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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 392356생성일: 2026년 10월 24일

Ethyl Acetate → HCID 22662859, 화합물

https://huagongshe.com/ko/reaction/392356

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물FluorineHCID 24524—
반응물Aminopyrazine carboxamideHCID 280292—
반응물Sodium BicarbonateHCID 516892—
용매Trifluoroacetic acidHCID 6422—
생성물HCID 22662859HCID 22662859—

반응 단계

In 9 mL of trifluoroacetic acid was dissolved 0.3 g of 3-amino-2-pyrazinecarboxamide. At an ice-cooled temperature, 10% fluorine gas (a fluorine gas diluted with nitrogen gas) was introduced into the solution at a rate of 45 ml per minute for a period of 22 minutes. After stirring the mixture at an ice-cooled temperature for 17 minutes, the temperature was elevated to room temperature. The reaction mixture was added to a mixture of 30 mL of saturated aqueous solution of sodium hydrogen carbonate and 30 mL of ethyl acetate, and the organic layer was separated. The remaining aqueous layer was acidified with 6 mol/L hydrochloric acid and then extracted with 20 ml of ethyl acetate. The organic layers thus obtained were united, washed successively with 10 mL of water and 10 mL of saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent: n-hexane:ethyl acetate=2:1] to obtain 0.015 g of 3-amino-6-fluoro-2-pyrazinecarboxamide as a light yellow-colored solid product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06800629B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-6e20edda12b6412e9052480c49ddde53
출처 메모uspto-grants-2004_10