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HRID 12128作成日:2026年10月26日

Pyridine → n-(5-Bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamide

https://huagongshe.com/reaction/12128

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Oxalyl chlorideHCID 65578—
反応物2-Amino-5-bromopyridineHCID 70622—
反応物3,4,5-Trimethoxy-2-nitrobenzoic acidHCID 97116—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物n-(5-Bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamideHCID 2259631998.3%

反応手順

To a solution of 3,4,5-trimethoxy-2-nitrobenzoic acid (0.5 g, 1.95 mmol) in dichloromethane (5 ml) was added oxalyl chloride (0.34 ml, 3.9 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-bromopyridine (0.81 g, 4.7 mmol) and pyridine (0.94 ml, 11.7 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-bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamide as a solid (790 mg, 98%). MS found for C15H14BrN3O6 M+=412, (M+2)+=414.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727982B2
出典データセットuspto-grants-2010_06
ORD IDord-2bbf6d4c24094021b4487360c5a0e84d
出典メモuspto-grants-2010_06