Ethyl 4-[2-(4-pyridyl)hydrazino]-1,6-naphthyridine-3-carboxylate hydrochloride → HCID 178479607、化合物
反応式
[ClH:1].[N:2]1[CH:7]=[CH:6][C:5]([NH:8][NH:9][C:10]2[C:19]3[C:14](=[CH:15][CH:16]=[N:17][CH:18]=3)[N:13]=[CH:12][C:11]=2[C:20]([O:22]CC)=O)=[CH:4][CH:3]=1>C(O)CCC>[ClH:1].[N:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:20](=[O:22])[C:11]3=[CH:12][NH:13][C:14]4[CH:15]=[CH:16][N:17]=[CH:18][C:19]=4[C:10]3=[N:9]2)=[CH:4][CH:3]=1参加物
3
実験手順
A suspension of ethyl 4-[2-(4-pyridyl)hydrazino]-1,6-naphthyridin-3-carboxylate hydrochloride (1.76 g) in 50 ml of n-butanol is refluxed for 20 hours. The mixture is cooled down to room temperature and filtered. Collected solid is dissolved in aqueous sodium hydroxide and stirred at room temperature for 21 hours, then filtered. The filtrate is acidified with 1N hydrochloric acid to precipitate a solid, which is collected, washed successively with aqueous methanol, methanol and acetone to yield 2-(4-pyridyl)-pyrazolo[4,3-c][1,6]naphthyridin-3(5H)-one hydrochloride, m.p. above 345°; IR (KBr) 726, 746, 791, 833, 898 cm-1.