Реакция #91263

ord-8f1f7bf5888d4b1898d637471491ae02

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-isopropylsulfanyl-pyridine (0.030 g, 0.149 mmol) obtained in Step C of Preparation Example 16 and 2-(4-hydroxy-2,3-dimethyl-phenyl)-cyclopropane carboxylic acid ethyl ester (0.035 g, 0.149 mmol) obtained in Step C of Preparation Example 48 were used to react sequentially in the same manner as in Steps A and B of Example 1 to obtain the title compound (0.046 g, 83%).

Источник

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