Reaktion #1685423

Reaktionsgleichung

5,10-dihydro-4H-pyrazolo[5,1-c][1,4]benzodiazepine

4-[(5-fluoro-2-methylbenzoyl)amino]-2-chlorobenzoyl chloride

diisopropylethylamine

→

N-[4-(4H-Pyrazolo[5,1-c][1,4]benzodiazepin-5(10H)ylcarbonyl)-3-chlorophenyl]-5-fluoro-2-methylbenzamide

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   WaschenThe mixture is washed with H2 O, 1N HCl, H2O, 1M NaHCO3, brine
2. 2
   Trocknendried (Na2SO4)
3. 3
   Waschenthe filter cake washed with dichloromethane
4. 4
   EinengenThe filtrate is concentrated
5. 5
   Sonstigethe solid crystallized from ethyl acetate
6. 6
   Sonstigeto give crystals, m.p. 137°-140° C.

Vorschrift

A mixture of 0.185 g of 5,10-dihydro-4H-pyrazolo[5,1-c][1,4]benzodiazepine, 0.391 g of 4-[(5-fluoro-2-methylbenzoyl)amino]-2-chlorobenzoyl chloride and 0.158 g of diisopropylethylamine in 10 ml of dichloromethane is stirred at room temperature overnight. The mixture is washed with H2 O, 1N HCl, H2O, 1M NaHCO3, brine and dried (Na2SO4). The solution is passed through a thin pad of hydrous magnesium silicate and the filter cake washed with dichloromethane. The filtrate is again passed through a thin pad of hydrous magnesium silicate. The filtrate is concentrated and the solid crystallized from ethyl acetate to give crystals, m.p. 137°-140° C.

Quelle