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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67385Generated: October 23, 2026

Sodium Carbonate Decahydrate → (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde-1-oxime

https://huagongshe.com/en/reaction/67385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium Carbonate DecahydrateHCID 151402—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant(S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehydeHCID 22822210—
SolventWaterHCID 962—
Product(S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde-1-oximeHCID 86738267—

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of 2.67 g (10 mmol) of (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde and 0.85 g (12.5 mmol) of hydroxylamine hydrochloride in 60 ml of water is treated dropwise at room temperature with a solution of 3.57 g (12.5 mmol) of sodium carbonate decahydrate in 10 ml of water. The mixture is stirred at 70° C. for 4 hours. After cooling, the separated material is filtered off under suction, washed with water and recrystallised directly from 50 ml of dimethylformamide. There is obtained (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde-1-oxime of melting point 285° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04346031
Source datasetuspto-grants-1982_08
ORD IDord-715e61470bf545069a2373ea3ea180a2
Source noteuspto-grants-1982_08