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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197166Generated: October 29, 2026

2-Chloro-5-pyridinesulfonyl chloride → HCID 86630978, compound

https://huagongshe.com/reaction/2197166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—
Reactant5-(2-Fluorophenyl)-1H-pyrrole-3-carboxaldehydeHCID 46908593—
ProductHCID 86630978HCID 86630978—

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 numberUS08338462B2
Source datasetuspto-grants-2012_12
ORD IDord-6b56f3d2e0194527a773ef10114f4d9b
Source noteuspto-grants-2012_12