Abstract: 10-(2-substituted-aminoethyl)-10,11-dihydro-5-methylene-2 or 3 7 or 8-substituted or unsubstituted-5H-dibenzo[a,d]cycloheptenes e.g., 10-(2-dimethylaminoethyl)-10,11-dihydro-5-methylene-5H-dibenzo[a,d]cyclohe ptene, prepared by various methods including acid dehydration of the corresponding dibenzo[a,d]cycloheptene-5-ols. The compounds are useful as anti-depressants.
Abstract: 2-Sec.-alkylaminobenzophenones are prepared by reacting a corresponding 2-aminobenzophenone with a ketone, a borohydride and carboxylic acid.
Type:
Grant
Filed:
January 29, 1976
Date of Patent:
April 11, 1978
Assignee:
Sandoz, Inc.
Inventors:
William J. Houlihan, Paul G. Mattner, Joseph A. Smith
Abstract: The compounds are 1-aryl-1-lower alkyl-substituted-1-buten-3-ols, butan-3-ols, and acylation products thereof, e.g., (p-biphenylyl)-2-penten-4-ol and are useful as pharmaceuticals.
Abstract: The compounds are 4-aryl substituted buta-2,3-dienoic acids and esters thereof which may also be lower alkyl-substituted at any of the 2- and 4- positions, e.g., 4-(p-methoxyphenyl)-2-methyl-buta-2,3-dienoic acid. The compounds are useful as pharmaceuticals, e.g., as antiinflammatory agents and hypolipidemic agents.
Type:
Grant
Filed:
November 17, 1976
Date of Patent:
February 14, 1978
Assignee:
Sandoz, Inc.
Inventors:
Eugene E. Galantay, Faizulla G. Kathawala
Abstract: Substituted aminophenyl ketones such as 2-alkylaminobenzophenones are prepared by reacting a corresponding 2-aminophenyl ketone with a ketone or aldehyde, a borohydride and strong acid.
Abstract: Anti-inflammatories and analgesics of the formula: ##STR1## wherein R.degree. is alkyl, R is hydrogen, alkyl, halo, nitro or R"' OOC--, R' is hydrogen, alkyl or halo, R" is a hydrolyzable carboxylic acid acyl group and R"' is hydrogen or alkyl.
Abstract: Anti-allergic 2-amino-quinolin-4-one-3-phosphonic acid esters are prepared by reacting an isatoic anhydride with the carbanion resulting from the treatment of an organo-methane phosphate with a proton abstracting agent.
Abstract: Compounds of the formula ##STR1## wherein R and R.sup.o are lower alkyl, R' is optionally substituted phenyl or 2-thienyl and n is 0 to 2, and their salt forms, are prepared by reacting a compound of the formula: ##STR2## with an aromatic nitrile and strong base, and quenching with water when the free base form is desired, said first mentioned compounds being intermediates for quinazolinones.
Abstract: Hypolipidemic agents of the formula: ##STR1## wherein X is C.dbd.O or CHOH,R.degree. is branched lower alkyl,R is hydrogen, alkyl, or halo,n is 1 or 2, andR' and R" are hydrogen, halo, alkyl or alkoxy, e.g., 4-phenoxy-pivalophenone.
Abstract: Hydroxymethyl-substituted-2(1H)-quinazolinones, e.g., 7-hydroxymethyl-1-isopropyl-4-phenyl-2(1H)-quinazolinone, are useful as anti-inflammatory agents.
Abstract: This disclosure describes novel compounds of the formula: ##STR1## where R is ##STR2## and R.sub.1 is straight chain lower alkyl, or ##STR3## where R.sub.3 is hydrogen or halo having an atomic weight of about 19 to 36,Which are useful as minor tranquilizers, sleep inducers and muscle relaxants.
Abstract: Substituted-iminodimethylene-di-tert-alkylophenones, e.g., 4",4"'-methyliminodimethylene-dipivalophenone, are prepared by treating a corresponding .alpha.-halo-p-tert-alkanoyl toluene with a substituted amine. The phenols are prepared from the corresponding phenones and both the phenones and the phenols are useful as hypolipidemic agents.
Abstract: This invention provides a single needle dialysis blood tubing occluder, comprising in a preferred aspect, a pair of pivotly mounted clamping arms having a leaf spring affixed to the non-pivot end of each occluder with the spring in slidable engagement with a symmetrical cam. Means are provided for actuating the cam, whereby the cam moves the tubing occluder to alternately occlude and non-occlude a pair of blood tubings.
Abstract: Derivatives of trifluoromethyl-substituted anthranilic acid amides, e.g., N-methyl-o-amino-.alpha.,.alpha.,.alpha.-trifluoromethyl-p-toluamide, are useful as minor tranquilizers and muscle relaxants.
Abstract: Pyranone carboxamides, e.g., 2,6-diphenyl-N-methyl-4-oxo-4H-pyran-3-carboxamide, are prepared by cyclizing and dehydrogenating 2-aminomethylene-5-hydroxy-N-methyl-3-oxo-alkylamides and are useful as anti-allergic agents.
Abstract: Hydroxyalkyl and aryl or heterocyclic substituted-4,5-dihydropyridazin(2H)-3-ones and diazobicyclo-ene-ones, e.g., 6-(p-chlorophenyl)-2-(2-hydroxybutyl)-4,5-dihydropyridazin(2H)-3-one are prepared by condensing 1-hydrazino-2-alkanols with aryl or heterocyclic-.gamma.-keto acids and are useful as central nervous system depressants.
Abstract: Compounds of the formula ##STR1## wherein R is secondary alkyl of 3 to 7 carbon atoms or tertiary alkyl of 4 to 7 carbon atoms,R' is secondary alkyl of 3 to 7 carbon atoms or tertiary alkyl of 4 to 7 carbon atoms,R.sub.1 is primary or secondary alkyl of 1 to 5 carbon atoms, andR.sub.2 is hydrogen, chloro or bromo,And the pharmaceutically acceptable acid addition salts thereof, are useful as anti-obesity and anti-diabetic agents. The compounds wherein R and R' are tertiary alkyl of 4 to 7 carbon atoms and R.sub.2 is hydrogen are synthesized from ketenimines and amidines, all of the compounds wherein R.sub.2 is hydrogen are synthesized by reduction of the corresponding 3-cyanopyridines, and the compounds wherein R.sub.2 is chloro or bromo are synthesized from the corresponding compounds wherein R.sub.2 is hydrogen and an N-halosuccinimide.
Type:
Grant
Filed:
February 5, 1976
Date of Patent:
October 25, 1977
Assignee:
Sandoz, Inc.
Inventors:
William R. Simpson, Robert J. Strohschein
Abstract: 5,5,7,7-tetramethyl-3-substituted or unsubstituted-phenylfuro[3,4-e]-as-triazines and corresponding 4-oxides, e.g., 5,7-dihydro-5,5,7,7-tetramethyl-3-phenylfuro[3,4-e]-as-triazine and 5,7-dihydro-5,5,7,7-tetramethyl-3-phenylfuro[3,4-e]-as-triazine-4-oxide, are prepared from 2,2,5,5-tetramethyl-3,4(2H,5H)-furandione-3-hydrazone-4-oximes and are useful as sleep inducers and minor tranquilizers.