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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329752Generated: October 28, 2026

m-Chloroperbenzoic acid → HCID 86743681, compound

https://huagongshe.com/reaction/329752

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 14719846HCID 14719846—
SolventChloroformHCID 6212—
ProductHCID 86743681HCID 86743681—

Reaction Steps

To a solution of 2.7 g of N-(1-benzyl-4-piperidyl)-6-chloro-3,4-dihydro-2,4-dimethyl-3-oxo-2H-1,4-benzoxazine-8-carboxamide in 150 ml of chloroform is added portionwise 2.7 g of metachloroperbenzoic acid under cooling and stirring. After 0.5 hour, ammonia gas is bubbled through the reaction solution under stirring and the precipitate is filtered off. The mother liquor is distilled off under reduced pressure followed by recrystallizing the residue from ethanolisopropyl ether to give N-(1-benzyl-4-piperidyl)-6-chloro-3,4-dihydro-2,4-dimethyl-3-oxo-2H-1,4-benzoxazine-8-carboxamide N-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892872
Source datasetuspto-grants-1990_01
ORD IDord-9f1aedced7b748c081ee67a620496c9f
Source noteuspto-grants-1990_01