関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | 6-bromo-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridine | HCID 57609300 | — |
| 溶媒 | Ethylene Glycol | HCID 174 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 6-Methoxy-5-(4-methyl-1H-imidazol-1-YL)pyridin-2-amine | HCID 53402967 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08637525B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-2bf927a7ae0046eca44869718d36c643 |
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| 出典メモ | uspto-grants-2014_01 |
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