Chemical compounds

Abstract

This invention relates to certain unsaturated fatty acid derivatives of therapeutically active 1,3-dioxolane nucleoside analogues and to pharmaceutical formulations containing them. The said derivatives are referred to as “Compounds of formula I” herein. Compounds of formula I can be used in the treatment of a cancerous disease. Treatment of both solid tumours and haematological cancers such as leukaemias, lymphomas and multiple myelomas are included.

Description

FIELD OF INVENTION

This invention relates to certain unsaturated fatty acid derivatives of therapeutically active 1,3-dioxolane nucleoside analogues and to pharmaceutical formulations containing them. The said derivatives are referred to as “Compounds of formula I” herein. Compounds of formula I can be used in the treatment of a cancerous disease. Treatment of both solid tumours and haematological cancers such as leukaemias, lymphomas and multiple myelomas are included.

TECHNICAL BACKGROUND

Nucleoside analogues, the derivatives of the natural nucleosides found as building blocks of DNA and RNA, are effective in the clinical treatment of human cancer or viral diseases, although in the early years such compounds were evaluated as antituberculosis agents. Such compounds have been registered in the market for more than 40 years, and approximately 35 products are currently in daily use. The natural nucleosides illustrated in the figure below, are constructed from two classes of nitrogen bases, the purines exemplified by adenine and guanine and the pyrimidines exemplified by thymine, uracil and cytosine, and from the monosaccharide ribose or deoxyribose.

The natural nucleosides all exist in the so called β-D configuration as illustrated in the formula A, below. The nitrogen base and the hydroxy-methyl side chain on the sugar ring are both on the same side (cis) of the plane of the sugar ring.

If the two groups are on either side (trans), it is referred to as the α isomer. In order to obtain nucleoside derivatives with anticancer or antiviral activity, chemical modifications in either the nitrogen base and/or the monosaccharide have been performed. For instance the addition of halogen atoms, the substitution of OH groups with other functional groups or a stereochemical change from ribose to arabinose may lead to products with a potential therapeutic benefit. In many products, the monosaccharide ring is conserved, while in others, the sugar ring has been changed into a chain. The nucleoside analogues are small molecules with fair to excellent aqueous solubility.

The extensive research and development effort put into the area of nucleoside analogues due to the worldwide AIDS epidemic bolstered the basic knowledge and understanding of mechanism of action, alterations in activity profile due to chemical modifications etc, also relevant to the field of cancer treatment.

A general weakness with many drugs, including nucleoside analogues, is low activity and inferior specificity for treatment of the actual disease in question. Some of these problems may be related to the inherent activity of the drug substance itself, some may be related to certain resistance mechanisms (either inherent in the patient or acquired during treatment e.g. MDR in cancer treatment). Some problems may be related to certain inferior transport or cellular uptake and activation mechanisms. Some problems may be related to rapid inactivation and/or excretion of the drug.

The efficacy of nucleoside analogues depends on a large extent on their ability to mimic natural nucleosides, thus interacting with viral and/or cellular enzymes and interfering with or inhibiting critical processes in the metabolism of nucleic acids. In order to exert their antiviral or anti cancer activity, the nucleoside analogues have to be transformed, via their mono- and di-phosphates, into their corresponding tri-phosphates through the action of viral and/or cellular kinases. As a general rule, the tri-phosphate is the active agent, but for some products, e.g. gemcitabine, even the di-phosphate may exert a clinically significant effect.

In order to reach the diseased, cancerous or virus infected cells or tissues, following either enteral or parenteral administration, the nucleoside analogues should have favourable pharmacokinetic characteristics. In addition to rapid excretion of the administered drug, many nucleoside analogues may be deactivated both in the blood stream and in tissues. For instance may cytosine derivatives, even at the mono-phosphate level, be rapidly deaminated through the action of a class of enzymes called deaminases, to the inactive uracil analogue. The cellular uptake and thus good therapeutic efficacy of many nucleoside analogues strongly depend on membrane bound nucleoside transport proteins (called concentrative and equilibrative nucleoside transporters). Hence compounds that do not rely on such specific uptake mechanisms are sought for. Yet another activity limiting factor, particularly within the anti cancer field, are the cellular repair mechanisms. When an anti-cancer nucleoside analogue mono-phosphate is incorporated into the cellular DNA, it should not be removed from the cancer cell DNA due to the exonuclease activity linked to the p53 protein. However, removal of a nucleoside analogue from the DNA of a healthy cell is favourable in order to limit the side effects of the drug.

