HCID 67237164, compound → HCID 67236605, compound
Reaction equation
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([C@H:15]2[C@@H:19]([O:20][CH3:21])[C@H:18]([O:22][CH3:23])[C@H:17]([C:24]3[CH:29]=[CH:28][C:27]([O:30]CC4C=CC=CC=4)=[CH:26][CH:25]=3)[N:16]2[C:38]2[CH:43]=[CH:42][C:41]([C:44]([CH3:47])([CH3:46])[CH3:45])=[CH:40][CH:39]=2)=[CH:11][CH:10]=1)C1C=CC=CC=1>C(OCC)(=O)C.[Pd]>[C:44]([C:41]1[CH:40]=[CH:39][C:38]([N:16]2[C@@H:17]([C:24]3[CH:29]=[CH:28][C:27]([OH:30])=[CH:26][CH:25]=3)[C@@H:18]([O:22][CH3:23])[C@H:19]([O:20][CH3:21])[C@@H:15]2[C:12]2[CH:13]=[CH:14][C:9]([OH:8])=[CH:10][CH:11]=2)=[CH:43][CH:42]=1)([CH3:47])([CH3:45])[CH3:46]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of the product from Example 48B (168 mg, 0.268 mmol) in ethyl acetate (3 ml) was added 10% palladium on carbon (17 mg) and the flask was evacuated and back-filled with H2 gas. The solution was stirred under a balloon of H2 gas for 20 h, filtered through Celite, and washed with ethyl acetate and methanol. The filtrate was concentrated and the residue was azeotroped with ether to give title compound (120 mg, 100%) as a white solid.
Workup
- customthe flask was evacuated
- additionback-filled with H2 gas
- filtrationfiltered through Celite
- washwashed with ethyl acetate and methanol
- concentrationThe filtrate was concentrated
- customthe residue was azeotroped with ether
Sources & evidence
- ORD record
- ord-2142e831e39d4f14b4eab00b4b85c644
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691938B2
Reaction notes
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