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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428808Generated: October 31, 2026

Methanesulfonyl chloride → HCID 71539337, compound

https://huagongshe.com/reaction/1428808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86680236HCID 86680236—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 71539337HCID 7153933761%

Reaction Steps

To a stirred solution of 2-(4-(aminomethyl)-3-methylphenyl)-N-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (83 mg, 0.19 mmol) in pyridine was added methanesulfonyl chloride (0.02 mL, 0.24 mmol) The reaction mixture was stirred for overnight at room temperature. The mixture was diluted with ethylacetate and washed with 1N HCl and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 2-(3-Methyl-4-(methylsulfonamidomethyl)phenyl)-N-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (example 97) (60 mg) was obtained as 61% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-03af2068d7c1431bbb52e82614de36f7
Source noteuspto-grants-2015_01