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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2215778생성일: 2026년 10월 26일

2-(1-methyl-1H-indol-7-yl)acetamide → 3-(6-Benzyloxy-1H-indol-3-yl)-4-(1-methyl-1H-indol-7-yl)-pyrrole-2,5-dione

https://huagongshe.com/reaction/2215778

반응식

참여 물질

역할이름HCID투입량
반응물2-(1-methyl-1H-indol-7-yl)acetamideHCID 11435397—
반응물(6-Benzyloxy-1H-indol-3-yl)-oxo-acetic acid methyl esterHCID 34181007—
반응물HCID 178418922HCID 178418922—
용매TetrahydrofuranHCID 8028—
생성물3-(6-Benzyloxy-1H-indol-3-yl)-4-(1-methyl-1H-indol-7-yl)-pyrrole-2,5-dioneHCID 2195008074%

반응 단계

To a suspension of (6-benzyloxy-1H-indol-3-yl}-oxo-acetic acid methyl ester (1.0 g, 3.2 mmol) and 2-(1-methyl-1H-indol-7-yl)-acetamide (608 mg, 3.2 mmol) in 15 ml THF was added 3.5 equiv. of tBuOK in THF at 0° C. (11.3 ml of 1.0 M solution in THF) under N2. The mixture was stirred at r.t overnight, quenched with conc. HCl 5.0 ml, and neutralized with 5 N NaOH to PH=8. The mixture was extracted with ethyl acetate, and the extract was washed with saturated NaHCO3, brine and water, dried over anhydrous MgSO4, filtered and concentrated. The residue was purified by flash chromatography with Hexane:Ethyl acetate (1:1) to yield the title compound (700 mg) as orange solid, 74% yield. MS(m/z): 448.2 (M++1), 446.1 (M−−1); 1HNMR (DMSO-d6) 11.62 (s, 1H), 11.07 (s, 1H), 7.77 (d, J=1.80 Hz, 1H), 7.57 (m, 1H ), 7.26 (m, 5H), 7.21 (d, J=2.40 Hz, 1H), 6.94 (tri, J=6.00 Hz, 1H), 6.84 (m, 2H), 6.44(d, J=2.40 Hz, 1H), 6.16 (s, 1H), 4.97 (s, 2H), 3.62 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07109229B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-e4bbb6fa380443e0aca38ac8e82bab94
출처 메모uspto-grants-2006_09