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HRID 216686作成日:2026年10月26日

Methyl 3-indoleglyoxylate → 3-(5-Dimethylaminomethyl-benzofuran-3-yl)-4-(1H-indol-3-yl)-pyrrole-2,5-dione

https://huagongshe.com/reaction/216686

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-indoleglyoxylateHCID 588944—
反応物Potassium tert-butoxideHCID 23665647—
反応物2-(5-Dimethylaminomethyl-benzofuran-3-yl)-acetamideHCID 59192034—
溶媒TetrahydrofuranHCID 8028—
生成物3-(5-Dimethylaminomethyl-benzofuran-3-yl)-4-(1H-indol-3-yl)-pyrrole-2,5-dioneHCID 2496823363%

反応条件

温度0 °C

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193236B2
出典データセットuspto-grants-2012_06
ORD IDord-756c81a104194b00a901d62a2ca5ceed
出典メモuspto-grants-2012_06