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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292030Generated: October 31, 2026

m-Chloroperbenzoic acid → 2-(3-chlorobenzoyloxy)-5-methyl-6-(4-pyridinyl)-2H-1,4-thiazin-3(4H)-one

https://huagongshe.com/reaction/2292030

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2H-1,4-Thiazin-3(4H)-one, 5-methyl-6-(4-pyridinyl)-HCID 3062532—
SolventDichloromethaneHCID 6344—
Product2-(3-chlorobenzoyloxy)-5-methyl-6-(4-pyridinyl)-2H-1,4-thiazin-3(4H)-oneHCID 1393603037.6%

Reaction Steps

m-Chloroperbenzoic acid (8.97 g, 70% purity) was added to a solution of 5-methyl-6-(4-pyridinyl)-2H-1,4-thiazin-3(4H)-one (5.0 g) in dichloromethane (120 ml) under ice/water-cooling and the mixture was stirred for 10 minutes under ice/water-cooling. The mixture was washed with saturated sodium bicarbonate aqueous solution (2 times) and successively with water (1 time) and was dried over magnsium sulfate. The solvent was removed under reduced pressure and the residue was recrystallized from ether-petrolem ether to give the titled compound (3.29 g, yield 37.6%) as pale yellow needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04800201
Source datasetuspto-grants-1989_01
ORD IDord-d72e1f4673334960b9298eb2c670d763
Source noteuspto-grants-1989_01