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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 277039생성일: 2026년 10월 23일

Ethyl p-methylbenzenesulfonate → Ethyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amine

https://huagongshe.com/ko/reaction/277039

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl p-methylbenzenesulfonateHCID 6638—
반응물Sodium hydrideHCID 24758—
반응물Sodium BicarbonateHCID 516892—
반응물2-Phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamineHCID 22629700—
용매DimethylformamideHCID 6228—
생성물Ethyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amineHCID 9904961117.3%

반응 단계

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. 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 0.37 g(17%) ethyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amine as beige crystals. MS m/e (%): 316 (M+H+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355653B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-3dd85b7dcf324760a84d78e13f421c26
출처 메모uspto-grants-2002_03