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	<dc:title xml:lang="en-US">Efficient synthesis of diversely substituted pyrazolo[1,5-a]pyrimidine derivatives promoted by ultrasound irradiation in water and their antibacterial activities</dc:title>
	<dc:creator>Das, Susma</dc:creator>
	<dc:creator>Khanikar, Shilpika</dc:creator>
	<dc:creator>Kaping, Shunan</dc:creator>
	<dc:creator>Roy, Jayanti Datta</dc:creator>
	<dc:creator>Sen, Arnab</dc:creator>
	<dc:creator>Helissey, Philippe</dc:creator>
	<dc:creator>Vishwakarma, Jai Narain</dc:creator>
	<dc:subject xml:lang="en-US">Enaminone</dc:subject>
	<dc:subject xml:lang="en-US">Single crystal</dc:subject>
	<dc:subject xml:lang="en-US">3-Aminopyrazole</dc:subject>
	<dc:subject xml:lang="en-US">Ultrasonic irradiation</dc:subject>
	<dc:subject xml:lang="en-US">X-ray crystallography</dc:subject>
	<dc:subject xml:lang="en-US">Antibacterial properties</dc:subject>
	<dc:description xml:lang="en-US">A green synthetic route leading to the discovery of a series of diversely substituted pyrazolo[1,5-a]pyrimidines, having CO2Et group embedded at position-2 has been unraveled in this article. A series of formylated active proton compounds that were chosen to react with a carboxylate substituted-3-aminopyrazole under ultrasonic irradiation in the presence of a mild acid as a catalyst and aqueous ethanol medium afforded the desired products. The molecular structures of all these synthesized compounds were established by their spectral and analytical data. A model molecule 3d, subjected to single-crystal X-ray crystallography analysis further confirms their molecular structure. The crystal crystallized to a monoclinic cell with P21/c space group, a = 7.468 (5) Å, b = 27.908 (17) Å, c = 7.232 (4) Å, β = 104.291 (7)o, V =1460.7(15) Å3, Z = 4, μ(MoKα) = 0.096 mm-1, Dcalc = 1.352 Mg/m3 16667 measured reflection (5.63 ≤ 2Θ ≤ 57.57°), 3720 unique (Rint = 0.0965, Rsigma = 0.0945) which were used in all calculations. The final R1 was 0.0750 (I &gt; 2σ(I)) and wR2 was 0.2226 (all data). These compounds were further explored for their antibacterial potential, and a few of them have exhibited encouraging results.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2020-12-31</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/2033</dc:identifier>
	<dc:identifier>10.5155/eurjchem.11.4.304-313.2033</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 11 No. 4 (2020): December 2020; 304-313</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/2033/pdf_2033</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2020 Authors</dc:rights>
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