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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426710Generated: November 3, 2026

Sodium hydride → HCID 67396593, compound

https://huagongshe.com/reaction/1426710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
Reactant3-Fluorobenzenesulfonyl ChlorideHCID 2734258—
ReactantHCID 67397020HCID 67397020—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67396593HCID 6739659391.2%

Reaction Steps

To a suspension of sodium hydride (60% in oil, 60 mg) in tetrahydrofuran (5 mL) were added dropwise a solution (5 mL) of tert-butyl {[5-(2-cyanopyridin-3-yl)-4-fluoro-1H-pyrrol-3-yl]methyl}methylcarbamate (330 mg) in tetrahydrofuran, 15-crown-5 (330 mg) and 3-fluorobenzenesulfonyl chloride (292 mg) under ice-cooling and the mixture was stirred for 3 hr. The reaction mixture was diluted with water, and extracted with ethyl acetate. The separated aqueous layer was extracted again with ethyl acetate. The combined organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=6:1→2:1) to give the title compound as a pale-yellow oil (yield 445 mg, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-3646e1cab39d4d40a1ef27999c6cd191
Source noteuspto-grants-2015_01