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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835360Generated: October 30, 2026

Dichloromethane → HCID 23502786, compound

https://huagongshe.com/reaction/1835360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-MethylimidazoleHCID 12749—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10299574HCID 10299574—
SolventDimethylformamideHCID 6228—
ProductHCID 23502786HCID 2350278646%

Reaction Steps

To a solution of 100 mg (0.207 mmol) N-(3,5-bis-trifluoromethyl-benzyl)-6-hydroxymethyl-N-methyl-4-o-tolyl-nicotinamide (Example 7) in 1 ml dichloromethane 0.03 ml (0.4 mmol) thionyl chloride were added at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 1 h. The solvent was evaporated and the light yellow residue was dried in high vacuo. The residue was dissolved in 1 ml dry N,N-dimethylformamide and added to a suspension of 2-methylimidazole sodium salt that had previously been prepared by addition of 54 mg (1.2 mmol) sodium hydride (55% dispersion in mineral oil) to a solution of 52 mg (0.62 mmol) 2-methylimidazole in 3 ml dry N,N-dimethylformamide under argon at room temperature. After stirring for 3 h the reaction was quenched by addition of excess water, followed by extraction with three portions of ethyl acetate. The combined organic extracts were dried with sodium sulfate and concentrated. Column chromatography afforded 52 mg (46%) of the title compound as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770637B2
Source datasetuspto-grants-2004_08
ORD IDord-65c9b0145ec440d6b72227a5bff97800
Source noteuspto-grants-2004_08