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HRID 2416010作成日:2026年10月25日

Acetic Acid → Diethyl 2-[3-chloro-5-(trifluoromethyl)-2-pyridyl]-2-[(1,3-dioxo-2,3-dihydro-1H-2-isoindolyl)methyl]malonate

https://huagongshe.com/reaction/2416010

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sodium hydrideHCID 24758—
反応物1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)-HCID 79244—
反応物Diethyl 2-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)malonateHCID 2774041—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Diethyl 2-[3-chloro-5-(trifluoromethyl)-2-pyridyl]-2-[(1,3-dioxo-2,3-dihydro-1H-2-isoindolyl)methyl]malonateHCID 22637220—

反応手順

To a suspension of 60% sodium hydride (0.65 g) in dry dimethylformamide (20 ml) at 0° C. was added a solution of diethyl 2-(3-chloro-5-trifluoromethyl-2-pyridyl)malonate (5 g) in dry dimethylformamide (10 ml) and the mixture was stirred for 15 minutes. A solution of N-bromomethylphthalimide (3.55 g) in dry dimethylformamide (10 ml) was added dropwise and the mixture was warmed with stirring to 22° C. over 18 hours. Glacial acetic acid (1 ml) was added and the mixture was poured into cold water (500 ml). The aqueous solution was extracted with diethyl ether (3×150 ml) and the combined extract was water washed (3×100 ml). The organic extract was dried (MgSO4) and evaporated to give a crude product. Trituration with diethyl ether/light petroleum (b.p. 40-60° C.) (1:1) gave the title compound, m.p. 159-61° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06821992B1
出典データセットuspto-grants-2004_11
ORD IDord-f1aba7d4c4da4213b07d2f2faed38b17
出典メモuspto-grants-2004_11