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Benzyl {2-[(2-(1H-Benzo[d][1,2,3]triazol-1-yl)-2-oxoethyl)amino]-2-oxoethyl} carbamate
Molbank 2014, 2014(3), M829; doi:10.3390/M829
Short Note

(1H-Benzo[d][1,2,3]triazol-1-yl)(5-bromo-1-hydroxy-1H-indol-3-yl)methanone

1, 1,* , 1, 1, 2 and 1,*
1 Dipartimento di Scienza e Alta Tecnologia, Università degli Studi dell'Insubria, via Valleggio 11, 22100, Como, Italy 2 Department of Chemistry and Biochemistry, University of Oklahoma, Stephenson Life Sciences Research Center, 101 Stephenson Parkway, Norman, OK 73019-5251, USA
In memory of Prof. Dr. Alan Roy Katritzky.
* Authors to whom correspondence should be addressed.
Received: 1 April 2014 / Accepted: 4 July 2014 / Published: 11 July 2014
Download PDF [234 KB, uploaded 11 July 2014]

Abstract

The title compound was easily prepared by a nitrosoarene-alkyne cycloaddition reaction carried out in toluene at 80 °C. The product is a highly functionalized compound that can be further derivatized through various functional group interconversion procedures.
Keywords: indoles; alkynones; nitrosoarenes; annulation indoles; alkynones; nitrosoarenes; annulation
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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Tibiletti, F.; Penoni, A.; Palmisano, G.; Maspero, A.; Nicholas, K.M.; Vaghi, L. (1H-Benzo[d][1,2,3]triazol-1-yl)(5-bromo-1-hydroxy-1H-indol-3-yl)methanone. Molbank 2014, 2014, M829.

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