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HRID 379392作成日:2026年10月27日

Dimethylformamide → 2-(3,5-Dimethoxy-phenyl)-N-methyl-N-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-acetamide

https://huagongshe.com/reaction/379392

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物(3,5-Dimethoxyphenyl)acetic acidHCID 138316—
反応物HCID 69138572HCID 69138572—
生成物2-(3,5-Dimethoxy-phenyl)-N-methyl-N-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-acetamideHCID 993400975%

反応手順

To a solution of 226 mg (1.15 mmol) 3,5-dimethoxy-phenylacetic acid in 7 ml N,N-dimethylformamide were added 244 mg (1.5 mmol) 1,1′-carbonyl-diimidazole and the solution was stirred for 30 min at room temperature. After addition of 283 mg (1 mmol) of methyl-(6-morpholin-4-yl-4-tolyl-pyridin-3-yl)-amine (as described in step f) for the preparation of Example 23), the reaction mixture was heated at 70° C. for 7 h. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved in 30 ml ethyl acetate. The organic phase was washed with water (2×30 ml), brine, dried (magnesium sulfate) and evaporated. Flash chromatography gave 347 mg (75%) of the title compound as a white foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06297375B1
出典データセットuspto-grants-2001_10
ORD IDord-867d8a06ea764c1f8bb01de3cf201f27
出典メモuspto-grants-2001_10