摘要
目的合成4-(4,6-二吗啉-1,3,5-三嗪-2-基)苯胺。方法三氯聚氰与吗啉在冰浴条件下经取代反应制得4,4’-(6-氯-1,3,5-三嗪-2,4-二基)二吗啉,再与苯胺-4-硼酸频那醇酯经Suzuki反应制得4-(4,6-二吗啉-1,3,5-三嗪-2-基)苯胺。结果与结论结构经核磁及质谱确证,总收率约61.7%。
Objective To synthesize 4 - (4,6 - dimorpholino - 1,3,5 - triazin - 2 - yl ) aniline. Methods 4,4' - ( 6 - chloro - 1,3,5 - triazine - 2,4 - diyl ) dimorpholine was synthesized with 2,4,6 - trichloro - 1,3,5 - triazine anti mor- pholine by substitution reaction under ice bath,and then reacting with amino - phenyl -4 - boronic acid pinacol ester to ob- tain 4 - ( 4,6 - dimorpholino - 1,3,5 - triazin - 2 - yl ) aniline by Suzuki reaction. Results and Conclusion The structure was confirmed by I H -NMR and ESI -MS,the overall yield was 61.7%.
出处
《药学研究》
CAS
2014年第4期242-243,共2页
Journal of Pharmaceutical Research
关键词
三氯聚氰
4-(4
6-二吗啉-1
3
5-三嗪-2-基)苯胺
中间体
合成
2,4,6 - trichloro - 1,3,5 - triazine
4 - ( 4,6 - dimorpholino - 1,3,5 - triazin - 2 - yl ) aniline
Interme-diates
Synthesis