Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393641생성일: 2026년 10월 24일
Potassium Hydroxide → 4-(4-Chloro-2-fluorophenoxy)-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline hydrochloride
https://huagongshe.com/ko/reaction/393641
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 4-Chloro-2-fluorophenol | HCID 181975 | — |
| 반응물 | 4-Chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline | HCID 22646554 | — |
| 생성물 | 4-(4-Chloro-2-fluorophenoxy)-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline hydrochloride | HCID 22646601 | 61% |
반응 단계
A mixture of 4-chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline (132 mg, 0.43 mmol), 4-chloro-2-fluorophenol (400 mg, 2.7 mmol) and potassium hydroxide (28 mg, 0.49 mmol) was head at 165° C. for 3 hours under argon. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with water, brine, dried (MgSO4) and the volatiles were removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol (95/5). The purified product was dissolved in methylene chloride and 2M ethereal hydrogen chloride (0.5 ml) was added. The volatiles were removed by evaporation and the residue was triturated with ether, collected by filtration and dried under vacuum to give 4-(4-chloro-2-fluorophenoxy)-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline hydrochloride (110 mg, 61%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06809097B1 |
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| 출처 데이터셋 | uspto-grants-2004_10 |
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| ORD ID | ord-e9ad687a37674a76836f2bf397f7b46e |
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| 출처 메모 | uspto-grants-2004_10 |
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