반응식
S1C2C=CC=CC=2N=C1NN=CC1OC([N+]([O-])=O)=CC=1.[N+:21]([C:24]1[S:28][C:27]([CH:29]=O)=[CH:26][CH:25]=1)([O-:23])=[O:22].[NH:31]([C:33]1[S:34][C:35]2[CH:41]=[C:40]([Cl:42])[CH:39]=[CH:38][C:36]=2[N:37]=1)[NH2:32]>>[Cl:42][C:40]1[CH:39]=[CH:38][C:36]2[N:37]=[C:33]([NH:31][N:32]=[CH:29][C:27]3[S:28][C:24]([N+:21]([O-:23])=[O:22])=[CH:25][CH:26]=3)[S:34][C:35]=2[CH:41]=1참가 물질
4
실험 절차
The compound 3n was prepared according procedure described for 3a by employing 5-nitrothiophen aldehyde (157 mg, 1 mmol) and 2-hydrazino-6-chloro-benzothiazole (199 mg, 1 mmol) at 70° C. for 2 h (yield 287 mg, 85%).
후처리
- customat 70° C.
- customfor 2 h
출처 및 근거
- ORD 기록
- ord-dcd6ac6ae27a4109be212ec35f340e81
- 출처 데이터셋
- uspto-grants-2016_03
- 특허 번호
- US09273039B2
연결된 노트
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