AU2001293817A1 - 4-amino-quinazolines - Google Patents

4-amino-quinazolines

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Publication number
AU2001293817A1
AU2001293817A1 AU2001293817A AU9381701A AU2001293817A1 AU 2001293817 A1 AU2001293817 A1 AU 2001293817A1 AU 2001293817 A AU2001293817 A AU 2001293817A AU 9381701 A AU9381701 A AU 9381701A AU 2001293817 A1 AU2001293817 A1 AU 2001293817A1
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Australia
Prior art keywords
phenyl
formula
het
methyl
compound
Prior art date
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Abandoned
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AU2001293817A
Inventor
Gerhard Barnickel
Sabine Bernotat-Danielowski
Bertram Cezanne
Dr. Ralf Devant
Daljit Dhanoa
Edward Jaeger
Werner Mederski
Mark R. Player
James Rinker
Richard Soll
James Vickers
Baoping Zhao
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Merck Patent GmbH
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Merck Patent GmbH
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Publication date
Application filed by Merck Patent GmbH filed Critical Merck Patent GmbH
Publication of AU2001293817A1 publication Critical patent/AU2001293817A1/en
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/94—Nitrogen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/95—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

Description

4-Amino-quinazolines
The invention relates to substituted 4-amino-quinazolines of the formula
in which R and R1 are independently of each other H, A, OH, OA, Hal, N(R5)2,
N02, CN, CHO, COA, CON(R5)2l COOR5, allyl, CH=CH- COOR5, CH=CHCON(R5)2, S02A or phenyl, which is unsubstituted or mono-, di- or trisubstituted by A, R2 and R3 are independently of each other H, A, cycloalkyl, -Het3, -(CH2)0-OR5, -(CH2)0-OR6, -(CH2)0-Het, -(CH2)0-NR5-Het,
-(CHA)p-(CH2)o-N(R5)2, -(CH2)p-(CHA)p-(CH2)m-ArJ -(CH2)0-Z-(CH2)q-N(R5)2l
provided that R and R together are not H, or NR2R3 together form a saturated monocyclic heterocyclic radical having
5 to 6 ring members, where 1 or 2 N atoms are present and the heterocyclic radical can be mono- or disubstituted by OH, Ar, OAr or arylalkyl, R4 is Ar or Het1, R5 is H or A,
R6 is benzo[1 ,3]dioxol-5-yl,
R7 is H, A, cycloalkyl or -(CH2)q-OR5, Q is O or S,
Y is a direct bond, (CH2)n or -NR5-(CH2)m-,
Z is phenylene, cyclohexylene, -NR5-, O, -CH(OH)-, -CA2- or
A is unbranched or branched alkyl having 1 to 6 carbon atoms,
Ar is phenyl, naphthyl or biphenyl, which is unsubstituted or mono-, di- or trisubstituted by A, OH, OA, cycloalkyloxy, 0-(CH2)p-Ph, CF3, OCF3, Hal, CN, CHO, COA, COOR5,
-(CH2)P-N(R7)2, NR5-COA, N02l S02N(R5)2, mor, S02-mor, 5-methyl-3-oxo-2,4-dihydropyrazol-2-yl, naphthyl or Het2, Het is a saturated, partially or completely unsaturated mono- or bicyclic heterocyclic radical having 5 to 10 ring members, where 1 or 2 N and/or 1 or 2 S or O atoms can be present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2, carbonyl oxygen, COOR5, benzyl, Het2 or phenyl which is unsubstituted or mono-, di- or trisubstituted by A, OH, OA, CF3, OCF3, Hal, CN, COOR5, N(R5)2, N02, S02N(R5)2,
Het1 is thiophen-2-yl which is substituted by Ar or He ttZ2
Het2 is a unsaturated mono- or bicyclic heterocyclic radical having
5 to 10 ring members, where 1 or 2 N and/or 1 or 2 S or
O atoms can be present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2)
-(CH2)p-(CHA)p-N(R5)-(CH2)q-COR5, CHO, COA or COOR5, Het3 is a partially or completely unsaturated mono- or bicyclic heterocyclic radical having 5 to 10 ring members, where 1 or 2
N atoms are present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2)
S02A or COOR5 provided that the heterocyclic radical is not bondend via an N atom, Hal is F, CI, Br or l, mor is morpholin-4-yl,
Ph is phenyl, n is 1 , 2, 3, 4, 5 or 6, m is O, 1 , 2, 3, 4, 5 or 6
0 is 1 , 2, 3, 4, 5, 6 or 7
P is O, 1 , 2, 3 or 4, q is 1 , 2, 3 or 4, and their pharmaceutically tolerable salts and solvates.
Similar 4-amino substituted quinazolines are disclosed in WO 99/09986, Mastafanova, Li et al, Khim.-Farm.Zh. 1982, 16, 938-42, US 5,436,233 or DE 2135172.
The invention is based on the object of finding novel compounds having valuable properties, in particular those which can be used for the production of medicaments.
It has been found that the compounds of the formula I and their salts or solvates have very valuable pharmacological properties together with good tolerability.
They act especially as GPIblX inhibitors, in particular inhibiting the interaction of this receptor with the ligand von Willebrand factor (vWF). This action can be demonstrated, for example, by a method which is described by S. Meyer et al. in J. Biol. Chem. 1993, 268, 20555-20562. The property as GPIblX alpha-thrombin receptor (N.J. Greco, Biochemistry 1996, 35, 915-921) can also be blocked by the compounds mentioned.
The significance of GPIblX as an adhesion receptor on platelets, which mediates the primary interaction of platelets with an arteriosclerotically modified vascular wall via binding to the vWF expressed there, has been described by many authors (e.g. Z.M. Ruggeri in Thromb. Hemost. 1997, 78, 611-616). The activation of another platelet adhesion receptor, GPIIbllla, following the GPIblX-vWF interaction, leads to platelet aggregation and thus to thrombotic vascular occlusion.
A GPIblX antagonist can thus prevent the start of thrombus formation and thus also release of active substances from the platelets which, for example, promote thrombus growth and have an additional trophic action on the vascular wall. This has been shown with inhibitory peptides or antibodies in various experimental models (e.g. H Yamamoto et al., Thromb. Hemost. 1998, 79, 202-210).
In the case of higher shear forces, the blocking action of GPIblX inhibitors exerts its maximum effect, as described by J.J. Sixma et al. in Arteriosclerosis, Thrombosis, and Vascular Biology 1996, 16, 64-71. According to the flow chamber method used there, the compounds of the formula I can be characterized as GPIblX inhibitors in whole blood.
The inhibition of thrombus formation of the GPIblX inhibitors can be measured by a modified Born method (Nature 1962, 4832, 927-929) using botrocetin or ristocetin as an aggregation stimulant.
The compounds of the formula I according to the invention can therefore be employed as pharmaceutical active compounds in human and veterinary medicine. They act as adhesion receptor antagonists, in particular as glycoprotein IblX antagonists, and are suitable for the prophylaxis and/or therapy of thrombotic disorders and sequelae deriving therefrom. The preferentially best action is to be expected in the case of thrombotic disorders in the arterial vascular system, but GPIblX inhibitors also have an effect in the case of thrombotic disorders in the venous vascular bed. The disorders are acute coronary syndromes, angina pectoris, myocardial infarct, peripheral circulatory disorders, stroke, transient ischaemic attacks, arteriosclerosis, reocclusion/restenosis after angioplasty/stent implantation. The compounds can furthermore be employed as anti-adhesive substances where the body comes into contact with foreign surfaces such as implants, catheters or cardiac pacemakers.
Therefore, the invention relates further to compounds of the formula I according to Claim 1 and their physiologically acceptable salts or solvates as pharmaceutical active compounds.
The invention relates to compounds of the formula I according to Claim 1 and their physiologically acceptable salts or solvates as glycoprotein IblX antagonists.
Comparison medication introduced onto the market which may be mentioned are aspirin and GPIIbllla antagonists.
The invention relates to the compounds of the formula I and their salts or solvates, and to a process for the preparation of these compounds and their salts or solvates, characterized in that a) a compound of the formula I is liberated from one of its functional derivatives by treating with a solvolysing or hydrogenolysing agent, or b) for compounds in which Y is a direct bond or (CH2)n in stage 1) a compound of the formula II
in which
R and R1 have a meaning indicated in Claim 1 , is reacted with a compound of the formula III
in which R4 has a meaning indicated in Claim 1 and Y is a direct bond or (CH2)n, and X is CI, Br, OH or a reactive esterified OH group followed by converting the cyano group to an amide group by conventional means to give a compound of formula IV
in which R, R1 and R4 have a meaning indicated in Claim 1 and Y is a direct bond or (CH2)n, in stage 2) a compound of formula IV as indicated above is reacted with a base to give a compound of formula V
in which R, R1 and R4 have a meaning indicated in Claim 1 and Y is a direct bond or (CH2)n, in stage 3) a compound of formula V as indicated above is reacted with a chlorinating agent to give a compound of formula VI
in which R, R1 and R4 have a meaning indicated in Claim 1 and Y is a direct bond or (CH2)n, and in stage 4) a compound of formula VI as indicated above is reacted with a compound of formula VII in which R2 and R3 or NR2R3 have a meaning indicated in Claim 1 , or b) for compounds in which Y is NR5-(CH2)m-, in stage 1) a compound of the formula VIII
in which
R and R1 have a meaning indicated in Claim 1 , is reacted with a compound of formula VII
in which R2 and R3 or NR2R3 have a meaning indicated in Claim 1 , to give a compound of formula IX
in which R, R1, R2, R3 and NR2R3 have a meaning indicated in Claim 1 , and in stage 2) a compound of formula IX as indicated above is reacted with a compound of formula X
R5
H-N— (CH2)— R4 X in which R •)4 , 0 R5 and m have a meaning indicated in Claim 1 or d) a radical R, R1, R2, R3 and/or R4 is converted into another radical R, R1, R2, R3 and/or R4 by, for example reducing a nitro group, sulfonyl group or sulfoxyl group, etherifying an OH group or subjecting an OA group to ether cleavage, alkylating a primary or secondary amino group, partially or completely hydrolysing a CN group, cleaving an ester group or esterifying a carboxylic acid radical, reacting an aryl bromide, aryl iodide, heteroaryl bromide or heteroaryliodide to give the corresponding coupling products by means of a Suzuki coupling with boronic acids, reacting a iodoquinazoline or bromoquinazoline to give the corresponding coupling products by means of a Stille coupling with allyltributyltin, - reacting a iodoquinazoline or bromoquinazoline to give the corresponding coupling products by means of a Heck coupling with acrylates, or carrying out a nucleophilic or electrophilic substitution, or a base or acid of the formula I is converted into one of its salts or solvates.
The compounds of the formula I can have a chiral center and therefore occur in a number of stereoisomeric forms. All these forms (e.g. R and S forms) and their mixtures (e.g. the RS forms) are included in the formula I.
The compounds according to the invention also include so-called prodrug derivatives, i.e. compounds of the formula I modified with, for example, alkyl or acyl groups, sugars or oligopeptides and which are rapidly cleaved in the body to give the active compounds according to the invention.
Furthermore, free amino groups as substituents of compounds of the formula I can be provided with appropriate conventional protective groups. Solvates of the compounds of the formula I are understood as meaning adducts of inert solvent molecules to the compounds of the formula I which are formed on account of their mutual power of attraction. Solvates are, for example, mono- or dihydrates or alcoholates.
The abbreviations used have the following meanings:
Ac acetyl,
Bu n-butyl,
DBU 1 ,8-diazabicyclo[5.4.0]undec-7-ene, DMA dimethylacetamide,
DMF dimethylformamide, dppf 1 ,1 '-bis(diphenylphosphino)ferrocene,
Et ethyl, iPr isopropyl, Me methyl,
Ph phenyl,
TEA triethylamine,
TFA trifluoroacetic acid.
In the above formulae, A is alkyl and has 1 to 6, preferably 1 , 2, 3 or 4 C atoms. Alkyl is preferably methyl, furthermore ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl or tert-butyl, additionally also pentyl, 1-, 2- or 3-methylbutyl, 1 ,1 -, 1 ,2- or 2,2-dimethylpropyl, 1 -ethylpropyl, hexyl, 1 -, 2-, 3- or 4-methylpentyl, 1 ,1 -, 1 ,2-, 1 ,3-, 2,2-, 2,3- or 3,3-dimethylbutyl, 1- or 2-ethylbutyl, 1 -ethyl-1 -methylpropyl, 1 -ethyl-2-methylpropyl, 1 ,1 ,2- or 1 ,2,2-trimethylpropyl. A is preferentially methyl, ethyl, propyl, isopropyl, butyl or pentyl.
