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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426675Generated: November 1, 2026

Sodium hydride → HCID 67395875, compound

https://huagongshe.com/reaction/1426675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
ReactantThiophene-3-sulfonyl ChlorideHCID 2776378—
ReactantHCID 67396538HCID 67396538—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67395875HCID 6739587594.2%

Reaction Steps

To a suspension of sodium hydride (97.9 mg, 60% in oil) in tetrahydrofuran (10 mL) were added a solution of tert-butyl {[5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate (311 mg) in tetrahydrofuran (3 mL), 15-crown-5 (449 mg), and thiophene-3-sulfonyl chloride (280 mg) under ice-cooling. The mixture was stirred at room temperature for 30 min, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=6:1→3:1) to give the title compound as a pale-yellow oil (yield 433 mg, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-cfb5c457bd224d2db60e5192d4ebd6dc
Source noteuspto-grants-2015_01