HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetyl chloride → 4,9-Dihydro-4-phenylacetyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | 4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one | HCID 12521641 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4,9-Dihydro-4-phenylacetyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one | HCID 20392249 | — |
Reaction Steps
A reaction mixture comprising 6.48 g. of 4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one and 25 g. of phenylacetyl chloride in 100 ml. of benzene is refluxed with stirring for 3 hours. The mixture is evaporated to an amber oil, combined with 100 ml. of ethanol and 6 ml. of 5 N sodium hydroxide and allowed to stand at room temperature for one hour. This solution is evaporated to an oily residue which is triturated with water and filtered, giving the desired product as pale pink crystals, mp. 165°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04168269 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-bff9e9a0063c4c5f86a50e2699e56d32 |
| Source note | uspto-grants-1979_09 |