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2-Amino-4-methylpyridine → 2-(4'-Chloropropoxy-2'-methylphenyl)-7-methylimidazo[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 | alpha-Bromo-2'-methyl-4'-chloropropoxyacetophenone | HCID 22015662 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Dichloromethane methanol | HCID 21226129 | — |
| 生成物 | 2-(4'-Chloropropoxy-2'-methylphenyl)-7-methylimidazo[1,2-a]pyridine | HCID 22015639 | — |
反応手順
A solution of the product of Step B (6.77 g) and 2-amino-4-picoline (2.4 g) in ethanol (22 mL) was heated at 72° C. for 10 hours. The reaction mixture was cooled to ambient temperature and dissolved in methanol/dichloromethane and treated with Dowex® 550A basic resin until the pH of the mixture was 7. The resin was removed via filtration and the filtrate evaporated. The title compound was precipitated from ethyl acetate upon addition of hexanes and used without further purification.
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-9e3c8858286e46a0b9d74b5d94f6f030 |
| 出典メモ | uspto-grants-2006_08 |