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HRID 344235作成日:2026年10月27日

N-tert-butyloxycarbonyl-4-(4-amino-5-chloro-2-methoxyphenylcarbonylaminomethyl)piperidine → 4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide hydrochloride

https://huagongshe.com/reaction/344235

反応式

関与物質

役割名称HCID仕込み量
反応物N-tert-butyloxycarbonyl-4-(4-amino-5-chloro-2-methoxyphenylcarbonylaminomethyl)piperidineHCID 11200348—
溶媒1,4-Dioxane hydrochlorideHCID 20443148—
生成物4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide hydrochlorideHCID 66780941192.7%

反応手順

4-amino-5-chloro-N-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)-2-methoxybenzamide (18.9 g) was dissolved in 4N hydrochloric acid-dioxane solution (150 ml). The mixture was stood at room temperature for 2 hr and the precipitated crystals were collected by filtration to give 15.3 g of 4-amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)-benzamide hydrochloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05864039
出典データセットuspto-grants-1999_01
ORD IDord-f96ccd0cf55d4751aaf72ed8595b57ac
出典メモuspto-grants-1999_01