NZ531928A - Novel dihydropteridinones, method for producing the same and the use thereof as medicaments - Google Patents

Abstract

Described are dihydropteridinone compounds of formula I that act as inhibitors of cell cycle kinases, wherein: R1 denotes a group selected from among hydrogen, NH2, XH, halogen and a C1-C3-alkyl group optionally substituted by one or more halogen atoms, R2 denotes a group selected from among hydrogen, CHO, XH, -X-C1-C2-alkyl and an optionally substituted C1-C3-alkyl group, R3, R4 may be identical or different and denote a group selected from among optionally substituted C1-C10-alkyl, C2-C10-alkenyl, C2-C10-alkynyl, aryl, heteroaryl, C3-C8-cycloalkyl, C3-C8-heterocycloalkyl, -X-aryl, -X-heteroaryl, -X-cycloalkyl, -X-heterocycloalkyl, -NR8-aryl, -NR8-heteroaryl, -NR8-cycloalkyl, - and -NR8-heterocycloalkyl, or a group selected from among hydrogen, halogen, COXR8, CON(R8)2, COR8 and XR8, or R3 and R4 together denote a 2- to 5-membered alkyl bridge which may contain 1 to 2 heteroatoms, R5 denotes hydrogen or a group selected from among optionally substituted C1-C10-alkyl, C2-C10-alkenyl, C2-C10-alkynyl, aryl, heteroaryl and -C3-C6-cycloalkyl, or R3 and R5 or R4 and R5 together denote a saturated or unsaturated C3-C4-alkyl bridge which may contain 1 to 2 heteroatoms, R6 denotes optionally substituted aryl or heteroaryl, R7 denotes hydrogen or -CO-X-C1-C4-alkyl, and X in each case independently of one another denotes O or S, and R8 in each case independently of one another denotes hydrogen or a group selected from among optionally substituted C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl and phenyl, or in the form of a tautomer, racemate, an enantiomer, a diastereomers and/or the mixtures thereof, and optionally the pharmacologically acceptable acid addition salt thereof. Also mentioned the processes for preparing a compound previously defined, and uses of this compound of formula I for the production of a medicament with an antiproliferative activity for the treatment and/or prevention of cancer, infections, inflammatory, and/or autoimmune diseases.

Description

New Zealand Paient Spedficaiion for Paient Number 531 923 1 1 531 J M 78947ffi.206 Novel dihydropteridinones, method for producing the same and the use thereof as medicaments The present invention relates to new dihydropteridinones of general formula (I) R1 R2 N r,"A- >r R6 Rs R wherein the groups X, R1, R2, R3, R4, R5, R6 and R7 have the meanings given in the claims and specification, the isomers thereof, processes for preparing these dihydropteridinones and the use thereof as pharmaceutical compositions.

Background to the invention Pteridinone derivatives are known from the prior art as active substances with an antiproliferative activity. WO 01/019825 describes the use of pteridinone derivatives for the treatment of neoplastic and viral diseases. The resistance of many types of tumours calls for the development of new pharmaceutical compositions for combating tumours.

The aim of the present invention is to prepare new compounds with an antiinflammatory and antiproliferative activity, or to at least provide a useful alternative.

Detailed description of the invention 25 Surprisingly it has been found that compounds of general formula (I) wherein the groups X and R1 to R7 have the meanings given hereinafter act as inhibitors of specific cell cycle kinases. Thus, the compounds according to the invention may be used for example to treat diseases connected with the activity of specific cell cycle kinases and characterised by excessive or abnormal cell proliferation. intellectual property office! of N.Z - 5 AUG 2005 .received 2 The present invention therefore relates to compounds of general formula (I) N Ft N R6 nn/ N N' (I) R wherein R1 denotes a group selected from among hydrogen, NH2, XH, halogen and a CrC3-alkyl group optionally substituted by one or more halogen atoms, R2 denotes a group selected from among hydrogen, CHO, XH, -X-Ci-C2-alkyl and an optionally substituted Ci-C3-alkyl group, R3, R4 which may be identical or different denote a group selected from among optionally substituted Ci-Cio-alkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, aryl, heteroaryl, 15 Cs-Cs-cycloalkyI, Ca-Cs-heterocycloalkyl, -X-aryl, -X-heteroaryl, -X-cycloalkyl, -X-heterocycloalkyl, -NR8-aryl, -NR8-heteroaryl, -NR8-cycloalkyl and -NR8-heterocycloalkyl, or a group selected from among hydrogen, halogen, COXR8, CON(R8)2, COR8 and XR8, or R3 and R4 together denote a 2- to 5-membered alkyl bridge which may contain 1 20 to 2 heteroatoms, R5 denotes hydrogen or a group selected from among optionally substituted Ci-Cio-alkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, aryl, heteroaryl and -C3-C6-cycloalkyl, or R3 and R5 or R4 and R5 together denote a saturated or unsaturated C3-C4-alkyl bridge which may contain 1 to 2 heteroatoms, 3 R6 denotes optionally substituted aryl or heteroaryl, R7 denotes hydrogen or -CO-X-CrC4-alkyl, and X in each case independently of one another denotes O or S, R8 in each case independently of one another denotes hydrogen or a group selected from among optionally substituted CrC4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl and phenyl, optionally in the form of the tautomers, the racemates, the enantiomers, the diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts thereof.

Preferred compounds of formula (I) are those wherein X and R6 have the meaning indicated, and R1 denotes hydrogen, R2 denotes a group selected from among a CHO, OH, and CH3 group, R3, R4 which may be identical or different denote a group selected from among hydrogen, optionally substituted CrC6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C7-cycloalkyl, or R3and R4 together denote a C2-Cs-alkyl bridge , R5 denotes a group selected from among optionally substituted Ci-Cio-alkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, C3-C6-cycloalkyl and C3-C6-cycloalkenyl, or R3 and R5 or R4 and R5 together denote a saturated or unsaturated C3-C4-alkyl 30 bridge which may contain 1 to 2 heteroatoms, and R7 denotes hydrogen, 4 optionally in the form of the tautomers, the racemates, the enantiomers, the diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts thereof.

Particularly preferred compounds of formula (I) are those wherein R1-R5, R7, R8 and X have the meaning indicated, and R6 denotes a group of general formula wherein n denotes 1, 2, 3 or 4, R9 denotes a group selected from among optionally substituted CrC6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, -CONH-CrCio-alkylene, -O-aryl, -O-heteroaryl, -O-cycloalkyl, -O-heterocycloalkyl, aryl, heteroaryl, cycloalkyl and heterocycloalkyl or a group selected from among -0-CrC6-alkyl-Q1, -CONR8-CrCio-alkyl-Q1, -CONR8-C2-Cio-alkenyl-Q1, -CONR8-Q2, halogen, OH, -S02R8, -S02N(R8)2, 0 20 -COR8, -COOR8, -N(R8)2, -NHCOR8, CONR8OCi-Ci0 alkylQ1 and CONR8OQ2, Q1 denotes hydrogen, -NHCOR8, or a group selected from among an optionally substituted -NH-aryl, -NH-heteroaryl, aryl, heteroaryl, C3-C8-cycloalkyl-and heterocycloalkyl group, Q2 denotes hydrogen or a group selected from among an optionally substituted aryl, heteroaryl, C3-C8-heterocycloaI kyl, C3-C8-cycloalkyl- and Ci-C4-alkyl-C3-C8-cycloalkyl group, R10 which may be identical or different denotes a group selected from among optionally substituted Ci-C6-alkyl, C2-C6-alkenyl and C2-C6-alkynyl, -0-Ci-C6-alkyl, -0-C2-C6-alkenyl, -0-C2-C6-alkynyl, C3-C6-heterocycloalkyl and C3-C6-cycloalkyl, or a group selected from among hydrogen, -CONH2, -COOR8,-OCON(R8)2, -N(R8)2, -NHCOR8,-NHCON(R8)2 , -N02and halogen, or adjacent groups R9 and R10 together denote a bridge of general formula Y denotes O, S or NR11, m denotes 0,1 or 2 R11 denotes hydrogen or Ci-C2-alkyl, and R12 denotes hydrogen or a group selected from among optionally substituted phenyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, -CrC3-alkyl-phenyl, -CrC3-alkyl-pyridyl, -CrC3-alkyl-pyrazinyl, -CrC3-alkyl-pyrimidinyl and -CrC3-alkyl-pyridazinyl, R13 denotes Ci-C6-alkyl, optionally in the form of the tautomers, the racemates, the enantiomers, the diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts thereof.

Particularly preferred are compounds of formula (I) wherein R3-R6, R8 and X have the meaning indicated, and R1 denotes hydrogen, R2 denotes CH3, and R7 denotes hydrogen, O 6 optionally in the form of the tautomers, the racemates, the enantiomers, the diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts thereof.

The invention further relates to compounds of formula (I), wherein X and R1-R7 have the meanings indicated, for use as pharmaceutical compositions.

Of particular importance according to the invention are compounds of formula (I), wherein X and R1-R7 have the meaning indicated, for use as pharmaceutical 10 compositions with an antiproliferative activity.

The invention also relates to the use of a compound of formula (I), wherein X and R1-R7 have the meaning indicated, for preparing a pharmaceutical composition for the treatment and/or prevention of cancer, infections, inflammatory and 15 autoimmune diseases.

The invention also relates to a method of treating and/or preventing cancer, infections, inflammatory and autoimmune diseases, characterised in that a patient is given an effective amount of a compound of formula (I), wherein Xand R1-R7 20 have the meanings indicated.

The invention also relates to pharmaceutical preparations, containing as active substance one or more compounds of general formula (I), wherein X and R1-R7 have the meanings indicated, or the physiologically acceptable salts thereof, 25 optionally combined with conventional excipients and/or carriers.

The invention also relates to a process for preparing a compound of general formula (I), 7 R1 N R N N' (I) TM' R wherein R1-R7 and X are as hereinbefore defined, characterised in that a compound of general formula (II) R1 R2 I 3 L N N D3 R (II) wherein R1-R5 and X are as hereinbefore defined and L is a leaving group, is reacted with an optionally substituted compound of general formula (III) HN' ,R (III) wherein R6 and R7are as hereinbefore defined.

I The invention also relates to a compound of formula (II), 8 N-VS*X CI ANA Jcj k (II) wherein R1-R5 and X are as hereinbefore defined. Compounds of formula (II) are important intermediate products for preparing the compounds of formula (I) according to the 5 invention.

The invention also relates to a process for preparing a compound of general formula (I), R 1 r->2 N R \ , N N R R 'N" R5 R (I) wherein R6 denotes a group of general formula, (R10)n R R9 denotes an optionally substituted group -CONH-CrCio-alkylene or a group selected from among -CONR8-CrCio-alkyl-Q1, -CONR8-C2-Cio-alkenyl-Q1, -CONR8-Q2 and -COOR8, and 20 R1-R5, R7, Ri0, n and X are as hereinbefore defined, 9 characterised in that a compound of general formula (IA) R1 R2 n/VnY° rv a x jcrs N N N Nr4 k R (r10>» 0* L (IA) wherein R1 to R5, R7 and R10 are as hereinbefore defined, and L denotes a leaving group, is reacted with a primary or secondary amine to form the corresponding amide or is reacted with an alcohol to form the corresponding ester.

The term alkyl groups, including alkyl groups which are a part of other groups, denotes branched and unbranched alkyl groups with 1 to 10 carbon atoms, preferably 1-6, most preferably 1-4 carbon atoms, such as, for example: methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl and decyl. Unless otherwise stated, the abovementioned terms propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl and decyl include all the possible isomeric forms. For example, the term propyl includes the two isomeric groups n-propyl and iso-propyl, the term butyl includes n-butyl, iso-butyl, sec. butyl and tert.-butyl, the term pentyl includes iso-pentyl, neopentyl, etc.

In the abovementioned alkyl groups one or more hydrogen atoms may optionally be replaced by other groups. For example these alkyl groups may be substituted by the halogen atoms fluorine, chlorine, bromine or iodine. The substituents fluorine and chlorine are preferred. The substituent chlorine is particularly preferred. All the hydrogen atoms of the alkyl group may optionally also be replaced.

Similarly, in the abovementioned alkyl groups, unless otherwise stated, one or more hydrogen atoms may optionally be replaced for example by an optionally substituted group selected from among CN, OCOCH3, aryl, preferably phenyl, heteroaryl, preferably thienyl, thiazolyl, imidazolyl, pyridyl, pyrimidyl or pyrazinyl, saturated or unsaturated heterocycloalkyl, preferably pyrazolyl, pyrrolidinyl, piperidinyl, piperazinyl or tetrahydro-oxazinyl, an amine group, preferably 5 methylamine, benzylamine, phenylamine or heteroarylamine, saturated or unsaturated bicyclic ring systems, preferably benzimidazolyl and cycloalkyl, preferably cyclohexyl or cyclopropyl.

The term alkyl bridge, unless otherwise stated, denotes branched and unbranched 10 alkyl groups with 2 to 5 carbon atoms, for example propylene, isopropylene, n-butylene, iso-butyl, sec. butyl and tert.-butyl etc. bridges. Propylene and butylene bridges are particularly preferred. In the alkyl bridges mentioned 1 to 2 C-atoms may optionally be replaced by one or more heteroatoms selected from among oxygen, nitrogen or sulphur.

The term alkenyl groups (including those which are a part of other groups) denotes branched and unbranched alkylene groups with 2 to 10 carbon atoms, preferably 2 - 6 carbon atoms, most preferably 2 - 3 carbon atoms, provided that they have at least one double bond. Examples include: ethenyl, propenyl, butenyl, pentenyl 20 etc. Unless otherwise stated, the abovementioned terms propenyl, butenyl, etc also include all the possible isomeric forms. For example, the term butylene includes n-butenyl, 1-methylpropenyl, 2-methylpropenyl, 1.1-dimethylethenyl, 1.2-dimethylethenyl etc.

