HCID 57589793, compound → HCID 57589800, compound
Reaction equation
[C:1]([O:5][C:6]([N:8]([C:40]([O:42][C:43]([CH3:46])([CH3:45])[CH3:44])=[O:41])[C:9]1[CH:14]=[C:13]([CH2:15][C@H:16]2[C:19](=[O:20])[N:18]([C:21](=[O:29])[NH:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C@@H:17]2[C:30]([O:32]CC2C=CC=CC=2)=[O:31])[CH:12]=[CH:11][N:10]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>CO.C(OCC)(=O)C.[Pd]>[C:43]([O:42][C:40]([N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[C:9]1[CH:14]=[C:13]([CH2:15][C@H:16]2[C:19](=[O:20])[N:18]([C:21](=[O:29])[NH:22][C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=3)[C@@H:17]2[C:30]([OH:32])=[O:31])[CH:12]=[CH:11][N:10]=1)=[O:41])([CH3:45])([CH3:46])[CH3:44]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Acylated lactam ester 20 (56 mg, 0.089 mmol) was dissolved in 2 mL of 1:1 methanol-ethyl acetate in a 20 mL glass vial. 10% palladium on carbon catalyst (10 mg) was added, and the solution was stirred under an atmosphere of hydrogen at room temperature overnight under argon, filtered, and then concentrated in vacuo. The residue was pure by HPLC/MS and was taken to the next step without purification. MS: 541.1 [M+H]+.
Workup
- filtrationfiltered
- concentrationconcentrated in vacuo
- customwas taken to the next step without purification
Sources & evidence
- ORD record
- ord-b2a8676c2be04af68bf78a251ae2b299
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07501404B2
Reaction notes
Loading…