138047-82-2Relevant academic research and scientific papers
Synthesis of 5-thioxo-6H-imidazo[1,2-c]quinazolines and related compounds based on cyclocondensations of 2-isothiocyanatobenzonitrile (ITCB) with α-aminoketones
Bodtke, Anja,Pfeiffer, Wolf-Diethard,G?rls, Helmar,Dollinger, Horst,Langer, Peter
, p. 11287 - 11298 (2008/03/12)
Pharmacologically relevant 5-thioxo-6H-imidazo[1,2-c]quinazolines and 5-oxo-6H-imidazo[1,2-c]quinazolines were prepared by sequential reactions of α-aminoketones with 2-isothiocyanatobenzonitrile (ITCB) and 2-isocyanatobenzonitrile (ICB), respectively. Th
Sequential cyclizations of 2-isothiocyanatobenzonitrile and 2-iso cyanatobenzonitrile with α-aminoketones
Langer, Peter,Bodtke, Anja
, p. 5965 - 5967 (2007/10/03)
Pharmacologically relevant 5-thioxo-6H-imidazo[1,2-c]quinazolines and 5-oxo-6H-imidazo[1,2-c]quinazolines were prepared by sequential reactions of α-aminoketones with 2-isothiocyanatobenzonitrile and 2-isocyanatobenzonitrile, respectively.
2-Isocyanatocyclohex-1-ene-carbonitrile and 2-isocyanatobenzonitrile as bifunctional electrophiles in the synthesis of [c]-heteroanellated quinazoline derivatives
Thom,Zinner
, p. 469 - 475 (2007/10/02)
N'-substituted N-(2-cyanophenyl)ureas afford [1,2,4]triazolo[1,5-c]-and imidazo[1,2-c]-quinazolin-5(6H)-ones. 2-Isocyanatocyclohex-1-ene-carbonitrile as starting compound leads to the 7,8,9,10-saturated structural analogues.
Imidazo [1,2-c] quinazoline compounds
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, (2008/06/13)
New imidazo [1,2-c] quinazoline compounds useful as coronary smooth muscle relaxants and corresponding to the formula: STR1 in which: Y is oxygen or sulfur;R 1 is (C 1 -C 6) alkyl optionally substituted by a phenyl itself optionally substituted, a (C 3 -C
