Реакция #302874

ord-c3bbc2a121cf4b6aa6d4c1b9b88221d7

Уравнение реакции

C=C(C(=O)OC)c1ccccc1
2-phenyl acrylic acid methyl ester
Nc1nc[nH]n1
3-amino-1,2,4-triazole
O=C1Nc2nncn2CC1c1ccccc1
6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on
Выход 19.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solvent was removed under reduced pressure
  2. 2
    workup.ADDITIONThe residue was treated with a small amount of ethanol and diethyl ether and cyclohexane
  3. 3
    workup.ADDITIONwere added
  4. 4
    ДругоеThe diethyl ether is slowly removed under reduced pressure
  5. 5
    ДругоеThe crude 6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on precipitated during evaporation
  6. 6
    Другоеwas isolated by filtration
  7. 7
    Промывкаwashed with diethyl ether
  8. 8
    Другое6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on was recrystallized from a small amount of ethanol

Методика

A solution of 9.01 g (55.6 mmol) 2-phenyl acrylic acid methyl ester and 4.24 g (50.4 mmol) 3-amino-1,2,4-triazole in 41 ml n-butanol was refluxed for 24 hours. The solvent was removed under reduced pressure. The residue was treated with a small amount of ethanol and diethyl ether and cyclohexane were added. The diethyl ether is slowly removed under reduced pressure. The crude 6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on precipitated during evaporation, was isolated by filtration and washed with diethyl ether. 6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on was recrystallized from a small amount of ethanol. 2.04 g (19%) 6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on was isolated (m.p. 184-186° C.).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08192918B2uspto-grants-2012_06