HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20329343, compound → HCID 20329304, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20329343 | HCID 20329343 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20329304 | HCID 20329304 | — |
Reaction Steps
44.6 g of 4-(benzyloxy)-1-methyl-8-chloro-6-phenyl-4H-s-triazolo[4,3-a][1,5]benzodiazepin-5-one in 400 ml of ethanol containing 2.0 g of Raney nickel is hydrogenated at an initial hydrogen pressure of 40 p.s.i. After 0.1 mole of hydrogen has been absorbed, the reaction is stopped, filtered and the solvent evaporated. The residue is triturated in ether and the title compound filtered off and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04133809 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-d27d686be8ed4b80aea538b63e7ddde7 |
| Source note | uspto-grants-1979_01 |