Реакция #50494

ord-b9abcddd57be425a9b079fbae3721260

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwas refluxed for 5 hours
  2. 2
    ДругоеAfter the reaction
  3. 3
    Другоеmost of the acetonitrile was removed by distillation and water
  4. 4
    workup.ADDITIONwas added to the residue
  5. 5
    ДругоеAs the solid product was separated
  6. 6
    Фильтрацияit was collected by filtration
  7. 7
    ДругоеThe crude material was recrystallized from ethanol

Методика

A mixture of 2.9 g of 2-nitroiminothiazolidine, 2.9 g of anhydrous potassium carbonate, 3.2 g of 2-chloro-5-pyridylmethylchloride and 50 ml of acetonitrile was refluxed for 5 hours with vigorously stirring. After the reaction, most of the acetonitrile was removed by distillation and water was added to the residue. As the solid product was separated, it was collected by filtration. The crude material was recrystallized from ethanol to give desired 3-(2-chloro-5-pyridylmethyl)-2-(nitroimino)thiazolidine.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05428032uspto-grants-1995_06