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HRID 1715613生成日期:2026年10月23日

碘化钠 → 5-(2,4-difluorophenoxy)-1-isobutyl-6-(piperidin-4-ylmethoxy)-1H-indazole

https://huagongshe.com/zh-CN/reaction/1715613

反应方程式

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-olHCID 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-indazoleHCID 4261114039.3%

反应条件

温度70 °C

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

DOI10.6084/m9.figshare.5104873.v1
专利号US07799782B2
来源数据集uspto-grants-2010_09
ORD IDord-227dd0eef5ea49f4bb697e42853ff06a
来源说明uspto-grants-2010_09