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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370728Generated: October 31, 2026

Hydroxyamine hydrochloride → 5-[4-[4-(4-Fluorophenyl)piperazin-1-yl]butyl]4-hydroxyimino-2-methyl-2,3,4,5-tetrahydropyrrolo[2,3-e][1,2]thiazine 1,1-dioxide

https://huagongshe.com/reaction/1370728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant5-[4-[4-(4-Fluorophenyl)piperazin-1-yl]butyl]-2-methyl-2,3,4,5-tetrahydropyrrolo[2,3-e][1,2]thiazin-4-one 1,1-dioxideHCID 9910796—
SolventPyridineHCID 1049—
Product5-[4-[4-(4-Fluorophenyl)piperazin-1-yl]butyl]4-hydroxyimino-2-methyl-2,3,4,5-tetrahydropyrrolo[2,3-e][1,2]thiazine 1,1-dioxideHCID 7261199988.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 174 mg (0.4 mmol) of Compound 23 and 111 mg (1.6 mmol) of hydroxylamine hydrochloride in 10 ml of pyridine was stirred for 24 hours over an oil bath of 80° C. Post-treatment and purification were conducted in a similar manner as in Example 21, whereby 159 mg of the title compound were obtained (yield: 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583296B2
Source datasetuspto-grants-2003_06
ORD IDord-1403673365d545a7abec767db7c4bd6c
Source noteuspto-grants-2003_06