HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369007Generated: October 30, 2026
Hydroxyamine hydrochloride → HCID 136391022, compound
https://huagongshe.com/reaction/2369007
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 66584720 | HCID 66584720 | — |
| Solvent | Pyridine ethanol | HCID 21975839 | — |
| Product | HCID 136391022 | HCID 136391022 | 109.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08703784B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-d56d1f2abcde42c1a505916187a36f46 |
|---|
| Source note | uspto-grants-2014_04 |
|---|