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

HRID 736227
Notes
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Reaction equation

HRID 736227 reaction equation
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
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
60 °C

Procedure

To a solution of 2-(4-Benzyl-piperazin-1-yl)-5-trifluoromethyl-pyrimidine (0.63 g) in methanol was added Palladium-C (Degussa EL101N; 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 of 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+).

Workup

  1. temperatureto cool down to room temperature
  2. filtrationthe catalyst was filtered of and solvent
  3. customwas removed in vacuo

Sources & evidence

ORD record
ord-fbbf7bc8f662401c9aab097c9dcff3a4
Source dataset
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07595314B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes