HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 54516569, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 54132851 | HCID 54132851 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54516569 | HCID 54516569 | 82.7% |
Reaction Steps
78 g (290 mmol) of (S)-9-oxo-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamide were suspended in 380 ml of dioxan and 68 ml of pyridine and treated dropwise at 0° with 59 ml (424 mmol) of trifluoroacetic anhydride. After stirring at 50° for two hours the reaction mixture was poured into 2 l of ice-water and the crystals were filtered off under suction, rinsed with water and dried. There were obtained 60 g (82%) of (S)-9-oxo-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carbonitrile of m.p. 232°-234°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665718 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-a06ef46278e045c9a245abd74feb9e4f |
| Source note | uspto-grants-1997_09 |