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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 868214생성일: 2026년 10월 27일

Pyridine → N-[[[1-(6-Fluoro-2-naphthalenylmethyl)-4-piperidinyl]amino]carbonyl]-6-quinoline carboxamide

https://huagongshe.com/reaction/868214

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Quinoline-6-carbonyl chlorideHCID 12391963—
반응물N-[[(6-fluoro-2-naphthalenyl)methyl]-4-piperidinyl]ureaHCID 21288076—
용매1,2-DichloroethaneHCID 11—
생성물N-[[[1-(6-Fluoro-2-naphthalenylmethyl)-4-piperidinyl]amino]carbonyl]-6-quinoline carboxamideHCID 13853618—

반응 단계

A mixture of 6-quinolinoyl chloride (4.77 g, 22 mmol), N-[[(6-fluoro-2-naphthalenyl)methyl]-4-piperidinyl]urea (6.02 g, 20 mmol), dry pyridine (2.5 ml) and 1,2-dichloroethane (30 ml) is stirred at reflux for 18 hours. The solution is then cooled, washed with aqueous sodium carbonate solution, dried and evaporated. The residue is crystallised from ethanol to give the title compound, mp 200°-201° C. (softens, maleate salt).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04778802
출처 데이터셋uspto-grants-1988_10
ORD IDord-fe4ffe43b4e3413780803c628c8a457f
출처 메모uspto-grants-1988_10