2009
DOI: 10.1107/s1600536809028025
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1′-Methyl-2,2′′-dioxoindoline-3-spiro-2′-pyrrolidine-3′-spiro-3′′-indoline-4′,4′-dicarbonitrile

Abstract: In the title compound, C21H15N5O2, the pyrrolidine ring adopts a twist conformation. Both the oxindole rings are planar [maximum deviations of 0.076 (1) and 0.029 (1) Å in the two rings] and are oriented at a dihedral angle of 72.7 (1)°. The crystal structure is stabilized by C—H⋯O, N—H⋯O, N—H⋯N and C—H⋯π inter­actions.

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Cited by 2 publications
(2 citation statements)
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“…The geometric parameters of the title molecule ( Fig. 1) agree well with those reported for a similar compound, 1′methyl-2,2′′-dioxoindoline-3-spiro-2′-pyrrolidine-3′-spiro-3′′-indoline-4′,4′-dicarbonitrile (Ramesh et al, 2009). The pyrrolidine ring (N2/C10/C11/C13/C21) adopts a twist conformation on bond N2-C21: puckering parameters and the asymmetry parameters for this ring are q 2 = 0.411 (2) Å, φ 2 = 160.3 3 Fig.…”
Section: S1 Structural Commentarysupporting
confidence: 83%
See 1 more Smart Citation
“…The geometric parameters of the title molecule ( Fig. 1) agree well with those reported for a similar compound, 1′methyl-2,2′′-dioxoindoline-3-spiro-2′-pyrrolidine-3′-spiro-3′′-indoline-4′,4′-dicarbonitrile (Ramesh et al, 2009). The pyrrolidine ring (N2/C10/C11/C13/C21) adopts a twist conformation on bond N2-C21: puckering parameters and the asymmetry parameters for this ring are q 2 = 0.411 (2) Å, φ 2 = 160.3 3 Fig.…”
Section: S1 Structural Commentarysupporting
confidence: 83%
“…For the biological activities of indole derivatives, see: Macor et al (1992); Andreani et al (2001); Quetin-Leclercq (1994); Mukhopadhyay et al (1981); Singh et al (2000). For the structure of a very similar compound, see: Ramesh et al (2009 Symmetry codes: (i) x þ 1 2 ; Ày þ 1 2 ; z þ 1 2 ; (ii) Àx þ 1 2 ; y þ 1 2 ; Àz þ 1 2 ; (iii) x; y; z þ 1.…”
Section: Related Literaturementioning
confidence: 99%