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HRID 1857622作成日:2026年10月27日

Sodium Iodide → 7-chloro-3-(3,5-dimethylphenyl)-4-[2-(1-methylpiperidin-2-yl)-ethoxy]-6-nitro-1H-quinolin-2-one

https://huagongshe.com/reaction/1857622

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Sodium BicarbonateHCID 516892—
反応物2-(2-Chloroethyl)-1-methylpiperidinium chlorideHCID 12432704—
反応物7-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-6-nitro-1H-quinolin-2-oneHCID 54711238—
溶媒DimethylformamideHCID 6228—
生成物7-chloro-3-(3,5-dimethylphenyl)-4-[2-(1-methylpiperidin-2-yl)-ethoxy]-6-nitro-1H-quinolin-2-oneHCID 998214749.1%

反応条件

温度80 °C

反応手順

A mixture of 7-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-6-nitro-1H-quinolin-2-one (100 mg) and sodium bicarbonate (54 mg) was suspended in 2 mL dry N,N-dimethylformamide and heated to 80° C. on an oil bath. After 30 minutes, sodium iodide (48 mg) was added followed by 2-(2-chloroethyl)-1-methylpiperidine hydrochloride (64 mg) and the mixture stirred at 80° C. for 7 hours. At this time the reaction was cooled to room temperature and quenched by the addition of 25 mL ice/water. The mixture was filtered and the residue washed (1×) with ice water then dried at 40° C. Purification of the crude product by flash chromatography on silica gel (chloroform:10% ammonium hydroxide in methanol, 95:5) gave the title compound (67 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06147088
出典データセットuspto-grants-2000_11
ORD IDord-cf5fe14dfd464d14a753b1d117efa825
出典メモuspto-grants-2000_11