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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426763Generated: November 3, 2026

Sodium hydride → HCID 67395405, compound

https://huagongshe.com/reaction/1426763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
Reactant1-Pyrrolidinesulfonyl chlorideHCID 6483902—
Reactanttert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamateHCID 67176761—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductHCID 67395405HCID 6739540592.1%

Reaction Steps

To a solution of tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate (200 mg) in tetrahydrofuran (20 mL) was added sodium hydride (60% in oil, 75 mg) at room temperature, and the mixture was stirred for 15 min. 15-Crown-5 (410 mg) was added, pyrrolidine-1-sulfonyl chloride (210 mg) was added and the mixture was further stirred for 6 hr. The reaction mixture was diluted with saturated aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The extract 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=4:1→1:1) to give the title compound as a colorless oil (yield 260 mg, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-8046045b24cc401d961dc6e4a68c8525
Source noteuspto-grants-2015_01