In the abovementioned alkenyl groups, unless otherwise stated, one or more 25 hydrogen atoms may optionally be replaced by other groups. For example, these alkyl groups may be substituted by the halogen atoms fluorine, chlorine, bromine or iodine. The substituents fluorine and chlorine are preferred. The substituent chlorine is particularly preferred. All the hydrogen atoms of the alkenyl group may optionally also be replaced.

The term alkynyl groups (including those which are a part of other groups) denotes branched and unbranched alkynyl groups with 2 to 10 carbon atoms, provided that 11 they have at least one triple bond, for example ethynyl, propargyl, butynyl, pentynyl, hexynyl etc., preferably ethynyl or propynyl.

In the abovementioned alkynyl groups, unless otherwise stated, one or more hydrogen atoms may optionally be replaced by other groups. For example, these alkyl groups may be substituted by the halogen atoms fluorine, chlorine, bromine or iodine. The substituents fluorine and chlorine are preferred. The substituent chlorine is particularly preferred. All the hydrogen atoms of the alkynyl group may optionally also be replaced.

The term aryl denotes an aromatic ring system with 6 to 14 carbon atoms, preferably 6 or 10 carbon atoms, preferably phenyl, which, unless otherwise stated, may carry one or more of the following substituents, for example: OH, NO2, CN, -OCHF2, -OCF3, -NH2, halogen, for example fluorine, chlorine, bromine or iodine, preferably fluorine or chlorine, CrCio-alkyl, preferably CrCs-alkyl, preferably CrC3-alkyl, most preferably methyl or ethyl, -0-Ci-C3-alkyl, preferably -O-methyl or-O-ethyl, - N-methyl -tetrahydro-oxazinyl, -COOH, -COO-CrC^alkyl, preferably -COOCH2CH3, -COO-C(CH3)3 or -COOCH3, -CONH2, -CONH-Ci-Cio-alkyl, while this alkyl may optionally be further substituted, optionally substituted -CONH-C3-C6-cycloalkyl, preferably optionally substituted -CONH-cyclopentyl, optionally substituted -CONH-heterocycloalkyl, preferably piperidinyl, pyrrolidinyl or piperazinyl, optionally substituted -CONH-heteroaryl, preferably optionally substituted -CONH-pyridyl, optionally substituted -CONH-aryl, preferably optionally substituted -CONH-phenyl, -CONMeCi-C3-alkyl, while this alkyl may optionally be further substituted, preferably -CONMeCH2-pyridyl, benzimidazole or a group of formula 12 x* Examples of 5-10-membered mono- or bicyclic heteroaryl rings wherein up to three C-atoms may be replaced by one or more heteroatoms selected from among oxygen, nitrogen or sulphur include furan, thiophene, pyrrole, pyrazole, imidazole, triazole, tetrazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazole, isoxazole, thiazole, thiadiazole and oxadiazole, while each of the abovementioned heterocycles may optionally also be anneilated onto a benzene ring, preferably benzimidazole, and unless otherwise stated these heterocycles may for example carry one or more of the following substituents: OH, N02, CN, -OCHF2, -OCF3) -NH2, halogen, preferably fluorine or chlorine, Ci-Cio-alkyl, preferably Ci-Cs-alkyl, preferably Ci-C3-alkyl, most preferably methyl or ethyl, -0-Ci-C3-alkyl, preferably -O-methyl or-O-ethyl, -methyl-N-tetrahydro-oxazinyl, -COOH, -COO-Ci-C4-alkyl, preferably -COO-C(CH3)3 or-COOCH3, -CONH2, optionally substituted phenyl, optionally substituted heteroaryl, preferably optionally substituted pyridyl or pyrazinyl, -CONH-CrCio-alkyl, while this alkyl may itself optionally be substituted, optionally substituted -CONH-C3-C6-cycloalkyl, preferably optionally substituted -CONH-cyclopentyl, optionally substituted -CONH-heteroaryl, preferably optionally substituted -CONH-pyridyl, optionally substituted -CONH-aryl, preferably optionally substituted -CONH-phenyl, -CONMeCi-C3-alkyl, while this alkyl may itself optionally be substituted, preferably -CONMeCH2-pyridyl, benzimidazole or a group of formula 13 The term cycloalkyl groups denotes, for example, saturated or unsaturated cycloalkyl groups with 3-8 carbon atoms, for example cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl or cyclooctyl, preferably cyclopropyl, cyclopentyl or cyclohexyl, while each of the abovementioned cycloalkyl groups may optionally also carry one or more substituents, preferably =0, or may be annellated to a benzene ring. "=0" denotes an oxygen atom linked via a double bond.

The term heterocycloalkyl groups, unless otherwise described in the definitions, may denote 5-, 6- or 7-membered, saturated or unsaturated heterocycles, which may contain nitrogen, oxygen or sulphur as heteroatoms, for example tetrahydrofuran, tetrahydrofuranon, y-butyrolactone, a-pyran, y-pyran, dioxolane, tetrahydropyran, dioxane, dihydrothiophene, thiolan, dithiolan, pyrroline, pyrrolidine, pyrazoline, pyrazolidine, imidazoline, imidazolidine, tetrazole, piperidine, pyridazine, pyrimidine, pyrazine, piperazine, triazine, tetrazine, morpholine, thiomorpholine, diazepan, oxazine, tetrahydro-oxazinyl, isothiazole and pyrazolidine, preferably pyrazolyl, pyrrolidinyl, piperidinyl, piperazinyl or tetrahydro-oxazinyl, while the heterocycle may optionally be substituted.

Generally, the term halogen denotes fluorine, chlorine, bromine or iodine.

The leaving group L denotes either identical or different leaving groups such as for example chlorine, bromine, iodine, methanesulphonyl, trifluoromethanesulphonyl or p-toluenesulphonyl, preferably chlorine.

The compounds according to the invention may be present in the form of the individual optical isomers, mixtures of the individual enantiomers, diastereomers or 14 racemates, in the form of the tautomers and also in the form of the free bases or the corresponding acid addition salts with pharmacologically acceptable acids -such as for example acid addition salts with hydrohalic acids, for example hydrochloric or hydrobromic acid, or organic acids, such as for example oxalic, fumaric, diglycolic or methanesulphonic acid.

The substituent R1 may denote a group selected from among hydrogen, NH2, XH, preferably OH, halogen, preferably fluorine or chlorine and a CrC3-alkyl group optionally substituted by one or more, preferably one, two or three halogen atoms, preferably fluorine or chlorine, preferably methyl or ethyl. Most preferably, the substituent R1 is hydrogen .

The substituent R2 may denote a group selected from among hydrogen, CHO, XH, preferably OH, -X-CrC2-alkyl, preferably -O-CH3 or -O-CH2CH3, and an optionally substituted CrC3-alkyl group, while the alkyl group preferably consists of 1 to 2 carbon atoms, particularly preferably a carbon atom and may optionally be substituted, preferably by halogen atoms, most preferably by fluorine atoms. In particular, the substituent R2 denotes methyl.

The substituents R3 and R4 may be identical or different and may represent a group selected from among optionally substituted CrCio-alkyl, preferably C1-C6-alkyl, preferably Ci-C4-alkyl, most preferably methyl, ethyl or propyl, particularly preferably methyl or ethyl, C2-Cio-alkenyl, preferably ethenyl or propenyl, preferably ethenyl, C2-C-io-alkynyl, preferably ethynyl or propynyl, aryl, preferably optionally substituted phenyl, heteroaryl, C3-C8-cycloalkyl, preferably cyclopropyl and cyclobutyl, Cs-Cs-heterocycloalkyl, -X-aryl, -X-heteroaryl, -X-cycloalkyl, -X-heterocydoalkyl, -NR8-aryl, -NR8-heteroaryl, -NR8-cycloalkyl and -NR8-heterocycloalkyl, or a group selected from among hydrogen, halogen, COXR8, CON(R8)2, COR8 and XR8, preferably hydrogen, or the groups R3 and R4 may together denote a 2- to 5-membered alkyl bridge, preferably an ethylene, propylene or butylene bridge , while the propylene or butylene bridge may contain 1 to 2 heteroatoms, preferably oxygen , nitrogen or sulphur, most preferably an ethylene bridge .

Most preferably, the substituent R3 denotes methyl or ethyl. The substituent R4 most preferably denotes hydrogen or methyl. Particularly preferred are compounds wherein R3 and R4 represent methyl.

All the groups mentioned in the definition of R3 and R4 may optionally be substituted.

The group R5 may contain hydrogen or a group selected from among optionally substituted CrCio-alkyl, for example Ci-C6-alkyl-aryl or CrC6-alkyl-heteroaryl, preferably CrC6-alkyl, most preferably CrCs-alkyl, particularly preferably propyl, butyl, pentyl, hexyl, -CH2-cyclohexyl, (CH2)i-2cyclopropyl or (CH2)4-OCOCH3, C2-Cio-alkenyl, preferably propenyl, butenyl, pentenyl or hexenyl, preferably propenyl or hexenyl, C2-Cio-alkynyl, preferably propynyl, butynyl or pentynyl, preferably propynyl, aryl, preferably phenyl, heteroaryl, -C3-C6-cycloalkyl, preferably cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl and -C3-C6-cycloalkenyl, preferably cyclohexenyl or cyclopentenyl, or the substituents R3and R5or R4and R5 together denote a saturated or unsaturated C3-C4-alkyl bridge which may contain 1 to 2 heteroatoms, preferably oxygen, sulphur or nitrogen.

All the groups mentioned in the definition of R5 may optionally be substituted.

The substituent R6 may denote optionally substituted aryl, or heteroaryl, preferably aryl, preferably phenyl.

Most preferably, the substituent R6 denotes a phenyl group, which may be substituted by one of the groups R9 and R10 described hereinafter, while the phenyl ring may carry one of the groups R9, preferably in the para position, and one, two, three or four, preferably one or two, of the groups R10, preferably in the ortho or meta position.

The substituent R7 may denote hydrogen or -CO-X-CrC4-alkyl, preferably hydrogen. 16 X denotes, in each case independently of one another, O or S, preferably O.

The groups R8 mentioned in the definitions of the substituents R3 and R4 represent, independently of one another in each case, hydrogen or a group selected from among optionally substituted CrC4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl and phenyl, preferably hydrogen or Ci-C2-alkyl.

The substituent R9 may represent a group selected from among optionally substituted Ci-C6-alkyl, preferably Ci-C4-alkyI, preferably methyl, ethyl or propyl, most preferably methyl, C2-C6-alkenyl, C2-C6-alkynyl, -CONH-Ci-Cio-alkylene, preferably -CONH-CrC3-alkylene, preferably -CONH-CrC2-alkylene, -O-aryl, preferably 0-C6-Cio-aryl, most preferably O-phenyl, -O-heteroaryl, -O-cycloalkyl, preferably 0-C3-C6-cycloalkyl, most preferably O-cyclopropyl, -O-heterocycloalkyl, aryl, preferably C6-Cio-aryl, most preferably phenyl, heteroaryl, cycloalkyl, preferably C3-C6-cycloalkyl, most preferably cyclopropyl, and heterocycloalkyl, or a group selected from among -0-CrC6-alkyl-Q1, -CONR8-CrCio-alkyl-Q1, -CONR8-CrCio-alkenyl-Q1, -CONR8-Q2, halogen, for example fluorine, chlorine, bromine or iodine, OH, -S02R8, -S02N(R8)2, -COR8-COOR8,-N(R8)2, -NHCOR8, CONR8OCrCio-alkylQ1 and CONR8OQ2, where Q1 and Q2 are as hereinbefore defined.

Preferably, R9 denotes one of the following groups -CONH-CrCio-alkyl, preferably -CONH-Ci-C3-alkyl, most preferably -CONH-CrC2-alkyl, while this alkyl may itself optionally be substituted, by CN, optionally substituted aryl, preferably optionally substituted phenyl, heteroaryl, preferably thienyl, thiazolyl, imidazolyl, pyridyl, pyrimidyl or pyrazinyl, saturated or unsaturated heterocycloalkyl, preferably pyrazolyl, pyrrolidinyl, piperidinyl, piperazinyl or tetrahydro-oxazinyl, an amine group, preferably methylamine, benzylamine, phenylamine or heteroarylamine, saturated or unsaturated bicyclic ring systems, preferably benzimidazolyl and cycloalkyl, preferably cyclohexyl.

Moreover R9 preferably denotes -CONH-heteroaryl, preferably -CONH-pyridyl, -CONH-C3-Cio-cycloalkyl, preferably -CONH-cyclopropyl -CONH-cyclobutyl or 17 -CONH-cyclopentyl, most preferably -CONH-cyclopropyl; -CONH-C3-C10-heterocycloalkyl, -CONH-C6-Cio-aryl, preferably -CONH-phenyl, COO-C1-C3-alkyl, most preferably COOCH3, COOH, halogen, preferably F or chlorine, OH or a group of formula All the groups mentioned in the definition of R9 may optionally be substituted, preferably by one or more of the groups selected from among OH, OCH3, CI, F, CH3, COOH, CONHCH2Ph and CONHCH2-pyrazinyl-CH3.