Over the years, many nucleoside analogues have been developed that to a large extent overcome some or many of the activity limiting features. As an example, acyclovir (ACV) can be given to illustrate a compound with great specificity. The ACV-mono-phosphate can only be formed by viral kinases meaning that ACV cannot be activated in uninfected cells. Despite this fact, ACV is not a particularly active product. In order to circumvent the often rate limiting step in the activation of a nucleoside analogue, the intracellular formation of the nucleoside analogue mono-phosphate, several phosphonate such as cidofovir or even mono-phosphate products, have been developed. In order to facilitate oral uptake or to secure a favourable drug disposition in the body, particular prodrugs such as Hepsera have been made.

In addition to the structural changes made to nucleoside analogues to facilitate enhanced clinical utility, further modifications have been made to improve the activity. The Applicant of the present invention (U.S. Pat. No. 6,153,594, U.S. Pat. No. 6,548,486 B1, U.S. Pat. No. 6,316,425 B1, U.S. Pat. No. 6,384,019 B1) and several other groups have modified nucleoside analogues through the addition of lipid moieties (EP-A-56265, EP-A-393920, WO 99/26958). This can be achieved by the linking of fatty acids through for instance an ester, amide, carbonate or carbamate bond. More elaborate products can be made, such as phospholipid derivatives (Eur J Pharm Sci (2000) 11b Suppl 2: p15-27, EP 545966 B1, CA 2468099 A1, U.S. Pat. No. 6,372,725 B1 and U.S. Pat. No. 6,670,341 B1) of the nucleoside analogues. Such analogues are described to have antiviral activity that is particularly suitable for the therapy and prophylaxis of infections caused by DNA, RNA or retroviruses. They are also suited for treatment of malignant tumours. The nucleoside analogue lipid derivatives may serve several purposes. They may be regarded as a prodrug that is not a substrate for deaminases, thereby protecting the nucleoside analogues from deactivation during transport in the bloodstream. The lipid derivatives may also be more efficiently transported across the cellular membrane resulting in enhanced intracellular concentration of the nucleoside analogue. Lipid derivatives may also be more suited for use in dermal preparations, oral products (U.S. Pat. No. 6,576,636 B2 and WO 01/18013 or particular formulations such as liposomes (U.S. Pat. No. 5,223,263) designed for tumour targeting.

Previously, some of the inventors of the present invention have demonstrated that for nucleoside analogues with a conserved β-D configuration of the monosaccharide ring, or for nucleoside analogues with a non-cyclic side chain, the antiviral or anticancer activity can be most efficiently improved through the formation of lipid derivatives of mono-unsaturated ω-9 C18 and C20 fatty acids (Antimicrobial Agents and Chemotherapy, January 1999, p. 53-61, Cancer Research 59, 2944-2949, Jun. 15, 1999, Gene Therapy (1998) 5, 419-426, Antiviral Research 45 (2000) 157-167, Biochemical Pharmacology 67 (2004) 503-511). Not only being more active than the poly-unsaturated counterparts, the preferred mono-unsaturated derivatives are more crystalline and chemically stabile towards oxidation of the lipid chain, hence being more favourable compounds from a chemical and pharmaceutical manufacturing point of view. The Applicant of the present invention has also demonstrated that the mono-unsaturated ω-9 C18 and C20 fatty acids are suited for improvement of the therapeutic activity of a large number of non-nucleoside biologically active compounds (EP 0977725 B1).

A relatively new subgroup of nucleoside analogues are the so called 1,3-dioxolane derivatives. In this class of compounds, the five-membered ring, analogues to the monosaccharide found in natural nucleosides, is conserved, but the CH₂ group in position 3 is exchanged with an O atom as shown in formula B below.

Several products within the 1,3-dioxolane class have shown promising antiviral and anti cancer activity in-vitro and in-vivo. For selected compounds, both enhanced, non-nucleoside transporter dependent, cellular uptake and reduced deamination (=inactivation) rate has been shown.

