发明名称 Quinoline and quinazoline compounds useful in therapy, particularly in the treatment of benign prostatic hyperplasia
摘要 <p>Compounds and pharmaceutically acceptable salts of formula I wherein, R1 is C1-4 alkoxy optionally substituted by one or more fluorine atoms, R2 is H or C1-4 alkoxy optionally substituted by one or more fluorine atoms, R3 is a 5 or 6 membered heterocyclic ring containing at least one heteroatom selected from N, 0 and S, the ring being optionally substituted by one or more groups selected from halogen, C1-4 alkoxy, C1-4 alkyl and CF3, R4 is a 4, 5, 6, or 7 membered heterocyclic ring containing at least one heteroatom selected from N, 0 and S, the ring being optionally fused to a benzene ring or a 5 or 6 membered heterocyclic ring containing at least one heteroatom selected from N, O and S, the ring system as a whole being optionally substituted by one or more groups independently selected from OH, C1-4 alkyl, C1-4 alkoxy, halogen, CONR8R9, SO2NR8R9, (CH2)bNR8R9 and NHSO2(C1-4 alkyl), and when S is a member of the ring system, it may be substituted by one or two oxygen atoms, R8 and R9 independently represent H or C1-4 alkyl, or together with the N atom to which they are attached they may represent a 5 or 6 membered heterocyclic ring containing at least one heteroatom selected from N, 0 and S, b is 0, 1,2 or 3, X is CH or N and L is absent or represents a cyclic group of formula Ia wherein, N is attached to the 2-position of the quinoline or quinazoline ring, A is absent or represents CO or SO2-, Z is CH or N, m is 1 or 2, and in addition, when Z represents CH, it may represent 0, n is 1, 2 or 3, provided that the sum of m and n is 2, 3, 4 or 5, or n is a chain of formula Ib wherein, N is attached to the 2-position of the quinoline or quinazoline ring, A' and Z' are the same as A and Z above, R6 and R7 independently represent H or C1-4 alkyl, p is 1, 2 or 3, and in addition, when Z' represents CH, it may represent 0. Also described is a method of manufacturing these compounds and the use of these compounds as medicaments for the treatment of benign prostatic hyperplasia.</p>
申请公布号 NZ336302(A) 申请公布日期 2000.08.25
申请号 NZ19980336302 申请日期 1998.01.06
申请人 PFIZER INC 发明人 FOX, DAVID NATHAN ABRAHAM
分类号 A61K31/47;A61K31/4725;A61K31/505;A61K31/517;A61K31/519;A61P13/08;C07D401/04;C07D401/14;C07D405/04;C07D409/04;C07D413/04;C07D471/04;(IPC1-7):A61K31/47;C07D239/00;C07D221/00 主分类号 A61K31/47
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