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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542628Generated: October 31, 2026

Hydrazine hydrate (1:1) → HCID 70393503, compound

https://huagongshe.com/reaction/542628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 13341543HCID 13341543—
SolventEthanolHCID 702—
ProductHCID 70393503HCID 7039350393%

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 hour 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04658024
Source datasetuspto-grants-1987_04
ORD IDord-470ea7ef6a1d4b3c8462c87c3cbadd3e
Source noteuspto-grants-1987_04