[NH:1]1[CH2:4][CH:3]([C:5]#[C:6][C:7]2[CH:16]=[C:15]3[C:10]([C:11](=[O:28])[C:12]([C:17]4[CH:22]=[CH:21][C:20]([NH:23][S:24]([CH3:27])(=[O:26])=[O:25])=[CH:19][CH:18]=4)=[CH:13][O:14]3)=[CH:9][CH:8]=2)[CH2:2]1.FC(F)(F)C(O)=O.[C:36](=O)([O:43]N1C(=O)CCC1=O)[O:37][CH:38]1[CH2:42][CH2:41][CH2:40][CH2:39]1.C(N(C(C)C)CC)(C)C>ClCCl>[CH:38]1([O:37][C:36]([N:1]2[CH2:4][CH:3]([C:5]#[C:6][C:7]3[CH:16]=[C:15]4[C:10]([C:11](=[O:28])[C:12]([C:17]5[CH:22]=[CH:21][C:20]([NH:23][S:24]([CH3:27])(=[O:26])=[O:25])=[CH:19][CH:18]=5)=[CH:13][O:14]4)=[CH:9][CH:8]=3)[CH2:2]2)=[O:43])[CH2:42][CH2:41][CH2:40][CH2:39]1To a mixture of N-(4-(7-(azetidin-3-ylethynyl)-4-oxo-4H-chromen-3-yl)phenyl)methanesulfonamide.trifluoroacetic acid salt (55 mgs, 0.140 mmol) in dichloromethane (3 mL) was added cyclopentyl 2,5-dioxopyrrolidin-1-yl carbonate (95 mgs, 0.42 mmol) and diisopropylethylamine (0.2 mL, 1.4 mmol), and the mixture was stirred at room temperature for 16 hours. The resulting mixture was concentrated under reduced pressure, and chromatographed (SiO2, 25% ethyl acetate/dichloromethane) to provide cyclopentyl-3-((3-(4-(methylsulfonamido)phenyl)-4-oxo-4H-chromen-7-yl)ethynyl)azetidine-1-carboxylate:
Wird geladen…