Реакция #2146771

ord-e58dfde0a0374274af02074f24a4e936

Уравнение реакции

OC1CCCNCC1
azepan-4-ol
[H-].[Na+]
sodium hydride
COc1ccc(Cn2ccc3cc(F)c(C)cc3c2=O)cc1
6-fluoro-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one
O
water
COc1ccc(Cn2ccc3cc(F)c(C)cc3c2=O)cc1
6-fluoro-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one
OC1CCCNCC1
azepan-4-ol
[H-].[Na+]
sodium hydride
COc1ccc(Cn2ccc3cc(OC4CCCNCC4)c(C)cc3c2=O)cc1
6-(azepan-4-yloxy)-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one
Выход 41.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеwas obtained
  2. 2
    Другоеwas isolated by filtration
  3. 3
    Другоеdried overnight in vacuum

Методика

A solution of 58 mg (0.51 mmol) azepan-4-ol in 5 ml dimethylacetamide was stirred with 45 mg (1.52 mmol) 80 percent sodium hydride for 45 minutes at room temperature. Then 150 mg (0.51 mmol) 6-fluoro-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one in dimethylacetamide was added. The reaction mixture was heated to 80° C. for 3 days during which additional amounts of azepan-4-ol and sodium hydride were added until complete conversion of the 6-fluoro-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one was obtained. The reaction mixture was slowly added to 10 ml water and after 1 h of stirring the product was isolated by filtration and dried overnight in vacuum. 82 mg of 6-(azepan-4-yloxy)-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one were obtained.

Источник

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