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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 744974생성일: 2026년 10월 25일

Dichloromethane → 2-cyclopropanecarboxamido-5-Bromo-4-Methyl-3-nitropyridine

https://huagongshe.com/reaction/744974

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물O-XyleneHCID 7237—
반응물Cyclopropanecarbonyl chlorideHCID 77637—
반응물2-Amino-5-bromo-4-methyl-3-nitropyridineHCID 7213207—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
생성물2-cyclopropanecarboxamido-5-Bromo-4-Methyl-3-nitropyridineHCID 1097948288.1%

반응 조건

온도110 °C

반응 단계

A mixture comprising 10 g (43.1 mmol) of 2-amino-5-bromo-4-methyl-3-nitropyridine, 6.3 g of 4-dimethylaminopyridine and xylene (50 ml) was heated at 110° C. in a nitrogen atmosphere. 5 g (47.4 mmol) of cyclopropanecarbonyl chloride was dropwise added thereto, followed by further stirring at 110° C. for 2 hours. The reaction mixture was brought to room temperature, followed by the addition of dichloromethane (200 ml) and water (50 ml). The organic phase was separated and the aqueous phase was further extracted with dichloromethane (50 ml). The organic phases were combined and washed with water (50 ml). The resulting organic phase was dried over anhydrous magnesium sulfate and concentrated to give a crude crystal. It was recrystallized from chloroform/ethyl acetate to give 11.4 g of the title compound (yield 88%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05559236
출처 데이터셋uspto-grants-1996_09
ORD IDord-77f3a031c1214ac984c3a0d640fdef40
출처 메모uspto-grants-1996_09