戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 10560作成日:2026年10月26日

Water → 4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/10560

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium MethoxideHCID 10942334—
反応物4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979972—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒MethanolHCID 887—
溶媒PyridineHCID 1049—
生成物4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979974—

反応条件

温度65 °C

反応手順

A suspension of Intermediate 71 (600 mg) and copper(I) iodide (141 mg, Kanto Chemicals) in methanol (5.5 ml) and pyridine (5.5 ml) was added with sodium methoxide (28% methanol solution, 1.7 ml, Wako Pure Chemical Industries) and stirred with heating at 65° C. for 24 hours. The reaction mixture was cooled to room temperature, then added with water (30 ml) and extracted three times with ethyl acetate (20 ml for each time). The combined organic layer was washed twice with saturated brine (30 ml for each time) and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:2) to obtain the title compound (364 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094789B2
出典データセットuspto-grants-2006_08
ORD IDord-e66b85a64f8c49938e94e99c298be080
出典メモuspto-grants-2006_08