Реакция #2336518
ord-090e5247b0a549bb915a20b3649cda76
Уравнение реакции
Реагенты
Нет
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ДругоеThe mixture was quenched with conc. HCl (1 mL)
- 2Экстракцияextracted with EtOAc (2×20 mL)
- 3ЭкстракцияThe combined organic extract
- 4Сушкаwas dried (MgSO4)
- 5Концентрированиеconcentrated
Методика
Ethyl 4-hydroxypyrimidine-5-carboxylate can be prepared following the procedure of M. Pesson et al., Eur. J. Med. Chem.—Chim. Ther. 1974, 9, 585. A solution of this ester (500 mg, 3 mmol) in THF (10 mL) and MeOH (5 mL) was treated with LiOH.H2O (373 mg, 8.9 mmol) and stirred overnight. The mixture was quenched with conc. HCl (1 mL) and extracted with EtOAc (2×20 mL). The combined organic extract was dried (MgSO4) and concentrated to give 260 mg of the title compound 19 as an orange solid, m.p. 220° C. (dec). 4-HYDROXY-2-METHYLPYRIMIDINE-5-CARBOXYLIC ACID (20).