Реакция #46116

ord-cc7cdf4d90fc4c72980716ddfe9808c6

Уравнение реакции

NS(=O)(=O)c1cc([N+](=O)[O-])ccc1Cl
2-Chloro-5-nitrobenzenesulphonamide
NC1CC1
cyclopropylamine
NS(=O)(=O)c1cc([N+](=O)[O-])ccc1NC1CC1
2-cyclopropylamino-5-nitrobenzenesulphonamide

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONabove is introduced into a hermetically closed vessel
  2. 2
    workup.ADDITIONcontaining
  3. 3
    ДругоеAfter this time period, the solvent and the reagent are removed
  4. 4
    Концентрированиеby concentrating under reduced pressure
  5. 5
    Фильтрацияis collected by filtration
  6. 6
    Промывкаwashed with methanol
  7. 7
    Другоеdried

Методика

2-Chloro-5-nitrobenzenesulphonamide (5 g) prepared in the Step above is introduced into a hermetically closed vessel containing a mixture of dioxane (70 mL) and cyclopropylamine (3.5 mL). The hermetically closed vessel is placed in an oven at 100° C. for 24 hours. After this time period, the solvent and the reagent are removed by concentrating under reduced pressure. The residue is taken up in methanol (20 mL) and the insoluble material, which contains the title product, is collected by filtration, washed with methanol and dried.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07741320B2uspto-grants-2010_06