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HRID 1261767作成日:2026年10月25日

Hydrochloric Acid → 3-methoxy-4-[(E)-3-oxo-3-(2-phenylamino-pyridin-3-yl)-propenyl]-benzoic acid methyl ester

https://huagongshe.com/reaction/1261767

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Methyl 4-formyl-3-methoxybenzoateHCID 10631650—
反応物Sodium MethoxideHCID 10942334—
反応物1-(2-(Phenylamino)pyridin-3-yl)ethanoneHCID 66815802—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物3-methoxy-4-[(E)-3-oxo-3-(2-phenylamino-pyridin-3-yl)-propenyl]-benzoic acid methyl esterHCID 8667205386.8%

反応条件

温度25 °C

反応手順

A mixture of 1-(2-phenylamino-pyridin-3-yl)-ethanone (833 mg, 3.92 mmol) in methanol (16.5 mL) at 25° C. was treated with 4-formyl-3-methoxy-benzoic acid methyl ester (508 mg, 2.61 mmol) and sodium methoxide in methanol (4.37M, 1.2 mL, 5.23 mmol). The reaction was stirred at 25° C. for 48 h. At this time, the reaction was diluted with water (100 mL), neutralized with a 1N aqueous hydrochloric acid solution, and extracted with methylene chloride (3×75 mL). The combined organics were dried over sodium sulfate filtered and concentrated in vacuo. Flash chromatography (40 g silica column, 10-50% ethyl acetate/hexanes) afforded 3-methoxy-4-[(E)-3-oxo-3-(2-phenylamino-pyridin-3-yl)-propenyl]-benzoic acid methyl ester (880 mg, 86.8%) as a red solid. ES+-HRMS m/e calcd for C23H20N2O4 [M+H+] 389.1496. Found 389.1494.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08471027B2
出典データセットuspto-grants-2013_06
ORD IDord-2a25fc279b5a4554b8578b6609bcaea1
出典メモuspto-grants-2013_06