دورية أكاديمية

Assembly of 4-aminoquinolines via palladium catalysis: a mild and convenient alternative to SNAr methodology.

التفاصيل البيبلوغرافية
العنوان: Assembly of 4-aminoquinolines via palladium catalysis: a mild and convenient alternative to SNAr methodology.
المؤلفون: Margolis BJ; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285, USA. margolis_brandon_j@lilly.com, Long KA, Laird DL, Ruble JC, Pulley SR
المصدر: The Journal of organic chemistry [J Org Chem] 2007 Mar 16; Vol. 72 (6), pp. 2232-5. Date of Electronic Publication: 2007 Feb 13.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: American Chemical Society Country of Publication: United States NLM ID: 2985193R Publication Model: Print-Electronic Cited Medium: Print ISSN: 0022-3263 (Print) Linking ISSN: 00223263 NLM ISO Abbreviation: J Org Chem Subsets: MEDLINE
أسماء مطبوعة: Publication: Columbus Oh : American Chemical Society
Original Publication: Easton, Pa. [etc.]
مواضيع طبية MeSH: Aminoquinolines/*chemical synthesis, Amines/chemistry ; Catalysis ; Methods ; Palladium/chemistry ; Quinolines/chemistry
مستخلص: 4-aminoquinolines, classically prepared via SNAr chemistry from an amine and 4-haloquinoline, are important scaffolds in medicinal chemistry. Interest in these compounds prompted us to explore palladium catalysis as an alternative to the existing methods for their preparation. Initial results followed by an iterative screening paradigm confirmed Pd(OAc)2/DPEphos/K3PO4 as a mild and convenient alternative for the formation of the C-N bond in 4-aminoquinolines. A description of the screen and the scope of this methodology are discussed herein.
المشرفين على المادة: 0 (Amines)
0 (Aminoquinolines)
0 (Quinolines)
5TWQ1V240M (Palladium)
E66400VT9R (quinoline)
تواريخ الأحداث: Date Created: 20070214 Date Completed: 20070531 Latest Revision: 20131121
رمز التحديث: 20240628
DOI: 10.1021/jo062168u
PMID: 17295543
قاعدة البيانات: MEDLINE
الوصف
تدمد:0022-3263
DOI:10.1021/jo062168u