Реакция #1605837

Уравнение реакции

isobutyryl chloride

aripiprazole

diisopropylamine

n-BuLi

→

7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1-isobutyryl-3,4-dihydroquinolin-2(1H)-one

Растворители

tetrahydrofuran

Условия реакции

Обработка

1. 1
   Температураwas re-cooled to 78° C.
2. 2
   ТемператураAfter 2 h the reaction mixture was warmed to room temperature
3. 3
   workup.STIRRINGstirred for 1 h
4. 4
   ДругоеA second reaction
5. 5
   ПромывкаThis mixture was washed with water
6. 6
   Сушкаdried over MgSO4
7. 7
   Фильтрацияfiltered
8. 8
   Другоеevaporated
9. 9
   workup.DISSOLUTIONThe residue was dissolved in diethyl ether
10. 10
    workup.ADDITION4M HCl in diethyl ether added
11. 11
    Другоеto form a precipitate
12. 12
    ДругоеThe mother liquor was decanted
13. 13
    Промывкаthe residual gum was washed with diethyl ether
14. 14
    ДругоеThe gum was then partitioned between ethyl acetate and saturated sodium bicarbonate
15. 15
    Другоеthe organic layer separated
16. 16
    СушкаAfter drying over MgSO4 and evaporation
17. 17
    Другоеthe residue was further purified on silica eluting with 1:1:0.1 dichloromethane/ethyl acetate/methanol
18. 18
    Другоеto give Compound-16 (1.3 g) as a yellow solid

Методика

To a solution of diisopropylamine (1.3 mL, 8.9 mmol) in tetrahydrofuran (25 mL) at 78° C. was added n-BuLi (2.2M in hexanes, 4.1 mL, 8.9 mmol). The reaction mixture was warmed to 0° C. and after 10 min was re-cooled to 78° C. and aripiprazole (2.0 g, 4.5 mmol) added. The reaction mixture was stirred for 30 min and then isobutyryl chloride (0.7 mL, 6.7 mmol) added. After 2 h the reaction mixture was warmed to room temperature and stirred for 1 h. A second reaction was carried out under exactly the same conditions and the two reactions were combined. This mixture was washed with water, dried over MgSO4, filtered and evaporated. The residue was dissolved in diethyl ether and 4M HCl in diethyl ether added to form a precipitate. The mother liquor was decanted and the residual gum was washed with diethyl ether. The gum was then partitioned between ethyl acetate and saturated sodium bicarbonate, and the organic layer separated. After drying over MgSO4 and evaporation, the residue was further purified on silica eluting with 1:1:0.1 dichloromethane/ethyl acetate/methanol to give Compound-16 (1.3 g) as a yellow solid.

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