WO2001046138A1 - Inhibitors of farnesyl protein transferase - Google Patents
Inhibitors of farnesyl protein transferase Download PDFInfo
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- WO2001046138A1 WO2001046138A1 PCT/GB2000/004875 GB0004875W WO0146138A1 WO 2001046138 A1 WO2001046138 A1 WO 2001046138A1 GB 0004875 W GB0004875 W GB 0004875W WO 0146138 A1 WO0146138 A1 WO 0146138A1
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- 0 Cc(cc(*)cc1)c1-c1cc(IC(C2)N(*)CC2S*)ccc1C(O)=O Chemical compound Cc(cc(*)cc1)c1-c1cc(IC(C2)N(*)CC2S*)ccc1C(O)=O 0.000 description 4
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/12—Oxygen or sulfur atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
Definitions
- This invention relates to compounds that inhibit farnesylation of mutant ras gene products through inhibition of the enzyme famesyl-protein transferase (FPTase).
- the invention also relates to methods of manufacturing the compounds, pharmaceutical compositions and methods of treating diseases, especially cancer, which are mediated through farnesylation.
- Ras genes are frequently mutated in tumours.
- Ras genes encode guanosine triphosphate (GTP) binding proteins which are believed to be involved in signal transduction, proliferation and malignant transformation.
- GTP guanosine triphosphate
- H-, K- and N-ras genes have been identified as mutant forms of ras (Barbacid M, Ann. Rev. Biochem. 1987, 56: 779-827).
- Post translational modification of ras protein is required for biological activity. Farnesylation of ras catalysed by FPTase is believed to be an essential step in ras processing.
- ras is able to attach to the cell membrane for relay of growth signals to the cell interior. In normal cells activated ras is believed to act in conjunction with growth factors to stimulate cell growth.
- tumour cells it is believed that mutations in ras cause it to stimulate cell division even in the absence of growth factors (Travis J, Science 1993, 260: 1877-1878), possibly through being permanently in GTP activated form rather than cycled back to GDP inactivated form. Inhibition of farnesylation of mutant ras gene products will stop or reduce activation.
- EP 696593 and PCT/GB96/01810 disclose further farnesyl transferase inhibitors, including pyrrolidine derivatives.
- R 1 and R 2 are independently selected from H or a prodrug moiety
- R 3 is hydrogen or halogen
- R 4 is hydrogen or halogen
- Y is S, S(O) or S(O) 2 ; or a salt thereof, provided that at least one of R 3 or R 4 is other than hydrogen.
- alkyl refers to straight or branched chain groups, which may, unless otherwise stated have from 1 to 20 and preferably from 1 to 6 carbon atoms.
- aryl includes phenyl.
- halo includes fluoro, chloro, bromo and iodo.
- heterocyclyl or “heterocyclic” include groups having from 4 to 10 ring atoms, up to 5 of which are selected from oxygen, sulphur and nitrogen.
- the rings may be mono-, or bicyclic and each ring may be aromatic or non-aromatic in character.
- Nitrogen atoms may be substituted if the valency of the ring allows it, with either a hydrogen or substituent group, such as a alkyl substituent.
- Sulphur atoms in a heterocyclic ring may be oxidised to S(O) or S(O) 2 groups.
- aromatic 5- or 6-membered heterocyclic ring systems include imidazole, triazole, pyrazine, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole and thiophene.
- a 9- or 10-membered bicyclic heteroaryl ring system is an aromatic bicyclic ring system comprising a 6-membered ring fused to either a 5 membered ring or another 6 membered ring.
- Examples of 5/6 and 6/6 bicyclic ring systems include benzofiiran, benzimidazole, benzthiophene, benzthiazole, benzisothiazole, benzoxazole, benzisoxazole, pyridoimidazole, pyrimidoimidazole, quinoline, isoquinoline, quinoxaline, quinazoline, phthalazine, cinnoline and naphthyridine.
- monocyclic heteroaryl rings contain upto 3 heteroatoms and bicyclic heteroaryl rings contain up to 5 heteroatoms.
- Preferred heteroatoms are N and S, especially N.
- attachment of heterocyclic rings to other groups is via carbon atoms.
- Suitable heterocyclic groups containing only N as the heteroatom are pyrrole, pyridine, indole, quinoline, isoquinoline, imidazole, pyrazine, pyrimidine, purine and pteridine.