The substituent R10 may be identical or different in each case and may denote a group selected from among optionally substituted CrC6-alkyl, preferably Ci-C3-alkyl, C2-C6-alkenyl, preferably C2-C3-alkenyl and C2-C6-alkynyl, preferably C2-C3-alkynyl, -0-Ci-C6-alkyl, preferably-0-Ci-C3-alkyl, -0-C2-C6-alkenyl, -0-C2-C6-alkynyl, C3-C6-heterocycloalkyl and C3-C6-cycloalkyl, or a group selected from among hydrogen, -CONH2, -COOR8, -OCON(R8)2, -N(R8)2, -NHCOR8, -NHCON(R8)2, -N02and halogen, for example fluorine, chlorine, bromine or iodine.

Preferably, the substituent R10 denotes hydrogen, methyl, methoxy, fluorine or chlorine, most preferably hydrogen or methoxy, particularly preferably methoxy.

Adjacent groups R9 and R10 may together denote a bridge of general formula O 18 wherein Y denotes O, S or NR11, preferably NR11, m denotes 0,1 or 2, preferably 1 , R11 denotes hydrogen or CrC2-alkyl, preferably hydrogen or methyl, most preferably hydrogen, R12 denotes hydrogen or a group selected from among optionally substituted phenyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, -Ci-C3-alkyl-phenyl, -CrC3-alkyl-10 pyridyl, -Ci-C3-alkyl-pyrazinyl, -Ci-C3-alkyl-pyrimidinyl and -Ci-C3-alkyl-pyridazinyl, preferably phenyl, pyridyl and pyrazinyl, and R13 denotes Ci-C6-alkyl, preferably methyl or ethyl.

The compounds according to the invention may be prepared by synthesis methods 15 A and B described hereinafter, while the substituents of general formulae (A1) to (A6) have the meanings given hereinbefore. These methods are to be understood as illustrations of the invention without restricting it to their subject matter.

Method A 20 Step 1A A compound of formula (A1) is reacted with a compound of formula (A2) to obtain a compound of formula (A3) (Diagram 1A). This reaction may be carried out according to WO 0043369 or WO 0043372. Compound (A1) is commercially obtainable, for example, from City Chemical LLC, 139 Allings Crossing Road, 25 West Haven, CT, 06516, USA. Compound (A2) may be prepared by procedures known from the literature: (a) F. Effenberger, U. Burkhart, J. Willfahrt LiebigsAnn. Chem. 1986, 314-333; b) T. Fukuyama, C.-K. Jow, M. Cheung, Tetrahedron Lett. 1995, 36, 6373-6374; c) R. K. Olsen, J. Org. Chem. 1970, 35, 1912-1915; d) F.E. Dutton, B.H. Byung Tetrahedron Lett. 1998, 30, 5313-5316; e) J. M. Ranajuhi, M. 30 M. Joullie Synth. Commun. 1996, 26,1379-1384.). 19 Diagram 1A o + HN R O rr R3 PR4 N^V^O" o R3 (A1) (A2) O (A3) In Step 1A, 1 equivalent of the compound (A1) and 1 to 1.5 equivalents, preferably 1.1 equivalents of a base, preferably potassium carbonate, potassium hydrogen carbonate, sodium carbonate or sodium hydrogen carbonate, calcium carbonate, most preferably potassium carbonate, are stirred in a diluent, for example acetone, aqueous acetone, tetrahydrofuran, diethylether or dioxane, preferably acetone or diethylether, most preferably acetone.

At a temperature of 0 to 15 °C, preferably 5 to 10 °C, 1 equivalent of an amino acid of formula (A2), dissolved in an organic solvent, for example acetone, tetrahydrofuran, diethylether or dioxane, preferably acetone, is added dropwise. The reaction mixture is heated to a temperature of 18°C to 30 °C, preferably about 22°C, with stirring and then stirred for a further 10 to 24 hours, preferably about 12 hours. Then the diluent is distilled off, the residue is combined with water and the mixture is extracted two to three times with an organic solvent, such as diethylether or ethyl acetate, preferably ethyl acetate. The combined organic extracts are dried and the solvent is distilled off. The residue (compound A3) may be used in Step 2 without any prior purification.

Step 2A The compound obtained in Step 1A (A3) is reduced at the nitro group and cyclised to form the compound of formula (A4) (Diagram 2A).

Diagram 2A R1 O R1 ]i A Rs ii J jLR4 CI^N^N' Reduction CI^N^N^V I i r1Jy0' R R & (A4) (A3) In Step 2A, 1 equivalent of the nitro compound (A3) is dissolved in an acid, 10 preferably glacial acetic acid, formic acid or hydrochloric acid, preferably glacial acetic acid, and heated to 50 to 70 °C, preferably about 60 °C. Then a reducing agent, for example zinc, tin or iron, preferably iron filings, is added to complete the exothermic reaction and the mixture is stirred for 0.2 to 2 hours, preferably 0.5 hours, at 100 to 125 °C, preferably at about 117 °C. After cooling to ambient 15 temperature the iron salt is filtered off and the solvent is distilled off. The residue is taken up in a solvent or mixture of solvents, for example ethyl acetate or dichloromethane/ methanol 9/1 and semisaturated NaCI solution, and filtered through kieselgur, for example. The organic phase is dried and evaporated down. The residue (compound (A4)) may be purified by chromatography or by 20 crystallisation or used as the crude product in Step 3A of the synthesis. 21 Step 3A The compound obtained in Step 2A (A4) may be reacted by electrophilic substitution as shown in Diagram 3A to obtain the compound of formula (A5). ,4 Diagram 3A R6 k (A4) (A5) In Step 3A 1 equivalent of the amide of formula (A4) is dissolved in an organic solvent, for example dimethylformamide or dimethylacetamide, preferably dimethylacetamide, and cooled to about -5 to 5 °C, preferably 0°C.

Then 0.9 to 1.3 equivalents of sodium hydride and 0.9 to 1.3 equivalents of alkyl halide, for example methyl iodide, are added. The reaction mixture is stirred for 0.1 - 3 hours, preferably about 1 hour, at about 0 to 10 °C, preferably at about 5 °C, and may optionally be left to stand for a further 12 hours at this temperature. The reaction mixture is evaporated down and extracted with water and an organic 15 solvent, preferably dichloromethane or ethyl acetate. The organic phases are evaporated down. The residue (compound (A5)) may be purified by chromatography, preferably over silica gel.

Step 4A The amination of the compound (A5) obtained in Step 3A to yield the compound of formula (A7) (Diagram 4A) may be carried out using the methods known from the literature of variants 4.1 A (a) M.P.V. Boarland, J.F.W. McOmie J. Chem. Soc. 1951,1218-1221; b) F. H. S. Curd, F. C. Rose J. Chem. Soc. 1946, 343-348., 4.2 25 A (a) Banks J. Am. Chem. Soc. 1944, 66,1131 b) Ghosh and Dolly J. Indian Chem. Soc. 1981, 58, 512-513. 22 Diagram 4A CI (A5) (A6) (A7) For example, in variant 4.1 A, 1 equivalent of the compound (A5) and 1 to 3 5 equivalents, preferably about 2 equivalents of the compound (A6) are heated without a solvent or in an organic solvent such as for example sulpholane, dimethylformamide, dimethylacetamide, toluene, N-methylpyrrolidone, dimethylsulphoxide or dioxane, preferably sulpholane, for 0.1 to 4 hours, preferably 1 hour, at 100 to 220 °C, preferably at about 160 °C. After cooling, the 10 product (A7) is crystallised by the addition of organic solvents or mixtures of solvents, e.g. diethylether/methanol, ethyl acetate, methylene chloride, or diethylether, preferably diethylether/methanol 9/1, or purified by chromatography.

For example, in variant 4.2 A , 1 equivalent of the compound (A5) and 1 to 3 15 equivalents of the compound (A6) are stirred with acid, for example 1-10 equivalents of 10-38% hydrochloric acid and/or an alcohol, for example ethanol, propanol, butanol, preferably ethanol, at reflux temperature for 1 to 48 hours, preferably about 5 hours.

The product precipitated (A7) is filtered off and optionally washed with water, dried 20 and crystallised from a suitable organic solvent.

If R6 denotes an optionally substituted benzimidazole, the preparation of the compounds (A6) using methods known from the literature may be carried out as shown in the following diagram, for example: 23 (Z1) (Z2) (Z4) Accordingly, for example, 33 mmol of the compound (Z1), 49 mmol of the compound (Z2) and 49 mmol of 1-ethoxycarbonyl-2-ethoxydihydroquinoline (EEDQ) are stirred into 50 ml of an organic solvent, preferably dimethylformamide, at about 100 to 130 °C, preferably at about 115 °C, 1 to 4 hours, preferably about 3 hours. Then the cooled reaction solution is added to 50 to 400 ml, preferably about 200 ml of a water/ethyl acetate mixture (mixing ratio about 1:1). The crystals formed (Z3) are suction filtered and washed.

Then 4.2 mmol of the compound (Z3) are stirred with 12.5 mmol of tin(ll)chloride and 30 mmol of potassium carbonate in about 50 ml of an organic diluent, preferably ethyl acetate, at about 22 °C for 4 to 48 hours, preferably about 24 hours. After the addition of 22 g of kieselgur the mixture is extracted with an organic diluent or mixture of diluents, preferably with a mixture of dichloromethane / methanol (9:1), the combined extracts are evaporated down and the precipitate formed (Z4) or the crystals produced (Z4) is or are isolated.

Step 5A If R9 denotes -CONR8-Ci-Cio-alkyl-Q1, -CONH-CrC5-alkylene or -CONR8-Q2, wherein the substituents have the meanings given hereinbefore, the compounds according to the invention may be prepared using methods known from the literature, for example as shown in Diagram 5A. * 24 The compound (A7^) obtained in Step 4A may be reacted either by saponification and subsequent amination to obtain the amide of general formula (A10) (Diagram (5A) variant 5.1 A), or by saponification, with subsequent conversion into the acid chloride (A9) and subsequent amination (Diagram (5A) variant 5.2A).

Diagram 5A J R9 Variant 5.1 A: In variant 5.1 A, for example, 20 mmol of the ester (A7') are heated in about 100 ml of a base, preferably 1N sodium hydroxide solution or lithium hydroxide solution and about 500 ml of an alcohol, for example with ethanol, dioxane or methanol, 15 preferably methanol, until the ester is completely reacted. Then the alcohol is distilled off. The residue is taken up in about 200 ml of water and acidified while cooling with acid, for example hydrochloric acid, preferably with 2 N hydrochloric acid. The product (A8) is filtered off and dried.

For example, about 0.5 mmol of the compound (A8) are dissolved with about 0.5 mmol of 0-benzotriazolyl-N,N,N',N'-tetramethyluronium tetrafluoroborate (TBTU) and about 1.4 mmol of diisopropylethylamine (DIPEA) in about 5 ml of an organic diluent, for example tetrahydrofuran, dimethylformamide, N-methylpyrrolidone, dimethylacetamide, preferably dimethylformamide. After the addition of about 0.75 mmol of an amine which forms the substituent R9, the reaction mixture is stirred for 0.1 to 24 hours, preferably about 12 hours at 20°C to 100°C. The product of formula (A10) is obtained for example by crystallisation or chromatographic purification.

Variant 5.2 A: In variant 5.2 A about 1 mmol of the acid (A8) for example is suspended in about 2.7 ml of thionyl chloride. The mixture is heated to 40°C to 80 °C, preferably about 50 °C, and at constant temperature 2 to 10 drops, preferably about 3 drops of 15 dimethylformamide are added to the reaction mixture with stirring. Then stirring is continued at 90°C until the reaction is complete. Excess thionyl chloride is distilled off. About 1 mmol of the acid chloride formed (A9) are dissolved in about 30 ml of an organic diluent, for example dichloromethane. After the addition of an amine which forms the substituent R9 the mixture is stirred at about 22°C. The precipitate 20 formed is filtered off and washed with water. The residue remaining is washed with an organic diluent, for example methanol. The mother liquor is purified, for example by chromatography, and evaporated down. The product (A10) remains.

Method B Alternatively to the methods described above, after Step 1A first the compound (A3) may be aminated and then the product (B1) may be cyclised to yield the compound (B2), as shown in Diagram B. Further substitution of the compound 30 (B2) to yield the compound (A7) may be carried out for example as in Step 3A. 26 Diagram B (A3) 27 The new compounds of general formula (I) may be synthesised analogously to the following examples of synthesis. These Examples are, however, intended only as examples of procedures to illustrate the invention further, without restricting the invention to their subject matter.

Example 63 and Example 109 : In order to synthesise the compounds 63 and 109 , first an intermediate compound 4 is prepared as described hereinafter. 38.9 ml (0.263 mol) of ethyl 2-bromobutyrate and 36.4 g (0.263 mol) of potassium carbonate were placed in 350 ml of ethyl acetate, and then 46.7 ml (0.402 mol) of isoamylamine, dissolved in 70 ml of ethyl acetate, were rapidly added dropwise. The mixture was refluxed for 20 h. The salt formed was filtered off, the filtrate was concentrated by evaporation, combined with 50 ml of toluene and again evaporated to dryness.

Yield: 54.3 g of a compound 1 (red oil) 54.3 g of compound 1, dissolved in 400 ml acetone, and 30.7 g (0.222 mol) of potassium carbonate were cooled to 8° C with stirring, combined with a solution of 43.1 g (0.222 mol) of 2,4-dichloro-5-nitropyrimidine in 250 ml acetone and then stirred for 24 h at RT. 4 28 The suspension formed was concentrated by evaporation, the residue was extracted with water and ethyl acetate, the organic phase was washed with water and NaCI solution, dried over MgS04 and evaporated to dryness.

Yield: 87.3 g of a compound 2 (brown oil) 44.1 g of compound 2 were dissolved in 800 ml glacial acetic acid and heated to 65°C and 36 g of iron filings were added batchwise. Then the mixture was stirred for 3 h at 70° C, the precipitate was filtered off and the filtrate was concentrated by evaporation.

