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HRID 392356作成日:2026年10月26日

Ethyl Acetate → HCID 22662859、化合物

https://huagongshe.com/reaction/392356

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物FluorineHCID 24524—
反応物Aminopyrazine carboxamideHCID 280292—
反応物Sodium BicarbonateHCID 516892—
溶媒Trifluoroacetic acidHCID 6422—
生成物HCID 22662859HCID 22662859—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06800629B2
出典データセットuspto-grants-2004_10
ORD IDord-6e20edda12b6412e9052480c49ddde53
出典メモuspto-grants-2004_10