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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 216686생성일: 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/216686

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-indoleglyoxylateHCID 588944—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-(5-Dimethylaminomethyl-benzofuran-3-yl)-acetamideHCID 59192034—
용매TetrahydrofuranHCID 8028—
생성물3-(5-Dimethylaminomethyl-benzofuran-3-yl)-4-(1H-indol-3-yl)-pyrrole-2,5-dioneHCID 2496823363%

반응 조건

온도0 °C

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, 1H), 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193236B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-756c81a104194b00a901d62a2ca5ceed
출처 메모uspto-grants-2012_06