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HRID 2408129作成日:2026年10月26日

5-Aminopyridine-2-carbonitrile → HCID 178510044、化合物

https://huagongshe.com/reaction/2408129

反応式

関与物質

役割名称HCID仕込み量
反応物5-Aminopyridine-2-carbonitrileHCID 3871395—
反応物3-MorpholinobenzaldehydeHCID 7164584—
触媒p-Toluenesulfonic acidHCID 6101—
溶媒TolueneHCID 1140—
生成物HCID 178510044HCID 17851004499.9%

反応手順

The mixture solution of 5-amino-pyridine-2-carbonitrile (9.3 g, 78.4 mmol), 3-morpholin-4-yl-benzaldehyde (15.0 g, 78.4 mmol) and p-toluenesulfonic acid (271.8 mg, 1.4 mmol) in toluene (150 mL) was heated to reflux for 12 h. Then the reaction mixture was cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 5-{[1-(3-morpholin-4-yl-phenyl)-meth-(E)-ylidene]-amino}-pyridine-2-carbonitrile (22.9 g, quant.) as a light yellow solid: MS (ESI) M+1=293.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08809369B2
出典データセットuspto-grants-2014_08
ORD IDord-c9d7d888639e442fab511ab3e82ecc93
出典メモuspto-grants-2014_08