Ar is phenyl, naphthyl or biphenyl, which is unsubstituted or mono-, di- or trisubstituted by A, OH, OA, cycloalkyloxy, 0-(CH2)p-Ph, CF3, OCF3, Hal, CN, CHO, COA, COOR5, -(CH2)P-N(R7)2) NR5-COA, N02, S02N(R5)2, mor, S02-mor, 5-methyl-3-oxo-2,4-dihydropyrazol-2-yl, naphthyl or Het2. Ar is preferentially phenyl, preferably - as indicated - mono- di- or trisubstituted phenyl, specifically preferentially phenyl, 2-, 3- or 4-methylphenyl, 2-, 3- or 4-ethylphenyl, 2-, 3- or 4-propylphenyl, 2-, 3- or 4-isopropylphenyl, 2-, 3- or 4-butylphenyl, 2-, 3- or 4-tert-butylphenyl, 2-, 3- or 4-aminophenyl, 2-, 3- or 4-N,N-dimethylaminophenyl, 2-, 3- or 4-sulfamoylphenyl, 2-, 3- or 4-nitrophenyl, 2-, 3- or 4-hydroxyphenyl, 2-, 3- or 4-methoxyphenyl, 2-, 3- or 4-ethoxyphenyl, 2-, 3- or 4-pentoxyphenyl, 2-, 3- or 4-phenoxyphenyl, 2-, 3- or 4-phenylmethoxyphenyl, 2-, 3- or 4- trifluoromethylphenyl, 2-, 3- or 4-trifluoromethoxyphenyl, 2-, 3- or 4- cycfopentyloxyphenyl, 2-, 3- or 4-carboxyphenyl, 2-, 3- or 4-(N,N- diethyl)sulfamoylphenyl, 4-(3-methyl-butyramido)-phenyl, 2-, 3- or 4- cyanophenyl, 2-, 3- or 4-fluorophenyl, 2-, 3- or 4-chlorophenyl, 2-, 3- or 4-bromophenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- or 3,5-dichlorophenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- or 3,5-dibromophenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- or 3,5- dimethoxyphenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- or 3,5-di(trifluoromethyl)phenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- or 3,5-di(phenylmethoxy)phenyl, 2-chloro-6- methylphenyl, 2-chloro-4-fluorophenyl, 3-bromo-6-fluorophenyl, 3,4,5- trimethoxyphenyl, 4-(morpholin-4-yl)phenyl, 4-(morpholin-4-yl- sulfonyl)phenyl, 4-(5-methyl-3-oxo-2,4-dihydropyrazol-2-yl)phenyl, 4-(4,6- dimethoxy-pyrimidin-2-yl)phenyl, 3-(4,6-dimethoxy-pyrimidin-2-yl)phenyl, 4- (pyrid-3-yl)phenyl, 3-(pyrid-3-yl)phenyl, 4-(thiophen-2-yl)phenyl, 4- (thiophen-3-yl)phenyl, 4-(2-formyl-thiophen-3-yl)phenyl, 3-(thiophen-2- yl)phenyl, 4-(benzo[c]thiophen-2-yl)phenyl, 4-(naphthalen-1 -yl)phenyl or
Furthermore, however, Ar is also preferentially unsubstituted naphthyl or biphenyl - as indicated - or alternatively mono-, di- or trisubstituted biphenyl, specifically preferentially biphenyl-4-yl or biphenyl-3-yl, 2'-methylbiphenyl-4-yl, 3'-methylbiphenyl-4-yl, 4'-methylbiphenyl-4-yl, 2'-methylbiphenyl-3-yl, 3'-methylbiphenyl-3-yl, 4'-methylbiphenyl-3-yl, 2-methylbiphenyl-4-yl, 3-methylbiphenyl-4-yl, 2-methylbiphenyl-3-yl, 4-methylbiphenyl-3-yi, 2'-tert-butylbiphenyl-4-yl, 3'-tert-butylbiphenyl-4-yl,
4'-tert-butylbiphenyl-4-yl, 2'-tert-butylbiphenyl-3-yl, 3'-tert-butylbiphenyl-3-yl, 4'-tert-butylbiphenyl-3-yl, 2-tert-butylbiphenyl-4-yl, 3-tert-butylbiphenyl-4-yl, 2-tertbutylbiphenyl-3-yl, 4-tert-butylbiphenyl-3-yl, 2'-isopropylbiphenyl-4-yl, 3'-isopropylbiphenyl-4-yl, 4'-isopropylbiphenyl-4-yl, 2'-isopropylbiphenyl-3- y|, 3'-isopropylbiphenyl-3-yl, 4'-isopropylbiphenyl-3-yl, 2-isopropylbiphenyl- 4-yl, 3-isopropylbiphenyl-4-yl, 2-isopropylbiphenyl), 4-isopropylbiphenyl-3- yl, 2'-fluorobiphenyl-4-yl, 3'-fluorobiphenyl-4-yl, 4'-fluorobiphenyl-4-yl, 2'-fluorobiphenyl-3-yl, 3'-fluorobiphenyl-3-yl, 4'-fluorobiphenyl-3-yl, 2-fluorobiphenyl-4-yl, 3-fluorobiphenyl-4-yl, 2-fluorobiphenyl-3-yl, 4-fluoro- biphenyl-3-yl, 2'-chlorobiphenyl-4-yl, 3'-chlorobiphenyl-4-yl, 4'-chloro- biphenyl-4-yl, 2'-chlorobiphenyl-3-yl, 3'-chlorobiphenyl-3-yl, 4'-chlorobiphenyl-3-yl, 2-chlorobiphenyl-4-yl, 3-chlorobiphenyl-4-yl, 2-chlorobiphenyl-3-yl, 4-chlorobiphenyl-3-yl, 2'-methoxybiphenyl-4-yI, 3'-methoxybiphenyl-4-yl, 4'-methoxybiphenyl-4-yl, 2'-methoxybiphenyl-3-yl, 3'-methoxybiphenyl-3-yl, 4'-methoxybiphenyl-3-yl, 2-methoxybiphenyl-4-yl, 3-methoxybiphenyl-4-yl, 2-methoxybiphenyl-3-yl, 4-methoxybiphenyl-3-yl, 2'-nitrobiphenyl-4-yl, 3'-nitrobiphenyl-4-yl, 4'-nitrobiphenyl-4-yl, 2'-nitro- biphenyl-3-yl, 3'-nitrobiphenyl-3-yl, 4'-nitrobiphenyl-3-yl, 2-nitrobiphenyl-4-yl, 3-nitrobiphenyl-4-yl, 2-nitrobiphenyl-3-yl, 4-nitrobiphenyl-3-yl, 2'-trifluoromethylbiphenyl-4-yl, 3'-trifluoromethylbiphenyl-4-yl, 4'-tri- fluoromethyl-biphenyl-4-yl, 2'-trifluoromethylbiphenyl-3-yI, 3'-trifluoromethylbiphenyl-3-yl, 4'-trifIuoromethylbiphenyl-3-yl, 2-trifluoromethylbiphenyl-4-yl, 3-trifluoromethylbiphenyl-4-yl, 2-trifluoromethylbiphenyl-3-yl, 4-trifluoromethylbiphenyl-3-yl, 2'-trifluoromethoxybiphenyl-4-yl, 3'-trifluoromethoxybiphenyl-4-yl, 4'-tri- fIuoromethoxybiphenyl-4-yl, 2'-trifluoromethoxybiphenyl-3-yl, 3'-trifluoromethoxybiphenyl-3-yl, 4'-trifIuoromethoxybiphenyl-3-yl, 2-trifluoromethoxybiphenyl-4-yl, 3-trifluoromethoxybiphenyl-4-yl, 2-trifluoromethoxybiphenyl-3-yl, 4-trifluoromethoxybiphenyl-3-yl, 3'- acetylbiphenyI-4-yl, 3'-acetylaminobiphenyl-4-yl, 3'-aminobiphenyl-4-yi, 31- formylbiphenyl-4-yl, 4'-formylbiphenyl-4-yl, 4'-propylaminomethylbiphenyl-4- yl, 3'-methoxyethylaminomethylbiphenyl-4-yl, 4'- cyclohexylmethylaminomethylbiphenyl-4-yl or 3'- hydroxypropylaminomethylbiphenyl-4-yl, furthermore preferentially disubstituted biphenyls, such as 2'-methyl-3'-nitrobiphenyl-4-yl, 2'-methyl-4'- nitrobiphenyl-4-yl, 2'-methyl-5'-nitrobiphenyl-4-yl, 2'-methyl-6'-nitrobiphenyl- 4-yl, 3'-methyl-2'-nitrobiphenyl-4-yl, 3'-methyl-4'-nitrobiphenyl-4-yl, 3'-methyl-5'-nitrobiphenyl-4-yl, 3'-methyl-6'- nitrobiphenyl-4-yl, 4'-methyl-2'- nitrobiphenyl-4-yl, 4'-methyl-3'-nitrobiphenyl-4-yl, 2'-methyl-3'-nitrobiphenyl- 3-yl, 2'-methyl-4'-nitrobiphenyl-3-yl, 2'-methyl-5'-nitrobiphenyl-3-yl, 2'-methyl-6'-nitrobiphenyl-3-yl, 3'-methyl-2'-nitrobiphenyl-3-yl, 3'-methyl-4'- nitrobiphenyl-3-yl, 3'-methyl-5'-nitrobiphenyl-3-yl, 3'-methyl-6'-nitrobiphenyl- 3-yl, 4'-methyl-2'-nitrobiphenyl-3-yl, 4'-methyl-3'-nitrobiphenyl-3-yl, 2'- methoxy-2-methylbiphenyl-4-yl, 3'-methoxy-2-methylbiphenyl-4-yl, 4,-methoxy-2-methylbiphenyl-4-yl, 4'-methoxy-3-nitrobiphenyl-4-yl, 2'-chloro-3'-fluorobiphenyl-4-yl, 2'-chloro-4'- fluorobiphenyl-4-yl, 2'-chloro-5'- fluorobiphenyl-4-yl, 2'-chloro-6'-fluorobiphenyl-4-yl, 3'-chioro-2'- fIuorobiphenyl-4-yl, 3'-chloro-4'-fIuorobiphenyl-4-yl, 3'-chloro-5'- fluorobiphenyl-4-yl, 3'-chloro-6'-fluorobiphenyl-4-yl, 4'-chloro-2'-fluoro- biphenyl-4-yl, 4'-chloro-3'-fluorobiphenyl-4-yl, 2'-chloro-3'-fluorobiphenyl-3- y|, 2'-chloro-4'-fluorobiphenyl-3-yl, 2'-chloro-5'-fluorobiphenyl-3-yl, 2'-chloro- 6'-fluorobiphenyl-3-yl, 3'-chloro-2'-fluorobiphenyl-3-yl, 3'-chloro-4'-fluoro- biphenyl-3-yl, 3'-chloro-5'-fluorobiphenyl-3-yl, 3'-chloro-6'-fluorobiphenyl-3- yl, 4'-chloro-2'-fluorobiphenyl-3-yl, 4'-chloro-3'- fluorobiphenyl-3-yl, (2,3'-diethyl)biphenyl-4-yl, (3,3'-diethyl)biphenyl-4-yl), (2,2'-diethyl)biphenyl- 4-yl, (2,4'-diethyl)biphenyl-4-yl, (2',3'-dimethoxy)biphenyl-4-yl, (2',4'- dimethoxy)biphenyl-4-yl, (2',5'-dimethoxy)biphenyl-4-yl, (2',6'-dimethoxy)- biphenyl-4-yl, (3',4'-dimethoxy)biphenyl-4-yl, (3',5'-dimethoxy)biphenyl-4-yl, (2',3'-dimethoxy)-biphenyl-3-yl, (2',4'-dimethoxy)biphenyl-3-yl, (2',5'-dimethoxy)biphenyl-3-yl, (2',6'-dimethoxy)-biphenyl-3-yI, (3',4'-dimethoxy)biphenyl)-3-yl, (3',5'-dimethoxy)biphenyl-3-yl, (3',5'-dichloro)biphenyl-4-yl, (3',5'-dichloro)biphenyl-3-yl, (2',4'-dichloro)biphenyl-4-yl, (3',4',5'-trimethoxy)biphenyl-4-yl,
(2',3'-di(trifluoromethyl))biphenyl-4-yl, (2',4'-di(trifluoromethyl))biphenyl-4-yl, (2',5'-di(trifluoromethyl))biphenyl-4-yl, (2',6'-di(trifluoromethyl))biphenyl-4-yl, (3',4'-di(trifluoromethyl))biphenyl-4-yl, (3',5'-di(trifluoromethyl))biphenyl-4-yl, (2',3'-di(trifluoromethyl))biphenyl-3-yl, (2',4'-di(trifluoromethyl))biphenyl-3-yl, (2',5'-di(trifluoromethyl))biphenyl-3-yl, (2,,6'-di(trifluoromethyl))biphenyl-3-yl, (3',4,-di(trifluoromethyl))biphenyl-3-yl, (3',5'-di(trifluoromethyl)biphenyl-3-yl, (2,2'-dimethyl)biphenyl-4-yl, (2,'3-dimethyl)biphenyl-4-yl, (2,4'-dimethyl)biphenyl-4-yl, (2,2'-dimethyl)biphenyl-3-yl, (2,3'-dimethyl)biphenyl-3-yl or (2,4'-dimethyl)biphenyl-3-yl.
Phenyl, 2-, 3- or 4-fluorophenyl, 2-, 3- or 4-chlorophenyl, 4-bromophenyl, 2,4- or 3,4-dichlorophenyl, 2,5- or 3,4-dimethoxyphenyl, 3,5-bis- (trifluoromethyl)phenyl, 4-aminophenyl, 4-dimethylaminophenyl, 2-, 3- or 4-methylphenyl, 2-, 3- or 4-methoxyphenyl, 4-propylphenyl, 4-isopropylphenyl, 4-butylphenyl, 4-tert.-butylphenyl, 2-, 3- or 4-nitrophenyl, 2-cyanophenyl, 2-, 3- or 4-pentoxyphenyl, 3- or 4-phenoxyphenyl, 2- or 4-benzyloxyphenyl, 2-, 3- or 4-trifluoromethylphenyl, 2-, 3- or 4- trifluoromethoxyphenyl, 2- or 4-cyclopentyloxyphenyl, 3- or 4- carboxyphenyl, 2-, 3- or 4-(N,N-diethyl)sulfamoylphenyl, 3,4- di(benzyloxy)phenyl, 4-(3-methyl-butyramido)-phenyl, 2-chloro-6- methylphenyl, 2-chloro-4-fluorophenyl, 3-bromo-6-fluorophenyl, 3,4,5- trimethoxyphenyl, 4-(morpholin-4-yl)phenyl, 4-(morpholin-4-yl- sulfonyl)phenyl, 4-(5-methyl-3-oxo-2,4-dihydropyrazol-2-yl)phenyl, 4-(4,6- dimethoxy-pyrimidin-2-yl)phenyl, 3-(4,6-dimethoxy-pyrimidin-2-yl)phenyl, 4- (pyridin-3-yl)phenyl, 3-(pyridin-3-yl)phenyl, 4-(thiophen-2-yl)phenyl, 3-
(thiophen-2-yl)phenyl, 4-(benzo[c]thiophen-2-yl)phenyl, 4-(naphthalen-1 - yl)phenyl, 4-(thiophen-3-yl)phenyl, 4-(2-formyl-thiophen-3-yl)phenyl, naphthyl, biphenyl-4-yl, 2'-fluorobiphenyl-4-yl, 4'-fluorobiphenyl-4-yl, 4'-fluorobiphenyl-3-yl, 4'-chlorobiphenyl-4-yl, 4'-chlorobiphenyl-3-yl, 4'-methoxybiphenyl-4-yl, 4'-methoxybiphenyl-3-yl, 3'-nitrobiphenyl-4-yl, 3'- acetylbiphenyl-4-yl, 3'-acetylaminobiphenyl-4-yl, 3'-aminobiphenyl-4-yl, 3'- formylbiphenyl-4-yl, 4'-formylbiphenyl-4-yl, 4'-propylaminomethylbiphenyl-4- yl, 3'-methoxyethyl-aminomethylbiphenyl-4-yl, 4'-cyclohexylmethyl- aminomethylbiphenyl-4-yl, 3'-hydroxypropylaminomethylbiphenyl-4-yl, (2,3'-diethyl)biphenyl-4-yl, (2,4'-diethyl)biphenyl-4-yl, (2,2'-diethyl)biphenyl- 4-yl, (3',5'-dichloro)biphenyl-3-yl, (3',4'-dimethoxy)biphenyl-4-yl, (2',4'-dichloro)biphenyl-4-yl, (3',4',5'-trimethoxy)biphenyl-4-yl, (3',5'- di(trifluoromethyl))biphenyl-4-yl or
is particularly preferred for Ar.
Arylalkyl is preferentially benzyl.
0-(CH2)p-Ph is phenylalkyloxy, in which p can be 0, 1 , 2, 3 or 4. Benzyloxy or phenyloxy is particularly preferred.
Cycloalkyl preferably has 3-7 C atoms and is preferably cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, and further also cyclopentylmethyl, cyclopentylethyl or cyclohexylmethyl; cyclopentyl, cyclohexylmethyl or cyclohexyl are particularly preferred.
Hal is preferably F, CI, Br or I.
Het is a saturated, partially or completely unsaturated mono- or bicyclic heterocyclic radical having 5 to 10 ring members, where 1 or 2 N and/or 1 or 2 S or O atoms can be present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2, carbonyl oxygen, COOR5, Het2, benzyl or phenyl which is unsubstituted or mono-, di- or trisubstituted by A, OH, OA, CF3, OCF3, Hal, CN, COOR5, N(R5)2, N02, S02N(R5)2.
Het is preferably unsubstituted 2- or 3-furyl, 2- or 3-thiophenyl, 1 -, 2- or 3-pyrrolyl, 1 -, 2-, 4- or 5-imidazolyl, 1-, 3-, 4- or 5-pyrazolyl, 2-, 4- or 5-oxazolyl, 3-, 4- or 5-isoxazolyl, 2-, 4- or 5-thiazolyl, 3-, 4- or 5-isothiazolyl, 2-, 3- or 4-pyridyl, 2-, 4-, 5- or 6-pyrimidinyl, furthermore preferably 1 ,2,3-triazol-1 -, -4- or -5-yl, 1 ,2,4-triazol-1 -, -4- or -5-yl, 1 - or 5-tetrazolyl, 1 ,2,3-oxadiazol-4- or -5-yl, 1 ,2,4-oxadiazol-3- or -5-yl, 1 ,3,4-thiadiazol-2- or -5-yl, 1 ,2,4-thiadiazol-3- or -5-yl, 1 ,2,3-thiadiazol-4- or -5-yl, 2-, 3-, 4-, 5- or 6-2H-thiopyranyl, 2-, 3- or 4-4H-thiopyranyl, 3- or 4-pyridazinyl, pyrazinyl, 2-, 3-, 4-, 5-, 6- or 7-benzofuryl, 2-, 3-, 4-, 5-, 6- or 7-benzothiophenyl, 1 -, 2-, 3-, 4-, 5-, 6- or 7-1 H-indolyl, 1 -, 2-, 4- or 5-benzimidazolyl, 1 -, 3-, 4-, 5-, 6- or 7-benzopyrazolyl, 2-, 4-, 5-, 6- or 7-benzoxazolyl, 3-, 4-, 5-, 6- or 7-benzisoxazolyl, 2-, 4-, 5-, 6- or 7-benzothiazolyl, 2-, 4-, 5-, 6- or 7-benzisothiazolyl, 4-, 5-, 6- or 7-benz-2,1 ,3-oxadiazolyl, 1-, 2-, 3-, 4-, 5-, 6-, 7- or 8-quinolinyl, 1 -, 3-, 4-, 5-, 6-, 7- or 8-isoquinolinyl, 1-,
2-, 3-, 4- or 9-carbazolyl, 1 -, 2-, 3-, 4-, 5-, 6-, 7-, 8- or 9-acridinyl, 3-, 4-, 5-, 6-, 7- or 8-cinnolinyl, 2-, 4-, 5-, 6-, 7- or 8-quinazolinyl. The heterocyclic radicals can also be partially or completely hydrogenated. Het can thus also be 2,3-dihydro-2-, -3-, -4- or -5-furyl, 2,5-dihydro-2-, -3-, -4- or -5-furyl, tetrahydro-2- or -3-furyl, 1 ,3-dioxolan-4-yl, tetrahydro-2- or -3-thiophenyl, 2,3-dihydro-1 -, -2-, -3-, -4- or -5-pyrrolyl, 2,5-dihydro-1 -, -2-, -3-, -4- or -5-pyrrolyl, 1 -, 2- or 3-pyrrolidinyl, tetrahydro-1 -, -2- or -3-pyrrolyl, tetrahydro-1-, -2- or 4-imidazolyl, 2,3-dihydro-1-, -2-, -3-, -4-, -5-, -6-, -7-1 H-indolyl, 2,3-dihydro-1 -, -2-, -3-, -4- or -5-pyrazolyl, tetrahydro-1 -, -3- or -4-pyrazolyl, 1 ,4-dihydro-1-, -2-, -3- or -4-pyridyl, 1 ,2,3,4-tetrahydro-1 -, -2-, -3-, -4-, -5- or -6-pyridyl, 1 ,2,3,6-tetrahydro-1 -, -2-, -3-, -4-, -5- or -6-pyridyl, 1 -, 2-, 3- or 4-piperidinyl, 1 -, 2-, 3- or 4-azepanyl, 2-, 3- or 4-morpholinyl, tetrahydro-2-, -3- or -4-pyranyl, 1 ,4-dioxanyl, 1 ,3-dioxan-2-, -4- or -5-yl, hexahydro-1 -, -3- or -4-pyridazinyl, hexahydro-1 -, -2-, -4- or -5-pyrimidinyl, 1 -, 2- or 3-piperazinyl, 1 ,2,3,4-tetrahydro-1-, -2-, -3-, -4-, -5-, -6-, -7- or -8-quinolinyl, 1 ,2,3,4-tetrahydro-1 -, -2-, -3-, -4-, -5-, -6-, -7- or -8-isoquinolinyl which can be substituted as indicated above or particularly substituted by A, OA, carbonyl oxygen, N02, Het2 or phenyl which is substituted by Hal, CN or OA.
