HCID 9824961, compound → HCID 9933529, compound
Reaction equation
[O:1]1[C:5]2=[N:6][C:7]([CH:10]([N:15]3[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][CH2:22][C:23]4[CH:32]=[CH:31][C:30]5[CH2:29][CH2:28][CH2:27][NH:26][C:25]=5[N:24]=4)[C:16]3=[O:33])[CH2:11][C:12]([OH:14])=[O:13])=[CH:8][CH:9]=[C:4]2[CH:3]=[CH:2]1>CO.[Pd]>[O:1]1[C:5]2=[N:6][C:7]([CH:10]([N:15]3[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][CH2:22][C:23]4[CH:32]=[CH:31][C:30]5[CH2:29][CH2:28][CH2:27][NH:26][C:25]=5[N:24]=4)[C:16]3=[O:33])[CH2:11][C:12]([OH:14])=[O:13])=[CH:8][CH:9]=[C:4]2[CH2:3][CH2:2]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 23-4 (360 mg, 0.80 mmol) in MeOH (10 mL) was treated with 10% Pd/C (100 mg) and stirred under a hydrogen atmosphere for 18 h. The catalyst was removed by filtration through celite and the residue chromatographed (75% 20:1:1 EtOH/NH4OH/H2O-25% EtOAc) to afford 23-5 as a colorless glass.
Workup
- customThe catalyst was removed by filtration through celite
- customthe residue chromatographed (75% 20:1:1 EtOH/NH4OH/H2O-25% EtOAc)
Sources & evidence
- ORD record
- ord-335ef4e5345c4f609a54c185f7019278
- Source dataset
- uspto-grants-2000_01
- Patent number
- US06017926
Reaction notes
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