HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377989Generated: October 31, 2026
Ammonia → (S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamide
https://huagongshe.com/reaction/1377989
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | (S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]-imidazo[1,5-a][1,4]benzodiazepine-1-carboxylic acid | HCID 22821781 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamide | HCID 53756795 | 78.9% |
Reaction Steps
40 g (124 mmol) of (S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxylic acid were suspended in 190 ml of N,N-dimethylformamide and treated portionwise at room temperature with 21 g (129.5 mmol) of 1,1'-carbonyldiimidazole. After completion of the CO2 evolution the clear brown solution was stirred at 50° for 30 min., cooled and treated dropwise with 30 ml of conc. ammonia at a temperature below 25° within about 10 min. After stirring for 30 minutes the suspension obtained was poured into 700 ml of ice-water, stirred at room temperature for 30 min. and filtered, whereupon the crystals were rinsed with a small amount of water. After drying there were obtained 31.36 g (78%) of (S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamide of m.p. 296°-298°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665718 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-1edb640ebbcf41a1ac5d6f55feebc76d |
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| Source note | uspto-grants-1997_09 |
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