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HRID 514718作成日:2026年10月25日

Pyridine → N-(5-chloropyridin-2-yl)-5-methyl-2-nitrobenzamide

https://huagongshe.com/reaction/514718

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物5-Methyl-2-nitrobenzoic acidHCID 18371—
反応物Oxalyl chlorideHCID 65578—
反応物2-Amino-5-chloropyridineHCID 66174—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-(5-chloropyridin-2-yl)-5-methyl-2-nitrobenzamideHCID 356251992%

反応手順

To a solution of 5-methyl-2-nitrobenzoic acid (1 g, 5.52 mmol) in dichloromethane (5 ml) was added oxalyl chloride (0.964 ml, 11.04 mmol) and a few drops of dimethylformamide. The mixture was stirred at r.t. for 2 hrs. After the evaporation of the solvent, the residue was dissolved in dichloromethane (5 ml). 2-amino-5-chloropyridine (852 mg, 6.62 mmol) and pyridine (1.34 ml, 16.56 mmol) were added to the solution. The mixture was stirred at r.t. overnight. After the evaporation of the solvent, the crude residue was purified by silica gel column chromatography using solvent system 25% ethyl acetate in hexane as eluent to give N-(5-chloro(2-pyridyl))(5-methyl-2-nitrophenyl)carboxamide as a solid (1.48 g, 92%). MS found for C13H10ClN3O3 M+=291, (M+2)+=293.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09108922B2
出典データセットuspto-grants-2015_08
ORD IDord-93b26794861d47f1a0e6ebccb94af737
出典メモuspto-grants-2015_08