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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426732Generated: November 1, 2026

Sodium hydride → HCID 67397601, compound

https://huagongshe.com/reaction/1426732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
ReactantFuran-2-sulfonyl ChlorideHCID 2795072—
Reactanttert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamateHCID 67176761—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67397601HCID 6739760187%

Reaction Steps

To a suspension of sodium hydride (60% in oil, 37 mg) in tetrahydrofuran (2 mL) were added dropwise a solution of tert-butyl {[5-(2-fluoropyridin-3-yl)-4-fluoro-1H-pyrrol-3-yl]methyl}methylcarbamate (200 mg) in tetrahydrofuran (1 mL), 15-crown-5 (205 mg) and 2-furansulfonyl chloride (132 mg) under ice-cooling and the mixture was stirred for 1 hr and half. 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 basic silica gel column chromatography (eluent: hexane-ethyl acetate=6:1→2:1) to give the title compound as a pale-yellow oil (yield 243 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-9d5c686ccf78482699b3fd88d08ef5cf
Source noteuspto-grants-2015_01