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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1270306생성일: 2026년 10월 25일

3,4,5-Trimethoxyphenol → 5,7-Dimethyl-2-(3-nitrophenyl)-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazine

https://huagongshe.com/reaction/1270306

반응식

참여 물질

역할이름HCID투입량
반응물3,4,5-TrimethoxyphenolHCID 69505—
반응물5,7-Dimethyl-2-(3-nitrophenyl)-4-(1H-1,2,4-triazol-1-yl)imidazo[5,1-f][1,2,4]triazineHCID 18449110—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물5,7-Dimethyl-2-(3-nitrophenyl)-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazineHCID 18449111—

반응 단계

A solution of 175.17 mg (1.04 mmol) of potassium tert-butoxide and 287.53 mg (1.56 mmol) of 3,4,5-trimethoxyphenol in 20 ml of tetrahydrofuran is stirred for 30 min. 350 mg (1.04 mmol) of 5,7-dimethyl-2-(3-nitrophenyl)-4-(1H-1,2,4-triazol-1-yl)imidazo[5,1-f][1,2,4]triazine from example 12A are added thereto and the mixture is heated for 2 h to 70° C. After cooling, the solvent is removed and the residue is taken up and extracted with dichloromethane and 1N sodium hydroxide solution. The organic phase is separated off, dried and the crude product is purified by flash chromatography. (Eluent: dichloromethane/methanol 100:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07202243B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-294f268b96ca4bffaec93c1bc25a8321
출처 메모uspto-grants-2007_04