Several types of lipophilic derivatives, including both poly-unsaturated and mono-unsaturated ω-9 C18 and C20 fatty acid ester and amides, of such 1,3,-dioxolane products are known (U.S. Pat. No. 5,817,667, U.S. 2001/0020026 A1 and U.S. 2003/0013660 A1). These references provide both a general teaching about the possible advantages obtained by making such lipid derivatives and the specific benefit of the same regarding activity in disease and mechanistic models. In particular, the in-vitro anti cancer activity of the N⁴-amide derivatives of (−)-β-L-dioxolane-cytidine (troxacitabine) made with the following fatty acids, oleic acid (cis-9-octadecenoic acid), elaidic acid (trans-9-octadecenoic acid) and linoleic acid (cis-9,12-octadecadienoic acid), have been compared in several cell lines. The three products have quite comparable activity, the oleic acid amid derivative being marginally better (2 to 5 times) than the elaidic counterpart.

DESCRIPTION OF THE INVENTION

There has now surprisingly been found that the activity of 1,3-dioxolane nucleoside derivatives can be significantly enhanced as compared to the prior art compounds through the formation of derivatives of certain unsaturated long chain fatty acids with at least one double bond in position 6 counted from the carbonyl carbon atom, commonly recognised as Δ⁶ unsaturated fatty acid. Both ester and amide derivatives of mono- and poly-Δ⁶-unsaturated fatty acid derivatives of 1,3-dioxolane nucleoside analogues have been examined, and are herein demonstrated with, and compared to the prior art compounds of the particular product troxacitabine. In detail, the ester and amide derivatives of petroselinic acid (cis-6-octadecenoic acid), petroselaidic acid (trans-6-octadecenoic acid), gamma-linolenic acid (cis-6,9,12-octadecatrienoic acid) and elaidic acid amide have been tested as a prior art comparator compound. The petroselaidic acid derivatives are the most potent. They are equally active, marginally better than the gamma-linolenic acid derivative, and 20 fold more active than the prior art product, troxacitabine-N⁴-elaidic acid amide.

In a separate experiment, the in-vitro activity of the amide derivative of petroselinic acid was compared to the prior art product troxacitabine-N⁴-elaidic acid amide in the breast tumour line MaTu and its adriamycin resistant subline MaTu/Adr. Surprisingly, there has been found that the good activity of the troxacitabine-petroselinic amide in the MaTu line was unchanged in the MaTu/Adr sub line while for the troxacitabine-N⁴-elaidic acid amide, a resistance factor of 6 was observed.

The compounds of this invention can be characterized by the general formula I:
wherein the substituents in position 2 and 5 of the 1,3dioxolane ring has the possibility to be above or below the plane of the five-membered ring. The said substituents can be in either a cis or a trans configuration. R₂ represents a hydrogen atom or a unsaturated fatty acid acyl group R₅C(O), R₅CH₂OC(O) or R₅CH₂NHC(O) where R₅ is a C_7-23 alkenyl residue of the general formula
CH₃—(CH₂)n-(CH═CH—CH₂)m-CH═CH—(CH₂)₄—  (II)
wherein m is a number from 0 to 2 and n is a number from 0 to 10.

R₁ denotes an optionally substituted nitrogen base possibly carrying a functional group such as an alcohol or an amino group, such group optionally being acylated with an unsaturated fatty acid.

More specifically, R₁ is
and R₃ is selected from the group consisting of hydrogen, methyl, trifluoromethyl, fluorine, chlorine, bromine or iodine; and Z and W are each independently Br, Cl, I, F, OR₄ or NHR₄ and at least one of Z and W is either OR₄ or NHR₄, and R₄ is H or R₅C(O), R₅CH₂OC(O) or R₅CH₂NHC(O) where R₅ is a C_7-23 alkenyl of the general formula II. R₂, R₃ and R₄ cannot simultaneously be hydrogen. X and Y can be either CH or a N atom with at least one of X or Y being N.

It is noted that the Δ⁶ unsaturated fatty acids contemplated in this invention can have both cis and trans stereochemistry of the double bonds.

