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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012476Generated: October 31, 2026

Sodium hydride → HCID 86630978, compound

https://huagongshe.com/reaction/1012476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
Reactant2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—
Reactant5-(2-Fluorophenyl)-1H-pyrrole-3-carboxaldehydeHCID 46908593—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86630978HCID 8663097866.2%

Reaction Steps

By a similar reaction as in Reference Example 65 and using 5-(2-fluorophenyl)-1H-pyrrole-3-carbaldehyde (893 mg) and 6-chloropyridine-3-sulfonyl chloride (1.30 g), the title compound was obtained as a pale-red solid (yield 1.14 g, 66%). More specifically, 5-(2-fluorophenyl)-1H-pyrrole-3-carbaldehyde (893 mg) was dissolved in tetrahydrofuran (10 mL), sodium hydride (60% in oil, 226 mg) was added and the mixture was stirred at room temperature for 15 min. 15-Crown-5 (1.1 mL) was added and the mixture was further stirred at the same temperature for 15 min. 6-Chloropyridine-3-sulfonyl chloride (1.30 g) was added. The reaction mixture was stirred at room temperature for 15 min. Water was added, and the mixture was extracted with ethyl acetate. The extract was washed with water and 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=19:1→3:2) to give the title compound as a pale-red solid (yield 1.14 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977488B2
Source datasetuspto-grants-2011_07
ORD IDord-4b4af3d8fce24a28a50120592c1b6aae
Source noteuspto-grants-2011_07