Реакция #165982

ord-dda31bf9a36b41a09868dd41bec7c59b

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеLC/MS [5.40 min; 469 (M+1)]

Методика

3-[(2-fluoro-4-iodophenyl)amino]-N-(2-piperidin-1-ylethyl)isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 2.5 mmol of 3-[(2-fluoro-4-iodophenyl)amino]isonicotinic acid (intermediate 1) and 4.0 mmol of 2-piperidin-1-ylethylamine. LC/MS [5.40 min; 469 (M+1)]

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08841459B2uspto-grants-2014_09