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1,2-Dimethoxyethane → Imidazo(4,5-b)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Aminopyridine | HCID 10439 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 生成物 | Imidazo(4,5-b)pyridine | HCID 67504 | — |
反応手順
Imidazopyridine salt E-3 is prepared from aminopyridine E-1 (also D-1) (refer to Chart D) (commercial source) or the amino pyridine A-2 (refer to Chart A) and dihaloacetone E-2 (Aldrich) either by a two-step procedure whereby E-1 and E-2 are stirred in a solvent such as dimethoxyethane with or without the addition of a base such as triethylamine or potassium carbonate to give imidazopyridine salt E-3. If dimethoxyethane alone is used as solvent, it is then replaced with alcoholic solvent and E-3 is heated until no additional E-4 is formed.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06013654 |
| 出典データセット | uspto-grants-2000_01 |
| ORD ID | ord-9a8146e705ca467fa81e6b7e20e0288b |
| 出典メモ | uspto-grants-2000_01 |