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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1095002생성일: 2026년 10월 26일

Pyridine → 3-(3-{[Bis-(2-hydroxy-propyl)-amino]-methyl}-benzoylamino)-naphthalene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1095002

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DiisopropanolamineHCID 8086—
반응물3-(Chloromethyl)benzoic acidHCID 241752—
반응물3-(3-Chloromethylbenzoylamino)-naphthalene-2-carboxylic acid methyl esterHCID 66638116—
용매DichloromethaneHCID 6344—
생성물3-(3-{[Bis-(2-hydroxy-propyl)-amino]-methyl}-benzoylamino)-naphthalene-2-carboxylic acid methyl esterHCID 66637804—

반응 단계

Subsequently, 3-(3-chloromethyl-benzoylamino)-naphthalene-2-carboxylic acid methyl ester (870 mg) was dissolved in anhydrous methylene chloride (15 ml). Pyridine (400 μl) and diisopropanolamine (compound B′) (1.0 g) were added to the solution at room temperature, and the mixture was then stirred at that temperature for 48 hr. After the completion of the reaction, distilled water was added thereto at room temperature, 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 under the reduced pressure. The residue was purified by column chromatography eluted with a hexane-acetone system to give 3-(3-{[bis-(2-hydroxy-propyl)-amino]-methyl}-benzoylamino)-naphthalene-2-carboxylic acid methyl ester as a useful intermediate (640 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08134015B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-b33e69d7d05747159e1ac4dc093c2c2f
출처 메모uspto-grants-2012_03