HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 22914455, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 22914329 | HCID 22914329 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22914455 | HCID 22914455 | 88.2% |
Reaction Steps
1.85 ml (13.4 mmol) of trifluoroacetic anhydride were added dropwise at <8° to a suspension of 3.72 g (12.8 mmol) of 8-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxamide in 17 ml of dioxan and 2 ml of pyridine. The beige solution obtained was stirred at 50°-60° for 4 hrs., cooled and treated with 80 ml of water. The white crystals were filtered off under suction and dried in a high vacuum. There were obtained 3.08 g (88%) of 8-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carbonitrile as colourless crystals of m.p. 272°-275°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665718 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-382ac4047bbb46fd970c817d59832ee8 |
| Source note | uspto-grants-1997_09 |