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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 721310생성일: 2026년 10월 25일

Nonan-5-ol → 1-Butylpentyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamate

https://huagongshe.com/reaction/721310

반응식

참여 물질

역할이름HCID투입량
반응물Nonan-5-olHCID 12202—
반응물TriphosgeneHCID 94429—
반응물Sodium BicarbonateHCID 516892—
반응물4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylanilineHCID 21890421—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물1-Butylpentyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamateHCID 2189000173.4%

반응 단계

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-dimethylaniline (50 mg) was added to toluene (5 ml), and triethylamine (0.5 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (68 mg) in methylene chloride was then added thereto, and the mixture was heated under reflux for 10 min. Next, 5-nonanol (33 mg) was added thereto, and the mixture was further stirred with heating under reflux for 3 hr. A saturated aqueous sodium bicarbonate solution was added to stop the reaction, and the reaction solution was then extracted with chloroform, followed by washing with a 1 N aqueous hydrochloric acid solution, water, and saturated brine in that order. The extract was dried over sodium sulfate and was then concentrated. The residue was purified on a column using chloroform/methanol to give the title compound (56 mg, yield 70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135466B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-58ee5ef0552546479bbc94c2895ee528
출처 메모uspto-grants-2006_11