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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182566Generated: November 3, 2026

Piperidine → HCID 17854627, compound

https://huagongshe.com/reaction/1182566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 17854639HCID 17854639—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
ProductHCID 17854627HCID 17854627—

Reaction Conditions

Temperature0 °C

Reaction Steps

44.0 mg (0.107 mmol) of 4-(3-chlorophenyl)-6-methyl-2-(methylthio)-N-(3-phenylpropyl)-5-pyrimidinecarboxamide was dissolved in 5 ml of dichloromethane. 36.9 mg (0.213 mmol) of mCPBA (m-chloroperbenzoic acid) was added thereto at 0° C. and stirred at the same temperature for 6 hours. 1 ml of saturated aqueous sodium bisulfite solution was added thereto at the same temperature and stirred for 30 minutes heating to room temperature. After the reaction mixture was diluted with dichloromethane, the organic layer was washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The obtained residue was dissolved in 5 ml of toluene and 91.1 mg (1.07 mmol) of piperidine was added at room temperature and stirred at 80° C. for 6 hours. After concentration under reduced pressure, the obtained residue was diluted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by the silica gel chromatography (hexane/ethyl acetate=10/1 to 1/1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288544B2
Source datasetuspto-grants-2007_10
ORD IDord-a9e37178a6d740b3a874f1beead309dc
Source noteuspto-grants-2007_10