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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572206생성일: 2026년 10월 27일

2,6-Dibromopyridine → 6-bromo-N-[(1S)-1-(3-nitrophenyl)ethyl]pyridin-2-amine

https://huagongshe.com/reaction/572206

반응식

참여 물질

역할이름HCID투입량
반응물2,6-DibromopyridineHCID 12274—
반응물(s)-1-(3-Nitrophenyl)ethanamineHCID 11292459—
반응물Bis(diphenylphosphino)-1,1'-binaphthylHCID 18630801—
반응물Sodium t-butoxideHCID 23676156—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물6-bromo-N-[(1S)-1-(3-nitrophenyl)ethyl]pyridin-2-amineHCID 8664185633%

반응 조건

온도80 °C

반응 단계

A mixture of (1S)-1-(3-nitrophenyl)ethanamine (365 mg, 2.2 mmol), 2,6-dibromopyridine (474 mg, 2 mmol), tris(dibenzylidene)dipalladium(0) (92 mg, 0.1 mmol), (+/−)-bis(diphenyphosphino)-1,1′-binaphthalene (125 mg, 0.2 mmol) and sodium tert-butoxide (270 mg, 2.8 mmol) in anhydrous toluene (4 mL) was heated at 80° C. for 17 hours. The mixture was cooled, diluted with ethyl acetate (50 mL), washed successively with saturated aqueous sodium hydrogen carbonate (3×30 mL) and brine (30 mL), dried (Na2SO4) and concentrated under reduced pressure to give a black oil which was purified by flash chromatography (silica, ethyl acetate/hexanes) to give 6-bromo-N-[(1S)-1-(3-nitrophenyl)ethyl]pyridin-2-amine (210 mg, 33%) and the di-addition product (205 mg, 50%) both as yellow oils.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029386B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-669d641cd5904fd7b163a83c97b03946
출처 메모uspto-grants-2015_05