3-Hydroxypiperidine → Rac-2-(3-hydroxy-piperidin-1-yl)-5-methylsulfamoyl-benzoic acid

HRID 32746

반응식

HRID 32746 반응식
CS(C1C=CC(N2CCCC2)=C(C=1)C(O)=O)(=O)=O.Cl[C:20]1[CH:28]=[CH:27][C:26]([S:29](=[O:33])(=[O:32])[NH:30][CH3:31])=[CH:25][C:21]=1[C:22]([OH:24])=[O:23].[OH:34][CH:35]1[CH2:40][CH2:39][CH2:38][NH:37][CH2:36]1>>[OH:34][CH:35]1[CH2:40][CH2:39][CH2:38][N:37]([C:20]2[CH:28]=[CH:27][C:26]([S:29](=[O:33])(=[O:32])[NH:30][CH3:31])=[CH:25][C:21]=2[C:22]([OH:24])=[O:23])[CH2:36]1

참가 물질

4

반응물 3

HCID 232933-HydroxypiperidineHCID 111724Benzoic acid, 2-chloro-5-[(methylamino)sulfonyl]-HCID 597934895-Methanesulfonyl-2-pyrrolidin-1-yl-benzoic acid

생성물 1

HCID 59793580Rac-2-(3-hydroxy-piperidin-1-yl)-5-methylsulfamoyl-benzoic acid수율 15%

실험 절차

The title compound was synthesised according to the procedure described for the synthesis of 5-Methanesulfonyl-2-pyrrolidin-1-yl-benzoic acid (Example S) from 2-Chloro-5-methylsulfamoyl-benzoic acid and rac-3-hydroxy-piperidine and obtained in 15% yield. MS (m/e): 312.9 (MH− 100%).

후처리

  1. customobtained in 15% yield

출처 및 근거

ORD 기록
ord-36919d26d00f4ef1a0e891b347c58139
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07427612B2

연결된 노트

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