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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2262115생성일: 2026년 10월 26일

Potassium Iodide → (2-(1H-indol-4-yl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-N-methyl,N-(3-morpholinopropylsulfonyl)methanamine

https://huagongshe.com/reaction/2262115

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물MorpholineHCID 8083—
반응물Potassium CarbonateHCID 11430—
반응물3-chloro-propane-1-sulfonic acid [2-(1H-indol-4-yl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl]-methyl-amideHCID 67190012—
용매AcetonitrileHCID 6342—
생성물(2-(1H-indol-4-yl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-N-methyl,N-(3-morpholinopropylsulfonyl)methanamineHCID 59593013—

반응 조건

온도80 °C

반응 단계

To a solution of 3-chloro-propane-1-sulfonic acid [2-(1H-indol-4-yl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl]-methyl-amide (18 mg) in acetonitrile (1 mL) at room temperature was added morpholine (15 μL), potassium carbonate (7 mg) and potassium iodide (2 mg). The reaction mixture was stirred at 80° C. for 72 h and allowed to cool to room temperature before quenching with water (30 mL) and extracting into dichloromethane (2×30 mL). The combined organics were washed with brine (30 mL), dried (MgSO4), reduced in vacuo and purified by column chromatography to give the title compound as an off-white solid (7 mg). NMR: CDCl3: 1.96 (m, 2H), 2.43-2.37 (m, 6H), 2.87 (s, 3H), 3.05 (m, 2H), 3.84 (t, J=4.8, 4H), 4.01 (t, J=4.8, 4H), 4.60 (s, 2H), 7.21-7.27 (m, 2H), 7.39 (s, 1H), 7.42-7.47 (m, 2H), 8.11 (d, J=7.2, 1H), 8.25 (s, 1H). MS: (ESI+): MH+ 571

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07846929B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-b0a48a7be94e499c89bdf181dba441b0
출처 메모uspto-grants-2010_12