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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38863생성일: 2026년 10월 24일

Sodium Iodide → 6-(1H-Indol-4-yl)-4-[5-({4-[2-(4-morpholinyl)ethyl]-1-piperazinyl}methyl)-1,3,4-oxadiazol-2-yl]-1H-indazole

https://huagongshe.com/ko/reaction/38863

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참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium HydroxideHCID 14798—
반응물DiisopropylethylamineHCID 81531—
반응물4-(2-Piperazin-1-yl-ethyl)-morpholineHCID 2734640—
반응물4-[5-(Chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazoleHCID 66776954—
용매IsopropanolHCID 3776—
용매AcetonitrileHCID 6342—
생성물6-(1H-Indol-4-yl)-4-[5-({4-[2-(4-morpholinyl)ethyl]-1-piperazinyl}methyl)-1,3,4-oxadiazol-2-yl]-1H-indazoleHCID 6677678150.5%

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온도70 °C

반응 단계

4-[2-(1-piperazinyl)ethyl]morpholine (14.1 mg, 0.11 mmol) and 4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazole (50 mg, 0.102 mmol) were dissolved in acetonitrile (0.5 ml) and N,N-diisopropylethylamine (0.026 ml, 0.15 mmol) was added, followed by sodium iodide (15.3 mg, 0.102 mmol). The solution was stirred at 70° C. for 18 h and blown to dryness under a stream of nitrogen. Isopropanol (0.3 ml) was added followed by 2M sodium hydroxide (0.3 ml) and stirred for 5 h when the mixture was neutralised and the solvent removed under a stream of nitrogen. The crude product was dissolved in dimethylsulphoxide (0.3 ml) and methanol (0.15 ml) with formic acid (0.05 ml) then purified by Mass Directed Automated Preparative HPLC (Method F) to give the title compound (26.4 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524751B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a395d4ab713344a8a1db6a2018ac61b2
출처 메모uspto-grants-2013_09