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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1403535생성일: 2026년 10월 26일

Pyridine → (S)-methyl 3-(methyl(1-phenylethyl)amino)-2-(trifluoromethylsulfonyloxy)quinoxaline-6-carboxylate

https://huagongshe.com/reaction/1403535

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물(S)-methyl 3-(methyl(1-phenylethyl)amino)-2-oxo-1,2-dihydroquinoxaline-6-carboxylateHCID 70665101—
용매DichloromethaneHCID 6344—
생성물(S)-methyl 3-(methyl(1-phenylethyl)amino)-2-(trifluoromethylsulfonyloxy)quinoxaline-6-carboxylateHCID 86670575—

반응 단계

To a solution of (S)-methyl 3-(methyl(1-phenylethyl)amino)-2-oxo-1,2-dihydroquinoxaline-6-carboxylate (320 mg, 0.95 mmol) in dichloromethane (30 mL) was added pyridine (313 mg, 3.96 mmol), and Tf2O (559 mg, 1.98 mmol). The resulting solution was stirred overnight at room temperature and then concentrated under vacuum to get a residue, which was purified via silica gel chromatography (1% to 5% ethyl acetate in petroleum ether) to give (S)-methyl 3-(methyl(1-phenylethyl)amino)-2-(trifluoromethylsulfonyloxy)quinoxaline-6-carboxylate as a yellow solid (432 mg, crude).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08912188B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-9e59c543b2b8438f87893d0b1aaece6b
출처 메모uspto-grants-2014_12