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HRID 475721作成日:2026年10月25日

Ammonia → 6-Methoxy-5-(4-methyl-1H-imidazol-1-YL)pyridin-2-amine

https://huagongshe.com/reaction/475721

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物MethanolHCID 887—
反応物6-bromo-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridineHCID 57609300—
溶媒Ethylene GlycolHCID 174—
溶媒WaterHCID 962—
生成物6-Methoxy-5-(4-methyl-1H-imidazol-1-YL)pyridin-2-amineHCID 53402967100%

反応条件

温度100 °C

反応手順

To a mixture of 6-bromo-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridine (1.000 g, 3.73 mmol) and cuprous oxide (0.053 g, 0.373 mmol) in 8.3 mL of ethylene glycol was added a 7 N solution of ammonia in methanol (7.99 mL, 55.9 mmol). The reaction mixture was heated in a high-pressure vessel at 100° C. overnight. Upon cooling to room temperature, the reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate and filtered. The solvent was removed in vacuum to give 6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-amine (762.0 mg, 3.73 mmol, 100% yield) as brown semisold. LC-MS (M+H)+=205.10. 1H NMR (500 MHz, CDCl3) δ ppm 7.53 (1H, s), 7.26 (1H, d, J=8.2 Hz), 6.78 (1H, s), 6.07 (1H, d, J=8.2 Hz), 3.86 (3H, s.), 2.25 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637525B2
出典データセットuspto-grants-2014_01
ORD IDord-2bf927a7ae0046eca44869718d36c643
出典メモuspto-grants-2014_01