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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641740Generated: November 1, 2026

Dimethylformamide → HCID 57736527, compound

https://huagongshe.com/reaction/1641740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHexaneHCID 8058—
ReactantHCID 57736451HCID 57736451—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 57736527HCID 5773652765.3%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of 2-bromo-5-[(2,5-difluorophenyl)[(3,5-difluorophenyl)thio]methyl]-4-methylpyridine (2.35 g, 5.31 mmol) in toluene (60 ml), a hexane solution of n-butyllithium (1.54 M, 4.14 ml, 6.38 mmol) was added in an argon atmosphere at −78° C. The reaction mixture was stirred for 30 minutes at −40° C., and then cooled again to −78° C., and N,N-dimethylformamide (0.494 ml, 6.38 mmol) was added. After completion of dropwise addition, the reaction mixture was Allowed to warm to 0° C., and water was added at the same temperature. Ethyl acetate was added to the reaction mixture, the organic layer was separated, and then the organic layer was washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate and filtered, then the filtrate was concentrated under reduced pressure, and the obtained residue was subjected to flash silica gel chromatography. The fraction obtained from an elution with hexane:ethyl acetate=10:1 was concentrated under reduced pressure to obtain the title compound (1.36 g, 3.47 mmol, 65%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114886B2
Source datasetuspto-grants-2012_02
ORD IDord-70121520adb44333b1a6af8b43a0e99b
Source noteuspto-grants-2012_02