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HRID 13994作成日:2026年10月26日

N-methyl-2-pyrrolidone → Methyl 3-(aminocarbonyl)-5-[(dipropylamino)carbonyl]benzoate

https://huagongshe.com/reaction/13994

反応式

関与物質

役割名称HCID仕込み量
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物HexamethyldisilazaneHCID 13838—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物DiisopropylethylamineHCID 81531—
反応物Methyl 3-bromo-5-(dipropylcarbamoyl)benzoateHCID 21939662—
触媒palladium(II) acetateHCID 167845—
生成物Methyl 3-(aminocarbonyl)-5-[(dipropylamino)carbonyl]benzoateHCID 22593626—

反応条件

温度100 °C

反応手順

To a mixture of methyl 3-bromo-5-[(dipropylamino)carbonyl]benzoate (XXI, PREPARATION 3, 0.5 g, 1.47 mmol) in dry N-methyl pyrrolidinone under a carbon monoxide atmosphere is added palladium (II) acetate (0.017 g, 0.074 mmol), 1,3-bis(diphenylphosphino)propane (0.045 g, 0.11 mmol), hexamethyldisilazane (1.0 mL, 4.7 mmol), and diisopropylethylamine (0.38 g, 2.94 mmol). The mixture is heated at 100 degrees C. for 24 hours. The mixture is cooled to 20-25 degrees C. and partitioned between water and ethyl acetate. The layers are separated and the aqueous phase is back-washed with ethyl acetate. The organic phases are combined and washed three times with saline, dried over anhydrous magnesium sulfate, filtered and concentrated. Column chromatography (silica gel, 75 mL; methanol/methylene chloride, 2.5/97.5) gives the title compound, NMR (CDCl3) delta 0.77, 1.02, 1.57, 1.71, 3.17, 3.49, 3.98, 5.78, 6.34, 8.07, 8.20 and 8.48.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727997B2
出典データセットuspto-grants-2010_06
ORD IDord-29f5d0eb949941ada3d0a5cf90557324
出典メモuspto-grants-2010_06