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HRID 270693作成日:2026年10月26日

4-Aminonicotinaldehyde → 2-(2,6-dichloro-3-nitro-phenyl)-N-(3-formyl-pyridin-4-yl)-acetamide

https://huagongshe.com/reaction/270693

反応式

関与物質

役割名称HCID仕込み量
反応物4-AminonicotinaldehydeHCID 2761033—
反応物2,6-Dichloro-3-nitrophenylacetic acidHCID 54265437—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
溶媒Thionyl ChlorideHCID 24386—
生成物2-(2,6-dichloro-3-nitro-phenyl)-N-(3-formyl-pyridin-4-yl)-acetamideHCID 5983385995.2%

反応手順

A solution of (2,6-dichloro-3-nitro-phenyl)-acetic acid (15.0 g, 60.0 mmol) in thionyl chloride (60 mL) is refluxed for one hour. The solvent is removed by concentration; dry toluene is added and concentrated to thoroughly remove thionyl chloride. To the solution of acid chloride in dry dichloromethane (200 mL) is added (drop-wise) a solution of 4-amino-pyridine-3-carbaldehyde (6.6 g, 54 mmol) in dichloromethane (50 mL) and DIEDA (10.7 mL, 60 mmol). The mixture is at room temperature for 2 hours. The reaction mixture is diluted with EtOAc (300 ml) and washed with saturated K2CO3 and brine. The organic layer is dried, filtered and concentrated to give crude product. Recrystallization with dichloromethane/hexane results in the titled compound as a solid (18.2 g, 95.2%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449582B2
出典データセットuspto-grants-2008_11
ORD IDord-c0ea74fc44c74a67a44b70cbc2269a15
出典メモuspto-grants-2008_11