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Table 2 Synthesis of 3-aryl- and 3-cyclohexyl-4-formylsydnone N-(tetra-O-acetyl-β-d-glucopyranosyl)thiosemicarbazones (4ao) under conventional and μ-wave heating

From: Synthesis and antibacterial and antifungal activities of N-(tetra-O-acetyl-β-d-glucopyranosyl)thiosemicarbazones of substituted 4-formylsydnones

Entry

R

Reaction time (min)

Yield (%)

Conventional heating

MW heating

Conventional heating

MW heating

4a

H

100

25

50

71

4b

2-Me

120

28

55

75

4c

3-Me

130

30

55

73

4d

4-Me

130

30

56

76

4e

2,3-diMe

130

35

55

70

4f

2,4-diMe

130

35

50

68

4g

4-Et

120

28

60

83

4h

3-OMe

130

30

60

78

4i

4-OMe

130

30

60

81

4j

4-OEt

130

25

60

82

4k

4-F

130

30

55

65

4l

4-Br

150

35

55

63

4m

4-I

130

35

57

68

4n

2-Me-5-Cl

140

45

50

43

4o

Cyclohexyla

130

30

60

85

  1. aCyclohexyl group is attached directly to sydnone ring at position 4