Thieno pyrazoles, electrophilic

Thieno[3,4-d]oxazole-3a(4H)-carboxylic acid, dihydro-2-methyl-synthesis, 6, 1020 Thieno[2,3-d Joxazoles synthesis, 6, 990 Thieno[3,2-g]pteridine structure, 3, 284 lH-Thieno[3,4-c]pyran-2-ones synthesis, 4, 1032 Thienopyrazines synthesis, 4, 1022-1024 Thieno[2,3-6]pyrazines, 4, 1023 electrophilic substitution, 4, 1024 Thieno[3,4-6]pyrazines, 4, 1024 Thieno[3,4-c]pyrazole, 4,6-dihydro-3-hydroxy-carbamates... 

Another electrophilic cyclization strategy is reported in which polyphosphoric acid cyclization of thienyl 2-hydrazones (89) affords l-(p-nitrophenyl)thieno[3,2-c]pyrazoles (90) (Equation (23)) <67CJC697>. On initial analysis, the process appears limited to p-nitrophenylhydrazones but the p-nitrophenyl unit is easily removed in a tandem reduction-oxidation sequence to afford the 1H-thieno[3,2-c]pyrazoles (3). 

Pyrazole-, Thiazole>, and Imidazole>fused Thiophens.—Starting from (410) and carrying out nucleophilic substitution with thioglycolate followed by ring-closure, as described for (384) and (408), the thieno[2,3-d]pyrazole system (411) was synthesized. Their ionization constants have been determined and the transmission of the influence of the substituents R has been studied and found to be more feeble than in naphthalene d benzo[b]thiophen. From the cyano-derivative (412), thiophen-fused derivatives such as (413) and (414) have been synthesized. Electrophilic... 

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