The residue was applied to silica gel in dichloromethane / methanol 90:10, concentrated by evaporation and purified by column chromatography (eluant: ethyl acetate / cyclohexane 1:1).

The residue was precipitated from ethyl acetate / petroleum ether.

Yield: 16.1 g of a compound 3 (beige powder) 16.1 g of compound 3 were dissolved in 75 ml of dimethylacetamide and cooled to 5°C under a nitrogen atmosphere with stirring. Then 2.51 g (0.063 mol) of NaH, 60% dispersion in mineral oil, was added, whereupon the temperature temporarily rose to 16°C. After 30 minutes 3.94 ml (0.063 mol) of methyl iodide, dissolved in 20 75 ml dimethylacetamide, were added, and the mixture was stirred for 24 h at 22°C.

The solvent was concentrated by evaporation, combined with 200 ml of water and the precipitate formed was suction filtered, then extracted by stirring with petroleum ether.

Yield: 15.1 g of a compound 4 (yellow powder) 1H-NMR (250 MHz): = 7.80 (1H, s), 4.35 (m, 1H), 3.92 (m, 1H), 3.22 (s, 3H), 3.14 (m, 1H), 1.81 (m, 2H), 1.60-1.40 (m, 3H), 0.90 (m, 6H), 0.70 (t, 3H).

Synthesis of Example 63 2.5 g of compound 4,1.43 g of 4-amino-3-methoxybenzoic acid, 1.25 mL of conc. hydrochloric acid, 150 mL of dist. water and 37.5 mL of ethanol were refluxed for 10 h. The precipitate was filtered off, washed with water and extracted by stirring 29 in methanol. Then the precipitate was recrystallised using petroleum ether and ether.

Yield: 1.6 g of a compound 5 (white powder) 0.2 g of compound 5, 5 mL of benzylamine, 0.16 g of TBTU, 0.17 g of DIPEA were dissolved in 2 ml of dimethylformamide (DMF) and stirred for 48 h at ambient temperature. Then the reaction mixture was taken up in methylene chloride, washed with water and the organic phase was evaporated down. When petroleum ether/ethyl acetate 9:1 was added the product was precipitated in the form of light 10 beige crystals.

Yield: 0.18 g. Melting point: 178°C Synthesis of Example 109 : 5 g of 2 amino-5-nitroaniline, 6.03 g of 4-pyridylcarboxylic acid, 12.1 g of EEDQ are dissolved in 50 mL of DMF and stirred at 115°C for 1.75 h, then the DMF is distilled off in vacuo and the reaction mixture is then heated to 180°C for 1 h. The residue is taken up in 30 mL of DMF and combined with 200 mL of water and 100 mL of ethyl acetate. The crystal slurry obtained is filtered off and washed with 20 water, ethyl acetate and ether.

Yield: 5.8 g of a compound 6 2 g of the compound 6 is combined with 0.2 g of 5 % Pd/C in 30 mL of ethanol and hydrogenated in the presence of hydrogen. It is then evaporated down and 25 crystallised from ethanol and toluene.

Yield: 1.75 g of white powder of a compound 7. 0.2 g of the compound 5, 0.28 g of the compound 7, 0.001 g of sodium-tert. butoxide, 2.5 mL of ethyleneglycol dimethylether, 0.006 g of palladium(ll) acetate 30 and 0.22 g of 2-(di-tert.-butylphospino)biphenyl are dissolved in 1.5 mL of N-methylpyrrolidone (NMP). Then the mixture is heated to 160°C for 0.5 h. The reaction mixture is then purified over 20 g of silica gel and the product is crystallised from ether, ethyl acetate and petroleum ether.

Yield: 0.04 g of yellow crystals. Melting point: 180°C Example 218 . 58 and 4: In order to synthesise the compounds 218, 58 and 4, first an intermediate compound 11 is prepared as described hereinafter. 55.8 g of DL-alanine methyl ester x HCI were dissolved in 500 ml of methanol, then 76.1 ml of 30% sodium methoxide solution was added and the salt was filtered off. 37.8 g of trimethylacetaldehyde were added to the filtrate, then it was left to stand for 22 h. Then 9.5 g of 10% Pd/C was added and the mixture was hydrogenated for 3.1 h at 0.5 bar and 20° C. The reaction mixture was suction filtered through kieselgur and concentrated by evaporation. The residue was taken up in diethylether, the salts were filtered through kieselgur and the filtrate was concentrated by evaporation.

Yield: 55.8 g of a compound 8 (clear liquid) 48.5 g of 2,4-dichloro-5-nitropyrimidine were placed in 400 ml of diethylether, 41.0 g of potassium hydrogen carbonate in 400 ml of water were added, and the mixture was cooled to -5°C. 43.3 g of compound 8 were dissolved in 400 ml of diethylether and added dropwise at -5° C. The mixture was stirred for 1 h at -5°C and for 2 h at 0° C, then heated to ambient temperature and the reaction mixture was left to stand for 24 h. 31 The organic phase was separated off, dried over MgSC>4 and evaporated to dryness.

Yield: 79.2 g of a compound 9 (yellow resin) 79.0 g of compound 9 were dissolved in 1000 ml of glacial acetic acid and heated to 70°C. After the removal of the heat source 52 g of iron was added batchwise. The temperature rose to about 110° C and the mixture was stirred for 1 h at this temperature. The suspension was filtered while hot and the filtrate was concentrated by evaporation.

The residue was taken up in ethyl acetate and combined with 150 ml of conc. HCI, the organic phase was separated off and the aqueous phase extracted several times with dichloromethane. The combined organic phases were concentrated by evaporation, applied to silica gel and purified by column chromatography (eluant: petroleum ether/ethyl acetate 1:1).

As the isolated substance was still highly contaminated, it was again purified over silica gel. The desired compound crystallised out, the crystals were suction filtered. The mother liquor was concentrated by evaporation and recrystallised from ethyl acetate / diethylether.

Yield: 17.63 g of a compound 10 7.6 g of the compound 10 and 6.4 ml of methyl iodide were placed in 75 ml of dimethylacetamide (DMA) and cooled to -15°C. 1.25 g of NaH, 60% dispersion in mineral oil, was added batchwise, and stirred for 30 min. at -10° to -5° C. Then 150 ml of ice water were added, the crystals were suction filtered and washed with 25 water and petroleum ether. The crystals were taken up in dichloromethane, filtered through kieselgur and the filtrate was evaporated to dryness. It was recrystallised from petroleum ether.

Yield: 6.3 g of compound 11 (beige crystals) 1H-NMR (250 MHz): = 7.73 (1H, s), 4.35 (d, 1H), 4.25 (m, 1H), 3.35 (s, 3H), 2.55 30 (d, 1H), 1.31 (d, 3H), 0.95 (s, 9H). 32 Synthesis of Example 218 0.2 g of compound 11, 3,5-difluoro-4-hydroxyaniline and 0.75 mL of sulpholane were heated to 130°C for 15 min, to 140°C for 15 min and to 170°C for 10 min. 5 Then the mixture was combined with ether, the supernatant solution was decanted off and the residue was crystallised from methanol/ether and recrystallised again from methanol.

Yield: 0.15 g of white crystals. Melting point:>250°C Synthesis of Example 4 6.3 g of compound 11 were dissolved in 25 mL of sulpholane at 100°C, then combined with 4.0 g of ethyl 4-aminobenzoate and heated to 170°C for 1 h. Then the mixture was combined with 50 mL of ether. After crystallisation started, a further 50 mL of ether and 50 mL of methanol were added. The crystals were recrystallised from methanol.

Yield: 6.6 g of a compound 12 (yellowish crystals), melting point: from 65°C decomposition sets in 3.55 g of compound 12 were suspended in 250 mL of methanol and at 60°C combined with 25 mL of 4N sodium hydroxide solution. After 6 h, 15 mL of glacial acetic acid were added, the resulting crystals were filtered off and washed with methanol/ether.

Yield: 1.2 g of a compound 13 (white crystals) 1.5 g of compound 13 were dissolved in 7.5 mL of thionyl chloride and heated to 80°C for 1 h. Then the thionyl chloride was eliminated by distillation, the residue was stirred with ether, the crystals were suction filtered and washed with ether. Yield: 1.7 g of a compound 14 (yellow crystals) 0.18 g of 3-aminopyridine were dissolved in 10 mL of tetrahydrofuran (THF) and combined with 0.4 mL of triethylamine. Then 0.22 g of compound 14 were added and the mixture was stirred for 16h at ambient temperature. The mixture was 33 evaporated to dryness, taken up in ethyl acetate, extracted with water, evaporated down again and the product was crystallised from ethyl acetate.

Yield: 0.07 g (beige crystals), Melting point: 215-216°C Synthesis of Example 58 0.05 g of compound 13 were suspended in 10 mL of dichloromethane, then combined with 0.15 mL of DIPEA and 0.05 g of TBTU. The solution was then stirred for 30 min and combined with 0.01 mL of 4-picolylamine. After 18 h the mixture was combined with 20 mL of water, the organic phase was separated off 10 and the product was purified by silica gel chromatography, then recrystallised from ethyl acetate /petroleum ether.

Yield: 0.044 g (white crystals), Melting point: 238-240°C Examples 65 and 125 In order to synthesise the compounds 65 and 125, first an intermediate compound 18 is prepared as described hereinafter. 28.3 g of isobutylamine, 36 g of ethyl R,S-2-bromopropionate and 28 g of potassium carbonate were refluxed in 150 ml of ethyl acetate for 6 h.

After cooling the salt was suction filtered, the mother liquor was concentrated by 25 evaporation.

The residue was combined with 100 ml of toluene and evaporated to dryness. Yield: 37.2 g of a compound 15 (yellow oil) 34 38.4 g of 2)4-dichloro-5-nitropyrimidine were placed in 300 ml of diethylether, 30 g of potassium hydrogen carbonate in 300 ml of water were added and the mixture was cooled to 0° C. 37.0 g of compound 15 were dissolved in 300 ml of diethylether and added dropwise at 0°-3° C. After 3 h the phases were separated, 5 the organic phase was dried and evaporated to dryness.

Yield: 71.6 g of a compound 16 40.0 g of compound 16 were dissolved in 300 ml of glacial acetic acid and heated to 70°C. After removal of the heat source, 30 g of iron was added batchwise. The 10 temperature rose to 110°C. The reaction mixture was cooled to 90°C and stirred for 20 min. at this temperature. Then it was filtered while hot and the filtrate was concentrated by evaporation. The residue was stirred with 300 ml of water and 300 ml of dichloromethane and filtered through kieselgur. The phases were separated. The organic phase was washed with water, dried over MgSC>4 and 15 evaporated to dryness. It was extracted from petroleum ether.

Yield: 26.7 g of a compound 17 .0 g of compound 17 were placed in 100 ml of DMA, 4.13 ml of methyl iodide were added and the mixture was cooled to 5° C. 2.60 g of NaH were added 20 batchwise as a 60% dispersion in mineral oil. The temperature rose to 13°C. After 30 min. 300 ml of ice water were added, the crystals precipitated were suction filtered and washed with petroleum ether.

Yield: 13.9 g of a compound 18 1H-NMR (250 MHz): = 7.95 (1H, s), 4.30 (m, 1H), 3.95 (m, 1H), 3.24 (s, 3H), 2.95 25 (m, 1H), 2.05 (m, 1H), 1.30 (d, 3H), 0.96 (d, 3H), 0.92 (d, 3H).

Synthesis of Example 65 2.1 g of compound 18 were combined with ethyl 4-aminobenzoate in 10 mL sulpholane and stirred for 2 h at 160°C. Then ether was added and the crystals 30 precipitated were washed with ether: Yield: 3.0 g of a compound 19 3 g of the compound 19 were combined with 200 mL of methanol and 25 mL of 4N NaOH and stirred for 4 h at 60°C. Then glacial acetic acid was added, the crystals precipitated were filtered off and washed with ether.

Yield: 2.3 g of a compound 20 (white crystals) 0.1 g of compound 20 were suspended in 3 mL of dichloromethane and 3 mL of DMF, and then combined with 0.13 g of DIPEA, 0.095 g of TBTU and 0.045 g of hydroxybenzotriazole (HOBt). Then the solution was stirred for 30 min and combined with 0.035 g of N-methyl-3-picolylamine. After 0.5 h the mixture was 10 combined with water and 1 g of potassium carbonate, the aqueous phase was extracted twice with 50 mL of ethyl acetate and the product was purified by silica gel chromatography and then recrystallised from ethanol/acetone.

Yield: 0.08 g Synthesis of Example 125 3.7 g of compound 20, 3.8 g of TBTU, 1.6 g of HOBt, 5 mL of DIPEA were dissolved in 40 mL of DMF and stirred for 4 h at ambient temperature. The mixture was evaporated down, taken up in 200 mL of ethyl acetate and extracted twice 20 with 5 mL of 5% potassium carbonate solution. The organic phase was evaporated down, the crystals precipitated were filtered off and washed with ethyl acetate and ether.

Yield: 1.65 g of a compound 21 (yellowish crystals) 0.486 g of compound 21 were refluxed with 0.33 g of 1,2- phenylenediamine in 10 mL of toluene for 0.5 h, then the mixture was evaporated down. The residue was combined with 100 mL ethyl acetate, the organic phase was extracted twice with water. The organic phase was evaporated down, the crystals precipitated were suction filtered and washed with a little ethyl acetate.

Yield: 0.25 g of a compound 22 (white crystals) 36 0.22 g of compound 22 were stirred into 20 g of polyphosphoric acid for 0.5 h at 150°C, then the mixture was poured onto ice and ammonia was added. It was then extracted twice with 100 mL of ethyl acetate, the organic phase was washed with water and evaporated down. The precipitated product (crystals) was suction 5 filtered and washed with ethyl acetate and ether.

