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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713813Generated: October 29, 2026

Methanesulfonyl chloride → HCID 59464028, compound

https://huagongshe.com/reaction/1713813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 68684444HCID 68684444—
SolventWaterHCID 962—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
ProductHCID 59464028HCID 59464028—

Reaction Steps

A solution of tert-butyl 4-(5-{[methoxy(oxo)acetyl]amino}pyridin-2-yl)piperazine-1-carboxylate (Intermediate 16, 4 g, 11 mmol) in 4N HCl/dioxan (25 mL) was stood for 16 h then concentrated by evaporation. The residue was dissolved in a mixture of DMF (20 mL) and pyridine (7 mL) then methanesulphonyl chloride (1.28 mL, 16.48 mmol) was added. The mixture was stirred for 3 hours then was diluted with water (50 mL) and extracted with dichloromethane (2×100 mL). The organic extracts were dried and concentrated by evaporation to give the title compound as a solid that was used without further purification; MS m/e MH+ 343.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795283B2
Source datasetuspto-grants-2010_09
ORD IDord-01441601eefc4a7e875bfb9b5d365ef4
Source noteuspto-grants-2010_09