Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 402905생성일: 2026년 10월 25일
Methyl 3-indoleglyoxylate → 3-(5-Dimethylaminomethyl-benzofuran-3-yl)-4-(1H-indol-3-yl)-pyrrole-2,5-dione
https://huagongshe.com/reaction/402905
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl 3-indoleglyoxylate | HCID 588944 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | 2-(5-Dimethylaminomethyl-benzofuran-3-yl)-acetamide | HCID 59192034 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(5-Dimethylaminomethyl-benzofuran-3-yl)-4-(1H-indol-3-yl)-pyrrole-2,5-dione | HCID 24968233 | 63% |
반응 단계
To a solution of 2-(5-dimethylaminomethyl-benzofuran-3-yl)-acetamide (91 mg, 0.39 mmol) and (1H-indol-3-yl)-oxo-acetic acid methyl ester (119 mg, 0.59 mmol) in anhydrous THF (5.0 mL) is added dropwise a 1 M solution of t-BuOK in THF (1.6 mL) under an argon atmosphere at 0° C. The resulting deep red reaction mixture is stirred for 5 min. at 0° C. and 30 min. at room temperature followed by partitioning between brine and EtOAc. The layers are separated and the aqueous layer is extracted twice with EtOAc. The combined organic layers are washed with brine, dried over Na2SO4, filtered and concentrated at reduced pressure to afford an orange solid. Purification by flash column chromatography (silica gel, EtOAc/acetic acid/water 7:1:1) affords the title compound as an orange solid (91.4 mg, 0.237 mmol, 63%). 1H NMR (400 MHz, DMSO-d6, 298 K): δ=11.90 (bs, 1H), 11.06 (bs, 1H), 8.28 (s, 1H), 7.89 (s, 1H), 7.47 (d, J=8.4 Hz, 1H), 7.33 (d, J=8.2 Hz, 1H), 7.06 (d, J=8.4 Hz, 1H), 6.94 (t, J=8.2 Hz, 1H), 6.82 (d, J=8.1 Hz, 1 H), 6.63 (d, J=8.2 Hz, 1H), 6.60 (s, 1H), 2.98 (s, 2H), 1.69 (s, 6H). MS (ES+): 386 (M(C23H19N3O3)+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08742132B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-245d7428811941ae95a98ee62d2298c0 |
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| 출처 메모 | uspto-grants-2014_06 |
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