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• 56278-50-3 2-cyanomethylbenzothiazole 
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Relevant academic research and scientific papers

Microwave-Assisted synthesis under solvent-free conditions of (E)-2-(Benzo[d]thiazol-2-yl)-3-arylacrylonitriles

A series of (E)-2-(benzo[d]thiazol-2-yl)-3-arylacrylonitriles was synthesized by microwave assisted Knoevenagel condensation under solvent-free conditions from the corresponding 2-(benzo[d]thiazol-2-yl)acetonitrile and aromatic aldehydes with electrondona

Ultrasound-assisted phase-transfer catalysis method in an aqueous medium to promote the Knoevenagel reaction: Advantages over the conventional and microwave-assisted solvent-free/catalyst-free method Dedicated to the memory of Professor Luis Astudillo Saavedra for his scientific career, support and fraternity.

Given the broad spectrum of uses of acrylonitrile derivatives as fluorescent probes, AChE inhibitors, and others, it is necessary to find easy, efficient and simple methods to synthesize and diversify these compounds. We report the results of a comparative study of the effects of three techniques on the reactions between heterocyclic aldehydes and 2-(benzo[d]thiazol-2-yl) acetonitrile: stirring; ultrasound coupled to PTC conditions (US-PTC); and MW irradiation (MWI) under solvent and catalyst-free conditions. The effects of conditions on reaction parameters were evaluated and compared in terms of reaction time, yield, purity and outcomes. The US-PTC method is more efficient than the MWI and conventional methods. The reaction times were considerably shorter, with high yields (>90%) and good levels of purity. In addition, X-ray diffraction analysis and quantum mechanical calculations, at the level of density functional theory (DFT), ratify obtaining acrylonitrile isomers with E configurations. The crystal structure of 3c is stabilized by weak C-H o?N intermolecular interactions (Ho?NC = 2.45 ?, Co?NC = 3.348(3) ?, Ho? NC = 162°), forming centrosymmetric ring R22 (20) along the crystallographic a axis.

Diels-Alder reaction of benzylidene(cyano)methyl-1,3-benzoxa/thiazoles as stable 1-azabuta-1,3-dienes

Diels-Alder reactions of benzylidene(cyano(methyl-1,3-benzothiazoles 2 and -1,3-benzoxazoles 3 as 1-azabuta-1,3-dienes are described.The dienes 2, 3, featuring stabilized imine moieties in the form of heteroaromatic rings, react with both electron-deficie

SYNTHESIS AND STRUCTURE ELUCIDATION OF BENZOTHIAZOLE-CONTAINING COMPOUNDS FOR ANTIMICROBIAL INVESTIGATION

Attempted cycloaddition of benzimidazole-2-thiol with arylidenemalononitriles 1 was unsuccessful. 2-Cyanomethyl-1,3-benzothiazole 6 condensed with certain aromatic aldehydes to produce 7, cycloaddition of which with cyanoacethydrazide 3 yielded 8. Structu