HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67483Generated: October 25, 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/reaction/67483
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate Decahydrate | HCID 151402 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde | HCID 22822210 | — |
| Solvent | Water | HCID 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-oxime | HCID 86738267 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04346034 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-bf09f41a8c194f0f87399c3ffd64e0e4 |
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| Source note | uspto-grants-1982_08 |
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