Реакция #46138

Уравнение реакции

1,5-dibromopentane

1,5-dibromopentane

3-(2-aminoethyl)-6-methoxy-2-methyl-4-phenylisoquinolin-1(2H)-one hydrochloride

triethylamine

→

HCl

6-Methoxy-2-methyl-4-phenyl-3-(2-piperidin-1-ylethyl)isoquinolin-1(2H)-one hydrochloride

Растворители

2-methyl-2-propanol

Условия реакции

Обработка

1. 1
   ТемператураAfter cooling to room temperature
2. 2
   Концентрированиеthe mixture was concentrated in vacuo
3. 3
   ДругоеThe crude residue was purified by preparative reversed phase HPLC
4. 4
   КонцентрированиеThe pure fractions were concentrated in vacuo
5. 5
   Промывкаwashed with saturated NaHCO3 solution and brine
6. 6
   Сушкаdried over Na2SO4
7. 7
   Фильтрацияfiltered
8. 8
   Концентрированиеconcentrated in vacuo
9. 9
   workup.ADDITIONtreated with excess ethereal HCl
10. 10
    Концентрированиеconcentrated in vacuo

Методика

To a solution of 3-(2-aminoethyl)-6-methoxy-2-methyl-4-phenylisoquinolin-1(2H)-one hydrochloride (100 mg, 0.290 mmol) in 15 mL of 2-methyl-2-propanol in a pressure tube was added triethylamine (0.142 mL, 1.02 mmol), followed by 1,5-dibromopentane (0.047 mL, 0.348 mmol). The mixture was heated at 150° C. overnight. Another portion of 1,5-dibromopentane was added (0.023 mL), and the heating continued for another 24 hours. After cooling to room temperature, the mixture was concentrated in vacuo. The crude residue was purified by preparative reversed phase HPLC. The pure fractions were concentrated in vacuo, taken up in EtOAc and washed with saturated NaHCO3 solution and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The product was taken up in dichloromethane, treated with excess ethereal HCl, and concentrated in vacuo to provide the HCl salt. Proton NMR for the product was consistent with the titled compound. ESI+MS: 377.19 [M+H]+.

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