Thiazoles can be synthesized through the reaction of α-haloketones with thioamides, followed by cyclization. The reaction can be performed under conventional heating in organic solvents.
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4-UREIDO-BENZOIC ACID
2,4-DIPHENYL-5-METHYLTHIAZOLE
4-Thiazolecarboxylic acid, 2-hydrazino-5-phenyl-, methyl ester
1-(4-benzyloxyphenyl)hexan-2-one
5-(p-bromophenyl)-2-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosylamino)thiazole
2-chloro-N-[4-(4-nitrophenyl)-1,3-thiazol-2-yl]acetamide
ethyl 3-(2-amino-1,3-thiazol-4-yl)benzoate
5-biphenyl-4-yl-2-methylthiazole
Benzamide, 4-chloro-N-[2,2-difluoro-1-(trifluoromethyl)ethenyl]-
2-((S)-1-Amino-5-benzyloxycarbonylamino-pentyl)-oxazole-4-carboxylic acid
