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HRID 393601作成日:2026年10月24日

Sodium Bicarbonate → HCID 22646584、化合物

https://huagongshe.com/ja/reaction/393601

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物5-Benzyloxy-2-fluoro-4-methylphenolHCID 21991049—
反応物4-Chloro-6-cyano-7-(2-methoxyethoxy)quinolineHCID 22646522—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物HCID 22646584HCID 2264658463%

反応条件

温度160 °C

反応手順

4-Chloro-6-cyano-7-(2-methoxyethoxy)quinoline (187 mg, 0.71 mmol), (prepared as described for the starting material in Example 1 but with an aqueous sodium hydrogen carbonate work up), was added to a solution of 5-benzyloxy-2-fluoro-4-methylphenol (248 mg, 1 mmol), (prepared as described for the starting material in Example 3), and potassium t-butoxide (120 mg, 1 mmol) in DMSO (5 ml) and the mixture then heated at 160° C. for 1.5 hours. The mixture was diluted with water and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/ethyl acetate (55/45) followed by preparative reverse-phase HPLC eluting with aqueous ammonium carbonate (2 g/1, adjusted to pH7 with carbon dioxide) and methanol (20/80) to give 4-(5-benzyloxy-2-fluoro-4-methylphenoxy)-6-cyano-7-(2-methoxyethoxy)quinoline (204 mg, 63%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06809097B1
出典データセットuspto-grants-2004_10
ORD IDord-694d6787e78e4946aa91d24d25588844
出典メモuspto-grants-2004_10