反应详情

The title compound was prepared analogously to step 7 of example B(29) where 4-[4-(pyridin-2-ylsulfanylcarbonyl)-butyl]-piperidine-1-carboxylic acid tert-butyl ester from step 5 above, was substituted in place 3-cyclohexyl-thiopropionic acid S-pyridin-2-yl ester. 1H NMR (400 MHz, CDCl3): δ 1–1.42 (m, 8H), 1.45 (s, 9H), 1.50–1.84 (m, 14H), 2.42–2.46 (m, 2H), 2.62–2.7 (m, 2H), 2.82–2.87 (m, 1H). ESIMS (MH+): 337.