HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Trityl Losartan Carboxaldehyde → 2-n-Butyl-1-[(2'-(N-triphenylmethyl-tetrazol-5-yl)biphenyl-4-yl)methyl]-1H-imidazole-5-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Trityl Losartan Carboxaldehyde | HCID 11657587 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-n-Butyl-1-[(2'-(N-triphenylmethyl-tetrazol-5-yl)biphenyl-4-yl)methyl]-1H-imidazole-5-carboxaldehyde | HCID 19094433 | — |
Reaction Steps
12.0 g (18.1 mmol) of 2-n-butyl-4-chloro-1-[(2'-(N-triphenylmethyltetrazol-5-yl)biphenyl-4-yl)methyl]-1H-imidazole-5-carboxaldehyde in 150 ml of methanol are hydrogenated at 25° C. for 1.5 h at a hydrogen pressure of about 3 bar in the presence of 1. 2 g of palladium on active carbon (5%) and 2.46 g (18.1 mmol) of sodium acetate trihydrate. The solution is then filtered off from the catalyst and concentrated, and the residue is chromatographed on silica gel 60 using ethyl acetate/petroleum ether (1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294633 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-a1365638ccc5488da9b094803df12262 |
| Source note | uspto-grants-1994_03 |