Yield: 0.115 g of yellowish crystals, Melting point: 287°C (decomposition) Example 171 In order to synthesise compound 171 first an intermediate compound 27 [sic] 34.4 g of N-isopentyl-benzylamine, 36.2 g of ethyl 2-bromo-propionate and 42.0 g of potassium carbonate were placed in 250 ml of DMF and stirred for 3 h at 110°C. After cooling the inorganic salts were filtered off, the filtrate was concentrated by evaporation. The residue was extracted with water and diethylether, the organic phase was washed with water, dried and evaporated to dryness.

Yield: 55.5 g of a compound 23 55.5 g of compound 23 were placed in 600 ml of ethanol, and hydrogenated with 25 20 ml of 32% HCI and 6 g of 10% Pd/C at 20°C under 5 bar for 20 min. Then it was filtered through kieselgur and concentrated by evaporation. The residue was combined with 400 ml of diethylether, the precipitate was suction filtered and washed with diethylether. 37 Yield: 23.5 g of a compound 24, melting point 105°C 23.5 g of compound 24 were dissolved in 200 ml of water and combined with 20.0 g (0.103 mol) of 2,4 -dichloro-5-nitropyrimidine in 400 ml of diethylether. After the reaction mixture had been cooled to -10° C , 50.0 g (0.499 mol) of potassium carbonate were added batchwise. The mixture was stirred at -5°C for 1 h and at 0°C for 1 h, then heated to ambient temperature. The aqueous phase was separated off, the organic phase was washed with water, dried and evaporated to dryness.

Yield: 36.9 g of a compound 25 .0 g of the compound 25 were dissolved in 280 ml of glacial acetic acid and heated to 70°C. After removal of the heat source 17 g of iron were added. The temperature rose to 100°C, then the mixture was stirred for 30 min. at this temperature.

It was then filtered while hot and the filtrate was concentrated by evaporation. The residue was combined with 300 ml of dichloromethane and 30 ml of 32% HCI, the phases were separated, the aqueous phase was extracted with dichloromethane, the combined organic phases were washed with water and aqueous ammonia solution, dried and evaporated to dryness. The residue was extracted with diethylether.

Yield: 10.5 g of a compound 26, melting point: 182°-185° C 2.7 g of the compound 26 and 2.5 ml of methyl iodide were placed in 27 ml of 25 DMA and cooled to -10° C. 0.45 g of NaH, 60% dispersion in mineral oil, was added and stirred for 30 min. at -5°C. Then 10 g of ice and 5 ml of 2N HCI were added and the mixture was concentrated by evaporation. The residue was extracted with ethyl acetate and water, the organic phase was dried, evaporated to dryness and filtered through silica gel.

Yield: 3.0 g of compound 27 (oil) 1H-NMR (250 MHz): = 7.67 (1H, s), 4.32-4.07 (m, 2H), 3.32 (s, 3H), 3.08 (m, 1H), 1.70-1.50 (m, 3H), 1.42 (d, 3H), 0.95 (m, 6H). 38 Synthesis of Example 171 0.28 g of compound 27, 0.9 mL of sulpholane and 0.22 g of p-aminobenzoic acid-benzylamide were stirred for 0.5 h at 170°C, then the mixture was combined with ether and the crystals were filtered off. The product was recrystallised from ethanol.

Yield: 0,15 g, melting point: 228-240°C (yellowish crystals) The compounds of formula (I) listed in Table 1 are obtained analogously to the process described above.

The abbreviations X2, X3, X4, X5 and X6 used in Table 1 in each case denote a link to a position in the general formula shown under Table 1 instead of the corresponding groups R2, R3, R4, R5 and R6.

Table 1 (Continued) 39 h f n^Y^Y° if ^ Ex. r2 r3 r4 config. r3 or r4 r5 r6 mp.[°C] 1 ¥■ ch3 h h rac.

CH3 X5 2 CH3 ch3 h rac. hjc^ch, •rVl 208 3 ch3 X. >u ch3 h rac.

V H3C^CH3 241 4 ? CH3 h,c. 3 ^ h rac.

CH, fW "Cu "X) N ch3 X.

^^°H3 H rac. h3c-^ch3 f cr^N 175 6 * ch3 HsC^ h r ^c^ch, ><5 O 190 7 * ch3 H rac. *5 "XX, "O N Table 1 (Continued) 40 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 8 CH3 X* Xj\ ch3 h rac. f "o 200 9 CH3 ><2 ^\^CH3 h rac. *5 h3c ^chj f o^Ni 0 168 CH3 ch3 h rac. v H3C-V-3 f ko 190 11 CH3 ch3 h rac. f CH3 £°* 12 ch3 /CH3 xr h rac.

^/CH3 XV CyV1 13 CH3 x>\ ch3 h rac.

F k/CH3 CH, O yvx Cr ^ N 145 14 ch3 X* ^\/CH3 h rac.

X5 ^yCH3 ch3 Table 1 (Continued) 41 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.rc] *■ CHj H,C.

H rac.

X5 55 16 CHs X* Xj^CH3 H rac. f Cr^N 6 250 17 CH3 X; Xb\/CH3 H rac.

\ H3C CH3 P i>c 0 204 18 CH3 X, X>\ CH3 H rac.

V f" """o 19 ? CHj H3C\y *3 H rac.

CH, (V *5 "TX. b CHj H3C^y *3 H R H3C^CH3 *5 XyO 221 21 X; Xs-^CH3 H rac. s.

H3C CH3 -^6 ct^N "o 172 Table 1 (Continued) 42 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.[°C] 22 CHs *2 X^CH, H rac.

X; ■x HjC CHj f" CT*N "o 221 23 fa Vs/CH, H rac. 24 * CHj H3C^y *3 H rac.

CH3 Y-o, ><5 X *r 210 * ch3 H,C. x, H R H3C^CH3 ^CH, 0 3 "ti n O 213 26 CH3 X* Xb^CHj H rac. x> ■x H3C CH3 v'°xJ) 188 27 ? CH, Xf^CH3 H rac.

X* ^C^N ci CH, 0 28 CH3 H S X, 0 29 ch3 X2 X3\^CH3 H rac.

V H3C^CH3 O^N 178 Table 1 (Continued) 43 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] CHj H R HsC^/CH, * ^Oy vjO 0 175 31 f ch3 H rac.

^/CHj * •jy </ 32 ch3 h rac.

HjC^CH, 221 33 CHj XJ\ chj H R * /CH, 0 3 O 124 34 ch, H3C. *3 h rac.

CHj Xs f^l O 136 CHj X* X^CHj H rac.

HjC^CHj ~b 162 36 CH3 X> X,\ CHj H rac.

HjC CH, cA 169 37 CH3 X, X,.

CHj H rac.

\ CT^N 219 Table 1 (Continued) 44 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[X] 38 CH3 ><2 ^^/CHj H rac.

V H3C^-CHj o^nhj 179 39 CH3 X, ^/CHj H rac.

V f or^N I °vch3 211 40 X2 Xrs.

CHj H rac. *s HsC^J CHj 41 * CHj H3C\ *3 H rac.

HaC^j *5 Xv 42 CH3 *3 H R H3C^CH3 ><5 q >? 100 43 * CHj h3c\y *3 H rac.

CH, (V °^r ch, 175 44 CHj X, ^CH3 H rac.

H3C CH3 *^6 o^nhj 203 Table 1 (Continued) 45 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 45 CH3 x.

X,\^CH3 H rac. <-Ax V-s 165 46 CH3 X,\/CH3 H rac.

H,(T^CH, (AN V) 47 chj X^CH, H rac.

Xs ayV^ 0 48 * CH, H3C\ H rac.

CH, fW yrQ* P * 49 ch3 H3C^y *3 H rac.

CH, **>< f^H, *5 "n A" 0 50 ch3 X* H rac.

H3c CH, I6 O<:?^NH2 212 51 * ch3 Xj-V. ch3 H S H3C^ch3 a"/7" 52 ch, X* ^ ch3 H rac.

H3C CH3 Table 1 (Continued) 46 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 53 ch3 h3cv H rac.

CH, rt *5 \j~0 p *»> 54 ch3 h3cx X, H rac. h3c^| Xs T)y ■I 55 CH3 X> CH, ^^CH, h rac.

V hjc^ch, 191 56 ch3 X* vs^ch, H rac. *6 9 "V 158 57 ch, X,\ chj H rac. k^ch3 chj t/XK 230 58 f" ch3 h3cv 3 x, H rac. h,c^| Xo b 59 chj H.C. 3 H R Xi o"013 0 125 Table 1 (Continued) 47 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.[°C] 60 ch3 h h rac. ch, f^ch, * 0 250 61 chs x* X,\ ch3 h rac. f k/ch3 ch3 f °°S3 62 ch3 x^-ch3 h rac. \ h3c' ch3 O i * 169 63 ch3 x* >^\/ch3 h rac.

V hjc chj (T^N "o 178 64 ch3 chj h rac. f ch, f 65 CH3 ch3 h rac. k^CH3 ch3 vn 66 * CH, )C\ ch, h R h3c^ch3 xi X) 0 225 Table 1 (Continued) 48 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.rc] 67 ch3 x* X,\ chj h rac. f hjc^j chj * 68 * ch3 H3C\w As h rac. ch, rW x> 69 x* xj\ ch3 h rac. x; chj 70 ch3 x* >U chj h rac. <r> f N 71 f2 ch3 «3<^y *3 h rac. ch, rt> * "xx, N=/ 72 ch3 x* W0"- h rac. *5 k^0". ch, X crNi S3 73 ch3 x* W0"- h rac. "l HjC CH3 cAN Table 1 (Continued) 49 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 74 CH3 H,C^CH, 9H, X, V N^J^N^O 167 75 ch3 H3CV. 3 ^Xj H rac.

?V H3C-^] *> *TX, nN T 76 CH, Xz X>\ CH, H rac.

Xs k^CH3 ch3 /a, 246 77 ch3 h3C.y *3 H rac. can, rW Xu "O.

N <p CH, 78 ch3 ><2 H rac. t H, ch3 </o. 172 79 <^3 H rac.

H3C^y CH, f CT^N So 170 80 CH3 ><2 rac.

V HjC^CH, Aa, H,C"° 222 81 CHj 'S*.

H rac.

HjC CHJ A H,C-V 187 Table 1 (Continued) 50 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 82 CH3 *2 CHj H rac. v H3C CH3 215 83 CH, *2 H3C^CH3 r i oi 199 84 CH* x, /CH-Xf 3 \\ CH3 rac. v HjC^CHj rvii H3C"0 H3C^° 127 85 f CHj h^y A3 H rac.

CH, fw- ty "xx 86 CHj x, X,\ CHj H rac.

CH, ** 169 87 CHj ><2 Xj\ CHj H rac.

CH, 0 u x\ 250 88 CHj x* xj\ CH3 H rac. v hsc^ % o^n a H,C ' 233 89 ch3 x, ^^/CHj H rac.

HjC^CHj 1> 160 Table 1 (Continued) 51 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.[°C] 90 ch3 x.

X,^ chj h rac. chj fvv 154 91 ch3 h,c. h rac. a1 xl* / oo 92 ch3 x,\/chj h rac. hjc^^chj * O'#5^N "0 93 f2 chj hj% h rac. ^c-^j x; xv .2) 94 f ch, h3% h R h3c^/ch3 x> /CHj o 3 0 95 chj x* wch3 h rac.

CHj f.

O^^N 150 96 ch, i 3 \ chj ch3 rac.

\ HjC CHj 0<#^NH2 300 97 chj h,c. 3 ^x, h rac. ch, rt x* "xv 4 243 Table 1 (Continued) 52 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 98 CH3 X»\ ^ CH, h rac. v hjc^ch, ca 209 99 C"3 x* ^/chj h rac. v hjctxh, * 182 100 ch3 /ch, 3 h rac. x> y0* 6 n 101 * ch, /ch, * h R ** 232 102 ch3 X.. ^ chj h rac. f chj f" x O f 103 *2 x,^ chj h rac. k^CH, chj 0 ftt"n ul f 104 *2 xr^/chj h rac. v hjc chj % 6 n 146 Table 1 (Continued) 53 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.rc] 105 ch3 x* X,\ chj h rac.

V ^0 H3C 209 106 chs *2 ch3 h rac. v a—0 286 107 ? CH3 /ch. 3 h rac.

^CH3 jy 6 108 ch3 /ch, xr^ 3 h R H3C^ch3 q 202 109 CH3 x* ^^-chj h rac.

V HJC CH, 4 \=N 180 110 CH3 x. ch3 h rac. \ ch, e/a. 111 $ chj h,c. 3 ^^x, h rac.

/S *5 o'CH* Ado 250 Table 1 (Continued) 54 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.[°C] 112 ch3 x* X,^ ch3 h rac.

V i_l p-^\~ch, h'c ch3 f" CT^N 113 f CHj xh3 3 h rac. y(X cS 114 ch3 X* *3 CHg blHj HjC^CH, O^N HjC'XHj 237 115 x* x3\^-ch3 h rac. *s \ h3c ch3 CAN 135 116 ch3 h rac. ch3 Y* xs 0 CH, 117 * ch3 A3 h rac. w* hac^s x* xy 118 ch, X* w0"- h rac. x* k^CH3 CH3 f Cr^N v Table 1 (Continued) 55 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 119 ch3 *2 xJ^chJ H rac. k^CH3 CH3 £ v=N 0 213 120 ch3 x* ^X/CHJ H rac. \ h3c ch3 ,N-\ - 0 198 121 ch3 xz x^ch, H rac.

