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4-(3,4-Dihydro-β-carbolin-1-yl)pyrimidin-2-amine

The mol­ecule of accanthomine A, C(15)H(13)N(5), is approximately planar, with the indolyl fused-ring and the pyrimidyl ring being twisted by 31.7 (1)° The amino group of the five-membered ring is an intramolecular hydrogen-bond donor to a nitro­gen acceptor of the pyrimide ring. The amino group of...

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Autores principales: Mukhtar, Mat Ropi, Zainal Abidin, Anissuhailin, Awang, Khalijah, A. Hadi, A. Hamid, Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968656/
https://www.ncbi.nlm.nih.gov/pubmed/21582249
http://dx.doi.org/10.1107/S160053680900600X
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author Mukhtar, Mat Ropi
Zainal Abidin, Anissuhailin
Awang, Khalijah
A. Hadi, A. Hamid
Ng, Seik Weng
author_facet Mukhtar, Mat Ropi
Zainal Abidin, Anissuhailin
Awang, Khalijah
A. Hadi, A. Hamid
Ng, Seik Weng
author_sort Mukhtar, Mat Ropi
collection PubMed
description The mol­ecule of accanthomine A, C(15)H(13)N(5), is approximately planar, with the indolyl fused-ring and the pyrimidyl ring being twisted by 31.7 (1)° The amino group of the five-membered ring is an intramolecular hydrogen-bond donor to a nitro­gen acceptor of the pyrimide ring. The amino group of the pyrimide ring is a hydrogen-bond donor to the N atoms of adjacent mol­ecules. These hydrogen-bonding inter­actions give rise to a layered network with a 4.8(2) topology.
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spelling pubmed-29686562010-12-30 4-(3,4-Dihydro-β-carbolin-1-yl)pyrimidin-2-amine Mukhtar, Mat Ropi Zainal Abidin, Anissuhailin Awang, Khalijah A. Hadi, A. Hamid Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of accanthomine A, C(15)H(13)N(5), is approximately planar, with the indolyl fused-ring and the pyrimidyl ring being twisted by 31.7 (1)° The amino group of the five-membered ring is an intramolecular hydrogen-bond donor to a nitro­gen acceptor of the pyrimide ring. The amino group of the pyrimide ring is a hydrogen-bond donor to the N atoms of adjacent mol­ecules. These hydrogen-bonding inter­actions give rise to a layered network with a 4.8(2) topology. International Union of Crystallography 2009-02-25 /pmc/articles/PMC2968656/ /pubmed/21582249 http://dx.doi.org/10.1107/S160053680900600X Text en © Mukhtar et al. 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Mukhtar, Mat Ropi
Zainal Abidin, Anissuhailin
Awang, Khalijah
A. Hadi, A. Hamid
Ng, Seik Weng
4-(3,4-Dihydro-β-carbolin-1-yl)pyrimidin-2-amine
title 4-(3,4-Dihydro-β-carbolin-1-yl)pyrimidin-2-amine
title_full 4-(3,4-Dihydro-β-carbolin-1-yl)pyrimidin-2-amine
title_fullStr 4-(3,4-Dihydro-β-carbolin-1-yl)pyrimidin-2-amine
title_full_unstemmed 4-(3,4-Dihydro-β-carbolin-1-yl)pyrimidin-2-amine
title_short 4-(3,4-Dihydro-β-carbolin-1-yl)pyrimidin-2-amine
title_sort 4-(3,4-dihydro-β-carbolin-1-yl)pyrimidin-2-amine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968656/
https://www.ncbi.nlm.nih.gov/pubmed/21582249
http://dx.doi.org/10.1107/S160053680900600X
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