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HRID 273224作成日:2026年10月27日

Potassium Carbonate → 7-bromo-3-{2-[(2R)-2-methyl-1-pyrrolidinyl]ethyl}isoquinoline

https://huagongshe.com/reaction/273224

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物(R)-2-MethylpyrrolidineHCID 641544—
反応物2-(7-Bromo-3-isoquinolinyl)ethyl 4-methylbenzenesulfonateHCID 86592226—
溶媒AcetonitrileHCID 6342—
生成物7-bromo-3-{2-[(2R)-2-methyl-1-pyrrolidinyl]ethyl}isoquinolineHCID 67104692—

反応条件

温度52.5 °C

反応手順

The product from Example 52F was dissolved in a solution of (2R)-2-methylpyrrolidine (0.26 g, 3.0 mmol) in acetonitrile (20 mL). The solution was treated with potassium carbonate (0.5 g, 3.6 mmol) and heated at 50-55° C. for 20 hours in a sealed flask. The mixture was allowed to cool to room temperature, filtered, and the filtrate was concentrated in vacuo. The residue was diluted with MTBE (20 mL) and water (20 mL) and the pH was adjusted to 3-3.5 with concentrated HCl. The aqueous layer was separated, extracted with MTBE (10 mL), adjusted to a pH of 8-8.5 with potassium carbonate, and extracted with isopropyl acetate (20 mL). The organic layer was separated and concentrated in vacuo. The residue was dissolved in heptane (20 mL), filtered, and the filtrate concentrated under vacuum to provide the title compound. 1H NMR (CDCl3) δ 1.10 (d, J=6.1 Hz, 3H); 1.35-1.49 (m, 1H); 1.62-1.85 (m, 2H); 1.85-1.98 (m, 1H); 2.23 (q, J=8.8. Hz, 1H); 2.28-2.42 (m, 1H); 2.46-2.57 (m, 1H), 3.04-3.19 (m, 2H); 3.19-3.30 (m, 2H); 7.47 (s, 1H); 7.60 (d, J=8.8 Hz, 1H), 7.647.70 (m, 1H), 8.05 (m, 1H); 9.09 (s, 1H); HRMS Calcd. for [C16H19BrN2+H+]: 319.0810. Found: 319.0795.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456196B2
出典データセットuspto-grants-2008_11
ORD IDord-7d6e6e6ee70f42939f9102d4c833a78f
出典メモuspto-grants-2008_11