HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20523293, compound → HCID 10013995, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20523293 | HCID 20523293 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10013995 | HCID 10013995 | — |
Reaction Steps
34 g (93.8 mmol) of benzyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carbamate are hydrogenated at room temperature and normal pressure in 300 ml of methanol in the presence of 4 g of 10 percent palladium/carbon. After removal of the catalyst and evaporation, the residue is recrystallized from ethyl acetate and hexane. There is obtained 3-amino-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 202°-204°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04352818 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-86bc812b8563416a81d53d9468f66fbf |
| Source note | uspto-grants-1982_10 |