Particularly preferred embodiments of this invention is exemplified with, but not limited to, troxacitabine-2′-hydroxymethyl-trans-6-octadecenoic acid ester, troxacitabine-N⁴-trans 6-octadecenoic acid amide, troxacitabine-2′-hydroxymethyl-gamma-linolenoic acid ester and troxacitabine-N⁴-cis6-octadecenoicacid amide.

EXAMPLE 1

The breast cancer cell line MaTu was seeded, 5×10³ cells per well, in 96-well-plates. The medium was RMPI 1640 with 2 mM Glutamine and 10% Foetal Bovine Serum. 24 hours later the test compounds were added in 6 concentrations. The cells were incubated for 4 days. The MTT solution was added to each well and incubated for 4 hours. The samples were read by an ELISA reader at 540 nm. The IC50 values were determined from growth curves. The test compounds were troxacitabine elaidic amid, troxacitabine petroselaidoate, troxacitabine-petroselaidic amide and troxacitabine γ-linolenoate. Surprisingly the activity of troxacitabine petroselaidoate and petroselaidic amide was 20 fold more active than troxacitabine elaidic amid.

                                 IC50 μM ±
Compound                         Standard Deviation
troxacitabine elaidic-amide      3.58 ± 2.56
troxacitabine petroselaidoate    0.18 ± 0.12
troxacitabine-petroselaidic amide 0.15 ± 0.07
troxacitabine γ-linolenoate      0.83 ± 0.59

EXAMPLE 2

The human breast carcinoma cancer cell line MaTu and the adriamycin resistant cell line MaTu/ADR were seeded, 5×10³ cells per well, in 96-well-plates. The medium was RMPI 1640 with 2 mM Glutamine and 10% Foetal Bovine Serum. 24 hours later the test compounds were added in a final volume of 20 μl to the cells, in six different concentrations. The cells were incubated for 4 days. MTT solution was added to each well and incubated for 4 hours. The samples were read by an ELISA reader at 540 nm. The IC50 values were determined from growth curves. The resistance factor is the IC50 in MaTu/Adr vs. IC50 in MaTu. The test compounds were troxacitabine-elaidic amide and troxacitabine-petroselinic amide. Surprisingly we found the troxacitabine-petroselinic amide to be independent of the adriamycin resistance, with a resistance factor of 1.0, compared to 5.8 for troxacitabine-elaidic amide.

                                 Resistance factor =
Compound                         (IC50 MaTu/Adr)/(IC50 MaTu)
troxacitabine- elaidic amide     5.8
troxacitabine-petroselinic amide 1.0

EXAMPLE 3

Troxacitabine N⁴-elaidic Acid Amide (Comparative Compound)

Troxacitabine (150 mg, 0.70 mmol), TEA (0.1 ml, 0.74 mmol) and DMAP (90 mg, 0.74 mmol) in dry DCM/DMF (5 ml/2 ml) was added elaidoyl chloride in DCM (5 ml). The acid chloride was prepared from elaidic acid (209 mg, 0.74 mmol), oxalyl chloride (0.4 ml, 2.96 mmol) and DMF (catalytic amount) in toluene (10 ml) by stirring at ambient temperature for 2 h and then evaporated to dryness. After stirring for 22 h at room temperature a saturated aqueous solution of NH₄Cl was added and the phases separated. The aqueous phase was extracted with DCM (3×), and the combined organic extracts were washed with saturated brine, dried (Na₂SO₄), filtered and evaporated in vacuuo. The product was purified by flash chromatography on silica gel eluting with MeOH/DCM (25:975) followed by MeOH/DCM (5:95) to give 208 mg (62%) of the desired product as colourless crystals.

¹H-NMR (200 MHz; CDCl₃); δ 8.51 (1H, d), 7.43 (1H, d), 6.21 (1H, m), 5.39 (2H, m), 5.18 (m, 1H), 4.40-4.12 (m, 2H), 4.01 (m, 2H), 2.44 (t, 2H), 2.2-1.9 (m, 6H), 1.8-1.1 (m, 22H), 0.96 (t, 3H). MS (electrospray); 500 [M+Na]⁺. HPLC: 99.4%

