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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047915Generated: November 3, 2026

Sodium hydride → HCID 67177939, compound

https://huagongshe.com/reaction/2047915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
Reactanttert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamateHCID 67176761—
Reactant6-methylpyridine-3-sulfonyl chloride hydrochlorideHCID 75366244—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67177939HCID 6717793983.1%

Reaction Steps

To a suspension of sodium hydride (60% in oil, 31 mg) in tetrahydrofuran (3 mL) were added tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate (100 mg), 15-crown-5 (170 mg), 6-methylpyridine-3-sulfonyl chloride hydrochloride (91 mg) at room temperature, and the mixture was stirred for 1.5 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The separated aqueous layer was extracted again with ethyl acetate. Combined organic layers were 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=17:3→1:1) to give the title compound as a pale-yellow oil (yield 123 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592597B2
Source datasetuspto-grants-2013_11
ORD IDord-9c22a0f650a249c285f8abbc9cdc75ef
Source noteuspto-grants-2013_11