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HRID 1690726作成日:2026年10月27日

Methyl iodide → 4-(5-Methoxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one

https://huagongshe.com/reaction/1690726

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物4-(5-Hydroxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-oneHCID 57781122—
溶媒DimethylformamideHCID 6228—
生成物4-(5-Methoxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-oneHCID 24802691—

反応手順

To a solution of 4-(5-hydroxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one (0.125 g, 0.495 mmol) (Example 6d) in DMF (2 mL) is added sodium hydride (0.018 g, 0.495 mmol). The reaction mixture is stirred at room temperature for 5 min and then methyl iodide (0.028 mL, 0.495 mmol) is added. The reaction is stirred for 2.5 h at room temperature. It is then washed with water and extracted with ethyl acetate twice. The organic layer is dried over Na2SO4 and concentrated in vacuo. The residue is purified by silica gel chromatography (dichloromethane-methanol, 19:1) to give 4-(5-methoxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one; MS (ESI) m/z 287.2 (M+H); 1H NMR (400 MHz, MeOD) δ ppm 1.70 (s, 3H), 1.77 (s, 3 H), 3.90 (s, 3 H), 4.39 (s, 2 H), 4.88 (br. s, 1 H), 6.99 (s, 1 H), 7.44-7.53 (m, 1H), 7.56-7.64 (m, 2 H), 7.76 (s, 1 H), 7.86 (d, J=7.6 Hz, 1 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08153674B2
出典データセットuspto-grants-2012_04
ORD IDord-42d2962b92d64e009480798e2fa586b5
出典メモuspto-grants-2012_04