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. 2017 Jan 30;22(2):213. doi: 10.3390/molecules22020213

Table 1.

Structures of TBZ derivatives.

No. R1 R2 R3 R4 R5 R6
TBZ H H H H H 4-thiazole
TBZ-01 H Me H H H 4-thiazole
TBZ-02 Me H H H H 4-thiazole
TBZ-03 H Me Me H H 4-thiazole
TBZ-04 H H Cl H H 4-thiazole
TBZ-05 H H F H H 4-thiazole
TBZ-06 a H H OMe H H 4-thiazole
TBZ-07 H Bz H H H 4-thiazole
TBZ-08 H graphic file with name molecules-22-00213-i001.jpg H H 4-thiazole
TBZ-09 H H NO2 H H 4-thiazole
TBZ-10 H H H H Me 4-thiazole
TBZ-11 H H H H Bn b 4-thiazole
TBZ-12 H H H H pMB b 4-thiazole
TBZ-13 H H H H mNB b 4-thiazole
TBZ-14 Me H H H H 2-Py b
TBZ-15 H graphic file with name molecules-22-00213-i002.jpg H H H 4-thiazole
TBZ-16 H H H graphic file with name molecules-22-00213-i003.jpg H 4-thiazole
TBZ-17 H H CF3 H H 4-thiazole
TBZ-18 H H H H graphic file with name molecules-22-00213-i004.jpg 4-thiazole
TBZ-19 H H H H Bn b Bn b
TBZ-20 H H H H 2-Py b 2-Py b

a Tautomer was determined by NMR spectroscopy analysis; b Bn= benzyl; pMB = p-methoxyl benzyl; m-NB = m-nitro benzyl; 2-Py = 2-pyridyl; Bz = benzoyl.