Реакция #40264

ord-ec8236a187c1419c973899f581646a85

Уравнение реакции

Cc1nc2ccccc2n1C
1,2-dimethyl-1H-benzimidazole
O=C(CCl)NCCSSCCNC(=O)CCl
N,N′-(disulfanediyldiethane-2,1-diyl)bis(2-chloroacetamide)
Cc1n(CC(=O)NCCSSCCNC(=O)Cn2c(C)[n+](C)c3ccccc32)c2ccccc2[n+]1C.[Cl-].[Cl-]
white powder
Выход 129.8%
Cc1n(CC(=O)NCCSSCCNC(=O)Cn2c(C)[n+](C)c3ccccc32)c2ccccc2[n+]1C.[Cl-].[Cl-]
1,1′-{disulfanediylbis[ethane-2,1-diylimino(2-oxoethane-2,1-diyl)]}bis(2,3-dimethyl-1H-benzimidazol-3-ium) chloride
Выход 129.8%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwas heated
  2. 2
    Температураto reflux for 24 h
  3. 3
    ТемператураAfter cooling
  4. 4
    Фильтрацияthe resulting white solids were collected by filtration
  5. 5
    Промывкаwashed with ethyl acetate and dichloromethane

Методика

A mixture of compound 1,2-dimethyl-1H-benzimidazole (2.93 g, 20 mmol) and N,N′-(disulfanediyldiethane-2,1-diyl)bis(2-chloroacetamide) (1.53 g, 5 mmol) in 20 ml of acetonitrile was heated to reflux for 24 h. After cooling, the resulting white solids were collected by filtration and washed with ethyl acetate and dichloromethane to afford 1.94 g of a white powder. Analyses were in accordance with the expected structure.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07727287B2uspto-grants-2010_06