Synthesis and crystal structures of 7-bromo-5-(2′-chloro)phenyl-3-hydroxy-1-methyl-1,2-dihydro-3H-1,4-benzodiazepin-2-one and 7-bromo-5-(2′-chloro)phenyl-1-hexyl-1,2,4,5-tetrahydro-3H-1,4-benzodiazepin-2,3-dione

► Synthesis and structural study of benzodiazepin-2-one derivatives. ► Influence of substituent in position 1 on heterocycle conformation and distortion. ► Proton migration. ► Contribution of H-bonds and halogen bond interaction to the overall structure organization and heterocycle distortion. Treat...

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Bibliographic Details
Published in:	Journal of molecular structure Vol. 1017; pp. 32 - 37
Main Authors:	Kravtsov, Victor Ch, Fonari, Marina S., Gdaniec, Мaria, Pavlovsky, Victor I., Andronati, Sergei A., Semenishyna, Ekaterina A.
Format:	Journal Article
Language:	English
Published:	Elsevier B.V 13-06-2012
Subjects:	1,4-Benzodiazepine Conformation Crystal structure hydrogen bonding Intermolecular interaction Synthesis X-ray diffraction Intermolecular interaction 1,4-Benzodiazepine Synthesis Crystal structure Conformation
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Summary:	► Synthesis and structural study of benzodiazepin-2-one derivatives. ► Influence of substituent in position 1 on heterocycle conformation and distortion. ► Proton migration. ► Contribution of H-bonds and halogen bond interaction to the overall structure organization and heterocycle distortion. Treatment of 7-bromo-5-(2′-chloro)phenyl-3-hydroxy-1,2-dihydro-3H-1,4-benzodiazepin-2-one (1) with methyl or hexyl tosylate resulted in 7-bromo-5-(2′-chloro)phenyl-3-hydroxy-1-methyl-1,2-dihydro-3H-1,4-benzodiazepin-2-one (2) and 7-bromo-5-(2′-chloro)phenyl-1-hexyl-1,2,4,5-tetrahydro-3H-1,4-benzodiazepin-2,3-dione (3). As confirmed by X-ray crystallography, the two products differ not only in the identity of the alkyl substituent in position 1 of the benzodiazepine fragment but also crystallize in different molecular forms resulting from proton migration. This alteration of the molecular structure leads to a significant change in the conformation of the central molecular fragment and influences the assembly mode in the crystal. In 3, centrosymmetric dimers formed via a pair of NH⋯O hydrogen bonds are further linked into chains via CBr⋯OC halogen bond interaction. In turn in 2 there are two symmetry independent molecules, each giving a different set of intermolecular interactions. One of the molecules forms a dimer via OH⋯O interactions whereas the second one generates chain via CBr⋯OC halogen bond that is also assisted by a weak OH⋯Br hydrogen bond.
Bibliography:	http://dx.doi.org/10.1016/j.molstruc.2012.02.071
ISSN:	0022-2860 1872-8014
DOI:	10.1016/j.molstruc.2012.02.071