Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426774Generated: November 2, 2026

Sodium hydride → HCID 67396861, compound

https://huagongshe.com/reaction/1426774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant6-Methoxypyridine-3-sulfonyl chlorideHCID 22344709—
ReactantHCID 67397275HCID 67397275—
SolventTetrahydrofuranHCID 8028—
Solvent15-Crown-5HCID 36336—
ProductHCID 67396861HCID 6739686197.3%

Reaction Steps

To a suspension of sodium hydride (60% in oil, 26 mg) in tetrahydrofuran (4 mL) were added dropwise a solution of tert-butyl {[5-(2-cyanopyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate (156 mg) in tetrahydrofuran (2 mL), 15-crown-5 (0.13 mL) and 6-methoxypyridine-3-sulfonyl chloride (135 mg) under ice-cooling, and the mixture was stirred for 30 min. The reaction mixture was diluted with ice 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=9:1→2:3) to give the title compound as a pale-yellow oil (yield 235 mg, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-d95b8556309c4f018f3e63dd5c9b98d3
Source noteuspto-grants-2015_01