a therapeutically effective does to achieve a vasodilatory or anti-hypertensive effect, the compound having the formula wherein: R 1 represents secondary alkyl having from 3 to 10 carbons; phenylalkyl, having from one to seven carbon atoms in the alkyl chain; mono- to penta-alkoxy phenylalkyl wherein said alkoxy contains from 1 to 3 carbons and said alkyl contains from 1 to 7 carbons; monohalophenylalkyl wherein said alkyl contains from 1 to 4 carbons; cycloalkyl wherein the ring contains from 3 to 8 carbons; bicycloalkyl wherein the rings together contain from 7 to 10 carbons; thienylalkyl wherein said alkyl contains from one to four carbons; pyridylalkyl wherein said alkyl contains from one to four carbons; R 2 and R 3 are hydrogen; R 4 is alkyl having 1 to 7 carbon atoms; or hydroxyalkyl which contains from 1 to 4 carbons; or secondary alkyl which contains from 3-8 carbons; or allylic alkenyl which contains from 3 to 7 carbons; or cycloalkyl wherein the ring contains from 3 to 7 carbons; or phenylalkyl wherein said alkyl contains from 1 to 4 carbons; or monoalkoxy phenylalkyl wherein said alkoxy and said alkyl each contain from 1 to 4 carbons; or thienylalkyl wherein said alkyl contains from 1 to 4 carbons; and R 5 is hydrogen, or straight chain lower alkyl having 1 to 4 carbons. 34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen. 35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.

34. The method of claim 33 wherein in the formula of the administered compound R 4 is ethyl and R 5 is hydrogen.

35. The method of claim 33 wherein in the formula of the administered compound R 1 is 3-pentyl.