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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1248761생성일: 2026년 10월 27일

Chloroform → N-[2-(N-methyl-N-benzylamino)ethyl]-5-isoquinolinesulfonamide

https://huagongshe.com/reaction/1248761

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물TriethylamineHCID 8471—
반응물(2-Aminoethyl)(benzyl)methylamineHCID 3014812—
반응물5-Isoquinolinesulfonyl chlorideHCID 3371655—
용매DichloromethaneHCID 6344—
생성물N-[2-(N-methyl-N-benzylamino)ethyl]-5-isoquinolinesulfonamideHCID 2025429584%

반응 단계

In 70 ml of methylene chloride were dissolved 3.24 g of 2-(N-methyl-N-benzylamino)ethylamine and 2.0 g of triethylamine, and to the solution was added dropwise 50 ml of a methylene chloride solution containing 3.0 g of 5-isoquinolinesulfonyl chloride under cooling with ice. After the dropwise addition of the methylene chloride solution, the mixed solution was stirred at a temperature of 15° C. to 25° C. for one hour, and then the reaction solution was washed with water and extracted with a 10% aqueous hydrochloric acid solution. The aqueous layer was washed with chloroform, rendered alkaline with a 1N aqueous sodium hydroxide solution, extracted with chloroform, and then the chloroform layer was washed with water, dried with anhydrous magnesium sulfate and the chloroform was distilled therefrom under reduced pressure. The residue thus obtained was subjected to a silica gel column chromatography (silica gel: 100 g; solvent: chloroform) to give 3.84 g of N-[2-(N-methyl-N-benzylamino)ethyl]-5-isoquinolinesulfonamide, i.e., Compound (65) in a yield of 84%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04525589
출처 데이터셋uspto-grants-1985_06
ORD IDord-5caaab0dca6b4a2ba1a3e0ddcac4bc2e
출처 메모uspto-grants-1985_06