Thiophen-2-yl, tetrahydro-furan-2-yl, 1 -methyl-octahydro-indol-3-yl, benzo[1 ,3]dioxol-5-yl, piperazin-1-yl, 4-methyl-piperazin-1-yl, piperidin-1 -yl, piperidin-4-yl, 1 -methyl-piperidin-3-yl, 4-benzyl-piperidin-1 -yl, 2-methyl- piperidin-1 -yl, 1-ethyl-pyrrolidin-2-yl, 1 -methyl-pyrrolidin-2-yl, 2-oxo- pyrrolidin-1 -yl, pyridin-2-yl, pyridin-4-yl, 5-nitro-pyridin-2-yl, imidazol-1 -yl, morpholin-4-yl, 5-methoxy-1 H-indol-2-yl is particularly preferred for Het.
Het1 is thiophen-2-yl which is substituted by Ar or Het2, in which Ar and Het2 have one of the above or below mentioned meanings. 5-(4- Fluorophenyl)-thiophen-2-yl, 5-(2-methoxyphenyl)-thiophen-2-yl, 5-(2- cyanophenyl)-thiophen-2-yl, 5-(2,5-dimethoxyphenyl)-thiophen-2-yl, 2- [2,2']bithiophenyl-5-yl, 5-(pyridin-4-yl)-thiophen-2-yl, 5-(1 H-indol-5-yl)- thiophen-2-yl, 5-quinolin-8-yl-thiophen-2-yl or 5-(benzo[b]thiophen-2-yl)- thiophen-2-yl is particularly preferred for Het1.
Het2 is a unsaturated mono- or bicyclic heterocyclic radical having 5 to
10 ring members, where 1 or 2 N and/or 1 or 2 S or O atoms can be present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2, -(CH2)p-(CHA)p-N(R5)-(CH2)q-COR5, CHO, COA or COOR5. Thiophen-2-yl, 2-formyl-thiophen-3-yl, pyridin-3-yl, pyridin-2-yl, pyridin-4-yl, indol-5-yl, quinolin-8-yl, 4,6-dimethoxy-pyrimidin-2-yl, benzo[b]thiophen-2-yl or
is particularly preferred for Het2.
Het3 is a partially or completely unsaturated mono- or bicyclic heterocyclic radical having 5 to 10 ring members, where 1 or 2 N atoms are present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2) S02A or COOR5 provided that the heterocyclic radical is not bondend via an N atom.
Quinolin-5-yl and 1 -methanesulfonyl-2,3-dihydro-1 H-indol-5-yl is particularly preferred for Het3.
(CH2)0-Het is preferentially thiophen-2-yl-ethyl, tetrahydro-furan-2-yl-methyl, 1 -methyl-octahydro-indol-3-yl-methyl, 1 -methyl-octahydro-indol-3-yl-ethyl benzo[1 ,3]dioxol-5-yl-methyl, benzo[1 ,3]dioxol-5-yl-ethyl, piperazin-1 -yl- ethyl, 4-methyl-piperazin-1 -yl-propyl, piperidin- -yl-ethyl, piperidin-4-yl- methyl, 1 -methyl-piperidin-3-yl-ethyl, 4-benzyl-piperidin-1 -yl-ethyl, 2-methyl- piperidin-1 -yl-propyl, 1 -ethyl-pyrrolidin-2-yl-methyl, 1 -methyl-pyrrolidin-2-yl- methyl, 2-oxo-pyrrolidin-1 -yl-propyl, pyridin-2-yl-ethyl, pyridin-4-yl-methyl, pyridin-4-yl-ethyl, imidazol-1 -yl-propyl, morpholin-4-yl-propyl or morpholin- 4-yl-ethyl.
(CH2)0-NR5-Het is preferentially (5-nitro-pyridin-2-yl)-amino-ethyl.
(CH2)o-OR5 is preferentially (CH2)2-OCH3, (CH2)3-OCH3 or (CH2)3-0(iPr). (CH2)o-OR6 is preferentially
(CH2)o-Z-(CH2)q-N(R5)2 is preferentially
CH- H
I
(CH2)3— N— (CH2)3-NH2 (CH2)2— — (CH2)2-NEt2
/ \
(CH2): N r — (CH2)3-NH2
\ / or -(CH2)3-0-(CH2)3-NH2.
(CH2)p-(CHA)p-(CH2)m-Ar is preferentially phenyl,
R and R1 are independently of each other H, A, OH, OA, Hal, N(R5)2, N02, CN, CHO, COA, CON(R5)2, COOR5, allyl, CH=CH-COOR5, .
CH=CHCON(R5)2, S02A or phenyl, which is unsubstituted or mono-, di- or trisubstituted by A, where A and Hal have a preferred meaning indicated beforehand and R5 have a preferred meaning indicated in the following.
R is preferentially H or OA. R1 is preferentially H, A, OA, Hal, allyl, CH=CH-COOR5, CH=CHCON(R5)2 or phenyl, which is unsubstituted or monosubstituted by A. H, A, OA or CI is particularly preferred for R1.
The preferred position of R1 is the 6- or 7-position of the quinazoline ring system.
R ,2 and , r R->3 are ; ind iepend ■en _tιl.y. o_f each o „._tιher ι H_ι, A Λ , cyc iloa ■l•ky ■l, - ιH_ιe«+t3 , -(CH2)0- OR5, -(CH2)o-OR6, -(CH2)0-Het, -(CH2)0-NR5-Het, -(CHA)p-(CH2)o-N(R5)2, -(CH2)p-(CHA)p-(CH2)m-Ar, -(CH2)o-Z-(CH2)q-N(R5)2,
provided that R and R3 together are not H, where A, Ar, cycloalkyl, Het or Het3 have a preferred meaning indicated beforehand and R5, R6, Q, Z, m, o, p and q have a preferred meaning indicated in the following. R2 is preferentially H or A.
R3 is preferentially A, cycloalkyl, -Het3, -(CH2)0-OR5, -(CH2)0-OR6, -(CH2)0- Het, -(CH2)0-NR5-Het, -(CHA)P-(CH2)0-N(R5)2, -(CH2)p-(CHA)p-(CH2)m-Ar, -(CH2)0-Z-(CH2)q-N(R5)2l
Furthermore NR2R3 together form a saturated monocyclic heterocyclic radical having 5 to 6 ring members, where 1 or 2 N atoms are present and the heterocyclic radical can be mono- or disubstituted by OH, Ar, OAr or arylalkyl, where Ar or arylalkyl have a preferred meaning indicated beforehand.
Preferred saturated monocyclic heterocyclic radicals can be piperidine or piperazine.
are particularly preferred for NR 2r R->3.
R4 is Ar or Het1, where Ar or Het1 have a preferred meaning indicated beforehand. Phenyl, 4-bromophenyl, 3,5-bis-(trifluoromethyl)phenyl, 4-tert.- butylphenyl, 3-bromo-6-fluorophenyl, 4-(pyridin-3-yl)phenyl, 3-(pyridin-3- yl)phenyl, 4-(thiophen-2-yl)phenyl, 3-(thiophen-2-yl)phenyl, naphthyl, biphenyl-4-yl, 4'-fluorobiphenyl-4-yl, 4'-fluorobiphenyl-3-yl, 4'-chloro- biphenyl-4-yl, 4'-chlorobiphenyl-3-yl, 4'-methoxybiphenyl-4-yl, 4'-methoxybiphenyl-3-yl, (3',5'-dichloro)biphenyl-3-yl is particularly preferred as Ar in R4.
Phenyl, 4-bromophenyl, 3,5-bis-(trifluoromethyl)phenyl, 4-tert.-butylphenyl, 3-bromo-6-fluorophenyl, 4-(pyridin-3-yl)phenyl, 3-(pyridin-3-yl)phenyl, 4- (thiophen-2-yl)phenyl, 3-(thiophen-2-yl)phenyl, naphthyl, biphenyl-4-yl, 4'-fluorobiphenyl-4-yl, 4'-fluorobiphenyl-3-yl, 4'-chlorobiphenyl-4-yl, 4'-chlorobiphenyl-3-yl, 4'-methoxybiphenyl-4-yl, 4'-methoxybiphenyl-3-yl, (3',5'-dichloro)biphenyl-3-yl, 5-(4-fluorophenyl)-thiophen-2-yl, 5-(2- methoxyphenyl)-thiophen-2-yl, 5-(2-cyanophenyl)-thiophen-2-yl, 5-(2,5- dimethoxyphenyl)-thiophen-2-yl, 2-[2,2']bithiophenyl-5-yl, 5-(pyridin-4-yl)- thiophen-2-yl, 5-(1 H-indol-5-yl)-thiophen-2-yl, 5-quinolin-8-yl-thiophen-2-yl or 5-(benzo[b]thiophen-2-yl)-thiophen-2-yl is particularly preferred for R4.
R5 is H or A, where A has a preferred meaning indicated beforehand.
R6 is benzo[1 ,3]dioxol-5-yl.
R7 is H, A, cycloalkyl or (CH2)q-OR5, where A, cycloalkyl and R5 have a preferred meaning indicated beforehand and q is preferrably 2 or 3.
Q is O or S, preferentially 0.
Y is a direct bond, (CH2)n or -NR5-(CH2)m-, where R5 has a preferred meaning indicated beforehand and n and m have a preferred meaning indicated in the following. Y is preferentially a direct bond or (CH2)n, very particularly preferably a direct bond.
Z is phenylene, cyclohexylene, -NR5-, O, -CH(OH)-, -CA2- or
, where R5 and A have a preferred meaning indicated beforehand. Phenylene and/or cyclohexylene are particularly bonded in 1 ,4- or 1 ,3-position.
n is 1 , 2, 3, 4, 5 or 6, preferentially 4. m is 0, 1 , 2, 3, 4, 5 or 6, preferentially 0, 1 , 2 or 3. o is 1 , 2, 3, 4, 5, 6 or 7, preferentially 1 , 2, 3 or 7. p is 0, 1 , 2, 3 or 4, preferentially 0, 1 or 2. q is 1 , 2, 3 or 4, preferentially 1 , 2 or 3.
Some preferred groups of compounds can be expressed by the following subformulae la to In, which correspond to the formula I and in which the radicals not designated in greater detail have the meanings indicated in formula I, but in which
in la R is H or OA and
R1 is H, A, OA or Hal;
in lb R is H or OA,
R1 is H, A, OA or Hal and Y is (CH2)n;
in lc R is H or OA,
R1 is H, A, OA or Hal,
R4 is Ar,
Ar is unsubstituted phenyl and Y is (CH2)n;
in ld R is H or OA,
R1 is H, A, OA or Hal and
Y is a direct bond;
in le R is H or OA,
R1 is H, A, OA or Hal and Y is -N(R5)-(CH2)m-;
in if R is H or OA,
R1 is H, A, OA or Hal,
R4 is Ar and
Y is a direct bond;
in lg R is H or OA,
R1 is H, A, OA or Hal,
R4 Ar,
Ar is phenyl or biphenyl, which is unsubstituted or substituted by Hal, Het2, OA or -(CH2)P-N(R7)2,
R7 is H, A, cycloalkyl, (CH2)3-OR5 or (CH2)2-OR5 and
Y is a direct bond;
in Ih R is H, R1 is Hal,
R2 is H,
R3 is -(CH2)0-Het, -(CHA)p-(CH2)o-N(R5)2 or
-(CH2)P-(CHA)p-(CH2)m-Ar,
R4 is Ar Ar is unsubstituted phenyl and
Y is a direct bond; ιn li R is H, R1 is Hal, R2 is H, Rs is -(CH2)0-Het, -(CHA)p-(CH2)o-N(R5)2l -(CH2)0-NR5-Het,
-(CH2)0-Z-(CH2)q-N(R5)2 or -(CH2)p-(CHA)p-(CH2)m-Ar,
R« is Ar,
Ar is biphenyl-4-yl and Y is a direct bond;
in lj R is H,
R1 is Hal,
R2 is H or A,
R3 is A, cycloalkyl, -Het3, -(CH2)0-OR5, -(CH2)0-OR6, -(CH2)0-Het, -(CH2)0-NR5-Het, -(CHA)P-(CH2)0-N(R5)2, -(CH2)P-(CHA)P- (CH2)m-Ar, -(CH2)o-Z-(CH2)q-N(R5)2,
or NR2R3 together form a saturated monocyclic heterocyclic radical having 5 to 6 ring members, where 1 or 2 N atoms are present and the heterocyclic radical can be mono- or disubstituted by OH, Ar, OAr or arylalkyl,
R4 is Ar,
Ar is phenyl which is substituted by Br and
Y is a direct bond;
in Ik R is H, R1 is Hal, R2 is H, R3 is -(CH2)0-Het or -(CHA)P-(CH2)0-N(R5)2,
R is Ar,
Ar is phenyl or biphenyl, which is unsubstituted or substituted by
Hal, Het2, OA or -(CH2)P-N(R7)2, R7 is H, A, cycloalkyl, (CH2)3-OR5 or (CH2)2-OR5 and Y is a direct bond;
R1 is Hal,
R2 is H,
R3 is -(CH2)0-Het or -(CHA)P-(CH2)0-N(R5)2,
R4 is Het1,
Het1 is thiophen-2-yl, which is substituted by Ar or Het2
R7 is H, A, cycloalkyl, (CH2)3-OR5 or (CH2)2-OR5 and
Y is a direct bond;
in In R is H,
R1 is Hal,
R^ is H,
R3 is -(CH2)0-Het or -(CHA)p-(CH2)o-N(R5)2,
R4 is Het1,
Het1 is 5-(4-fluoro-phenyl)-thiophen-2-yl, 5-(2-methoxy-phenyl)- thiophen-2-yl, 5-(2-cyano-phenyl)-thiophen-2-yl, 5-(2,5- dimethoxy-phenyl)-thiophen-2-yl, 2-[2,2']bithiophenyl-5-yl, 5- (1 H-indol-5-yl)-thiophen-2-yl, 5-pyridine-4-yl-thiophen-2-yl, 5- quinolin-8-yl-thiophen-2-yl or 5-benzo[b]thiophen-2-yl- thiophen-2-yl
R7 is H, A, cycloalkyl, (CH2)3-OR5 or (CH2)2-OR5 and
Y is a direct bond.
The compounds of the formula I and also the starting substances for their preparation are otherwise prepared by methods known per se, such as are described in the literature (e.g. in the standard works such as Houben- Weyl, Methoden der organischen Chemie [Methods of Organic Chemistry], Georg-Thieme-Verlag, Stuttgart), namely under reaction conditions which are known and suitable for the reactions mentioned. In this case, use can also be made of variants which are known per se, but not mentioned here in greater detail.
The starting substances, if desired, can also be formed in situ such that they are not isolated from the reaction mixture, but immediately reacted further to give the compounds of the formula I.
The compounds of the formula I can be obtained by liberating them from their functional derivatives by solvolysis, in particular hydrolysis or by hydrogenolysis.
