Arkivoc

A new protocol for the synthesis of primary, secondary and tertiary anthranilamides utilizing N-(2-aminoarylacyl) benzotriazoles

N Kanışkan, Ş Kökten, İ Çelik

Index: Kaniskan, Nevin; Koekten, Sule; Celik, Ilhami Arkivoc, 2012 , vol. 2012, # 8 p. 198 - 213

Full Text: HTML

Citation Number: 5

Abstract

Abstract A convenient route for efficient conversion of unprotected anthranilic acids into the corresponding N-(2-aminoarylacyl) benzotrazoles is described. N-(2-Aminoarylacyl)- benzotrazoles have been successfully used to synthesize primary, secondary and tertiary anthranilamides in high yields (71-96%). Keywords: Anthranilic acid, benzotriazole, N-(2- aminoarylacyl) benzotrazoles, anthranilamides

Related Articles:

Efficient and practical transition metal-free catalytic hydration of organonitriles to amides

[Tu, Tao; Wang, Zhixun; Liu, Zelong; Feng, Xike; Wang, Qingyi Green Chemistry, 2012 , vol. 14, # 4 p. 921 - 924]

The intramolecular Diels-Alder reaction: recent advances and synthetic applications

[Hossain; Borthakur Indian Journal of Chemistry - Section B Organic Chemistry Including Medicinal Chemistry, 1990 , vol. 29, # 11 p. 1062 - 1063]

Regioselective reduction of substituted dinitroarenes using baker's yeast

[Davey, Claire L.; Powell, Lawson W.; Turner, Nicholas J.; Wells, Andrew Tetrahedron Letters, 1994 , vol. 35, # 42 p. 7867 - 7870]

Formamide as an Ammonia Synthon in Amination of Acid Chlorides

[Srinivasan; Manisankar Synthetic Communications, 2010 , vol. 40, # 23 p. 3538 - 3543]

Copper-catalyzed direct amination of ortho-functionalized haloarenes with sodium azide as the amino source

[Zhao, Haibo; Fu, Hua; Qiao, Renzhong Journal of Organic Chemistry, 2010 , vol. 75, # 10 p. 3311 - 3316]

More Articles...