Реакция #7601

ord-cbd7290e07da4dfdac2dff3ae8a033b9

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe solid was filtered off
  2. 2
    Промывкаwashed with isopropanol
  3. 3
    Сушкаether and dried under vacuum

Методика

A solution of 4-chloro-7-(2-methoxyethoxy)cinnoline (156 mg, 0.65 mmol) and 2-fluoro-5-hydroxy-4-methylaniline (111 mg, 0.78 mmol), (prepared as described for the starting material in Example 11), in 2-pentanol (8 ml) and 5M isopropanolic hydrogen chloride (1 ml) was heated at 120° C. for 2.5 hours. The solid was filtered off, washed with isopropanol and then ether and dried under vacuum to give 4-(2-fluoro-5-hydroxy-4-methylanilino)-7-(2-methoxyethoxy)cinnoline hydrochloride (207 mg, 84%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07087602B2uspto-grants-2006_08