Convenient synthesis of disubstituted tacrine derivatives via electrophilic and copper induced reactions
dc.contributor.author | Ekiz, Makbule | |
dc.contributor.author | Tutar, Ahmet | |
dc.contributor.author | Ökten, Salih | |
dc.date.accessioned | 2020-04-30T22:41:43Z | |
dc.date.available | 2020-04-30T22:41:43Z | |
dc.date.issued | 2016 | |
dc.department | DÜ, Fen-Edebiyat Fakültesi, Kimya Bölümü | en_US |
dc.description | Okten, Salih/0000-0001-9656-1803; Tutar, Ahmet/0000-0001-5524-8001 | en_US |
dc.description | WOS: 000381530900009 | en_US |
dc.description.abstract | The bromination of 2-aminobenzonitrile (2) with molecular bromine (2 equiv) furnished 2-amino-3,5-dibromobenzonitrile (7) in 98% yield. One-pot syntheses are described for dibromotacrine derivatives (6,14-18) utilizing Friedlander reactions. A convenient route is described for disubstituted derivatives of tacrines from dibromotacrine 6 and 15 by various substitution reactions. Several disubstituted tacrines were synthesized by treatment of dibromo 6 and 15 derivatives with n-BuLi followed by trapping with an electrophile [Si(Me)(3)Cl, S-2(Me)(2)]. Both were converted to the corresponding cyano derivatives (21-23) via copper-assisted nucleophilic substitution reactions in moderate yields (30%, 50%, and 60%, respectively). Copper-induced nucleophilic substitution of dibromide 15 with NaOMe afforded mono methoxide 31 in 25% yield. (C) 2016 Elsevier Ltd. All rights reserved. | en_US |
dc.description.sponsorship | Sakarya University Research FundSakarya University [2014-02-04-008] | en_US |
dc.description.sponsorship | This study was supported by grants from the Sakarya University Research Fund (Project number: 2014-02-04-008). | en_US |
dc.identifier.doi | 10.1016/j.tet.2016.07.012 | en_US |
dc.identifier.endpage | 5330 | en_US |
dc.identifier.issn | 0040-4020 | |
dc.identifier.issue | 35 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 5323 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.tet.2016.07.012 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/3236 | |
dc.identifier.volume | 72 | en_US |
dc.identifier.wos | WOS:000381530900009 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Pergamon-Elsevier Science Ltd | en_US |
dc.relation.ispartof | Tetrahedron | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Tacrine | en_US |
dc.subject | Bromotacrine | en_US |
dc.subject | Cyanotacrine | en_US |
dc.subject | Lithium-bromine exchange | en_US |
dc.subject | Thiomethyltacrine | en_US |
dc.subject | Methoxytacrine | en_US |
dc.title | Convenient synthesis of disubstituted tacrine derivatives via electrophilic and copper induced reactions | en_US |
dc.type | Article | en_US |
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