Реакция #48600

ord-abb1c6f593064b278921ff370239f3b1

Уравнение реакции

COc1ccc(CCl)cc1
4-methoxybenzyl chloride
O=C(Nc1ccccc1)c1n[nH]cc1I
4-iodo-1H-pyrazole-3-carboxylic acid phenylamide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COc1ccc(Cn2cc(I)c(C(=O)Nc3ccccc3)n2)cc1
4-iodo-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide
Выход 71.2%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthen evaporated under reduced pressure
  2. 2
    ДругоеThe residue was partitioned between ethyl acetate and brine
  3. 3
    Другоеthe ethyl acetate layer was separated
  4. 4
    Сушкаdried (MgSO4)
  5. 5
    Фильтрацияfiltered
  6. 6
    Другоеevaporated
  7. 7
    ДругоеThe crude material was purified by flash column chromatography
  8. 8
    Промывкаeluting with 1:3 ethyl acetate/hexane
  9. 9
    workup.ADDITIONthe product containing fractions
  10. 10
    Другоеevaporated

Методика

A solution of 4-iodo-1H-pyrazole-3-carboxylic acid phenylamide (670 mg; 2.14 mmol) in acetonitrile (10 ml) was treated with potassium carbonate (360 mg; 2.57 mmol)) followed by 4-methoxybenzyl chloride (320 μl; 2.35 mmol). The mixture was stirred at room temperature overnight then evaporated under reduced pressure. The residue was partitioned between ethyl acetate and brine; the ethyl acetate layer was separated, dried (MgSO4), filtered and evaporated. The crude material was purified by flash column chromatography eluting with 1:3 ethyl acetate/hexane and the product containing fractions combined and evaporated to give 660 mg of 4-iodo-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07745638B2uspto-grants-2010_06