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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 277011생성일: 2026년 10월 25일

Methanol → 2-Furan-2-yl-7-pyridin-4-yl-[1,2,4]triazolo [1,5-a]pyridin-5-ylamine

https://huagongshe.com/reaction/277011

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium hydrideHCID 24758—
반응물3-Pyridin-4-YL-acrylonitrileHCID 53407808—
반응물3-benzenesulfonyl-methyl-5-furan-2-yl-1H-[1,2,4]triazoleHCID 70170246—
용매TetrahydrofuranHCID 8028—
생성물2-Furan-2-yl-7-pyridin-4-yl-[1,2,4]triazolo [1,5-a]pyridin-5-ylamineHCID 988208113%

반응 단계

To a boiling suspension of 5.9 g(0.12 mol) sodiumhydride (55%) in 100 ml tetrahydrofuran was slowly added over a period of 6 hours a mixture of 10.1 g (0.035 mol) 3-benzenesulfonyl-methyl-5-furan-2-yl-1H-[1,2,4]triazole and 4.56 g (0.035 mol) 3-(4-pyridinyl)-2-propenenitrile in 400 ml tetrahydrofuran. Boiling was continued for 15 hours and then 50 ml methanol were added at room temperature. Evaporation of the solvent and chromatography on silicagel with dichloromethane/methanol 95/5 gave 1.3 g (13%) 2-furan-2-yl-7-pyridin-4-yl-[1,2,4]triazolo [1,5-a]pyridin-5-ylamine as yellow crystals with mp. 294-296° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355653B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-c380808d2e1f4b5990ee50f4ac7eebb4
출처 메모uspto-grants-2002_03