Issue 0, 1972

Reactive intermediates. Part XVI. Dihydrobenz[cd]indazoles and attempted routes to benz[cd]indazole

Abstract

Attempted synthesis of 1,2-dihydrobenz[cd]indazole from dimethyl 1,2-dihydrobenz[cd]indazole-1,2-dicarboxylate yielded only the more stable 1,3- and 1,5-dihydro-forms, (7) and (8), with the indazole rather than the naphthalene nucleus aromatic. These indazoles can be reconverted into NN-disubstituted dihydrobenzindazole derivatives but cannot be oxidised to benz[cd]indazole. Several other unsuccessful attempts to obtain the elusive benz[cd]indazole system are described.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 68-71

Reactive intermediates. Part XVI. Dihydrobenz[cd]indazoles and attempted routes to benz[cd]indazole

S. Bradbury, C. W. Rees and R. C. Storr, J. Chem. Soc., Perkin Trans. 1, 1972, 68 DOI: 10.1039/P19720000068

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