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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345043Generated: October 27, 2026

m-Chloroperbenzoic acid → 6-Methanesulphonamido-2-methylquinoline-1-oxide

https://huagongshe.com/reaction/345043

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN-(2-Methylquinolin-6-yl)methanesulfonamideHCID 19813426—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product6-Methanesulphonamido-2-methylquinoline-1-oxideHCID 19813436—

Reaction Steps

m-Chloroperbenzoic acid ("MCPBA") (5.2 g) was added portionwise to a solution of 6-methanesulphonamido-2-methylquinoline (6 g) in methylene chloride and stirring was continued for 17 hours. The reaction mixture was then diluted with aqueous sodium bicarbonate and the organic layer was separated. The aqueous layer was extracted with methylene chloride. The combined organic layers were washed with aqueous sodium bicarbonate, dried (MgSO4) and evaporated in vacuo to give a solid which was recrystallised from ethanol to give the title compound, yield 1.6 g, m.p. 241°-243°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055473
Source datasetuspto-grants-1991_10
ORD IDord-c02addb57b82406b9d8249336e29e103
Source noteuspto-grants-1991_10