methyl N-(tert-butoxycarbonyl)-4-[4-{6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}but-1-en-1-yl]-L-phenylalaninate 在
钯 氢气 作用下,
以
乙醇 为溶剂,
反应 16.0h,
以to afford methyl N-(tert-butoxycarbonyl)-4-(4-{6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}butyl)-L-phenylalaninate as a clear colourless oil (1.02 g, 71%)的产率得到methyl N-(tert-butoxycarbonyl)-4-(4-{6-[(tert-butoxycarbonyl)(methyl)amino]pyridin-2-yl}butyl)-L-phenylalaninate