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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641742Generated: November 2, 2026

Formaldehyde → HCID 11999692, compound

https://huagongshe.com/reaction/1641742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
Reactant5-[[(4-Fluorophenyl)sulfonyl](2,3,6-trifluorophenyl)methyl]-4-methylpyridine-2-carboxamideHCID 57736541—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 11999692HCID 11999692106%

Reaction Steps

To a solution of 5-[[(4-fluorophenyl)sulfonyl](2,3,6-trifluorophenyl)methyl]-4-methylpyridine-2-carboxamide (150 mg, 0.34 mmol) obtained in Example 39 in ethylene glycol dimethyl ether (3 ml), an aqueous solution of formaldehyde (37%, 0.1 ml) and 5% aqueous sodium hydroxide (0.4 ml) were added at 0° C., and the mixture was stirred overnight at room temperature. Sodium carbonate (20 mg) was added to the reaction mixture, and the mixture was stirred for 20 minutes at room temperature. The mixture was concentrated under reduced pressure, and then the residue was dissolved in chloroform, dried over magnesium sulfate, and filtered. Subsequently, the filtrate was concentrated under reduced pressure, and the resulting residue was subjected to silica gel chromatography. The fraction obtained from an elution with hexane:ethyl acetate=1:1 was concentrated under reduced pressure, and the resulting residue was washed with diethyl ether, and then was collected by filtration, to obtain the title compound (93 mg, 0.20 mmol, 58%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114886B2
Source datasetuspto-grants-2012_02
ORD IDord-8696e9e7f0254063a8374ec59bc97381
Source noteuspto-grants-2012_02