HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088799Generated: November 1, 2026
Hydroxyamine hydrochloride → HCID 73867443, compound
https://huagongshe.com/reaction/1088799
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 5,6-Dihydro-1H,3H,7H-[1,3]oxazino[5,4,3-ij]quinoline-3,7-dione | HCID 14685727 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 73867443 | HCID 73867443 | — |
Reaction Steps
6,7-Dihydro-3,7-dioxo-1H,3H,5H-pyrido[3,2,1-ij][3,1]benzoxazine (5 g), hydroxylamine hydrochloride (2.1 g) and sodium acetate (7.5 g) were dissolved in a mixed solvent of ethanol-water (5:1) (90 ml) and the mixture was refluxed for 2 hours. After completion of the reaction, the solvent was distilled off and the resulting residue was poured into water. Crystals which precipitated were collected by filtration and dried to give 6,7-dihydro-3-oxo-7-hydroxyimino-1H,3H,5H-pyrido[3,2,1-ij][3,1]benzoxazine. The compound was dissolved in acetic acid (150 ml) and platinum oxide (250 mg) was added thereto. The mixture was subjected to catalytic reduction at 50° C. and 4 atmospheres. After completion of the catalytic reduction, catalyst was filtered off and the filtrate was concentrated to give 6,7-dihydro-3-oxo-7-amino-1H,3H,5H-pyrido [3,2,1-ij][3,1]benzoxazine (5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04963566 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-473411a1fc2f4cb3b8044329dc83bde5 |
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| Source note | uspto-grants-1990_10 |
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