119337-29-0Relevant academic research and scientific papers
Synthesis, biological evaluation and molecular docking study of 1,2,3-1H-triazoles having 4H-pyrano[2,3-d]pyrimidine as potential Mycobacterium tuberculosis protein tyrosine phosphatase B inhibitors
Thanh, Nguyen Dinh,Hai, Do Son,Ha, Nguyen Thi Thu,Tung, Do Tien,Le, Cao Thi,Van, Hoang Thi Kim,Toan, Vu Ngoc,Toan, Duong Ngoc,Dang, Le Hai
, p. 164 - 171 (2019)
Some heterocycles, namely 2-amino-4H-pyran-3-carbonitriles, were synthesized in a three-component reaction from substituted benzaldehydes, malononitrile, and ethyl acetoacetate. These heterocycles have been converted subsequently into 4H-pyrano[2,3-d]pyri
Functionalization of Ethyl 6-Amino-4-(4-chlorophenyl)-5-cyano-2-methyl-4H-pyran-3-carboxylate: Facile Synthesis of a New Series of Pyrano[2,3-d]pyrimidine Derivatives
Amr, A. E.,El-Hamid, A. Abd,El-Sayed, H. A.,Mohamed, A. S. A.,Morsy, H. A.,Said, S. A.
, p. 1403 - 1408 (2021/08/13)
Abstract: Herein, synthesis of a new series of pyrano[2,3-d]pyrimidine scaffolds is presented. Ethyl 6-amino-4-(4-chlorophenyl)-5-cyano-2-methyl-4H-pyran-3-carboxylate has been reacted with formamide, formic acid, urea, thiourea, semicarbazide, and thiose
Polyazanaphthalenes, I. The Reaction of Ethyl 6-Amino-5-cyano-4-aryl-2-methyl-4H-pyran-3-carboxylate with Nucleophilic Reagents
Harb, Abdel-Fattah A.,Hesien, Abdel-Haleem M.,Metwally, Saoud A.,Elnagdi, Mohamed Hilmy
, p. 585 - 588 (2007/10/02)
Ethyl 6-amino-5-cyano-4-aryl-2-methyl-4H-pyran-3-carboxylates 4 could be converted into 1,6-diazanaphthalene, pyranopyrazole, isoxazolopyridine, pyranopyridine, 1,8-diazanaphthalene, and pyranopyridine derivatives on treatment
