HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20329298, compound → HCID 20329311, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20329298 | HCID 20329298 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20329311 | HCID 20329311 | — |
Reaction Steps
33.5 g of 1-methyl-8-nitro-6-phenyl-4H-s-triazolo[4,3-a][1,5] benzodiazepin-5-one in 100 ml of ethanol containing 2.0 g of Raney nickel is hydrogenated at room temperature at an initial hydrogen pressure of 50 p.s.i. The reaction is stopped when 0.3 moles of hydrogen has been absorbed; the suspension is filtered and the filtrate evaporated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04133809 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-fdf356f2d7634356964b89d4836c98fa |
| Source note | uspto-grants-1979_01 |