反应 #2267087

反应方程式

iodine

(rac)-2-(2,3,5,6-tetrahydro[1,4]oxazino[2,3,4-hi]indol-6-ylmethyl)-1H-isoindole-1,3(2H)-dione

iodine

iodine

→

title compound

(rac)-2-[(8-iodo-2,3,5,6-tetrahydro[1,4]oxazino[2,3,4-hi]indol-6-yl)methyl]-1H-isoindole-1,3(2H)-dione

溶剂

CHCl3

CHCl3

CHCl3

CHCl3

反应条件

后处理

1. 1
   workup.STIRRINGThe mixture was stirred at rt for 4 h
2. 2
   workup.STIRRINGAfter stirring for another 2 h
3. 3
   过滤the mixture was filtered through a pad of celite
4. 4
   洗涤washed with CHCl3
5. 5
   洗涤The filtrate was washed with Na2SO3 solution
6. 6
   干燥dried (MgSO4)
7. 7
   过滤After filtration
8. 8
   浓缩the filtrate was concentrated in vacuo to dryness

实验过程

To a suspension of (rac)-2-(2,3,5,6-tetrahydro[1,4]oxazino[2,3,4-hi]indol-6-ylmethyl)-1H-isoindole-1,3(2H)-dione (0.081 g, 0.253 mmol) and silver trifluoroacetate (0.059 g, 0.266 mmol) in CHCl3 (2.0 mL) was added a solution of iodine (0.067 g, 0.266 mmol) in CHCl3 (8.0 mL) dropwise at rt. The mixture was stirred for 68 h. Silver trifluoroacetate (0.03 g, 0.136 mmol) and solution of iodine (0.035 g, 0.136 mmol) in CHCl3 (6.0 mL) were added. The mixture was stirred at rt for 4 h and added again silver trifluoroacetate (0.02 g, 0.09 mmol) and solution of iodine (0.025 g, 0.10 mmol) in CHCl3 (5.0 mL). After stirring for another 2 h, the mixture was filtered through a pad of celite and washed with CHCl3. The filtrate was washed with Na2SO3 solution and dried (MgSO4). After filtration, the filtrate was concentrated in vacuo to dryness and the residue was subjected to prep TLC (EtOAc/hexane, 1:2) to give 0.046 g (41%) of light yellow oil as the title compound: 1H NMR (400 MHz, CDCl3) δ 7.81-7.78 (m, 2 H), 7.69-7.65 (m, 2 H), 6.98 (s, 1 H), 6.86 (s, 1 H), 4.34-4.29 (m, 2 H), 3.91-3.80 (m, 2 H), 3.62-3.58 (m, 1 H), 3.24-3.14 (m, 2 H), 3.04-3.00 (m, 1 H), 2.97-2.92 (m, 1 H); MS (EI) m/z 447 (M++H).

来源