Preferred starting substances for the solvolysis or hydrogenolysis are those which otherwise correspond to the formula I, but instead of one or more free amino and/or hydroxyl groups contain corresponding protected amino and/or hydroxyl groups, in particular those which instead of an H-N- group carry an R'-N- group, in which R' is an amino protective group and/or those which instead of the H atom of a hydroxyl group carry a hydroxyl protective group, e.g. those which correspond to the formula I, but instead of a group -COOH carry a group -COOR", in which R" is a hydroxyl protective group.
A number of - identical or different - protected amino and/or hydroxyl groups can also be present in the molecule of the starting substance. If the protective groups present are different from one another, in many cases they can be removed selectively (lit.: T.W. Greene, P.G.M. Wuts, Protective Groups in Organic Chemistry, 2nd ed., Wiley, New York 1991 or P.J. Kocienski, Protecting Groups, 1st ed., Georg Thieme Verlag, Stuttgart - New- York, 1994). The expression "amino protective group" is generally known and relates to groups which are suitable for protecting (for blocking) an amino group against chemical reactions, but which are easily removable after the desired chemical reaction has been carried out at other positions in the molecule. Typical groups of this type are, in particular, unsubstituted or substituted acyl, aryl, aralkoxymethyl or aralkyl groups. Since the amino protective groups are removed after the desired reaction (or reaction sequence), their nature and size is otherwise not critical; however, those having 1-20, in particular 1-8, C atoms are preferred. The expression "acyl group" is to be interpreted in the widest sense in connection with the present process. It includes acyl groups derived from aliphatic, araliphatic, aromatic or heterocyclic carboxylic acids or sulfonic acids and, in particular, alkoxycarbonyl groups, aryloxycarbonyl groups and especially aralkoxycarbonyl groups. Examples of acyl groups of this type are alkanoyl such as acetyl, propionyl, butyryl; aralkanoyl such as phenylacetyl; aroyl such as benzoyl or toluyl; aryloxyalkanoyl such as POA; alkoxycarbonyl such as methoxycarbonyl, ethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, BOC, 2-iodoethoxycarbonyl; aralkyloxycarbonyl such as CBZ ("carbobenzoxy"), 4-methoxybenzyloxycarbonyl (MOZ), 4-Nitro- benzyloxycarbonyl oder 9-fluorenylmethoxycarbonyl (Fmoc); 2-
(phenylsulfonyl)ethoxycarbonyl; trimethylsilylethoxycarbonyl (Teoc) or arylsulfonyl such as 4-methoxy-2,3,6-trimethyiphenyl-sulfonyl (Mtr). Preferred amino protective groups are BOC, furthermore CBZ, Fmoc, benzyl and acetyl; particularly preferred Fmoc.
The expression "hydroxyl protective group" is also generally known and relates to groups which are suitable for protecting a hydroxyl group against chemical reactions, but which are easily removable after the desired chemical reaction has been carried out at other positions in the molecule.
Typical groups of this type are the above mentioned unsubstituted or substituted aryl, aralkyl, aroyl or acyl groups, furthermore also alkylgroups, alkyl-, aryl- or aralkylsilylgroups or 0,0- or 0,S-acetals. The nature and size of the hydroxyl protective groups is not critical, since they are removed again after the desired chemical reaction or reaction sequence; groups having 1-20, in particular 1-10 C atoms, are preferred. Examples of hydroxyl protective groups are, inter alia, benzyl, 4-methoxybenzyl or 2,4- dimethoxybenzyl, aroyl groups such as benzoyl or p-nitrobenzoyl, acyl groups such as acetyl or pivaloyl, p-toluolsulfonyl, alkyl groups such as methyl or tert-butyl, but also allyl, alkylsilyl groups such as trimethylsilyl (TMS), triisopropylsilyl (TIPS), tert-butyldimethylsilyl (TBS) or triethylsilyl, trimethylsilylethyl, aralkylsilyl groups such as tert-butyldiphenylsilyl (TBDPS), cyclic acetals such as isopropylidene-, cyclopentylidene-, cyclohexylidene-, benzylidene-, p-methoxybenzylidene- or o,p- dimethoxybenzylideneacetal, acyclic acetales such as tetrahydropyranyl (Thp), methoxymethyl (MOM), methoxyethoxymethyl (MEM), benzyloxymethyl (BOM) or methylthiomethyl (MTM). Acetyl, benzyl, tert- butyl or TBS being particularly preferred.
The liberation of the compounds of the formula I from their functional derivatives depending on the protective group used is known in the present literature such as T.W. Greene, P.G.M. Wuts, Protective Groups in Organic Chemistry, 2nd ed., Wiley, New York 1991 , P.J. Kocienski, Protecting Groups, 1 st ed., Georg Thieme Verlag, Stuttgart - New- York, 1994. In this case, use can also be made of variants which are known per se, but not mentioned here in greater detail.
The groups BOC and O-tert-butyl can preferably be removed, for example, using TFA in dichloromethane or using approximately 3 to 5N HCI in dioxane at 15-30°C, the Fmoc group using an approximately 5 to 50% solution of dimethylamine, diethylamine or piperidine in DMF at 15-30°C.
Preferred starting substances for the solvolysis or hydrogenolysis includes also those which otherwise correspond to the formula I, but are attached to a solid phase. The liberation of the compounds of the formula I from the solid phase is known in the present literature such as Novabiochem - The Combinatorial Chemistry Catalog, March 99 and cited literature.
The solid phase with a carbonate moiety as terminal functional group can preferably be removed, for example, using TFA (50%) in dichloromethane.
The quinazolines of formula I can also preferably be prepared, using either solution or solid-phase techniques.
The term solid phase indicates a resin for solid-phase chemistry, especially for combinatorial chemistry, i.e. by robot- and computer-assisted syntheses, and subjected to mass screening as indicated in US 5,463,564; M. A. Gallop et al., J. Med. Chem. 1994, 37, 1233-1251 and 1385-1401 and M.J. Sofia, Drug Discovery Today 1996, 1 , 27-34). The polymeric material of the solid phase is generally chosen from the group consisting of cross-linked polystyrene, cross-linked polyacrylamide or other resins, natural polymers or silicagels.
The group of cross-linked polystyrene, cross-linked polyacrylamide or other resins includes e.g. polyacrylamide, poLymethacrylamide, polyhydroxyethylmethacrylate, polyamide, polystyrene, (meth)acrylate copolymers, for instance from (methy) acrylic acid, esters of (meth)acrylic acid and/or 2-methylene-succinic acid, but-2-enoic acid or maleic acid, polyurethanes or other copolymers.
Suitable terminal functional groups or linkers on the surface of the resin have to be chosen to attach the compounds to the resin. There exists a variety of commercially available resins, e.g. in Novabiochem - The Combinatorial Chemistry Catalog, March 99. Examples for suitable resins are carbonate resins with a modified carbonate group as terminal functional group like p-nitrophenylcarbonate resin, halogenated resins like Merrifield resin (chloromethylpolystyrene) or carboxy resins like carboxy polystyrene resin or NovaSyn® TG Carboxy Resin. p-Nitrophenylcarbonate resin is particularly preferred. These and other types of resins well known in the art can be used in the subject invention.
The quinazoiines of formula I, in which Y is a direct bond or (CH2)n, can preferably be prepared by combining and reacting a 2-amino-benzonitrile of formula II with an aldehyde of formula III followed by converting the cyano group to an amide group, reacting the given formula IV with a base, chlorinating the given quinazolin-4-one of formula V and reacting the given formula VI with an amine of formula VII. The conversion of the cyano group to the amide group occurs by conventional means which are known to a skilled artisan. Particularly, the conversion occurs via oxidation within the presence of a base. The quinazoiines of formula I, in which Y is -N(R5)-(CH2)m-, can be prepared by reacting a 2,4-dichloro-quinazoline of formula VIII with an amine of formula VII and reacting the given formula IX with an amine of formula X.
As a rule, the starting compounds of the formulae II, III, VII, VIII and X are known or commercially available.
The unknown compounds, however, can be prepared by methods known per se. The 2,4-dichloro-quinazolines of formula II in which R and R1 have a meaning indicated in claim 1 can be prepared by reacting a substituted anthranilic acid with KOCN/acetic acid in the presence of a base and chlorinating the given 1 H-quinazoline-2,4-dione. The aldehydes of formula III, as a rule, are also commercially available. Furthermore, syntheses for the preparation of aldehydes of formula III, such as, for example, the oxidation of an alcohol, can be used.
The amines of formula VII or X in which R2, R3, NR R3, R5, R4 and m have a meaning indicated in claim 1 , as a rule, are also commercially available and can be attached to the suitable resin or to a compound of formula VI, VIII or IX by coupling procedures well known in the art and as described in the ensuing Examples. Furthermore, syntheses for the preparation of amines of formula VII or X, such as, for example, the Gabriel synthesis, can be used.
For the preparation of compounds of the formula I in which R4 is unsubstituted or substituted biphenyl, heteroarylsubstituted phenyl or aryl- or heteroaryl-substituted thiophenyl, an appropriate compound of the formula I in which R4 is phenyl chloride, phenyl bromide, phenyl iodide, thiophenyl chloride, thiophenyl bromide or thiophenyl iodide can be reacted with the appropriate boronic acid derivatives in a Suzuki type coupling reaction. This reaction is expediently carried out under Palladium catalysis with different phosphines as coordination ligands, e.g. Pd(P(Ph)3)2,
Pd(ll)CI2dppf, PdOAc2 + P(R*)3 (R* = phenyl, cyclohexyl, tert-butyl) etc. in the presence of a base such as potassium carbonate, cesium carbonate, DBU, NaOH, in an inert solvent or solvent mixture, e.g. DMF or 1 ,4-dioxane at temperatures between 0° and 150°, preferably between 60° and 120°. Depending on the conditions used, the reaction time is between a few minutes and a number of days. The boronic acid derivatives can be prepared by conventional methods or are commercially available. The reactions can be carried out in analogy to the methods indicated in Suzuki et al., J. Am. Chem. Soc. 1989, 111 , 314ff., Suzuki et al., Chem. Rev. 1995, 95, 2457ff and G.C. Fu et al. Angew. Chem 1998, 110, 3586.
The Suzuki type coupling reaction can be furthermore used to convert radicals R and R1 into other radicals R and R1, for e.g. to convert a halogen substituted quinazoiines to a quinazoline substituted by substituted or unsubstituted phenyl.
For the preparation of compounds of the formula I in which R or R1 is allyl, an appropriate compound of the formula I in which R4 is quinazoline chloride, quinazoline bromide or quinazoline iodide can be reacted with allyltributyltin in a Stille type coupling reaction. This reaction is expediently carried out under Palladium catalysis with different phosphines as coordination ligands, e.g. Pd(P(Ph)3)2, Pd(ll)CI2dppf, PdOAc2 + P(R*)3 (R* = phenyl, cyclohexyl, tert-butyl) etc. in an inert solvent or solvent mixture, e.g. DMF or 1 ,4-dioxane at temperatures between 0° and 150°, preferably between 60° and 120°. Depending on the conditions used, the reaction time is between a few minutes and a number of days.
For the preparation of compounds of the formula I in which R or R1 is CH=CH-COOR5 or CH=CH-CON(R5)2, an appropriate compound of the formula I in which R4 is quinazoline chloride, quinazoline bromide or quinazoline iodide can be reacted with substituted acrylate in a Heck type coupling reaction. This reaction is expediently carried out under Palladium catalysis with different phosphines as coordination ligands, e.g.
Pd(P(Ph)3)2, Pd(ll)CI2dppf, PdOAc2 + P(R*)3 (R* = phenyl, cyclohexyl, tert- butyl) etc. in the presence of a base such as triethyl amine or a catalyst tetrabutylammonium iodide, in an inert solvent or solvent mixture, e.g. DMF or 1 ,4-dioxane at temperatures between 0° and 150°, preferably between 60° and 120°. Depending on the conditions used, the reaction time is between a few minutes and a number of days.
A base of the formula I can be converted into the associated acid addition salt using an acid, for example by reaction of equivalent amounts of the base and of the acid in an inert solvent such as ethanol and subsequent evaporation. Acids which give physiologically acceptable salts are particularly suitable for this reaction. Thus inorganic acids can be used, e.g. sulfuric acid, nitric acid, hydrohalic acids such as hydrochloric acid or hydrobromic acid, phosphoric acids such as orthophosphoric acid, sulfamic acid, furthermore organic acids, in particular aliphatic, alicyclic, araliphatic, aromatic or heterocyclic mono- or polybasic carboxylic, sulfonic or sulfuric acids, e.g. formic acid, acetic acid, propionic acid, pivalic acid, diethylacetic acid, malonic acid, succinic acid, pimelic acid, fumaric acid, maleic acid, lactic acid, tartaric acid, malic acid, citric acid, gluconic acid, ascorbic acid, nicotinic acid, isonicotinic acid, methane- or ethanesulfonic acid, p-toluenesulfonic acid, naphthalenemono- and disulfonic acids or laurylsulfuric acid. Salts with physiologically unacceptable acids, e.g. picrates, can be used for the isolation and/or purification of the compounds of the formula I. On the other hand, compounds of the formula I with bases (e.g sodium or potassium hydroxide or carbonate) can be converted into the corresponding metal salts, in particular alkali metal or alkaline earth metal salts, or into the corresponding ammonium salts.
The invention furthermore relates to pharmaceutical preparations comprising at least one compound of the formula I and/or one of its physiologically acceptable salts, which are prepared, in particular, in an non-chemical way. In this case, the compounds of the formula I according to the invention can be brought into a suitable dose form together with at least one solid, liquid and/or semi-liquid excipient or auxiliary and, if appropriate, in combination with one or more other active compounds.
These preparations can be used as medicaments in human or veterinary medicine. Possible excipients are organic or inorganic substances which are suitable for enteral (e.g. oral) or parenteral administration or topical application and do not react with the novel compounds, for example water, vegetable oils, benzyl alcohols, alkylene glycols, polyethylene glycols, glyceryl triacetate, gelatin, carbohydrates such as lactose or starch, magnesium stearate, talc and petroleum jelly. Tablets, pills, coated tablets, capsules, powders, granules, syrups, juices or drops are used, in particular, for oral administration, suppositories are used for rectal administration, solutions, preferably oily or aqueous solutions, furthermore suspensions, emulsions or implants, are used for parenteral administration, and ointments, creams or powders are used for topical application. The novel compounds can also be lyophilized and the lyophilizates obtained used, for example, for the production of injection preparations. The preparations indicated can be sterilized and/or can contain auxiliaries such as lubricants, preservatives, stabilizers and/or wetting agents, emulsifiers, salts for affecting the osmotic pressure, buffer substances, colorants, flavorings and/or one or more other active compounds, e.g. one or more vitamins.
The compounds of the formula I and their physiologically acceptable salts act as adhesion receptor antagonists, in particular glycoprotein IblX antagonists, and can be employed for the prophylaxis and/or therapy of thrombotic disorders and sequelae deriving therefrom. The disorders are acute coronary syndromes, angina pectoris, myocardial infarct, peripheral circulatory disorders, stroke, transient ischaemic attacks, arteriosclerosis and reocclusion/restenosis after angioplasty/stent implantation.
In this case, the substances according to the invention are as a rule administered in the dose of the glycoprotein llbllla antagonist ReoPro® of preferably between approximately 1 and 500 mg, in particular between 5 and 100 mg, per dose unit. The daily dose is preferably between approximately 0.02 and 10 mg/kg of body weight. The specific dose for each patient depends, however, on all sorts of factors, for example on the efficacy of the specific compound employed, on the age, body weight, general state of health and sex, on the diet, on the time and route of administration, and on the excretion rate, pharmaceutical combination and severity of the particular disorder to which the therapy applies. Oral administration is preferred.
Above and below, all temperatures are indicated in °C. In the following examples, "customary working-up" for solution reactions means: if necessary, water is added, if necessary, depending on the constitution of the final product, the mixture is adjusted to pHs between 2 and 10 and extracted with ethyl acetate or dichloromethane, the organic phase is separated off, dried over sodium sulfate and evaporated, and the residue is purified by chromatography on silica gel and/or by crystallization.
"Customary working-up" for solid-phase reactions means: the crude reaction is filtered and washed with DMF twice, then sucessively with methanol and methylene chloride three times, and finally once with methyl tert-butyl ether. The resin is then dried in vacuo.
Mass spectrometry (MS) apparatuses Kratos OMIT and Finnigan LCQ. (M+H)+ values or M+ values are determined.
