Synthesis of tetrazolo [1,5-a]quinoxaline derivatives

Design, synthesis, and SAR study of isopropoxy allylbenzene derivatives as 15-lipoxygenase inhibitors

Objective(s): Allylbenzenes have been recently developed as inhibitors of lipoxygenases. They decrease peroxidation activity via mimicking 1,4-unsaturated bonds of fatty acids by their allyl portion. We designed and synthesized new derivatives of allyl benzenes (6a-f) with isopropoxy and amide substituents at ortho and meta positions towards allyl group, respectively. ...

An Efficient Protocol for Synthesis of 2-amino-3cyanopyridine Derivatives using Nano-modified SBA-15

Condensation reaction of chalcones with malononitrile and ammonium acetate in the presence of the green nano-modified SBA-15 affords the corresponding 2-amino-3-cyanopyridine derivatives in excellent yield. This approaches claimed to be an environment friendly protocol as it afforded some advantages such as excellent yields and cleaner reaction.

Effiecient Synthesis of tetrazoloquinoxaline derivatives

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.

an efficient protocol for synthesis of 2-amino-3cyanopyridine derivatives using nano-modified sba-15

Synthesis of novel derivatives of chromenone bearing an N -carbamothioyl moiety as soybean 15-LOX inhibitors

Novel derivatives of chromenone bearing an N -carbamothioyl moiety were synthesized and evaluated for their soybean 15-LOX inhibitory activity. Synthesis of the target compounds was started from 7-hydroxy-2H -chromen-2-one. It was reacted with 1-fluoro-2(4)-nitrobenzene to obtain the corresponding nitrophenoxy-chromenone derivative. Reduction of the nitro group was achieved in the presence of Z...

synthesis of new heterocyclic system n7-ethyl-5-methyl[1,2,4]triazolo[4,3:1,2]pyrimido[4,5d][1,3]thiazol-7-amine & synthesis of novel 7-methyl-3,5-di(alkhylsulfanyl) [1,2,4]triazolo[4,3-c]pyrimidine derivatives

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...