5′-Methyl-4′-oxo-7′-phenyl-3′,4′-dihydro-1′H-spiro[cyclohexane-1,2′-quinazoline]-8′-carbonitrile

The title compound, C21H21N3O, was obtained by cyclocondensation of 3-amino-5-methyl-[1,1′-biphenyl]-2,4-dicarbonitrile with cyclohexanone. The six-membered 1,3-diaza ring assumes an envelope conformation [with the flap atom displaced by 0.511 (7) &#...

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Main Authors: Jianhong Tang, Daxin Shi, Liupan Yan, Xuan Liu, Jiarong Li
Format: Article
Language:English
Published: International Union of Crystallography 2011-07-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S160053681102188X
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spelling doaj-1652abb9cb334112adf7f26d9d7ad2092020-11-24T21:29:02ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682011-07-01677o1672o167210.1107/S160053681102188X5′-Methyl-4′-oxo-7′-phenyl-3′,4′-dihydro-1′H-spiro[cyclohexane-1,2′-quinazoline]-8′-carbonitrileJianhong TangDaxin ShiLiupan YanXuan LiuJiarong LiThe title compound, C21H21N3O, was obtained by cyclocondensation of 3-amino-5-methyl-[1,1′-biphenyl]-2,4-dicarbonitrile with cyclohexanone. The six-membered 1,3-diaza ring assumes an envelope conformation [with the flap atom displaced by 0.511 (7) Å from the plane through the other ring atoms] and the cyclohexane ring displays a chair conformation. The dihedral angle between the aromatic rings is 42.61 (7)°.In the crystal, the molecules form hydrogen-bonded bands along [011].http://scripts.iucr.org/cgi-bin/paper?S160053681102188X
collection DOAJ
language English
format Article
sources DOAJ
author Jianhong Tang
Daxin Shi
Liupan Yan
Xuan Liu
Jiarong Li
spellingShingle Jianhong Tang
Daxin Shi
Liupan Yan
Xuan Liu
Jiarong Li
5′-Methyl-4′-oxo-7′-phenyl-3′,4′-dihydro-1′H-spiro[cyclohexane-1,2′-quinazoline]-8′-carbonitrile
Acta Crystallographica Section E
author_facet Jianhong Tang
Daxin Shi
Liupan Yan
Xuan Liu
Jiarong Li
author_sort Jianhong Tang
title 5′-Methyl-4′-oxo-7′-phenyl-3′,4′-dihydro-1′H-spiro[cyclohexane-1,2′-quinazoline]-8′-carbonitrile
title_short 5′-Methyl-4′-oxo-7′-phenyl-3′,4′-dihydro-1′H-spiro[cyclohexane-1,2′-quinazoline]-8′-carbonitrile
title_full 5′-Methyl-4′-oxo-7′-phenyl-3′,4′-dihydro-1′H-spiro[cyclohexane-1,2′-quinazoline]-8′-carbonitrile
title_fullStr 5′-Methyl-4′-oxo-7′-phenyl-3′,4′-dihydro-1′H-spiro[cyclohexane-1,2′-quinazoline]-8′-carbonitrile
title_full_unstemmed 5′-Methyl-4′-oxo-7′-phenyl-3′,4′-dihydro-1′H-spiro[cyclohexane-1,2′-quinazoline]-8′-carbonitrile
title_sort 5′-methyl-4′-oxo-7′-phenyl-3′,4′-dihydro-1′h-spiro[cyclohexane-1,2′-quinazoline]-8′-carbonitrile
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2011-07-01
description The title compound, C21H21N3O, was obtained by cyclocondensation of 3-amino-5-methyl-[1,1′-biphenyl]-2,4-dicarbonitrile with cyclohexanone. The six-membered 1,3-diaza ring assumes an envelope conformation [with the flap atom displaced by 0.511 (7) Å from the plane through the other ring atoms] and the cyclohexane ring displays a chair conformation. The dihedral angle between the aromatic rings is 42.61 (7)°.In the crystal, the molecules form hydrogen-bonded bands along [011].
url http://scripts.iucr.org/cgi-bin/paper?S160053681102188X
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AT daxinshi 5amp8242methyl4amp8242oxo7amp8242phenyl3amp82424amp8242dihydro1amp8242hspirocyclohexane12amp8242quinazoline8amp8242carbonitrile
AT liupanyan 5amp8242methyl4amp8242oxo7amp8242phenyl3amp82424amp8242dihydro1amp8242hspirocyclohexane12amp8242quinazoline8amp8242carbonitrile
AT xuanliu 5amp8242methyl4amp8242oxo7amp8242phenyl3amp82424amp8242dihydro1amp8242hspirocyclohexane12amp8242quinazoline8amp8242carbonitrile
AT jiarongli 5amp8242methyl4amp8242oxo7amp8242phenyl3amp82424amp8242dihydro1amp8242hspirocyclohexane12amp8242quinazoline8amp8242carbonitrile
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