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以２，４－二氧六氢－１，３，５－三嗪为先导化合物，引入不同的酰基，进行Ｎ－酰化结构改造，合成了７个新化合物，抗病毒活性测试表明，其中４个化合物对ＴＭＶ的抑制率达到５０％～５３％，与参照物ＤＡＤＨＴ接近．
Using 2,4-dioxo-1,3,5-triazine as the lead compound, different acyl groups were introduced and the N-acylation structure was modified to synthesize seven new compounds. The antiviral activity test showed that 4 The inhibition rate of the compounds to TMV reached 50% ~ 53%, which was close to the reference DADHT.