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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12307생성일: 2026년 10월 24일

Bromine → 2-Bromo-6-methoxypyridin-3-amine

https://huagongshe.com/ko/reaction/12307

반응식

참여 물질

역할이름HCID투입량
반응물BromineHCID 24408—
반응물Sodium ThiosulfateHCID 24477—
반응물6-Methoxy-3-pyridinylamineHCID 81121—
반응물Sodium AcetateHCID 517045—
용매Acetic AcidHCID 176—
생성물2-Bromo-6-methoxypyridin-3-amineHCID 15209324—

반응 단계

A mixture of 1.83 g (14.7 mM) of 5-amino-2-methoxypyridine and 1.21 g (14.7 mM) of sodium acetate in 12 ml of acetic acid is prepared and 0.75 ml (14.7 mM) of bromine is added gently, with stirring and while maintaining at room temperature. The reaction mixture is kept stirring for 30 minutes, at room temperature, and 200 ml of saturated sodium thiosulfate solution are then added. The aqueous phase obtained is extracted twice with ethyl acetate. The combined organic phases are dried over magnesium sulfate and concentrated under reduced pressure. 3 g of the expected compound are obtained in the form of a violet-colored solid (quantitative yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728002B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-27352282c0af4dfbb16addeee00b36b0
출처 메모uspto-grants-2010_06