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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 425894생성일: 2026년 10월 24일

N-bromobutanimide → 3-(Benzyloxy)-5-bromopyridin-2-amine

https://huagongshe.com/ko/reaction/425894

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물2-Amino-3-benzyloxypyridineHCID 90334—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물3-(Benzyloxy)-5-bromopyridin-2-amineHCID 2062655453%

반응 단계

To a stirred solution of 2-amino-3-benzyloxypyridine (42.0 g, 0.21 mol) in CH3CN (600 mL) at 0° C. was added N-bromosuccinimide (37.1 g, 0.21 mol) over 30 minutes. The mixture was stirred for 0.5 hr, after which the reaction was then diluted with EtOAc (900 mL) and partitioned with H2O (900 mL). The organic layer was, washed with brine and dried (Na2SO4), filtered and concentrated to dryness under vacuum to yield 3-benzyloxy-5-bromo-pyridin-2-ylamine (31.0 g, 0.11 mol, 53%). 1H NMR (CDCl3, 300 MHz) δ 4.63-4.78 (brs, 2H), 5.04 (s, 2H), 7.07 (d, 1H, J, 1.8 Hz), 7.33-7.42 (m, 5H), 7.73 (d, 1H, J, 1.8 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08106197B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-c82cf1b949b640d692dc8323f8b26d6f
출처 메모uspto-grants-2012_01