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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 563951생성일: 2026년 10월 27일

N-pyridin-3-ylpyridin-3-amine → N-(1-(2-bromophenyl)ethyl)-N-(pyridin-3-yl)pyridin-3-amine

https://huagongshe.com/reaction/563951

반응식

참여 물질

역할이름HCID투입량
반응물N-pyridin-3-ylpyridin-3-amineHCID 598775—
반응물Lithium diisopropylamideHCID 2724682—
반응물1-Bromo-2-(1-bromoethyl)benzeneHCID 12350146—
용매TetrahydrofuranHCID 8028—
생성물N-(1-(2-bromophenyl)ethyl)-N-(pyridin-3-yl)pyridin-3-amineHCID 59138884237.5%

반응 단계

To a cooled solution (−78° C.) of N-pyridin-3-ylpyridin-3-amine (0.886 g, 5.23 mmol) in dry tetrahydrofuran (20 mL) was added LDA (3.8 mL of a 1.5 M solution, 5.75 mmol) to form a light yellow suspension. After stirring for 30 min, 1-bromo-2-(1-bromoethyl)benzene (3-1) (1.38 g, 5.23 mmol) was added in one portion. The reaction was stirred for 30 min at −78° C. then allowed to warmn to 0° C. and quenched with NH4Cl sat. solution (6 mL). The mixture was diluted with water and extracted with THF (2×20 mL), washed with brine and the organic layer was dried over Na2SO4. The solution was then filtered, concentrated, and dried under vacuum to give crude N-(1-(2-bromophenyl)ethyl)-N-(pyridin-3-yl)pyridin-3-amine (3-2) as a light brown solid (4.40 g): Analytical LCMS: (214 nm), 2.043 min. m/e (m+1): 356.1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067607B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-be3737b2942b43e28351a99aa0d767a0
출처 메모uspto-grants-2011_11