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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38862생성일: 2026년 10월 24일

Sodium Iodide → 4-(5-{[(2R,6S)-2,6-Dimethyl-4-morpholinyl]methyl}-1,3,4-oxadiazol-2-yl)-6-(1H-indol-4-yl)-1H-indazole

https://huagongshe.com/ko/reaction/38862

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참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium HydroxideHCID 14798—
반응물DiisopropylethylamineHCID 81531—
반응물2,6-Dimethylmorpholine, cis-HCID 641500—
반응물4-[5-(Chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazoleHCID 66776954—
용매IsopropanolHCID 3776—
용매AcetonitrileHCID 6342—
생성물4-(5-{[(2R,6S)-2,6-Dimethyl-4-morpholinyl]methyl}-1,3,4-oxadiazol-2-yl)-6-(1H-indol-4-yl)-1H-indazoleHCID 667768289%

반응 조건

온도70 °C

반응 단계

(2R,6S)-2,6-Dimethylmorpholine (12.57 mg, 0.11 mmol) and 4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazole (51 mg, 0.104 mmol) were dissolved in acetonitrile (0.5 ml) and N,N-diisopropylethylamine (0.0262 ml, 0.15 mmol) was added, followed by sodium iodide (14.99 mg, 0.1 mmol). The solution was stirred at 70° C. for 18 h and blown to dryness under a stream of nitrogen. Isopropanol (0.5 ml) was added followed by 2M sodium hydroxide (0.5 ml) and stirred for 18 h when the mixture was neutralised and the solvent removed under a stream of nitrogen. The crude product was dissolved in dimethylsulphoxide (0.5 ml) and purified by Mass Directed Automated Preparative HPLC (Method F) and the solvent was evaporated in vacuo using Genevac to give the title compound (4 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524751B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c756c05db4ff44339989f36d54ca88a2
출처 메모uspto-grants-2013_09