参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 碘化钠 | HCID 5238 | — |
| 反应物 | 碳酸钾 | HCID 11430 | — |
| 反应物 | 1-N-BOC-4-(4-甲基苯磺酰氧甲基)哌啶 | HCID 10642851 | — |
| 反应物 | 5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-ol | HCID 136163662 | — |
| 溶剂 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 溶剂 | 乙醚 | HCID 3283 | — |
| 溶剂 | N,N-二甲基甲酰胺 | HCID 6228 | — |
| 产物 | 5-(2,4-difluorophenoxy)-1-isobutyl-6-(piperidin-4-ylmethoxy)-1H-indazole | HCID 42611140 | 39.3% |
反应步骤
To a solution of 5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-ol (0.06 g, 0.19 mmol) and 4-(toluene-4-sulfonyloxymethyl)-piperidine-1-carboxylic acid tert-butyl ester (0.08 g, 0.20 mmol) in DMF (3 mL) was added NaI (0.014 g, 0.009 mmol) and K2CO3 (0.08 g, 0.56 mmol). The reaction mixture was heated to 70° C. for 20 hours. The mixture was diluted with ether and water and the layers were separated. The aqueous layer was extracted with ether (2×) and the combined organic layers were washed with water and brine, and dried over Na2SO4. The crude mixture was concentrated under reduced pressure and purified by reverse phase HPLC. The desired fraction was concentrated to 0.037 g that was then treated with HCl (4N in dioxane) for 7 hours. The solvent was removed under reduced pressure and the final product was dried under high vacuum to obtain 0.031 g solid (37% yield). MS (APCI+) m/z 416 (M+1) detected.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07799782B2 |
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| 来源数据集 | uspto-grants-2010_09 |
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| ORD ID | ord-227dd0eef5ea49f4bb697e42853ff06a |
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| 来源说明 | uspto-grants-2010_09 |
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