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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 389977생성일: 2026년 10월 25일

Benzyl isocyanate → 1-Benzyl-3-{5-[4-(2-trifluoromethylbenzoyl)piperazin-1-YL]pyridin-2-YL}urea

https://huagongshe.com/reaction/389977

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl isocyanateHCID 76639—
반응물[4-(6-Aminopyridin-3-YL)piperazin-1-YL]-(2-trifluoromethylphenyl)methanoneHCID 67419145—
용매DichloromethaneHCID 6344—
생성물1-Benzyl-3-{5-[4-(2-trifluoromethylbenzoyl)piperazin-1-YL]pyridin-2-YL}ureaHCID 1144308030%

반응 단계

To a solution of [4-(6-aminopyridin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)-methanone (0.035 g, 0.12 mmol) in dichloromethane (3 mL) was added benzylisocyanate (0.4 mL, 0.3 mmol). After stirring for 66 h, dichloromethane was removed in vacuo and the residue was diluted with ethyl acetate (20 mL). The organic phase was washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. Purification by preparative thin layer chromatography afforded the title compound as a pale white solid (14.6 mg, 30% yield). 1H NMR (300 MHz, CDCl3) δ 9.61, 8.78, 7.73, 7.58, 7.25, 6.78, 4.59, 3.95, 3.32, 3.13, 2.94. MS (ES+) m/z 484.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383628B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-edbbd4dd5a484c41a7e61bcf140a532e
출처 메모uspto-grants-2013_02