HCID 14858794, compound → HCID 14858793, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH:9]([C:11]2[CH:19]=[CH:18][CH:17]=[CH:16][C:12]=2[C:13]([OH:15])=[O:14])[OH:10])=[CH:4][CH:3]=1>CO.[Pd]>[C:5]1([CH2:8][N:1]([CH2:9][C:11]2[CH:12]=[CH:16][CH:17]=[CH:18][CH:19]=2)[C:2]2[CH:3]=[CH:4][C:5]([CH2:8][CH:9]([C:11]3[CH:19]=[CH:18][CH:17]=[CH:16][C:12]=3[C:13]([OH:15])=[O:14])[OH:10])=[CH:6][CH:7]=2)[CH:6]=[CH:7][CH:2]=[CH:3][CH:4]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Compound VII (32 mg), obtained in Example 10, was dissolved in methanol (2 ml). Pd/C (10 mg) was added and the reaction mixture flushed with hydrogen and stirred for about 1.5 hours until all spotting material was gone, as determined by TLC in CH2Cl2 :ethylacetate (1:1), yielding 16.2 mg (86 percent yield) of Compound 5b.
Workup
- customthe reaction mixture flushed with hydrogen
Sources & evidence
- ORD record
- ord-2e4ffcfa218d421a9b022bb2bdb1eed0
- Source dataset
- uspto-grants-1993_02
- Patent number
- US05187086
Reaction notes
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