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HRID 430985作成日:2026年10月24日

m-Chloroperbenzoic acid → tert-butyl 2-[2-(2-butyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate

https://huagongshe.com/ja/reaction/430985

反応式

関与物質

役割名称HCID仕込み量
反応物m-Chloroperbenzoic acidHCID 70297—
反応物Sodium BicarbonateHCID 516892—
反応物tert-butyl 2-[2-(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamateHCID 21898025—
溶媒DichloromethaneHCID 6344—
生成物tert-butyl 2-[2-(2-butyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamateHCID 2189803185.9%

反応手順

A solution of tert-butyl 2-[2-(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate (4.12 g, 10.0 mmol) in 50 mL of CH2Cl2 was treated with 3-chloroperoxybenzoic acid (MCPBA, 77%, 2.5 g, 11.2 mmol). After stirring for 5 h, the reaction mixture was treated with saturated NaHCO3 solution and the layers were separated. The organic portion was washed with H2O and brine then dried over Na2SO4 and concentrated to give 3.68 g of tert-butyl 2-[2-(2-butyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate as a light brown foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06656938B2
出典データセットuspto-grants-2003_12
ORD IDord-998bdc43df004b70b3c578b1ff0ecdb5
出典メモuspto-grants-2003_12