- Hydrogenated or other substituted forms of the above aromatic rings, (which are not aromatic), such as tetrahydropyridyl rings are examples of non-aromatic heterocyclic groups.
- Various forms of prodrugs are known in the art. For examples of such prodrug derivatives, see: a) Design of Prodrugs, edited by H. Bundgaard, (Elsevier, 1985) and Methods in Enzymology, Vol. 42, p. 309-396, edited by K. Widder, et al. (Academic Press, 1985); b) A Textbook of Drug Design and Development, edited by Krogsgaard-Larsen; c) H. Bundgaard, Chapter 5 "Design and Application of Prodrugs", by H.
- R 5 C(O) -where R 5 is an optionally substituted aryl or heterocyclyl group.
- R 5 is optionally substituted phenyl, optionally substituted pyridyl, optionally substituted furyl, optionally substituted isoxazole, optionally substituted tetrahydropyridyl or optionally substituted tetrahydrofuryl.
- Suitable substituents for R 5 include alkyl groups such as methyl, haloalkyl groups such as trifluoromethyl, hydroxy, alkoxy such as methoxy or cyano.
- R 5 is phenyl, pyridyl or N-methyl-tetrahydropyridyl.
- Examples of prodrugs groups for R 2 are in vivo cleavable ester groups of a pharmaceutically-acceptable ester which is cleaved in the human or animal body to produce the parent acid.
- R 2 together with the carboxy group to which it is attached forms a pharmaceutically-acceptable esters such as C, .6 alkyl esters or C, .6 cycloalkyl esters, for example methyl, ethyl, propyl, iso-propyl, n-butyl or cyclopentyl ; C,. 6 alkoxymethyl esters, for example methoxymethyl; Ci.
- alkanoyloxymethyl esters for example pivaloyloxymethyl; phthalidyl esters; C 3.8 cycloalkoxycarbonyloxyC,. 6 alkyl esters, for example 1-cyclohexylcarbonyloxyethyl; l,3-dioxolan-2-ylmethyl esters, for example 5-methyl-l,3-dioxolan-2-ylmethyl; C,. 6 alkoxycarbonyloxyethyl esters, for example 1-methoxycarbonyloxyethyl; aminocarbonylmethyl esters and mono- or di- N-(C,.
- R 2 together with the carboxy group to which it is attached forms a pharmaceutically-acceptable amide, preferably an N-C, .6 alkylamide and an N,N-di-(C, .6 alkyl)amide, such as N-methyl, N-ethyl, N-propyl, N,N-dimethyl, N-ethyl-N-methyl or N,N-diethylamide.
- R 2 is selected from hydrogen, a C alkyl group such as isopropyl or cyclopentyl, or an optionally substituted heterocyclic group such as N-methyl -tetrahydropyridyl .
- R 3 is suitably a halo atom such as fluoro or chloro group, in particular fluorine.
- R 4 is preferably a hydrogen or fluorine, and in particular is hydrogen.
- the linking group L is suitably a group of formula CH 2 -Z- where Z is NH or O.
- Z is NH or O.
- Both E and Z isomeric forms of such compounds form part of the invention together with mixtures thereof. In particular, compounds were geometrical isomerism is possible are preferably in E form.
- Group Y is preferably a group S or S(O) 2 .
- optically active or racemic forms by virtue of one or more asymmetric carbon atoms
- the invention includes in its definition any such optically active or racemic form which possesses the property of inhibiting FTPase.
- the synthesis of optically active forms may be carried out by standard techniques of organic chemistry well known in the art, for example by synthesis from optically active starting materials or by resolution of a racemic form.
- inhibitory properties against FTPase may be evaluated using the standard laboratory techniques referred to hereinafter.
- Compounds of Formula I may form salts which are within the ambit of the invention. Pharmaceutically acceptable salts are preferred although other salts may be useful in, for example, isolating or purifying compounds. When the compound contains a basic moiety it may form pharmaceutically acceptable salts with a variety of inorganic or organic acids, for example hydrochloric, hydrobromic, sulphuric, phosphoric, trifluoroacetic, citric or maleic acid.
- inorganic or organic acids for example hydrochloric, hydrobromic, sulphuric, phosphoric, trifluoroacetic, citric or maleic acid.
