The invention relates to the technical field of biological
medicine, in particular to a synthesis method and application of pinenyl thiazolidone derivatives, and the synthesis method comprises the step of synthesizing thiosemicarbazide A at the yield of 90% under the promotion of
hydrochloric acid through
condensation reaction between myrtenal and 4-methyl-3-thiosemicarbazide. Cyclizing the
compound A and
chloroacetic acid to obtain a key intermediate thiazolidone B; then, the intermediate reacts with substituted
benzaldehyde, and the target
compound C1-C13 is obtained. The adopted substrate myrtenal has a better anti-proliferation effect on
malignant cells, strong water
solubility is enhanced by introducing
thiazolidines, and remarkably enhanced anti-
cancer activity can be shown by introducing the
thiazolidine derivative modified by
Schiff base. The series of products are novel in structure, high in yield, simple in separation and purification operation and suitable for
mass production, and part of products such as C5 have good
biological activity.