HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 8-Chloro-6-(2-fluorophenyl)-1-methyl-3-morpholino-4H-imidazo[1,5-a][1,4]benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-N-hydroxy-alpha-(4-morpholinyl)-1H-1,4-benzodiazepine-2-methanimine | HCID 53925677 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Chloro-6-(2-fluorophenyl)-1-methyl-3-morpholino-4H-imidazo[1,5-a][1,4]benzodiazepine | HCID 13046989 | — |
Reaction Steps
A mixture of 0.4 g of 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-N-hydroxy-α-(4-morpholinyl)-1H-1,4-benzodiazepine-2-methanimine, 5 ml of glacial acetic acid and 0.4 ml of acetaldehyde was heated to reflux for 5 minutes. The usual workup and chromatography of the crude reaction mixture on 5 g of silica gel using 5% (v/v) of ethanol in methylene chloride gave yellow crystalline product identical with that described above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04244867 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-64a5660871d04c1eb344c169211976d0 |
| Source note | uspto-grants-1981_01 |