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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641756Generated: November 2, 2026

Water → HCID 57736462, compound

https://huagongshe.com/reaction/1641756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 57736499HCID 57736499—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 57736462HCID 5773646252.5%

Reaction Steps

To a solution of 5-[hydroxy(2,3,6-trifluorophenyl)methyl]-4-methylpyridine-2-carboxamide (7.11 g, 24.0 mmol) in N,N-dimethylformamide (150 ml), methanesulfonyl chloride (3.72 ml, 48.0 mmol) and then triethylamine (13.4 ml, 96.0 mmol) were added in a nitrogen atmosphere at 0° C., and the mixture was stirred for 2 hours at room temperature. Water and ethyl acetate were added to the reaction mixture at 0° C., the organic layer was separated, and the organic layer was washed sequentially with 1 N hydrochloric acid, saturated aqueous sodium hydrogencarbonate and saturated brine. The organic layer was dried over anhydrous sodium sulfate and filtered, and then the filtrate was concentrated under reduced pressure. The resulting residue was subjected to flash silica gel chromatography, and the fraction obtained from an elution with dichloromethane:methanol=49:1 was concentrated under reduced pressure, to obtain the title compound (4.71 g, 12.6 mmol, 52%) as a pale brown foamy substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114886B2
Source datasetuspto-grants-2012_02
ORD IDord-f999a02a5024450db723aa39944c4791
Source noteuspto-grants-2012_02