[C:1]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]([N:14]([CH2:34][C:35]2[CH:46]=[CH:45][C:38]([O:39][CH2:40][C:41]([O:43]C)=[O:42])=[CH:37][CH:36]=2)[CH2:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]#[C:23][C:24]3[CH:29]=[CH:28][C:27]([CH2:30][CH2:31][CH2:32][CH3:33])=[CH:26][CH:25]=3)=[CH:18][CH:17]=2)=[O:13])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>CO.C1COCC1>[C:1]([C:5]1[CH:6]=[CH:7][C:8]([NH:11][C:12]([N:14]([CH2:34][C:35]2[CH:46]=[CH:45][C:38]([O:39][CH2:40][C:41]([OH:43])=[O:42])=[CH:37][CH:36]=2)[CH2:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]#[C:23][C:24]3[CH:29]=[CH:28][C:27]([CH2:30][CH2:31][CH2:32][CH3:33])=[CH:26][CH:25]=3)=[CH:18][CH:17]=2)=[O:13])=[CH:9][CH:10]=1)([CH3:2])([CH3:3])[CH3:4]To a solution of methyl {4-[({[(4-tert-butylphenyl)amino]carbonyl}{4-[(4-butylphenyl)-ethynyl]benzyl}amino)methyl]phenoxy}acetate (70 mg, 0.11 mmol) in MeOH (1 mL) and THF (1 mL) was added an aqueous solution of NaOH (0.5 mL, 5N) and the resulting mixture was stirred at it for 3 hrs. Then the solvents were removed under reduced pressure. The residue was taken up in EtOAc and washed with an aqueous solution of HCl (1N) and brine. The organic layer was dried over MgSO4 and the solvent was removed to give 46 mg (67%) of the title compound. HPLC, Rt: 5.67 min (purity: 97.4%). 1H NMR (CD3OD) δ: 7.48 (d, J=8.3 Hz, 2H), 7.40 (d, J=7.5 Hz, 2H), 7.18-7.33 (m, 10H), 6.93 (d, J=8.7 Hz, 2H), 4.66 (s, 2H), 4.66 (s, 2H), 4.54 (s, 2H), 2.63 (t, J=7.5 Hz, 2H), 1.60 (m, 2H), 1.37 (m, 2H), 1.30 (s, 9H), 0.95 (t, J=7.2 Hz, 3H). M+(ESI): 603.4, M−(ESI): 601.3.
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