HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → HCID 53926064, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 53855200 | HCID 53855200 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 53926064 | HCID 53926064 | 21.3% |
Reaction Steps
The procedure is similar to that described in Example 1, but starting with 1.36 g of benzyl (2R,4R)-3-[3-{2-[4-tert-butoxycarbonyl-2-(2-phenylphenyl)-3-thiazolidinyl]-2-oxoethyl}ureido]phenylacetate, 0.44 g of ammonium formate and 0.6 g of palladium on charcoal (10% Pd). 0.25 g of (2R,4R)-3-[3-{2-[4-tert-butoxycarbonyl-2-(2-phenylphenyl)-3-thiazolidinyl]-2-oxoethyl}ureido]phenylacetic acid, melting point 128° C., is thereby obtained; [α]D25 =-26.2°±0.9° (C %=0.56; MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633270 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-b47779451583489f80b26bac401c4f5d |
| Source note | uspto-grants-1997_05 |