- a suitable pharmaceutically-acceptable salt of the invention when the compound contains an acidic moiety is an alkali metal salt, for example a sodium or potassium salt, an alkaline earth metal salt, for example a calcium or magnesium salt, an ammonium salt or a salt with an organic base which affords a pharmaceutically-acceptable cation, for example a salt with methylamine, dimethylamine, trimethylamine, piperidine, morpholine or tris-(2-hydroxyethyl)amine.
- Particular salts of compounds of the invention are acetates, alkyl sulphonates such as methyl or ethyl sulphonate, fumarates, formates, succinates and gluconates.
- Solvates for example hydrates, are also within the ambit of the invention and may be prepared by generally known methods. Particular examples of compounds of formula (I) are shown in Table 1
- a compound of Formula I for use in preparation of a medicament for treatment of a disease mediated through farnesylation of ras, in particular cancer.
- the compound is suitably formulated as a pharmaceutical composition for use in this way.
- composition comprising a compound of formula I listed above together with a pharmaceutically acceptable diluent or carrier.
- a method of treating ras mediated diseases, especially cancer by administering an effective amount of a compound of Formula I to a mammal in need of such treatment.
- a compound of Formula I, or a pharmaceutically-acceptable salt thereof for use in a method of treatment of the human or animal body by therapy.
- the invention also provides the use of a compound of formula (I) in the preparation of a medicament for use in treating famesylated ras mediated disease or medical condition such as cancers.
- Specific cancers which may be treated by the compound or composition of the invention include:
- - carcinoma including that of the bladder, breast, colon, kidney, liver, lung, ovary, pancreas, stomach, cervix, thyroid and skin;
- - hematopoietic tumors of lymphoid lineage including acute lymphocytic leukemia, B-cell lymphoma and Burketts lymphoma;
- - hematopoietic tumors of myeloid lineage including acute and chronic myelogenous leukemias and promyelocytic leukemia; - tumors of mesenchymal origin, including fibrosarcoma and rhabdomyosarcoma; and
- the compounds of Formula I are especially useful in treatment of tumors having a high incidence of ras mutation, such as colon, lung, and pancreatic tumors.
- a composition having one (or a combination) of the compounds of this invention development of tumors in a mammalian host is reduced.
- Compounds of Formula I may also be useful in the treatment of diseases other than cancer that may be associated with signal transduction pathways operating through Ras, e.g., neuro-fibromatosis.
- Compounds of Formula I may also be useful in the treatment of diseases associated with CAAX-containing proteins other than Ras (e.g., nuclear lamins and transducin) that are also post-translationally modified by the enzyme farnesyl protein transferase.
- Ras e.g., nuclear lamins and transducin
- compositions of the invention may be in a form suitable for oral use (for example as tablets, lozenges, hard or soft capsules, aqueous or oily suspensions, emulsions, dispersible powders or granules, syrups or elixirs), for topical use (for example as creams, ointments, gels, or aqueous or oily solutions or suspensions), for administration by inhalation (for example as a finely divided powder or a liquid aerosol), for administration by insufflation (for example as a finely divided powder) or for parenteral administration (for example as a sterile aqueous or oily solution for intravenous, subcutaneous, intramuscular or intramuscular dosing or as a suppository for rectal dosing).
- oral use for example as tablets, lozenges, hard or soft capsules, aqueous or oily suspensions, emulsions, dispersible powders or granules, syrups or elixir
- compositions of the invention may be obtained by conventional procedures using conventional pharmaceutical excipients, well known in the art.
- compositions intended for oral use may contain, for example, one or more colouring, sweetening, flavouring and/or preservative agents.
- Suitable pharmaceutically acceptable excipients for a tablet formulation include, for example, inert diluents such as lactose, sodium carbonate, calcium phosphate or calcium carbonate, granulating and disintegrating agents such as corn starch or algenic acid; binding agents such as starch; lubricating agents such as magnesium stearate, stearic acid or talc; preservative agents such as ethyl or propyl p-hydroxybenzoate, and anti- oxidants, such as ascorbic acid. Tablet formulations may be uncoated or coated either to modify their disintegration and the subsequent absorption of the active ingredient within the gastrointestinal tract, or to improve their stability and/or appearance, in either case, using conventional coating agents and procedures well known in the art.
- inert diluents such as lactose, sodium carbonate, calcium phosphate or calcium carbonate
- granulating and disintegrating agents such as corn starch or algenic acid
- binding agents such as starch
- Compositions for oral use may be in the form of hard gelatin capsules in which the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules in which the active ingredient is mixed with water or an oil such as peanut oil, liquid paraffin, or olive oil.
