戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 656867作成日:2026年10月26日

Sodium Bicarbonate → 7-Fluoro-2-methoxy-1,5-naphthyridine

https://huagongshe.com/reaction/656867

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8-Bromo-7-fluoro-2-methoxy-1,5-naphthyridineHCID 45480320—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物7-Fluoro-2-methoxy-1,5-naphthyridineHCID 4690080287%

反応手順

8-Bromo-7-fluoro-2-(methoxy)-1,5-naphthyridine (for a synthesis see WO2004058144, Example 53(g)) (5.040 g, 19.61 mmol) was stirred in MeOH (200 ml) with sodium hydrogen carbonate (3.29 g, 39.22 mmol) and 10% palladium on carbon (2.5 g), and the resulting suspension was hydrogenated at 1 atmosphere of hydrogen pressure under for 4 h. The mixture was filtered with suction through celite and the solids were washed with MeOH (500 ml). The combined filtrate plus washings were concentrated to about 50 ml under reduced pressure and then treated with water (200 ml) and DCM (300 ml). The aqueous phase was separated and extracted twice more with DCM (300 ml). The combined organic phases were separated, dried over anhydrous magnesium sulphate, filtered and evaporated to give the desired compound as an off-white solid (3.044 g, 87%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08071592B2
出典データセットuspto-grants-2011_12
ORD IDord-0da16db5eb034e5b957f54a901bcd029
出典メモuspto-grants-2011_12