HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570915Generated: October 30, 2026
O-ethylhydroxylamine hydrochloride → HCID 89601426, compound
https://huagongshe.com/reaction/570915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-ethylhydroxylamine hydrochloride | HCID 76850 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 89601756 | HCID 89601756 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 89601426 | HCID 89601426 | — |
Reaction Steps
To a solution of tert-butyl 4-[acetyl(tert-butoxycarbonyl)amino]-6-formyl-3-oxo-5H-1,2,4-triazine-2-carboxylate (192 mg, 0.500 mmol) and sodium acetate (45 mg, 0.55 mmol) in EtOH (1.0 mL) at room temperature was added O-ethylhydroxylamine HCl-salt (54 mg, 0.55 mmol). The mixture was heated to 70° C. and stirred for 2 h. The obtained reaction mixture was filtered hot and the solid residual washed with EtOH. The filtrate was concentrated to give the desired product which was used without further purification. LCMS (Method I) RT 1.94 min. [M+Na]+ 450.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09024019B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-b1c458658af54ea59dbe546f4c61b6b7 |
|---|
| Source note | uspto-grants-2015_05 |
|---|