A comparison of the structures of some 2- and 3-substituted chromone derivatives: a structural study on the importance of the secondary carboxamide backbone for the inhibitory activity of MAO-B

Acta Crystallographica Section E: Crystallographic Communications

Gomes, L.R.³  Borges, F.⁴  Gaspar, A.⁵  Cagide, F.⁶  Low, J.N.⁹ 

[1]CIQUP/Departamento de Quí

[2]Department of Chemistry, University of Aberdeen, Meston Walk, Old Aberdeen, AB24 3UE, Scotland

[3]FP-ENAS-Faculdade de Ciê

[4]REQUIMTE/Departamento de Quí

[5]de da UFP, Universidade Fernando Pessoa, Rua Carlos da Maia, 296, P-4200-150 Porto, Portugal

[6]de, Escola Superior de Saú

[7]mica e Bioquí

[8]mica, Faculdade de Ciê

[9]ncias de Saú

[10]ncias, Universidade do Porto, 4169-007 Porto, Portugal

关键词: CRYSTAL STRUCTURE;    CHROMONES;    PHARMALOGICAL ACTIVITY;    SUPRAMOLECULAR STRUCTURE;    HYDROGEN BONDING;   

DOI  :  10.1107/S2056989015017958

学科分类：数学（综合）

来源: International Union of Crystallography

【 摘 要 】

The crystal structures of the 3-substituted tertiary chromone carboxamide derivative, C17H13NO3, N-methyl-4-oxo-N-phenyl-4H-chromene-3-carboxamide (1), and the chromone carbonyl pyrrolidine derivatives, C14H13NO3, 3-(pyrrolidine-1-carbon­yl)-4H-chromen-4-one (3) and 2-(pyrrolidine-1-carbon­yl)-4H-chromen-4-one (4) have been determined. Their structural features are discussed and compared with similar compounds namely with respect to their MAO-B inhibitory activities. The chromone carboxamide presents a –syn conformation with the aromatic rings twisted with respect to each other [the dihedral angle between the mean planes of the chromone system and the exocyclic phenyl ring is 58.48 (8)°]. The pyrrolidine derivatives also display a significant twist: the dihedral angles between the chromone system and the best plane formed by the pyrrolidine atoms are 48.9 (2) and 23.97 (12)° in (3) and (4), respectively. Compound (3) shows a short C—H⋯O intra­molecular contact forming an S(7) ring. The supra­molecular structures for each compound are defined by weak C—H⋯O hydrogen bonds, which link the mol­ecules into chains and sheets. The Cambridge Structural Database gave 45 hits for compounds with a pyrrolidinecarbonyl group. A simple statistical analysis of their geometric parameters is made in order to compare them with those of the mol­ecules determined in the present work.

【 授权许可】

CC BY