HCID 66592460, compound → 1-(1-Fluoro-2-methylpropan-2-yl)piperazine
Reaction equation
C(OC([N:11]1[CH2:16][CH2:15][N:14]([C:17]([CH3:21])([CH3:20])[CH2:18][F:19])[CH2:13][CH2:12]1)=O)C1C=CC=CC=1>C(O)C.[OH-].[OH-].[Pd+2]>[CH3:21][C:17]([N:14]1[CH2:13][CH2:12][NH:11][CH2:16][CH2:15]1)([CH3:20])[CH2:18][F:19]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
4-(1,1-Dimethyl-2-fluoroethyl)piperazine-1-carboxylic acid benzyl ester (270 mg, 0.92 mmol) was dissolved in ethanol (20 mL), and 10% palladium hydroxide/carbon (100 mg) was added thereto. The mixture was stirred for two days at room temperature under a hydrogen stream at normal pressure. The catalyst was separated by filtration, and then the reaction liquor was concentrated under reduced pressure, and dried to obtain the title compound (97 mg, 66%) as an oily matter. This compound was used in the subsequent reaction without performing further purification.
Workup
- customThe catalyst was separated by filtration
- concentrationthe reaction liquor was concentrated under reduced pressure
- customdried
Sources & evidence
- ORD record
- ord-2535447a3f624fa795eb2d5d2bff3578
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08129366B2
Reaction notes
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