- an inert solid diluent for example, calcium carbonate, calcium phosphate or kaolin
- water or an oil such as peanut oil, liquid paraffin, or olive oil.
- Aqueous suspensions generally contain the active ingredient in finely powdered form together with one or more suspending agents, such as sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, polyvinyl-pyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents such as lecithin or condensation products of an alkylene oxide with fatty acids (for example polyoxethylene stearate), or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol
- the aqueous suspensions may also contain one or more preservatives (such as ethyl or propyl p-hydroxybenzoate, anti-oxidants (such as ascorbic acid), colouring agents, flavouring agents, and/or sweetening agents (such as sucrose, saccharine or aspartame).
- preservatives such as ethyl or propyl p-hydroxybenzoate, anti-oxidants (such as ascorbic acid), colouring agents, flavouring agents, and/or sweetening agents (such as sucrose, saccharine or aspartame).
- Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil (such as arachis oil, olive oil, sesame oil or coconut oil) or in a mineral oil (such as liquid paraffin).
- the oily suspensions may also contain a thickening agent such as beeswax, hard paraffin or cetyl alcohol.
- Sweetening agents such as those set out above, and flavouring agents may be added to provide a palatable oral preparation.
- These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.
- Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water generally contain the active ingredient together with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients such as sweetening, flavouring and colouring agents, may also be present.
- the pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions.
- the oily phase may be a vegetable oil, such as olive oil or arachis oil, or a mineral oil, such as for example liquid paraffin or a mixture of any of these.
- Suitable emulsifying agents may be, for example, naturally-occurring gums such as gum acacia or gum tragacanth, naturally-occurring phosphatides such as soya bean, lecithin, an esters or partial esters derived from fatty acids and hexitol anhydrides (for example sorbitan monooleate) and condensation products of the said partial esters with ethylene oxide such as polyoxyethylene sorbitan monooleate.
- the emulsions may also contain sweetening, flavouring and preservative agents.
- Syrups and elixirs may be formulated with sweetening agents such as glycerol, propylene glycol, sorbitol, aspartame or sucrose, and may also contain a demulcent, preservative, flavouring and/or colouring agent.
- sweetening agents such as glycerol, propylene glycol, sorbitol, aspartame or sucrose, and may also contain a demulcent, preservative, flavouring and/or colouring agent.
- compositions may also be in the form of a sterile injectable aqueous or oily suspension, which may be formulated according to known procedures using one or more of the appropriate dispersing or wetting agents and suspending agents, which have been mentioned above.
- a sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example a solution in 1,3-butanediol.
- Suppository formulations may be prepared by mixing the active ingredient with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug. Suitable excipients include, for example, cocoa butter and polyethylene glycols.
- Topical formulations such as creams, ointments, gels and aqueous or oily solutions or suspensions, may generally be obtained by formulating an active ingredient with a conventional, topically acceptable, vehicle or diluent using conventional procedure well known in the art.
- Compositions for administration by insufflation may be in the form of a finely divided powder containing particles of average diameter of, for example, 30 ⁇ or much less, the powder itself comprising either active ingredient alone or diluted with one or more physiologically acceptable carriers such as lactose.
- the powder for insufflation is then conveniently retained in a capsule containing, for example, 1 to 50mg of active ingredient for use with a turbo-inhaler device, such as is used for insufflation of the known agent sodium cromoglycate.
- Compositions for administration by inhalation may be in the form of a conventional pressurised aerosol arranged to dispense the active ingredient either as an aerosol containing finely divided solid or liquid droplets.
- Conventional aerosol propellants such as volatile fluorinated hydrocarbons or hydrocarbons may be used and the aerosol device is conveniently arranged to dispense a metered quantity of active ingredient.
- the amount of active ingredient that is combined with one or more excipients to produce a single dosage form will necessarily vary depending upon the host treated and the particular route of administration.
- a formulation intended for oral administration to humans will generally contain, for example, from 0.5 mg to 2 g of active agent compounded with an appropriate and convenient amount of excipients which may vary from about 5 to about 98 percent by weight of the total composition.
- Dosage unit forms will generally contain about 1 mg to about 500 mg of an active ingredient.
- the size of the dose for therapeutic or prophylactic purposes of a compound of the Formula I will naturally vary according to the nature and severity of the conditions, the age and sex of the animal or patient and the route of administration, according to well known principles of medicine.
- compounds of the Formula I are useful in treating diseases or medical conditions which are due alone or in part to the effects of farnesylation of ras.
- a daily dose in the range for example, 0.5 mg to 75 mg per kg body weight is received, given if required in divided doses. In general lower doses will be administered when a parenteral route is employed.
- a dose in the range for example, 0.5 mg to 30 mg per kg body weight will generally be used.
- a dose in the range for example, 0.5 mg to 25 mg per kg body weight will be used.
- Oral administration is however preferred.
- Compounds of this invention may be useful in combination with known anti-cancer and cyto toxic agents. If formulated as a fixed dose such combination products employ the compounds of this invention within the dosage range described herein and the other pharmaceutically active agent within its approved dosage range. Sequential use is contemplated when a combination formulation is inappropriate.
- the compounds of the Formula I are primarily of value as therapeutic agents for use in warm-blooded animals (including man), they are also useful whenever it is required to inhibit the effects of activation of ras by farnesylation. Thus, they are useful as pharmacological standards for use in the development of new biological tests and in the search for new pharmacological agents.
- a compound of the invention, or a salt thereof may be prepared by any process known to be applicable to the preparation of such compounds or structurally related compounds. Such processes are illustrated by the following representative schemes in which variable groups have any of the meanings defined for Formula I unless stated otherwise.
- Functional groups may be protected and deprotected using conventional methods. For examples of protecting groups such as amino and carboxylic acid protecting groups (as well as means of formation and eventual deprotection), see T.W. Greene and P.G.M. Wuts, "Protective Groups in Organic Synthesis", Second Edition, John Wiley & Sons, New York, 1991. Note abbreviations used have been listed immediately before the Examples below.
- Protecting groups may be removed by any convenient method as described in the literature or known to the skilled chemist as appropriate for the removal of the protecting group in question, such methods being chosen so as to effect removal of the protecting group with minimum disturbance of groups elsewhere in the molecule.
- Specific examples of protecting groups are given below for the sake of convenience, in which "lower” signifies that the group to which it is applied preferably has 1-4 carbon atoms. It will be understood that these examples are not exhaustive. Where specific examples of methods for the removal of protecting groups are given below these are similarly not exhaustive. The use of protecting groups and methods of deprotection not specifically mentioned is of course within the scope of the invention.
- a carboxy protecting group may be the residue of an ester- forming aliphatic or araliphatic alcohol or of an ester- forming silanol (the said alcohol or silanol preferably containing 1-20 carbon atoms).
- carboxy protecting groups include straight or branched chain (l-12C)alkyl groups (e.g. isopropyl, t-butyl); lower alkoxy lower alkyl groups (e.g. methoxymethyl, ethoxymethyl, isobutoxymethyl; lower aliphatic acyloxy lower alkyl groups, (e.g. acetoxymethyl, propionyloxymethyl, butyryloxymethyl, pivaloyloxym ethyl); lower alkoxycarbonyloxy lower alkyl groups (e.g. 1-methoxycarbonyloxyethyl, 1-ethoxycarbonyloxyethyl); aryl lower alkyl groups (e.g.
- tri(lower alkyl)silyl groups e.g. trimethylsilyl and t-butyldimethylsilyl
- tri(lower alkyl)silyl lower alkyl groups e.g. trimethylsilylethyl
- (2-6C)alkenyl groups e.g. allyl and vinylethyl
- Methods particularly appropriate for the removal of carboxyl protecting groups include for example acid-, metal- or enzymically-catalysed hydrolysis.
- hydroxy protecting groups include lower alkenyl groups (e.g. allyl); lower alkanoyl groups (e.g. acetyl); lower alkoxycarbonyl groups (e.g. t-butoxycarbonyl); lower alkenyloxycarbonyl groups (e.g. allyloxycarbonyl); aryl lower alkoxycarbonyl groups (e.g.
- amino protecting groups include formyl, aralkyl groups (e.g. benzyl and substituted benzyl, e.g.
- lower alkoxycarbonyl e.g. t-butoxycarbonyl
- lower alkenyloxycarbonyl e.g
- Methods appropriate for removal of hydroxy and amino protecting groups include, for example, acid-, base, metal- or enzymically-catalysed hydrolysis, or photolytically for groups such as s-nitrobenzyloxycarbonyl, or with fluoride ions for silyl groups.
