돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248901생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/248901

반응식

참여 물질

역할이름HCID투입량
반응물N-(((1-(2-Naphthalenylmethyl)-4-piperidinyl)amino)carbonyl)benzamideHCID 72002—
용매Sodium HydroxideHCID 14798—
생성물[1-(Naphth-2-ylmethyl)piperid-4-yl]ureaHCID 13145794—

반응 단계

1-Benzoyl-3-[1-(naphth-2-ylmethyl)piperid-4-yl]urea (prepared according 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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05212179
출처 데이터셋uspto-grants-1993_05
ORD IDord-471cc0bfbc9b40e7b7522546f7f5128a
출처 메모uspto-grants-1993_05