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HRID 515552作成日:2026年10月25日

2-Aminopyridine → N-(5-pyrimidinylmethylene)-2-pyridinamine

https://huagongshe.com/reaction/515552

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminopyridineHCID 10439—
反応物Pyrimidine-5-carboxaldehydeHCID 2761034—
溶媒ChloroformHCID 6212—
生成物N-(5-pyrimidinylmethylene)-2-pyridinamineHCID 6828215599.8%

反応手順

A solution of 2-aminopyridine (11.314 g, 120.3 mmol) and pyrimidine-5-carboxaldehyde (14.0 g, 129.6 mmol) in chloroform (300 mL) was stirred at room temperature for 15 min. The volatiles were then removed under reduced pressure (1 h at 75° C.) to yield a yellow solid. The crude solid was dissolved in chloroform (300 mL) and the solution was stirred for 15 min. The volatiles were then removed under reduced pressure (1 h at 75° C.) to yield a yellow solid. The crude solid was again dissolved in chloroform (300 mL), the solution was stirred for 15 min, and the volatiles were removed under reduced pressure (1 h at 85° C.) to yield a yellow solid. This solid was dried in a vacuum oven overnight at 80° C. to yield 22.090 g (99.8%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09108965B2
出典データセットuspto-grants-2015_08
ORD IDord-8448ac91cd3e43139bff4f0665ee5357
出典メモuspto-grants-2015_08