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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972223Generated: October 31, 2026

Methanesulfonyl chloride → HCID 59485956, compound

https://huagongshe.com/reaction/1972223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 59485645HCID 59485645—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59485956HCID 5948595685.2%

Reaction Steps

To a solution of 3-(4-(4-chlorophenoxy)phenyl)-1-(2-hydroxyethyl)-4-(3-(trifluoromethyl)phenyl)imidazolidin-2-one (340 mg, 0.713 mmol) in DCM (3.5 mL) at 0° C. are added MsCl (111 μL, 1.43 mmol) and TEA (199 μL, 1.43 mmol). The reaction mixture is stirred at room temperature overnight before removal of the solvent. The residue is taken in H2O (40 mL) and extracted with EtOAc (3×20 mL). The combined organic layer is washed with brine, dried over MgSO4, concentrated, and purified by silica gel chromatography (20˜70% EtOAc/hexanes) to provide the title compound (337 mg, 85% yield) as a colorless oil-like product; HPLC-MS calculated for C25H22ClF3N2O5S (M+H+) 555.1, found 555.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431607B2
Source datasetuspto-grants-2013_04
ORD IDord-8a19788079314730b0fcc7e132038644
Source noteuspto-grants-2013_04