EXAMPLES
Example 1 :
1. Pyridine (0,144 mole) is given to a solution of 2-amino-4- chlorobenzonitrile (0,131 mole) in 100 ml tetrahydrofuran (THF) and a solution of 4-bromobenzoylchloride (31 ,6 g, 0,144 mole) in 50 ml THF is added under nitrogen. After addition of 100 ml THF, the mixture is stirred for 6 h at room temperature (rt). The crude reaction is then customary worked up for solution reactions affording 4-bromo-N-(5-chloro-2-cyano- phenyl)-benzamide as a solid; m.p. 151-152°. MS calc: 335,6 ; found: 336, 338. 2. A suspension of 4-bromo-N-(5-chloro-2-cyano-phenyl)-benzamide (30 g, 89,4 mmol) in 500 ml methanol is mixed with 130 ml NaOH (2N) and perhydrite tablets [(H202), 50 g]. The mixture is heated to boiling for 2 hrs. After cooling to rt and customary working up 4-bromo-N-(5-chloro-2- aminocarbonyl-phenyl)-benzamide is obtained as a solid; m.p. 172-173°.
MS calc: 354 ; found: 354.
3. 4-Bromo-N-(5-chloro-2-aminocarbonyl-phenyl)-benzamide (18,25 g, 51 ,6 mmol) is solved in 250 ml dioxane and 250 ml NaOH (1 N) are added. The mixture is heated to boiling for 5 days. After cooling to rt and customary working up 2-(4-bromo-phenyl)-7-chloro-3H-quinazolin-4-one is obtained as a solid; m.p. > 300°.
MS calc: 336 ; found: 336.
4. 2-(4-Bromo-phenyl)-7-chloro-3H-quinazolin-4-one (38,7 mmol) is added to 50 ml thionylchloride and is heated at 40°. The mixture is treated with 6 ml dimethylformamide (DMF). After cooling to rt the mixture is stirred for 3 hrs. Customary working up gives 2-(4-bromo-phenyl)-4,7-dichloro- quinazoline as a solid; m.p. 189-190°. MS calc: 354.0 ; found: 355.
5. A solution of 2-(4-bromo-phenyl)-4,7-dichloro-quinazoline (0,085 mmol, 30 mg) in 2 ml THF is treated with aniline (0,01 ml, 0,11 mmol). The suspension is heated to 60° and stirred for 18 hrs. The reaction mixture is filtered and the crystals are washed with THF and dried. [2-(4-Bromo- phenyl)-7-chloro-quinazolin-4-yl]-phenyl-amine is obtained. MS calc: 410,7 ; found: 411.
Example 2: Analogously to example 1, 1-(4-bromo-phenyl)-4,7-dichloro-quinazoline is reacted with HNR2R3 to obtain compounds of formula 11 according to table 1.
Table 1 : 4-bromophenyl-quinazolines of formula 11
Example 3:
A solution of 2-(4-bromo-phenyl)-4,7-dichloro-quinazoline (0,085 mmol, 30 mg) [prepared analogously to example 1] in 2 ml THF is treated with benzylamine (0,174 mmol, 0,019 ml). The mixture is heated at 60° for 6 hrs. After cooling to rt, the reaction mixture is filtered through a tentacle ion exchanger (LiChrolut® SCX: Merck ChromBook, 2nd ed. page 31).
Evaporation of the solvent afforded benzyl-[2-(4-bromo-phenyl)-7-chloro- quinazolin-4-yl]-amine.
MS calc: 424,7 ; found: 425.
Example 4: Analogously to example 3, 2-(4-bromo-phenyl)-4,7-dichloro-quinazoline is reacted with HNR •>2 Rr-ι3 to obtain compounds of formula 11
according to table 2.
Table 2: 4-bromophenyl-quinazolines of formula 11
Example 5:
Analogously to example 3, 2-(4-bromo-phenyl)-4-chloro-6-methyl- quinazoline is reacted
with 1-propyl-pyrrolidin-2-one to obtain 1-{3-[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-ylamino]-propyl}- pyrrolidin-2-one; MS calc: 439,4 ; found: 439,6;
with [2-(2-aminomethyl-phenylsulfanyl)-phenyl]-methanol to obtain
[2-(2-{[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-ylamino]-methyl}- phenylsulfanyl)-phenyl]-methanol; MS calc: 542,5 ; found: 544,2;
with 3-(2-methyl-piperidin-1-yl)-propylamine to obtain
[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-[3-(2-methyl-piperidin-1- yl)-propyl]-amine; MS calc: 453,4 ; found: 453,3;
with 2-pyridin-2-yl-ethylamine to obtain
[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-(2-pyridin-2-yl-ethyl)- amine; MS calc: 419,3 ; found: 419,3;
with 1-(3-trifluoromethyl-phenyl)-piperazine to obtain
2-(4-bromo-phenyl)-6-methyl-4-[4-(3-trifluoromethyl-phenyl)-piperazin-1- yl]-quinazoline; MS calc: 419,3 ; found: 419,3; with C-(1-ethyl-pyrrolidin-2-yl)-methylamine to obtain
[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-(1 -ethyl-pyrrolidin-2- ylmethyl)-amine;
MS calc: 425,4 ; found: 425,6;
with 4-benzyl-piperidin-4-ol to obtain
4-benzyl-1 -[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-piperidin-4-ol;
MS calc: 488,4 ; found: 490,3;
with 1 -phenyl-piperazine to obtain
2-(4-bromo-phenyl)-6-methyl-4-(4-phenyl-piperazin-1 -yl)-quinazoline; MS calc: 459,4 ; found: 459,4;
with 3-morpholin-4-yl-propylamine to obtain [2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-(3-morpholin-4-yl-propyl)- amine; MS calc: 441 ,4 ; found: 441 ,3;
with 2-(1-methyl-pyrrolidin-2-yl)-ethylamine to obtain [2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-[2-(1-methyl-pyrrolidin-2- yl)-ethyl]-amine; MS calc: 425,4 ; found: 425,4;
with 3-(4-methyl-piperazin-1 -yl)-propyIamine to obtain [2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-[3-(4-methyl-piperazin-1- yl)-propyl]-amine; MS calc: 454,4 ; found: 454,4;
with 3,4,5-trimethoxy-benzylamine to obtain [2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-(3,4,5-trimethoxy-benzyl)- amine; MS calc: 494,4 ; found: 496,1 ; with 2-fluoro-benzylamine to obtain
[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-(2-fluoro-benzyl)-amine; MS calc: 422,3 ; found: 422,4;
with benzyl-methyl-amine to obtain benzyl-[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-methyl-amine; MS calc: 418,3 ; found: 418,4;
with methyl-(1 -methyl-piperidin-4-ylmethyl)-amine to obtain
[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-methyl-(1-methyl-piperidin- 4-ylmethyl)-amine; MS calc: 425,3 ; found: 425,2;
with cyclohexyl-methyl-amine to obtain
[2-(4-bromo-phenyl)-6-methyl-quinazolin-4"-yl]-cyclohexyl-methyl-amine; MS calc: 410,4 ; found: 412,1;
with N1,N1-dimethyl-ethane-1 ,2-diamine to obtain N'-[2-(4-bromo-phenyi)-6-methyl-quinazolin-4-yI]-N,N-dimethyl-ethane-
1 ,2-diamine; MS calc: 385,3 ; found: 386,3;
with butyl-methyl-amine to obtain [2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-butyl-methyl-amine;
MS calc: 384,3 ; found: 384,4;
with N,N,N'-trimethyl-propane-1 ,3-diamine to obtain
N-[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-N,N',N,-trimethyl- ρropane-1 ,3-diamine;
MS calc: 413,4 ; found: 415,2; with 4-benzyl-piperidine to obtain
4-(4-benzyl-piperidin-1-yl)-2-(4-bromo-phenyl)-6-methyl-quinazoline; MS calc: 472,4 ; found: 474,3;
with N1,N1-diethyl-pentane-1 ,4-diamine to obtain
N4-[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-N1,N1-diethyl-pentane- 1 ,4-diamine; MS calc: 455,4 ; found: 455,3;
with butylamine to obtain
[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-butyl-amine;
with N,N-diethyl-propane-1 ,3-diamine to obtain
N'-[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-N,N-diethyl-propane- 1 ,3-diamine;
with benzylamine to obtain benzyl-[2-(4-bromo-phenyl)-6-methyl-quinazolin-4-yl]-amine.
Example 6:
Analogously to example 3, 2-(4-bromo-phenyl)-4,6-dichloro-quinazoline is reacted
with N1,N1-diethyl-pentane-1 ,4-diamine to obtain N4-[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-N1,N1-diethyl-pentane-
1 ,4-diamine; MS calc: 475,86 ; found: 476;
with 4-benzyl-piperidine to obtain 4-(4-benzyl-piperidin-1-yl)-2-(4-bromo-phenyl)-6-chloro-quinazoline;
MS calc: 492,84; found: 493; with N,N,N'-trimethyl-propane-1 ,3-diamine to obtain
N-[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-N,N',N'-trimethyl- propane-1 ,3-diamine; MS calc: 433,78; found: 434;
with butyl-methyl-amine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-butyl-methyl-amine; MS calc: 404,74 ; found: 405;
with N1,N1-dimethyl-ethane-1 ,2-diamine to obtain
N'-[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-N,N-dimethyl-ethane- 1 ,2-diamine;
with N1,N1-diethyl-ethane-1 ,2-diamine to obtain N'-[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-N,N-diethyl-ethane-1 ,2- diamine;
with cyclohexyl-methyl-amine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-cyclohexyl-methyl-amine; MS calc: 430,77; found: 431 ;
with methyl-(1 -methyl-piperidin-4-ylmethyl)-amine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-methyl-(1-methyl-piperidin- 4-ylmethyl)-amine; MS calc: 445,79; found: 446;
with benzyl-methyl-amine to obtain benzyl-[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-methyl-amine; MS calc: 438,75; found: 439;
with 2-fluoro-benzylamine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-(2-fluoro-benzyl)-amine; MS calc: 442,72; found: 443;
with 3,4,5-trimethoxy-benzylamine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-(3,4,5-trimethoxy-benzyl)- amine;
MS calc: 514,80; found: 515;
with 3-(4-methyl-piperazin-1-yl)-propylamine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-[3-(4-methyl-piperazin-1- yl)-propyl]-amine;
MS calc: 474,8 ; found: 474;
with 2-(1-methyl-pyrrolidin-2-yl)-ethylamine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-[2-(1-methyl-pyrrolidin-2- yl)-ethyl]-amine;
MS calc: 445,79; found: 446;
with 3-morpholin-4-yl-propylamine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-(3-morpholin-4-yl-propyl)- amine;
MS calc: 461 ,78; found: 462;
with 1-phenyl-piperazine to obtain
2-(4-bromo-phenyl)-6-chloro-4-(4-phenyl-piperazin-1-yl)-quinazoline; MS calc: 479,81 ; found: 480;
with 4-benzyl-piperidin-4-ol to obtain
4-benzyl-1-[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-piperidin-4-ol; MS calc: 508,84; found: 509;
with C-(1 -ethyl-pyrrolidin-2-yl)-methylamine to obtain [2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-(1 -ethyl-pyrrolidin-2- ylmethyl)-amine; MS calc: 445,78; found: 446;
with 1-(3-trifluoromethyI-phenyl)-piperazine to obtain
2-(4-bromo-phenyl)-6-chloro-4-[4-(3-trifluoromethyl-phenyl)-piperazin-1- yl]-quinazoline; MS calc: 547,80; found: 549;
with 2-pyridin-2-yl-ethylamine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-(2-pyridin-2-yl-ethyl)- amine; MS calc: 439,74; found: 440;
with 3-(2-methyl-piperidin-1 -yl)-propylamine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-[3-(2-methyl-piperidin-1-yl)- propylj-amine; MS calc: 472,83; found: 473;
with [2-(2-aminomethyl-phenylsulfanyl)-phenyl]-methanol to obtain [2-(2-{[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-ylamino]-methyl}- phenylsulfanyl)-phenyl]-methanol; MS calc: 562,92; found: 563;
with 1-propyl-pyrrolidin-2-one to obtain
1-{3-[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-ylamino]-propyl}- pyrrolidin-2-one; MS calc: 459,77; found: 460;
with butylamine to obtain
[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-butyl-amine; with N,N-diethyl-propane-1 ,3-diamine to obtain
N'-[2-(4-bromo-phenyl)-6-chloro-quinazolin-4-yl]-N,N-diethyl-propane- 1 ,3-diamine;
with benzylamine to obtain benzyl-[2-(4-bromo-phenyl)-6-chIoro-quinazolin-4-yl]-amine.
Example 7: Analogously to example 3, 2-(4-bromo-phenyl)-4-chloro-6,7-dimethoxy- quinazoline is reacted
with 1 -propyl-pyrrolidin-2-one to obtain
1-{3-[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazoIin-4-ylamino]-propyl}- pyrrolidin-2-one;
with [2-(2-aminomethyl-phenylsulfanyl)-phenyl]-methanol to obtain
[2-(2-{[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-ylamino]-methyl}- phenylsulfanyl)-phenyl]-methanol; MS calc: 588,52; found: 589;
with 3-(2-methyI-piperidin-1 -yl)-propylamine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-[3-(2-methyl- piperidin-1 -yl)-propyl]-amine; MS calc: 499,45; found: 500;
with 2-pyridin-2-yl-ethylamine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-(2-pyridin-2-yl-ethyl)- amine; MS calc: 465,35; found: 466;
with 1-(3-trifluoromethyl-phenyl)-piperazine to obtain 2-(4-bromo-phenyl)-6,7-dimethoxy-4-[4-(3-trifluoromethyl-phenyl)- piperazin-1 -yl]-quinazoline; MS calc: 573,41 ; found: 574;
with C-(1 -ethyl-pyrrolidin-2-yl)-methylamine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-(1-ethyl-pyrrolidin-2- ylmethyl)-amine; MS calc: 483,41 ; found: 484;
with 4-benzyl-piperidin-4-ol to obtain
4-benzyl-1 -[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-piperidin- 4-ol; MS calc: 534,45; found: 535;
with 1 -phenyl-piperazine to obtain
2-(4-bromo-phenyl)-6,7-dimethoxy-4-(4-phenyl-piperazin-1-yl)- quinazoline; MS calc: 505,41 ; found: 506;
with 3-morpholin-4-yl-propylamine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-(3-morpholin-4-yl- propyl)-amine; MS calc: 487,39; found: 488;
with 2-(1-methyl-pyrrolidin-2-yl)-ethylamine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-[2-(1-methyl- pyrrolidin-2-yl)-ethyl]-amine; MS calc: 471 ,39; found: 472;
with 3-(4-methyl-piperazin-1 -yl)-propylamine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-[3-(4-methyl- piperazin-1 -yl)-propyl]-amine; MS calc: 486,43; found: 487;
with 3,4,5-trimethoxy-benzylamine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-(3,4,5-trimethoxy- benzyl)-amine;
MS calc: 540,41 ; found: 541 ;
with 2-fluoro-benzylamine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-(2-fluoro-benzyl)- amine;
MS calc: 468,32; found: 469;
with benzyl-methyl-amine to obtain benzyl-[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-methyl-amine; MS calc: 464,36; found: 465;
with methyl-(1-methyl-piperidin-4-ylmethyl)-amine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-methyl-(1-methyl- piperidin-4-ylmethyl)-amine; MS calc: 471 ,40; found: 472;
with cyclohexyl-methyl-amine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-cyclohexyl-methyl- amine; MS calc: 456,38; found: 457;
with N1,N1-dimethyl-ethane-1 ,2-diamine to obtain
N'-[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-N,N-dimethyl- ethane-1 ,2-diamine; MS calc: 431 ,33; found: 432;
with N1,N1-diethyl-ethane-1 ,2-diamine to obtain N'-[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-N,N-diethyl- ethane-1 ,2-diamine;
with butyl-methyl-amine to obtain [2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-butyl-methyl-amine;
MS calc: 431 ,35; found: 432;
with N,N,N'-trimethyl-propane-1 ,3-diamine to obtain
N-[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-N,N',N'-trimethyl- propane-1 ,3-diamine;
MS calc: 459,38; found: 460;
with 4-benzyl-piperidine to obtain
4-(4-benzyl-piperidin-1 -yl)-2-(4-bromo-phenyl)-6,7-dimethoxy- quinazoline;
MS calc: 518,45; found: 519;
with N1,N1-diethyl-pentane-1 ,4-diamine to obtain
N4-[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-N1,N1-diethyl- pentane-1 ,4-diamine;
MS calc: 501 ,47; found: 502;
with butylamine to obtain
[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-butyl-amine;
with N,N-diethyl-propane-1 ,3-diamine to obtain
N'-[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-N,N-diethyl- propane-1 ,3-diamine;
with benzylamine to obtain benzyl-[2-(4-bromo-phenyl)-6,7-dimethoxy-quinazolin-4-yl]-amine. Example 8:
Analogously to example 3, 2-phenyl-4,7-dichloro-quinazoline [prepared analogously to example 1 , starting compounds 2-amino-4- chlorobenzonitrile and benzoylchloride] is reacted
with 3-imidazol-1-yl-propylamine to obtain
(7-chloro-2-phenyl-quinazolin-4-yl)-(3-imidazol-1-yl-propyl)-amine;
with N1,N1-diethyl-pentane-1 ,4-diamine to obtain N4-(7-chloro-2-phenyl-quinazolin-4-yl)-N1,N -diethyl-pentane-1 ,4- diamine;
with 3-morpholin-4-yl-propylamine to obtain
(7-chloro-2-phenyl-quinazolin-4-yl)-(3-morpholin-4-yl-propyl)-amine;
with phenyl-amine to obtain
(7-chloro-2-phenyl-quinazolin-4-yl)-phenyl-amine.
