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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727888Generated: November 4, 2026

Isobutylamine → HCID 17854676, compound

https://huagongshe.com/reaction/1727888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 17854639HCID 17854639—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
ProductHCID 17854676HCID 17854676—

Reaction Conditions

Temperature0 °C

Reaction Steps

83.8 mg (0.203 mmol) of 4-(3-chlorophenyl)-6-methyl-2-(methylthio)-N-(3-phenylpropyl)-5-pyrimidinecarboxamide was dissolved in 5 ml of dichloromethane. 70.2 mg (0.407 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 excessive amounts of 74.2 mg (1.02 mmol) of isobutylamine 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 numberUS07494989B2
Source datasetuspto-grants-2009_02
ORD IDord-48205809ce9048f693d221ca1e5bf6d1
Source noteuspto-grants-2009_02