[C:1]([NH:8][CH:9]([CH2:16][CH2:17][CH2:18][CH3:19])[C:10]([CH3:15])([CH3:14])[C:11]([OH:13])=O)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].CN(C(ON1N=N[C:30]2[CH:31]=[CH:32][CH:33]=[N:34][C:29]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(C(C)C)CC)(C)C.[CH3:53][O:54][C:55](=[O:63])[CH2:56]C1CCNCC1>ClCCl>[CH3:53][O:54][C:55](=[O:63])[CH2:56][N:34]1[CH2:29][CH2:30][CH2:31][CH2:32][CH:33]1[C:11](=[O:13])[C:10]([CH3:15])([CH3:14])[CH:9]([CH2:16][CH2:17][CH2:18][CH3:19])[NH:8][C:1]([O:3][C:4]([CH3:5])([CH3:6])[CH3:7])=[O:2]To a solution of N-Boc-β-n-butyl-α,α-dimethyl-β-alanine (1.68 g, 6.13 mmol) in dichloromethane (30 ml) was added HATU reagent (2.8 g, 7.37 mmol) and di-i-propylethylamine (6.58 ml, 36.8 mmol) under cooling with ice. After being stirred for 30 min, to the reaction mixture was added 4-piperidineacetic acid methyl ester (1.45 g, 9.19 mmol) and stirred overnight at room temperature. After the solvent was distilled off, the resulting residue was dissolved into ethyl acetate and washed with 5% aqueous citric acid, 5% aqueous sodium bicarbonate, and brine for three times respectively. The organic layer was dried over anhydrous sodium sulfate. After the solvent was distilled off, the residue was subjected to the silica gel column chromatography (2.2×20 cm) and eluted with hexane:ethyl acetate=2:1 to give powder of N-Boc-β-n-butyl-α,α-dimethyl-β-alanyl-piperidineacetic acid methyl ester (1.70 g, 67.2%).
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