HCID 178514258, compound → HCID 178514264, compound

HRID 1393931Notes

Reaction equation

HRID 1393931 reaction equation
C(OC([NH:11][C:12]1([PH:20]([NH:22][C:23](=[O:32])[CH:24]=[CH:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[O:21])[CH2:17][CH2:16][CH2:15][N:14]([NH2:18])[C:13]1=[O:19])=O)C1C=CC=CC=1>C(O)C.[Pd]>[NH2:11][C:12]1([PH:20]([NH:22][C:23](=[O:32])[CH2:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[O:21])[CH2:17][CH2:16][CH2:15][N:14]([NH2:18])[C:13]1=[O:19]

Participants

4

Reactant 1

HCID 178514258HCID 178514258, compound

Product 1

HCID 178514264HCID 178514264, compound

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

Palladium black (20.0 mg) was added to a solution of (3S, P (SR))-3-benzyloxycarbonylamino-1-amino(cinnamoylamino)phosphinyl-2-piperidone (201.0 mg, 0.4404 mmol) in ethanol (6 mL), and the resulting mixture was stirred at room temperature for 20 hours under a hydrogen atmosphere.

Sources & evidence

ORD record
ord-000cfeed64284693b1df0ffa6c5b7efb
Source dataset
uspto-grants-2008_03
Patent number
US07348318B2

Reaction notes

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