JOURNAL ARTICLE

3′-[Hydroxy(4-oxo-4H-chromen-3-yl)methyl]-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carbonitrile

E. GovindanK. SakthiMurugesanA. SubbiahPandiP. YuvarajBoreddy S. R. Reddy

Year: 2011 Journal:   Acta Crystallographica Section E Structure Reports Online Vol: 68 (1)Pages: o136-o137   Publisher: International Union of Crystallography

Abstract

In the title compound, C23H19N3O4, the pyran ring adopts a half-chair conformation, while the pyrrolidine (with a C atom as the flap atom) and the five-membered ring in the indoline (with a C atom as the flap atom) ring system adopt slight envelope conformations. The pyrrolidine ring makes dihedral angles of 83.3 (1) and 60.4 (1)° with the mean plane through all non-H atoms of the indoline and chromene ring systems, respectively. In the crystal, mol­ecules are connected by two unique N—H⋯O and O—H⋯O hydrogen-bonding inter­actions, which form centrosymmetric patterns described by graph-set motifs R 2 2(18) and R 2 2(14). These two motifs combine to form a hydrogen-bonded chain which propagates in the a-axis direction. The crystal structure is also stablized by C—H⋯O inter­actions and by aromatic π–π stacking inter­actions between the pyran and benzene rings of neighbouring mol­ecules [centroid–centroid distance = 3.755 (1) Å and slippage = 1.371 (2) Å].

Keywords:
Pyrrolidine Indoline Ring (chemistry) Dihedral angle Chemistry Pyran Atom (system on chip) Stacking Crystallography Hydrogen bond Crystal structure Benzene Bioinformatics Stereochemistry Molecule Organic chemistry Computer science

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Topics

Synthesis of Organic Compounds
Health Sciences →  Medicine →  Pharmacology
Crystal structures of chemical compounds
Physical Sciences →  Chemistry →  Inorganic Chemistry
Synthesis and biological activity
Physical Sciences →  Chemistry →  Organic Chemistry

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