تفاعل #48596

ord-c01a70bd6cf64212a1ffd3d3a4856a47

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction was evaporated
  2. 2
    أخرىthen purified by flash column chromatography
  3. 3
    غسيلeluting with 1:3
  4. 4
    workup.ADDITIONProduct containing fractions
  5. 5
    أخرىevaporated

الإجراء التجريبي

A solution of 4-phenyl-1H-pyrazole-3-carboxylic acid (75 mg; 0.4 mmol) (prepared according to Example 228C), aniline (45 μl; 0.48 mmol), EDAC (92 mg; 0.48 mmol) and HOBt (65 mg; 0.48 mmol) in 5 ml of DMF was stirred at room temperature overnight. The reaction was evaporated then purified by flash column chromatography eluting with 1:3 then 1:2 ethyl acetate/hexane. Product containing fractions were combined and evaporated to give 30 mg of 4-phenyl-1H-pyrazole-3-carboxylic acid phenylamide as a white solid. (LC/MS: Rt 3.12 [M+H]+ 264).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745638B2uspto-grants-2010_06