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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448882생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/448882

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참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물4-[2-(3-Bromo-4-chloro-benzoylamino)-phenyl]-butyric acid methyl esterHCID 68602147—
용매DimethylformamideHCID 6228—
생성물4-{2-[(3-Bromo-4-chloro-benzoyl)-methyl-amino]-phenyl}-butyric acid methyl esterHCID 6860262092.7%

반응 조건

온도0 °C

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481738B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-c5d8f1bb921c4c79a7b7f9eb13115d3a
출처 메모uspto-grants-2013_07