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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345042Generated: October 25, 2026

Methanesulfonyl chloride → N-(2-Methylquinolin-6-yl)methanesulfonamide

https://huagongshe.com/reaction/345042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Methylquinolin-6-amineHCID 103148—
SolventPyridineHCID 1049—
ProductN-(2-Methylquinolin-6-yl)methanesulfonamideHCID 19813426—

Reaction Steps

Methanesulphonyl chloride (6.2 ml) was added dropwise to a stirred solution of 6-amino-2-methylquinoline (12.5 g) in pyridine (100 ml) cooled to 5°. Stirring was continued for 17 hours at room temperature. The pyridine was then removed by evaporation in vacuo, the residue diluted with aqueous sodium bicarbonate, and extracted three times with methylene chloride. The combined organic extracts were combined, dried (MgSO4) and evaporated in vacuo to give the title compound, yield 13.0 g, m.p. 151°-153°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055473
Source datasetuspto-grants-1991_10
ORD IDord-791cb89a953e43a6977715154fc64535
Source noteuspto-grants-1991_10