反应 #70244

反应方程式

4-Methylsulfonyl-piperidine hydrochloride

sodium tert-butoxide

4-bromo-1-(2-(methylthio)pyrimidin-4-yl)-1H-indole

→

desired compound

收率 43.6%

4-(4-methanesulfonyl-piperidin-1-yl)-1-(2-methylsulfanyl-pyrimidin-4-yl)-1H-indole

收率 43.6%

溶剂

dioxane

dioxane

dioxane

反应条件

后处理

1. 1
   其他the mixture was bubbled with argon for 10 minutes
2. 2
   其他The mixture was bubbled with argon for 5 minutes
3. 3
   其他sealed
4. 4
   其他The sealed thick wall bottle was put into oil bath at 65° C.
5. 5
   workup.STIRRINGThe mixture was stirred at 120° C. for 1.5 hr
6. 6
   温度The resulting mixture was cooled to 50° C.
7. 7
   过滤filtered through a thin layer of Celite
8. 8
   洗涤rinsed with dioxane (100 mL)
9. 9
   浓缩The filtrate was concentrated
10. 10
    萃取extracted with dichloromethane and saturated ammonium chloride solution
11. 11
    其他The organic layer was dried
12. 12
    浓缩concentrated to a volume about 25 mL
13. 13
    workup.ADDITIONThe mixture was treated with ethyl acetate (150 mL)
14. 14
    过滤the yellow solid was filtered

实验过程

4-Methylsulfonyl-piperidine hydrochloride (6.89 g, 34.5 mmol) was grinded into fine powder and mixed with fine powder of sodium tert-butoxide (7.65 g, 79.6 mmol) in dry dioxane (180 mL). After 30 minutes of stirring, 4-bromo-1-(2-(methylthio)pyrimidin-4-yl)-1H-indole (8.5 g, 26.5 mmol) was added followed by dry dioxane (10 mL) and the mixture was bubbled with argon for 10 minutes. Bis(tri-tert-butylphosphine)palladium (1.02 g, 2.0 mmol) was added followed by dry dioxane (10 mL). The mixture was bubbled with argon for 5 minutes and then sealed. The sealed thick wall bottle was put into oil bath at 65° C. and heated to 120° C. The mixture was stirred at 120° C. for 1.5 hr. The resulting mixture was cooled to 50° C. and filtered through a thin layer of Celite, rinsed with dioxane (100 mL). The filtrate was concentrated and extracted with dichloromethane and saturated ammonium chloride solution. The organic layer was dried and concentrated to a volume about 25 mL. The mixture was treated with ethyl acetate (150 mL) and the yellow solid was filtered to give the desired compound (4.65 g). The filtrate was concentrated and dissolved in dichloromethane and purified through ISCO flash column chromatography (200 g silica gel, 20% to 100% ethyl acetate in hexanes) to give second batch of desired product as a yellow solid (1.67 g, combined total 6.32 g, yield 59.1%). LC-MS calcd for C19H22N4O2S2 (m/e) 402.12, obsd 402.9 (M+H).

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