HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 20523282, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20523292 | HCID 20523292 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 20523282 | HCID 20523282 | — |
Reaction Steps
1.30 g (5 mmol) of 3-(chloromethyl)-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one and 200 mg (5 mmol) of sodium hydroxide are hydrogenated at room temperature and normal pressure in 20 ml of alcohol and in the presence of 100 mg of 10 percent palladium/carbon. The catalyst is removed, the solvent is evaporated and the residue is taken up in chloroform. The solution is washed with water, dried over magnesium sulphate and evaporated. There is obtained 4,5-dihydro-3,5-dimethyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 184.5°-185.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04352818 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-662b440fb487489999036b1bfd2082a9 |
| Source note | uspto-grants-1982_10 |