tetrahydro-1-(5-t-butyl-1,3,4-thiadiazol-2-yl)-3-methyl-6-hydroxy-2(1H)-pyrimidinone 、
三乙胺 、
3-(4-chlorophenyl)propanoyl chloride 在
Tetrahydro-1-(5-t-butyl-1,3,4-thiadiazol-2-yl)-3-methyl-6-[ β-(4-chlorophenyl)propionyloxy]-2(1H)-pyrimidinone 作用下,
以
苯 为溶剂,
反应 0.5h,
以to yield the desired product tetrahydro-1-(5-t-butyl- 1,3,4-thiadiazol-2-yl)-3-methyl-6-[β-(4-chlorophenyl)propionyloxy] -2 (1H)-pyrimidinone as the residue的产率得到Tetrahydro-1-(5-t-butyl-1,3,4-thiadiazol-2-yl)-3-methyl-6-[ β-(4-chlorophenyl)propionyloxy]-2(1H)-pyrimidinone