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1-Ethyl-4-(2-fluoro-4-nitrophenyl)piperazine → 4-(4-Ethylpiperazin-1-yl)-3-fluoroaniline

HRID 2066712
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인쇄 미리보기

반응식

HRID 2066712 반응식
[CH2:1]([N:3]1[CH2:8][CH2:7][N:6]([C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[CH:11][C:10]=2[F:18])[CH2:5][CH2:4]1)[CH3:2]>[Ni].CO>[CH2:1]([N:3]1[CH2:4][CH2:5][N:6]([C:9]2[CH:14]=[CH:13][C:12]([NH2:15])=[CH:11][C:10]=2[F:18])[CH2:7][CH2:8]1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 29478391-Ethyl-4-(2-fluoro-4-nitrophenyl)piperazine

생성물 1

HCID 107515754-(4-Ethylpiperazin-1-yl)-3-fluoroaniline

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

A suspension of 1-ethyl-4-(2-fluoro-4-nitro-phenyl)-piperazine (1.24 g, 15.1 mmol) and Raney Nickel (13 mg) in MeOH (6 mL) is stirred for 17 h at RT, under a hydrogen atmosphere. The reaction mixture is filtered through a pad of celite and concentrated to afford the title compound as a purple oil: ESI-MS: 224.1 [MH]+; tR=0.90 min (system 1).

후처리

  1. filtrationThe reaction mixture is filtered through a pad of celite
  2. concentrationconcentrated

출처 및 근거

ORD 기록
ord-459a7d94ba0545fcabd92cb3711d8fc0
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08293746B2

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