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Synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidine hybrids: synthetic sequence and the molecular and supramolecular structures of two intermediates and three final products
A concise and versatile synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidines has been developed, starting from 4-(1H-benzo[d]imidazol-1-yl)pyrimidines, and we report here the synthesis and spectroscopic and structural characterization of three such products, along wit...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240168/ https://www.ncbi.nlm.nih.gov/pubmed/37140891 http://dx.doi.org/10.1107/S2053229623003728 |
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author | Vicentes, Daniel E. Rodríguez, Ricaurte Cobo, Justo Glidewell, Christopher |
author_facet | Vicentes, Daniel E. Rodríguez, Ricaurte Cobo, Justo Glidewell, Christopher |
author_sort | Vicentes, Daniel E. |
collection | PubMed |
description | A concise and versatile synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidines has been developed, starting from 4-(1H-benzo[d]imidazol-1-yl)pyrimidines, and we report here the synthesis and spectroscopic and structural characterization of three such products, along with those of two intermediates in the reaction pathway. The intermediates 4-[2-(4-chlorophenyl)-1H-benzo[d]imidazol-1-yl]-6-methoxypyrimidine-2,5-diamine, (II), and 4-[2-(4-bromophenyl)-1H-benzo[d]imidazol-1-yl]-6-methoxypyrimidine-2,5-diamine, (III), crystallize as the isostructural monohydrates C(18)H(15)ClN(5)O·H(2)O and C(18)H(15)BrN(5)O·H(2)O, respectively, in which the components are linked into complex sheets by O—H⋯N and N—H⋯O hydrogen bonds. In the product (E)-4-methoxy-5-[(4-nitrobenzylidene)amino]-6-[2-(4-nitrophenyl)-1H-benzo[d]imidazol-1-yl]pyrimidin-2-amine, which crystallizes as a 1:1 solvate with dimethyl sulfoxide, C(25)H(18)N(8)O(5)·C(2)H(6)OS, (IV), inversion-related pairs of the pyrimidine component are linked by N—H⋯N hydrogen bonds to form cyclic centrosymmetric R (2) (2)(8) dimers to which pairs of solvent molecules are linked by N—H⋯O hydrogen bonds. (E)-4-Methoxy-5-[(4-methylbenzylidene)amino]-6-[2-(4-methylphenyl)-1H-benzo[d]imidazol-1-yl]pyrimidin-2-amine, C(27)H(24)N(6)O, (V), crystallizes with Z′ = 2 and the molecules are linked into a three-dimensional framework structure by a combination of N—H⋯N, C—H⋯N and C—H⋯π(arene) hydrogen bonds. The analogous product (E)-4-methoxy-5-[(4-chlorobenzylidene)amino]-6-[2-(4-methylphenyl)-1H-benzo[d]imidazol-1-yl]pyrimidin-2-amine, C(26)H(21)ClN(6)O, (VI), crystallizes from dimethyl sulfoxide in two forms: one, denoted (VIa), is isostructural with (V), and the other, denoted (VIb), crystallizes with Z′ = 1, but as an unknown solvate in which the pyrimidine molecules are linked by N—H⋯N hydrogen bonds to form a ribbon containing two types of centrosymmetric ring. |
format | Online Article Text |
id | pubmed-10240168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-102401682023-06-06 Synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidine hybrids: synthetic sequence and the molecular and supramolecular structures of two intermediates and three final products Vicentes, Daniel E. Rodríguez, Ricaurte Cobo, Justo Glidewell, Christopher Acta Crystallogr C Struct Chem Research Papers A concise and versatile synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidines has been developed, starting from 4-(1H-benzo[d]imidazol-1-yl)pyrimidines, and we report here the synthesis and spectroscopic and structural characterization of three such products, along with those of two intermediates in the reaction pathway. The intermediates 4-[2-(4-chlorophenyl)-1H-benzo[d]imidazol-1-yl]-6-methoxypyrimidine-2,5-diamine, (II), and 4-[2-(4-bromophenyl)-1H-benzo[d]imidazol-1-yl]-6-methoxypyrimidine-2,5-diamine, (III), crystallize as the isostructural monohydrates C(18)H(15)ClN(5)O·H(2)O and C(18)H(15)BrN(5)O·H(2)O, respectively, in which the components are linked into complex sheets by O—H⋯N and N—H⋯O hydrogen bonds. In the product (E)-4-methoxy-5-[(4-nitrobenzylidene)amino]-6-[2-(4-nitrophenyl)-1H-benzo[d]imidazol-1-yl]pyrimidin-2-amine, which crystallizes as a 1:1 solvate with dimethyl sulfoxide, C(25)H(18)N(8)O(5)·C(2)H(6)OS, (IV), inversion-related pairs of the pyrimidine component are linked by N—H⋯N hydrogen bonds to form cyclic centrosymmetric R (2) (2)(8) dimers to which pairs of solvent molecules are linked by N—H⋯O hydrogen bonds. (E)-4-Methoxy-5-[(4-methylbenzylidene)amino]-6-[2-(4-methylphenyl)-1H-benzo[d]imidazol-1-yl]pyrimidin-2-amine, C(27)H(24)N(6)O, (V), crystallizes with Z′ = 2 and the molecules are linked into a three-dimensional framework structure by a combination of N—H⋯N, C—H⋯N and C—H⋯π(arene) hydrogen bonds. The analogous product (E)-4-methoxy-5-[(4-chlorobenzylidene)amino]-6-[2-(4-methylphenyl)-1H-benzo[d]imidazol-1-yl]pyrimidin-2-amine, C(26)H(21)ClN(6)O, (VI), crystallizes from dimethyl sulfoxide in two forms: one, denoted (VIa), is isostructural with (V), and the other, denoted (VIb), crystallizes with Z′ = 1, but as an unknown solvate in which the pyrimidine molecules are linked by N—H⋯N hydrogen bonds to form a ribbon containing two types of centrosymmetric ring. International Union of Crystallography 2023-05-05 /pmc/articles/PMC10240168/ /pubmed/37140891 http://dx.doi.org/10.1107/S2053229623003728 Text en © Vicentes et al. 2023 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Research Papers Vicentes, Daniel E. Rodríguez, Ricaurte Cobo, Justo Glidewell, Christopher Synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidine hybrids: synthetic sequence and the molecular and supramolecular structures of two intermediates and three final products |
title | Synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidine hybrids: synthetic sequence and the molecular and supramolecular structures of two intermediates and three final products |
title_full | Synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidine hybrids: synthetic sequence and the molecular and supramolecular structures of two intermediates and three final products |
title_fullStr | Synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidine hybrids: synthetic sequence and the molecular and supramolecular structures of two intermediates and three final products |
title_full_unstemmed | Synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidine hybrids: synthetic sequence and the molecular and supramolecular structures of two intermediates and three final products |
title_short | Synthesis of 5-(arylmethylideneamino)-4-(1H-benzo[d]imidazol-1-yl)pyrimidine hybrids: synthetic sequence and the molecular and supramolecular structures of two intermediates and three final products |
title_sort | synthesis of 5-(arylmethylideneamino)-4-(1h-benzo[d]imidazol-1-yl)pyrimidine hybrids: synthetic sequence and the molecular and supramolecular structures of two intermediates and three final products |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240168/ https://www.ncbi.nlm.nih.gov/pubmed/37140891 http://dx.doi.org/10.1107/S2053229623003728 |
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