EXAMPLE 4

Troxacitabine-2′-hydroxymethyl-petroselaidoate

Troxacitabine (0.5 g, 2.4 mmol) in dry DMF (10 ml) was added a solution of HCl in DMF (1.3 M, 2.2 ml, 2.8 mmol), which had been prepared by bubbling HCl-gas through DMF. After some seconds a colourless solid precipitated from the solution. The resulting mixture was stirred for 30 min. and petroselaidoyl chloride in DMF (5 ml) was then added. The acid chloride had previously been prepared from petroselaidic acid (1.0 g, 3.5 mmol), oxalyl chloride (1.9 ml, 14 mmol) and DMF (catalytic amount) in DCM (30 ml) by stirring at ambient temperature for 1 h and then evaporated to dryness. After stirring for 64 h at room temperature the mixture was poured into water and extracted with DCM (3×). The combined organic extracts were washed with a saturated aqueous solution of NaHCO₃, brine, dried (Na₂SO₄), filtrated and evaporated in vacuuo. The product was purified by flash chromatography on silica gel eluting with MeOH/DCM (5:95) to give 0.52 g (46%) of the desired product as colourless crystals.

¹H-NMR (200 MHz; CDCl₃); δ 7.74 (d, 1H), 6.27 (m, 1H), 5.87 (d, 1H), 5.40 (m, 2H), 5.22 (m, 1H), 4.6-4.2 (m, 4H), 2.42 (t, 2H), 2.00 (m, 4H), 1.65 (m, 2H), 1.5-1.2 (m, 22H), 0.87 (t, 3H). MS (electrospray); 478 [M+H]⁺, 500 [M+Na]⁺. HPLC; 93.7%

EXAMPLE 5

Troxacitabine N⁴-petroselaidic Acid Amide

Petroselaidic acid (662 mg, 2.35 mmol) in DCM (20 ml) was added TEA (0.33 ml, 2.35 mmol) followed by TBTU (753 mg, 2.35 mmol), and stirred for 40 min. at RT before troxacitabine (0.5 g, 2.35 mmol) in DMF (2 ml) was added. After stirring for 22 h at RT a saturated aqueous solution of NH₄Cl was added and the phases separated. The aqueous phase was extracted with DCM (3×), and the combined organic extracts were washed with saturated NaHCO₃, brine, dried (Na₂SO₄), filtered and evaporated in vacuuo. The product was purified by flash chromatography on silica gel eluting with MeOH/DCM (25:975) to give 650 mg (58%) of the desired product as colourless crystals.

¹H-NMR (200 MHz; CDCl₃); δ 8.57 (d, 1H), 7.47 (d, 1H), 6.21 (d, 1H), 5.42 (m, 2H), 5.16 (s, 1H), 4.4-4.2 (m, 2H), 4.01 (m, 2H), 2.49 (t, 2H), 2.02 (m, 4H), 1.71 (m, 2H), 1.5-1.2 (m, 22H), 0.87 (t, 3H). MS (electrospray); 478 [M+H]⁺, 500 [M+Na]⁺. HPLC; 93.8%

EXAMPLE 6

Troxacitabine 2′-hydroxymethyl-6,9,12-linolenoate

Troxacitabine (0.7 g, 3.3 mmol) in dry DMF (17 ml) was added a solution of HCl in DMF (1.3 M, 3.0 ml, 3.9 mmol), which had been prepared by bubbling HCl-gas through DMF. After some seconds a colourless solid precipitated from the solution. The resulting mixture was stirred for 30 min. before acid chloride in DMF (4 ml) was added. The acid chloride had previously been prepared from GLA (2.19 g, 7.9 mmol), oxalyl chloride (2.66 ml, 31.4 mmol) and DMF (catalytic amount) in DCM (50 ml) by stirring at ambient temperature for 3 h and then evaporated to dryness. After stirring for 48 h at room temperature the mixture was poured into aqueous NaHCO₃ and extracted with DCM (3×). The combined organic extracts were washed with brine, dried (Na₂SO₄), filtered and evaporated in vacuuo. The product was purified by flash chromatography on silica gel eluting with MeOH/DCM (3:100) to give 0.85 g (54%) of the desired product as a pale yellow solid.

