戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 542211作成日:2026年10月27日

Chloroform → 4-Amino-6,7-dimethoxy-2-(piperazin-1-yl)quinoline

https://huagongshe.com/reaction/542211

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物4-Amino-6,7-dimethoxy-2-(4-benzylpiperazin-1-yl)quinolineHCID 13359991—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物4-Amino-6,7-dimethoxy-2-(piperazin-1-yl)quinolineHCID 1406899851.2%

反応手順

4-Amino-6,7-dimethoxy-2-(4-benzylpiperazin-1-yl)quinoline (6.2 g) in ethanol (300 ml) with 5% Pd/C catalyst was stirred at 50° under an atmosphere of hydrogen (50 p.s.i.) for 20 hours. The mixture was cooled, chloroform (100 ml) added and the solution filtered through "Solkafloc". The solid was washed with chloroform-methanol (1:1, 4×100 ml) and the combined filtrates evaporated in vacuo. The residue was partitioned between chloroform-sodium carbonate solution (10%), the organic layer removed, the aqueous phase saturated with salt and further extracted with chloroform. The combined organic extracts were washed with brine, dried (Na2SO4) and evaporated in vacuo to yield 4-amino-6,7-dimethoxy-2-(piperazin-1-yl)quinoline (2.42 g). Spectroscopy showed this product to be the same as that of Example 32.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04656174
出典データセットuspto-grants-1987_04
ORD IDord-6479889b16bc45df8345a373e0507f3d
出典メモuspto-grants-1987_04