V h3c^chj 4 ,N-\ H5C \ \D 122 ch3 x> ^\/CH3 H rac. hjc chJ cr^N 123 * CHj H3C— X, H rac.

CH3 O sO h3c" 124 * ch3 xr-^ch, H rac.

Xs 0 125 CH3 x* x,\ chj h rac. x* chj 287 Table 1 (Continued) 56 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 126 CH3 X* ^\/CH3 H rac.

V H3C^CH3 ,N~\ H3C \—N o 195 127 CH3 Xz CHj H rac. k/CHj CHj 6y 6 128 CHj H,C. 3 Xj H rac.

HaC^ X* 129 CHj X* ^CHj H rac. hc-TCti CHj Cr^N 247 130 CHa Xz H rac. k^CHj CHj A X 131 CH3 Xz X3—CHj CHj H,C^CH, °6 281 132 CH3 Xz >U CHj H rac. f CHj O'^NHj Table 1 (Continued) 57 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.rC] 133 ch3 x, CHj H rac. k/-CHs CHj r^i) kyj O"^NH2 134 ch3 xz x)\ CHj H rac. f ^0 208 135 $ CHj /CHj xf 3 H rac.

^/CH, ocr* <s 136 * CHj /CHj V 3 H R o 192 137 CHj /CHj xf * H rac.

^/CHj -a- 212 138 * CHj h3ck 3 ^ H rac.

F^O 139 CH3 X, H rac. k^CHj CHj Cx^~W Table 1 (Continued) 58 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 140 CH3 *2 xs\zch3 h rac. hjc ^chj $> N=\ 148 141 ch3 H3C\w *3 h rac. ^hj H3C^ *5 * CI 142 ch3 H3C\y h rac.

CH3 xs 0 a 143 CHj x* x3v. ch3 h rac. v h3C^ v.

X HjC 186 144 chj ><2 x,/\ X4 HjCT^CH, f v anx0 199 145 CHa xz chj h rac. •v c«3 214 146 CH3 *2 chj h rac. f 0 y^~) 155 Table 1 (Continued) 59 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 147 CH3 x> X,\/CHj H rac.

\ CH, f" O^N ~o 148 * CHj H rac.

CH, xs "toyh O 149 CHj H rac.

^/CH» xi 245 150 ch3 ><2 X,\ CHj H rac. f chj & & 151 CHj x* *3\ CHj H rac. v HjG CHJ cr n ^ch, 152 CHj x* xj\ CHj H rac. hJc chJ 0 f)x" ul F 153 * CHj /CH, 3 H rac. ^/chJ H,N. M XXf 154 CH3 x* CHj H rac. v 1 Table 1 (Continued) 60 Ex.

R2 R3 R4 config. R3 or R4 R® R6 mp.[°C] 155 f2 CHj H3C\y H rac.

CH, i^CHj I CHj 3 *5 "cv "a 156 ch3 X,\/CH3 H rac.

CHj y—f ^S—,* cf " 265 157 cho Xz Xi\ CH3 H rac.

J lo CHJ 192 158 cha Xz Xj\ CHj H rac. \ 0 xxx 0 * N 222 159 ch3 Xz CHj H rac. v HjC CHj rvx a 221 160 * CHj ^CHj hA^CH, NH, 298 161 <fhj Xz CHj H rac. v I4 Cr"H o 181 162 * chj chj h s HA^CH, * ^CH3 O 3 ,N. X. X, yy n. » O Table 1 (Continued) 61 Ex.

R2 R3 R4 config. R3 or R4 R® R6 mp.[°C] 163 ch3 x* hjc chj % ^X 172 164 ch* *2 ^chj h rac. t kc^ch, CH o<!^N >cch> ch, * 227 165 ch3 ><2 x)\ chj h rac. h3c' ch3 X^XK r,c n oh 258 166 ch3 x* ch3 x, chj kjc chj 0 x hjc oij 266 167 chj h rac. o^^nh, 168 ch3 x* ^chj \\ chj rac. v hjc^ch, 0 159 169 ch3 x* hjc chj o-o 0>~ca 250 Table 1 (Continued) 62 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 170 CH3 CH, H rac. *> S, 213 171 CH3 *2 CHj H rac.

V O 228 172 *2 Xj\ CHj H rac.

J X, /vVS k^CH, 181 173 *2 V CHj H rac.

V \ 182 174 CHj *3 H rac. tk HaC^ * 175 CHa ^^CHj H rac.

„,Jych' CHj * O^N 197 176 * CH, HjC. 3 Xx, H rac.

'Oh H,C^| *5 "(V *0 Table 1 (Continued) 63 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.rc] 177 ch3 x. h rac. ch, N 216 178 ch3 x> X,\ ch3 h rac. f Cr^N "0 200 179 ch3 x* ^CH, h rac.

J O'^N/N^S\ hj 197 180 ch3 X.. ch, rac. \ 0 f] T* N HjC^° 143 181 ch3 x* x4— v HjC CHJ T3 f $ 234 182 r chj •vs h rac. hsc^J x* *oy £ NH, 183 cha x* h rac.

V f °v x> 169 Table 1 (Continued) 64 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.rC] 184 * ch3 HsC^y As h rac.

CHj uYn^aq o 185 ch3 X* *3\ chj h rac. v) 9 •v 198 186 ch, X, H.C^CH, ri H3CX 3 XN ^O 202 187 ch3 X, >U chj h rac. v * 200 188 ch3 xj\ chj h rac. v "\a 189 CH* X* Xs\ chj h rac. </ 198 190 CH. X* x4-— v HjC CHj CH, X si H.N^O 196 Table 1 (Continued) 65 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.rC] 191 ch3 X* CH3 \ ch, 1 1" b 253 192 * ch3 hsc\^x) h rac. xv y 193 ch, X> Xs\ chj h rac. <r> 0' H3C>=n 201 194 ch3 X* X^CHj h rac. a °~h SN>=0 250 195 ch3 X, X,\ CHj h rac.

J * F 198 196 X, ^ch, h rac.

J !* Cr^H 245 197 * chj h rac. ^/ch3 Xs ur £ Table 1 (Continued) 66 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.[°C] 198 * ch3 h,c. 3 Xj h rac. h3c^| x* xv 2nf 199 CH, ch, h rac.

V f 200 <*3 X* xi-ch, \ ch, H.C^CH, o ¥ 198 201 ch, h h rac. o *J¥ 202 * ch, HjC^ * x, h rac. >5 "^v 0 203 ch, X* ch, h rac.

X; I* ° "^9 O—Olj 198 204 $ ch, h3c^\^ h rac. *s xu.

N. 0 Table 1 (Continued) 67 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.[°C] 205 CHj H,C.

H rac. x> "tv a 206 fr CHj H,C.

H rac. 0^*3 xv "to 207 xj\ CHj H rac.

J * ji r* -^xi 184 208 CHj .CH, xf^ 3 H rac. * 0 . . \ / ^ 253 209 CH3 X*\/CHj H rac.

^CH, 0 * 240 210 f CHj H,C^ 3 ^X, H rac.

|^F F^"F 211 ch3 ><2 CHj \ CHj CH. 266 Table 1 (Continued) 68 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 212 fHs ^\/CH3 H rac. a 213 ?Hs Xj\ ch3 H rac.

X v CHj 6v 6 214 ?H3 ><2 ^ ch3 H rac. f Sy^OW 215 ?H3 X* CHj H rac. <o "xi, 232 216 CH* H rac. k/CH3 CHj 6v 6 217 * ch3 '*S H rac.

H»C^| * xv F^S 218 CH3 H rac.

CH, F >250 Table 1 (Continued) 69 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 219 CH3 *2 H3C^ x, H rac.

H3C CH, "a 260 (Zers.) 220 ch3 H3C\ X, h R HjCv^-CH, X. q^CH3 xy NHj 190 221 * ch3 H3C\ X, h R HJCVXH, "cv nh2 228 222 * CH, H3C\ X, h R ^CyCH, NH, 223 CH3 h R y HjC CH, f fj^ K,N^^O 243 224 ch3 X* h R HjC CHJ ;-p^ O—O 258 225 * ch3 H3C^ X, H R HJO/CK, 'oc^nh, 0 226 * ch3 H3C\ 3 x. h R HjO/CHJ x> CH, 0 Table 1 (Continued) 70 Ex.

R2 R3 R4 config. R3 or R4 Rs R6 mp.rc] 227 ch3 a3 h R CH, * 0^ *ys 0 241 228 * ch3 H3C\ 3 x, h R CH, f^CH, * xy* 0 229 CH, H3C^ 3 X, H R f o^NH, 300 230 ch3 X, H3C\ 3 X, H R X; jl h3c^^ch3 O^NH2 200 231 ch3 x, x,\ZCH3 h R jl h3c^-ch3 f8 O^NH2 232 232 ch3 h R x; jl h3c^~ch3 "^6 O^NH, 149 234 x, H3C^ 3 *3 h R £ cn3 x ¥ H2N'^O 197 235 CH3 h3c\ 3 X, h R 6 f HjN'^O 226 Table 1 (Continued) 71 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp[°C] 236 CH3 Xz H3C^ 3 *3 H R O—O 182 237 CH3 *2 H3Cv. 3 X, H R I O^^NHj 238 CH3 Xz Xs^/CHj H R 6 f 239 fa Xz H R 6 HjN^O 240 fa Xz H3C\y *3 H R 6 HjN^^O 241 CH3 h3C\ 3 X, H R 6 O—O J= 194 242 ch3 X* H3C\y *3 H R I f O^^NHj 200 243 ch3 Xz H3C^ 3 X3 H R \ HjC' CH, H3C 156 Table 1 (Continued) 72 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.[°C] 244 CHs H R / HjC CHJ •v 195 245 CH3 X,\^ch3 H R H3C'^CHj .0 147 246 * ch3 H3C\y H R ".CyCH, CH, 247 CH3 X! H3C\ *3 H R X; Jr H3C CH3 T> J V oAj. <> 85 248 f2 ch3 H3C\ *3 H R l"3 f^CH, ** 0 249 ch3 Xz H3C\y *3 H R V- 6^ O^N <i> 250 ch3 X! H3C-. 3 X, H R Jt H3C ch3 f1 ^2> 158 251 CH3 X. *3 H R 6 CH, S v coc 188 Table 1 (Continued) 73 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.[°C] 252 ch3 ><2 h3c\ x.

H R 6 f a,X 245 253 ch3 xz h3cv.

X, H R 1 f I 254 CH3 h3c\y H R X ct^n 128 255 CH3 xz h3c\ x.

H R 1 6r°^ o^n 256 CH3 xz Xj^/CH, H R JL H3C CHj x, 181 257 CH, xz Xj^/CH, H R JL H3C CH, cAn 217 258 ch3 xz h3c^ 3 x, H R 6 *-16 259 ch3 xz h3c\y *3 H R 6 cn, * V o^n <6 Table 1 (Continued) 74 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 260 fa x* h3c^ 3 x, h R 6 I" <6 261 ch3 H3C\ X, h R "A^CH, x* xi/ 0 230 262 ch3 h3c\y *3 h R "A^CH, x> ^CH, 0 3 ^vv 193 263 chj H3C\ 3 X, h R O 264 ch3 Xz xJ-^/chJ h R <AN A 152 265 ch3 x^-ch3 h R HjC^CHJ f" CT^Tjl A 207 266 chj h3c\y *3 h R 229 267 * chj ^Y *3 h R x, ch3 Table 1 (Continued) 75 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 268 ch3 h3c\y a3 h R h,c ch, ch, x, o^n 183 269 * ch3 h3cv. 3 x, H R CH. f^ch, * /> 270 * ch3 h3c^ 3 x H R CH, ^cJ * 161 271 ch3 Xz H3C^ 3 x, h R h,c^-ch3 x. 282 272 *2 x^^/ch, h R jl h3cch, 0 157 273 ch, Xz h R h,c^-ch, x. i 129 274 ch3 Xz h3°v.y *3 H R 6 ch, x, i 3 ? V 164 275 ch3 Xz h3c\y *3 h R 6 f n o 219 Table 1 (Continued) 76 Ex.

R2 R® R4 config. R3 or R4 R5 R6 mp.rc] 276 ch3 H3C^ 3 *3 H R I A 277 X* H3Cv X, H R £ % * i. 200 278 ch3 X* H3C\ 3 X3 H R <?> f" O^N 200 279 ch3 X* H3C\ X, H R 1 Ar°^ O^N A 280 X* ^\^CH3 H R 6 W'°T^ hAo A 281 CHa *2 Xr^/C^ H R f N""^0 A 282 ch3 x> H3C\ X, H R 6 ■"A ^nX) 283 ch3 H3C\ X, H R ?; CH, 277 Table 1 (Continued) 77 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 284 ch3 h3c\ 3 *3 H R 6 \ V O^N a 197 285 ch3 ><2 H3CNy *3 H R 6 a 286 ch3 ^3CSy *3 H R HjC CHj h3C° 182 287 * CHj H3C\y *3 H R HP CH, 0^ xv X^fNLJ H,C CH3 288 ch3 V^/CHj H R I HjC CHj /k, /CH, o n 3 163 289 ch3 Xrv ^CHj H R HJC'^CHJ f 212 290 * CHj H3C\ 3 x, H R HjC^CHJ X, <fh, O 291 CHj h3c\y As H R V* *=4h3 o^ljl chj Table 1 (Continued) 78 Ex.

