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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5740생성일: 2026년 10월 24일

N-(2-Aminoethyl)isoquinoline-5-sulfonamide → N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamide

https://huagongshe.com/ko/reaction/5740

반응식

참여 물질

역할이름HCID투입량
반응물N-(2-Aminoethyl)isoquinoline-5-sulfonamideHCID 3544—
반응물Ethyl AcetateHCID 8857—
반응물p-ChlorocinnamaldehydeHCID 3794977—
반응물SodiumHCID 5360545—
용매MethanolHCID 887—
생성물N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamideHCID 17615671.5%

반응 단계

2.01 g of N-(2-aminoethyl]-5-isoquinolinesulfonamide was dissolved in 30 ml of methanol, to the solution was added 1.60 g of p-chlorocinnamaldehyde, and the mixture was stirred for one hour at a room temperature. After an addition of 350 mg of sodium tetrahydrideborate in portions with ice cooling, the mixture was stirred for 30 minutes. After an addition of ethyl acetate, the reaction mixture was sequentially washed three times with water, and then twice with a saturated sodium chloride aqueous solution, and dried over magnesium sulfate. The mixture was filtered and evaporated to remove the solvent under a reduced pressure. A residue was purified using a silica gel column (silica gel 80 g, eluant: 5% methanol in chloroform), and resulting crystals were washed with benzene/hexane (1:1), to obtain 2.30 g of the title compound as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245034
출처 데이터셋uspto-grants-1993_09
ORD IDord-972b7e9615b641608f2fd7c85b62dfc9
출처 메모uspto-grants-1993_09