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HRID 868214作成日:2026年10月27日

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

https://huagongshe.com/reaction/868214

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Quinoline-6-carbonyl chlorideHCID 12391963—
反応物N-[[(6-fluoro-2-naphthalenyl)methyl]-4-piperidinyl]ureaHCID 21288076—
溶媒1,2-DichloroethaneHCID 11—
生成物N-[[[1-(6-Fluoro-2-naphthalenylmethyl)-4-piperidinyl]amino]carbonyl]-6-quinoline carboxamideHCID 13853618—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04778802
出典データセットuspto-grants-1988_10
ORD IDord-fe4ffe43b4e3413780803c628c8a457f
出典メモuspto-grants-1988_10