Реакция #2336518

ord-090e5247b0a549bb915a20b3649cda76

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe mixture was quenched with conc. HCl (1 mL)
  2. 2
    Экстракцияextracted with EtOAc (2×20 mL)
  3. 3
    ЭкстракцияThe combined organic extract
  4. 4
    Сушкаwas dried (MgSO4)
  5. 5
    Концентрированиеconcentrated

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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE039991E1uspto-grants-2008_01