Analogously to example 3, N-[4-(4,7-dichloro-quinazolin-2-yl)-phenyl]-3- methyl-butyramide [prepared analogously to example 1 , starting compounds 2-amino-4-chlorobenzonitrile and 4-(3-methyl-butyrylamino)- benzoyl chloride] is reacted
with N1,N1-diethyl-propane-1 ,3-diamine to obtain N-{4-[7-chloro-4-(3-diethylamino-propylamino)-quinazolin-2-yl]-phenyl}-3- methyl-butyramide.
Example 9:
Analogously to example 3, 2-biphenyl-4-yl-4,7-dichloro-quinazoline [prepared analogously to example 1 , starting compounds 2-amino-4- chlorobenzonitrile and biphenyl-4-carbonyl chloride] is reacted with N1,N1-diethyl-pentane-1 ,4-diamine to obtain
N4-(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-N1,N1-diethyl-pentane-1 ,4- diamine;
with 3-imidazol-1-yl-propylamine to obtain
(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-(3-imidazol-1-yl-propyl)-amine;
with N1,N1-diethyl-ethane-1 ,2-diamine to obtain
N'-(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-N,N-diethyl-ethane-1 ,2- diamine;
with N1,N1-diethyi-propane-1 ,3-diamine to obtain
N'-(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-N,N-diethyl-propane-1 ,3- diamine;
with 3-morpholin-4-yl-propylamine to obtain
(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-(3-morpholin-4-yl-propyl)- amine;
with 1 -(3-amino-propyl)-pyrrolidin-2-one to obtain
1-[3-(2-biphenyl-4-yl-7-chloro-quinazolin-4-ylamino)-propyl]-pyrrolidin-2- one;
with 4-(2-amino-ethyl)-phenylamine to obtain [2-(4-amino-phenyl)-ethyl]-(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)- amine;
with N1-(5-nitro-pyridin-2-yl)-ethane-1 ,2-diamine to obtain
N-(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-N'-(5-nitro-pyridin-2-yl)- ethane-1 ,2-diamine;
with 2-piperazin-1-yl-ethylamine to obtain (2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-(2-piperazin-1-yl-ethyl)-amine;
with (4-aminomethyl-phenyl)-dimethyl-amine to obtain
(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-(4-dimethylamino-benzyl)- amine;
with 2-pyridin-2-yl-ethylamine to obtain
(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-(2-pyridin-2-yI-ethyl)-amine;
with C-(3-aminomethyl-cyclohexyl)-methylamine to obtain
(3-aminomethyl-cyclohexylmethyl)-(2-biphenyl-4-yl-7-chloro-quinazolin-4- yl)-amine;
with heptane-1 ,7-diamine to obtain N1-(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-heptane-1 ,7-diamine;
with propane-1 ,3-diamine to obtain
N1-(2-biphenyl-4-yl-7-chloro-quinazolin-4-yl)-propane-1 ,3-diamine.
Example 10:
Analogously to example 3, 2-(4-bromo-phenyl)-4,7-dichloro-quinazoline [prepared analogously to example 1 , starting compounds 2-amino-4- chlorobenzonitrile and 4-bromobenzoylchloride] is reacted with N1,N1-diethyl-propane-1 ,3-diamine to obtain N'-[2-(4-bromo-phenyl)-7-chloro-quinazolin-4-yl]-N,N-diethyl-propane-1 ,3- diamine.
1 ,2 Equivalents of K2C03, 1 ,2 equivalents of 4-chlorophenylboronic acid and 10 mol% of Pd((PPh3)4 are added to a solution of N'-[2-(4-bromo- phenyl)-7-chloro-quinazolin-4-yl]-N,N-diethyl-propane-1 ,3-diamine (16,5 mmol) in 80 ml of DMF and it is heated at 80° until conversion is complete. After filtering off the catalyst and customary working up for solution reactions, N'-[7-chloro-2-(4'-chloro-biphenyl-4-yl)-quinazolin-4-yl]-N,N- diethyl-propane-1 ,3-diamine is obtained.
Example 11 : Analogously to example 10, N'-[2-(4-bromo-phenyl)-7-chloro-quinazolin-4- yl]-N,N-diethyl-propane-1 ,3-diamine is reacted
with 4-methoxyphenylboronic acid to obtain
N'-[7-chloro-2-(4'-methoxy-biphenyl-4-yl)-quinazolin-4-yl]-N,N-diethyl- propane-1 ,3-diamine;
with 3-acetylaminophenylboronic acid to obtain
N-{4'-[7-chloro-4-(3-diethylamino-propylamino)-quinazolin-2-yl]-biphenyl- 3-yl}-acetamide;
with 3-formylphenylboronic acid to obtain
4'-[7-chloro-4-(3-diethylamino-propylamino)-quinazolin-2-yl]-biphenyl-3- carbaldehyde;
with 4-[(cyclohexylmethyl-amino)-methyl]-phenylboronic acid to obtain N-(7-chloro-2-{4'-[(cyclohexylmethyl-amino)-methyl]-biphenyl-4-yl}- quinazolin-4-yl)-N',N'-diethyl-propane-1 ,3-diamine.
Analogously to example 10, N'-[2-(3-bromo-phenyl)-7-chloro-quinazolin-4- yl]-N,N-diethyl-propane-1 ,3-diamine is reacted
with 3,5-dichlorophenylboronic acid to obtain
N'-[7-chloro-2-(3',5'-dichloro-biphenyl-3-yl)-quinazolin-4-yl]-N,N-diethyl- propane-1 ,3-diamine;
with 4-fluorophenylboronic acid to obtain N'-[7-chloro-2-(4'-fluoro-biphenyl-3-yl)-quinazolin-4-yl]-N,N-diethyl- propane-1 ,3-diamine.
Example 12:
Analogously to example 10, N4-[2-(4-bromo-phenyl)-7-chloro-quinazolin-4- yl]-N1,N1-diethyl-pentane-1 ,4-diamine (prepared according to example 3) is reacted
with 4-chlorophenylboronic acid to obtain N4-[7-chloro-2-(4'-chloro-biphenyl-4-yl)-quinazolin-4-yl]-N1 ,N1-diethyl- pentane-1 ,4-diamine;
with 3-formylphenylboronic acid to obtain
4'-[7-chloro-4-(4-diethylamino-1-methyl-butylamino)-quinazolin-2-yl]- biphenyl-3-carbaldehyde;
with 3-[(hydroxypropyl-amino)-methyl]-phenylboronic acid to obtain
3-({4'-[7-chloro-4-(4-diethylamino-1-methyl-butylamino)-quinazolin-2-yl]- biphenyl-3-ylmethyl}-amino)-propan-1-ol.
Analogously to example 10, N4-[2-(3-bromo-phenyl)-7-chloro-quinazolin-4- yl]-N1,N1-diethyl-pentane-1 ,4-diamine is reacted
with 4-methoxyphenylboronic acid to obtain N4-[7-chloro-2-(4'-methoxy-biphenyl-3-yl)-quinazolin-4-yl]-N1,N1-diethyl- pentane-1 ,4-diamine;
with (pyridin-3-yl)boronic acid to obtain
N4-[7-chloro-2-(3-pyridin-3-yl-phenyl)-quinazolin-4-yl]-N1,N1-diethyl- pentane-1 ,4-diamine.
Example 13: Analogously to example 3, 2-(4-bromo-phenyl)-4,7-dichIoro-quinazoline [prepared analogously to example 1 , starting compounds 2-amino-4- chlorobenzonitrile and 4-bromobenzoylchloride] is reacted with 2-(1-methyl- octahydro-indol-3-yl)-ethylamine to obtain
[2-(4-bromo-phenyl)-7-chloro-quinazolin-4-yl]-[2-(1 -methyl-octahydro-indol- 3-yl)-ethyl]-amine.
Analogously to example 10, [2-(4-bromo-phenyl)-7-chloro-quinazolin-4-yl]- [2-(1-methyl-octahydro-indol-3-yl)-ethyl]-amine is reacted
with 4-fluorophenylboronic acid to obtain
[7-chloro-2-(4'-fIuoro-biphenyl-4-yl)-quinazolin-4-yl]-[2-(1-methyl- octahydro-indol-3-yl)-ethyl]-amine;
with (thiophen-2-yl)boronic acid to obtain
[7-chloro-2-(4-thiophen-2-yl-phenyl)-quinazolin-4-yl]-[2-(1-methyl- octahydro-indol-3-yl)-ethyl]-amine;
with (pyridin-3-yl)boronic acid to obtain [7-chloro-2-(4-pyridin-3-yl-phenyl)-quinazolin-4-yl]-[2-(1-methyl- octahydro-indol-3-yl)-ethyl]-amine.
Analogously to example 10, [2-(3-bromo-phenyl)-7-chloro-quinazolin-4-yl]- [2-(1 -methyl-octahydro-indol-3-yl)-ethyl]-amine is reacted with (thiophen-2-yl)boronic acid to obtain
[7-chloro-2-(3-thiophen-2-yl-phenyl)-quinazolin-4-yl]-[2-(1-methyl- octahydro-indoI-3-yl)-ethyl]-amine;
with 3-(acetylamino)-phenylboronic acid to obtain N-(3'-{7-chloro-4-[2-(1-methyl-octahydro-indol-3-yl)-ethylamino]- quinazolin-2-yl}-biphenyl-3-yl)-formamide. Example 14:
Analogously to example 3, 2-(4-bromo-phenyl)-4,7-dichloro-quinazoline [prepared analogously to example 1 , starting compounds 2-amino-4- chlorobenzonitrile and 4-bromobenzoylchloride] is reacted with 2-(1-methyl- piperidin-3-yl)-ethylamine to obtain
[7-chloro-2-(4-bromo-phenyl)-quinazolin-4-yl]-[2-(1-methyl-piperidin-3-yl)- ethyl]-amine.
Analogously to example 10, [7-chloro-2-(4-bromo-phenyl)-quinazolin-4-yl]- [2-(1 -methyl-piperidin-3-yl)-ethyl]-amine is reacted
with 3-formylphenylboronic acid to obtain
4'-{7-chloro-4-[2-(1-methyl-piperidin-3-yl)-ethylamino]-quinazolin-2-yl}- biphenyl-3-carbaldehyde;
with (thiophen-3-yl)boronic acid to obtain
[7-chloro-2-(4-thiophen-3-yl-phenyl)-quinazolin-4-yl]-[2-(1-methyl- piperidin-3-yl)-ethyl]-amine;
with 2-(formyl-thiophen-3-yl)boronic acid to obtain
3-(4-{7-chloro-4-[2-(1-methyl-piperidin-3-yl)-ethylamino]-quinazolin-2-yl}- phenyl)-thiophene-2-carbaldehyde;
with 3-[(2-methoxy-ethylamino)-methyl]-phenylboronic acid to obtain (7-chloro-2-{3'-[(2-methoxy-ethylamino)-methyl]-biphenyl-4-yl}- quinazolin-4-yl)-[2-(1-methyl-piperidin-3-yl)-ethyl]-amine;
with {2-[1 -(methoxycarbonylmethyl-amino)-ethyl]-thiophen-3-yl}-boronic acid to obtain {1 -[3-(4-{7-chloro-4-[2-(1 -methyl-piperidin-3-yl)-ethylamino]-quinazolin-2- yI}-phenyl)-thiophen-2-yl]-ethylamino}-acetic acid methyl ester
Analogously to example 3, 2-(4-bromo-phenyl)-4,7-dichloro-quinazoline [prepared analogously to example 1] is reacted with 2-morpholin-4-yl- ethylamine to obtain
[2-(4-bromo-phenyl)-7-chloro-quinazolin-4-yl]-(2-morpholin-4-yl-ethyl)- amine.
Analogously to example 10, [2-(4-bromo-phenyl)-7-chloro-quinazolin-4-yl]-
(2-morpholin-4-yl-ethyl)-amine is reacted
with 3,4-dimethoxyphenylboronic acid to obtain [7-chloro-2-(3',4'-dimethoxy-biphenyl-4-yl)-quinazolin-4-yl]-(2-morpholin-
4-yl-ethyl)-amine;
with 4-formylphenylboronic acid to obtain
4'-[7-chloro-4-(2-morpholin-4-yl-ethylamino)-quinazolin-2-yl]-biphenyI-4- carbaldehyde;
with 2-(formyl-thiophen-3-yl)boronic acid to obtain
3-{4-[7-chloro-4-(2-morpholin-4-yl-ethylamino)-quinazolin-2-yI]-phenyl}- thiophene-2-carbaldehyde;
with 4-(propylaminomethyl)-phenylboronic acid to obtain [7-chloro-2-(4'-propylaminomethyl-biphenyl-4-yl)-quinazolin-4-yl]-(2- morpholin-4-yl-ethyl)-amine.
Example 15: Analogously to example 3, 2-(5-bromo-thiophen-2-yl)-4,7-dichloro- quinazoline [prepared analogously to example 1 , starting compounds 2-amino-4-chlorobenzonitrile and 5-bromo-thiophene-2-carbonyl chloride] is reacted with 2-(1-methyl-octahydro-indol-3-yl)-ethylamine to obtain [2-(5-bromo-thiophen-2-yl)-7-chloro-quinazolin-4-yl]-[2-(1-methyl-octahydro- indol-3-yl)-ethyl]-amine.
Analogously to example 10, [2-(5-bromo-thiophen-2-yl)-7-chloro-quinazolin- 4-yl]-[2-(1 -methyl-octahydro-indol-3-yl)-ethyl]-amine is reacted
with 4-fluorophenylboronic acid to obtain
{7-chloro-2-[5-(4-fluoro-phenyl)-thiophen-2-yl]-quinazolin-4-yl}-[2-(1- methyl-octahydro-indol-3-yl)-ethyl]-amine;
with 2-methoxyphenylboronic acid to obtain {7-chloro-2-[5-(2-methoxy-phenyl)-thiophen-2-yl]-quinazolin-4-yl}-[2-(1- methyl-octahydro-indol-3-yl)-ethyl]-amine;
with (1 H-indol-5-yl)boronic acid to obtain
{7-chloro-2-[5-(1 H-indol-5-yl)-thiophen-2-yl]-quinazolin-4-yI}-[2-(1-methyl- octahydro-indol-3-yl)-ethyl]-amine;
with (quinolin-8-yl)boronic acid to obtain
[7-chloro-2-(5-quinolin-8-yl-thiophen-2-yl)-quinazolin-4-yl]-[2-(1-methyl- octahydro-indol-3-yl)-ethyl]-amine. Analogously to example 3, 2-(5-bromo-thiophen-2-yl)-4,7-dichloro- quinazoline [prepared analogously to example 1] is reacted with N1,N1-diethyl-propane-1 ,3-diamine to obtain
N'-[2-(5-bromo-thiophen-2-yl)-7-chloro-quinazolin-4-yl]-N,N-diethyl-propane- 1 ,3-diamine.
Analogously to example 10, N'-[2-(5-bromo-thiophen-2-yl)-7-chloro- quinazolin-4-yl]-N,N-diethyl-propane-1 ,3-diamine is reacted
with (thiophen-2-yl)boronic acid to obtain
N'-(2-[2,2']bithiophenyl-5-yl-7-chloro-quinazolin-4-yl)-N,N-diethyl- propane-1 ,3-diamine;
with (pyridin-4-yl)boronic acid to obtain N'-[7-chloro-2-(5-pyridin-4-yi-thiophen-2-yl)-quinazolin-4-yl]-N,N-diethyl- propane-1 ,3-diamine;
with (2,5-dimethoxy)phenylboronic acid to obtain
N'-{7-chloro-2-[5-(2,5-dimethoxy-phenyl)-thiophen-2-yl]-quinazolin-4-yl}- N,N-diethyl-propane-1 ,3-diamine.
