Synthesis of pyrazolone derivatives. XXIX. Synthesis of 1,3-dioxolane-indazole derivatives.
نویسندگان
چکیده
منابع مشابه
Synthesis of pyrazolone derivatives and their biological activities
3-Methyl-1-phenylpyrazol-5-one and its derivatives prepared using ethyl acetoacetate, phenyl hydrazine and its derivatives. Ethyl acetoacetate reacted with phenylhydrazine at reflux temperature to give 3-methyl-1-phenylpyrazol-5-one crude and recrystlized from diluted ethanol to give pure 3-methyl1-phenylpyrazol-5-one. Different pyrazolone derivatives were prepared by using different phenyl hyd...
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3-Methyl-5-chloro-1-phenylpyrazol and its derivatives were prepared by the reaction with 3methyl -1-phenylpyrazol-5-one, phosphorous oxytrichloride and N-N dimethyl aniline respectively using catalyst. These compounds were further treated with alcohols and sodium hydroxide to form ether linkage. Ethyl acetoacetate reacted with phenylhydrazine at reflux temprature to give 3-methyl-1phenylpyrazol...
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An efficient and convenient synthesis of pyrrolidinones and pyridinones utilizing enamino esters as starting material has been described. The structures of the compounds obtained were confirmed by spectral and elemental analyses.
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Displacement reaction of 2,3-dichloroquinoxaline with secondary amines in boiling ethanol afforded it`s mono aminoquinoxaline derivatives. Further reaction of the latter compounds with sodium azide in warm dimethylsulfoxide achieved a group of 4-amino tetrazolo[1,5-a]quinoxaline derivatives. 1HNMR spectra of these compounds are discussed.
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در این تحقیق، ابتدا از واکنش 5-برمو-2-کلرو-6- متیل-4-پیریمیدین آمین (1) با هیدرازین هیدرات در حلال اتانول، 5-برومو-2-هیدرازینو -6-متیل -4-پیریمیدین آمین (2) به دست آمد. سپس از واکنش این ترکیب با تری اتیل اورتو استر های مختلف در حلال استیک اسید محصولات تری آزولوپیریمیدین (a,b3) حاصل گردید. همچنین از واکنش مشتق هیدرازین دار (2) با سدیم نیتریت در حلال استیک اسید و آب حد واسطی ایجاد شده است که از ر...
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ژورنال
عنوان ژورنال: Chemical and Pharmaceutical Bulletin
سال: 1977
ISSN: 0009-2363,1347-5223
DOI: 10.1248/cpb.25.1124