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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351286생성일: 2026년 10월 25일

4-tert-Butylcyclohexylamine → N-(4-tert-Butylcyclohexyl)-N'-(7-hydroxynaphthalen-1-yl)urea

https://huagongshe.com/reaction/351286

반응식

참여 물질

역할이름HCID투입량
반응물4-tert-ButylcyclohexylamineHCID 79396—
반응물(7-Hydroxy-naphthalen-1-yl)-carbamic acid phenyl esterHCID 20090380—
용매Dimethyl SulfoxideHCID 679—
생성물N-(4-tert-Butylcyclohexyl)-N'-(7-hydroxynaphthalen-1-yl)ureaHCID 18435880—

반응 단계

4-tert-Butyl-cyclohexylamine (69 mg, 0.44 mmol) and (7-hydroxy-naphthalen-1-yl)-carbamic acid phenyl ester (125 mg, 0.44 mmol) were combined and stirred at ambient temperature in DMSO (3 mL) overnight. The product was purified by directly injecting the crude reaction onto a reverse phase prep-HPLC (90–10% water:acetonitrile gradient). The appropriate fractions were lyophilized to yield 1-(4-tert-Butyl-cyclohexyl)-3-(7-hydroxy-naphthalen-1-yl)-urea

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07183411B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-75db14825a1f48a6961e36069b97b72c
출처 메모uspto-grants-2007_02