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2-Amino-4-methylpyridine → 2-[3-(3-Chloro-propoxy)-phenyl]-7-methyl-imidazo[1,2-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Amino-4-methylpyridine | HCID 1533 | — |
| 反応物 | 2-Bromo-1-[3-(3-chloro-propoxy)-phenyl]-ethanone | HCID 22015592 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-[3-(3-Chloro-propoxy)-phenyl]-7-methyl-imidazo[1,2-a]pyridine | HCID 22015609 | 48.7% |
反応手順
A solution of the product of Step B (2.6 g) and 2-amino-4-picoline (0.96 g) in ethanol (10 mL) was heated at 73° C. for 2 hours. The reaction mixture was cooled to ambient temperature and the solvent evaporated in vacuo. The residue was dissolved in dichloromethane (75 mL), washed with saturated sodium bicarbonate solution (2×75 mL), brine (75 mL), dried over magnesium sulfate, filtered and evaporated. The residue was purified via silica gel chromatography (ethyl acetate/hexane) to give the title compound (1.3 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07087757B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-47a419c279bd4298997bf49bc82a7f5a |
| 出典メモ | uspto-grants-2006_08 |