تفاعل #91267

ord-4b9a8b2ef709491abe4fe00f58bc3137

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىobtained in Preparation Example 54
  2. 2
    أخرىto react sequentially in the same manner as in Steps A and B of Example 1

الإجراء التجريبي

3-Chloromethyl-2-cyclopentylsulfanyl-pyridine (21 mg, 0.09 mmol) obtained in Step C of Preparation Example 8 and (6-hydroxy-7-methyl-benzofuran-3-yl)-acetic acid methyl ester (21 mg, 0.09 mmol) obtained in Preparation Example 54 were used to react sequentially in the same manner as in Steps A and B of Example 1 to obtain the title compound (30 mg, 83%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09447044B2uspto-grants-2016_09