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

HRID 32743

반응식

HRID 32743 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]([CH3:32])(=[O:31])=[O:30])=[CH:25][C:21]=1[C:22]([OH:24])=[O:23].[OH:33][CH:34]1[CH2:39][CH2:38][CH2:37][NH:36][CH2:35]1>>[OH:33][CH:34]1[CH2:39][CH2:38][CH2:37][N:36]([C:20]2[CH:28]=[CH:27][C:26]([S:29]([CH3:32])(=[O:31])=[O:30])=[CH:25][C:21]=2[C:22]([OH:24])=[O:23])[CH2:35]1

참가 물질

4

반응물 3

HCID 232933-HydroxypiperidineHCID 23291322-Chloro-5-(methylsulphonyl)benzoic acidHCID 597934895-Methanesulfonyl-2-pyrrolidin-1-yl-benzoic acid

생성물 1

HCID 59793490Rac-2-(3-hydroxy-piperidin-1-yl)-5-methanesulfonyl-benzoic acid수율 9%

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 Y) from 2-Chloro-5-methanesulfonyl-benzoic acid and rac-3-hydroxy-piperidine and obtained in 9% yield. MS (m/e): 298.1 (M−H 100%).

후처리

  1. customobtained in 9% yield

출처 및 근거

ORD 기록
ord-d594005021914311880238702fbd4221
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07427612B2

연결된 노트

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