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Hydrazine hydrate (1:1) → HCID 67960143, 화합물

HRID 1529357
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HRID 1529357 반응식
[C:1]([O:5][C:6]([NH:8][CH:9]1[CH2:14][CH2:13][N:12]([C:15]2[N:20]=[C:19]([C:21]3[C:29]4[C:24](=[CH:25][CH:26]=[C:27]([N+:30]([O-])=O)[CH:28]=4)[N:23]([C:33]([O:35][C:36]([CH3:39])([CH3:38])[CH3:37])=[O:34])[CH:22]=3)[CH:18]=[N:17][CH:16]=2)[CH2:11][CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].O.NN>CO.[Ni]>[NH2:30][C:27]1[CH:28]=[C:29]2[C:24](=[CH:25][CH:26]=1)[N:23]([C:33]([O:35][C:36]([CH3:39])([CH3:38])[CH3:37])=[O:34])[CH:22]=[C:21]2[C:19]1[CH:18]=[N:17][CH:16]=[C:15]([N:12]2[CH2:13][CH2:14][CH:9]([NH:8][C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[CH2:10][CH2:11]2)[N:20]=1
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참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 67959775HCID 67959775, 화합물

생성물 1

HCID 67960143HCID 67960143, 화합물수율 85%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

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온도
50 °C

실험 절차

To a solution of tert-butyl 3-(6-(4-(tert-butoxycarbonylamino)piperidin-1-yl)pyrazin-2-yl)-5-nitro-1H-indole-1-carboxylate (200 mg, 0.37 mmol) in MeOH (2 mL) was added Raney Ni (30 mg) and then heated at 50° C. for 5 min. Hydrazine hydrate (0.2 mL) was added and the resulting mixture was stirred at the same temperature for another 10 min. The reaction mixture was cooled to RT and filtered off the Raney Ni through Celite. The filtrate was concentrated to obtain the title compound as a pale brown solid (160 mg, 85%). MS (ESI, pos. ion) m/z: 509.3 (M+1).

후처리

  1. temperatureThe reaction mixture was cooled to RT
  2. filtrationfiltered off the Raney Ni through Celite
  3. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-62e1b21f9d664698bfa834abb214f06a
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09090593B2

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