HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-chloro-8-fluoro-5-methyl-3-(5-piperidin-1-ylmethyl-1,2,4-oxadiazol-3-yl)-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 22914252 | HCID 22914252 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-chloro-8-fluoro-5-methyl-3-(5-piperidin-1-ylmethyl-1,2,4-oxadiazol-3-yl)-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one hydrochloride | HCID 22914251 | 175% |
Reaction Steps
1.37 g (3.18 mmol) of 7-chloro-8-fluoro-5-methyl-3-(5-piperidin-1-ylmethyl-1,2,4-oxadiazol-3-yl)-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one were dissolved in 50 ml of hot ethanol and treated at 40° with 0.95 ml (3.5 mol) of 3.7N ethanolic hydrochloric acid. After stirring at 0° for 30 minutes the solution was concentrated to a volume of ~20 ml and treated with 100 ml of ether. The white suspension obtained was suction filtered. There were obtained 1.30 g (88%) of 7-chloro-8-fluoro-5-methyl-3-(5-piperidin-1-ylmethyl-1,2,4-oxadiazol-3-yl)-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one hydrochloride (1:1) as white crystals; m.p. 240°-243° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665718 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-e7e013bec5f44ba784bb094d080c931d |
| Source note | uspto-grants-1997_09 |