Ethyl-2-[4-trifluoromethyl-piperidinyl]-4-methylamino-5-nitro-benzoate → Ethyl-2-[4-trifluoromethyl-piperidinyl]-4-methylamino-5-amino-benzoate
반응식
[CH2:1]([O:3][C:4](=[O:26])[C:5]1[CH:10]=[C:9]([N+:11]([O-])=O)[C:8]([NH:14][CH3:15])=[CH:7][C:6]=1[N:16]1[CH2:21][CH2:20][CH:19]([C:22]([F:25])([F:24])[F:23])[CH2:18][CH2:17]1)[CH3:2]>[Ni].C1COCC1>[CH2:1]([O:3][C:4](=[O:26])[C:5]1[CH:10]=[C:9]([NH2:11])[C:8]([NH:14][CH3:15])=[CH:7][C:6]=1[N:16]1[CH2:17][CH2:18][CH:19]([C:22]([F:23])([F:24])[F:25])[CH2:20][CH2:21]1)[CH3:2]참가 물질
4
실험 절차
A mixture of ethyl-2-[4-trifluoromethyl-piperidinyl]-4-methylamino-5-nitro-benzoate (380 mg, 1.01 mmol), Ra—Ni (500 mg) and THF (20 mL) is stirred overnight under 10 bar H2-atmosphere. The mixture is filtered, and the filtrate is concentrated.
후처리
- filtrationThe mixture is filtered
- concentrationthe filtrate is concentrated
출처 및 근거
- ORD 기록
- ord-4d0e7f2c602243429fbfb5fb8f03c6b1
- 출처 데이터셋
- uspto-grants-2014_03
- 특허 번호
- US08674113B2
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