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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426768Generated: November 1, 2026

Sodium hydride → HCID 67396943, compound

https://huagongshe.com/reaction/1426768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant15-Crown-5HCID 36336—
Reactant2,6-Difluorobenzenesulfonyl chlorideHCID 2734271—
ReactantHCID 67397275HCID 67397275—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67396943HCID 6739694387.3%

Reaction Steps

To a suspension of sodium hydride (60% in oil, 26.0 mg) in tetrahydrofuran (3 mL) was added tert-butyl {[5-(2-cyanopyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate (156 mg) at room temperature, and the mixture was stirred for 15 min. After stirring, 15-crown-5 (143 mg) and 2,6-difluorobenzenesulfonyl chloride (159 mg) were added dropwise and the mixture was further stirred at room temperature for 2 hr. Saturated aqueous ammonium chloride solution was added, and the mixture was concentrated under reduced pressure. The residue was 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=9:1→3:2) to give the title compound as a colorless oil (yield 213 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-3270a290f9664ef5bbed04446701e1fb
Source noteuspto-grants-2015_01