HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 54435252, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 53829958 | HCID 53829958 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54435252 | HCID 54435252 | 52.8% |
Reaction Steps
7.5 g (22.3 mmol) of (S)-8-trifluoromethyl-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamide were suspended in 40 ml of dioxan and 4 ml of pyridine and treated dropwise with 3.6 ml of trifluoroacetic anhydride at 7 to 10° within 10 min. The mixture was stirred at room temperature for 3/4 hour and poured into 300 ml of water. The suspension obtained was filtered and, after drying the residue, there were obtained 3.75 g (52%) of (S)-8-trifluoromethyl-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carbonitrile of m.p. 115°-119°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665718 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-e0b0a88001c64d5dbfbcd5d9f53506ee |
| Source note | uspto-grants-1997_09 |