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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40652생성일: 2026년 10월 24일

Triethylamine → N-(4-Methoxybenzyl)-2-bromo-5-nitropyridin-4-amine

https://huagongshe.com/ko/reaction/40652

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-MethoxybenzylamineHCID 75452—
반응물2-Bromo-4-chloro-5-nitropyridineHCID 59613418—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물N-(4-Methoxybenzyl)-2-bromo-5-nitropyridin-4-amineHCID 5692646877.2%

반응 단계

A solution of 4-methoxybenzylamine (0.756 g, 5.51 mmol) in acetonitrile (2 mL) was added to a mixture of 2-bromo-4-chloro-5-nitropyridine (1.19 g, 5.01 mmol) and triethylamine (0.768 mL, 5.51 mmol) in acetonitrile (8 mL). After stirring for 1.5 hours, the solution was diluted with ethyl acetate (100 mL) which was then washed successively with water and brine before being concentrated in vacuo to a light brown oil which solidified on standing to give the title compound (1.31 g, 3.87 mmol, 77%). 1H NMR (d6-DMSO, 400 MHz) δ 9.00 (br t, 1H, J=6.3 Hz), 8.80 (s, 1H), 7.35 (d, 2H, J=8.7 Hz), 7.10 (s, 1H), 6.95 (d, 2H, J=8.8 Hz), 4.60 (d, 2H, J=6.0 Hz), 3.70 (s, 3H). LCMS (1) Rt=2.13 min; m/z (ESI−) 336, 338 (M−H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530468B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-2e3d4c2515ea484f98336fd06b5114a8
출처 메모uspto-grants-2013_09