반응식
[NH2:1][CH2:2][CH2:3][CH2:4][C@H:5]1[O:9][C:8](=[O:10])[N:7]([C:11]2[CH:12]=[CH:13][C:14]3[S:19][CH2:18][C:17](=[O:20])[NH:16][C:15]=3[CH:21]=2)[CH2:6]1.[Cl:22][C:23]1[C:28]2[NH:29]C(=O)[O:31][C:32](=O)[C:27]=2[CH:26]=[CH:25][CH:24]=1>>[NH2:29][C:28]1[C:23]([Cl:22])=[CH:24][CH:25]=[CH:26][C:27]=1[C:32]([NH:1][CH2:2][CH2:3][CH2:4][C@H:5]1[O:9][C:8](=[O:10])[N:7]([C:11]2[CH:12]=[CH:13][C:14]3[S:19][CH2:18][C:17](=[O:20])[NH:16][C:15]=3[CH:21]=2)[CH2:6]1)=[O:31]참가 물질
3
실험 절차
Starting from 6-[(R)-5-(3-amino-propyl)-2-oxo-oxazolidin-3-yl]-4H-benzo[1,4]thiazin-3-one (described in WO 2010/041219) and 8-chloro-1H-benzo[d][1,3]oxazine-2,4-dione and using Procedure A, the title compound was obtained as a colourless solid (97 mg; 70% yield).
출처 및 근거
- ORD 기록
- ord-ceaf159ad0b1494997a2beba31aa605c
- 출처 데이터셋
- uspto-grants-2014_12
- 특허 번호
- US08916573B2
연결된 노트
불러오는 중…