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Synthesis and Biological Activity of Some New 2-(2,4 dimethoxyphenylpyrrolo [2,3-d] Pyrimidine Compounds

المصدر: مجلة جامعة الزيتونة
الناشر: جامعة الزيتونة
المؤلف الرئيسي: Musa, Suliman M. (Author)
المجلد/العدد: ع12
محكمة: نعم
الدولة: ليبيا
التاريخ الميلادي: 2014
الصفحات: 66 - 79
DOI: 10.35778/1742-000-012-023
ISSN: 2523-1006
رقم MD: 840427
نوع المحتوى: بحوث ومقالات
قواعد المعلومات: EcoLink, EduSearch, IslamicInfo, HumanIndex
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عدد مرات التحميل

7

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المستخلص: The present work is aimed to synthesize some new heterocyclic compounds containing pyrrolo[2,3-d]pyrimidines, Our approach to the synthesis of the target compounds started through the hydrolysis of 6-ethylthio-4-methyl-2-(2'',4'- dimethoxyphenyl)pyi imidine-5-carbonitrile (2) by refluxing in ethanol containing sodium hydroxide to give the corresponding sodium salt derivative (3) which in turn wais acidified to give 5-cyano-4-niethyl-2-(2 A- dimethoxyphenyl)pyrimidin-6(H)one (4). Chlorination of the hydroxy derivative (4) afforded 6-Chloro-4-methyl-2-(2\4'- dimethoxyphenyl)pyrimidin-5-carbonitrile (5), which reacted with ethyl glycinate hydrochloride.to give Ethyl (5-cyano-4-methyl-2-(2\4'- dimethoxyphenyl)yrimidin-6-yloxy)acetate (6),which underwent cyclization to give the ethyl 5-amino-4-methyl-2-(2,4'-dimethoxyphenyl)-7H- pyrrolo[2,3-d]pyrimidine-6-carboxylate (10). Also the reaction of compound (5) with piperidine, and morpholine, gave the piperidino- and morphilino- derivatives (7) and (8) respectively. The compound (10) was used as key intermediates in the synthesis of other new pyrrolo[2,3-d]pyrimidine derivatives (11-13), pyrimido[4\5\4,5]pyrrolo[2,3-d]pyrimidines (14-17a-c) and triazolopyrrolopyrimidines (18, 19) by reaction with different reagents . Eight compounds were selected and screened in vitro for their

ISSN: 2523-1006

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