Реакция #94294
ord-8a708d5803164077b7f4629a7c0c7d9b
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Температураrefluxed for 3 hrs
- 2Температураreflux
- 3ДругоеThe solids which precipitate
- 4Температураon cooling
- 5Фильтрацияare filtered
- 6workup.DISSOLUTIONpartially dissolved
- 7Фильтрацияfiltered
- 8ТемператураThe isopropanol filtrate is cooled
- 9workup.ADDITIONtreated with diethyl ether
- 10ФильтрацияThe crystallized product is filtered
- 11Другоеdried
- 12Другоеto 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.