Five closely related 4-chloro-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepines: similar molecular structures but different supramolecular assemblies

Dibenz[ b , f ]azepine (DBA) is a privileged 6-7-6 tricyclic ring system of importance in both organic and medicinal chemistry. Benzo[ b ]pyrimido[5,4- f ]azepines (BPAs), which also contain a privileged 6-7-6 ring system, are less well investigated, probably because of a lack of straightforward and...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Acta crystallographica. Section C, Structural chemistry Structural chemistry, 2015-12, Vol.71 (12), p.1062-1068
Hauptverfasser: Acosta, Lina M., Jurado, Jorge, Palma, Alirio, Cobo, Justo, Glidewell, Christopher
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1068
container_issue 12
container_start_page 1062
container_title Acta crystallographica. Section C, Structural chemistry
container_volume 71
creator Acosta, Lina M.
Jurado, Jorge
Palma, Alirio
Cobo, Justo
Glidewell, Christopher
description Dibenz[ b , f ]azepine (DBA) is a privileged 6-7-6 tricyclic ring system of importance in both organic and medicinal chemistry. Benzo[ b ]pyrimido[5,4- f ]azepines (BPAs), which also contain a privileged 6-7-6 ring system, are less well investigated, probably because of a lack of straightforward and versatile methods for their synthesis. A simple and versatile synthetic approach to BPAs based on intramolecular Friedel–Crafts alkylation has been developed. A group of closely-related benzo[ b ]pyrimido[5,4- f ]azepine derivatives, namely (6 RS )-4-chloro-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 14 H 14 ClN 3 , (I), (6 RS )-4-chloro-8-hydroxy-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 14 H 14 ClN 3 O, (II), (6 RS )-4-chloro-8-methoxy-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 15 H 16 ClN 3 O, (III), and (6 RS )-4-chloro-8-methoxy-6,11-dimethyl-2-phenyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 21 H 20 ClN 3 O, (IV), has been prepared and their structures compared with the recently published structure [Acosta-Quintero et al. (2015). Eur. J. Org. Chem. pp. 5360–5369] of (6 RS )-4-chloro-2,6,8,11-tetramethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, (V). All five compounds crystallize as racemic mixtures and they have very similar molecular conformations, with the azepine ring adopting a boat-type conformation in each case, although the orientation of the methoxy substituent in each of (III) and (IV) is different. The supramolecular assemblies in (II) and (IV) depend upon hydrogen bonds of the O—H...N and C—H...π(arene) types, respectively, those in (I) and (V) depend upon π–π stacking interactions involving pairs of pyrimidine rings, and that in (III) depends upon a π–π stacking interaction involving pairs of phenyl rings. Short C—Cl...π(pyrimidine) contacts are present in (I), (II) and (IV) but not in (III) or (V).
doi_str_mv 10.1107/S2053229615020811
format Article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1107_S2053229615020811</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1107_S2053229615020811</sourcerecordid><originalsourceid>FETCH-LOGICAL-c901-49db06457618541d1eab36d87c60bb38d61fd4239a6e3cfe914b7d98901b60623</originalsourceid><addsrcrecordid>eNplUNtKw0AUXETBUvsBvu0HdHVPLpvENynWCgUf7FspYS8ndGXThN1ESP_EvzVBQcGnM2fOzMAZQm6B3wHw7P4t4mkcRYWAlEc8B7ggs4liE3f5B1-TRQjvnHOAKM0ymJHPtf1Aql0T0A3Uo5MdGpowfXSNb5hYAjBjj4MZl5RuKFN4Ojd7quihHbytrWn26TJhtKIHecbWnjA80DAenPS0bhzqfkKh873ueo-Bqr6jxlYVejx1NPStl786GQLWylkMN-Sqki7g4mfOyW79tFtt2Pb1-WX1uGW64MCSwigukjQTkKcJGECpYmHyTAuuVJwbAZVJoriQAmNdYQGJykyRj14luIjiOYHvWO2bEDxWZTu-Jf1QAi-ndst_7cZfPCptng</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Five closely related 4-chloro-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepines: similar molecular structures but different supramolecular assemblies</title><source>Wiley Online Library All Journals</source><source>Alma/SFX Local Collection</source><creator>Acosta, Lina M. ; Jurado, Jorge ; Palma, Alirio ; Cobo, Justo ; Glidewell, Christopher</creator><creatorcontrib>Acosta, Lina M. ; Jurado, Jorge ; Palma, Alirio ; Cobo, Justo ; Glidewell, Christopher</creatorcontrib><description>Dibenz[ b , f ]azepine (DBA) is a privileged 6-7-6 tricyclic ring system of importance in both organic and medicinal chemistry. Benzo[ b ]pyrimido[5,4- f ]azepines (BPAs), which also contain a privileged 6-7-6 ring system, are less well investigated, probably because of a lack of straightforward and versatile methods for their synthesis. A simple and versatile synthetic approach to BPAs based on intramolecular Friedel–Crafts alkylation has been developed. A group of closely-related benzo[ b ]pyrimido[5,4- f ]azepine derivatives, namely (6 RS )-4-chloro-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 