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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-(1-methyl-1H-indol-7-yl)acetamide | HCID 11435397 | — |
| 반응물 | (6-Benzyloxy-1H-indol-3-yl)-oxo-acetic acid methyl ester | HCID 34181007 | — |
| 반응물 | HCID 178418922 | HCID 178418922 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(6-Benzyloxy-1H-indol-3-yl)-4-(1-methyl-1H-indol-7-yl)-pyrrole-2,5-dione | HCID 21950080 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07109229B2 |
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| 출처 데이터셋 | uspto-grants-2006_09 |
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| ORD ID | ord-e4bbb6fa380443e0aca38ac8e82bab94 |
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| 출처 메모 | uspto-grants-2006_09 |
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