¹H-NMR (200 MHz, CDCl₃); δ 7.78 (d, 1H), 6.30 (m, 1H), 6.85 (d, 1H), 5.6-5.1 (m, 7H), 4.6-4.1 (m, 5H), 2.9-2.7 (m, 4H), 2.4 (t, 2H), 2.2-2.0 (m, 3H), 1.8-1.2 (m, 10H), 0.95 (t, 3H). MS (electrospray); 496 [M+Na⁺]. HPLC; 93.9%

EXAMPLE 7

Troxacitabine N⁴-petroselinic Acid Amide

Petroselinic acid (666 mg, 2.36 mmol) in DCM (20 ml) was added TEA (0.33 ml, 2.37 mmol) followed by TBTU (753 mg, 2.35 mmol), and stirred for 40 min. at RT before troxacitabine (0.501 g, 2.35 mmol) in DMF (2 ml) was added. After stirring for 22 h at RT a saturated aqueous solution of NH₄Cl (25 mL) was added and the phases separated. The aqueous phase was extracted with DCM (3×50 mL), and the combined organic extracts were washed with saturated NaHCO₃ (25 mL), brine (25 mL), dried (Na₂SO₄), filtered and evaporated in vacuuo. The product was purified by flash chromatography on silica gel eluting with MeOH/DCM (25:975-50:950) to give 599 mg (53%) of the desired product as colourless crystals.

¹H-NMR (200 MHz; CDCl₃); δ 8.48 (bs, 1H), 8.42 (d, J=7.4 Hz, 1H), 7.39 (d, J=7.5 Hz, 1H), 6.16 (d, J=4.7 Hz, 1H), 5.31 (m, 2H), 5.09 (s, 1H), 4.18-4.33 (m, 2H), 3.94 (d, J=4.8 Hz, 2H), 2.40 (t, J=7.3 Hz, 2H), 2.02 (m, 4H), 1.63 (m, 2H), 1.23-1.44 (m, 21H), 0.84 (t, J=6.0 Hz, 3H). MS (electrospray, pos.); 500 [M+Na]⁺. MS (electrospray, neg.); 477 [M+]⁺. HPLC; 93%

EXAMPLE 8

Troxacitabine-2′-hydroxymethyl-petroselinoate

Troxacitabine (0.503 g, 2.36 mmol) in dry DMF (7 mL) was added a solution of HCl in DMF (1.3 M, 2.2 ml, 2.86 mmol), which had been prepared by bubbling HCl-gas through DMF. After some seconds a colourless solid precipitated from the solution. The resulting mixture was stirred for 30 min. and petroselinic acid chloride in DMF (12 mL) was then added. The acid chloride had previously been prepared from petroselinic acid (1.59 g, 5.6 mmol), oxalyl chloride (4.5 mL, 53 mmol) and DMF (0.1 mL catalytic amount) in toluene (35 mL) by stirring at ambient temperature for 2 h and then evaporated to dryness. After stirring for 43 h at room temperature the mixture was poured into water (50 mL) and extracted with DCM (3×100 mL) The combined organic extracts were washed with a saturated aqueous solution of NaHCO₃ (50 mL), brine (50 mL), dried (Na₂SO₄), filtrated and evaporated in vacuuo. The product was purified by flash chromatography on silica gel eluting with MeOH/DCM (25:975-50:950) to give 0.686 g (61%) of the desired product as pale yellow crystals.

¹H-NMR (200 MHz; CDCl₃); δ 7.69 (d, J=7.4 Hz, 1H), 6.21 (m, 1H), 5.70 (d, J=7.4 Hz, 1H), 5.30 (m, 2H), 5.16 (m, 1H), 4.45 (dd, J=3.4Hz, 12.3 Hz, 1H), 4.16-4.28 (m, 3H), 2.34 (t, J=7.4 Hz, 2H), 1.99 (m, 4H), 1.68 (m, 2H), 1.22-1.38 (m, 22H), 0.84 (t, J=6.4 Hz, 3H). MS (electrospray, pos); 500 [M+Na]⁺. MS (electrospray, neg); 477 [M+]⁺. HPLC; 94%

EXAMPLE 9

Troxacitabine N⁴-6,9,12-linolenic Acid Amide

Gamma linolenic acid (GLA) (0.38 g, 1.8 mmol) dissolved in DCM (4 ml) was added TEA (245 uL, 1.8 mmol) and TBTU (0.57 g, 1.8 mmol). The solution was allowed to stir for 30 min. at RT before troxacitabine (0.38 g, 1.8 mmol) in DCM (2 ml) was added. The reaction mixture was stirred for 70 h at RT before a saturated aqueous solution of NH₄Cl was added and the mixture extracted with DCM (3×). The combined organic phases were washed with brine, dried (NaSO₄), filtered and evaporated in vacuuo. The desired product was isolated by flash chromatography on silica gel eluting with MeOH/DCM (3:200) to give 0.30 g (35%) of the title compound as a pale yellow solid.

