Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613630Generated: October 29, 2026

Hydroxyamine hydrochloride → HCID 18321776, compound

https://huagongshe.com/reaction/613630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
ReactantHCID 18321810HCID 18321810—
SolventEthanolHCID 702—
ProductHCID 18321776HCID 18321776—
ProductHCID 86755000HCID 86755000—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-[2,4-dichloro-3-[2-methyl-4-(pyrazol-1-yl)quinolin-8-yloxymethyl]phenyl]-2-formylpyrrole (80 mg), hydroxylamine hydrochloride (18 mg), sodium acetate (21 mg) and ethanol (60° solution in water, 1.5 ml) was stirred at 60° C. for 1 hour. After cooling to ambient temperature, the reaction mixture was concentrated in vacuo. The residue was dissolved in ethyl acetate, washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by preparative thin-layer chromatography (n-hexane:ethyl acetate=1:1, V/V) to give 1-[2,4-dichloro-3-[2-methyl-4-(pyrazol-1-yl)quinolin-8-yloxymethyl]phenyl]-2-((E)-hydroxyiminomethyl)pyrrole (45 mg) as an amorphous powder and 1-[2,4-dichloro-3-[2-methyl-4-(pyrazol-1-yl)quinolin-8-yloxymethyl]phenyl]-2-((Z) -hydroxyiminomethyl)pyrrole (14 mg) as an amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008229
Source datasetuspto-grants-1999_12
ORD IDord-2d3b0b48dba247b2805cd8bc909443c4
Source noteuspto-grants-1999_12