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HRID 23941作成日:2026年10月26日

1-Piperazinecarboxylic acid, ethyl ester → Ethyl 4-[(8-hydroxyquinolin-5-yl)methyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/23941

反応式

関与物質

役割名称HCID仕込み量
反応物1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
反応物DiisopropylethylamineHCID 81531—
反応物8-Quinolinol, 5-(chloromethyl)-, hydrochloride (1:1)HCID 12269596—
溶媒ChloroformHCID 6212—
生成物Ethyl 4-[(8-hydroxyquinolin-5-yl)methyl]piperazine-1-carboxylateHCID 109030542.9%

反応手順

N-Ethoxycarbonylpiperazine (1.5 ml, 10.2 mmol) was added to a mixture of 5-chloromethyl-8-hydroxyquinoline hydrochloride (2.36 g, 10.2 mmol) and diisopropylethylamine (3.6 ml, 20.6 mmol) in CHCl3 (50 ml) at 5° C. The mixture was stirred for 24 h at room temperature. CHCl3 (100 ml) was then added and the solution was washed with 5% NaHCO3 (3×50 ml) and brine (2×50 ml) and then dried over Na2SO4. The solution was filtered and evaporated to dryness. The residue was crystallized from a mixture of benzene hexane and gave 1.38 g (42%) of the title product. M.p. −96° C. TLC (CHCl3-MeOH-NH3 9:1:0.1) Rf=0.6; TLC (CHCl3-MeOH-Me3 9:0.5:0.05) Rf−0.4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855711B1
出典データセットuspto-grants-2005_02
ORD IDord-42f95f73faf44ca99a56964d76d6bf47
出典メモuspto-grants-2005_02