R2 R3 R4 config. R3orR4 R5 R6 mp.[°C] 292 ch3 H3C\ 3 X, H R f^CH, *5 0 293 ch3 Xz H3C\ X, h R jl h3c chj -c'0^ 0 N CH3 200 294 ch3 Xz Xj\^CH3 H R hjc ch3 l" hrt, 144 295 ch3 Xz H3C\y A3 h R 6 "X O O-O 221 296 CH3 Xz H3C\ X, H R --CM / X 150 297 ch3 Xz H3C\y *3 H R A !* 298 CH. Xz Xs\^CH3 H R hjc-^chj f* "^xjj k 163 299 ch3 Xz H3C\ 3 X, h R <*> f* * V O^N CH, Table 1 (Continued) 79 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 300 ch3 x, a3 H R £ f CH, 98 301 ch. ** h3c\y ^3 H R i cjw O^-N 302 ch3 x! H R 6 f* k° 303 ch3 H R o 304 ch3 h3c\y a3 H R 6 "■6 |vsa> 305 ch3 x* h3c\y a3 H R 6 Or^N CH, 306 ch3 H.C. ^ x3 H R 6 T* f o^n CHj 307 ch3 H3C^ 3 x, H R HjC CHj ch3 0 h3c^ 179 Table 1 (Continued) 80 Ex.

R2 R3 R4 config. R3 or R4 Rs R6 mp.[°C] 308 CH3 h R hjct^ch, o^n h3c^chs 174 309 ch3 ^^-ch3 h R HjCT^CH, is ty^ch, 231 310 CH. ><2 h3c\ 3 x, h R h3c chj % ct^n 311 ch3 h3c\ 3 x, h R x, O HjC 312 k h3c\y h R <*3 hjc-^ f^chj *tVv 313 ch3 h3c\ 3 x, h R V- ">c\ ir0^ cAn 314 ch3 x* xb^/chj h R jL !w=v/-/ "j_h * 0 \> x 69 315 ch. x* H3C\ x3 h r JL l» 9 V-v 200 Table 1 (Continued) 81 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.[°C] 316 ch3 *2 H3C\ x, H R ch, x 1 3 ? H;x> 210 317 ch3 x, H3C\ H R f ha hjc—/v 1 n o 131 318 ch3 x* "sg^y *3 H R A i5, O^N HjC^CH, 319 ch3 x* h3c\y *3 H R <*> i" HjC^ 145 320 ch3 x> h3c\y ^3 H R £ /°"3 1 321 ch3 x* H3C^y *3 H R I Ar0"1 CaN H,C 'CM, 322 ch3 x> ^^chj H R jl & ° a H.C CHj 149 323 CHj x, XS^/CH3 H R 6 * N"^0 HjC^CHJ Table 1 (Continued) 82 Ex. r2 r3 r4 config. r3orr4 r® r6 mp.rc] 324 ch3 ^^chj h r 6 N^O HjC^CHj 325 ch3 ><2 H3C\ X, h r 6 h3C3\x 3 N^^O 326 ch3 x.

H3C\y h r 6 O—O 327 ch3 H3C^y *3 h r 6 f. 0 i H,C CHj 328 * chj H3C\y *3 h r H.C^/CH, X. v^l ^ ^\--n ch,' 0 176 329 * chj H3C\y A3 h r VyeH, x.

^CH, 0 3 0H3C CH, 330 chj H3CV.y *3 h r HCyOi, X, 0h3c chj 331 chj ><2 x.^chj h r / HjC CHj f3 f X>c Table 1 (Continued) 83 Ex.

R2 R3 R4 config. R3 or R4 R5 R6 mp.rC] 332 ch3 ><2 V^CH, H R I CH3 333 ¥■ ch3 H3C\W *3 H R * CH3 ^yy° 0 HJC 334 ch3 Xj CHj CH3 1 % O^N CH. 250 335 ch3 X2 >^—CHj CHj tyrTH, f1 Ci^N A 236 I In the preceding Table the abbreviations X1 to X6 in the groups specified denote the bond which links the particular group to the corresponding group R1 to R6. 84 As has been found, the compounds of general formula (I) are characterised by their wide range of applications in the therapeutic field. Particular mention should be made of those applications in which the inhibition of specific cell cycle kinases, particularly the inhibiting effect on the proliferation of cultivated human tumour cells 5 but also the proliferation of other cells, such as endothelial cells, for example, plays a part.

As could be demonstrated by FACS analysis, the inhibition of proliferation brought about by the compounds according to the invention is mediated by the arrest of the 10 cells, particularly at the G2/M phase of the cell cycle. The cells arrest, independently of the cells used, for a specific length of time in this phase of the cell cycle before programmed cell death is initiated. An arrest in the G2/M phase of the cell cycle is ^ triggered, for example, by the inhibition of specific cell cycle kinases. Studies in model organisms such as Schizosaccharomyces pombe or Xenopus, or 15 investigations in human cells have shown that the transition from the G2 phase to mitosis is regulated by the CDK1/cyclin B kinase (Nurse, 1990). This kinase, which is also known as the "mitosis promoting factor" (MPF), phosphorylates and thereby regulates a number of proteins, such as e.g. nuclear lamins, kinesin-like motor proteins, condensins and Golgi matrix proteins, which play an important part in the 20 breakdown of the nuclear envelope, in centrosome separation, the formation of the mitotic spindle apparatus, chromosome condensation and the breakdown of the Golgi apparatus (Nigg. E., 2001). A murine cell line with a temperature-sensitive CDK1 kinase mutant shows a rapid breakdown of the CDK1 kinase and a subsequent arrest in the G2/M phase after a temperature increase (Th'ng et al., 25 1990). The treatment of human tumour cells with inhibitors against CDK1/cyclin B such as e.g. butyrolactone also leads to an arrest in the G2/M phase and subsequent apoptosis (Nishio, et al. 1996). Another kinase which is involved in the G2 and mitosis phase is polo-like kinase 1 (Plk1), which is responsible for the maturation of the centrosomes, for the activation of the phosphatase Cdc25C, as well as for the 30 activation of the anaphase promoting complex (Glover et al., 1998, Qian, et al., 2001). The injection of Plk1 antibodies leads to a G2 arrest in untransformed cells whereas tumour cells arrest in the mitosis phase (Lane and Nigg, 1996). In addition, the protein kinase aurora B has been described as having an essential function during entry into mitosis. Aurora B phosphorylates histone H3 at Ser11 and thereby 85 initiates chromosome condensation (Hsu, J.Y. et al., 2000). A specific cell cycle arrest in the G2/M phase may, however, also be triggered e.g. by the inhibition of specific phosphatases such as e.g. Cdc25C (Russell and Nurse, 1986). Yeasts with a defective cdc25 gene arrest in the G2 phase, while overexpression of cdc25 leads to early entry into the mitosis phase (Russell and Nurse, 1987). However, an arrest in the G2/M phase can also be triggered by the inhibition of certain motor proteins, so-capped kinesins such as e.g. Eg5 (Mayer et al., 1999), or by agents which stabilise or destabilise microtubules (e.g. colchicin, taxol, etoposide, vinblastin, vincristin) (Schiff and Horwitz, 1980).

In view of their biological properties the compounds of general formula I according to the invention, their isomers and their physiologically acceptable salts are suitable for " the treatment of diseases characterised by excessive or abnormal cell proliferation.

Such diseases include, for example: viral infections (e.g. HIV and Kaposi's sarcoma); inflammatory and autoimmune diseases (e.g. colitis, arthritis, Alzheimer's disease, glomerulonephritis and wound healing); bacterial, fungal and/or parasitic infections; leukaemias, lymphoma and solid tumours; skin diseases (e.g. psoriasis); bone diseases; cardiovascular diseases (e.g. restenosis and hypertrophy). They are also 20 suitable for protecting proliferating cells (e.g. hair, intestinal, blood and progenitor cells) from damage to their DNA caused by radiation, UV treatment and/or cytostatic treatment (Davis et al., 2001).

The new compounds may be used for the prevention, short-term or long-term treatment of the abovementioned diseases, also in combination with other active 25 substances used for the same indications, e.g. cytostatics.

The activity of the compounds according to the invention was determined in the cytotoxicity test on cultivated human tumour cells and/or in a FACS analysis, for example on HeLaS3 cells. In both test methods, the compounds exhibited a good to 30 very good activity, i.e. for example an EC50 value in the HeLaS3 cytotoxicity test of less than 5 pmol, generally less than 1 pmol.

Measurement of cytotoxicity on cultivated human tumour cells To measure the cytotoxicity on cultivated human tumour cells, cells of the cervical cancer tumour cell line HeLaS3 (obtained from American Type Culture Collection 86 (ATCC)) in Ham's F12 Medium (Life Technologies) and 10% foetal calf serum (Life Technologies) were cultivated and harvested in the logarithmic growth phase. Then the HeLaS3 cells were placed in 96-well plates (Costar) at a density of 1000 cells per well and incubated overnight in an incubator (at 37°C and 5 % CO2), while on each 5 plate 6 wells were filled only with medium (3 wells as a control of the medium, 3 wells for incubation with reduced AlamarBlue). The active substances were added to the cells in various concentrations (dissolved in DMSO; final concentration: 1%) (in each case as a triple measurement). After 72 hours' incubation, 20 pi of AlamarBlue (AccuMed International) were added to each well, and the cells were incubated for a 10 further 7 hours. As a control, 20 pi of reduced Alamar Blue (AlamarBlue reagent which had been autoclaved for 30 min) were added to 3 wells. After 7 h incubation the colour change of the AlamarBlue reagent in the individual wells was determined " in a Perkin Elmer fluorescence spectrophotometer (excitation 530 nm, emission 590 nm, slits 15, integrate time 0.1). The amount of AlamarBlue reagent reacted 15 represents the metabolic activity of the cells. The relative cell activity was calculated as a percentage of the control (HeLa S3 cells without inhibitor) and the active substance concentration which inhibits the cell activity by 50% (IC50) was obtained. The values were calculated from the average of three individual measurements, correcting for the control value (medium control).

FACS Analysis Propidium iodide (PI) binds stoichiometrically to double-stranded DNA, and is thus suitable for determining the percentage of cells in the G1, S and G2/M phase of the cell cycle on the basis of the cell DNA content. Cells in the GO and G1 phase have a 25 diploid DNA content (2N), whereas cells in G2 or mitosis have a 4N DNA content. For PI staining, 0.4 million HeLaS3 cells were seeded, for example, on a 75 cm2 cell culture flask, and after 24 h either 1 % DMSO was added as control or the substance was added in various concentrations (in 1 % DMSO). The cells were incubated for 24 h with the substance or with DMSO, before the cells were washed with 2 x PBS and 30 detached with trypsin /EDTA. The cells were centrifuged (1000 rpm, 5 min, 4°C), and the cell pellet was washed 2 x with PBS, before the cells were resuspended in 0.1 ml of PBS. Then the cells were fixed with 80% ethanol for 16 hours at 4°C or alternatively for 2 hours at -20°C. The fixed cells (106 cells) were centrifuged (1000 rpm, 5 min, 4°C), washed with PBS and then centrifuged again . The cell pellet was 87 resuspended in 2 ml of Triton X-100 in 0.25 % PBS, and incubated for 5 min on ice, before 5 ml of PBS were added and the mixture was centrifuged again. The cell pellet was resuspended in 350 pi of PI stain solution (0.1 mg/ml of Raze A, 10 pg/ml of presidium iodide in 1 x PBS). The cells were incubated for 20 min in the dark with 5 the stain buffer before being transferred into sample measuring vessels for the FACS scan. The DNA measurement was carried out in a Becton Dickinson FACS Analyzer, with an argon laser (500 mW, emission 488 nm), and the DNA Cell Quest Program (BD). The logarithmic PI fluorescence was determined with a band-pass filter (BP 585/42). The cell populations in the individual phases of the cell cycle were quantified 10 with the ModFit LT program of Becton Dickinson.

The compounds of general formula (I) may be used on their own or combined with other active substances according to the invention, optionally also in conjunction with 15 other pharmacologically active substances. Suitable preparations include for example tablets, capsules, suppositories, solutions, particularly solutions for injection (s.c., i.v., i.m.) and infusion, syrups, emulsions or dispersible powders. The amount of pharmaceutically active compound in each case should be in the range from 0.1 - 90 wt.%, preferably 0.5 - 50 wt.% of the total composition, i.e. in amounts which are 20 sufficient to achieve the dosage range given below. The doses specified may, if necessary, be given several times a day.

Suitable tablets may be obtained, for example, by mixing the active substance(s) with known excipients, for example inert diluents such as calcium carbonate, calcium 25 phosphate or lactose, disintegrants such as corn starch or alginic acid, binders such as starch or gelatine, lubricants such as magnesium stearate or talc and/or agents for delaying release, such as carboxymethyl cellulose, cellulose acetate phthalate, or polyvinyl acetate. The tablets may also comprise several layers.

Coated tablets may be prepared accordingly by coating cores produced analogously to the tablets with substances normally used for tablet coatings, for example collidone or shellac, gum arabic, talc, titanium dioxide or sugar. To achieve delayed release or prevent incompatibilities the core may also consist of a number of layers. Similarly the tablet coating may consist of a number of layers to achieve delayed 35 release, possibly using the excipients mentioned above for the tablets. 88 Syrups or elixirs containing the active substances or combinations thereof according to the invention may additionally contain a sweetener such as saccharin, cyclamate, glycerol or sugar and a flavour enhancer, e.g. a flavouring such as vanillin or orange 5 extract. They may also contain suspension adjuvants or thickeners such as sodium carboxymethyl cellulose, wetting agents such as, for example, condensation products of fatty alcohols with ethylene oxide, or preservatives such as p-hydroxybenzoates.

