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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 496660생성일: 2026년 10월 25일

Ethyl isocyanate → N-(1-Boc-piperidin-3-yl-methyl)-N-phenyl-N'-ethylurea

https://huagongshe.com/reaction/496660

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl isocyanateHCID 8022—
반응물N-(1-Boc-piperidin-3-ylmethyl)anilineHCID 12972131—
용매DichloromethaneHCID 6344—
생성물N-(1-Boc-piperidin-3-yl-methyl)-N-phenyl-N'-ethylureaHCID 1297213295%

반응 단계

To a solution of N-(1-Boc-piperidin-3-ylmethyl)aniline 1 (102 mg, 0.35 mmol) in 1 mL of dry CH2Cl2 was added ethyl isocyanate (95%, 35 μL, 1.2 eq.) at room temperature. After being shaken at room temperature for overnight, the reaction mixture was passed through an aminopropyl NH2 cartridge and washed with CH2Cl2. Removal of the CH2Cl2 afforded N-(1-Boc-piperidin-3-yl-methyl)-N-phenyl-N′-ethylurea (2) (120 mg, 95%). LRMS 285 (M−100)+ 261.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06946477B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-45242b6f677f4e619f9e707e4be62ec0
출처 메모uspto-grants-2005_09