Реакция #2146766

ord-45b9030d93c5416ab4974e38ef3e7cfa

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe solvent was removed i
  2. 2
    workup.DISSOLUTIONand the residue was dissolved in water
  3. 3
    workup.ADDITIONby adding 2 N HCl
  4. 4
    ФильтрацияFiltration of the precipitate
  5. 5
    Другоеdrying

Методика

1.56 g (4.27 mmol) [4-(7-Chloro-1-oxo-1,2-dihydro-isoquinolin-6-yloxy)-piperidin-1-yl]-acetic acid ethyl ester (41) were dissolved in 20 mL of methanol and 20 ml of 2N NaOH were added. After stirring for 1 h at room temperature, the solvent was removed i. vac. and the residue was dissolved in water. The aqueous solution was neutralized by adding 2 N HCl. Filtration of the precipitate and drying gave 856 mg of the title compound. Rt=0.82 min (Method B). Detected mass: 337.1 (M+H+).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08278294B2uspto-grants-2012_10