Volume 53, Issue 5 pp. 1611-1616
Article

AgNO3 Catalyzed Regio-Selective Synthesis of 3-Alkyl/Aryl-idene-3,4-dihydro-4-tosyl-2H-1,4-Benzoxazine: Novel Anti-Tubercular Scaffolds

Sivanandhan Karunanidhi

Sivanandhan Karunanidhi

Department of Pharmaceutical Chemistry, Discipline of Pharmaceutical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa

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Rajshekhar Karpoormath

Corresponding Author

Rajshekhar Karpoormath

Department of Pharmaceutical Chemistry, Discipline of Pharmaceutical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa

E-mail: [email protected]; [email protected]Search for more papers by this author
Milan Bera

Corresponding Author

Milan Bera

Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai, 400076 India

E-mail: [email protected]; [email protected]Search for more papers by this author
Rajesh A. Rane

Rajesh A. Rane

Department of Pharmaceutical Chemistry, Discipline of Pharmaceutical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa

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Mahesh B. Palkar

Mahesh B. Palkar

Department of Pharmaceutical Chemistry, Discipline of Pharmaceutical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa

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First published: 28 August 2015
Citations: 4

Abstract

A facile and efficient method for the construction of 3-alkyl/aryl substituted 1,4-benzoxazine and benzoxazepine via AgNO3 catalyzed cyclization of propargyloxy sulfonamides and their anti-tubercular activity against Mycobacterium tuberculosis H37RV is described. This cyclization proceeds through 6-exo-dig manner to generate the products in moderate to good yields.

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