- protecting groups for amide groups include aralkoxymethyl (e.g.. benzyloxymethyl and substituted benzyloxymethyl); alkoxymethyl (e.g. methoxymethyl and trimethylsilylethoxymethyl); tri alkyl/arylsilyl (e.g. trimethylsilyl, t-butyldimethylsily, t- butyldiphenylsilyl); tri alkyl/arylsilyloxymethyl (e.g. t-butyldimethylsilyloxymethyl, t-butyldiphenylsilyloxymethyl); 4-alkoxyphenyl (e.g.
- Alkoxymethyl, tri alkyl/arylsilyl and tri alkyl/silyloxymethyl groups may be introduced by reacting the amide with the appropriate chloride and removing with acid; or in the case of the silyl containing groups, fluoride ions.
- the alkoxyphenyl and alkoxybenzyl groups are conveniently introduced by arylation or alkylation with an appropriate halide and removed by oxidation with eerie ammonium nitrate.
- alk-1-enyl groups may be introduced by reacting the amide with the appropriate aldehyde and removed with acid.
- the invention also provides a process for preparing a compound of formula (I) as defined above which process
- the invention also provides a process for preparing a compound of formula (I) as defined above which process comprises reacting a compound of formula (II)
- R 1 is a group R 1 as defined in relation to formula (I) or a precursor thereof
- R 5 is a protecting group such as BOC or ALLOC with a compound of formula (III) where Y is as defined in relation to formula (I) and R 2' is a group R 2 as defined in relation to formula (I) or a precursor thereof; and thereafter if desired or necessary, carrying out one or more of the following steps: a) removing protecting groups R 5 ; a) converting any precursor groups R 1 and R 2 to groups R 1 and R 2 ; and b) changing said groups to different R 1 , R 2 groups.
- reaction between compounds of formula (II) and (III) is suitably effected in an organic solvent such as dichloromethane in the presence of a base such as DMAP and EDC.
- a base such as DMAP and EDC.
- Moderate temperatures for example of from 0 to 50°C, conveniently ambient temperature, are employed.
- Precursor groups R 1 and R 2 may include protecting groups such as esters, which are not pharmaceutically acceptable. These may be converted to hydrogen or other prodrug groups using conventional methods as illustrated below. Removal of protecting groups R 5 can be carried out using conventional methods such as reaction with TFA and/or triethylsilane.
- R 1 , R 3 , R 4 , R 5 and L are as defined in relation to formula (II) and R 6 is a protecting group, in particular an alkyl group such as methyl.
- Deprotection is suitably effected using a strong base such as an alkali metal hydroxide, in particular sodium hydroxide.
- the reaction is suitably effected in a solvent such as aqueous alcohol and in particular aqueous methanol, at elevated temperatures, conveniently at the reflux temperature of the solvent.
- Suitable coupling conditions include the use of a reducing agent (e.g. NaCNBH3, BH3, hydrogen plus catalyst, LiHBEt3, di-isobutyl-aluminiumhydride, lithium aluminium hydride, sodium borohydride) in the presence of a suitable solvent e.g.methanol or ethanol & acetic acid.
- a reducing agent e.g. NaCNBH3, BH3, hydrogen plus catalyst, LiHBEt3, di-isobutyl-aluminiumhydride, lithium aluminium hydride, sodium borohydride
- a suitable solvent e.g.methanol or ethanol & acetic acid.
- Aldehydes of formula (VI) may be prepared by reduction of the compounds of formula (VII)
- R 1 and R 5 are as defined above and R 6 is alkyl such as methyl and R 7 is alkoxy such as methoxy.
- reaction is suitably effected in an organic solvent such as dichloromethane in the presence of a weak base such as triethylamine. Moderate to low temperatures, for example, from -10 to 0°C are suitably employed.
- Compounds of formula (XIV) are suitably prepared by reacting a compound of formula (XV) (XV) where R 6 is as defined above and Z' is a leaving group such as halogen and in particular bromine, with a compound of formula (XVI) where R 3 and R 4 are as defined above.
- the reaction is suitably effected in the presence of a reagent such as ceasium fluoride, and a catalyst such as a palladium catalyst (e.g. tetrakis(triphenylphsophine) palladium(O).
- a suitable solvent for the reaction is dimethoxyethane and the reaction can be effected under reflux conditions.
- Compounds of formula (XNIII) are suitably prepared by reduction of a compound of formula (VI), for example using a reducing agent such as lithium aluminium hydride. Reduction is carried out under conventional conditions in a solvent such as tetrahydrofuran.
