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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1014277생성일: 2026년 10월 26일

Tetrahydrofuran → 1-[2-(dimethylamino)ethyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine

https://huagongshe.com/reaction/1014277

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참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Aluminium lithium hydrideHCID 21226445—
반응물1-(6-Amino-5-methoxy-2,3-dihydro-1H-indol-1-yl)-2-(dimethylamino)ethan-1-oneHCID 53414764—
용매Diethyl EtherHCID 3283—
용매Ethyl AcetateHCID 8857—
생성물1-[2-(dimethylamino)ethyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-amineHCID 5944212925%

반응 조건

온도50 °C

반응 단계

A 1.0M solution of lithium aluminum hydride in diethyl ether (Aldrich, 11 mL, 11 mmol, 10 equiv.) was added dropwise to a solution of 1-[(dimethylamino)acetyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine (0.280 g, 1.12 mmol) in diethyl ether (10 mL). The solids failed to dissolve, so anhydrous tetrahydrofuran was added (10 mL) and the solution was maintained at 50° C. for 12 hours. The solution was cooled, poured into ice water, diluted with ethyl acetate, and the organic layer was dried, taken to a residue under reduced pressure, and purified by chromatography on SiO2 to afford 1-[2-(dimethylamino)ethyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine (0.065 g, 25% Yield). 1H NMR (400 MHz, CDCl3) δ ppm 6.66 (s, 1 H), 6.05 (s, 1 H), 3.77 (s, 3 H), 3.28 (t, J=8.07 Hz, 2 H), 3.16 (t, J=6.97 Hz, 2 H), 2.86 (t, J=8.25 Hz, 2H), 2.64 (s, 2 H), 2.39 (s, 6 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07981903B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-06825cde5e48477bb6ac4c73b7d0421c
출처 메모uspto-grants-2011_07