Реакция #2146773

ord-2f73221be65042c0b0c23944c7e81392

Уравнение реакции

COc1ccc(Cn2ccc3cc(O[C@H]4CCN(C(=O)OC(C)(C)C)C4)c(C)cc3c2=O)cc1
(S)-3-[2-(4-Methoxy-benzyl)-7-methyl-1-oxo-1,2-dihydro-isoquinolin-6-yloxy]-pyrrolidine-1-carboxylic acid tert-butyl ester
O=C(O)C(F)(F)F
trifluoroacetic acid
Cc1cc2c(=O)[nH]ccc2cc1O[C@H]1CCNC1
7-Methyl-6-((S)-pyrrolidin-3-yloxy)-2H-isoquinolin-1-one
Выход 87.3%

Условия реакции

Температура
150°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.DISTILLATIONThen the excess trifluoroacetic acid was distilled off in vacuo
  2. 2
    workup.ADDITIONthe residue was diluted with 10 ml 1 M hydrochloric acid
  3. 3
    ПромывкаThe aqueous phase was washed with methylene chloride twice
  4. 4
    Другоеdried

Методика

0.54 g (1.2 mmol) (S)-3-[2-(4-Methoxy-benzyl)-7-methyl-1-oxo-1,2-dihydro-isoquinolin-6-yloxy]-pyrrolidine-1-carboxylic acid tert-butyl ester were dissolved in 2.7 g (23 mmol) trifluoroacetic acid. After 1 h at room temperature the mixture was heated for 2 h in a microwave oven at 150° C. Then the excess trifluoroacetic acid was distilled off in vacuo and the residue was diluted with 10 ml 1 M hydrochloric acid. The aqueous phase was washed with methylene chloride twice and then it was freeze dried to give 0.256 g 7-Methyl-6-((S)-pyrrolidin-3-yloxy)-2H-isoquinolin-1-one as the hydrochloride. Rt=0.90 min (Method B). Detected mass: 245.2 (M+H+).

Источник

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