Реакция #91569

ord-ccba2ea0d9d942d7ab0a3ba174906e24

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted with ethyl acetate
  2. 2
    СушкаThe organics were dried over sodium sulphate
  3. 3
    Концентрированиеconcentrated in vacuo

Методика

To an ice cooled solution of, 1,1-dimethylethyl 7-(5-chloro-2-{[(4-methyl-2-pyridinyl)methyl]oxy}phenyl)-3,4-dihydro-2(1H)-isoquinolinecarboxylate, (0.28 g) in DCM (1 ml) was added TFA (1 ml) and this was stirred at room temperature overnight. The reaction mixture was dissolved in water and backwashed with ethyl acetate. The aqueous layer was neutralised with aqueous sodium bicarbonate and extracted with ethyl acetate. The organics were dried over sodium sulphate and concentrated in vacuo to yield the title compound, 0.12 g

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09447074B2uspto-grants-2016_09