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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393642생성일: 2026년 10월 25일

Triphenylphosphine → 4-Chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline

https://huagongshe.com/reaction/393642

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물1H-1,2,4-Triazole-1-ethanolHCID 550925—
반응물4-Chloro-6-methoxyquinolin-7-olHCID 135583731—
용매DichloromethaneHCID 6344—
생성물4-Chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinolineHCID 2264655445%

반응 단계

Diethyl azodicarboxylate (1 ml, 6.5 mmol) was added dropwise to a solution of 4-chloro-7-hydroxy-6-methoxyquinoline (845 mg, 4.0 mmol), (prepared as described for the starting material in Example 3), 2-([1,2,4]-triazol-1-yl)ethanol (500 mg, 4.4 mmol), (Ann. Pharm. Fr. 1977, 35, 503-508), and triphenylphosphine (1.7 g, 6.5 mmol) in methylene chloride (40 ml) under argon. After stirring for 4 days at ambient temperature, the insoluble materials were removed by filtration. The volatiles were removed by evaporation and the residue was purified by column chromatography on silica eluting with methylene chloride/acetonitrile/methanol (75/20/5). The product was purified by a second chromatography on neutral alumina eluting with methylene chloride/acetonitrile/methanol (75/20/5). The purified product was triturated with ether, collected by filtration and dried under vacuum to give 4-chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline (544 mg, 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809097B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-8d3f5f227766422fabf12c317ca2b63e
출처 메모uspto-grants-2004_10