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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1162912생성일: 2026년 10월 24일

Dichloromethane → 7-(3-hydroxypropylamino)-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one

https://huagongshe.com/ko/reaction/1162912

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물7-[3-(tert-butyldimethylsilyloxy)propylamino]-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-oneHCID 57558101—
용매TetrahydrofuranHCID 8028—
생성물7-(3-hydroxypropylamino)-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-oneHCID 23156776101.9%

반응 단계

The 7-[3-(tert-butyldimethylsilyloxy)propylamino]-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one (435 mg, 0.913 mmol) obtained in step A was dissolved in THF (9 ml). Thereafter, a 1 M tetrabutylammonium fluoride THF solution (1.1 ml, 1.1 mmol) was added to the obtained solution at a room temperature. The obtained mixture was stirred for 5 hours. Thereafter, methylene chloride was added to the reaction solution. An organic layer thereof was washed with a saturated saline solution, and was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel chromatography (methylene chloride:methanol=30:1), so as to obtain 7-(3-hydroxypropylamino)-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one (337 mg, 95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07820693B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-1fa931e1f50d42229998f1077252e940
출처 메모uspto-grants-2010_10