反应 #991

反应方程式

(R)-4-methyl-3-pyridin-2-yl-[1,2,3]-oxathiazolidine-2,2-dioxide

4-piperazinoindole

→

(R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine

收率 67.5%

溶剂

acetonitrile

反应条件

后处理

1. 1
   其他then evaporated in vacuo
2. 2
   温度cooled
3. 3
   洗涤washed with ethyl acetate (2×100 ml)
4. 4
   萃取extracted into dichioromethane (3×100 ml)
5. 5
   干燥dried (MgSO4)
6. 6
   其他then evaporated in vacuo
7. 7
   其他to give a brown glass
8. 8
   其他This was purified on a silica column
9. 9
   洗涤eluting with 10% propan-2-ol in dichloromethane

实验过程

A solution of (R)-4-methyl-3-pyridin-2-yl-[1,2,3]-oxathiazolidine-2,2-dioxide (4.04 g 0.019 moles) and 4-piperazinoindole (3.80 g 0.019 moles) in acetonitrile (200 ml) was heated to 60° C. for 0.5 h then evaporated in vacuo. The residue was taken up into dilute HCl (100 ml), warmed to 60° C. for 0.5 h, cooled, washed with ethyl acetate (2×100 ml), made basic with potassium carbonate, extracted into dichioromethane (3×100 ml), dried (MgSO4) then evaporated in vacuo to give a brown glass. This was purified on a silica column eluting with 10% propan-2-ol in dichloromethane to give (R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine (4.3 g) as a clear glass.

来源