반응식
C[S:2]([C:5]1[CH:6]=[CH:7][C:8]([N:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11])(=[O:4])=[O:3].ClC1C=CC(S(=O)(=O)[NH:30][CH2:31][CH:32]2[CH2:34][CH2:33]2)=CC=1C(O)=O.N1CCCC1>>[CH:32]1([CH2:31][NH:30][S:2]([C:5]2[CH:6]=[CH:7][C:8]([N:14]3[CH2:18][CH2:17][CH2:16][CH2:15]3)=[C:9]([CH:13]=2)[C:10]([OH:12])=[O:11])(=[O:4])=[O:3])[CH2:34][CH2:33]1참가 물질
4
실험 절차
The title compound was synthesised according to the procedure described for the synthesis of 5-Methanesulfonyl-2-pyrrolidin-1-yl-benzoic acid from 2-Chloro-5-(cyclopropylmethyl-sulfamoyl)-benzoic acid and pyrrolidine and obtained in 38% yield.
후처리
- customobtained in 38% yield
출처 및 근거
- ORD 기록
- ord-4ca8d71b6dbb4d62b9c25dc812bff8fb
- 출처 데이터셋
- uspto-grants-2009_09
- 특허 번호
- US07595314B2
연결된 노트
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