戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 277055作成日:2026年10月27日

p-Toluenesulfonic acid → Diethyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amine

https://huagongshe.com/reaction/277055

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Ethyl p-methylbenzenesulfonateHCID 6638—
反応物Sodium hydrideHCID 24758—
反応物Sodium BicarbonateHCID 516892—
反応物2-Phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamineHCID 22629700—
溶媒DimethylformamideHCID 6228—
生成物Diethyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amineHCID 990610915%

反応手順

A solution of 0.29 g (0.001 mol) 2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine in 50 ml dimethylformamide was treated with 0.05 g (0.001 mol) sodiumhydride(55%) for 15 minutes at room temperature. Then 0.22 g (0.001 mol) ethyl-p-toluenesulfonate were added and stirring was continued for 22 hours. Addition of sodiumhydride and p-toluenesulfonate was repeated three times. After each addition stirring was continued at 50° C. for 20 hours. Saturated aqueous sodiumbicarbonate was added and the mixture was extracted with dichloromethane. Evaporation of the solvent and chromatography on silicagel with dichloromethane/methanol 96/4 gave 0.05 g (15%) diethyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amine as yellow oil. MS m/e (%): 343 (M+, 59), 314 (100), 300 (73), 104 (51).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355653B1
出典データセットuspto-grants-2002_03
ORD IDord-38f8a5076cc64aeeac9ae0163886b886
出典メモuspto-grants-2002_03