发明名称 IRREVERSIBLE INHIBITORS OF TYROSINE KINASES.
摘要 1. A nitrogen-containing heterocyclic compound having the Formula I wherein X is -D-E-F and Y is -SR<4>, -OR<4>, -NHR<3>, or hydrogen, or X is -SR<4>, -OR<4>, -NHR<3>, or hydrogen, and Y is -D-E-F; D is or absent; E is F is provided that when E is D is not R<1> is hydrogen, halogen, or alkyl with the number of carbon atoms from 1 to 6; R<2>, R<3>, and R<4> are independently hydrogen, alkyl with the number of carbon atoms from 1 to 6, -(CH2)n-N-piperidinyl, -(CH2)n-N-piperazinyl, -(CH2)n-N1-piperazinyl[N4-(C1-C6)alkyl], -(CH2)n-N-pyrrolidyl,-(CH2)n-pyridinyl, -(CH2)n-N-imidazolyl,-(CH2)n-imidazolyl, -(CH2)n-N-morpholino-,-(CH2)n-N-thiomorpholino-, -(CH2)n-N-hexahydroazepine or substituted alkyl with the number of carbon atoms from 1 to 6, wherein the substituents are selected from -OH, -NH2, or A and B are independently hydrogen, alkyl with the number of hydrogen atoms from 1 to 6, -(CH2)nOH, -(CH2)n-N-piperidinyl, -(CH2)n-N-piperazinyl, -(CH2)n-N1-piperazinyl[N4-(C1-C6)alkyl], -(CH2)n-N-pyrrolidyl,-(CH2)n-N-pyridyl, -(CH2)n-imidazolyl or -(CH2)n-N-imidazolyl; Z<1>, Z<2>, or Z<3> are independently hydrogen, halogen, alkyl with the number of carbon atoms from 1 to 6, cycloalkyl with the number of carbon atoms from 3 to 8, alkoxy-group with the number of carbon atoms from 1 to 6, cycloalkoxy-group with the number of carbon atoms from 3 to 8, nitro, perfluoroalkyl with the number of carbon atoms from 1 to 6, hydroxyl, acyloxy-group with the number of carbon atoms from 1 to 6, -NH2, -NH(C1-C6 alkyl), -N(C1-C6 alkyl)2, -NH(C3-C8cycloalkyl), -N(C3-C8 cycloalkyl)2, hydroxymethyl, acyl with the number of carbon atoms from 1 to 6, cyano-group, azido-group, thioalkyl with the number of carbon atoms from 3 to 8, sulfonylcycloalkyl with the number of carbon atoms from 3 to 8, mercapto-group, alkoxycarbonyl with the number of carbon atoms from 1 to 6, cycloalkoxycarbonyl with the number of carbon atoms from 3 to 8, alkenyl with the number of carbon atoms from 2 to 4, cycloalkenyl with the number of carbon atoms from 4 to 8, or alkynyl with the number of carbon atoms from 2 to 4; and R<5> is hydrogen, halogen, perfluoroalkyl with the number of carbon atoms from 1 to 6, 1,1-difluoroalkyl with the number of carbon atoms from 1 to 6, alkyl with the number of carbon atoms from 1 to 6, -(CH2)n-N-piperidinyl, -(CH2)n-piperazinyl, -(CH2)n-piperazinyl[N4-(C1-C6)alkyl], -(CH2)n-N-pyrrolidyl, -(CH2)n-pyridinyl, -(CH2)n-N-imidazolyl, -(CH2)n-N-morpholino-, -(CH2)n-N-thiomorpholino-, , -CH=CH-(C1-C6)alkyl, -(CH2)n-N-hexahydroazepine, -(CH2)nNH2,-(CH2)nNH(C1-C6 alkyl), -(CH2)nN(C1-C6 alkyl)2, -1-oxo(C1-C6)alkyl, carboxy-, alkyloxycarbonyl with the number of carbon atoms from 1 to 6, N-alkylcarbamoyl with the number of carbon atoms from 1 to 6, phenyl or substituted phenyl, wherein the substituted phenyl can have from one to three substituents independently selected from Z<1>, Z<2>, Z<3> or a monocyclic heteroaryl group with 5 or 6 ring atoms, comprising at least one geteroatom selected from N, O, S and P, and each alkyl group with the number of carbon atoms from 1 to 6 can be substituted by -OH, -NH2, or NAB, where A and B are as defined above, R<6> is hydrogen or alkyl with the number of carbon atoms from 1 to 6; n is 1 to 4, p is 0 or 1, and the pharmaceutically acceptable salts, esters, amides, and prodrugs thereof. 