نتایج جستجو برای: hexahydroquinoline 3 carboxamide

تعداد نتایج: 1812884  

2009
Long He Hong-Mei Qin Lian-Mei Chen

There are two independent mol-ecules in the asymmetric unit of the title compound, C(15)H(12)BrNO(2). In both mol-ecules, the two benzene rings adopt a cis configuration with respect to the ep-oxy ring. In one mol-ecule, the ep-oxy ring makes dihedral angles of 60.5 (2) and 77.92 (19)° with the two benzene rings; in the other mol-ecule, the values are 61.0 (2) and 81.43 (19)°. Inter-molecular N...

Journal: :Molecules 2007
Yehya M Elkholy

2-Oxo-4-phenyl-1,2,5,6,7,8-hexahydroquinoline-3-carbonitrile (10) reacted with hydrazine hydrate, phenylisothiocyanate or benzoyl chloride to give derivatives 12, 13 and 15, respectively. The latter two products were treated with hydrazine hydrate to afford pyrozole[3,4-b]quinolines derivatives 14 and 16, respectively. Compound 10 also reacted with acetonitrile dimer or malononitrile dimer to y...

Journal: :Journal of the Korean Chemical Society 2014

2011
Xiao-Hui Deng Jing-Wen Ran

In the title dinuclear compound, [Zn(2)(C(6)H(6)N(3)O)(2)(C(6)H(7)N(3)O)(2)](NO(3))(2), the Zn(II) cation is N,N'-chelated by one pyridine-2-carboxamide oximate anion and one pyridine-2-carboxamide oxime mol-ecule, and is further bridged by an oxime O atom from the adjacent pyridine-2-carboxamide oximate anion, forming a distorted trigonal bipyramidal coordination. Two pyridine-2-carboxamide ox...

Journal: :Acta Crystallographica Section E Structure Reports Online 2011

Journal: :Acta Crystallographica Section E Structure Reports Online 2010

Journal: :Acta Crystallographica Section E Structure Reports Online 2009

Journal: :Acta Crystallographica Section E Crystallographic Communications 2018

2012
Cosmas O. Okoro Tasneem Siddiquee

This article describes one-pot synthesis of new fluorinated hexahydroquinoline derivatives via unsymmetric Hantzsch reaction involving 5-trifluoromethyl-1,3cyclohexanedione, aldehydes, acetoacetate ester, and ammonium acetate in trifluoroethanol (TFE). The reaction is simple and rapid with high yield.

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