- Compounds of formula (XVII) may be prepared by protection of the corresponding carboxylic acid, for example by esterifying the acid using an alcohol, in particular an alkyl alcohol such as methanol.
- the reaction is suitably effected in the presence of sulphuryl chloride or the like, at elevated temperatures, conveniently at the reflux temperature of the solvent.
- the acid itself may be prepared by deprotection of a compound of formula
- Suitable deprotection conditions include heating the compound with a suitable reagent such as pyridine hydrochloride to high temperatures such, for example from 200 to 250°C, and preferably at about 220°C.
- THF, toluene, DMSO optionally in the presence of an aqueous solvent (2 -phase system) and optionally in the presence of a catalyst complexing agent which solubilises alkali metal ions in non-polar solvents such as 1,4,7,10,13-pentaoxacyclopentadecane (also called 15-Crown-5) or 1,4,7, 10,13, 16-hexaoxacyclooctadecane (also called 18-Crown-6).
- a catalyst complexing agent which solubilises alkali metal ions in non-polar solvents such as 1,4,7,10,13-pentaoxacyclopentadecane (also called 15-Crown-5) or 1,4,7, 10,13, 16-hexaoxacyclooctadecane (also called 18-Crown-6).
- groups R 1 and R 2 may be changed for different such groups after any of the above preparation methods using conventional chemistry and examples of this are provided hereinafter.
- FPT Farnesyl protein transferase
- the substrate for FPT was Kras (CVIM C-terminal sequence).
- the cDNA for oncogenic val 12 variant of human c-Ki-ras-2 4B was obtained from the plasmid pSWl 1-1 (ATCC). This was then subcloned into the polylinker of a suitable expression vector e.g.
- melting points are uncorrected and were determined using a Mettler SP62 automatic melting point apparatus or an oil-bath apparatus; melting points for the end-products of the Formula I were determined after crystallisation from a conventional organic solvent such as ethanol, methanol, acetone, ether or hexane, alone or in admixture; and
- Triethylamine (29 ml.) was added to a solution of methyl 4-methoxysalicylate (Compound xxvi in Scheme 3)(25.0 g.) in dichloromethane(500 ml.) and the solution cooled to 0°C.
- Trifluoromethanesulphonic anhydride (29 ml.) was added dropwise and the reaction stirred at ambient temperature for lhour. Additional portions of triethylamine and trifluoromethanesulphonic anhydride were added over l ⁇ hours until HPLC showed absence of starting material. The reaction was washed with 2N hydrochloric acid and the organic phase evaporated to give a brown oil.
- Compound X the active ingredient being termed "Compound X"
- Citric acid 0.38% w/v
- the above formulations may be obtained by conventional procedures well known in the pharmaceutical art.
- the tablets (a)-(c) may be enteric coated by conventional means, for example to provide a coating of cellulose acetate phthalate.
- the aerosol formulations (h)-(k) may be used in conjunction with standard, metered dose aerosol dispensers, and the suspending agents sorbitan trioleate and soya lecithin may be replaced by an alternative suspending agent such as sorbitan monooleate, sorbitan sesquioleate, polysorbate 80, polyglycerol oleate or oleic acid.
