Реакция #2145397

ord-aec2b1d65877483d8944db4c052c7df0

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеwas evaporated to an oil which
  2. 2
    Другоеwas crystallised from aqueous ethanol

Методика

A solution of 2-(2-aminoethylthiomethyl)-4-methoxypyridine (3.28 g) in methanol (40 cc) was added over 70 minutes to a stirred solution of 1-methylthio-1-methylsulphinyl-2-nitroethylene (3.01 g) in methanol (200 cc) at 30°. The mixture was allowed to stand overnight at room temperature and was evaporated to an oil which was crystallised from aqueous ethanol to give 1-methylthio-1-[2-(4-methoxy-2-pyridylmethylthio)ethylamino)-2-nitroethylene monohydrate (3.04 g) m.p. 52.5°-54.5°.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04215126uspto-grants-1980_07