z-logo
open-access-imgOpen Access
The polyfunctionalized enaminone ethyl [( Z )‐2‐(2,2‐dimethyl‐4,6‐dioxo‐1,3‐dioxan‐5‐ylidenemethyl)‐1‐methyl‐3‐oxo‐but‐1‐enylamino]acetate
Author(s) -
Vencato Ivo,
Cunha Silvio,
Ferrari Jailton,
Napolitano Hamilton B.,
Lariucci Carlito
Publication year - 2004
Publication title -
acta crystallographica section e
Language(s) - English
Resource type - Journals
ISSN - 1600-5368
DOI - 10.1107/s1600536804030211
Subject(s) - adduct , moiety , intramolecular force , chemistry , hydrogen bond , intermolecular force , amine gas treating , stereochemistry , medicinal chemistry , molecule , organic chemistry
The solid‐state structure of the title enaminone, C 15 H 17 N 1 O 7 , the C adduct obtained from the reaction of 4‐aminopent‐3‐en‐2‐one with methoxymethylene Meldrum's acid, has been investigated by X‐ray diffraction, and several structural features are different from the previously described structure of the corresponding N adduct. The carbonyl group of the enaminone moiety of the C adduct is not coplanar with the enamine fragment. One bifurcated intramolecular N—H⋯O hydrogen bond [2.688 (2) and 2.668 (2) Å] and two intermolecular C—H⋯O hydrogen bonds [3.339 (3) and 3.379 (3) Å] are observed. The structure packs in a linear fashion along the [100] direction.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom