HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sarmazenil | HCID 71231 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid | HCID 14590421 | — |
Reaction Steps
A mixture of 3.11 g (9.72 mmol) of ethyl 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate, 10 ml of ethanol, 2 ml of water and 400 mg of sodium hydroxide is heated to boiling under reflux for 1 hour. After evaporation of the ethanol, the residue is treated with 10 ml of 1 N hydrochloric acid. The colourless material obtained is filtered off under suction, washed with water and dried. There is obtained 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid with a decomposition point of 283°-284°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04352818 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-04d660b749e44f96b13eb7d1e2871a9f |
| Source note | uspto-grants-1982_10 |