3-Furoic acid → N-(4-Ethoxy-2-nitrophenyl)-3-furancarboxamide
반응식
[O:1]1[CH:5]=[CH:4][C:3]([C:6]([OH:8])=O)=[CH:2]1.[CH2:9]([O:11][C:12]1[CH:18]=[CH:17][C:15]([NH2:16])=[C:14]([N+:19]([O-:21])=[O:20])[CH:13]=1)[CH3:10]>>[CH2:9]([O:11][C:12]1[CH:18]=[CH:17][C:15]([NH:16][C:6]([C:3]2[CH:4]=[CH:5][O:1][CH:2]=2)=[O:8])=[C:14]([N+:19]([O-:21])=[O:20])[CH:13]=1)[CH3:10]참가 물질
3
실험 절차
The title compound was prepared from 3-furoic acid and 4-ethoxy-2-nitroaniline as a yellow solid as described in Example 15. 1H NMR (DMSO-d6): 10.25 (s, 1H), 8.36 (d, J=2.4, 1H), 7.83-7.81 (m, 1H), 7.53-7.47 (m, 2H), 7.35-7.31 (m, 1H), 6.94 (d, J=2.4, 1H), 4.12 (q, J=6.9, 2H), 1.35 (t, J=6.9, 3H).
출처 및 근거
- ORD 기록
- ord-7ea257e44ccf41158ff9d536679e2aac
- 출처 데이터셋
- uspto-grants-2004_09
- 특허 번호
- US06794397B2
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