Regioselectivity of the substitution for the nitro group in 2,4,6-trinitrobenzonitrile under the action of thiols. The synthesis of 4,6-dinitro derivatives of benzo-annelated sulfur-containing heterocycles

Mendeleev Communications Pub Date: DOI: 10.1070/MC2000v010n02ABEH001220

Abstract

Conditions for the regioselective substitution for a nitro group in the ortho-position in 2,4,6-trinitrobenzonitrile under the action of thiols (PhCH2SH, HSCH2CO2Et or PhSH) in the presence of K2CO3 or KOH were found, and the intramolecular cyclization of the ortho-fragments –SX and –CN (X = Cl or CH2CO2Et) was performed to afford 3-chloro-4,6-dinitrobenzo[d]isothiazole and 3-amino-2-ethoxycarbonyl-4,6-dinitrobenzo[b]thiophene, respectively.

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