تفاعل #586104

ord-2ef4725139d742d496e09cfb23d1adca

معادلة التفاعل

C=Cc1c(N)cccc1C(C)(C)C
3-tert-butyl-2-vinyl-phenylamine
Cn1cc(C(=O)O)c(C(F)(F)F)n1
1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid
CCN(CC)CC
triethylamine
CN(C)C=O
dimethylformamide
C=Cc1c(NC(=O)c2cn(C)nc2C(F)(F)F)cccc1C(C)(C)C
1-Methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (3-tert-butyl-2-vinylphenyl)amide

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter this the solution is slowly added to a solution
  2. 2
    أخرىThe resulting reaction mixture
  3. 3
    أخرىAfter removal of the solvent in a water jet vacuum
  4. 4
    أخرىthe residue is purified by flash chromatography over silicagel (eluent: hexane/ethylacetate 2:1)

الإجراء التجريبي

197 mg (1,01 mmol) 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid and 135 mg (1,07 mmol) oxalylic acid chloride are dissolved in 8 ml methylenechloride. The solution is stirred for 3 hours at room temperature in the presence of a catalytic amount of dimethylformamide (DMF). After this the solution is slowly added to a solution consisting of 180 mg (1,01 mmol) 3-tert-butyl-2-vinyl-phenylamine, 155 mg (1,52 mmol) triethylamine and 7 ml methylenechloride. The resulting reaction mixture is then stirred at room temperature for 16 hours. After removal of the solvent in a water jet vacuum, the residue is purified by flash chromatography over silicagel (eluent: hexane/ethylacetate 2:1). This gives 0,27 g 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (3-tert-butyl-2-vinylphenyl)amide in the form of a colourless solid (m.p. 118-119° C.; 76% of theory).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07767625B2uspto-grants-2010_08