2. A nitrogen-containing heterocyclic compound having the Formula II wherein Q is X is -D-E-F and Y is -SR<4>, -OR<4>, -NHR<3> or hydrogen, or X is -SR<4>, -OR<4>, -NHR<3> or hydrogen, and Y is -D-E-F; D is or absent; E is F is provided that when E is D is not R<1> is hydrogen, halogen, or alkyl with the number of carbon atoms from 1 to 6; R<2>, R<3>, and R<4> are independently hydrogen, alkyl with the number of carbon atoms from 1 to 6, -(CH2)n-N-piperidinyl,-(CH2)n-N-piperazinyl, -(CH2)n-N1-piperazinyl[N4-(C1-C6)alkyl], -(CH2)n-N-pyrrolidyl, -(CH2)n-pyridinyl, -(CH2)n-N-imidazolyl, -(CH2)n-imidazolyl, -(CH2)n-N-morpholino-,-(CH2)n-N-thiomorpholino-, -(CH2)n-N-hexahydroazepine or substituted alkyl with the number of carbon atoms from 1 to 6, wherein the substituents are selected from -OH, -NH2, or A and B are independently hydrogen, alkyl with the number of carbon atoms from 1 to 6, -(CH2)nOH, -(CH2)n-N-piperidinyl, -(CH2)n-N-piperazinyl, -(CH2)n-N1-piperazinyl[N4-(C1-C6)alkyl], -(CH2)n-N-pyrrolidyl, -(CH2)n-N-pyridyl, -(CH2)n-imidazolyl or -(CH2)n-N-imidazolyl; E<1>, E<2>, and E<3> are independently halogen, alkyl with the number of carbon atoms from 1 to 6, cycloalkyl with the number of carbon atoms from 3 to 8, alkoxy-group with the number of carbon atoms from 1 to 6, cycloalkoxy-group with the number of carbon atoms from 3 to 8, nitro-group, perfluoroalkyl with the number of carbon atoms from 1 to 6, hydroxyl, acyloxy-group with the number of carbon atoms from 1 to 6, -NH2, -NH(C1-C6alkyl), -N(C1-C6 alkyl)2, -NH(C3-C8cycloalkyl), -N(C3-C8 cycloalkyl)2, hydroxymethyl, acyl with the number of carbon atoms from 1 to 6, cyano-group, azido-group, thioalkyl with the number of carbon atoms from 1 to 6, sulfinylalkyl with the number of carbon atoms from 1 to 6, sulfonylalkyl with the number of carbon atoms from 1 to 6, thiocycloalkyl with the number of carbon atoms from 3 to 8, sulfinylcycloalkyl with the number of carbon atoms from 3 to 8, sulfonylcycloalkyl with the number of carbon atoms from 3 to 8, mercapto-group, alkoxycarbonyl with the number of carbon atoms from 1 to 6, cycloalkoxycarbonyl with the number of carbon atoms from 3 to 8, alkenyl with the number of carbon atoms from 2 to 4, cycloalkenyl with the number of carbon atoms from 4 to 8, or alkynyl with the number of carbon atoms from 2 to 4; and R<5> is hydrogen, halogen, perfluoroalkyl with the number of carbon atoms from 1 to 6, 1,1-difluoroalkyl with the number of carbon atoms from 1 to 6, alkyl with the number of carbon atoms from 1 to 6, -(CH2)n-N-piperidinyl, -(CH2)n-piperazinyl, -(CH2)n-piperazinyl[N4-(C1-C6)alkyl], -(CH2)n-N-pyrrolidyl, -(CH2)n-pyridinyl, -(CH2)n-N-imidazolyl, -(CH2)n-N-morpholino-, -(CH2)n-N-thiomorpholino-, -CH=CH-(C1-C6)alkyl, -(CH2)n-N-hexahydroazepine, -(CH2)nNH2,-(CH2)nNH(C1-C6 alkyl), -(CH2)nN(C1-C6 alkyl)2, -1-oxo(C1-C6)alkyl, carboxy-, alkyloxycarbonyl with the number of carbon atoms from 1 to 6, N-alkylcarbamoyl with the number of carbon atoms from 1 to 6, phenyl or substituted phenyl, wherein the substituted phenyl can have from one to three substituents independently selected from Z<1>, Z<2>, Z<3> or a monocyclic heteroaryl group with 5 or 6 ring atoms, comprising at least one heteroatom selected from N, O, S and P, and each alkyl-group with the number of carbon atoms from 1 to 6 can be substituted with -OH, -NH2 or -NAB, where A and B are as defined above, R<6> is hydrogen or alkyl with the number of carbon atoms from 1 to 6; n is 1 to 4, p is 0 or 1 and the pharmaceutically acceptable salts, esters, amides, and prodrugs thereof. 