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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641759Generated: November 1, 2026

Formaldehyde → HCID 57736529, compound

https://huagongshe.com/reaction/1641759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 57736408HCID 57736408—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 57736529HCID 5773652932%

Reaction Steps

To a solution of 4-methyl-5-[[[4-(trifluoromethoxy)phenyl]sulfonyl](2,3,6-trifluorophenyl) methyl]pyridine-2-carboxamide (177 mg, 0.350 mmol) in ethylene glycol dimethyl ether (3 ml), an aqueous solution of formaldehyde (37%, 78.9 μl) and 1 N aqueous sodium hydroxide (17.5 μl) were added at room temperature, and the mixture was stirred for 2 days. Ethyl acetate was added to the reaction mixture, and the mixture was washed with saturated aqueous ammonium chloride. Subsequently, 1 N hydrochloric acid was added to the organic layer, and the mixture was stirred for 1 hour. After the organic layer was separated, the organic layer was washed with saturated brine, 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 hexane:ethyl acetate=1:1 was concentrated under reduced pressure. The resulting residue was washed with a mixed solvent of ethyl acetate and diethyl ether, and then was collected by filtration, to obtain the title compound (59.4 mg, 0.111 mmol, 32%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114886B2
Source datasetuspto-grants-2012_02
ORD IDord-71d9af9b6ac3425589e5c1516e278be0
Source noteuspto-grants-2012_02