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Table 1 The physicochemical properties of synthesized benzimidazole derivatives

From: Design, synthesis and biological profile of heterocyclic benzimidazole analogues as prospective antimicrobial and antiproliferative agents

Comp.

IUPAC name

Mol. structure

Mol. formula

Rf valuea

m. p. (oC)

% yield

Z1

1H-Benzo[d]imidazol-2-yl 2-(2,4-dinitrophenyl-amino) ethanethioate

C15H11N5O5S

0.48

180–183

83.64

Z2

1H-Benzo[d]imidazol-2-yl 2-(2-nitrophenylamino)ethanethioate

C15H12N4O3S

0.82

212–215

73.93

Z3

1H-Benzo[d]imidazol-2-yl 2-(3-nitrophenylamino)ethanethioate

C15H12N4O3S

0.75

217–220

85.74

Z4

1H-Benzo[d]imidazol-2-yl 2-(3-bromophenylamino)ethanethioate

C15H12N3OSBr

0.47

257–260

73.19

Z5

1H-Benzo[d]imidazol-2-yl 2-(4-bromophenylamino)ethanethioate

C15H12N3OSBr

0.65

260–263

57.48

Z6

1H-Benzo[d]imidazol-2-yl 2-(4-chloro-2-nitrophenylamino) ethanethioate

C15H11N4O3SCl

0.66

140–143

94.19

Z7

1H-Benzo[d]imidazol-2-yl 2-(2-chlorophenylamino)ethanethioate

C15H12N3OSCl

0.60

277–280

60.63

Z8

1H-Benzo[d]imidazol-2-yl 2-(3-chlorophenylamino)ethanethioate

C15H12N3OSCl

0.68

265–268

65.87

Z9

1H-Benzo[d]imidazol-2-yl 2-(2,6-dimethyyphenylamino) ethanethioate

C17H17N3OS

0.59

274–277

65.52

Z10

1H-Benzo[d]imidazol-2-yl 2-(2-chloro-4-nitrophenylamino) ethanethioate

C15H11N4O3SCl

0.74

180–183

91.45

Z11

1H-Benzo[d]imidazol-2-yl 2-(2-florophenylamino)ethanethioate

C15H12N3OSF

0.73

272–275

72.43

Z12

1H-Benzo[d]imidazol-2-yl 2-(4-florophenylamino)ethanethioate

C15H12N3OSF

0.55

270–273

68.60

Z13

1H-Benzo[d]imidazol-2-yl 2-(4-methylphenylamino)ethanethioate

C16H15N3OS

0.61

266–269

64.13

Z14

1H-Benzo[d]imidazol-2-yl 2 (methyl (phenyl)amino)ethanethioate

C17H17N3OS

0.70

245–248

53.40

Z15

H-Benzo[d]imidazol-2-yl 2-(ethy l(phenyl)amino)ethanethioate

C16H15N3OS

0.75

261–264

56.95

Z16

1H-Benzo[d]imidazol-2-yl 2-(2-(2-nitrobenzylidene)hydrazinyl) ethanethioate

C16H13N5O3S

0.58

258–260

59.40

Z17

1H-Benzo[d]imidazol-2-yl 2-(2-(3-nitrobenzylidene)hydrazinyl) ethanethioate

C16H13N5O3S

0.54

262–265

82.89

Z18

1H-Benzo[d]imidazol-2-yl 2-(2-(4-nitrobenzylidene)hydrazinyl) ethanethioate

C16H13N5O3S

0.59

250–253

65.04

Z19

1H-Benzo[d]imidazol-2-yl 2-(2-(4-hydroxy-3-methoxybenzylidene) hydrazinyl)ethanethioate

C17H16N4O3S

0.53

263–266

53.93

Z20

1H-Benzo[d]imidazol-2-yl 2-(2-(3-ethoxy-4-hydoxybenzylidene) hydrazinyl)ethanethioate

C18H18N4O3S

0.52

269–272

60.65

Z21

1H-Benzo[d]imidazol-2-yl 2-(2-(4-bromobenzylidene)hydrazinyl) ethanethioate

C16H13N4OSBr

0.50

277–280

65.52

Z22

1H-Benzo[d]imidazol-2-yl 2-(2-(2-hydroxybenzylidene)hydrazinyl) ethanethioate

C16H14N4O2S

0.57

259–262

63.60

Z23

1H-Benzo[d]imidazol-2-yl 2-(2-(3,4-dimethoxybenzylidene) hydrazinyl)ethanethioate

C18H18N4O3S

0.46

264–267

72.30

Z24

1H-Benzo[d]imidazol-2-yl 2-(2-(2-bromo-3-phenylallylidene) hydrazinyl)ethanethioate

C18H15N4OSBr

0.51

160–163

78.68

Z25

1H-Benzo[d]imidazol-2-yl 2-(2-(4-(dimethylamino)benzylidene) hydrazinyl)ethanethioate

C17H14N4O2S

0.57

250–253

72.58

Z26

1H-Benzo[d]imidazol-2-yl 2-(2-(4-formylbenzylidene) hydrazinyl)ethanethioate

C18H19N5OS

0.65

200–203

87.45

Z27

1H-Benzo[d]imidazol-2-yl 2-(2-(2,4-dichlorobenzylidene) hydrazinyl) ethanethioate

C16H12N4OSCl2

0.49

255–257

81.69

Z28

1H-Benzo[d]imidazol-2-yl 2-(2-(2-chlorobenzylidene)hydrazinyl) ethanethioate

C16H13N4OSCl

0.64

259–262

74.33

Z29

1H-Benzo[d]imidazol-2-yl 2-(2-(3-phenylallylidene)hydrazinyl) ethanethioate

C18H16N4OS

0.56

264–267

64.68

Z30

1H-Benzo[d]imidazol-2-yl 2-(2-(2-methoxylbenzylidene) hydrazinyl)ethanethioate

C17H16N4O2S

0.48

267–270

57.12

  1. aTLC mobile phase-ethyl acetate