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Table 1 The physicochemical properties of the synthesized analogous

From: Design, synthesis and biological potentials of novel tetrahydroimidazo[1,2-a]pyrimidine derivatives

Comp.

M. Formula

M. Wt.

m.p. (°C)

R f valuea

% yield

1

C30H28N4O8

572

121–123

0.58

86

2

C29H32N4O10

596

169–171

0.31

83

3

C26H25N5O9

551

159–161

0.53

80

4

C30H35N5O7

577

150–153

0.68

84

5

C26H25N5O9

551

122–124

0.63

91

6

C26H25N5O9

551

159–161

0.51

64

7

C28H31N5O7

549

161–163

0.56

88

8

C26H26N4O8

522

170–172

0.61

84

9

C27H28N4O9

552

146–148

0.41

80

10

C26H24Cl2N4O7

574

148–150

0.42

83

11

C27H28N4O8

536

174–176

0.45

78

12

C26H25BrN4O7

584

144–146

0.66

72

13

C27H28N4O8

536

148–150

0.39

78

14

C26H25BrN4O7

584

155–157

0.38

72

15

C26H25BrN4O8

601

119–121

0.62

90

16

C27H28N4O8

536

149–151

0.47

91

17

C27H26N4O8

534

140–142

0.25

79

18

C26H25ClN4O7

540

150–153

0.59

73

19

C26H26N4O7

506

144–146

0.47

83

20

C26H25ClN4O7

540

151–153

0.55

75

21

C28H30N4O9

566

146–148

0.66

85

22

C26H26N4O8

522

100–102

0.61

74

23

C26H25ClN4O7

540

141–143

0.56

77

24

C28H28N4O7

532

143–145

0.53

81

  1. aTLC mobile phase-Benzene