Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 11223028 | HCID 11223028 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58858426 | HCID 58858426 | — |
Reaction Steps
6.0 g (15.4 mmoles) of 4′-(4-isopropyl-5-oxo-3-pentanoyl-oxazolidin-2-yl)-biphenyl-2-carbonitrile is reacted in 30 ml of ethanol with 3.8 g of ammonium formate (61.6 mmoles) and 2 g of 5% Pd/C catalyst. The temperature is raised to 75° C., keeping these conditions for 3 hours. The mixture is cooled and the catalyst is filtered off. The organic phase is concentrated under reduced pressure to a residue to obtain 2-[(2′-cyano-biphenyl-4-yl-methyl)-pentanoyl-amino]-3-methylbutyric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07439261B2 |
|---|
| Source dataset | uspto-grants-2008_10 |
|---|
| ORD ID | ord-b630129e96bc4526a89da13cfbe23241 |
|---|
| Source note | uspto-grants-2008_10 |
|---|