Réaction #2254158

ord-c60899a56d664d62ae11942440e68bea

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    ConcentrationThe reaction was concentrated in vacuo
  2. 2
    Autreused directly in the following reaction step

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09044016B2uspto-grants-2015_06