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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426664Generated: November 1, 2026

Sodium hydride → 4-fluoro-5-(2-fluoropyridin-3-yl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/1426664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
ReactantPyridine-3-sulfonyl chlorideHCID 3164136—
ReactantHCID 58349833HCID 58349833—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
Product4-fluoro-5-(2-fluoropyridin-3-yl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 8662398149%

Reaction Steps

To a solution of 4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrole-3-carbaldehyde (110 mg) in tetrahydrofuran (11 mL) was added sodium hydride (60% in oil, 43 mg) at room temperature and the mixture was stirred for 5 min. 15-Crown-5 (233 mg) was added dropwise, and the mixture was stirred for 5 min. Pyridine-3-sulfonyl chloride (141 mg) was added, and the mixture was further stirred for 1 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=1:1→1:4) to give the title compound as a colorless oil (yield 90 mg, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-f9282585b2fa40e5a9f6b975b0f97919
Source noteuspto-grants-2015_01