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HRID 10561作成日:2026年10月25日

Hydrochloride methanol → 4-(4-Methoxy-5-isoquinolyl)aminopiperidine hydrochloride

https://huagongshe.com/reaction/10561

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloride methanolHCID 21893726—
反応物4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979974—
生成物4-(4-Methoxy-5-isoquinolyl)aminopiperidine hydrochlorideHCID 21979814—

反応手順

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 96 (358 mg) and 10% hydrogen chloride/methanol solution (10 ml). The reaction mixture was cooled to room temperature, and then the solvent was evaporated under reduced pressure. The residue was added with methanol (2 ml) and diethyl ether (6 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (336 mg) as light yellow powdery solid.

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-b56a0268b051416cac8d42612a0103b2
出典メモuspto-grants-2006_08