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    101.
    发明专利
    未知

    公开(公告)号：DE60001190D1

    公开(公告)日：2003-02-20

    申请号：DE60001190

    申请日：2000-04-14

    Applicant: SERVIER LAB

    Inventor： FAUCHERE JEAN-LUC ,  ORTUNO JEAN-CLAUDE ,  DUHAULT JACQUES ,  BOUTIN JEAN ALBERT ,  LEVENS NIGEL

    IPC: C07D249/08 ,  A61K31/4196 ,  A61K31/4427 ,  A61K31/443 ,  A61K31/4433 ,  A61K31/4439 ,  A61K31/501 ,  A61P3/00 ,  A61P3/04 ,  A61P3/10 ,  A61P9/00 ,  A61P9/12 ,  A61P15/00 ,  A61P15/10 ,  A61P25/00 ,  A61P25/08 ,  A61P25/20 ,  A61P25/22 ,  A61P25/24 ,  A61P43/00 ,  C07D249/12 ,  C07D249/14 ,  C07D401/04 ,  C07D401/12 ,  C07D401/14 ,  C07D403/12 ,  C07D405/12 ,  C07D409/12

    Abstract: 1,2,4-Triazolylamino-substituted carboxamide or hydrazide derivatives (I) are new. Triazole derivatives of formula G-NH-A- CO-NH-(NH)n-W-Z (I) and their enantiomers, diastereoisomers and acid or base addition salts are new. G = 1,2,4-triazolyl group of formula (G1)-(G4); n = 0 or 1; W = CO, S, SO or SO2; Z, R1 = alkyl or (all optionally substituted) aryl, heteroaryl, aralkyl, aralkenyl, aralkynyl, heteroaralkyl, heteroaralkenyl or heteroaralkynyl; A = -A2-, -A1-A-2-, -A2-A1- or -A1-A2-A1-; A1 = alkylene; A2 = phenylene, naphthylene, cycloalkylene or heteroarylene (all optionally substituted); R = H or as Z. Alkyl or alkylene groups have 1-6C; alkenyl/alkynyl groups have 2-6C and 1-3 double/triple bonds; cycloalkylene groups have 3-6C; aryl groups are phenyl, naphthyl, biphenylyl, dihydronaphthyl or tetrahydronaphthyl; heteroaryl moieties are 5-11 membered, mono- or bicyclic and unsaturated or partially unsaturated, and contain 1-4 of O, S and N as heteroatoms; arylene or heteroarylene moieties are the divalent analogs of arylene and heteroarylene respectively; optionally substituted, in the case of aryl, aralkyl, heteroaryl and heteroaralkyl, indicates that the groups are optionall ring-substituted by 1-5 of alkyl, alkoxy, halo, OH, perhaloalkyl, NO2, NH2, mono- or dialkylamino, 1-6C acyl, CONH2, mono- or di-alkylaminocarbonyl, 1-6C acylamino, alkoxycarbonyl, CHO, COOH, SO3H, CN, aminoalkyl, mono- or dialkylaminoalkyl, thioalkyl, alkylthioalkyl, hydroxyalkyl or alkoxyalkyl; optionally substituted, in the case of phenylene, naphthylene and heteroarylene, indicates that the groups are optionally substituted by 1-3 of alkyl, alkoxy, halo, OH, perhaloalkyl, NO2, NH2, mono- or dialkylamino, 1-6C acyl, CHO, COOH, alkoxycarbonyl, CONH2, mono- or di-alkylaminocarbonyl, 1-6C acylamino or CN. An Independent claim is included for the preparation of (I).

    102.
    发明专利
    未知

    公开(公告)号：AT231133T

    公开(公告)日：2003-02-15

    申请号：AT00401039

    申请日：2000-04-14

    Applicant: SERVIER LAB

    Inventor： FAUCHERE JEAN-LUC ,  ORTUNO JEAN-CLAUDE ,  DUHAULT JACQUES ,  BOUTIN JEAN ALBERT ,  LEVENS NIGEL

    IPC: C07D249/08 ,  A61K31/4196 ,  A61K31/4427 ,  A61K31/443 ,  A61K31/4433 ,  A61K31/4439 ,  A61K31/501 ,  A61P3/00 ,  A61P3/04 ,  A61P3/10 ,  A61P9/00 ,  A61P9/12 ,  A61P15/00 ,  A61P15/10 ,  A61P25/00 ,  A61P25/08 ,  A61P25/20 ,  A61P25/22 ,  A61P25/24 ,  A61P43/00 ,  C07D249/12 ,  C07D249/14 ,  C07D401/04 ,  C07D401/12 ,  C07D401/14 ,  C07D403/12 ,  C07D405/12 ,  C07D409/12

    Abstract: 1,2,4-Triazolylamino-substituted carboxamide or hydrazide derivatives (I) are new. Triazole derivatives of formula G-NH-A- CO-NH-(NH)n-W-Z (I) and their enantiomers, diastereoisomers and acid or base addition salts are new. G = 1,2,4-triazolyl group of formula (G1)-(G4); n = 0 or 1; W = CO, S, SO or SO2; Z, R1 = alkyl or (all optionally substituted) aryl, heteroaryl, aralkyl, aralkenyl, aralkynyl, heteroaralkyl, heteroaralkenyl or heteroaralkynyl; A = -A2-, -A1-A-2-, -A2-A1- or -A1-A2-A1-; A1 = alkylene; A2 = phenylene, naphthylene, cycloalkylene or heteroarylene (all optionally substituted); R = H or as Z. Alkyl or alkylene groups have 1-6C; alkenyl/alkynyl groups have 2-6C and 1-3 double/triple bonds; cycloalkylene groups have 3-6C; aryl groups are phenyl, naphthyl, biphenylyl, dihydronaphthyl or tetrahydronaphthyl; heteroaryl moieties are 5-11 membered, mono- or bicyclic and unsaturated or partially unsaturated, and contain 1-4 of O, S and N as heteroatoms; arylene or heteroarylene moieties are the divalent analogs of arylene and heteroarylene respectively; optionally substituted, in the case of aryl, aralkyl, heteroaryl and heteroaralkyl, indicates that the groups are optionall ring-substituted by 1-5 of alkyl, alkoxy, halo, OH, perhaloalkyl, NO2, NH2, mono- or dialkylamino, 1-6C acyl, CONH2, mono- or di-alkylaminocarbonyl, 1-6C acylamino, alkoxycarbonyl, CHO, COOH, SO3H, CN, aminoalkyl, mono- or dialkylaminoalkyl, thioalkyl, alkylthioalkyl, hydroxyalkyl or alkoxyalkyl; optionally substituted, in the case of phenylene, naphthylene and heteroarylene, indicates that the groups are optionally substituted by 1-3 of alkyl, alkoxy, halo, OH, perhaloalkyl, NO2, NH2, mono- or dialkylamino, 1-6C acyl, CHO, COOH, alkoxycarbonyl, CONH2, mono- or di-alkylaminocarbonyl, 1-6C acylamino or CN. An Independent claim is included for the preparation of (I).

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