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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18215생성일: 2026년 10월 25일

2-Amino-5-bromo-3-nitropyridine → 5-Bromopyridine-2,3-diamine

https://huagongshe.com/reaction/18215

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-5-bromo-3-nitropyridineHCID 138878—
용매EthanolHCID 702—
생성물5-Bromopyridine-2,3-diamineHCID 69115698%

반응 단계

To a suspension of 2-amino-5-bromo-3-nitropyridine (2.0 g, 9.17 mmole) in absolute EtOH (50 mL) was added SnCl2 hydrate (9.3 g, 41.3 mmole), then the mixture was heated to reflux. After 3 hr the mixture was cooled to RT and concentrated. The residue was taken up in 2.0 M NaOH and extracted with EtOAc (3×). The combined organic layers were dried (MgSO4), filtered, and concentrated to give the title compound (1.69 g, 98%) which was sufficiently pure for use in the next step: MS (ES) m/e 188/190 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741339B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a6d97c126179416eac70759d445f8bf5
출처 메모uspto-grants-2010_06