Synthesis of 1-(2-(4-Substitutedphenylamino)-Imidazo[2,1-B] Benzothiazole-3-Yl) Propan-1-One

Authors

  • Chalak Azimi

isoxazolones; 2-chlorobenzothiazole; imidazobenzothiazoles; triethylamine (tea)

Abstract

4-propionyl-3-(4-substitutedphenylamino) isoxazol-5(2H)-one, substituted on nitrogen with a 2-chlorobenzot-hiazole group, reacts with triethylamine (TEA) in ethanol under reflux conditions to provide a convenient synthesis of 1-(2-(4-substitutedphenyl amino) -imidazo [2,1b] benzothiazole-3-yl) propan-1-one.

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How to Cite

Synthesis of 1-(2-(4-Substitutedphenylamino)-Imidazo[2,1-B] Benzothiazole-3-Yl) Propan-1-One. (2014). Global Journal of Science Frontier Research, 14(B2), 51-56. https://www.journalofscience.org/index.php/GJSFR/article/view/1122

References

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(2-(4-bromophenylamino)-imidazo[2,1-b] benzothiazole-3-yl) propan-1-one (15, X. 1.

mmol) and triethylamine (0.3 mL) were refluxed in ethanol (10 mL) for 24 hours. The reaction mixture was left to cool to room tempreture and resulting precipitate was colleted to afford 1-(2-(4-bromophenylamino)imidazo [2, 1-b] benzothiazole-3-yl) propan-1-one as white needles. 49(55%), 177-182.

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Synthesis of 1-(2-(4-Substitutedphenylamino)-Imidazo[2,1-B] Benzothiazole-3-Yl) Propan-1-One

Published

2014-05-28

How to Cite

Synthesis of 1-(2-(4-Substitutedphenylamino)-Imidazo[2,1-B] Benzothiazole-3-Yl) Propan-1-One. (2014). Global Journal of Science Frontier Research, 14(B2), 51-56. https://www.journalofscience.org/index.php/GJSFR/article/view/1122