Реакция #78819

ord-45b050ef2cc34fdbb9b9b60df9738e49

Уравнение реакции

Clc1nc(Nc2ccccc2)c2ccccc2n1
2-chloro-4-phenylamino-quinazoline
CNS(=O)(=O)Cc1ccc(N)cc1
N-methyl-(4-aminophenyl)-methanesulfonamide
CNS(=O)(=O)Cc1ccc(Nc2nc(Nc3ccccc3)c3ccccc3n2)cc1.Cl
N-methyl-[4-(4-phenylamino-quinazolin-2-ylamino)-phenyl]-methanesulfonamide hydrochloride

Растворители

Условия реакции

Температура
170°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe warm reaction mixture
  2. 2
    Другоеthe hydrochloride salt, which is crystallizing
  3. 3
    Температураon cooling
  4. 4
    Фильтрацияis filtered off

Методика

A solution of 2-chloro-4-phenylamino-quinazoline (0.92 g) (prepared as described in Example 1a and N-methyl-(4-aminophenyl)-methanesulfonamide (0.80 g) in 10 ml of isopentylalcohol is stirred under nitrogen at 170° C. for 15 min in a sealed vessel. The warm reaction mixture is diluted with 10 ml ethanol and the hydrochloride salt, which is crystallizing on cooling, is filtered off to yield N-methyl-[4-(4-phenylamino-quinazolin-2-ylamino)-phenyl]-methanesulfonamide hydrochloride as light yellow crystals melting at 259-263° C.; Rf (A2) 0.11, FAB-MS: (M+H)+=420. Analytical data: C22H21N5O2S+HCl.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06713265B1uspto-grants-2004_03