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HRID 339467作成日:2026年10月26日

Hydrochloric Acid → 2-[5-(6-Chloroquinoxalin-2-yloxy)-2-ethylphenyl]hexahydro-4,7-ethanoindene-1,3-dione

https://huagongshe.com/reaction/339467

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium CarbonateHCID 11430—
反応物2,6-DichloroquinoxalineHCID 87748—
反応物2-(2-Ethyl-5-hydroxyphenyl)hexahydro-4,7-ethanoindene-1,3-dioneHCID 66677814—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物2-[5-(6-Chloroquinoxalin-2-yloxy)-2-ethylphenyl]hexahydro-4,7-ethanoindene-1,3-dioneHCID 66676721—

反応条件

温度140 °C

反応手順

To a mixture of 2-(2-ethyl-5-hydroxyphenyl)hexahydro-4,7-ethanoindene-1,3-dione (83 mg, 0.28 mmol) and anhydrous potassium carbonate (90 mg, 0.56 mmol) is added a solution of 2,6-dichloroquinoxaline (67 mg, 0.34 mmol) in anhydrous dimethylformamide (2.0 ml), and the mixture is heated at 140° C. for 40 minutes under microwave irradiation. The mixture is acidified with 2M aqueous hydrochloric acid and diluted with dichloromethane then filtered. The organic phase is concentrated under reduced pressure and the residue is purified by preparative reverse phase HPLC to afford 2-[5-(6-chloroquinoxalin-2-yloxy)-2-ethylphenyl]hexahydro-4,7-ethanoindene-1,3-dione.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895474B2
出典データセットuspto-grants-2014_11
ORD IDord-b30b327cf88748a5a0b2a419f8867806
出典メモuspto-grants-2014_11