Unknown

Dataset Information

0

Crystal structure of (E)-9-({[4-(di-ethyl-amino)-phen-yl]imino}-meth-yl)-2,3,6,7-tetra-hydro-1H,5H-pyrido[3,2,1-ij]quinolin-8-ol.


ABSTRACT: The title compound, C23H29N3O, was synthesized from the condensation reaction of 8-hy-droxy-julolidine-9-carbaldehyde and N,N-diethyl-p-phenyl-enedi-amine. The hy-droxy group forms a intra-molecular hydrogen bond to the imine N atom and generates an S(6) ring motif. The conformation about the C=N bond is E, and the aromatic ring of the julolidine moiety is inclined to the benzene ring by 3.74?(14)°. One of the fused non-aromatic rings of the julolidine moiety adopts an envelope conformation and the other has a screw-boat conformation. In the crystal, mol-ecules are linked by C-H?? inter-actions involving the aromatic julolidine ring, forming slabs parallel to the bc plane. The tricyclic fragment of the julolidine ring and the azomethine C=N bond are disordered over two sets of sites with a refined occupancy ratio of 0.773?(3):0.227?(3).

SUBMITTER: Faizi MS 

PROVIDER: S-EPMC5209767 | biostudies-literature | 2017 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Crystal structure of (<i>E</i>)-9-({[4-(di-ethyl-amino)-phen-yl]imino}-meth-yl)-2,3,6,7-tetra-hydro-1<i>H</i>,5<i>H</i>-pyrido[3,2,1-<i>ij</i>]quinolin-8-ol.

Faizi Md Serajul Haque MS   Ahmad Musheer M   Kapshuk Anatoly A AA   Golenya Irina A IA  

Acta crystallographica. Section E, Crystallographic communications 20170101 Pt 1


The title compound, C<sub>23</sub>H<sub>29</sub>N<sub>3</sub>O, was synthesized from the condensation reaction of 8-hy-droxy-julolidine-9-carbaldehyde and <i>N</i>,<i>N</i>-diethyl-<i>p</i>-phenyl-enedi-amine. The hy-droxy group forms a intra-molecular hydrogen bond to the imine N atom and generates an <i>S</i>(6) ring motif. The conformation about the C=N bond is <i>E</i>, and the aromatic ring of the julolidine moiety is inclined to the benzene ring by 3.74 (14)°. One of the fused non-aromatic  ...[more]

Similar Datasets

| S-EPMC3685040 | biostudies-literature
| S-EPMC5050754 | biostudies-literature
| S-EPMC2983933 | biostudies-literature
| S-EPMC5418808 | biostudies-literature
| S-EPMC2969442 | biostudies-literature
| S-EPMC3588512 | biostudies-literature
| S-EPMC3588293 | biostudies-other
| S-EPMC3515293 | biostudies-literature
| S-EPMC2977288 | biostudies-literature
| S-EPMC3006987 | biostudies-literature