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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426709Generated: November 1, 2026

Sodium hydride → HCID 67396609, compound

https://huagongshe.com/reaction/1426709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
Reactant3-Methoxybenzenesulfonyl chlorideHCID 2737504—
ReactantHCID 67397020HCID 67397020—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67396609HCID 6739660995.4%

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-methoxybenzenesulfonyl chloride (310 mg) under ice-cooling and the mixture was stirred for 15 min. 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 477 mg, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-71a92e3a3b5e45418fc646f6dd84d168
Source noteuspto-grants-2015_01