Ethyl bromoacetate → Ethyl 3-acetylamino-3-(2-furylcarbonyl)propionate
반응식
[C:1]([NH:4][CH2:5][C:6]([C:8]1[O:9][CH:10]=[CH:11][CH:12]=1)=[O:7])(=[O:3])[CH3:2].[H-].[Na+].Br[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18]>>[C:1]([NH:4][CH:5]([C:6]([C:8]1[O:9][CH:10]=[CH:11][CH:12]=1)=[O:7])[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])(=[O:3])[CH3:2]참가 물질
4
실험 절차
2.6 g of N-acetyl-(2-furylcarbonyl)methylamine, 0.74 g of 61% sodium hydride and 2.9 g of ethyl bromoacetate are treated in the same manner as described in Preparation 1-(2). 1.6 g of ethyl 3-acetylamino-3-(2-furylcarbonyl)propionate are thereby obtained. Yield: 41%
후처리
- customas described in Preparation 1-(2)
출처 및 근거
- ORD 기록
- ord-cf7a9daec9664351b0543f3116ef2ab9
- 출처 데이터셋
- uspto-grants-1987_02
- 특허 번호
- US04642313
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