Formic Acid → Thiazolo[4,5-c]quinoline
反応式
[NH2:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([C:11]=1[SH:12])=[CH:9][CH:8]=[CH:7][CH:6]=2.[CH:13](O)=O.S(S([O-])=O)([O-])(=O)=O.[Na+].[Na+].[OH-].[Na+]>O.Cl>[S:12]1[C:11]2[C:10]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=3[N:4]=[CH:3][C:2]=2[N:1]=[CH:13]1参加物
7
実験手順
A mixture of 17.62 g (0.1 mole) of 3-amino-4-mercapto-quinoline, 150 ml of 100% formic acid and 1.5 g of sodium pyrosulfite is refluxed for 3 hours. The reaction mixture is cooled, diluted with a mixture of 800 ml of water and 40 ml of concentrated hydrochloric acid, made alkaline to pH 10 by adding a sodium hydroxide solution and extracted three times with 200 ml of benzene each. The benzene solution is evaporated. Thus 15.0 g of thiazolo[4,5-c]quinoline are obtained, m.p.: 114°-116° C., yield 80%.
後処理
- temperatureis refluxed for 3 hours
- temperatureThe reaction mixture is cooled
- extractionextracted three times with 200 ml of benzene each
- customThe benzene solution is evaporated
出典と根拠
- ORDレコード
- ord-b77ffacd016f4f97be2a8a9d57b06ba6
- 出典データセット
- uspto-grants-1990_02
- 特許番号
- US04904669
反応ノート
読み込み中…