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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2254302생성일: 2026년 10월 26일

Sodium Iodide → N-[3-(Quinolin-7-yloxy)propyl]-2,3-dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine

https://huagongshe.com/reaction/2254302

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물DiisopropylethylamineHCID 81531—
반응물7-(3-Bromopropoxy)quinolineHCID 19745014—
반응물2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamineHCID 19745017—
용매DimethylformamideHCID 6228—
생성물N-[3-(Quinolin-7-yloxy)propyl]-2,3-dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamineHCID 993051857.6%

반응 조건

온도80 °C

반응 단계

2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine (1.3 g, 6.2 mmole), 7-(3-bromopropoxy)quinoline (1.53 g, 5.5 mmole), diisopropylethylamine 2.6 g, 20 mmole) and sodium iodide (5.5 g, 37 mmole) were combined in 200 ml of DMF and heated at 80° C. for 15 hours under a nitrogen atmosphere. The solvent was then removed in vacuum and replaced with 500 ml of dichloromethane. The mixture was washed with 250 ml each of saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride, dried over sodium sulfate, filtered, and concentrated in vacuum. The residue was column chromatographed on 250 g of silica gel using 3% methanol/dichloromethane as eluant. The product-containing fractions were combined and concentrated in vacuum and the residue (2.25 g) recrystallized from ethanol with the addition of 6 ml of 4N isopropanolic HCl to give 1.25 g of the title compound as a yellow solid dihydrochloride salt, m.p. 224°-226° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05235055
출처 데이터셋uspto-grants-1993_08
ORD IDord-1f3b8dd37368441c944a3642b06276fb
출처 메모uspto-grants-1993_08