Abstract
The title compound, C14H11ClN2O, was synthesized by the reaction of 2-chlorobenzaldehyde and 2-aminobenzamide in an ionic liquid. The pyrimidine ring adopts a skew-boat conformation and the two benzene rings make a dihedral angle of 87.1 (1)°. In the crystal, N—H⋯O and C—H⋯N hydrogen bonding links the molecules along b.
Highlights
The title compound, C14H11ClN2O, was synthesized by the reaction of 2-chlorobenzaldehyde and 2-aminobenzamide in an ionic liquid
H atoms treated by a mixture of independent and constrained refinement max = 0.20 e Å3
We report here the crystal structure of 2-(2-chlorophenyl)-2,3-dihydroquinazolin-4(1H)-one, (I)
Summary
H atoms treated by a mixture of independent and constrained refinement max = 0.20 e Å3. R factor = 0.030; wR factor = 0.082; data-to-parameter ratio = 12.5. The title compound, C14H11ClN2O, was synthesized by the reaction of 2-chlorobenzaldehyde and 2-aminobenzamide in an ionic liquid. The pyrimidine ring adopts a skew-boat conformation and the two benzene rings make a dihedral angle of 87.1 (1). N—H O and C—H N hydrogen bonding links the molecules along b
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More From: Acta Crystallographica Section E Structure Reports Online
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