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HRID 1403535作成日:2026年10月26日

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

https://huagongshe.com/reaction/1403535

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物(S)-methyl 3-(methyl(1-phenylethyl)amino)-2-oxo-1,2-dihydroquinoxaline-6-carboxylateHCID 70665101—
溶媒DichloromethaneHCID 6344—
生成物(S)-methyl 3-(methyl(1-phenylethyl)amino)-2-(trifluoromethylsulfonyloxy)quinoxaline-6-carboxylateHCID 86670575—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08912188B2
出典データセットuspto-grants-2014_12
ORD IDord-9e59c543b2b8438f87893d0b1aaece6b
出典メモuspto-grants-2014_12