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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426720Generated: November 2, 2026

Methanesulfonyl chloride → HCID 67396174, compound

https://huagongshe.com/reaction/1426720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67399475HCID 67399475—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67396174HCID 6739617455%

Reaction Steps

To a solution of tert-butyl [(4-fluoro-5-(2-fluoropyridin-3-yl)-1-{[3-(hydroxymethyl)phenyl]sulfonyl}-1H-pyrrol-3-yl)methyl]methylcarbamate (683 mg) in tetrahydrofuran (5 mL) were added methanesulfonyl chloride (174 mg) and diisopropylethylamine (215 mg) under ice-cooling, and the mixture was stirred at room temperature for 60 hr. The solvent was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→3:1) to give the title compound as a pale-yellow oil (yield 386 mg, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-cd15dc2eda5c4f16b25d019398dfe8fa
Source noteuspto-grants-2015_01