623113-98-4Relevant articles and documents
Synthesis of some novel azetidino[2,3-b][1,8]naphthyridin-2(1H)-ones and 1,2,4-triazolo [4,3-a][1,8] naphthyridines
Mogilaiah,Reddy, P. Raghotham,Rao, R. Babu,Reddy, N. Vasudeva
, p. 1746 - 1749 (2007/10/03)
Ethyl 1.8-naphthyridin-2-one-3-carboxylate 1 on fusion with different anilines at 200°C affords N-aryl-1,8-naphthyridin-2-one-3-carboxamides 2, which undergo smooth cyclization with POCl3 yielding 1-arylazetidino [2,3-b][1,8]naphthyridin-2(1H)-ones 3. Compound 1 on treatment with POCl 3 yield ethyl 2-chloro-1,8-naphthyridine-3-carboxylate 4, which on reaction with aromatic acid hydrazides in methanol furnishes respective N-aroyl-N'-(3-carbethoxy-1,8-naphthyridin-2-yl) hydrazines 5. Cyclization of 5 with POCl3 under reflux result in the formation of 1-aryl-4-carbethoxy-1,2,4-triazol [4,3-a][1,8]naphthyridines 6. Compounds 3 and 6 have been evaluated for their antibacterial activity using streptomycin as a reference compound.