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公开(公告)号:NO128275B
公开(公告)日:1973-10-22
申请号:NO332668
申请日:1968-08-26
Applicant: HOFFMANN LA ROCHE
Inventor: BRETSCHNEIDER H , KLOETZER W , FRANZMAIR R , SCHMIDT B
IPC: C07D27/14
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公开(公告)号:ZA7203032B
公开(公告)日:1973-02-28
申请号:ZA7203032
申请日:1972-05-04
Applicant: HOFFMANN LA ROCHE
Inventor: BROSSI A , KLOETZER W , TEITEL S
IPC: C07D20060101 , C07D
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公开(公告)号:SE340460B
公开(公告)日:1971-11-22
申请号:SE1698068
申请日:1968-12-11
Applicant: HOFFMANN LA ROCHE
Inventor: BRETSCHNEIDER H , KLOETZER W
IPC: C07D51/44
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公开(公告)号:SE310683B
公开(公告)日:1969-05-12
申请号:SE1052360
申请日:1960-11-02
Applicant: HOFFMANN LA ROCHE
Inventor: BRETSCHNEIDER H , KLOETZER W
IPC: C07D51/44
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公开(公告)号:NO129571B
公开(公告)日:1974-04-29
申请号:NO332768
申请日:1968-08-26
Applicant: HOFFMANN LA ROCHE
Inventor: BRETSCHNEIDER H , KLOETZER W , FRANZMAIR R
IPC: C07D27/04
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公开(公告)号:ZA723031B
公开(公告)日:1973-02-28
申请号:ZA723031
申请日:1972-05-04
Applicant: HOFFMANN LA ROCHE
Inventor: BROSSI A , KLOETZER W , TEITEL S
IPC: C07D20060101 , C07D
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公开(公告)号:SE340620B
公开(公告)日:1971-11-29
申请号:SE1150468D
申请日:1968-08-27
Applicant: HOFFMANN LA ROCHE
Inventor: BRETSCHNEIDER H , KLOETZER W , FRANZMAIR R , SCHMIDT B
IPC: C07D207/22 , C07D207/38 , C07D27/14
Abstract: (A) Cmpds. (I) and (III): and tautomeric forms of I and III, where R' = Ph opt. substd. by (1-6Ce alkyl, (1-6C) Oalkyl, or halogen. R2 = Ph opt. substd. by (1-6C) alkyl, (1-6C)O alkyl, or halogen, (5-6C) cycloalkyl, or (5-6C) cycloalkenyl. R3, R4, R5 and R6 = H or (1-6C) alkyl. R7 = H, (1-6C) alkyl, lower carbalkoxy, lower alkyl, N(alkyl)2-lower alkyl, lower alkoxyphenyl, or lower alkoxy-lower alkyl. R8 = H or (1-6C) alkyl. X = O, S, or NH. (B) Acid addn. salts (II) of I. I and II Hypoglycaemics. III Intermediates for I.
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公开(公告)号:SE340454B
公开(公告)日:1971-11-22
申请号:SE1150568D
申请日:1968-08-27
Applicant: HOFFMANN LA ROCHE
Inventor: FRANZMAIR R , BRETSCHNEIDER H , KLOETZER W
IPC: C07D27/04
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公开(公告)号:SE331996B
公开(公告)日:1971-01-25
申请号:SE245168
申请日:1968-02-26
Applicant: HOFFMANN LA ROCHE
Inventor: BRETSCHNEIDER H , FRANZMAIR B , KLOETZER W , SCHMIDT B
IPC: C07D207/22 , C07D207/38 , C07D27/14
Abstract: (A) Cmpds. (I) and (III): and tautomeric forms of I and III, where R' = Ph opt. substd. by (1-6Ce alkyl, (1-6C) Oalkyl, or halogen. R2 = Ph opt. substd. by (1-6C) alkyl, (1-6C)O alkyl, or halogen, (5-6C) cycloalkyl, or (5-6C) cycloalkenyl. R3, R4, R5 and R6 = H or (1-6C) alkyl. R7 = H, (1-6C) alkyl, lower carbalkoxy, lower alkyl, N(alkyl)2-lower alkyl, lower alkoxyphenyl, or lower alkoxy-lower alkyl. R8 = H or (1-6C) alkyl. X = O, S, or NH. (B) Acid addn. salts (II) of I. I and II Hypoglycaemics. III Intermediates for I.
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公开(公告)号:YU40388A
公开(公告)日:1990-02-28
申请号:YU40388
申请日:1988-03-01
Applicant: HOFFMANN LA ROCHE
Inventor: KLOETZER W , MONTAVON M , MUESSNER R , SINGEWALD N
IPC: A61K31/415 , A61K31/4164 , C07D233/56 , A61K31/417 , A61P3/00 , A61P29/00 , C07D233/61 , C07D233/64 , C07D233/80 , C07D233/84 , C07D233/88 , C07D521/00
Abstract: Imidazole derivatives of the formula I wherein R1 and R2 each is lower alkyl, X is a residue of the formula R3 is hydrogen and R4 is hydrogen or lower alkyl or R3 and R4 taken together are an additional carbon-nitrogen bond; R5 is hydrogen or lower alkyl; R6 is hydrogen, lower alkyl, lower alkylthio or a residue of the formula -NR7R8; and R7 and R8 each is lower alkyl or taken together with the nitrogen atom are a 5- or 6-membered saturated heterocycle; and pharmaceutically acceptable acid addition salts thereof are described. The compounds of formula I possess valuable pharmacodynamic properties, especially inflammation-inhibiting and edema-inhibiting properties, so that they can be used for the control or prevention of illnesses, especially for the control or prevention of inflammations and edemas.
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