Реакция #91243

ord-9e5b11e716fc4473ac1fcffbd2150981

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеto react sequentially in the same manner as in Steps A and B of Example 1

Методика

3-Chloromethyl-2-cyclobutylsulfanyl-pyridine (0.040 g, 0.18 mmol) obtained in Step C of Preparation Example 23 and 2-(3-fluoro-4-hydroxy-phenyl)-cyclopropane carboxylic acid ethyl ester (0.046 g, 0.18 mmol) obtained in Step C of Preparation Example 44 were used to react sequentially in the same manner as in Steps A and B of Example 1 to obtain the title compound (0.069 g, 98%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09447044B2uspto-grants-2016_09