2-羟基-5-硝基吡啶置于sodium Cyanide,溴,三溴化磷,铁粉,溶剂黄146体系中,用 乙酸乙酯,1,2-二氯乙烷,N,N-二甲基甲酰胺 作为反应溶剂,化学反应 6.5H,反应生成 3-氨基-6-氰基吡啶
参考文献:The Synthesis Of The High-Potency Sweetener,Nc-00637. Part 2: Preparation Of The Pyridine Moiety
标题:The Synthesis Of The High-Potency Sweetener,Nc-00637. Part 2: Preparation Of The Pyridine Moiety
摘要:The Pyridine Moiety Within The High-Potency Sweetener,Nc-00637 (1),5-Amino-2-Cyanopyridine (4),Was Prepared From 2-Hydroxy-5-Nitropyridine (10). The Sequence Involved The Conversion Of The Hydroxy Group To Bromide Followed By Substitution With Cyanide To Give 2-Cyano-5-Nitropyridine (8). Reduction Of The Nitro Group Proved To Be Troublesome When Catalytic Hydrogenation Was Used. Iron With An Acid Gave A Reproducible Reaction That Could Be Used At Scale.
DOI:10.1021/op034110C