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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44243생성일: 2026년 10월 23일

Triethylamine → N-(5-bromo-2-chloropyridin-3-yl)-2-nitrobenzamide

https://huagongshe.com/ko/reaction/44243

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Nitrobenzoyl chlorideHCID 11875—
반응물3-Amino-5-bromo-2-chloropyridineHCID 21858354—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매Sodium BicarbonateHCID 516892—
생성물N-(5-bromo-2-chloropyridin-3-yl)-2-nitrobenzamideHCID 86658034—

반응 단계

To a solution of 5-bromo-2-chloropyridine-3-amine (3.9 g, 18.9 mmol) and triethylamine (5.3 mL, 37.9 mmol) in tetrahydrofuran (60 mL) was added 2-nitrobenzoylchloride (2.49 mL, 18.9 mmol). The reaction was stirred for 24 hours. The reaction mixture was diluted with ethyl acetate (200 mL) and saturated aqueous sodium bicarbonate (60 mL). The organic layer was separated and washed with water (50 mL), brine (50 mL), dried over sodium sulfate, filtered and concentrated to dryness under reduced pressure. The crude product was purified by flash chromatography (SiO2, 25% ethyl acetate in hexanes). The N-(5-bromo-2-chloropyridin-3-yl)-2-nitrobenzamide was obtained as a yellow solid (1.5 g). LCMS [M+H]: 356.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541407B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ab89fc2dc2b24ffea8f46cdcfcbc29fa
출처 메모uspto-grants-2013_09