Реакция #91240

ord-af95432e448d4808903cfc77069b1d82

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

2-Chloromethyl-6-cyclopentylsulfanyl-pyridine (0.040 g, 0.17 mmol) obtained in Step C of Preparation Example 27 and 2-(3-fluoro-4-hydroxy-phenyl)-cyclopropane carboxylic acid ethyl ester (0.040 g, 0.17 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 (0.061 g, 89%).

Источник

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