반응식
NC1C=CC(C([NH:8][CH:9]([CH2:27][S:28]([CH3:31])(=[O:30])=[O:29])[C:10]([N:12]2[CH2:16][CH2:15][CH2:14][CH:13]2[C:17]([NH:19][CH:20]([CH:25]=[O:26])[CH2:21][C:22]([OH:24])=[O:23])=[O:18])=[O:11])=O)=CC=1Cl.[Cl:35][C:36]1[CH:37]=[C:38]([CH:42]=[C:43]([Cl:46])[C:44]=1[OH:45])[C:39]([OH:41])=O>>[Cl:46][C:43]1[CH:42]=[C:38]([CH:37]=[C:36]([Cl:35])[C:44]=1[OH:45])[C:39]([NH:8][CH:9]([CH2:27][S:28]([CH3:31])(=[O:30])=[O:29])[C:10]([N:12]1[CH2:16][CH2:15][CH2:14][CH:13]1[C:17]([NH:19][CH:20]([CH:25]=[O:26])[CH2:21][C:22]([OH:24])=[O:23])=[O:18])=[O:11])=[O:41]참가 물질
3
반응물 2
생성물 1
실험 절차
Compound 20s was prepared according to the procedure used for the preparation of 20i, using 3,5-dichloro-4-hydroxybenzoic acid in place of 1-isoquinolinecarboxylic acid.
출처 및 근거
- ORD 기록
- ord-5e08b25201134761ab3b9297ce971fa1
- 출처 데이터셋
- uspto-grants-2008_04
- 특허 번호
- US07358273B2
연결된 노트
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