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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51972생성일: 2026년 10월 23일

Diisopropyl Ether → 7-[(4'-Trifluoromethyl-biphenyl-2-carbonyl)-amino]-quinoline-3-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/51972

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참여 물질

역할이름HCID투입량
반응물Diisopropyl EtherHCID 7914—
반응물DiisopropylethylamineHCID 81531—
반응물Ethyl 7-aminoquinoline-3-carboxylateHCID 9877801—
반응물4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chlorideHCID 11066000—
용매TolueneHCID 1140—
용매1,1-DichloroethaneHCID 6365—
생성물7-[(4'-Trifluoromethyl-biphenyl-2-carbonyl)-amino]-quinoline-3-carboxylic acid ethyl esterHCID 1018327158.4%

반응 조건

온도84 °C

반응 단계

To a mixture of 7-amino-quinoline-3-carboxylic acid ethyl ester (11 g, 51 mmol, 1 equiv), dichloroethane (220 mL, 20 volumes), and diisopropylethylamine (13.15 g, 101.7 mmol, 2 equiv) was slowly added a solution of 4′-trifluoromethyl-biphenyl -2-carbonyl chloride (17.38 g, 61 mmol, 1.2 equiv) dissolved in dichloroethane (30 mL, 2.7 volumes). The reaction was heated at 84° C. overnight and then cooled to room temperature. The reaction mixture was washed with 1 N hydrochloric acid (2×150 mL) and the aqueous layer was back extracted with dichloroethane (1×150 mL). The combined organic layers were washed with 1 N sodium hydroxide (2×150 mL), water (150 mL), and saturated sodium chloride (2×150 mL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo to give a red-brown oil. The oil was dissolved in hot toluene (32 mL) and isopropyl ether (16 mL) and the resulting solution was allowed to cool with stirring to give a beige slurry. The solids were collected by filtration to give 7-[(4′-trifluoromethyl-biphenyl-2-carbonyl)-amino]-quinoline-3-carboxylic acid ethyl ester (13.8 g, 58.4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713489B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-ca88576402484af4b76b9d01a0bfce8c
출처 메모uspto-grants-2004_03