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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369007Generated: October 30, 2026

Hydroxyamine hydrochloride → HCID 136391022, compound

https://huagongshe.com/reaction/2369007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 66584720HCID 66584720—
SolventPyridine ethanolHCID 21975839—
ProductHCID 136391022HCID 136391022109.1%

Reaction Steps

A solution of 1-[7-(bis{[2-(trimethylsilyl)ethoxy]methyl}amino)pyrazolo[1,5-a]pyrimidin-5-yl]ethanone (4.34 g, 9.94 mmol) in 1:1 EtOH/pyridine (50 mL) was treated with hydroxylamine hydrochloride (3.45 g, 49.7 mmol). The resulting mixture was stirred at room temperature for 1.5 h and then concentrated under reduced pressure to remove most solvent. The residue was partitioned between EtOAc (100 mL) and water (60 mL), the layers were separated, and the organic phase was washed with water (60 mL) and brine (20 mL), dried over Na2SO4 and concentrated under reduced pressure to give the title compound, 1-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)ethanone oxime (4.90 g, 85% purity, 93% yield) as an off-white semisolid: MS (ESI+) for C20H37N5O3Si2 m/z 452 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703784B2
Source datasetuspto-grants-2014_04
ORD IDord-d56d1f2abcde42c1a505916187a36f46
Source noteuspto-grants-2014_04