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2-(4-Benzylpiperazin-1-yl)-5-trifluoromethylpyrimidine → 2-(Piperazin-1-YL)-5-(trifluoromethyl)pyrimidine

HRID 1820731
노트
인쇄 미리보기

반응식

HRID 1820731 반응식
C([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[N:19]=[CH:18][C:17]([C:20]([F:23])([F:22])[F:21])=[CH:16][N:15]=2)[CH2:10][CH2:9]1)C1C=CC=CC=1>CO>[N:11]1([C:14]2[N:15]=[CH:16][C:17]([C:20]([F:22])([F:21])[F:23])=[CH:18][N:19]=2)[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 468388822-(4-Benzylpiperazin-1-yl)-5-trifluoromethylpyrimidine

생성물 1

HCID 163147972-(Piperazin-1-YL)-5-(trifluoromethyl)pyrimidine수율 90.3%

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
60 °C

실험 절차

To a solution of 2-(4-Benzyl-piperazin-1-yl)-5-trifluoromethyl-pyrimidine (0.63 g) in methanol was added Palladium-C (Degussa E101N; 5%), and the reaction mixture was heated at 60° C. under hydrogen atmosphere. The reaction mixture was then allowed to cool down to room temperature, the catalyst was filtered off, and solvent was removed in vacuo to yield the title compound as a colorless solid (0.41 g). MS (m/e): 233.1 (M+H+).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureto cool down to room temperature
  2. filtrationthe catalyst was filtered off
  3. customsolvent was removed in vacuo

출처 및 근거

ORD 기록
ord-95ee7e19a4c544118c72b7160c2fde85
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07605163B2

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