돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3890생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물N-(Aminocarbonyl)-2-thiophenecarboxamideHCID 395032—
반응물4-Amino-1-(2-naphthyl)methylpiperidineHCID 11195823—
용매PyridineHCID 1049—
생성물1-[1-(Naphth-2-ylmethyl)piperid-4-yl]-3-(then-2-oyl)ureaHCID 12942334—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04722930
출처 데이터셋uspto-grants-1988_02
ORD IDord-b9261355c50f45a3ac126c2d60770352
출처 메모uspto-grants-1988_02