Реакция #2254158

ord-c60899a56d664d62ae11942440e68bea

Уравнение реакции

O=C(Cl)c1cc(C(F)(F)F)nn1-c1ncccc1Cl
2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carbonyl chloride
Nc1c(Cl)cc(Cl)cc1C(=O)O
3,5-dichloroanthranilic acid
CCN(CC)CC
triethylamine
O=C(O)c1cc(Cl)cc(Cl)c1NC(=O)c1cc(C(F)(F)F)nn1-c1ncccc1Cl
2-(3-chloro-2-pyridyl)-N-[2,4-dichloro-6-hydroxycarbonyl-phenyl]-5-(trifluoromethyl)pyrazole-3-carboxamide

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеThe reaction was concentrated in vacuo
  2. 2
    Другоеused directly in the following reaction step

Методика

To a solution of 3,5-dichloroanthranilic acid (7.89 g, 38.3 mmol) in methylene chloride (130 mL) at 0° C. was added triethylamine (18.6 mL, 134.0 mmol). A solution of 2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carbonyl chloride (13.7 g, 44.0 mmol) in methylene chloride (130 mL) at 0° C. was then added, the reaction allowed to warm to room temperature and then stirred further for 16 h. The reaction was concentrated in vacuo and used directly in the following reaction step.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09044016B2uspto-grants-2015_06