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HRID 1160454作成日:2026年10月26日

Cesium carbonate → Methyl 3-[methyl(methylsulfonyl)amino]-5-(2-oxo-4-phenylpyrrolidin-1-yl)benzoate

https://huagongshe.com/reaction/1160454

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物1,4-DioxaneHCID 31275—
反応物4-Phenyl-2-pyrrolidinoneHCID 121397—
反応物Methyl 3-bromo-5-[methyl(methylsulfonyl)amino]benzoateHCID 57529331—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 3-[methyl(methylsulfonyl)amino]-5-(2-oxo-4-phenylpyrrolidin-1-yl)benzoateHCID 5781512482%

反応条件

温度110 °C

反応手順

A mixture of methyl 3-bromo-5-[methyl(methylsulfonyl)amino]benzoate obtained in Reference Example 15 322 mg (1.0 mmol), 4-phenyl-2-pyrrolidinone 177 mg (1.1 mmol), cesium carbonate 456 mg (1.4 mmol), tris(dibenzylideneacetone)dipalladium(0) 4.6 mg (0.005 mmol), Zandphos 8.7 mg (0.015 mmol) and 1,4-dioxane (2 mL) was stirred at 110° C. under argon atmosphere for 7 hours. The reaction solution was diluted with ethyl acetate and the resulting precipitates were filtered. The solvent was evaporated and the residual solid was purified by a column chromatography on silica gel (eluted with hexane/ethyl acetate=3:1→1:1) to give 329 mg (0.817 mmol) of the title compound (yield: 82%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07816387B2
出典データセットuspto-grants-2010_10
ORD IDord-aeaa676f33c5463f8539c4bef597e2ff
出典メモuspto-grants-2010_10