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HRID 507991作成日:2026年10月27日

Dimethylformamide → methyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoate

https://huagongshe.com/reaction/507991

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物2-Methyl-1,2,3,4-tetrahydroquinolineHCID 96289—
反応物Methyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoateHCID 23157330—
溶媒Ethyl AcetateHCID 8857—
生成物methyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoateHCID 2315748875%

反応条件

温度70 °C

反応手順

A mixture of methyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoate (0.70 g, 2.2 mmol), 2-methyl-1,2,3,4-tetrahydroquinoline (0.39 g, 2.6 mmol), potassium carbonate (0.60 g, 4.3 mmol) and N,N-dimethylformamide (14 mL) was stirred at 70° C. for 23 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-2/1) to give the title compound (0.63 g, yield 75%) as a pale-yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07786165B2
出典データセットuspto-grants-2010_08
ORD IDord-6312856ef23848778fe07efbc22e69ae
出典メモuspto-grants-2010_08