82137-61-9Relevant academic research and scientific papers
Some reactions of 2-functionalized 3-amino-4-aryl-6-(2′-thienyl)-thieno[2,3-B]-pyridines: Synthesis of new pyridothienopyrimidines, pyridothienotriazines and related fused tetracyclic systems
Abdel-Rahman,Bakhite,Mohamed,Thabet
, p. 89 - 106 (2007/10/03)
4-Aryl-3-cyano-6-(2′-thienyl)-pyridine-2(1H)-thiones (2a-c) were prepared and reacted with chloroacetonitrile or chloroacetamide to furnish 3-amino-4-aryl-6-(2′-thienyl)-thieno[2,3-b]pyridine-2-carbonitriles (4a-c) and 2-carboxamide analogs 6a-c respectiv
Synthesis of some new pyridothienopyrimidines and related [1,2,4]triazolopyridothienopyrimidines
Bakhite, E.A.,Abdel-Rahman, A.E.,Mohamed, O.S.,Thabet, E.A.
, p. 236 - 247 (2007/10/03)
3-Amino-4-phenyl-6-(2-thienyl)thieno[2,3-b]pyridine-2-carboxamide (3a) reacted with triethyl orthoformate to give the pyrimidinone derivative 4. Reaction of 4 with phosphorus oxychloride produced the corresponding 4-chloropyrimidine derivative 5 which underwent some nucleophilic displacements upon treatment with thiourea, morpholine or aniline to give the pyridothienopyrimidine derivatives 6, 8 and 9 respectively. Similarly, the reaction of 5 with hydrazine hydrate afforded 4-hydrazino-9-phenyl-7-(2-thienyl)pyrido[3',2':4,5]thieno[3,2-d]pyrimidine (10). The condensation of 3-amino-4-phenyl-6-(2-thienyl)thieno[2,3-b]pyridine-2-carbonitrile (3b) with triethyl orthoformate led to the methanimidate derivative 18 which upon treatment with hydrazine hydrate furnished 3-amino-3,4-dihydro-4-imino-9-phenyl-7-(2-thienyl)pyrido[3',2':4,5]thieno[3,2-d]pyrimidine (19). The compounds 10 and 19 were used as precursors for synthesizing the isomeric [1,2,4]triazolopyridothienopyrimidines via Dimroth rearrangements.
CYCLIZATION REACTIONS OF NITRILES. 2-ARYL-3-(2-THENOYL)-1,1-DICYANOPROPANES AND PYRIDINE DERIVATIVES BASED ON THEM
Sharanin, Yu. A.,Promonenkov, V. K.,Shestopalov, A. M.
, p. 548 - 556 (2007/10/02)
In the reaction of 1,1,1-trifluoro-3-(2-thenoyl)acetone with arylidenemalononitriles acid cleavage of the products from Michael addition takes place with the formation of 2-aryl-3-(2-thenoyl)-1,1-dicyanopropanes.They were used for the synthesis of 4-aryl-2-bromo-6-(2-thienyl)-3-cyanopyridines and 4-aryl-6-(2-thienyl)-3-cyano-2(1H)-pyridinethiones and condensed heterocyclic compounds based on them.
