3-Benzyl-6-benzyl­amino-1-methyl-5-nitro-1,2,3,4-tetra­hydro­pyrimidine

In the title compound, C(19)H(22)N(4)O(2), the tetra­hydro­pyrimidine ring adopts an envelope conformation (with the N atom connected to the benzyl group representing the flap). This benzyl group occupies a quasi-axial position. The two benzyl groups lie over the tetra­hydro­pyridimidine ring. The a...

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Detalles Bibliográficos
Autores principales: Kannan, M., Manivel, P., Sarathbabu, M., Sathishkumar, R., Surya Prakash Rao, H., Krishna, R.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983565/
https://www.ncbi.nlm.nih.gov/pubmed/21580289
http://dx.doi.org/10.1107/S160053681000348X
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author Kannan, M.
Manivel, P.
Sarathbabu, M.
Sathishkumar, R.
Surya Prakash Rao, H.
Krishna, R.
author_facet Kannan, M.
Manivel, P.
Sarathbabu, M.
Sathishkumar, R.
Surya Prakash Rao, H.
Krishna, R.
author_sort Kannan, M.
collection PubMed
description In the title compound, C(19)H(22)N(4)O(2), the tetra­hydro­pyrimidine ring adopts an envelope conformation (with the N atom connected to the benzyl group representing the flap). This benzyl group occupies a quasi-axial position. The two benzyl groups lie over the tetra­hydro­pyridimidine ring. The amino group is a hydrogen-bond donor to the nitro group.
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spelling pubmed-29835652010-12-30 3-Benzyl-6-benzyl­amino-1-methyl-5-nitro-1,2,3,4-tetra­hydro­pyrimidine Kannan, M. Manivel, P. Sarathbabu, M. Sathishkumar, R. Surya Prakash Rao, H. Krishna, R. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(22)N(4)O(2), the tetra­hydro­pyrimidine ring adopts an envelope conformation (with the N atom connected to the benzyl group representing the flap). This benzyl group occupies a quasi-axial position. The two benzyl groups lie over the tetra­hydro­pyridimidine ring. The amino group is a hydrogen-bond donor to the nitro group. International Union of Crystallography 2010-02-03 /pmc/articles/PMC2983565/ /pubmed/21580289 http://dx.doi.org/10.1107/S160053681000348X Text en © Kannan et al. 2010 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
Kannan, M.
Manivel, P.
Sarathbabu, M.
Sathishkumar, R.
Surya Prakash Rao, H.
Krishna, R.
3-Benzyl-6-benzyl­amino-1-methyl-5-nitro-1,2,3,4-tetra­hydro­pyrimidine
title 3-Benzyl-6-benzyl­amino-1-methyl-5-nitro-1,2,3,4-tetra­hydro­pyrimidine
title_full 3-Benzyl-6-benzyl­amino-1-methyl-5-nitro-1,2,3,4-tetra­hydro­pyrimidine
title_fullStr 3-Benzyl-6-benzyl­amino-1-methyl-5-nitro-1,2,3,4-tetra­hydro­pyrimidine
title_full_unstemmed 3-Benzyl-6-benzyl­amino-1-methyl-5-nitro-1,2,3,4-tetra­hydro­pyrimidine
title_short 3-Benzyl-6-benzyl­amino-1-methyl-5-nitro-1,2,3,4-tetra­hydro­pyrimidine
title_sort 3-benzyl-6-benzyl­amino-1-methyl-5-nitro-1,2,3,4-tetra­hydro­pyrimidine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983565/
https://www.ncbi.nlm.nih.gov/pubmed/21580289
http://dx.doi.org/10.1107/S160053681000348X
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