돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339467생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/339467

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물2,6-DichloroquinoxalineHCID 87748—
반응물2-(2-Ethyl-5-hydroxyphenyl)hexahydro-4,7-ethanoindene-1,3-dioneHCID 66677814—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-[5-(6-Chloroquinoxalin-2-yloxy)-2-ethylphenyl]hexahydro-4,7-ethanoindene-1,3-dioneHCID 66676721—

반응 조건

온도140 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895474B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-b30b327cf88748a5a0b2a419f8867806
출처 메모uspto-grants-2014_11