Реакция #4666

ord-a4b80bde42b64cf99f5959c49c2e964f

Уравнение реакции

CCOC([O-])[O-]
ethyl orthoformate
CCOC(=O)CC(=O)c1cc(F)c(-n2cccc2)cc1F
ethyl 2,5-difluoro-4-(pyrrol-1-yl)benzoylacetate
NC1CC1
cyclopropylamine
CCOC(=O)C(=CNC1CC1)C(=O)c1cc(F)c(-n2cccc2)cc1F
crystals
Выход 36.1%
CCOC(=O)C(=CNC1CC1)C(=O)c1cc(F)c(-n2cccc2)cc1F
ethyl 3-cyclopropylamino-2-(2,5-difluoro-4-pyrrol-1-ylbenzoyl)acrylate
Выход 36.1%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe mixture is refluxed for 3 hours
  2. 2
    ДругоеIt is evaporated to dryness
  3. 3
    workup.DISSOLUTIONthe residue is dissolved in 10 ml of ethanol
  4. 4
    ДругоеIt is evaporated to dryness
  5. 5
    Экстракцияthe oily residue is extracted with 3×30 ml of boiling hexane
  6. 6
    КонцентрированиеThe hexane fractions are concentrated to 20 ml
  7. 7
    workup.WAITleft for 12 hours at 5° C.

Методика

1 g (0.0068 mol) of ethyl orthoformate is added to a solution of 1.1 g (0.00315 mol) of ethyl 2,5-difluoro-4-(pyrrol-1-yl)benzoylacetate in 3 ml of acetic anhydride and the mixture is refluxed for 3 hours. It is evaporated to dryness, the residue is dissolved in 10 ml of ethanol, 0.3 ml (0.0034 mol) of cyclopropylamine is added and the mixture is left at room temperature for 1 hour. It is evaporated to dryness and the oily residue is extracted with 3×30 ml of boiling hexane. The hexane fractions are concentrated to 20 ml and left for 12 hours at 5° C. to give 0.41 g of crystals melting at 90°-2° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04727080uspto-grants-1988_02