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Hydrazine hydrate (1:1) → 1,1-Dimethylethyl 4-[(2-amino-4-chloro-5-methoxyphenyl)amino]-1-piperidinecarboxylate

HRID 2064153
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HRID 2064153 반응식
[CH3:1][O:2][C:3]1[C:4]([Cl:26])=[CH:5][C:6]([N+:23]([O-])=O)=[C:7]([NH:9][CH:10]2[CH2:15][CH2:14][N:13]([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[CH2:12][CH2:11]2)[CH:8]=1.O.NN>C(O)C.[Ni]>[NH2:23][C:6]1[CH:5]=[C:4]([Cl:26])[C:3]([O:2][CH3:1])=[CH:8][C:7]=1[NH:9][CH:10]1[CH2:11][CH2:12][N:13]([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[CH2:14][CH2:15]1
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참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 598501431,1-Dimethylethyl 4-[(5-methoxy-4-chloro-2-nitrophenyl)amino]-piperidinecarboxylate

생성물 1

HCID 598502131,1-Dimethylethyl 4-[(2-amino-4-chloro-5-methoxyphenyl)amino]-1-piperidinecarboxylate

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

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온도
40 °C

실험 절차

1,1-Dimethylethyl 4-[(5-methoxy-4-chloro-2-nitrophenyl)amino]-piperidinecarboxylate (D47) (400 mg) was dissolved in ethanol (10 ml) and Raney nickel (50% aqueous suspension, 1.0 ml) was added at room temperature; the mixture was heated to 40° C. and hydrazine monohydrate (0.5 ml) was added over 30 min. After 30 min more, the reaction mixture was cooled to room temperature, filtered through Celite evaporated and chromatographed on silica gel eluting with ethyl acetate-hexane mixtures to yield the title compound, 300 mg.

후처리

  1. temperaturethe reaction mixture was cooled to room temperature
  2. filtrationfiltered through Celite
  3. customevaporated
  4. customchromatographed on silica gel eluting with ethyl acetate-hexane mixtures

출처 및 근거

ORD 기록
ord-757b8a5e1d1d488b936178e4f44e59fa
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08288412B2

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