HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178435512, compound → HCID 178435511, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178435512 | HCID 178435512 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178435511 | HCID 178435511 | — |
Reaction Steps
A solution of 1 g of 7-ethyl-1,2-dihydro-4-methyl-3-o-nitrobenzyl-2-oxo-1-[2'-(1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]quinoline in 25 ml of ethanol is hydrogenated on 0.3 g of 5% Pd-on-charcoal at 20° and normal pressure until the calculated amount of H2 has been taken up. The catalyst is filtered off, the filtrate is evaporated and the 3-o-aminobenzyl-7-ethyl-1,2-dihydro-4-methyl-2-oxo-1-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl-methyl]quinoline obtained is purified by chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371226 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-3b4b001e43164052b683d9a016e2e677 |
| Source note | uspto-grants-1994_12 |