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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12153생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/12153

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물5-Methyl-2-nitrobenzoic acidHCID 18371—
반응물Oxalyl chlorideHCID 65578—
반응물2-Amino-5-chloropyridineHCID 66174—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-(5-chloropyridin-2-yl)-5-methyl-2-nitrobenzamideHCID 356251992%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727981B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-bd09f05c6fa3401a81f8a51176430386
출처 메모uspto-grants-2010_06