Реакция #323010
ord-4ed7c62a3b6340d280c753bb6995acab
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Температура
4°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ПромывкаAfter treatment with caustic soda and washing
- 2Другоеthe product produced (24 g; m.p. 202° C.)
- 3workup.DISSOLUTIONis dissolved
- 4Другоеthe crystallised solid is separated by filtration
- 5Промывкаwashed with ethanol (2×15 cc)
- 6Другоеdried at 40° C. under reduced pressure (0.067 kPa)
Методика
The procedure is similar to that described in Example 37, but starting with 2-amino-7-chloro-1,8-naphthyridine (18 g), 2-fluorophenol (44.8 g) and potassium hydroxide pellets (13.2 g; 85% purity). After treatment with caustic soda and washing, the product produced (24 g; m.p. 202° C.) is dissolved in boiling ethanol (200 cc). After 16 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with ethanol (2×15 cc) and dried at 40° C. under reduced pressure (0.067 kPa). 2-Amino-7-(2-fluorophenoxy)-1,8-naphthyridine (14.9 g) is produced, m.p. 206° C.