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1-Methyl-4-(1-(4-nitrophenyl)piperidin-4-yl)piperazine → 4-(4-(4-Methyl-1-piperazinyl)-1-piperidinyl)benzenamine

HRID 2189267
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인쇄 미리보기

반응식

HRID 2189267 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH:8]2[CH2:13][CH2:12][N:11]([C:14]3[CH:19]=[CH:18][C:17]([N+:20]([O-])=O)=[CH:16][CH:15]=3)[CH2:10][CH2:9]2)[CH2:4][CH2:3]1>CO.[Pd]>[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH:8]2[CH2:13][CH2:12][N:11]([C:14]3[CH:19]=[CH:18][C:17]([NH2:20])=[CH:16][CH:15]=3)[CH2:10][CH2:9]2)[CH2:4][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 580159221-Methyl-4-(1-(4-nitrophenyl)piperidin-4-yl)piperazine

생성물 1

HCID 580157484-(4-(4-Methyl-1-piperazinyl)-1-piperidinyl)benzenamine수율 102%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A suspension of 1-Methyl-4-[1-(4-nitro-phenyl)-piperidin-4-yl]-piperazine-(46 mg, 0.15 mmol) and Pd/C (10%, 8 mg) in MeOH (2 mL) is stirred at room temperature under H2 (balloon pressure) for 16 hours, then filtered through celite, washed with EtOAc, concentrated under reduced pressure to give 42 mg of the title compound as a light grey solid.

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후처리

  1. filtrationfiltered through celite
  2. washwashed with EtOAc
  3. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-cfbce55ba50f463fbfe303b9c609dbb8
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08324225B2

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