Unknown

Dataset Information

0

6,7,8,9,10,11-Hexahydro-13H-azocino[2,1-b]quinazolin-13-one.


ABSTRACT: The title compound, C(14)H(16)N(2)O, is a synthetic analogue of quinazolone alkaloids with pyrrilo, pyrido and azopino rings. The quinazolinic part of the mol-ecule is generally planar within 0.037?(3)?Å; the eight-membered ring exhibits an inter-mediate conformation between the chair and boat forms as it is typical for cyclo-octene rings. An ethyl-ene group of the azopino ring is disordered over two positions with a refined occupancy ratio of 0.910?(7):0.090?(7). In the crystal, the H atoms of the aromatic rings form weak C-H?O and C-H?N hydrogen bonds. One C-H?O hydrogen bond leads to the formation of a one-dimensional chain. Another C-H?O and a C-H?N bond link these chains, generating a three-dimensional network.

SUBMITTER: Okmanov RY 

PROVIDER: S-EPMC2977403 | biostudies-literature | 2009 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

6,7,8,9,10,11-Hexahydro-13H-azocino[2,1-b]quinazolin-13-one.

Okmanov Rasul Ya RY   Samarov Zafir U ZU   Turgunov Kambarali K KK   Tashkhodjaev Bakhodir B   Shakhidoyatov Khusniddin M KM  

Acta crystallographica. Section E, Structure reports online 20090704 Pt 8


The title compound, C(14)H(16)N(2)O, is a synthetic analogue of quinazolone alkaloids with pyrrilo, pyrido and azopino rings. The quinazolinic part of the mol-ecule is generally planar within 0.037 (3) Å; the eight-membered ring exhibits an inter-mediate conformation between the chair and boat forms as it is typical for cyclo-octene rings. An ethyl-ene group of the azopino ring is disordered over two positions with a refined occupancy ratio of 0.910 (7):0.090 (7). In the crystal, the H atoms of  ...[more]

Similar Datasets

| S-EPMC3200730 | biostudies-literature
| S-EPMC2979261 | biostudies-literature
| S-EPMC3006833 | biostudies-literature
| S-EPMC3151818 | biostudies-other
| S-EPMC2983797 | biostudies-other
| S-EPMC3151778 | biostudies-literature
| S-EPMC3201358 | biostudies-literature
| S-EPMC4120575 | biostudies-literature
| S-EPMC2960321 | biostudies-other
| S-EPMC3379507 | biostudies-other