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HRID 1084729作成日:2026年10月27日

3-Quinolinecarboxylic acid, 4-chloro-8-methoxy-, ethyl ester → Ethyl 8-methoxy-4-(4-methoxy-3-thienylamino)quinoline-3-carboxylate

https://huagongshe.com/reaction/1084729

反応式

関与物質

役割名称HCID仕込み量
反応物3-Quinolinecarboxylic acid, 4-chloro-8-methoxy-, ethyl esterHCID 304557—
反応物4-Methoxythiophen-3-amineHCID 14989685—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl 8-methoxy-4-(4-methoxy-3-thienylamino)quinoline-3-carboxylateHCID 1498968676.2%

反応手順

Ethyl 8-methoxy-4-chloroquinoline-3-carboxylate (1.5 g, 0.0056 mol) and 4-methoxy-3-aminothiophene (1.46 g, 0.0112 mol) in 1,4 dioxan (20 ml) were heated under reflux for 4 hours. The solid which had formed was collected by filtration and dried. The solid was dissolved in chloroform, washed with sodium carbonate solution (50 ml), then water, dried over magnesium sulphate, filtered and evaporated under reduced pressure to give a yellow solid. Recrystallization from ethyl acetate gave the title compound, (1.53 g) m.p. 176°-178°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05006535
出典データセットuspto-grants-1991_04
ORD IDord-749dbe78ec7e49cc892975268f9012ca
出典メモuspto-grants-1991_04