公开(公告)号：JPH0770082A

公开(公告)日：1995-03-14

申请号：JP11296094

申请日：1994-05-26

Applicant: UCB SA

Inventor： FUIRITSUPU MISHIERU ,  ERITSUKU KOSUMAN ,  JIYAN GOBEERU ,  ERUNSUTO BURUFUERUTO

IPC: A61K31/415 ,  A61K31/4164 ,  A61K31/4174 ,  A61K31/4178 ,  A61P27/02 ,  A61P27/06 ,  C07D233/54 ,  C07D233/56 ,  C07D233/64 ,  C07D403/10

公开(公告)号：JPH01313467A

公开(公告)日：1989-12-18

申请号：JP10903089

申请日：1989-04-27

Applicant: UCB SA

Inventor： ERITSUKU KOSUMEN ,  JIYANNPIEERU GEERUTO ,  JIYAN KOBEERU ,  FUIRITSUPU MISHIERU ,  ERUNSUTO URUFUEERU

IPC: C07D233/56 ,  A61K31/415 ,  A61K31/4164 ,  A61P9/08 ,  A61P9/10 ,  A61P9/12 ,  A61P25/02 ,  A61P29/00 ,  C07D233/54 ,  C07D233/64

Abstract: New substituted 1-(1H-imidazol-4-yl)alkyl-benzamides and their salts, processes for the preparation thereof and pharmaceutical compositions. These compounds have the formula wherein R1, R2=hydrogen or C1-C4-alkyl, R3=hydrogen, amino, hydroxyl, C1-C4-alkyl or C1-C4-hydroxyalkyl, R4=hydrogen or C1-C4-alkyl, or R3R4N=pyrrolidino, piperidino or morpholino, R5 and R6=hydrogen, hydroxyl, C1-C4-alkyl or C1-C4-alkoxy, at least one of R5 and R6 being other than hydrogen. These compounds are prepared either by reacting a nitrogen compound with an alkyl 1-(1H-imidazol-4-yl)alkyl-benzoate or with a 1-(1H-imidazol-4-yl)alkyl-benzoic acid, or by hydrolyzing in an acid medium a 2-hydroxy-3-[1-(1H-imidazol-4-yl)alkyl]-benzonitrile. The compounds have anti-ischemic and alpha 2-adrenoceptor agonist activities.

公开(公告)号：JPS63132876A

公开(公告)日：1988-06-04

申请号：JP27814487

申请日：1987-11-02

Applicant: UCB SA

Inventor： ERITSUKU KOSEMENTO ,  JIYAN PIEERU GEERUTSU ,  JIYAN GOBEERU ,  FUIRITSUPU MISHIERU

IPC: A61K31/415 ,  A61K31/4164 ,  A61K31/495 ,  A61P9/08 ,  A61P9/10 ,  A61P9/12 ,  C07D233/54 ,  C07D233/58 ,  C07D233/64 ,  C07D405/06 ,  C07D413/06