Реакция #3660

ord-f0f4f088cd0d48ca83f5762cc569ed4f

Уравнение реакции

Cc1cc(C(=O)N2Cc3cccn3Cc3ccccc32)ccc1N
10,11-dihydro-10-(3-methyl-4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine
O=C(Cl)c1ccc(Cl)cc1Cl
2,4-dichlorobenzoyl chloride
CCN(C(C)C)C(C)C
diisopropylethylamine
Cc1cc(C(=O)N2Cc3cccn3Cc3ccccc32)ccc1NC(=O)c1ccc(Cl)cc1Cl
crystals
Выход 84.1%
Cc1cc(C(=O)N2Cc3cccn3Cc3ccccc32)ccc1NC(=O)c1ccc(Cl)cc1Cl
N-[4-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)-2-methylphenyl]-2,4-dichlorobenzamide
Выход 84.1%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ПромывкаThe mixture is washed with water
  2. 2
    Сушкаdried (MgSO4)
  3. 3
    КонцентрированиеThe filtrate is concentrated
  4. 4
    workup.ADDITIONhexane added
  5. 5
    Другоеto give crystals
  6. 6
    ДругоеRecrystallization from dichloromethane-hexane

Методика

A mixture of 0.40 g of 10,11-dihydro-10-(3-methyl-4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine, 0.40 g of 2,4-dichlorobenzoyl chloride and 0.75 g of diisopropylethylamine in 50 ml of dichloromethane is stirred at room temperature for 16 hours. The mixture is washed with water, dried (MgSO4) and the solution passed through a thin pad of hydrous magnesium silicate. The filtrate is concentrated and hexane added to give crystals. Recrystallization from dichloromethane-hexane gives 0.52 g of crystals, m.p. 213°-215° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05733905uspto-grants-1998_03