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HRID 3890作成日:2026年10月24日

N-(Aminocarbonyl)-2-thiophenecarboxamide → 1-[1-(Naphth-2-ylmethyl)piperid-4-yl]-3-(then-2-oyl)urea

https://huagongshe.com/ja/reaction/3890

反応式

関与物質

役割名称HCID仕込み量
反応物N-(Aminocarbonyl)-2-thiophenecarboxamideHCID 395032—
反応物4-Amino-1-(2-naphthyl)methylpiperidineHCID 11195823—
溶媒PyridineHCID 1049—
生成物1-[1-(Naphth-2-ylmethyl)piperid-4-yl]-3-(then-2-oyl)ureaHCID 12942334—

反応手順

4-Amino-1-(naphth-2-ylmethyl)piperidine (1.0 g, 0.0047 m) and 1-(then-2-oyl)urea (0.65 g, 0.0042 m) in pyridine (5 cm3) was refluxed for 9.5 hours. The solvent was evaporated, water added, and the precipitated title compound filtered and washed well with water. This was recrystallised from ethanol, converted to the hydrochloride salt in ethanol with ethanolic HCl, and recrystallised from ethanol, 0.5 g, at the hydrochloride, m.p. 217°-219° 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-b9261355c50f45a3ac126c2d60770352
出典メモuspto-grants-1988_02