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HRID 2262115作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物MorpholineHCID 8083—
反応物Potassium CarbonateHCID 11430—
反応物3-chloro-propane-1-sulfonic acid [2-(1H-indol-4-yl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl]-methyl-amideHCID 67190012—
溶媒AcetonitrileHCID 6342—
生成物(2-(1H-indol-4-yl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-N-methyl,N-(3-morpholinopropylsulfonyl)methanamineHCID 59593013—

反応条件

温度80 °C

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07846929B2
出典データセットuspto-grants-2010_12
ORD IDord-b0a48a7be94e499c89bdf181dba441b0
出典メモuspto-grants-2010_12