Benzyl 4-(cyclopropylcarbonyl)piperazine-1-carboxylate → 1-(Cyclopropylcarbonyl)piperazine
Reaction equation
[CH:1]1([C:4]([N:6]2[CH2:11][CH2:10][N:9](C(OCC3C=CC=CC=3)=O)[CH2:8][CH2:7]2)=[O:5])[CH2:3][CH2:2]1>C(O)C.[C].[Pd]>[CH:1]1([C:4]([N:6]2[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]2)=[O:5])[CH2:2][CH2:3]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
In 100 mL of ethanol was dissolved benzyl 4-(cyclopropylcarbonyl)piperazine-1-carboxylate (3.00 g, 10.4 mmol), and 1.5 g of 10% palladium-carbon was added thereto, followed by stirring at room temperature under hydrogen atmosphere overnight. The palladium-carbon was removed by filtration, and the filtrate was evaporated to give the title compound (1.50 g, 97.3%) as a colorless oil.
Workup
- additionwas added
- customThe palladium-carbon was removed by filtration
- customthe filtrate was evaporated
Sources & evidence
- ORD record
- ord-82ab1b217edd4a61af11c48f6b174f2c
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07619100B2
Reaction notes
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