Analogously to example 3, 2-(5-bromo-thiophen-2-yl)-4,7-dichloro- quinazoline [prepared analogously to example 1] is reacted with N1,N1-diethyl-pentane-1 ,4-diamine to obtain N4-[2-(5-bromo-thiophen-2-yl)-7-chloro-quinazolin-4-yl]-N1,N1-diethyl- pentane-1 ,4-diamine.
Analogously to example 10, N4-[2-(5-bromo-thiophen-2-yl)-7-chloro- quinazolin-4-yl]-N1,N1-diethyl-pentane-1 ,4-diamine is reacted
with 2-cyanophenylboronic acid to obtain 2-{5-[7-chloro-4-(4-diethylamino-1 -methyl-butylamino)-quinazolin-2-yl]- thiophen-2-yl}-benzonitrile;
with (benzo[b]thiophen-2-yl)boronic acid to obtain N4-[2-(5-benzo[b]thiophen-2-yl-thiophen-2-yl)-7-chloro-quinazolin-4-yl]-
N1,N1-diethyl-pentane-1 ,4-diamine.
Example 16:
Analogously to example 3, 4-chloro-2-(4-phenyl-butyl)-quinazoline [prepared analogously to example 1 , starting compounds 2-amino- benzonitrile and 5-phenyl-pentanoyl chloride] is reacted
with N1,N1-diethyl-pentane-1 ,4-diamine to obtain
N1,N -diethyl-N4-[2-(4-phenyl-butyl)-quinazolin-4-yl]-pentane-1 ,4- diamine;
with C-(3-aminomethyl-cyclohexyl)-methylamine to obtain
(3-aminomethyl-cyclohexylmethyl)-[2-(4-phenyl-butyl)-quinazolin-4-yl]- amine;
MS calc: 402,6 ; found: 403,6.
Example 17:
1. A solution of 2,4,7-trichloro-quinazoline (38,7 mmol) in 50 ml DMF is treated with N1,N1-diethyl-pentane-1 ,4-diamine (50 mmol). The mixture is stirred at rt for 4 hrs. A solution of C-(5-methoxy-1 H-indol-3-yl)-methylamine (50 mmol) in 10 ml DMF is added and the mixture is heated to 80-100° for 3 days. Customary working up gives 7-chloro-N -(4-diethylamino-1-methyl- butyl)-N2-(5-methoxy-1 H-indol-3-ylmethyl)-quinazoline-2,4-diamine
Analogously to example 17, 2,4,7-trichloro-quinazoline is reacted with N l11,,NN11--diethyl-pentane-1 ,4-diamine to give N4-(2,7-dichloro-quinazolin-4-yl)- N1,N1-diethyl-pentane-1 ,4-diamine and is further reacted
with 5-bromo-2-fluoro-benzylamine to obtain
N2-(5-bromo-2-fluoro-benzyl)-7-chloro-N4-(4-diethylamino-1-methyl- butyl)-quinazoline-2,4-diamine;
with 3,5-bis-trifluoromethyl-benzylamine to obtain
N2-(3,5-bis-trifluoromethyl-benzyl)-7-chloro-N4-(4-diethylamino-1-methyl- butyl)-quinazoline-2,4-diamine;
with 4-tert-butyl-benzylamine to obtain
N N22--((44--tteertrt--bbuuttyyll--bbeennzzyyll)-7-chloro-N4-(4-diethylamino-1-methyl-butyl)- quinazoline-2,4-diamine.
Analogously to example 17, 2,4,7-trichloro-quinazoline is reacted with 2- pyridin-2-yl-ethylamine to give (7-chloro-quinazolin-4-yl)-(2-pyridin-2-yl- ethyl)-amine and is further reacted
with phenethylamine to obtain 7-chloro-N2-phenethyl-N4-(2-pyridin-2-yl-ethyl)-quinazoline-2,4-diamine; with 3-morpholin-4-yl-propylamine to obtain
7-chloro-N2-(3-morpholin-4-yl-propyl)-N4-(2-pyridin-2-yl-ethyl)- quinazoline-2,4-diamine.
Analogously to example 17, 2,4,7-trichloro-quinazoline is reacted with diethylamine to give (2,7-dichloro-quinazolin-4-yl)-diethyl-amine and is further reacted
with biphenyl-4-ylamine to obtain N2-biphenyl-4-yl-7-chloro-N ,N4-diethyl-quinazoline-2,4-diamine.
The following examples relate to pharmaceutical preparations:
Example A: Injection vials
A solution of 100 g of an active compound of the formula I and 5 g of disodium hydrogenphosphate is adjusted to pH 6.5 in 3 I of double-distilled water using 2N hydrochloric acid, sterile-filtered, dispensed into injection vials, lyophilized under sterile conditions and aseptically sealed. Each injection vial contains 5 mg of active compound.
Example B: Suppositories
A mixture of 20 g of an active compound of the formula I is melted with 100 g of soya lecithin and 1400 g of cocoa butter, poured into moulds and allowed to cool. Each suppository contains 20 mg of active compound.
Example C: Solution
A solution is prepared from 1 g of an active compound of the formula I, 9.38 g of NaH2P04.2H20, 28.48 g of Na2HP0 .12H20 and 0.1 g of benzalkonium chloride in 940 ml of double-distilled water. The mixture is adjusted to pH 6.8, made up to 1 I and sterilized by irradiation. This solution can be used in the form of eye drops.
Example D: Ointment 500 mg of an active compound of the formula I is mixed with 99.5 g of petroleum jelly under aseptic conditions.
Example E: Tablets A mixture of 1 kg of active compound of the formula I, 4 kg of lactose,
1.2 kg of potato starch, 0.2 g of talc and 0.1 kg of magnesium stearate is compressed in a customary manner to give tablets such that each tablet contains 10 mg of active compound.
Example F: Coated tablets
Analogously to Example E, tablets are pressed which are then coated with a coating of sucrose, potato starch, talc, tragacanth and colorant in a customary manner.
Example G: Capsules
2 kg of active compound of the formula I are dispensed into hard gelatin capsules in a customary manner such that each capsule contains 20 mg of the active compound.
Example H: Ampules
A solution of 1 kg of active compound of the formula I in 60 ml of double- distilled water is sterile-filtered, dispensed into ampoules, lyophilized under sterile conditions and aseptically sealed. Each ampule contains 10 mg of active compound.

Claims (14)

What is claimed is:
1. Compounds of the formula
in which R an R1 are independently of each other H, A, OH, OA, Hal, N(R5) ,
N02, CN, CHO, COA, CON(R5)2, COOR5, allyl, CH=CH- COOR5, CH=CHCON(R5)2, S02A or phenyl, which is unsubstituted or mono-, di- or trisubstituted by A, R2 and R3 are independently of each other H, A, cycloalkyl, -Het3, -(CH2)0-OR5, -(CH2)o-OR6, -(CH2)0-Het, -(CH2)0-NR5-Het,
-(CHA)p-(CH2)0-N(R5)2l -(CH2)p-(CHA)p-(CH2)m-Ar, -(CH2)o-Z-(CH2)q-N(R5)2,
provided that R2 and R together are not H, or NR2R3 together form a saturated monocyclic heterocyclic radical having 5 to 6 ring members, where 1 or 2 N atoms are present and the heterocyclic radical can be mono- or disubstituted by OH, Ar, OAr or arylalkyl, R4 is Ar or Het1, R5 is H or A,
Rs is benzo[1 ,3]dioxol-5-yl,
R7 is H, A, cycloalkyl or (CH2)q-OR5, Q is O or S,
Y is a direct bond, (CH2)n or -NR5-(CH2)m-,
Z is phenylene, cyclohexylene, -NR5-, O, -CH(OH)-, -CA2- or
A is unbranched or branched alkyl having 1 to 6 carbon atoms,
Ar is phenyl, naphthyl or biphenyl, which is unsubstituted or mono-, di- or trisubstituted by A, OH, OA, cycloalkyloxy, 0-(CH2)p-Ph, CF3, OCF3, Hal, CN, CHO, COA, COOR5,
-(CH2)P-N(R7)2, NR5-COA, N02, S02N(R5)2, mor, S02-mor, 5-methyl-3-oxo-2,4-dihydropyrazol-2-yl, naphthyl or Het2, Het is a saturated, partially or completely unsaturated mono- or bicyclic heterocyclic radical having 5 to 10 ring members, where 1 or 2 N and/or 1 or 2 S or O atoms can be present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2, carbonyl oxygen, COOR5, benzyl, Het2 or phenyl which is unsubstituted or mono-, di- or trisubstituted by A, OH, OA, CF3, OCF3, Hal, CN, COOR5, N(R5)2, N02, S02N(R5)2,
Het1 is thiophen-2-yl substituted with Ar or Het2,
Het2 is a unsaturated mono- or bicyclic heterocyclic radical having
5 to 10 ring members, where 1 or 2 N and/or 1 or 2 S or O atoms can be present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2,
-(CH2)p-(CHA)p-N(R5)-(CH2)q-COR5, CHO, COA or COOR5, Het3 is a partially or completely unsaturated mono- or bicyclic heterocyclic radical having 5 to 10 ring members, where 1 or 2 N atoms are present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3l N(R5)2,
S02A or COOR5 provided that the heterocyclic radical is not bondend via an N atom, Hal is F, CI, Br or l, mor is morpholin-4-yl,
Ph is phenyl, n is 1 , 2, 3, 4, 5 or 6, m is O, 1 , 2, 3, 4, 5 or 6,
0 is 1 , 2, 3, 4, 5, 6 or 7,
P is O, 1 , 2, 3 or 4, q is 1 , 2, 3 or 4, and their pharmaceutically tolerable salts and solvates.
2. A compound of claim 1 , wherein R is H or OA.
3. A compound according to claims 1 or 2, wherein R1 is H, A, OA or Hal.
4. A compound according to at least one of claims 1 to 3, wherein Y is (CH2)n and n is 1 , 2, 3, 4, 5 or 6.
5. A compound according to at least one of claims 1 to 3, wherein Y is a direct bond.
6. A compound according to at least one of claims 1 to 3, wherein Y is -N(R5)-(CH2)m- and R5 is H or A.
7. Compounds of the formula I according to at least one of claims 1 to 6 a) [2-(benzo[1 ,3]dioxol-5-yloxy)-ethyl]-[2-(4-bromo-phenyl)-7-chloro- quinazolin-4-yl]-amine, b) [2-(4-bromo-phenyi)-7-chloro-quinazolin-4-yl]-[2-(1-methyl-octahydro- indol-3-yl)-ethyl]-amine, and their physiologically acceptable salts and solvates.
8. Process for the preparation of the compounds of the formula I in which
R and R1 are independently of each other H, A, OH, OA, Hal, N(R5)2, N02, CN, CHO, COA, CON(R5)2, COOR5, allyl, CH=CH- COOR5, CH=CHCON(R5)2, S02A or phenyl, which is unsubstituted or mono-, di- or trisubstituted by A,
R2 and R3 are independently of each other H, A, cycloalkyl, -Het3, -(CH2)0-OR5, -(CH2)0-OR6, -(CH2)0-Het, -(CH2)0-NR5-Het, -(CHA)p-(CH2)0-N(R5)2, -(CH2)p-(CHA)p-(CH2)m-Ar,
-(CH2)0-Z-(CH2)q-N(R5)2,
provided that R2 and R3 together are not H, or NR2R3 together form a saturated monocyclic heterocyclic radical having 5 to 6 ring members, where 1 or 2 N atoms are present and the heterocyclic radical can be mono- or disubstituted by OH, Ar, OAr or arylalkyl,
R4 is Ar or Het1,
R5 is H or A,
R6 is benzo[1 ,3]dioxol-5-yl,
R R77 is H, A, cycloalkyl or -(CH2)q-OR5
Q Q is O or S,
Y is a direct bond, (CH2)n or -NR5-(CH2)m-,
Z is phenylene, cyclohexylene, -NR5-, O, -CH(OH)-, -CA2- or
A is unbranched or branched alkyl having 1 to 6 carbon atoms, Ar is phenyl, naphthyl or biphenyl, which is unsubstituted or mono-, di- or trisubstituted by A, OH, OA, cycloalkyloxy, 0-(CH2)p-Ph, CF3, OCF3, Hal, CN, CHO, COA, COOR5, -(CH2)p-N(R7)2, NR5-COA, N02, S02N(R5)2, mor, S02-mor, 5-methyl-3-oxo-2,4-dihydropyrazol-2-yl, naphthyl or Het2, Het is a saturated, partially or completely unsaturated mono- or bicyclic heterocyclic radical having 5 to 10 ring members, where 1 or 2 N and/or 1 or 2 S or O atoms can be present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2, carbonyl oxygen, COOR5, benzyl, Het2 or phenyl which is unsubstituted or mono-, di- or trisubstituted by A, OH, OA, CF3, OCF3, Hal, CN, COOR5, N(R5)2, N02, S02N(R5)2, Het1 is thiophen-2-yl substituted with Ar or Het2,
Het2 is a unsaturated mono- or bicyclic heterocyclic radical having 5 to 10 ring members, where 1 or 2 N and/or 1 or 2 S or
O atoms can be present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3, N(R5)2, -(CH2)p-(CHA)p-N(R5)-(CH2)q-COR5, CHO, COA or COOR5, Het3 is a partially or completely unsaturated mono- or bicyclic heterocyclic radical having 5 to 10 ring members, where 1 or 2
N atoms are present and the heterocyclic radical can be mono- or disubstituted by A, Hal, OH, OA, CF3, OCF3> N(R5)2, S02A or COOR5 provided that the heterocyclic radical is not bondend via an N atom, Hal is F, CI, Br or l, mor is morpholin-4-yl,
Ph is phenyl, n is 1 , 2, 3, 4, 5 or 6, m is 0, 1 , 2, 3, 4, 5 or 6, o is 1 , 2, 3, 4, 5, 6 or 7, p is 0, 1 , 2, 3 or 4, q is 1 , 2, 3 or 4, and their pharmaceutically tolerable salts and solvates according to at least one of claims 1 to 7, characterized in that a) a compound of the formula I is liberated from one of its functional derivatives by treating with a solvolysing or hydrogenolysing agent, or b) for compounds in which Y is a direct bond or (CH2)n in stage 1) a compound of the formula II
in which
R and R1 have a meaning indicated in Claim 1 , is reacted with a compound of the formula III
X. P<— R4
Y O »'
in which R4 has a meaning indicated in Claim 1 and Y is a direct bond or (CH2)n, and X is CI, Br, OH or a reactive esterified OH group followed by converting the cyano group to an amide group by conventional means to give a compound of formula IV
in which R, R1 and R4 have a meaning indicated in Claim 1 and Y is a direct bond or (CH2)n, in stage 2) a compound of formula IV as indicated above is reacted with a base to give a compound of formula V
in which R, R1 and R4 have a meaning indicated in Claim 1 and Y is a direct bond or (CH2)n, in stage 3) a compound of formula V as indicated above is reacted with a chlorinating agent to give a compound of formula VI
in which R, R1 and R4 have a meaning indicated in Claim 1 and Y is a direct bond or (CH2)n, and in stage 4) a compound of formula VI as indicated above is reacted with a compound of formula VII
in which R and R or NR ι2 Rr-,3 have a meaning indicated in Claim 1 , or b) for compounds in which Y is NR5-(CH2)m- in stage 1) a compound of the formula VIII
in which R and R1 have a meaning indicated in Claim 1 , is reacted with a compound of formula VII
in which R2 and R3 or NR2R3 have a meaning indicated in Claim 1 , to give a compound of formula IX
in which R, R1, R2, R3 and NR2R3 have a meaning indicated in Claim 1 , and in stage 2) a compound of formula IX as indicated above is reacted with a compound of formula X
in which R4, R5 and m have a meaning indicated in Claim 1 or d) a radical R, R1, R2, R3 and/or R4 is converted into another radical R,
R1, R2, R3 and/or R4 by, for example reducing a nitro group, sulfonyl group or sulfoxyl group, etherifying an OH group or subjecting an OA group to ether cleavage, alkylating a primary or secondary amino group, partially or completely hydrolysing a CN group, cleaving an ester group or esterifying a carboxylic acid radical, reacting an aryl bromide, aryl iodide, heteroaryl bromide or heteroaryliodide to give the corresponding coupling products by means of a Suzuki coupling with boronic acids, reacting a iodoquinazoline or bromoquinazoline to give the corresponding coupling products by means of a Stille coupling with allyltributyltin, reacting a iodoquinazoline or bromoquinazoline to give the corresponding coupling products by means of a Heck coupling with acrylates, or carrying out a nucleophilic or electrophilic substitution, or a base or acid of the formula I is converted into one of its salts or 10 solvates.
9. Compounds of the formula I according to at least one of claims 1 to 7 and their physiologically acceptable salts or solvates as pharmaceutical active compounds.
15
10. Compounds of the formula I according to claim 9 and their physiologically acceptable salts or solvates as glycoprotein IblX antagonists.
20 11. Compounds of the formula I according to claim 9 and their physiologically acceptable salts or solvates as glycoprotein IblX antagonists for the control of thrombotic disorders and sequelae deriving therefrom.
25 12. Pharmaceutical preparation characterized in that it contains at least one compound of the formula I according to at least one of claims 1 to 7 or one of its physiologically acceptable salts or solvates.
13. Use of compounds of the formula I according to at least one of claims 1 to 7 and/or their physiologically acceptable salts or solvates for the on production of a pharmaceutical preparation for the control of thrombotic disorders and sequelae deriving therefrom or for use as anti-adhesive substances.
14. Use of compounds of the formula I according to at least one of claims 1 to 7 and/or their physiologically acceptable salts or solvates for the production of a pharmaceutical preparation for the treatment of illnesses, such as for the prophylaxis and/or therapy of thrombotic disorders, as well as sequelae such as, for example, myocardial infarct, arteriosclerosis, angina pectoris, acute coronary syndromes, peripheral circulatory disorders, stroke, transient ischaemic attacks, reocclusion/restenosis after angioplasty/stent implantations or as anti- adhesive substances for implants, catheters or heart pacemakers.
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Families Citing this family (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6660731B2 (en) 2000-09-15 2003-12-09 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
CA2422354C (en) 2000-09-15 2009-12-08 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
AU2001293817A1 (en) 2000-09-20 2002-04-02 Merck Patent Gmbh 4-amino-quinazolines
NZ526469A (en) 2000-12-21 2005-10-28 Vertex Pharma Pyrazole compounds useful as protein kinase inhibitors
PE20030008A1 (en) 2001-06-19 2003-01-22 Bristol Myers Squibb Co DUAL INHIBITORS OF PDE 7 AND PDE 4
US7829566B2 (en) 2001-09-17 2010-11-09 Werner Mederski 4-amino-quinazolines
JP2005516005A (en) * 2001-12-07 2005-06-02 バーテクス ファーマスーティカルズ インコーポレイテッド Pyrimidine-based compounds useful as GSK-3 inhibitors
DE60320933D1 (en) 2002-01-10 2008-06-26 Bayer Healthcare Ag RHO-KINASE INHIBITORS
EP1470122B1 (en) 2002-01-23 2007-12-19 Bayer Pharmaceuticals Corporation Rho-kinase inhibitors
CA2473510A1 (en) 2002-01-23 2003-07-31 Bayer Pharmaceuticals Corporation Pyrimidine derivatives as rho-kinase inhibitors
US7645878B2 (en) * 2002-03-22 2010-01-12 Bayer Healthcare Llc Process for preparing quinazoline Rho-kinase inhibitors and intermediates thereof
CN1319968C (en) 2002-08-02 2007-06-06 沃泰克斯药物股份有限公司 Compositions useful as inhibitors of GSK-3
US7312239B2 (en) * 2002-09-04 2007-12-25 Mitsubishi Pharma Corporation Medicament for prevention and/or therapy of arterial wall disorder
US7713983B2 (en) 2003-03-03 2010-05-11 Vertex Pharmaceuticals Incorporated Quinazolines useful as modulators of ion channels
CL2004000409A1 (en) 2003-03-03 2005-01-07 Vertex Pharma COMPOUNDS DERIVED FROM 2- (REPLACED CILO) -1- (AMINO OR REPLACED OXI) -CHINAZOLINE, INHIBITORS OF IONIC SODIUM AND CALCIUM VOLTAGE DEPENDENTS; PHARMACEUTICAL COMPOSITION; AND USE OF THE COMPOUND IN THE TREATMENT OF ACUTE PAIN, CHRONIC, NEU
WO2004103270A2 (en) 2003-04-02 2004-12-02 Suntory Pharmaceutical Research Laboratories Llc Compounds and methods for treatment of thrombosis
AU2004230928B2 (en) * 2003-04-09 2010-12-02 Exelixis, Inc. Tie-2 modulators and methods of use
BRPI0411514A (en) * 2003-06-20 2006-08-01 Coley Pharm Gmbh small molecule toll-like receptor antagonists
CA2530312A1 (en) 2003-07-02 2005-01-20 F. Hoffmann-La Roche Ag Arylamine-substituted quinazolinone compounds
US8309562B2 (en) 2003-07-03 2012-11-13 Myrexis, Inc. Compounds and therapeutical use thereof
WO2006074147A2 (en) 2005-01-03 2006-07-13 Myriad Genetics, Inc. Nitrogen containing bicyclic compounds and therapeutical use thereof
US7928107B2 (en) 2004-09-02 2011-04-19 Vertex Pharmaceuticals Incorporated Quinazolines useful as modulators of ion channels
US8283354B2 (en) 2004-09-02 2012-10-09 Vertex Pharmaceuticals Incorporated Quinazolines useful as modulators of ion channels
US7718658B2 (en) 2004-09-02 2010-05-18 Vertex Pharmaceuticals Incorporated Quinazolines useful as modulators of ion channels
US8153630B2 (en) 2004-11-17 2012-04-10 Miikana Therapeutics, Inc. Kinase inhibitors
US8258145B2 (en) 2005-01-03 2012-09-04 Myrexis, Inc. Method of treating brain cancer
ES2535854T3 (en) 2005-09-30 2015-05-18 Miikana Therapeutics, Inc. Substituted Pyrazole Compounds
AU2007303846B2 (en) * 2006-10-04 2011-03-10 Pfizer Products Inc. Pyrido[4,3-d]pyrimidin-4(3H)-one derivatives as calcium receptor antagonists
US20090209536A1 (en) * 2007-06-17 2009-08-20 Kalypsys, Inc. Aminoquinazoline cannabinoid receptor modulators for treatment of disease
SI2410844T1 (en) 2009-03-27 2016-06-30 Merck Sharp & Dohme Corp. Inhibitors of hepatitis c virus replication
US20190127365A1 (en) 2017-11-01 2019-05-02 Merck Sharp & Dohme Corp. Inhibitors of hepatitis c virus replication
AU2010249080A1 (en) 2009-05-12 2012-01-12 Merck Sharp & Dohme Corp. Fused tricyclic aryl compounds useful for the treatment of viral diseases
EP2435424B1 (en) 2009-05-29 2015-01-21 Merck Sharp & Dohme Corp. Antiviral compounds composed of three linked aryl moieties to treat diseases such as hepatitis c
US8772505B2 (en) 2009-05-29 2014-07-08 Merck Sharp & Dohme Corp. Antiviral compounds composed of three aligned aryl moieties to treat diseases such as hepatitis C
MX2012002099A (en) 2009-09-03 2012-04-11 Bristol Myers Squibb Co Quinazolines as potassium ion channel inhibitors.
CN102574817A (en) 2009-09-24 2012-07-11 巴斯夫欧洲公司 Aminoquinazoline compounds for combating invertebrate pests
US20130156731A1 (en) 2009-12-22 2013-06-20 Kevin X. Chen Fused tricyclic compounds and methods of use thereof for the treatment of viral diseas
US8732671B2 (en) * 2010-02-26 2014-05-20 Red Hat, Inc. Generating stack traces of call stacks that lack frame pointers
AU2011224698A1 (en) * 2010-03-09 2012-11-01 Merck Sharp & Dohme Corp. Fused Tricyclic Silyl Compounds and methods of use thereof for the treatment of viral diseases
CA2812779A1 (en) 2010-09-29 2012-04-19 Merck Sharp & Dohme Corp. Fused tetracycle derivatives and methods of use thereof for the treatment of viral diseases
WO2012122716A1 (en) 2011-03-17 2012-09-20 Merck Sharp & Dohme Corp. Tetracyclic xanthene derivatives and methods of use thereof for treatment of viral diseases
WO2014100501A1 (en) * 2012-12-20 2014-06-26 Sanford-Burnham Medical Research Institute Small molecule agonists of neurotensin receptor 1
WO2014110687A1 (en) 2013-01-16 2014-07-24 Merck Sharp & Dohme Corp. Thiazolyl-substitued tetracyclic compounds and methods of use thereof for treatment of viral diseases
CA2952732C (en) 2014-06-25 2024-01-02 Sanford-Burnham Medical Research Institute Small molecule agonists of neurotensin receptor 1
CN104496915B (en) * 2014-12-19 2017-05-03 华侨大学 Synthetic method of quinazolinone aromatic compound
SG11201705184PA (en) 2014-12-24 2017-07-28 Gilead Sciences Inc Isoquinoline compounds for the treatment of hiv
TWI770552B (en) 2014-12-24 2022-07-11 美商基利科學股份有限公司 Quinazoline compounds
BR112017013491A2 (en) 2014-12-24 2018-01-09 Gilead Sciences, Inc. fused pyrimidine compounds for the treatment of hiv
US11787783B2 (en) 2016-12-13 2023-10-17 Beta Therapeutics Pty Ltd Heparanase inhibitors and use thereof
US11718609B2 (en) 2016-12-13 2023-08-08 Beta Therapeutics Pty Ltd Heparanase inhibitors and use thereof
EP4017492A4 (en) * 2019-08-22 2023-10-11 Biohaven Therapeutics Ltd. Molecules that bind to tdp-43 for the treatment of amyotrophic lateral sclerosis and related disorders
WO2022241186A1 (en) * 2021-05-13 2022-11-17 Duke University Compositions for and methods of treating and/or preventing pain

Family Cites Families (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3669968A (en) * 1970-05-21 1972-06-13 Pfizer Trialkoxy quinazolines
US4642347A (en) 1985-05-21 1987-02-10 American Home Products Corporation 3(2-quinolinylalkoxy)phenols
IL89027A (en) * 1988-01-29 1993-01-31 Lilly Co Eli Quinazoline derivatives, process for their preparation and fungicidal, insecticidal and miticidal compositions containing them
IL89029A (en) 1988-01-29 1993-01-31 Lilly Co Eli Fungicidal quinoline and cinnoline derivatives, compositions containing them, and fungicidal methods of using them
US4952567A (en) 1988-05-09 1990-08-28 City Of Hope Inhibition of lipogenesis
US6004979A (en) 1991-02-07 1999-12-21 Hoechst Marion Roussel Nitrogenous bicycles
MX9200299A (en) 1991-02-07 1992-12-01 Roussel Uclaf NEW NITROGENATED BICYCLE DERIVATIVES, THEIR PROCEDURE FOR PREPARING THE NEW INTERMEDIATE COMPOUNDS OBTAINED THEIR APPLICATION AS MEDICINES AND THE PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM.
DK0498722T3 (en) 1991-02-07 1998-03-09 Roussel Uclaf New bicyclic nitrogen compounds substituted with a benzyl group, process for their preparation, the novel intermediates obtained, their use as drugs and the pharmaceutical compositions contained in them.
US5245036A (en) 1992-05-07 1993-09-14 Dowelanco Process for the preparation of 4-phenoxyquinoline compounds
US5972598A (en) 1992-09-17 1999-10-26 Board Of Trustess Of The University Of Illinois Methods for preventing multidrug resistance in cancer cells
EP1195372A1 (en) 1994-04-18 2002-04-10 Mitsubishi Pharma Corporation N-heterocyclic substituted benzamide derivatives with antihypertensive activity
US5840695A (en) 1994-10-07 1998-11-24 Heska Corporation Ectoparasite saliva proteins and apparatus to collect such proteins
US5658902A (en) * 1994-12-22 1997-08-19 Warner-Lambert Company Quinazolines as inhibitors of endothelin converting enzyme
JP3290666B2 (en) 1995-06-07 2002-06-10 ファイザー・インコーポレーテッド Heterocyclic fused-ring pyrimidine derivatives
US5598994A (en) 1995-06-29 1997-02-04 Panduit Corp. Stud engaging device
GB9514265D0 (en) 1995-07-13 1995-09-13 Wellcome Found Hetrocyclic compounds
US5906819A (en) 1995-11-20 1999-05-25 Kirin Beer Kabushiki Kaisha Rho target protein Rho-kinase
DE19608653A1 (en) 1996-03-06 1997-09-11 Thomae Gmbh Dr K Pyrimido [5,4-d] pyrimidines, medicaments containing these compounds, their use and processes for their preparation
US6391874B1 (en) 1996-07-13 2002-05-21 Smithkline Beecham Corporation Fused heterocyclic compounds as protein tyrosine kinase inhibitors
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
KR100576148B1 (en) 1996-08-12 2006-05-03 미쯔비시 웰 파마 가부시키가이샤 Medicines Comprising Rho Kinase Inhibitor
AR012634A1 (en) 1997-05-02 2000-11-08 Sugen Inc QUINAZOLINE BASED COMPOUND, FAMACEUTICAL COMPOSITION THAT UNDERSTANDS IT, METHOD TO SYNTHESIZE IT, ITS USE, METHODS OF MODULATION OF THE DESERINE / TREONIN PROTEIN-KINASE FUNCTION AND IN VITRO METHOD TO IDENTIFY COMPOUNDS THAT MODULATE
US5885803A (en) 1997-06-19 1999-03-23 Incyte Pharmaceuticals, Inc. Disease associated protein kinases
ZA986729B (en) 1997-07-29 1999-02-02 Warner Lambert Co Irreversible inhibitors of tyrosine kinases
WO1999009986A1 (en) * 1997-08-22 1999-03-04 Kyowa Hakko Kogyo Co., Ltd. 4-aminoquinazoline derivatives
CA2214841A1 (en) 1997-10-31 1999-04-30 Lisa Mckerracher Rho antagonists and their use to block inhibition of neurite outgrowth
EP1028964A1 (en) 1997-11-11 2000-08-23 Pfizer Products Inc. Thienopyrimidine and thienopyridine derivatives useful as anticancer agents
DE19756388A1 (en) * 1997-12-18 1999-06-24 Hoechst Marion Roussel De Gmbh New 2-aryl-4-amino-6,7-di:methoxy-quinazoline derivatives useful as guanylate cyclase activators for treating cardiovascular diseases, etc.
RS49779B (en) 1998-01-12 2008-06-05 Glaxo Group Limited, Byciclic heteroaromatic compounds as protein tyrosine kinase inhibitors
GB9800575D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
JPH11209287A (en) * 1998-01-23 1999-08-03 Ono Pharmaceut Co Ltd Inhibitor of nitrogen monoxide production
ID26698A (en) 1998-06-19 2001-02-01 Pfizer Prod Inc PIROLO COMPOUNDS [2,3-d] PYRIMIDINE
EP1459743B9 (en) 1998-08-17 2012-08-01 Senju Pharmaceutical Co., Ltd. Agent for prophylaxis and treatment of glaucoma
HUP0103386A3 (en) 1998-08-21 2002-07-29 Parker Hughes Inst St Paul Use of quinazoline derivatives for producing pharmaceutical compositions having jak 3-inhibitor effect
US6184226B1 (en) 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
SE515247C2 (en) 1998-09-04 2001-07-02 Alfa Laval Agri Ab Animal booth with locking means
US6080747A (en) 1999-03-05 2000-06-27 Hughes Institute JAK-3 inhibitors for treating allergic disorders
KR100704704B1 (en) 1999-03-25 2007-04-09 미쯔비시 웰 파마 가부시키가이샤 Preventives/Remedies for interstitial pneumonia and pulmonary fibrosis
AU3328600A (en) 1999-03-25 2000-10-16 Santen Pharmaceutical Co. Ltd. Ocular tension-lowering agents
EP1174150A4 (en) 1999-04-22 2004-06-16 Mitsubishi Pharma Corp Preventives/remedies for angiostenosis
AU4144400A (en) 1999-04-27 2000-11-10 Mitsubishi Pharma Corporation Preventives/remedies for liver diseases
GB9918035D0 (en) 1999-07-30 1999-09-29 Novartis Ag Organic compounds
NZ522989A (en) * 2000-06-30 2005-06-24 Glaxo Group Ltd Quinazoline ditosylate salt compounds
AU2001293817A1 (en) 2000-09-20 2002-04-02 Merck Patent Gmbh 4-amino-quinazolines
WO2002030465A2 (en) 2000-10-12 2002-04-18 University Of Rochester Compositions that inhibit proliferation of cancer cells
WO2002053143A2 (en) 2001-01-05 2002-07-11 The Medical College Of Georgia Research Institute, Inc. Treatment of erectile dysfunction with rho-kinase inhibitors

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