CCO.[CH3:4][O:5][C:6]1[CH:7]=[C:8]([CH:27]=[CH:28][C:29]=1[O:30][CH3:31])[O:9][CH2:10][C:11](=O)[C:12]#[C:13][C@@H:14]1[CH2:18][CH2:17][CH2:16][N:15]1C(OC(C)(C)C)=O.Cl.[NH2:33][OH:34].C(O)(C(F)(F)F)=O>C(Cl)(Cl)Cl>[CH3:4][O:5][C:6]1[CH:7]=[C:8]([CH:27]=[CH:28][C:29]=1[O:30][CH3:31])[O:9][CH2:10][C:11]1[CH:12]=[C:13]([C@@H:14]2[CH2:18][CH2:17][CH2:16][NH:15]2)[O:34][N:33]=1
To an EtOH (10 mL) solution of the compound (390 mg) obtained in Example 14-(2), hydroxylamine hydrochloride (139 mg) was added and the mixture was heated under reflux for 20 hours. The reaction mixture was concentrated to give a brown oil, to which CHCl3 (1.0 mL) and TFA (5.0 mL) were added, followed by stirring at room temperature for 21 hours. After concentrating the reaction mixture, saturated aqueous sodium bicarbonate (50 mL) was added and the organic layer extracted with CHCl3 (50 mL×2) was dried (Na2SO4), filtered and concentrated to give the titled compound (326 mg, brown oil) as a mixture with impurities.
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