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HRID 10502作成日:2026年10月26日

4-Methoxybenzylamine → 3-[(1-Amino-5-isoquinolyl)oxy]propylamine hydrochloride

https://huagongshe.com/reaction/10502

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethoxybenzylamineHCID 75452—
反応物2-(Di-tert-butylphosphino)biphenylHCID 2734215—
反応物N-(tert-butoxycarbonyl)-3-[(1-chloro-5-isoquinolyl)oxy]propylamineHCID 21979957—
反応物Sodium t-butoxideHCID 23676156—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物3-[(1-Amino-5-isoquinolyl)oxy]propylamine hydrochlorideHCID 21979858—

反応条件

温度80 °C

反応手順

The title compound was synthesized from Intermediate 18 according to the method described in a reference (Buchwald, S. L., J. Org. Chem., 65, 1158 (2000)). That is, a suspension of Intermediate 18 (674 mg), tris (dibenzylideneacetone)dipalladium(0) (92 mg, Aldrich), 2-(di-tert-butylphosphino)biphenyl (119 mg, Strem Chemicals), 4-methoxybenzylamine (329 mg, Tokyo Kasei Kogyo) and sodium tert-butoxide (269 mg, Tokyo Kasei Kogyo) in toluene (5 ml) was stirred with heating at 80° C. under nitrogen atmosphere for 2 hours. The reaction mixture was cooled to room temperature and added with ethyl acetate (5 ml). The insoluble matters were removed by filtration through Celite. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to obtain the title compound (525 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-2e01521f8a6a49748b5268aa0846e201
出典メモuspto-grants-2006_08