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HRID 1009752作成日:2026年10月23日

Dimethyl Sulfate → N-methyl-N-(3-pyridyl)-2-[4-(6-cyano-7-methoxyquinolin-4-yloxy)phenyl]acetamide

https://huagongshe.com/ja/reaction/1009752

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfateHCID 6497—
反応物Lithium bis(trimethylsilyl)amideHCID 57426343—
反応物N-(3-pyridyl)-2-[4-(6-cyano-7-methoxyquinolin-4-yloxy)phenyl]acetamideHCID 67304801—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物N-methyl-N-(3-pyridyl)-2-[4-(6-cyano-7-methoxyquinolin-4-yloxy)phenyl]acetamideHCID 67304576—

反応条件

温度-5 °C

反応手順

Under an atmosphere of argon, a 1M solution of lithium hexamethyldisilazane in THF (0.27 ml) was added dropwise to a stirred solution of N-(3-pyridyl)-2-[4-(6-cyano-7-methoxyquinolin-4-yloxy)phenyl]acetamide (0.1 g) in DMF (2 ml) that had been cooled to −5° C. After 5 minutes, a solution of dimethyl sulphate (0.026 ml) in DMF (0.5 ml) was added dropwise and the resultant mixture was stirred at 0° C. for 30 minutes. The mixture was evaporated and the residue was purified by preparative HPLC using a Waters ‘Xterra’ reversed-phase column (5 microns silica) using decreasingly polar mixtures of water (containing 0.2% ammonium carbonate) and acetonitrile as eluent. There was thus obtained the title compound (0.04 g); 1H NMR: (CDCl3) 3.34 (s, 3H), 3.52 (s, 2H), 4.08 (s, 3H), 6.51 (d, 1H), 7.07 (d, 2H), 7.18 (d, 2H), 7.42 (m, 1H), 7.53 (br s, 2H), 8.5 (br s, 1H), 8.65 (br s, 1), 8.67 (d, 1H), 8.69 (s, 1H); Mass Spectrum: M+H+ 425.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07973164B2
出典データセットuspto-grants-2011_07
ORD IDord-611a837bb71f41b9be447a419dbd6771
出典メモuspto-grants-2011_07