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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53443생성일: 2026년 10월 24일

Pyridine → 2-Valerylamino-5-bromo-4-methyl-3-nitropyridine

https://huagongshe.com/ko/reaction/53443

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DichloromethaneHCID 6344—
반응물Valeryl chlorideHCID 61186—
반응물2-Amino-5-bromo-4-methyl-3-nitropyridineHCID 7213207—
용매WaterHCID 962—
생성물2-Valerylamino-5-bromo-4-methyl-3-nitropyridineHCID 2146417381%

반응 조건

온도110 °C

반응 단계

A mixture comprising 10 g (43.1 mmol) of 2-amino-5-bromo-4-methyl-3-nitropyridine and 6.8 g of pyridine was heated to 110° C. in a nitrogen atmosphere. 5.7 g (47.4 mmol) of valeroyl chloride was dropwise added thereto and the mixture was stirred at 110° C. for 5 hours. The reaction mixture was brought to room temperature, followed by the addition of methylene chloride (50 ml) and water (50 ml). The organic phase was separated. The aqueous phase was further extracted with methylene chloride (50 ml). The organic phases were combined, dried over anhydrous magnesium sulfate and subjected to vacuum concentration to give a crude crystal. It was recrystallized from ethyl acetate to give 11 g of 2-valerylamino-5-bromo-4-methyl-3-nitropyridine (yield 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618969
출처 데이터셋uspto-grants-1997_04
ORD IDord-1da1f522f51f4cdfa04c306c6fee3dc0
출처 메모uspto-grants-1997_04