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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426713Generated: October 28, 2026

Sodium hydride → HCID 67396710, compound

https://huagongshe.com/reaction/1426713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
Reactant3-Cyanobenzene-1-sulfonyl chlorideHCID 2801360—
Reactanttert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamateHCID 67176761—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67396710HCID 6739671091.4%

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 {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate (323 mg) in tetrahydrofuran, 15-crown-5 (330 mg) and 3-cyanobenzenesulfonyl chloride (302 mg) under ice-cooling and the mixture was stirred for 17 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 446 mg, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-4eb081d187ba47a38965099fec368d9f
Source noteuspto-grants-2015_01