¹H-NMR (200 MHz, CDCl₃); δ 8.5 (d, 1H), 7.45 (d, 1H), 6.20 (d, 1H), 6.6-6.3 (m, 6H), 5.15 (s, 1H), 4.3 (m, 2H), 4.0 (s, 2H), 2.8 (m, 5 H), 3.5 (m, 3H), 2.1 (m, 4H), 1.7 (m, 2H), 1.4 (m, 6H), 0.95 (m, 3H). MS (electrospray); 496 [M+Na⁺]. HPLC; 97.0%

HPLC-parameters:

HPLC-system:      Agilent 1100
Column:           Cromolith Speedrod RP-C18e 50 × 4.6 mm
Time of analysis: 15 min
Flow:             2 ml/min
Mobil phase:      A: 5% MeOH in water added phosphate-buffer
                  (pH = 6)
                  B: MeOH added phosphate-buffer (pH = 6)
Temperature:      40° C.
Detector:         UV 240-300 nm

Claims

1. A compound having the following formula (I): wherein: R1 is and R3 is selected from the group consisting of hydrogen, methyl, trifluoromethyl, fluorine, chlorine, bromine and iodine; and

X and Y can be either CH or a N atom with at least one of X or Y being N, and

Z and W are each independently Br, Cl, I, F, OR4 or NHR4 and at least one of Z and W is either OR4 or NHR4, and R4 is H or R5C(O), R5CH2OC(O) or R5CH2NHC(O) where R5 is a C7-23 alkenyl of the general formula

CH3—(CH2)n-(CH═CH—CH2)m-CH═CH—(CH2)4—  (II)

wherein m is a number from 0 to 2 and n is a number from 0 to 10,

R2 is H or R5C(O), R5CH2OC(O) or R5CH2NHC(O) where R5 is a C7-23 alkenyl of the general formula

CH3—(CH2)n-(CH═CH—CH2)m-CH═CH—(CH2)4—  (II)

wherein m is a number from 0 to 2 and n is a number from 0 to 10, with the proviso that R2, R3 and R4 cannot simultaneously be hydrogen, or a pharmaceutically acceptable salt thereof.

2. A compound according to claim 1, wherein R1 is cytosine-analogue wherein R2 is H or R5C(O), R5CH2OC(O) or R5CH2NHC(O) and R4 is H or R5C(O), R5CH2OC(O) or R5CH2NHC(O) where R5 is a C7-23 alkenyl of the general formula CH3—(CH2)n-(CH═CH—CH2)m-CH═CH—(CH2)4—  (II) wherein m is a number from 0 to 2 and n is a number from 0 to 10, with the proviso that R2 and R4 cannot simultaneously be hydrogen, or a pharmaceutically acceptable salt thereof.

3. A compound according to claim 1, defined as: wherein R2 is H or R5C(O), R5CH2OC(O) or R5CH2NHC(O) and R4 is H or R5C(O), R5CH2OC(O) or R5CH2NHC(O) where R5 is a C7-23 alkenyl of the general formula CH3—(CH2)n-(CH═CH—CH2)m-CH═CH—(CH2)4—  (II) wherein m is a number from 0 to 2 and n is a number from 0 to 10, with the proviso that R2 and R4 cannot simultaneously be hydrogen, or a pharmaceutically acceptable salt thereof.

4. A compound according to claim 1, selected from the group consisting of: or a pharmaceutically acceptable salt thereof.

5-9. (canceled)

10. A method for, treating cancer in a subject in need of such treatment, which comprises administering to such subject a therapeutically effective amount of a compound of formula (I) as defined in claim 1 or a pharmaceutically acceptable salt thereof.

11. A pharmaceutical preparation, comprising a compound of formula (I) as defined in claim 1, and a pharmaceutically acceptable excipient diluent and/or carrier therefor.