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HRID 3891作成日:2026年10月24日

N-(((1-(2-Naphthalenylmethyl)-4-piperidinyl)amino)carbonyl)benzamide → [1-(Naphth-2-ylmethyl)piperid-4-yl]urea

https://huagongshe.com/ja/reaction/3891

反応式

関与物質

役割名称HCID仕込み量
反応物N-(((1-(2-Naphthalenylmethyl)-4-piperidinyl)amino)carbonyl)benzamideHCID 72002—
溶媒Sodium HydroxideHCID 14798—
生成物[1-(Naphth-2-ylmethyl)piperid-4-yl]ureaHCID 13145794—

反応手順

1-Benzoyl-3-[1-(naphth-2-ylmethyl)piperid-4-yl]urea (prepared acccording to Example 1) is hydrolysed by refluxing in 2N sodium hydroxide to give [1-(naphth-2-ylmethyl)piperid-4-yl]urea(m.p. 183°-5° C.). The product is acylated by reaction with 4-methoxybenzoyl chloride to give the title compound, m.p. of HCL, quarterhydrate=193°-193.5° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04722930
出典データセットuspto-grants-1988_02
ORD IDord-f835042249204abe88c806390379a6a4
出典メモuspto-grants-1988_02