HCID 58022609, compound → HCID 58022560, compound
Reaction equation
[CH2:1]([C@@:4]([NH:31][C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])([CH2:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([S:19][C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=2)=[CH:15][C:14]=1[Cl:30])[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH:2]=[CH2:3]>C(OCC)(=O)C.[Pd]>[C:35]([O:34][C:32]([NH:31][C@:4]([CH2:1][CH2:2][CH3:3])([CH2:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([S:19][C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:27])[F:28])[CH:21]=2)=[CH:15][C:14]=1[Cl:30])[C:5]([O:7][CH2:8][CH3:9])=[O:6])=[O:33])([CH3:38])([CH3:36])[CH3:37]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of the compound of Example 13 (400 mg) in ethyl acetate (20 mL) was added palladium, on activated carbon/ethylene diamine complex (100 mg), and the resultant solution was stirred at room temperature for 24 hours under hydrogen atmosphere. The reaction solution was filtered through Celite, and the solvent was evaporated. The resultant residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1) to obtain the target product (293 mg) as a colorless oil.
Workup
- filtrationThe reaction solution was filtered through Celite
- customthe solvent was evaporated
- customThe resultant residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1)
Sources & evidence
- ORD record
- ord-ca9bcf63f05e49d4a815fdd376fe17b2
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08273748B2
Reaction notes
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