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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393643생성일: 2026년 10월 24일

Hydrochloric Acid → 4-(4-Chloro-2-fluoroanilino)-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline hydrochloride

https://huagongshe.com/ko/reaction/393643

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Chloro-2-fluoroanilineHCID 93898—
반응물4-Chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinolineHCID 22646554—
용매IsopropanolHCID 3776—
용매DimethylformamideHCID 6228—
생성물4-(4-Chloro-2-fluoroanilino)-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline hydrochlorideHCID 2264662620.2%

반응 조건

온도150 °C

반응 단계

A solution 2 4-chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline (203 mg, 0.66 mmol), (prepared as described for the starting material in Example 38), and 4-chloro-2-fluoroaniline (74 μl, 0.66 mmol) in DMF (10 ml) containing 5M hydrogen chloride in isopropanol (0.4 ml) was heated at 150° C. for 8 hours. The volatiles were removed by evaporation and the residue was partitioned between water and methylene chloride. The aqueous layer was adjusted to pH9 with I M sodium hydroxide. The organic layer was washed with brine, dried (MgSO4) and the volatiles were removed by evaporation. The residue was dissolved in methylene chloride/methanol and 2M ethereal hydrogen chloride (1 ml) was added. After removal of the volatiles by evaporation, the residue was triturated with ether, collected by filtration, washed with ether and dried under vacuum to give 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline hydrochloride (60 mg, 17%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809097B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-b0e4b2581daf4c2ab67a502ee4c7af75
출처 메모uspto-grants-2004_10