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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426771Generated: November 2, 2026

Sodium hydride → HCID 67396571, compound

https://huagongshe.com/reaction/1426771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant15-Crown-5HCID 36336—
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantHCID 67397275HCID 67397275—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67396571HCID 6739657187%

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-chlorobenzenesulfonyl chloride (214 mg) were added dropwise and the mixture was further stirred at room temperature for 1 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→2:1) to give the title compound as a pale-yellow oil (yield 211 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-1eeaf90a1a624f1ca9011cd4ab8ee374
Source noteuspto-grants-2015_01