14 H 14 ClN 3 , (I), (6 RS )-4-chloro-8-hydroxy-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 14 H 14 ClN 3 O, (II), (6 RS )-4-&lt;!?tlsb=-0.14pt&gt;chloro-8-methoxy-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 15 H 16 ClN 3 O, (III), and (6 RS )-4-chloro-8-methoxy-6,11-dimethyl-2-phenyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 21 H 20 ClN 3 O, (IV), has been prepared and their structures compared with the recently published structure [Acosta-Quintero et al. (2015). Eur. J. Org. Chem. pp. 5360–5369] of (6 RS )-4-chloro-2,6,8,11-tetramethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, (V). All five compounds crystallize as racemic mixtures and they have very similar molecular conformations, with the azepine ring adopting a boat-type conformation in each case, although the orientation of the methoxy substituent in each of (III) and (IV) is different. The supramolecular assemblies in (II) and (IV) depend upon hydrogen bonds of the O—H...N and C—H...π(arene) types, respectively, those in (I) and (V) depend upon π–π stacking interactions involving pairs of pyrimidine rings, and that in (III) depends upon a π–π stacking interaction involving pairs of phenyl rings. Short C—Cl...π(pyrimidine) contacts are present in (I), (II) and (IV) but not in (III) or (V).</description><identifier>ISSN: 2053-2296</identifier><identifier>EISSN: 2053-2296</identifier><identifier>DOI: 10.1107/S2053229615020811</identifier><language>eng</language><ispartof>Acta crystallographica. Section C, Structural chemistry, 2015-12, Vol.71 (12), p.1062-1068</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c901-49db06457618541d1eab36d87c60bb38d61fd4239a6e3cfe914b7d98901b60623</citedby><cites>FETCH-LOGICAL-c901-49db06457618541d1eab36d87c60bb38d61fd4239a6e3cfe914b7d98901b60623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Acosta, Lina M.</creatorcontrib><creatorcontrib>Jurado, Jorge</creatorcontrib><creatorcontrib>Palma, Alirio</creatorcontrib><creatorcontrib>Cobo, Justo</creatorcontrib><creatorcontrib>Glidewell, Christopher</creatorcontrib><title>Five closely related 4-chloro-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepines: similar molecular structures but different supramolecular assemblies</title><title>Acta crystallographica. Section C, Structural chemistry</title><description>Dibenz[ b , f ]azepine (DBA) is a privileged 6-7-6 tricyclic ring system of importance in both organic and medicinal chemistry. Benzo[ b ]pyrimido[5,4- f ]azepines (BPAs), which also contain a privileged 6-7-6 ring system, are less well investigated, probably because of a lack of straightforward and versatile methods for their synthesis. A simple and versatile synthetic approach to BPAs based on intramolecular Friedel–Crafts alkylation has been developed. A group of closely-related benzo[ b ]pyrimido[5,4- f ]azepine derivatives, namely (6 RS )-4-chloro-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 14 H 14 ClN 3 , (I), (6 RS )-4-chloro-8-hydroxy-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 14 H 14 ClN 3 O, (II), (6 RS )-4-&lt;!?tlsb=-0.14pt&gt;chloro-8-methoxy-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 15 H 16 ClN 3 O, (III), and (6 RS )-4-chloro-8-methoxy-6,11-dimethyl-2-phenyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 21 H 20 ClN 3 O, (IV), has been prepared and their structures compared with the recently published structure [Acosta-Quintero et al. (2015). Eur. J. Org. Chem. pp. 5360–5369] of (6 RS )-4-chloro-2,6,8,11-tetramethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, (V). All five compounds crystallize as racemic mixtures and they have very similar molecular conformations, with the azepine ring adopting a boat-type conformation in each case, although the orientation of the methoxy substituent in each of (III) and (IV) is different. The supramolecular assemblies in (II) and (IV) depend upon hydrogen bonds of the O—H...N and C—H...π(arene) types, respectively, those in (I) and (V) depend upon π–π stacking interactions involving pairs of pyrimidine rings, and that in (III) depends upon a π–π stacking interaction involving pairs of phenyl rings. Short C—Cl...π(pyrimidine) contacts are present in (I), (II) and (IV) but not in (III) or (V).</description><issn>2053-2296</issn><issn>2053-2296</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNplUNtKw0AUXETBUvsBvu0HdHVPLpvENynWCgUf7FspYS8ndGXThN1ESP_EvzVBQcGnM2fOzMAZQm6B3wHw7P4t4mkcRYWAlEc8B7ggs4liE3f5B1-TRQjvnHOAKM0ymJHPtf1Aql0T0A3Uo5MdGpowfXSNb5hYAjBjj4MZl5RuKFN4Ojd7quihHbytrWn26TJhtKIHecbWnjA80DAenPS0bhzqfkKh873ueo-Bqr6jxlYVejx1NPStl786GQLWylkMN-Sqki7g4mfOyW79tFtt2Pb1-WX1uGW64MCSwigukjQTkKcJGECpYmHyTAuuVJwbAZVJoriQAmNdYQGJykyRj14luIjiOYHvWO2bEDxWZTu-Jf1QAi-ndst_7cZfPCptng</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Acosta, Lina M.