95546-66-0Relevant articles and documents
CYCLIZATION OF NITRILES. XIV. SYNTHESIS AND REACTIONS OF 1-ALKYL-4-CYANO-5,6,7,8-TETRAHYDRO-3(2H)-ISOQUINOLINETHIONES AND SOME OF THEIR ANALOGS
Sharanin, Yu. A.,Shestopalov, A. M.,Promonenkov, V. K.,Rodinovskaya, L. A.
, p. 2216 - 2224 (2007/10/02)
1-Alkyl-4-cyano-5,6,7,8-tetrahydro-3(2H)-isoquinolinethiones and 6-methyl-4,5-trimethylene-3-cyano-2(1H)-pyridinethione were synthesized by the reaction of cyclic enamino ketones and 1,3-diketones with nitriles containing an active methylene group.The products are readily alkylated by halogen derivatives of the sulfur atom with the formation of substituted 3-alkylthio-4-cyano-5,6,7,8-tetrahydroisoquinolines, 3-aminothienopyridines, and 3-aminothienoquinolines, which were used in the synthesis of various heterocyclic systems.The corresponding 1-alkyl-4-cyano-5,6,7,8-tetrahydro-3(2H)-isoquinolines are alkylated preferentially at the ring nitrogen atom.