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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1094983생성일: 2026년 10월 26일

Pyridine → 2-(3-Chloromethyl-benzoylamino)-5-dipropylamino-benzoic acid methyl ester

https://huagongshe.com/reaction/1094983

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DichloromethaneHCID 6344—
반응물Veratroyl chlorideHCID 77070—
반응물2-Amino-5-dipropylamino-benzoic acid methyl esterHCID 61313650—
생성물2-(3-Chloromethyl-benzoylamino)-5-dipropylamino-benzoic acid methyl esterHCID 66637743—

반응 조건

온도0 °C

반응 단계

2-Amino-5-dipropylamino-benzoic acid methyl ester (compound A) (243 mg) produced by the above reaction was dissolved in anhydrous methylene chloride (3.0 ml). Subsequently, pyridine (170 μl) and 3-(chloromethyl)benzoyl chloride (compound B) (166 μl) were added to the solution at 0° C., and the mixture was stirred at 0° C. for one hr. After the completion of the reaction, distilled water was added thereto, and the mixture was subjected to separatory extraction with chloroform. The organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated. The residue was purified by column chromatography using a hexane-acetone system to give 2-(3-chloromethyl-benzoylamino)-5-dipropylamino-benzoic acid methyl ester as a useful intermediate (280 mg, yield 64%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08134015B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-c368aed5d7bb4f9cbc810a6899df9373
출처 메모uspto-grants-2012_03