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HRID 501047作成日:2026年10月25日

Triethylamine → 6-(5-Methoxy-benzofuran-2-yl)-pyridazin-3-ylamine

https://huagongshe.com/reaction/501047

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物6-Bromopyridazin-3-amineHCID 2794779—
反応物(5-Methoxy-1-benzofuran-2-yl)boronic acidHCID 22221596—
触媒HCID 178418476HCID 178418476—
溶媒EthanolHCID 702—
生成物6-(5-Methoxy-benzofuran-2-yl)-pyridazin-3-ylamineHCID 2501492821.1%

反応条件

温度140 °C

反応手順

5-methoxybenzofuran boronic acid 1.2 mmol), 6-bromo-3-pyridazinamine (1.0 mmol), Pd(PPh3)2Cl2 (0.024 mmol) and NEt3 (317 μL) were mixed in EtOH (10 mL) in a 20 mL microwave vial. The mixture was stirred at 140° C. for 10 min in a microwave reactor. The solvent was removed under vacuum, water was added and the solution was extracted with EtOAc. The organic layer was dried over Na2SO4, filtered and the solvent removed under vacuum. The crude substance was purified by preparative HPLC to afford the title compound as a white solid (51 mg). 1H NMR δ ppm 7.77 (d, 1 H) 7.52 (d, 1 H) 7.35 (s, 1H) 7.19 (d, 1 H) 6.79-6.98 (m, 2 H) 6.72 (s, 2 H) 3.80 (s, 3 H); MS m/z 242 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772256B2
出典データセットuspto-grants-2010_08
ORD IDord-e336682ef11347baaef493fc5392dfac
出典メモuspto-grants-2010_08