HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 70053231, compound → HCID 20142995, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 70053231 | HCID 70053231 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Product | HCID 20142995 | HCID 20142995 | — |
Reaction Steps
A solution of 5.2 g (0.015 m) of 7-chloro-1,3-dihydro-5-(2-fluorophenyl)-3-methyl-2-nitromethylene-2H-1,4-benzodiazepine in 450 ml of 2:1 tetrahydrofuran-methanol was hydrogenated for 3 hrs. using a Parr apparatus, Raney nickel catalyst (3 teaspoonsful) and an initial pressure of 18 psi. The mixture was filtered and evaporated at reduced pressure to give crude 2-aminomethyl-7-chloro-2,3-dihydro-5-(2-fluorophenyl)-3-methyl-1H-1,4-benzodiazepine as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04739049 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-ef37cfcc1349468bacff6b93b468708a |
| Source note | uspto-grants-1988_04 |