Synthesis ,Characterization and Study Biological Activity of Some New 1, 3, 4-Thiadiazole and Pyrazolone Derivatives Containing Indole Ring

Autor: Khalid F. Ali, Kadhim M. Lazim, Jumbad H. Tomma
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Zdroj: Ibn Al-Haitham Journal for Pure and Applied Sciences, Vol 27, Iss 3 (2017)
Druh dokumentu: article
ISSN: 1609-4042
2521-3407
Popis: This work involves synthesis and characterization of some new 1, 3, 4-thiadiazole or pyrazoline derivatives heterocyclic containing indole ring. The new 2-amino-1, 3, 4thiadiazole derivatives[IV] and [V]a, b were synthesized by cyclization reaction of 2-methyl1H-indole-carbothiosemicarbazide[III] in H2SO4 acid or by reaction of indole-3-acetic acid or indole-3-butanoic acid with thiosemicarbazide in the presence of phosphorous oxychloride, respectively. Amide derivatives [VI]-[VIII] were synthesized by the reaction equimolar of 2amino-1, 3, 4-thiadiazoles and (acetyl chloride, benzoyl chloride, anisoyl chloride and heptanoyl chloride) in DMF and pyridine as accepter. The new pyrazolone derivatives [XI]a, b were synthesized from heating under reflux equimolar from a mixture of acid hydrazides [X]a or [X]b and ethylacetoacetate in absolute ethanol. Acetyl pyrazolone compounds[XII]a, b were synthesized by the reaction of pyrazolone derivatives [X]a or [X]b with acetyl chloride in 1,4-Dioxane in present of calcium hydroxide to give 4-acetyl pyrazolone derivatives[XI]a, b. The new aryl hydrazone derivatives of pyrazoline [XIII] and [XIV] were synthesized by the reaction of one mole of compounds [XII]a or [XII]b with one mole of phenyl hydrazine or substituted phenyl hydrazine in ethanol. All the synthesized compounds have been characterized by melting points , FTIR, 1HNMR and Mass spectroscopy (of some of theme).
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