Please use this identifier to cite or link to this item:
Title: Synthesis of novel 1,2,4-oxadiazole heterocyclic compounds containing 2-H pyranopyridine-2-one moiety and related compounds
Authors: Kumar, N Vasanth
Mashelker, Uday C
Keywords: 1,2,4-oxadiazole;Carboxamide;2H-pyranopyridine -2-one;Anti-hypertensive;Hydroxyl amine;Tyrosine kinase;Cyclocondensation;Carboxamidoxime
Issue Date: Jan-2007
Publisher: CSIR
IPC Code: Int. Cl.⁸ C07D
Abstract: 7-Hydroxy/Amino-5-methyl-6-(5-substituted-[1,2,4]oxadiazol-3-yl)-2-oxo-2H-pyrano[2,3-b]pyridine-3-carboxylic acid amides 5a-c and 6a-c have been prepared starting from ethyl 2H-pyrano [2,3-b] pyridine-3-carboxylate 1 and 2, compounds 1 and 2 are treated with aqueous ammonia solution to afford 2H-pyrano[2,3-b] pyridine-3-carboxamide 3a-b, which are converted to 6-carboxamidoxime 2H-pyrano [2,3-b] pyridine-3-carboxamide 4a-b by treating with hydroxyl amine in refluxing ethanol. Carboxamidoximes 4a-b are treated with various acid chlorides to obtain 1,2,4-oxadiazole derivatives 5a-c and 6a-c. Carboxamide 3a is reacted with triethyl orthoformate to give 4-amino-5-methyl pyrano [3",2':5,6] pyrido [2,3-d] pyrimidine-7-carboximde 7. Carboxamidoxime 4a is allowed to react with N,N-dimethyl formamide dimethyl acetal under reflux to obtain N-(6-carbonyl-4-methyl-7-oxo-1,7-dihydropyrano[2,3-b]pyrazolo[4,3-e]pyri¬dine-3-yl)methanamide 8. These compounds are expected to have better hypertensive activity.
Page(s): 216-220
ISSN: 0376-4699
Appears in Collections:IJC-B Vol.46B(01) [January 2007]

Files in This Item:
File Description SizeFormat 
IJCB 46B(1) (2007) 216-220.pdf130.14 kBAdobe PDFView/Open

Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.