반응식
[CH:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([CH:14]([CH3:16])[CH3:15])[C:11]=1[O:12][CH3:13])[CH:7]=O)([CH3:3])[CH3:2].[F:17][C:18]1[CH:19]=[C:20]2[C:24](=[CH:25][CH:26]=1)[NH:23][C:22](=[O:27])[CH2:21]2>>[CH:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([CH:14]([CH3:16])[CH3:15])[C:11]=1[O:12][CH3:13])[CH:7]=[C:21]1[C:20]2[C:24](=[CH:25][CH:26]=[C:18]([F:17])[CH:19]=2)[NH:23][C:22]1=[O:27])([CH3:3])[CH3:2]참가 물질
3
실험 절차
3,5-Diisopropyl-4-methoxybenzaldehyde was condensed with 5-fluoro-2-oxindole to give 0.3 g of 3-(3,5-diisopropyl-4methoxybenzylidene)-5-fluoro-1,3-dihydroindol-2-one as a yellow-orange solid.
출처 및 근거
- ORD 기록
- ord-c1496f9aa97c4332b07eb4ab5d85d9f9
- 출처 데이터셋
- uspto-grants-2005_02
- 특허 번호
- US06855730B2
연결된 노트
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