3. A nitrogen-containing heterocyclic compound having the Formula III wherein Q is X is -D-E-F, and Y is -OR<4>, -NHR<3> or hydrogen, or X is -OR<4>, -NHR<3> or hydrogen, and Y is -D-E-F; D is or absent; E is F is wherein when E is D is not R<1> is hydrogen, halogen, or alkyl with the number of carbon atoms from 1 to 6; R<2>, R<3>, and R<4> are independently hydrogen, alkyl with the number of carbon atoms from 1 to 6, -(CH2)n-N-piperidinyl, -(CH2)n-N-piperazinyl, -(CH2)n-N1-piperazinyl[N4-(C1-C6)alkyl], -(CH2)n-N-pyrrolidyl, -(CH2)n-pyridinyl, -(CH2)n-N-imidazolyl, -(CH2)n-imidazolyl, -(CH2)n-N-morpholino-, -(CH2)n-N-thiomorpholino-, -(CH2)n-N-hexahydroazepine or substituted alkyl with the number of carbon atoms from 1 to 6, wherein the substituents are selected from -OH, -NH2, or A and B are independently hydrogen, alkyl with the number of hydrogen atoms from 1 to 6, -(CH2)nOH, -(CH2)n-N-piperidinyl, -(CH2)n-N-piperazinyl, -(CH2)n-N1-piperazinyl[N4-(C1-C6)alkyl], -(CH2)n-N-pyrrolidyl, -(CH2)n-N-pyridyl, -(CH2)n-imidazolyl, or -(CH2)n-N-imidazolyl; E<1>, E<2>, and E<3> are independently halogen, alkyl with the number of carbon atoms from 1 to 6, cycloalkyl with the number of carbon atoms from 3 to 8, alkoxy-group with the number of carbon atoms from 1 to 6, cycloalkoxy-group with the number of carbon atoms from 3 to 8, nitro-group, perfluoroalkyl with the number of carbon atoms from 1 to 6, hydroxyl, acyloxy-group with the number of carbon atoms from 1 to 6, -NH2, -NH(C1-C6alkyl), -N(C1-C6 alkyl)2, -NH(C3-C8cycloalkyl), -N(C3-C8 cycloalkyl)2, hydroxymethyl, acyl with the number of carbon atoms from 1 to 6, cyano-group, azido-group, thioalkyl with the number of carbon atoms from 1 to 6, sulfinylalkyl with the number of carbon atoms from 1 to 6, sulfonylalkyl with the number of carbon atoms from 1 to 6, thiocycloalkyl with the number of carbon atoms from 3 to 8, sulfinylcycloalkyl with the number of carbon atoms from 3 to 8, sulfonylcycloalkyl with the number of carbon atoms from 3 to 8, mercapto-group, alkoxycarbonyl with the number of carbon atoms from 1 to 6, cycloalkoxycarbonyl with the number of carbon atoms from 3 to 8, alkenyl with the number of carbon atoms from 2 to 4, cycloalkenyl with the number of carbon atoms from 4 to 8, or alkynyl with the number of carbon atoms from 2 to 4; R<5> is hydrogen, halogen, perfluoroalkyl with the number of carbon atoms from 1 to 6, 1,1-difluoroalkyl with the number of carbon atoms from 1 to 6, alkyl with the number of carbon atoms from 1 to 6, -(CH2)n-N-piperidinyl, -(CH2)n-piperazinyl, -(CH2)n-piperazinyl[N4-(C1-C6)alkyl], -(CH2)n-N-pyrrolidyl, -(CH2)n-pyridinyl, -(CH2)n-N-imidazolyl, -(CH2)n-N-morpholino-, -(CH2)n-N-thiomorpholino-, -CH=CH-(C1-C6)alkyl, -(CH2)n-N-hexahydroazepine, -(CH2)nNH2,-(CH2)nNH(C1-C6 alkyl), -(CH2)nN(C1-C6 alkyl)2, -1-oxo(C1-C6)alkyl, carboxy-, alkyloxycarbonyl with the number of carbon atoms from 1 to 6, N-alkylcarbamoyl with the number of carbon atoms from 1 to 6, phenyl or substitute
申请公布号 EA001595(B1) 申请公布日期 2001.06.25
申请号 EA19980000887 申请日期 1997.04.08
申请人 WARNER-LAMBERT COMPANY 发明人 BRIDGES, ALEXANDER, JAMES;DENNY, WILLIAM, ALEXANDER;DOBRUSIN, ELLEN, MYRA;DOHERTY, ANNETTE, MARIAN;FRY, DAVID, W.;MCNAMARA, DENNIS, JOSEPH;SHOWALTER, HOWARD, DANIEL, HOLLIS;SMAILL, JEFFREY, B.;ZHOU, HAIRONG
分类号 A61K31/00;A61K31/505;A61K31/517;A61K31/519;A61K31/529;A61P9/10;A61P15/00;A61P17/06;A61P35/00;A61P43/00;C07D239/94;C07D403/04;C07D471/04;C07D487/04;C07D495/04;C07D521/00;C07F9/6561 主分类号 A61K31/00
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