HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 20333033, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 57279629 | HCID 57279629 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20333033 | HCID 20333033 | — |
Reaction Steps
An amount of 3.67 g (0.010 mole) of 6-phenyl-8-chloro-4H-s-triazolo[1,5-a][1,4]-benzodiazepine-2-carboxylic acid ethyl ester is dissolved at 40° in 300 ml of ethanol, and 50 ml of conc. aqueous ammonia solution is then added. The clear solution is allowed to stand for 24 hours at room temperature and thereupon concentrated at 40° in vacuo. The red residue is suspended in 100 ml of water, filtered under suction, and the filter residue subsequently washed with water. The resulting product is recrystallised from methanol and dried at 100°-120° in vacuo to obtain 6-phenyl-8-chloro-4H-s-triazolo[1,5-a][1,4]benzodiazepine-2-carboxamide, M.P. 252°-254°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04111950 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-48252f3521114077b7002e43359bd4dc |
| Source note | uspto-grants-1978_09 |