A series of (5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl derivatives 6a–6e have been synthesized and screened for in vitro anti-leishmanial activity against the promastigote form of L. major. The structure of Schiff bases were confirmed by 1H NMR, IR. Screening results indicate that all of the designed and synthesized final compounds (6a-6e) significantly reduced the viability of promastigotes ...

In this work, we studied the processes of vinyl ester formation by addition benzoic acid to phenylacetylene in presence complex catalysts diacetate-di (2-amino-5-methylthio-1,3,4-thiadiazolo) cobalt(II) ([Co(C3H5N3S2)2(CH3COO)2] and tetrakis(2-amino-5-ethylthio-1,3,4-thiadiazole)-zinc(II) dinitrate ([Zn(C4H7S2)4](NO3)2): 1-phenylvinyl benzoate anti-Markovnikov coupling product - styryl were obt...

An efficient one-pot synthesis of novel β-amino acid derivatives containing a thiadiazole moiety was developed using a chiral squaramide cinchona alkaloid as organocatalyst. The reactions afforded chiral β-amino acid derivatives in moderate yields and with moderate to excellent enantioselectivities. The present study demonstrated for the first time the use of a Mannich reaction catalyzed by a ch...

Human carbonic anhydrases (CAs) are well studied targets for the development of inhibitors for pharmaceutical applications. The crystal structure of human CA II has been determined in complex with two CA inhibitors (CAIs) containing conventional sulfonamide and thiadiazole moieties separated by a -CF2- or -CHNH2- spacer group. The structures presented here reveal that these spacer groups allow ...

The present synthetic strategy involves the synthesis of indolyl-triazolo-thiadiazole heterocyclic ring systems 8–13 from condensation 4-amino-5-(1H-indol-2-yl)-3H-1,2,4-triazole-3-thione 1 with aromatic carboxylic acid derivatives 2–7 in presence POCl3 for h. All compounds were obtained very good yields and have been well-characterized using spectroscopic techniques. Exclusively, quality cryst...

An improved procedure for isolation of 5-amino-3-methyl-1,2,4-thiadiazole in pure form on a multi-gram scale without chromatography is reported. Its 1H and 13C-NMR and IR data are presented and previously published erroneous data corrected. The molecular structure is confirmed by X-ray diffraction which shows layers consisting of an elaborate two-dimensional hydrogen bonded network of molecules.