HCID 57624619, compound → HCID 57624592, compound
Reaction equation
[C:1]([O:4][CH2:5][C:6]([NH:38][C:39](=[O:41])[CH3:40])([CH2:33][O:34][C:35](=[O:37])[CH3:36])[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[C:24]3[C:19](=[C:20]([O:25]CC4C=CC=CC=4)[CH:21]=[CH:22][CH:23]=3)[CH:18]=[CH:17][CH:16]=2)=[CH:11][CH:10]=1)(=[O:3])[CH3:2]>C(OCC)(=O)C.CO.[C].[Pd]>[C:35]([O:34][CH2:33][C:6]([NH:38][C:39](=[O:41])[CH3:40])([CH2:5][O:4][C:1](=[O:3])[CH3:2])[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[C:24]3[C:19](=[C:20]([OH:25])[CH:21]=[CH:22][CH:23]=3)[CH:18]=[CH:17][CH:16]=2)=[CH:11][CH:10]=1)(=[O:37])[CH3:36]Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
The compound (1.45 g) of Example (1-1) was dissolved in ethyl acetate (30 mL) and methanol (10 mL), 10% palladium carbon (500 mg) was added, and the mixture was stirred at room temperature for 5 hr under a hydrogen atmosphere. After celite filtration, the filtrate was concentrated, and the residue was washed with diethyl ether to give the object product (0.99 g) as white crystals.
Workup
- filtrationAfter celite filtration
- concentrationthe filtrate was concentrated
- washthe residue was washed with diethyl ether
Sources & evidence
- ORD record
- ord-cc9527716e954987a918fc00db2de0f4
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08114902B2
Reaction notes
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