Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272074Generated: October 31, 2026

Methanesulfonyl chloride → HCID 12149978, compound

https://huagongshe.com/reaction/272074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 12149979HCID 12149979—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 12149978HCID 12149978—

Reaction Steps

To a solution of 30 mg of (2R)-N-{((3R)-1-cyclohexylmehyl-3-piperidyl)methyl}-1-{(2S,4R)-4-hydroxy-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonylpyrrolidine-2-carboxamide in 0.6 ml of chloroform, 0.018 ml of triethylamine and 0.004 ml of methanesulfonyl chloride were added under cooling with ice, followed by 50 minutes' stirring at room temperature. The reaction liquid was diluted with chloroform, washed with saturated aqueous sodium bicarbonate solution and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the resultant residue was purified by means of a preparative thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (Merck), chloroform/methanol/28% aqueous ammonia=100/10/1) to provide 33 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452908B2
Source datasetuspto-grants-2008_11
ORD IDord-a70f3ec82faa426ab73d3301d36d43c2
Source noteuspto-grants-2008_11