Solutions for injection and infusion are prepared in the usual way, e.g. with the 10 addition of preservatives such as p-hydroxybenzoates, or stabilisers such as alkali metal salts of ethylenediamine tetraacetic acid, optionally using emulsifiers and/or dispersants, while if water is used as the diluent organic solvents may optionally be ) used as solubilisers or auxiliary solvents, and transferred into injection vials or ampoules or infusion bottles.

Capsules containing one or more active substances or combinations of active substances may for example be prepared by mixing the active substances with inert carriers such as lactose or sorbitol and packing them into gelatine capsules.

Suitable suppositories may be made for example by mixing with carriers provided for this purpose, such as neutral fats or polyethyleneglycol or the derivatives thereof.

Suitable excipients may be, for example, water, pharmaceutically acceptable organic solvents, such as paraffins (e.g. petroleum fractions), oils of vegetable origin 25 (e.g. groundnut or sesame oil), mono- or polyfunctional alcohols (e.g. ethanol or glycerol), carriers such as e.g. natural mineral powders (e.g. kaolin, clays, talc, chalk), synthetic mineral powders (e.g. highly dispersed silica and silicates), sugar (e.g. glucose, lactose and dextrose), emulsifiers (e.g. lignin, spent sulphite liquors, methylcellulose, starch and polyvinylpyrrolidone) and lubricants (e.g. magnesium 30 stearate, talc, stearic acid and sodium lauryl sulphate).

The preparations are administered in the usual way, preferably by oral or transdermal route, particularly preferably by oral route. When administered orally the tablets may, of course, contain additives, such as e.g. sodium citrate, calcium 35 carbonate and dicalcium phosphate together with various additives, such as starch, 89 preferably potato starch, gelatine and the like, in addition to the abovementioned carriers. Lubricants such as magnesium stearate, sodium laurylsulphate and talc may also be used to form tablets. In the case of aqueous suspensions the active substances may be combined with various flavour enhancers or colourings in addition to the abovementioned excipients.

For parenteral use, solutions of the active substances may be prepared using suitable liquid carrier materials.

The dosage for intravenous use is 1 -1000 mg per hour, preferably between 5 - 500 mg per hour.

However, it may optionally be necessary to deviate from the amounts specified, depending on the body weight or method of administration, the individual response to the medication, the nature of the formulation used and the time or interval over which it is administered. Thus, in some cases, it may be sufficient to use less than the 15 minimum quantity specified above, while in other cases the upper limit specified will have to be exceeded. When large amounts are administered it may be advisable to spread them over the day in a number of single doses.

The formulation examples that follow illustrate the present invention without 20 restricting its scope: Examples of pharmaceutical formulations A) Tablets per tablet active substance 100 mg lactose 140 mg corn starch 240 mg polyvinylpyrrolidone 15 mg magnesium stearate 5 mg 500 mg The finely ground active substance, lactose and some of the com starch are mixed together. The mixture is screened, then moistened with a solution of polyvinylpyrrolidone in water, kneaded, wet-granulated and dried. The granules, the

Claims (22)

90 remaining corn starch and the magnesium stearate are screened and mixed together. The mixture is compressed to produce tablets of suitable shape and size. B) Tablets per tablet 5 active substance 80 mg lactose 55 mg cornstarch 190 mg microcrystalline cellulose 35 mg 10 polyvinylpyrrolidone 15 mg sodium-carboxymethyl starch 23 mg magnesium stearate 2 mg 15 400 mg The finely ground active substance, some of the com starch, lactose, microcrystalline cellulose and polyvinylpyrrolidone are mixed together, the mixture is screened and worked with the remaining corn starch and water to form a granulate which is dried and screened. The sodiumcarboxymethyl starch and the magnesium stearate are 20 added and mixed in and the mixture is compressed to form tablets of a suitable size. C) Ampoule solution active substance 50 mg 25 sodium chloride 50 mg water for inj. 5 ml The active substance is dissolved in water at its own pH or optionally at pH 5.5 to 6.5 and sodium chloride is added to make it isotonic. The solution obtained is filtered free 30 from pyrogens and the filtrate is transferred under aseptic conditions into ampoules which are then sterilised and sealed by fusion. The ampoules contain 5 mg, 25 mg and 50 mg of active substance. 91 Patent Claims 1) A compound of general formula (I), R1 R2 N r\ n n n i 6 is r r
1. (I) ■r r wherein 10 R1 denotes a group selected from among hydrogen, NH2, XH, halogen and a Ci-C3-alkyl group optionally substituted by one or more halogen atoms, 15 20 25 R2 denotes a group selected from among hydrogen, CHO, XH, -X-Ci-C2-alkyl and an optionally substituted C-i-C3-alkyl group, R3, R4 which may be identical or different denote a group selected from among optionally substituted Ci-Cio-alkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, aryl, heteroaryl, C3-Cs-cycloalkyl, Cs-Cs-heterocycloalkyl, -X-aryl, -X-heteroaryl, -X-cycloalkyl, -X-heterocycloalkyl, -NR8-aryl, -NR8-heteroaryl, -NR8-cycloalkyl, - and -NR8-heterocycloalkyl, or a group selected from among hydrogen, halogen, COXR8, CON(R8)2, COR8 and XR8, or R3 and R4 together denote a 2- to 5-membered alkyl bridge which may contain 1 to 2 heteroatoms, R5 denotes hydrogen or a group selected from among optionally substituted Ci-Cio-alkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, aryl, heteroaryl and -C3-C6-cycloalkyl, or R3and R5or R4and R5 together denote a saturated or unsaturated C3-C4-alkyl bridge which may contain 1 to 2 heteroatoms, intellectual property office of n.z - 5 AUG 2005 RECEI VPn 92 R6 denotes optionally substituted aryl or heteroaryl, R7 denotes hydrogen or -CO-X-Ci-C4-alkyl, and 5 X in each case independently of one another denotes O or S, R8 in each case independently of one another denotes hydrogen or a group selected from among optionally substituted CrC4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl 10 and phenyl, optionally in the form of a tautomer, a racemate, an enantiomer, a diastereomer and/or a mixture thereof, and optionally a pharmacologically acceptable acid addition salt thereof. 15
2. 2) A compound according to claim 1, wherein X and R6 have the meaning indicated, and 20 R1 denotes hydrogen, R2 denotes a group selected from among a CHO, OH, and CH3 group, 25 R3, R4 which may be identical or different denote a group selected from among hydrogen, optionally substituted C-i-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C7-cycloalkyl, or 30 R3 and R4 together denote a C2-Cs-alkyl bridge , R5 denotes a group selected from among optionally substituted Ci-Cio-alkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, C3-C6-cycloalkyl and C3-C6-cycloalkenyl, or R3 and R5 or R4 and R5 together denote a saturated or unsaturated C3-C4-alkyl bridge which may contain 1 to 2 heteroatoms, and INTELLECTUAL m^PERTY office -5 AUG 2005 -6-ECElVEn 93 R7 denotes hydrogen, optionally in the form of a tautomer, a racemate, an enantiomer, a diastereomer and/or a mixture thereof, and optionally a pharmacologically acceptable acid addition salt thereof.
3. 3) A compound according to claim 1 or claim 2, wherein R1-R5, R7, R8 and X have the meaning indicated, and R6 denotes a group of general formula wherein n denotes 1, 2, 3 or 4, R9 denotes a group selected from among optionally substituted C-i-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, -CONH-Ci-Cio-alkylene, -O-aryl, -O-heteroaryl, -O-cycloalkyl, -O-heterocycloalkyl, aryl, heteroaryl, cycloalkyl and heterocycloalkyl or a group selected from among -0-Ci-C6-alkyl-Q1, -CONR8-Ci-Cio-alkyl-Q1, -CONR8-C2-Ci0-alkenyl-Q1, -CONR8-Q2, halogen, OH, -S02R8, -S02N(R8)2, -COR8 -COOR8 -N(R8)2, -NHCOR8, CONR^CrC-io alkylQ1 and CONR8OQ2, Q1 denotes hydrogen, -NHCOR8, or a group selected from among an optionally substituted -NH-aryl, -NH-heteroaryl, aryl, heteroaryl, Cs-Cs-cycloalkyl- and heterocycloalkyl group, Q2 denotes hydrogen or a group selected from among an optionally substituted aryl, heteroaryl, Cs-Cs-heterocycloalkyl, Cs-Cs-cycloalkyl- and Ci-C4-alkyl-C3-C8-cycloalkyl group, INimtUUAL WjOPERTY OFFICE - 5 AUG 2005 94 R10 which may be identical or different denotes a group selected from among optionally substituted CrC6-alkyl, C2-C6-alkenyl and C2-C6-alkynyl, -0-C-i-C6-alkyl, -0-C2-C6-alkenyl, -0-C2-C6-alkynyl, C3-C6-heterocycloalkyl and C3-C6-cycloalkyl, or a group selected from among hydrogen, -CONH2, -COOR8 -OCON(R8)2, -N(R8)2, -5 NHCOR8 -NHCON(R8)2 , -N02 and halogen, Y denotes O, S or NR11, 10 m denotes 0,1 or 2 R11 denotes hydrogen or Ci-C2-alkyl, and R12 denotes hydrogen or a group selected from among optionally substituted 15 phenyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, -Ci-C3-alkyl-phenyl, -Ci-C3-alkyl-pyridyl, -CrC3-alkyl-pyrazinyl, -Ci-C3-alkyl-pyrimidinyl and -Ci-C3-alkyl-pyridazinyl, R13 denotes CrC6-alkyl £ 20 optionally in the form of a tautomer, a racemate, an enantiomer, a diastereomer and/or a mixture thereof, and optionally a pharmacologically acceptable acid addition salt thereof. 25
4. 4) A compound according to any one of claims 1 to 3, wherein r3_r6 p8 anc| x have meaning indicated, and R1 denotes hydrogen, R2 denotes CH3, and R7 denotes hydrogen, 30 optionally in the form of a tautomer, a racemate, an enantiomer, a diastereomer and/or a mixture thereof, and optionally a pharmacologically acceptable acid addition or adjacent groups R9 and R10 together denote a bridge of general formula salt thereof. intellectual property office - 5 AUG 2005 Received 95
5. 5) Use of a compound of formula (I) according to any one of claims 1 to 4 for the production of a medicament with an antiproliferative activity. 5
6. 6) Use of a compound of formula (I) according to any one of claims 1 to 4 for the production of a medicament for the treatment and/or prevention of cancer, infections, inflammatory and/or autoimmune diseases.
7. 7) Method of treating and/or preventing cancer, infections, inflammatory and/or 10 autoimmune diseases in non-human animals, wherein an effective quantity of a compound of formula (I) according to any one of claims 1 to 4 is administered.
8. 8) A pharmaceutical preparation, containing as active substance one or more compounds of general formula (I) according to any one of claims 1 to 4 or a 15 physiologically acceptable salt thereof, optionally combined with conventional excipients and/or carriers.
9. 9) Process for preparing a compound of general formula (I), in which R1-R7 and X have the meanings given in any one of claims 1 to 4, wherein a compound of general formula (II) lAXJc? l n n r3 25 (id in which intellectual property office! of n.z - 5 AUG 2005 -received 96 R1-R5 and X have the meanings given in any one of claims 1 to 4 and L is a leaving group, is reacted with an optionally substituted compound of general formula (III) R\ /R n H 5 (I") in which R6 and R7 have the meanings given in any one of claims 1 to 4.
10. 10) A compound of formula (II), R1 R2 N ll XR< N^r3 10 ("0 wherein R1-R5 and X have the meanings given in claims 1 to 4.
11. 11) A process for preparing a compound of general formula (I), 15 N r\ N N' R' 6 (I) r 'n !5R R5 ■r in which R6 denotes a group of general formula, 20 I'NItLLfcCTUAL PROPERTY OF N.Z. " 5 AUG 2005 -R ECFiypp OFFICE] 97 R9 denotes an optionally substituted group -CONH-CrCio-alkylene or a group selected from among -CONR8-Ci-Cio-alkyl-Q1, -CONR8-C2-Cio-alkenyl-Q1, -CONR8-Q2, and -COOR8, and R1-R5, R7, R10, n and X are as defined as in claims 1 to 4, wherein a compound of general formula (IA) R1 R2 ivr, k1 n n p4 If (IA) io in which R1 to R5, R7, R10 and n are as defined as in claims 1 to 4, and L denotes a leaving group, is reacted with a primary or secondary amine to form the corresponding amide or is 15 reacted with an alcohol to form the corresponding ester.
12. 12) A compound of the general formula (I) according to any one of claims 1 to 4, substantially as herein described with reference to any one of the Examples, Table 1 or part thereof. 20
13. 13) A compound of the general formula (I) to any one of claims 1 to 4, substantially as herein described.
14. 14) Use according to claim 5 or claim 6 wherein the compound of the general 25 formula (I) is substantially as herein described with reference to any one of the Examples, Table 1 or part thereof. intellectual property office i of n.z. 1 - 5 AUG 2005 RECEIVED 98
15. 15) Use according to claim 5 or claim 6, substantially as herein described.
16. 16) A method according to claim 7 wherein the compound of the general formula (I) 5 is substantially as herein described with reference to any one of the Examples, Table 1 or part thereof.
17. 17) A method according to claim 7, substantially as herein described.
18. 18) A pharmaceutical preparation according to claim 8 wherein the compound of the general formula (I) is substantially as herein described with reference to any one of the Examples, Table 1 or part thereof.
19. 19) A pharmaceutical preparation according to claim 8, substantially as herein 15 described.
20. 20) A process according to claim 9 or claim 11, substantially as herein described with reference to any one of the Examples, Table 1 or part thereof. 20
21. 21) A process according to claim 9 or claim 11, substantially as herein described.
22. 22) A compound of general formula (II), substantially as herein described.