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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Detalles Bibliográficos
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:
Organic Papers
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
Descripción
Sumario: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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