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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400574생성일: 2026년 10월 24일

Sodium Hydroxide → 5-Amino-6-bromo-2-pyridinecarbonitrile

https://huagongshe.com/ko/reaction/400574

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물BromineHCID 24408—
반응물5-Aminopyridine-2-carbonitrileHCID 3871395—
용매Acetic AcidHCID 176—
생성물5-Amino-6-bromo-2-pyridinecarbonitrileHCID 2421389235.9%

반응 단계

5-Aminopyridine-2-carbonitrile (2.38 g, 20 mmol) was dissolved in 6 mL of glacial acetic acid. A solution of bromine (1 mL, 20 mmol) in 2.5 mL of glacial acetic acid was added dropwise over a period of 30 minutes while the room temperature was maintained with a water bath. The resulting slurry was stirred for 1 hour at room temperature, treated with 50 mL of aqueous 20% sodium hydroxide solution and extracted with three 160 mL portions of dichloromethane. The combined organic layers were dried over sodium sulfate (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by crystallization from ethyl acetate-hexanes to give 5-amino-6-bromopyridine-2-carbonitrile (1.42 g, 35% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741897B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-3f12eec8677b4ebf8019de91e1881cd1
출처 메모uspto-grants-2014_06