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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 638375생성일: 2026년 10월 26일

1-(5-Isoquinolinylsulfonyl)piperazine → HCID 13116936, 화합물

https://huagongshe.com/reaction/638375

반응식

참여 물질

역할이름HCID투입량
반응물1-(5-Isoquinolinylsulfonyl)piperazineHCID 3545—
반응물Ethyl BromideHCID 6332—
반응물Potassium CarbonateHCID 11430—
반응물Chloroform methanolHCID 21584188—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
생성물HCID 13116936HCID 1311693674.1%

반응 단계

In 100 ml of ethanol were added 2.77 g of 1-(5-isoquinolinesulfonyl)piperazine, i.e., Compound (35), 1.66 g of anhydrous potassium carbonate and 5.45 g of ethyl bromide, and the reaction was carried out at an external temperature of 70° C. for 24 hours. After the reaction solution was filtered, the filtrate was condensed and the residue was dissolved in 50 ml of chloroform, and the solution was extracted twice with a 2N aqueous hydrochloric acid solution. The aqueous hydrochloric acid layer was rendered alkaline, extracted twice with 50 ml of chloroform, and the chloroform layer extracted was washed with water and dried with anhydrous magnesium sulfate. After the chloroform was distilled therefrom, the residue obtained was subjected to a silica gel column chromatography (silica gel: 100 g; solvent: 2% methanol-chloroform) to give 2.26 g of 1-(5-isoquinolinesulfonyl)-4-ethylpiperazine, i.e., Compound (42) in a yield of 74%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04560755
출처 데이터셋uspto-grants-1985_12
ORD IDord-118dcab10db243cba38965d8a598788b
출처 메모uspto-grants-1985_12