HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 8-Chloro-6-(2-fluorophenyl)-1-methyl-3-morpholino-4H-imidazo[1,5-a][1,4]benzodiazepine 5-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 178526225 | HCID 178526225 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 8-Chloro-6-(2-fluorophenyl)-1-methyl-3-morpholino-4H-imidazo[1,5-a][1,4]benzodiazepine 5-oxide | HCID 13046988 | — |
Reaction Steps
A mixture of 4.2 g (0.01 mole) of 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-N-hydroxy-α-(4-morpholinyl)-1H-1,4-benzodiazepine-2-methanimine 4-oxide, 50 ml of glacial acetic acid and 4 ml of acetaldehyde was heated to reflux for 5 minutes. The cooled reaction mixture was poured on ice, made alkaline with ammonia and extracted with methylene chloride. The extracts were dried and evaporated and the residue was crystallized from ether/2-propanol to yield yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04259241 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-b513e2526b0442d5ae6d866ccf1a83f4 |
| Source note | uspto-grants-1981_03 |