Academic Journal

A New Method for the Synthesis of 3-Thiocyanatopyrazolo[1,5-a]pyrimidines

التفاصيل البيبلوغرافية
العنوان: A New Method for the Synthesis of 3-Thiocyanatopyrazolo[1,5-a]pyrimidines
المؤلفون: Vladimir A. Kokorekin, Sergey V. Neverov, Vera N. Kuzina, Vladimir A. Petrosyan
المصدر: Molecules; Volume 25; Issue 18; Pages: 4169
بيانات النشر: Multidisciplinary Digital Publishing Institute
سنة النشر: 2020
المجموعة: MDPI Open Access Publishing
مصطلحات موضوعية: thiocyanate group, 5-aminopyrazoles, 1,3-dicarbonyl compounds, pyrazolo[1,5- a ]pyrimidines, anodic C–H thiocyanation, condensation, cyclic voltammetry
جغرافية الموضوع: agris
الوصف: In this article, we demonstrate how an original effective “metal-free” and “chromatography-free” route for the synthesis of 3-thiocyanatopyrazolo[1,5-a]pyrimidines has been developed. It is based on electrooxidative (anodic) C–H thiocyanation of 5-aminopyrazoles by thiocyanate ion leading to 4-thiocyanato-5-aminopyrazoles (stage 1, yields up to 87%) following by their chemical condensation with 1,3-dicarbonyl compounds or their derivatives (stage 2, yields up to 96%). This method is equally effective for the synthesis of 3-thiocyanatopyrazolo[1,5-a]pyrimidines, both without substituents and with various donor (acceptor) substituents in the pyrimidine ring.
نوع الوثيقة: text
وصف الملف: application/pdf
اللغة: English
Relation: Organic Chemistry; https://dx.doi.org/10.3390/molecules25184169
DOI: 10.3390/molecules25184169
الاتاحة: https://doi.org/10.3390/molecules25184169
Rights: https://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.A7EC6B01
قاعدة البيانات: BASE
الوصف
DOI:10.3390/molecules25184169