Réaction #3671

ord-b059c77beaae4653998ed401d032340b

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureWhile cooling in an ice bath
  2. 2
    Lavagethe separated organic layer washed with saturated sodium bicarbonate
  3. 3
    Séchagedried with Na2SO4
  4. 4
    AutreThe methylene chloride is removed in vacuo

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05733905uspto-grants-1998_03