반응 #2186220

ord-18ec271f997f4e3dbed88f19dfc3ea03

반응 방정식

Nc1c(SC(F)(F)F)c(C(=O)O)nn1-c1c(Cl)cc(C(F)(F)F)cc1Cl
5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthio-1H-pyrazole-3-carboxylic acid
NC1CC1
Cyclopropylamine
Nc1c(SC(F)(F)F)c(C(=O)NC2CC2)nn1-c1c(Cl)cc(C(F)(F)F)cc1Cl
title compound
수율 87.0%
Nc1c(SC(F)(F)F)c(C(=O)NC2CC2)nn1-c1c(Cl)cc(C(F)(F)F)cc1Cl
5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthio-1H-pyrazole-3-carboxylic acid cyclopropylamide
수율 87.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated to
  2. 2
    workup.WAITcontinued at 55° C. for 6 hours
  3. 3
    추출extracted with ethyl acetate
  4. 4
    세척washed with aqueous potassium hydrogensulfate (5%)
  5. 5
    건조dried over magnesium sulfate
  6. 6
    기타evaporated

실험 절차

A mixture of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthio-1H-pyrazole-3-carboxylic acid (0.85 g, 1.83 mmol) and 1,1-dicarbonylimidazole (0.36 g, 2.20 mmol) in dioxane was heated to. 55° C. for 2 hours. Cyclopropylamine (0.20 ml, 2.83 mmol) was then added and stirring continued at 55° C. for 6 hours. The cooled mixture was diluted with water, extracted with ethyl acetate, washed with aqueous potassium hydrogensulfate (5%), dried over magnesium sulfate and evaporated to give the title compound (0.762 g, yield 87%) as off-white crystals, mp 193° C., 1H NMR (CDCl3): 0.64 (m, 2H, cyclopropyl), 0.83 (m, 2H, cyclopropyl), 2,87 (m,1H, cyclopropyl), 4.31 (bs, 2H, NH2), 6.82 (bs,1 H, C(O)NH), and 7.80 (s, 2H, Ar—H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07569516B2uspto-grants-2009_08