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公开(公告)号:KR800001279B1
公开(公告)日:1980-10-26
申请号:KR760000422
申请日:1976-02-20
Applicant: HOFFMANN LA ROCHE
Inventor: BERNAUER K , SCHNEIDER F , PFOERTNER K
IPC: C07D207/10
Abstract: Analgesic pyrrolidine derivs. (I; R1 = pyridy1; R2 = H, lower alky1; R3 = H, lower alky1, benzy1; R4 = halogen, lower alcohol, lower alkoxy, nitro, and amino-substituted pheny1) were prepd. by the redn. of pyrrolines II. Thus, 4-methy1-4-nitro-3-(4-pytidy1)-valerophenon was reduced by Zn in CH3COOH followed by treating with 1n-HC1 and crystallizing with EtOH/(CH3)2CO gave trans-4-(2,2-dimethy1-5-pheny1-pyrolidy1)-pyridine dihydrochloride. I are useful as non-addictive analgesic agent, 3.0g., racemic 4-(cis-2,2-dimethy1-5-pheny1-3-pyrrolidiny1)-pyridine dihydrochloride had ED50 47mg/kg.
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公开(公告)号:ZA7704345B
公开(公告)日:1978-06-28
申请号:ZA7704345
申请日:1977-07-19
Applicant: HOFFMANN LA ROCHE
Inventor: SCHMID H , BERNAUER K , PFOERTNER K , SCHNEIDER F
IPC: C07D207/08 , C07C , C07D
CPC classification number: C07D207/08
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公开(公告)号:SE7708536L
公开(公告)日:1978-01-27
申请号:SE7708536
申请日:1977-07-25
Applicant: HOFFMANN LA ROCHE
Inventor: BERNAUER K , PFOERTNER K , SCHNEIDER F , SCHMID H
IPC: C07D207/08 , C07D409/04
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公开(公告)号:SE7708536A
公开(公告)日:1978-01-27
申请号:SE7708536
申请日:1977-07-25
Applicant: HOFFMANN LA ROCHE
Inventor: BERNAUER K , PFOERTNER K , SCHNEIDER F , SCHMID H
IPC: C07D207/08 , C07D409/04
CPC classification number: C07D207/08
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公开(公告)号:BR7601094A
公开(公告)日:1976-09-14
申请号:BR7601094
申请日:1976-02-20
Applicant: HOFFMANN LA ROCHE
Inventor: BERNAUER K , SCHMID H , PFOERTNER K , SCHNEIDER F
IPC: C07D213/50 , C07D401/04
Abstract: Compounds represented by the formula +q,10 WHEREIN R1 is a pyridyl, R2 is hydrogen or lower alkyl, R3 is hydrogen, lower alkyl or benzyl and R4 is phenyl or phenyl substituted at one or more carbon atoms with one or more of halogen, lower alkyl, lower alkoxy, nitro or amino AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF, HAVING ANALGESIC ACTIVITY ARE DISCLOSED.
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公开(公告)号:SE7602069L
公开(公告)日:1976-08-23
申请号:SE7602069
申请日:1976-02-20
Applicant: HOFFMANN LA ROCHE
Inventor: BERNAUER K , PFOERTNER K , SCHNEIDER F , SCHMID H
IPC: C07D213/50 , C07D401/04
Abstract: Compounds represented by the formula +q,10 WHEREIN R1 is a pyridyl, R2 is hydrogen or lower alkyl, R3 is hydrogen, lower alkyl or benzyl and R4 is phenyl or phenyl substituted at one or more carbon atoms with one or more of halogen, lower alkyl, lower alkoxy, nitro or amino AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF, HAVING ANALGESIC ACTIVITY ARE DISCLOSED.
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公开(公告)号:SE424988B
公开(公告)日:1982-08-23
申请号:SE7708536
申请日:1977-07-25
Applicant: HOFFMANN LA ROCHE
Inventor: BERNAUER K , PFOERTNER K , SCHNEIDER F , SCHMID H
IPC: C07D207/08 , C07D207/09 , C07D401/10 , C07D403/10 , C07D409/04 , C07D413/10 , C07D417/10
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公开(公告)号:ZA807852B
公开(公告)日:1981-12-30
申请号:ZA807852
申请日:1980-12-15
Applicant: HOFFMANN LA ROCHE
Inventor: PFOERTNER K , BERNAUER K
IPC: C07D263/10 , A61K20060101 , A61K31/42 , A61K31/421 , A61P3/08 , C07D20060101 , C07D , A61K
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公开(公告)号:DK545980A
公开(公告)日:1981-06-22
申请号:DK545980
申请日:1980-12-19
Applicant: HOFFMANN LA ROCHE
Inventor: BERNAUER K , PFOERTNER K
IPC: C07D263/10 , C07D
Abstract: Compounds of the formula I wherein R1 and R2, independently, are hydrogen, halogen or lower alkyl; R3, R4, R5, R6 and R7, independently, are hydrogen or lower alkyl; R8 is hydrogen, lower alkyl or formyl; R9 and R10, independently, are methyl or trifluoromethyl; and n is 0 (zero) or, when both R7 and R8 are lower alkyl, n is 0 (zero) or 1, prepared, inter alia, from p-aminobenzaldehydes which may be N-alkyl substituted, are described. The compounds of formula I are orally active antidiabetic agents.
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公开(公告)号:AU500184B2
公开(公告)日:1979-05-10
申请号:AU1062976
申请日:1976-01-29
Applicant: HOFFMANN LA ROCHE
Inventor: BERNAUER K , PFOERTNER K , SCHNEIDER F , SCHMID H
IPC: C07D213/50 , C07D401/04 , A61K31/44
Abstract: Compounds represented by the formula +q,10 WHEREIN R1 is a pyridyl, R2 is hydrogen or lower alkyl, R3 is hydrogen, lower alkyl or benzyl and R4 is phenyl or phenyl substituted at one or more carbon atoms with one or more of halogen, lower alkyl, lower alkoxy, nitro or amino AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF, HAVING ANALGESIC ACTIVITY ARE DISCLOSED.
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