Реакция #94294

ord-8a708d5803164077b7f4629a7c0c7d9b

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураrefluxed for 3 hrs
  2. 2
    Температураreflux
  3. 3
    ДругоеThe solids which precipitate
  4. 4
    Температураon cooling
  5. 5
    Фильтрацияare filtered
  6. 6
    workup.DISSOLUTIONpartially dissolved
  7. 7
    Фильтрацияfiltered
  8. 8
    ТемператураThe isopropanol filtrate is cooled
  9. 9
    workup.ADDITIONtreated with diethyl ether
  10. 10
    ФильтрацияThe crystallized product is filtered
  11. 11
    Другоеdried
  12. 12
    Другоеto give 1.03 g

Методика

To 2.23 g. of 2-(4-methoxyphenyl)imidazo[1,2-a]pyridine in 50 ml. of acetonitrile is added 2.84 g. of methyl iodide, and the resulting reaction mixture refluxed for 3 hrs. Additional methyl iodide (2 ml.) is added and reflux continued for one hour. The solids which precipitate on cooling are filtered and partially dissolved in boiling isopropanol and filtered. The isopropanol filtrate is cooled and treated with diethyl ether. The crystallized product is filtered and dried to give 1.03 g., m.p. 194-196° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04129567uspto-grants-1978_12