HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → HCID 54366979, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 86750877 | HCID 86750877 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 54366979 | HCID 54366979 | 48.3% |
Reaction Steps
The procedure is similar to that described in Example 1, but starting with 2.58 g of benzyl (4R)-3-{3-[2-(4-tert-butoxycarbonyl-2-benzyl-3-thiazolidinyl)-2-oxoethyl]ureido}phenylacetate (isomer A) , 1.6 g of ammonium formate and 1.3 g of palladium on charcoal (10% Pd). 1.06 g of (4R) -3-{3-[2-(4-tert-butoxycarbonyl-2-benzyl-3-thiazolidinyl)-2-oxoethyl]ureido}phenylacetic acid (isomer A), melting point 110° C., are thereby obtained; [α]D25 =-89.0°±1.6° (C %=0.51; methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633270 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-ffb54698da8d46458dc9823e743c6180 |
| Source note | uspto-grants-1997_05 |