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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1162901생성일: 2026년 10월 24일

Triethylamine → 2-Oxo-3-[1-oxo-3-(2-trifluoromethylphenyl)-1,2-dihydroisoquinolin-7-yl]oxazolidin-5-ylmethyl methanesulfonate

https://huagongshe.com/ko/reaction/1162901

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ammonium ChlorideHCID 25517—
반응물Methanesulfonyl chlorideHCID 31297—
반응물7-(5-Hydroxymethyl-2-oxooxazolidin-3-yl)-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-oneHCID 57558151—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물2-Oxo-3-[1-oxo-3-(2-trifluoromethylphenyl)-1,2-dihydroisoquinolin-7-yl]oxazolidin-5-ylmethyl methanesulfonateHCID 5755787576%

반응 단계

Triethylamine (128 μl) and methanesulfonyl chloride (71 μl) were added to a solution obtained by dissolving the 7-(5-hydroxymethyl-2-oxooxazolidin-3-yl)-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one (186.7 mg, 0.462 mmol) obtained in step B in methylene chloride (2.3 ml), under cooling on ice. The obtained mixture was stirred for 30 minutes. Thereafter, a saturated ammonium chloride aqueous solution was added to the reaction solution, followed by extraction with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and was then concentrated. The obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=2:1, and then methylene chloride:methanol=30:1), so as to obtain 2-oxo-3-[1-oxo-3-(2-trifluoromethylphenyl)-1,2-dihydroisoquinolin-7-yl]oxazolidin-5-ylmethyl methanesulfonate (169.1 mg; yield: 76%) in the form of a colorless foaming substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07820693B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-559eb20379a84280b24188a05a533278
출처 메모uspto-grants-2010_10