HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 66920127, compound → HCID 66920231, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 66920127 | HCID 66920127 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66920231 | HCID 66920231 | 83.2% |
Reaction Steps
7 g of (S)-4-Benzyloxycarbonylamino-5-oxo-5-[4-(3-trifluoromethyl-phenyl)-piperazin-1-yl]-pentanoic acid tert-butyl ester were dissolved in 120 ml of EtOH and 70 mg of Pd/C 10% was added. Hydrogenation under 3 bar of hydrogen was continued until full conversion of the reaction was obtained. After filtration of the catalyst all volatiles were evaporated under reduced pressure to give 4.4 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598179B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-f7ab6adfe59f493a8a14a73ff86609b1 |
| Source note | uspto-grants-2013_12 |