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2-(6-Methylpyridin-2-yl)-1-(quinoxalin-6-yl)ethanone synthesis

1synthesis methods
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Yield:356560-90-2 65%

Reaction Conditions:

Stage #1: 2,6-dimethylpyridinewith n-butyllithium in tetrahydrofuran;hexane at -60; for 0.5 h;
Stage #2: with diethylaluminium chloride in tetrahydrofuran;hexane at -60 - 20;
Stage #3: quinoxaline-6-carbonyl chloride in tetrahydrofuran;hexane at -60; for 0.333333 h;Further stages.;

References:

Kim, Dae-Kee;Jang, Yoojeung;Ho, Soon Lee;Park, Hyun-Ju;Yoo, Jakyung [Journal of Medicinal Chemistry,2007,vol. 50,# 13,p. 3143 - 3147] Kim, Dae-Kee;Choi, Joon Hun;An, Young Jae;Lee, Ho Soon [Bioorganic and Medicinal Chemistry Letters,2008,vol. 18,# 6,p. 2122 - 2127]