HCID 10114545, compound → HCID 10204152, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9](=[O:33])[C:10]1[CH:15]=[CH:14][C:13]([CH:16]2[CH:20]=[CH:19][CH:18]([C:21]3[CH:26]=[C:25]([O:27][CH3:28])[C:24]([O:29][CH3:30])=[C:23]([O:31][CH3:32])[CH:22]=3)[O:17]2)=[CH:12][CH:11]=1>CCOC(C)=O.O=[Pt]=O>[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9](=[O:33])[C:10]1[CH:11]=[CH:12][C:13]([CH:16]2[CH2:20][CH2:19][CH:18]([C:21]3[CH:22]=[C:23]([O:31][CH3:32])[C:24]([O:29][CH3:30])=[C:25]([O:27][CH3:28])[CH:26]=3)[O:17]2)=[CH:14][CH:15]=1Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a degazed solution of 289 (43 mg, 0.096 mmol) in AcOEt (4 mL) was added PtO2 (3 mg, 0.01 mmol) and the reaction mixture was stirred at room temperature under a 1 atm pressure of H2 for 16 h. The reaction flask was purged with N2 then the reaction mixture was filtered through celite, rinsed with MeOH and concentrated. The crude residue was purified three times by flash chromatography on silica gel (MeOH/DCM: 2/98, AcOEt/DCM: 30/70 and AcOEt/CHCl3: 30/70) to afford the title compound 290 (10 mg, 0.22 mmol, 23% yield). 1H NMR (CDCl3) δ (ppm): 8.10 (s, 1H), 7.91 (d, J=8.0 Hz, 2H), 7.50 (d, J=8.0 Hz, 2H), 7.34 (d, J=7.5 Hz, 1H), 7.10 (t, J=7.5 Hz, 1H), 6.96-6.85 (m, 2H), 6.64 (s, 2H), 5.33 (t, J=7.0 Hz, 1H), 5.21 (t, J=7.0 Hz, 1H), 3.89 (s, 6H), 3.85 (s, 3H), 2.59-2.40 (m, 2H), 2.09-1.88 (m, 2H).
Workup
- customThe reaction flask was purged with N2
- filtrationthe reaction mixture was filtered through celite
- washrinsed with MeOH
- concentrationconcentrated
- customThe crude residue was purified three times by flash chromatography on silica gel (MeOH/DCM: 2/98, AcOEt/DCM: 30/70 and AcOEt/CHCl3: 30/70)
Sources & evidence
- ORD record
- ord-a710cad8c4844f78936d43a9a9c25468
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07868204B2
Reaction notes
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