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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428756Generated: November 1, 2026

Methanesulfonyl chloride → HCID 71539430, compound

https://huagongshe.com/reaction/1428756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86680221HCID 86680221—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 71539430HCID 7153943022%

Reaction Steps

To a stirred solution of 2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (151 mg, 0.33 mmol) in pyridine, cooled to 0° C., were added methanesulfonyl chloride (151 mg). The resulting reaction mixture was stirred for 15 h at room temperature. The mixture dissolved in dichloromethane and washed with 1N HCl. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 2-(3-Methoxy-4-(methylsulfonamidomethyl)phenyl)-N-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (example 78) (38 mg) was obtained as 22% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-a2808897121243f380b80daf755a2551
Source noteuspto-grants-2015_01