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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 7-(3-Bromopropoxy)quinoline | HCID 19745014 | — |
| 반응물 | 2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine | HCID 19745017 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-[3-(Quinolin-7-yloxy)propyl]-2,3-dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine | HCID 9930518 | 57.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05235055 |
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| 출처 데이터셋 | uspto-grants-1993_08 |
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| ORD ID | ord-1f3b8dd37368441c944a3642b06276fb |
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| 출처 메모 | uspto-grants-1993_08 |
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