Реакция #3671

ord-b059c77beaae4653998ed401d032340b

Уравнение реакции

O
Water
Cc1ccc(F)cc1C(=O)Nc1ccc(C(=O)Cl)c(Cl)c1
4-[(2-methyl-5-fluorobenzoyl)amino]-2-chlorobenzoyl chloride
c1ccc2c(c1)Cn1cccc1CN2
10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
Cc1c(F)cccc1C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)c(Cl)c1
glass
Cc1c(F)cccc1C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)c(Cl)c1
N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)-3-chlorophenyl]-3-fluoro-2-methylbenzamide

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураWhile cooling in an ice bath
  2. 2
    Промывкаthe separated organic layer washed with saturated sodium bicarbonate
  3. 3
    Сушкаdried with Na2SO4
  4. 4
    ДругоеThe methylene chloride is removed in vacuo

Методика

To a solution of 1.50 g of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine in 25 ml of methylene chloride is added 1.23 g of N,N-diisopropylethylamine. While cooling in an ice bath, a solution of 3.08 g of [4-[(2-methyl-5-fluorobenzoyl)amino]-2-chlorobenzoyl chloride in 50 ml of methylene chloride is added. The reaction mixture becomes homogeneous and is stirred at room temperature for 18 hours. Water is added and the separated organic layer washed with saturated sodium bicarbonate, dried with Na2SO4 and passed through a short pad of hydrous magnesium silicate two times. The methylene chloride is removed in vacuo to give 3.81 g of a glass. A sample is crystallized from ethyl acetate to give crystalline solid, m.p. 200°-205° C.

Источник

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