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公开(公告)号:IT1119193B
公开(公告)日:1986-03-03
申请号:IT6888779
申请日:1979-09-28
Applicant: CARTER WALLACE
Inventor: STIEFEL FRANK J
Abstract: A process for the production of 2-methyl-2-sec. butyl-1,3-propanediol from crotyl alcohol is disclosed. The diol obtained is useful in the manufacture of 2-methyl-2-(1-methylpropyl)-1,3-propanediol dicarbamate a valuable antihypertensive agent.
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公开(公告)号:FI69304C
公开(公告)日:1986-01-10
申请号:FI833016
申请日:1983-08-23
Applicant: CARTER WALLACE
Inventor: STIEFEL FRANK J
IPC: A61K31/40 , C07D295/08 , A61P9/08 , A61P9/10 , C07D20060101 , C07D207/00 , C07D295/088 , C07D295/12 , C07D295/13
Abstract: A novel, efficient, economical procedure for the synthesis of ethers of n-propanoldiamine having the formula: wherein R is a straight or branched chain lower alkyl group or an aralkyl group, Ar is an aromatic group, Ar1 is an aromatic or heterocyclic group, A is a tertiary aliphatic, cycloaliphatic or heterocyclic amino group and addition salts thereof with pharmacologically acceptable acids.
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公开(公告)号:CA1192907A
公开(公告)日:1985-09-03
申请号:CA418556
申请日:1982-12-23
Applicant: CARTER WALLACE
Inventor: STIEFEL FRANK J
IPC: C07D295/08 , A61K31/40 , A61P9/08 , A61P9/10 , C07D20060101 , C07D207/00 , C07D295/088 , C07D295/12 , C07D295/13 , C07D207/04
Abstract: SYNTHESIS OF ETHERS OF N-PROPANOLDIAMINES A process for preparing .beta.-¢(2-methylpropoxy) methyl!-N-phenyl-N-(phenylmethyl)-l-pyrrolidineethanamine hydrochloride hydrate in which isobutanol is reacted with epichlorohydrin, the product is reacted with thionyl chloride, and the compound thus obtained condensed with n-benzylaniline. In accordance with the invention, the condensing step is carried out using sodium hydride as the condensing agent.
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公开(公告)号:BR8208033A
公开(公告)日:1983-11-22
申请号:BR8208033
申请日:1982-12-10
Applicant: CARTER WALLACE
Inventor: STIEFEL FRANK J
IPC: C07D295/08 , A61K31/40 , A61P9/08 , A61P9/10 , C07D20060101 , C07D207/00 , C07D295/088 , C07D295/12 , C07D295/13 , C07D207/04
Abstract: A novel, efficient, economical procedure for the synthesis of ethers of n-propanoldiamine having the formula: wherein R is a straight or branched chain lower alkyl group or an aralkyl group, Ar is an aromatic group, Ar1 is an aromatic or heterocyclic group, A is a tertiary aliphatic, cycloaliphatic or heterocyclic amino group and addition salts thereof with pharmacologically acceptable acids.
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公开(公告)号:NO833071A
公开(公告)日:1983-08-26
申请号:NO833071
申请日:1983-08-26
Applicant: CARTER WALLACE
Inventor: STIEFEL FRANK J
IPC: C07D295/08 , A61K31/40 , A61P9/08 , A61P9/10 , C07D20060101 , C07D207/00 , C07D295/088 , C07D295/12 , C07D295/13 , C07D
CPC classification number: C07D295/088 , C07D295/13
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公开(公告)号:IT8249760D0
公开(公告)日:1982-12-28
申请号:IT4976082
申请日:1982-12-28
Applicant: CARTER WALLACE
Inventor: STIEFEL FRANK J
IPC: A61K31/40 , C07D295/08 , A61P9/08 , A61P9/10 , C07D20060101 , C07D207/00 , C07D295/088 , C07D295/12 , C07D295/13 , A61K
Abstract: A novel, efficient, economical procedure for the synthesis of ethers of n-propanoldiamine having the formula: wherein R is a straight or branched chain lower alkyl group or an aralkyl group, Ar is an aromatic group, Ar1 is an aromatic or heterocyclic group, A is a tertiary aliphatic, cycloaliphatic or heterocyclic amino group and addition salts thereof with pharmacologically acceptable acids.
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公开(公告)号:CA1123011A
公开(公告)日:1982-05-04
申请号:CA336678
申请日:1979-09-28
Applicant: CARTER WALLACE
Inventor: STIEFEL FRANK J
Abstract: IN THE CANADIAN PATENT OFFICE By: Frank J. Stiefel For: Chemical Process A process for the production of 2-methyl-2-sec. butyl-1,3-propanediol from crotyl alcohol is disclosed. The diol obtained is useful in the manufacture of 2-methyl-2(1-methylpropyl)-1,3-propanediol dicarbamate a valuable antihypertensive agent.
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公开(公告)号:AU5423579A
公开(公告)日:1980-07-03
申请号:AU5423579
申请日:1979-12-28
Applicant: CARTER WALLACE
Inventor: STIEFEL FRANK J
IPC: C07D498/04
Abstract: The compound 7-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo(3,2-b)(1,3)-benzoxazin- 9-one is produced by reacting a mixture of tetrahydrofuran and crotonaldehyde with 5-chlorosalicylhydroxamic acid. The compound has demonstrated utility as a uricosuric agent.
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