📜2,5-二氨基-4,6-二氯嘧啶置于ammonium Hydroxide体系中,化学反应 24.0H,以93%的收率获得2,4,5-三氨基-6-氯嘧啶 参考文献: Compounds For Treating Cystic Fibrosis[fr] Composés Pour Le Traitement De La Fibrose Kystique 标题: Compounds For Treating Cystic Fibrosis[fr] Composés Pour Le Traitement De La Fibrose Kystique
专利信息
专利号:US-10676445-B1 优先权日:2019-06-06 标 题:Synthesis of aminopyrimidine-based energetic materials 发明人:WILHELM CHRISTOPHER; FOROHAR FARHAD; SOTO DENISSE 权利人:US NAVY 摘要:A new azido compound, 5-amino-6-chloro-2,4-diazido-pyrimidine, and a process for synthesizing. The synthesis may include reacting 5-amino-2,4,6-trichloropyrimidine and sodium azide. There is an excess molar amount of sodium azide for each chloro fractional molar amount on the 5-amino-2,4,6-trichloropyrimidine. The synthesis is a two phase reaction that is a dispersion. The 5-amino-2,4,6-trichloropyrimidine dissolved in acetone is a liquid phase, and the sodium azide is insoluble in acetone and is a solid phase, that is present in excess of chemical equivalents. The reaction product is soluble in acetone, and the reaction by-product, sodium chloride is also insoluble in acetone, and the crude yield is about 92%. Unreacted sodium azide and formed sodium chloride are removed by filtration.
参考文献:10.1016/s0166-3542(99)00019-4 摘要:Hisaki M, Imabori H, Azuma M, Suzutani T, Iwakura F, Ohta Y, Kawanishi K, Ichigobara Y, Node M, Nishide K, Yoshida I, Ogasawara M. Synthesis and anti-influenza virus activity of novel pyrimidine derivatives. Antiviral Res. 1999 Jun;42(2):121–37. doi: 10.1016/s0166-3542(99)00019-4.