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HRID 849478作成日:2026年10月23日

1,2-Dimethoxyethane → Imidazo(4,5-b)pyridine

https://huagongshe.com/ja/reaction/849478

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethoxyethaneHCID 8071—
反応物TriethylamineHCID 8471—
反応物2-AminopyridineHCID 10439—
反応物Potassium CarbonateHCID 11430—
生成物Imidazo(4,5-b)pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06013654
出典データセットuspto-grants-2000_01
ORD IDord-9a8146e705ca467fa81e6b7e20e0288b
出典メモuspto-grants-2000_01