Synthesis of Novel Spiro-oxindole compounds by Reaction of 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1,2-dione in green solvent
محل انتشار: بیست و هفتمین کنفرانس شیمی آلی ایران
سال انتشار: 1398
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 171
نسخه کامل این مقاله ارائه نشده است و در دسترس نمی باشد
- صدور گواهی نمایه سازی
- من نویسنده این مقاله هستم
استخراج به نرم افزارهای پژوهشی:
شناسه ملی سند علمی:
ISOC27_294
تاریخ نمایه سازی: 19 اسفند 1399
چکیده مقاله:
Most Reactions concerted on useful tools for the synthesis of biologically active compounds. One of these reactions is the multi-step syntheses conducted in a one-pot fashion that can contain various compounds with biological effects. Multicomponent reactions (MCRs) can dramatically reduce the generation of chemical waste and reduce the cost of the starting materials.1 The Uracil, Pyrazole, Pyrazolone and their analogs occupy a unique place in the field of medicinal chemistry as anticancer, anti-inflammatory, antiviral drugs and so all. 2-4 As a part of our continued interest in the synthesis of novel Spiro compounds,5-6 we decided to demonstrate the one-pot reaction of 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolone-1,2-dione 1, 3-methylpyrazol-5-one 2 or 5-amine-3-methyl-pyrazole 3 with 6-aminouracil 4 in the green solvent such as Water, Ethanol and Ethanol/Water (1:1) (scheme 1). The resulting structure 5a were produced in very good yields and the structures were confirmed by the 1H & 13C-NMR and FT-IR spectra,s.
کلیدواژه ها:
نویسندگان
Hadi Zare Fazlelahi
Department of Organic Chemistry, Faculty of Chemistry, Urmia University, Urmia, Iran
Peyman Najafi Moghadam
Department of Organic Chemistry, Faculty of Chemistry, Urmia University, Urmia, Iran
Mohammad Mehdi Baradarani
Department of Organic Chemistry, Faculty of Chemistry, Urmia University, Urmia, Iran