반응식
C(N=[N+]=[N-])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1.[N+:12]([C:15]1[CH:16]=[C:17]2[C:21](=[CH:22][CH:23]=1)[NH:20][CH2:19][CH2:18]2)([O-:14])=[O:13].[NH2:24][C:25](N)=[O:26].[ClH:28]>CCOCC>[ClH:28].[N+:12]([C:15]1[CH:16]=[C:17]2[C:21](=[CH:22][CH:23]=1)[N:20]([C:25](=[O:26])[NH:24][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1)[CH2:19][CH2:18]2)([O-:14])=[O:13]참가 물질
6
실험 절차
This material was prepared from nicotinoyl azide (0.43 g, 2.9 mmol) and 5-nitroindoline (0.38 g, 2.3 mmol), and conversion of the precipitated urea to the salt using excess HCl in ether, following the procedure of Example 2. This gave the title compound (0.64 g, 76%) as a light yellow powder, m.p. 244°-7° C. (dec.).
출처 및 근거
- ORD 기록
- ord-aafc92b2637a4682a1f40d81e42fab24
- 출처 데이터셋
- uspto-grants-1998_11
- 특허 번호
- US05834494
연결된 노트
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