HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981127Generated: October 28, 2026
Hydrazine hydrate (1:1) → HCID 70393503, compound
https://huagongshe.com/reaction/1981127
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 13341543 | HCID 13341543 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70393503 | HCID 70393503 | 93% |
Reaction Steps
2.48 g of tert.butyl 2,3,6,7,8,9-hexahydro-5,9-dioxo-8(S)-phthalimido-1H,5H-pyrazolo[1,2-a][1,2]diazepine-1(S)-carboxylate [prepared as described in Example 3(D)] were stirred at room temperature for 0.5 hours in 80 ml of ethanol with 0.3 g of hydrazine hydrate and the mixture was then evaporated. 90 ml of 2N acetic acid were added, the mixture was stirred at room temperature for 1 hour and was then filtered. The filtrate was made basic with solid sodium carbonate and then extracted twice with dichloromethane. The combined dichloromethane extracts were dried over magnesium sulphate and evaporated to give 1.58 g (93%) of tert.butyl 8(S)-amino-2,3,6,7,8,9-hexahydro-5,9-dioxo-1H,5H-pyrazolo[1,2-a][1,2]diazepine-1(S)-carboxylate in the form of a gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04512924 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-1349cb812f974b42a4fc054324676165 |
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| Source note | uspto-grants-1985_04 |
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