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HRID 1019812作成日:2026年10月25日

Water → (S)-2-(1-(5-chloro-3-(2-(methylsulfonyl)phenyl)quinoxalin-2-yl)ethyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/1019812

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium hydroxy sulfiteHCID 23707502—
反応物BentoniteHCID 71586775—
反応物2-((1S)-1-(5-chloro-3-(2-(methylthio)phenyl)quinoxalin-2-yl)ethyl)isoindoline-1,3-dioneHCID 86698513—
溶媒DichloromethaneHCID 6344—
生成物(S)-2-(1-(5-chloro-3-(2-(methylsulfonyl)phenyl)quinoxalin-2-yl)ethyl)isoindoline-1,3-dioneHCID 8669851582%

反応手順

A 5 L three-necked round-bottomed flask equipped with an addition funnel, nitrogen inlet, overhead stirrer and thermocouple was charged with Montmorillonite K10 (274 g, 274 mmol) and water (54.2 mL). The mixture was vigorously stirred for ˜10 min, when a free flowing powder was obtained. At this time DCM (1.26 mL) was added followed by Oxone (421 g, 685 mmol). The reaction temperature dropped to 15° C. A solution of 2-((1S)-1-(5-chloro-3-(2-(methylthio)phenyl)quinoxalin-2-yl)ethyl)isoindoline-1,3-dione (126 g, 274 mmol) in DCM (630 mL) was added at rt (18-20° C.) to the montmorillonite/oxone suspension through an addition funnel and the internal temperature was controlled below 21° C. by a water/ice bath. The reaction was stirred at rt (19-21° C.) and monitored by LC. It was deemed completion after 96 h. The reaction mixture was filtered and the solids were washed with DCM (2×250 mL). The combined organic solution was washed with 10 wt % aq. solution of Na2SO3 (2×250 mL), concentrated and dried to afford the product as a light yellow solid 110 g with 97.6% LC purity and 82% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.14-8.29 (m, 1H), 7.64-8.14 (m, 8H), 7.52 (dd, J=5.5, 3.0 Hz, 1H), 7.21-7.38 (m, 1H), 5.59-5.94 (m, 1H), 3.10-3.27 (m, 3H), 1.66-1.91 (m, 3H) Mass Spectrum (ESI) m/z=492.0 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08716290B2
出典データセットuspto-grants-2014_05
ORD IDord-ea7cc998a310487da36a049b79b3237d
出典メモuspto-grants-2014_05