参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 反应物 | 2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-iodobenzaldehyde | HCID 23078419 | — |
| 反应物 | HCID 178418443 | HCID 178418443 | — |
| 溶剂 | 四氢呋喃 | HCID 8028 | — |
| 产物 | 1-{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-iodophenyl}-1-propanol | HCID 68832550 | — |
反应步骤
2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-iodobenzaldehyde was dissolved in anhydrous tetrahydrofuran (1 ml) to prepare a solution. A 1 M tetrahydrofuran solution (0.5 ml) of ethylmagnesium bromide was added to the solution at 0° C., and the mixture was stirred at 0° C. for one hr. Water (1 ml) was added dropwise to the reaction solution to stop the reaction. The mixture was extracted with ethyl acetate, and the ethyl acetate layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure to give 1-{2-[(6,7-dimethoxy-4-quinolyl)oxy]-5-iodophenyl}-1-propanol.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07560558B2 |
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| 来源数据集 | uspto-grants-2009_07 |
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| ORD ID | ord-4ad7f767f5a347988f581a69730af127 |
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| 来源说明 | uspto-grants-2009_07 |
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