Reaktion #1583820

ord-88b83d26ba4340d3a383441a52ae6a09

Reaktionsgleichung

Cc1c(C(=O)Cl)cnn1C(C(F)(F)F)C(F)(F)F
5-methyl-1-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]pyrazole-4-carbonyl chloride
Nc1ccnnc1
pyridazin-4-amine
CCN(CC)CC
triethylamine
Cc1c(C(=O)Nc2ccnnc2)cnn1C(C(F)(F)F)C(F)(F)F
title compound
Ausbeute 90.0%
Cc1c(C(=O)Nc2ccnnc2)cnn1C(C(F)(F)F)C(F)(F)F
5-methyl-1-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-1H-pyrazole-4-carboxylic acid pyridazin-4-ylamide
Ausbeute 90.0%

Reaktionsbedingungen

Temperatur
22.5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with 3×15 ml sat. aq. NH4Cl solution
  2. 2
    Trocknendried over MgSO4
  3. 3
    Sonstigeevaporated
  4. 4
    SonstigePurification by flash chromatography (CH2Cl2/MeOH)

Vorschrift

A solution of 398 mg 5-methyl-1-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]pyrazole-4-carbonyl chloride in 10 ml CH2Cl2 was added dropwise to a solution of 185 mg pyridazin-4-amine and 750 mg triethylamine in 30 ml CH2Cl2 at 0° C. The mixture was stirred at 20-25° C. for about 68 h, diluted with 25 ml ethylacetate, washed with 3×15 ml sat. aq. NH4Cl solution, dried over MgSO4 and evaporated. Purification by flash chromatography (CH2Cl2/MeOH) gave 160 mg of the title compound (90% purity). HPLC-MS (Method 1): RT 2.278 min, m/z [MH]+ 354.1.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09198422B2uspto-grants-2015_12