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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2112182생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2112182

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-NaphthylalanineHCID 185915—
반응물1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidineHCID 10642851—
반응물5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-olHCID 136163662—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물5-(2,4-difluorophenoxy)-1-isobutyl-6-(piperidin-4-ylmethoxy)-1H-indazoleHCID 4261114039.3%

반응 조건

온도70 °C

반응 단계

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 Nal (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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07521447B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-5db3053aa1d4415390a3041fe30bc36e
출처 메모uspto-grants-2009_04