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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 653574생성일: 2026년 10월 24일

Hydrogen Bromide → 2-Bromo-5-methyl-7-phenyl-1,2,4-triazolo[1,5-a]pyrimidine

https://huagongshe.com/ko/reaction/653574

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물WaterHCID 962—
반응물Ethyl AcetateHCID 8857—
반응물5-Methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidin-2-amineHCID 975713—
반응물Sodium NitriteHCID 23668193—
용매Acetic AcidHCID 176—
용매DichloromethaneHCID 6344—
용매Dichloromethane ethylacetateHCID 21226138—
생성물2-Bromo-5-methyl-7-phenyl-1,2,4-triazolo[1,5-a]pyrimidineHCID 19889044—

반응 단계

To 2.0 g (8.9 mmol) of 5-methyl-7-phenyl-1,2,4-triazolo[1,5-a]pyrimidin-2-amine stirring in a mixture of 20 ml of 48% hydrobromic acid and 10 ml of glacial acetic acid, 2.0 g (29.0 mmol) of sodium nitrite was slowly added portionwise with good stirring at ambient temperature. The thick suspension was stirred at about 60° C. for 15 minutes followed by stirring another 10 minutes without heat. Ethyl acetate (150 ml) and excess water were added. The ethyl acetate layer was separated whereby a certain amount of insoluble material present was ignored and the extract washed with water (2X), saturated sodium bicarbonate, brine, dried over magnesium sulfate, and evaporated in vacuo to give a solid residue. Silica gel column chromatography (methylene chloride followed by 10:1 methylene chloride/ethyl acetate) afforded the title compound, 15 m.p. 178°-180° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05127936
출처 데이터셋uspto-grants-1992_07
ORD IDord-036e294f664e440a8ac4cae1a142c2aa
출처 메모uspto-grants-1992_07