Реакция #91239

ord-6e8690af860246bba24af5ea12711eef

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-isopropylsulfanyl-pyridine (0.040 g, 0.20 mmol) obtained in Step C of Preparation Example 1 and 2-[3-fluoro-4-hydroxy-phenyl]-cyclopropane carboxylic acid ethyl ester (0.044 g, 0.20 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 (0.060 g, 84%).

Источник

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