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HRID 231076생성일: 2026년 10월 26일

Sodium hydride → 8-(3-(4-(2-Methoxyphenyl)piperazin-1-yl)propoxy)-1-nicotinoyl-1,2,3,4-tetrahydroquinoline-trihydrochloride

https://huagongshe.com/reaction/231076

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-(3-Chloropropyl)-4-(2-methoxyphenyl)piperazineHCID 622669—
반응물1,2,3,4-Tetrahydro-1-(3-pyridylcarbonyl)quinolin-8-olHCID 3018739—
용매DimethylformamideHCID 6228—
생성물8-(3-(4-(2-Methoxyphenyl)piperazin-1-yl)propoxy)-1-nicotinoyl-1,2,3,4-tetrahydroquinoline-trihydrochlorideHCID 20034517—

반응 단계

0.53 (11.0 mmol) of a 50% strength sodium hydride dispersion is introduced in portions into a solution of 2.54 g (10.0 mmol) of 8-hydroxy-1-nicotinoyl-1,2,3,4-tetrahydroquinoline in 20 ml of anhydrous dimethylformamide and the mixture is subsequently stirred at 40°-50° C. for 30 minutes. After cooling to room temperature, a solution of 4.03 g (15.0 mmol) of 1-(3-chloropropyl)-4-(2-methoxyphenyl)piperazine in 20 ml of anhydrous dimethylformamide is added dropwise and the mixture is subsequently stirred at room temperature for 16 hours. The reaction solution is poured onto 150 ml of ice-water and extracted with methylene chloride and the extracts are washed several times with water, dried and concentrated. The crude product is further purified by column chromatography on silica gel (mobile phase toluene:ethanol 9:1) and converted into the dihydrochloride as described under Example 2(a). The product thus obtained is identical to the product described under 2(a).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04845099
출처 데이터셋uspto-grants-1989_07
ORD IDord-9393e4b407154a35ba3fa509557bbd05
출처 메모uspto-grants-1989_07