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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329749Generated: October 25, 2026

Azasetron → HCID 131716241, compound

https://huagongshe.com/reaction/329749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzasetronHCID 2264—
Reactantm-Chloroperbenzoic acidHCID 70297—
SolventChloroformHCID 6212—
ProductHCID 131716241HCID 131716241—

Reaction Steps

To a solution of 5.0 g of 6-chloro-3,4-dihyro-4-methyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide in 100 ml of chloroform with cooling at -30° C. is added 4.02 g of 80% metachloroperbenzoic acid, and the system stirred at -20° C. to -25° C. for about 30 minutes. The resultant solution is stirred at room temperature for 20 minutes and ammonia gas is bubbled into the solution at 10°-18° C. The precipitated crystals are filtered off and the filtrate is concentrated under reduced pressure. The residue is purified with column chromatography with a mixed eluent of chloroform and methanol (10:1) and to the residue is added acetonictile. The crystals are collected by filtration and recrystallized form acetonitrile to give 6-chloro-3,4-dihydro-4-methyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide N-oxide hemihydrate, melting at 198°-200° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892872
Source datasetuspto-grants-1990_01
ORD IDord-70babcd0159a493cbcafe0acc272effd
Source noteuspto-grants-1990_01