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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1743396생성일: 2026년 10월 26일

Triethylamine → 6,7-Dimethyl-5-methoxy-3-(methylthio)-1,3-dihydro-2H-indole-2-one

https://huagongshe.com/reaction/1743396

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sulfuryl chlorideHCID 24648—
반응물Methyl (methylthio)acetateHCID 85522—
반응물Proton spongeHCID 88675—
반응물4-Methoxy-2,3-dimethylanilineHCID 11094809—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물6,7-Dimethyl-5-methoxy-3-(methylthio)-1,3-dihydro-2H-indole-2-oneHCID 2223807746%

반응 단계

To a solution of methyl (methylthio)acetate (40.8 mL, 317 mmol) in dichloromethane (1100 mL) was added sulfuryl chloride (26.6 mL, 331 mmol) at −78° C., and the mixture was stirred for 15 minutes. Further, a solution of 4-methoxy-2,3-dimethylaniline (41.7 g, 276 mmol) and proton sponge (62.1 g, 290 mmol) in dichloromethane (200 mL) was added dropwise over 1 hour and mixture was stirred at the same temperature for 1 hour. Triethylamine (43 mL, 380 mmol) was added, and the temperature was gradually raised to room temperature. After stirring at room temperature for 2 hours, water was added, the organic layer was washed with an aqueous saturated solution of sodium bicarbonate and saturated brine, dried over sodium sulfate, and the solvent was distilled off under reduced pressure. To the residue was added toluene (300 mL), and the mixture was stirred at reflux for 1 hour. The solvent was distilled off under reduced pressure, which was recrystallized from ethyl acetate to obtain 30.0 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07008940B1
출처 데이터셋uspto-grants-2006_03
ORD IDord-d7c675b9ee8e41cd9e3d5f36d3576b26
출처 메모uspto-grants-2006_03