반응식
[Cl:1][C:2]1[CH:30]=[CH:29][C:5]([CH2:6][N:7]([C:13]2[C:18]([C:19]([F:22])([F:21])[F:20])=[CH:17][C:16]([N+:23]([O-])=O)=[CH:15][C:14]=2[N+:26]([O-])=O)[C:8](=[O:12])[O:9][CH2:10][CH3:11])=[CH:4][CH:3]=1>C(OCC)(=O)C.[Pd]>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][N:7]([C:13]2[C:18]([C:19]([F:22])([F:20])[F:21])=[CH:17][C:16]([NH2:23])=[CH:15][C:14]=2[NH2:26])[C:8](=[O:12])[O:9][CH2:10][CH3:11])=[CH:29][CH:30]=1참가 물질
4
실험 절차
Ethyl 4-chlorobenzyl[2,4-dinitro-6-(trifluoromethyl)phenyl]carbamate (294.7 mg) was dissolved in ethyl acetate (20 ml), and to the solution was added 10% Pd—C (267.7 mg). The reaction mixture was stirred under hydrogen atmosphere for 7 hours. The catalyst was filtered, and washed with ethyl acetate. The filtrate was concentrated in vacuo to give the title compound (248.7 mg).
후처리
- filtrationThe catalyst was filtered
- washwashed with ethyl acetate
- concentrationThe filtrate was concentrated in vacuo
출처 및 근거
- ORD 기록
- ord-22e9506486f448879edec20695904024
- 출처 데이터셋
- uspto-grants-2005_09
- 특허 번호
- US06939887B2
연결된 노트
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