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HRID 703853作成日:2026年10月26日

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

https://huagongshe.com/reaction/703853

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US04985438
出典データセットuspto-grants-1991_01
ORD IDord-e374e0a09e0a47fea24a78939de7697b
出典メモuspto-grants-1991_01