</creator><creator>Jurado, Jorge</creator><creator>Palma, Alirio</creator><creator>Cobo, Justo</creator><creator>Glidewell, Christopher</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20151201</creationdate><title>Five closely related 4-chloro-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepines: similar molecular structures but different supramolecular assemblies</title><author>Acosta, Lina M. ; Jurado, Jorge ; Palma, Alirio ; Cobo, Justo ; Glidewell, Christopher</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c901-49db06457618541d1eab36d87c60bb38d61fd4239a6e3cfe914b7d98901b60623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Acosta, Lina M.</creatorcontrib><creatorcontrib>Jurado, Jorge</creatorcontrib><creatorcontrib>Palma, Alirio</creatorcontrib><creatorcontrib>Cobo, Justo</creatorcontrib><creatorcontrib>Glidewell, Christopher</creatorcontrib><collection>CrossRef</collection><jtitle>Acta crystallographica. Section C, Structural chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Acosta, Lina M.</au><au>Jurado, Jorge</au><au>Palma, Alirio</au><au>Cobo, Justo</au><au>Glidewell, Christopher</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Five closely related 4-chloro-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepines: similar molecular structures but different supramolecular assemblies</atitle><jtitle>Acta crystallographica. Section C, Structural chemistry</jtitle><date>2015-12-01</date><risdate>2015</risdate><volume>71</volume><issue>12</issue><spage>1062</spage><epage>1068</epage><pages>1062-1068</pages><issn>2053-2296</issn><eissn>2053-2296</eissn><abstract>Dibenz[ b , f ]azepine (DBA) is a privileged 6-7-6 tricyclic ring system of importance in both organic and medicinal chemistry. Benzo[ b ]pyrimido[5,4- f ]azepines (BPAs), which also contain a privileged 6-7-6 ring system, are less well investigated, probably because of a lack of straightforward and versatile methods for their synthesis. A simple and versatile synthetic approach to BPAs based on intramolecular Friedel–Crafts alkylation has been developed. A group of closely-related benzo[ b ]pyrimido[5,4- f ]azepine derivatives, namely (6 RS )-4-chloro-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 14 H 14 ClN 3 , (I), (6 RS )-4-chloro-8-hydroxy-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 14 H 14 ClN 3 O, (II), (6 RS )-4-&lt;!?tlsb=-0.14pt&gt;chloro-8-methoxy-6,11-dimethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 15 H 16 ClN 3 O, (III), and (6 RS )-4-chloro-8-methoxy-6,11-dimethyl-2-phenyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, C 21 H 20 ClN 3 O, (IV), has been prepared and their structures compared with the recently published structure [Acosta-Quintero et al. (2015). Eur. J. Org. Chem. pp. 5360–5369] of (6 RS )-4-chloro-2,6,8,11-tetramethyl-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepine, (V). All five compounds crystallize as racemic mixtures and they have very similar molecular conformations, with the azepine ring adopting a boat-type conformation in each case, although the orientation of the methoxy substituent in each of (III) and (IV) is different. The supramolecular assemblies in (II) and (IV) depend upon hydrogen bonds of the O—H...N and C—H...π(arene) types, respectively, those in (I) and (V) depend upon π–π stacking interactions involving pairs of pyrimidine rings, and that in (III) depends upon a π–π stacking interaction involving pairs of phenyl rings. Short C—Cl...π(pyrimidine) contacts are present in (I), (II) and (IV) but not in (III) or (V).</abstract><doi>10.1107/S2053229615020811</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 2053-2296
ispartof Acta crystallographica. Section C, Structural chemistry, 2015-12, Vol.71 (12), p.1062-1068
issn 2053-2296
2053-2296
language eng
recordid cdi_crossref_primary_10_1107_S2053229615020811
source Wiley Online Library All Journals; Alma/SFX Local Collection
title Five closely related 4-chloro-6,11-dihydro-5 H -benzo[ b ]pyrimido[5,4- f ]azepines: similar molecular structures but different supramolecular assemblies
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T14%3A32%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Five%20closely%20related%204-chloro-6,11-dihydro-5%20H%20-benzo%5B%20b%20%5Dpyrimido%5B5,4-%20f%20%5Dazepines:%20similar%20molecular%20structures%20but%20different%20supramolecular%20assemblies&rft.jtitle=Acta%20crystallographica.%20Section%20C,%20Structural%20chemistry&rft.au=Acosta,%20Lina%20M.&rft.date=2015-12-01&rft.volume=71&rft.issue=12&rft.spage=1062&rft.epage=1068&rft.pages=1062-1068&rft.issn=2053-2296&rft.eissn=2053-2296&rft_id=info:doi/10.1107/S2053229615020811&rft_dat=%3Ccrossref%3E10_1107_S2053229615020811%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true