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HRID 1485949作成日:2026年10月24日

Methyl iodide → 4-{2-[(3-Bromo-4-chloro-benzoyl)-methyl-amino]-phenyl}-butyric acid methyl ester

https://huagongshe.com/ja/reaction/1485949

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物4-[2-(3-Bromo-4-chloro-benzoylamino)-phenyl]-butyric acid methyl esterHCID 68602147—
溶媒DimethylformamideHCID 6228—
生成物4-{2-[(3-Bromo-4-chloro-benzoyl)-methyl-amino]-phenyl}-butyric acid methyl esterHCID 6860262092.7%

反応条件

温度0 °C

反応手順

To 4-[2-(3-bromo-4-chloro-benzoylamino)-phenyl]-butyric acid methyl ester (1.04 g, 2.54 mmol) in DMF (10 mL) at 0-5° C., was added NaH (152 mg, 3.81 mmol, 60% in mineral oil) in two portions. The mixture was stirred for 15 min at 0° C. and 15 min at rt. After addition of iodomethane (316 μl, 5.08 mmol), the mixture was stirred at room temperature for 12 hrs and was partitioned between ethyl acetate and citric acid. The separated organic layer was then washed with brine and dried over Na2SO4. Concentration and purification by silica gel column chromatography eluting with hexane/ethyl acetate (4/1) up to hexane/ethyl acetate (3/2) yielded 4-{2-[(3-bromo-4-chloro-benzoyl)-methyl-amino]-phenyl}-butyric acid methyl ester (1.0 g). MS [M+H]+: 426.0; tR=2.46 min. (method 1)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09422310B2
出典データセットuspto-grants-2016_08
ORD IDord-96a31d542c644845889de818de7a31db
出典メモuspto-grants-2016_08