HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464863Generated: October 29, 2026
Hydrazine hydrate (1:1) → HCID 13622590, compound
https://huagongshe.com/reaction/464863
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 13622568 | HCID 13622568 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13622590 | HCID 13622590 | 159.7% |
Reaction Steps
A mixture of tert-butyl 3(S)-[1(S)-ethoxycarbonyl-9-phthalimidononyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetate (0.46 g), hydrazine hydrate (0.18 g) and ethanol (10 ml) is allowed to stand overnight at room temperature. The mixture is concentrated under reduced pressure, diluted with water (50 ml) and extracted with ethyl acetate (50 ml×4). Water (50 ml) and sodium bicarbonate (0.5 g) are added to the organic extract, and to the resulting mixture is added dropwise di-tert-butyl dicarbonate (0.24 g) with stirring. After stirring for 30 minutes at room temperature, the ethyl acetate layer is dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue is purified by silica gel column chromatography using hexane-ethyl acetate (2:1) as an eluent to yield tert-butyl 3(S)-[9-tert-butoxycarbonylamino-1(S)-ethoxycarbonylnonyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetate (0.35 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04548932 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-e8283dbb05af4af0904a01e151a9a6fb |
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| Source note | uspto-grants-1985_10 |
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