Research Article

Synthesis of Substituted Thieno[2,3-d]pyrimidin-4-ones and Their Testing for Evaluation of Cytotoxic Activity on Mammalian Cell Models

Table 1

Some physical-chemical parameters of synthesized compounds (1–16).

Compound no.Yield, %
(%, [Lit.])
Mp, °C (solvent)
(Mp, [Lit.])

(Eluent)
Empiric formula

186
(42, [17])
90–92 (cyclohexane)
(88–90, [17])
0.70
(A)
C9H13NO2S
281
(45, [17])
87–89 (hexane)
(87–89, [17])
0.65
(A)
C10H13NO2S
385
(82, [17])
98–100 (hexane)
(96–98, [17])
0.43
(B)
C11H15NO2S
48270-71 (hexane)
(68–70, [17])
0.74
(B)
C12H17NO2S
586144-145 (hexane)
(144-145, [17])
0.70
(A)
C11H12N2OS
690
(54, [14])
202-203 (methanol)
(200-201, [14])
0.65
(A)
C12H12N2OS
792
(60, [14])
214-215 (ethanol)
(212–214, [14])
0.43
(B)
C13H14N2OS
892
(62, [14])
157-158 (ethanol)
(156–158, [14])
0.74
(B)
C14H16N2OS
985115–117 (heptane)
(115–117, [14])
0.75
(B)
C12H14N2OS
1082
(80, [14])
182-183 (heptane)
(180–183, [14])
0.75
(B)
C13H14N2OS
1188
(85, [14])
218–220 (ethanol)
(215-216, [14])
0.76
(B)
C14H16N2OS
1292
(78, [14])
156–158 (ethanol)
(155–157, [14])
0.80
(B)
C15H18N2OS
1388159–161 (heptane)
(158–160, [15])
0.82
(B)
C13H16N2OS
1485
(75, [15])
197-198 (heptane)
(196–198, [14])
0.80
(B)
C14H16N2OS
1591
(67, [14])
155–157 (ethanol)
(150–152, [14])
0.81
(B)
C15H18N2OS
1690
(65, [14])
161–163 (heptane)
(159-160, [14])
0.86
(B)
C16H20N2OS