Abstract
Description
Claims
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00985621A EP1242372A1 (en) | 1999-12-22 | 2000-12-18 | Inhibitors of farnesyl protein transferase |
BR0016667-7A BR0016667A (en) | 1999-12-22 | 2000-12-18 | Compound and pharmaceutical composition |
KR1020027008023A KR20020063249A (en) | 1999-12-22 | 2000-12-18 | Inhibitors of farnesyl protein transferase |
IL14987000A IL149870A0 (en) | 1999-12-22 | 2000-12-18 | Inhibitors of farnesyl protein transferase |
MXPA02006110A MXPA02006110A (en) | 1999-12-22 | 2000-12-18 | Inhibitors of farnesyl protein transferase. |
US10/168,379 US6777438B2 (en) | 1999-12-22 | 2000-12-18 | Inhibitors of farnesyl protein transferase |
JP2001547049A JP2003518092A (en) | 1999-12-22 | 2000-12-18 | Farnesyl protein transferase inhibitor |
AU22029/01A AU2202901A (en) | 1999-12-22 | 2000-12-18 | Inhibitors of farnesyl protein transferase |
CA002388669A CA2388669A1 (en) | 1999-12-22 | 2000-12-18 | Inhibitors of farnesyl protein transferase |
NO20022923A NO20022923L (en) | 1999-12-22 | 2002-06-18 | Inhibitors of farnesyl protein transferase |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9930317.4A GB9930317D0 (en) | 1999-12-22 | 1999-12-22 | Novel compounds |
GB9930317.4 | 1999-12-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2001046138A1 true WO2001046138A1 (en) | 2001-06-28 |
Family
ID=10866833
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2000/004875 WO2001046138A1 (en) | 1999-12-22 | 2000-12-18 | Inhibitors of farnesyl protein transferase |
Country Status (14)
Country | Link |
---|---|
US (1) | US6777438B2 (en) |
EP (1) | EP1242372A1 (en) |
JP (1) | JP2003518092A (en) |
KR (1) | KR20020063249A (en) |
CN (1) | CN1411441A (en) |
AU (1) | AU2202901A (en) |
BR (1) | BR0016667A (en) |
CA (1) | CA2388669A1 (en) |
GB (1) | GB9930317D0 (en) |
IL (1) | IL149870A0 (en) |
MX (1) | MXPA02006110A (en) |
NO (1) | NO20022923L (en) |
WO (1) | WO2001046138A1 (en) |
ZA (1) | ZA200202907B (en) |
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WO1998050029A1 (en) * | 1997-05-07 | 1998-11-12 | University Of Pittsburgh | Inhibitors of protein isoprenyl transferases |
WO1999041235A1 (en) * | 1998-02-10 | 1999-08-19 | Astrazeneca Uk Limited | Farnesyl transferase inhibitors |
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1999
- 1999-12-22 GB GBGB9930317.4A patent/GB9930317D0/en not_active Ceased
-
2000
- 2000-12-18 CA CA002388669A patent/CA2388669A1/en not_active Abandoned
- 2000-12-18 CN CN00817419A patent/CN1411441A/en active Pending
- 2000-12-18 US US10/168,379 patent/US6777438B2/en not_active Expired - Fee Related
- 2000-12-18 JP JP2001547049A patent/JP2003518092A/en active Pending
- 2000-12-18 AU AU22029/01A patent/AU2202901A/en not_active Abandoned
- 2000-12-18 WO PCT/GB2000/004875 patent/WO2001046138A1/en not_active Application Discontinuation
- 2000-12-18 MX MXPA02006110A patent/MXPA02006110A/en active IP Right Grant
- 2000-12-18 BR BR0016667-7A patent/BR0016667A/en not_active IP Right Cessation
- 2000-12-18 EP EP00985621A patent/EP1242372A1/en not_active Withdrawn
- 2000-12-18 IL IL14987000A patent/IL149870A0/en unknown
- 2000-12-18 KR KR1020027008023A patent/KR20020063249A/en not_active Application Discontinuation
-
2002
- 2002-04-12 ZA ZA200202907A patent/ZA200202907B/en unknown
- 2002-06-18 NO NO20022923A patent/NO20022923L/en unknown
Patent Citations (3)
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WO1997006138A1 (en) * | 1995-08-04 | 1997-02-20 | Zeneca Limited | 4-mercaptopyrrolidine derivatives as farnesyl transferase inhibitors |
WO1998050029A1 (en) * | 1997-05-07 | 1998-11-12 | University Of Pittsburgh | Inhibitors of protein isoprenyl transferases |
WO1999041235A1 (en) * | 1998-02-10 | 1999-08-19 | Astrazeneca Uk Limited | Farnesyl transferase inhibitors |
Also Published As
Publication number | Publication date |
---|---|
EP1242372A1 (en) | 2002-09-25 |
US20030096842A1 (en) | 2003-05-22 |
MXPA02006110A (en) | 2002-12-05 |
CA2388669A1 (en) | 2001-06-28 |
CN1411441A (en) | 2003-04-16 |
NO20022923D0 (en) | 2002-06-18 |
BR0016667A (en) | 2002-09-03 |
GB9930317D0 (en) | 2000-02-09 |
KR20020063249A (en) | 2002-08-01 |
JP2003518092A (en) | 2003-06-03 |
ZA200202907B (en) | 2003-07-14 |
AU2202901A (en) | 2001-07-03 |
IL149870A0 (en) | 2002-11-10 |
US6777438B2 (en) | 2004-08-17 |
NO20022923L (en) | 2002-06-18 |
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