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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2119487생성일: 2026년 10월 27일

Potassium Carbonate → 2-(4-Fluorophenyl)-1-(4-[2-(1-methyl(2-piperidyl))ethoxy]benzyl)-6-(phenylmethoxy)-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/2119487

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-(2-Chloroethyl)-1-methylpiperidineHCID 3016566—
반응물Dichloromethane methanolHCID 21226129—
반응물2-(4-Fluorophenyl)-1-(4-hydroxybenzyl)-6-(phenylmethoxy)-1,2,3,4-tetrahydroisoquinolineHCID 23440767—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(4-Fluorophenyl)-1-(4-[2-(1-methyl(2-piperidyl))ethoxy]benzyl)-6-(phenylmethoxy)-1,2,3,4-tetrahydroisoquinolineHCID 693163417%

반응 단계

To a solution of 2-(4-fluorophenyl)-1-(4-hydroxybenzyl)-6-(phenylmethoxy)-1,2,3,4-tetrahydroisoquinoline (0.500 g, 1.14 mmol) in DMF (5 ml) was added potassium carbonate (0.236 g, 1.7 nmmol) and the resulting mixture allowed to stir for twenty minutes. To the reaction mixture was added 2-(2-chloroethyl)-N-methyl piperidine (0.271 g, 1.37 mmol). The reaction was allowed to stir overnight. The reaction was diluted with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered, and concentrated. The product was purified by radial chromatography (100% CH2Cl2, then CH2Cl2/MeOH, 95:5) to yield the title compound (0.043 g, 7% yield): ES−MS (m/z) 565 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06686351B2
출처 데이터셋uspto-grants-2004_02
ORD IDord-ebbe60d92a97464bae3327034f63f199
출처 메모uspto-grants-2004_02