A one-pot synthetic approach for construction of thiazolo[3,2- a]benzimidazole-linked quinoxaline scaffold via palladium-catalyzed reactions
Publish place: 20th Iranian Chemical Congress
Publish Year: 1397
نوع سند: مقاله کنفرانسی
زبان: English
View: 315
متن کامل این Paper منتشر نشده است و فقط به صورت چکیده یا چکیده مبسوط در پایگاه موجود می باشد.
توضیح: معمولا کلیه مقالاتی که کمتر از ۵ صفحه باشند در پایگاه سیویلیکا اصل Paper (فول تکست) محسوب نمی شوند و فقط کاربران عضو بدون کسر اعتبار می توانند فایل آنها را دریافت نمایند.
- Certificate
- من نویسنده این مقاله هستم
استخراج به نرم افزارهای پژوهشی:
شناسه ملی سند علمی:
IRANCC20_713
تاریخ نمایه سازی: 28 اردیبهشت 1398
Abstract:
Nitrogen heterocyclic compounds are the most abundant and integral scaffolds that occur ubiquitously in a variety of synthetic drugs, bio-active natural products, pharmaceuticals, and agrochemicals. Due to their broad applications, these compounds have long been a subject of great interest, and fundamental efforts have been made for the development of synthetic strategies that could lead to the discovery of new bioactive compounds in medicinal chemistry. [1]In this research work, a novel thiazolo[3,2-a]benzimidazole-linked quinoxaline system were synthesized by a multi-component reaction of 3-amine substituted 2-chloroquinoxalines, terminal alkynes and 1H-benzo[d]imidazole-2(3H)-thione in the presence of the palladium-copper catalyst. This one-pot process provided an efficient and successful approach for the construction of new thiazolo[3,2-a]benzimidazole-based quinoxaline scaffold with good-to-high yields. All the new synthesized compounds were characterized by the analytical spectral data
Authors
Saeed Lashkari
Faculty of Chemistry, Shahrood University of Technology, Shahrood, Iran;
Ali Keivanloo
Faculty of Chemistry, Shahrood University of Technology, Shahrood, Iran;
Mohammad Bakherad
Faculty of Chemistry, Shahrood University of Technology, Shahrood, Iran;
Mahsa Fakharian
Faculty of Chemistry, Shahrood University of Technology, Shahrood, Iran;