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HRID 51971作成日:2026年10月25日

Hydrochloric Acid → Ethyl 7-aminoquinoline-3-carboxylate

https://huagongshe.com/reaction/51971

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物7-(Benzhydrylidene-amino)-quinoline-3-carboxylic acid ethyl esterHCID 10287230—
溶媒EthanolHCID 702—
生成物Ethyl 7-aminoquinoline-3-carboxylateHCID 987780168.3%

反応手順

Concentrated hydrochloric acid (1 mL, 2.5 volumes) was added to a solution of 7-(benzhydrylidene-amino)-quinoline-3-carboxylic acid ethyl ester (400 mg, 1.05 mmol, 1 equiv) in ethanol (4 mL, 10 volumes). The solution was stirred at room temperature for three hours and then concentrated. The residue was dissolved in ethyl acetate (20 mL, 50 volumes) and the organic layer was washed with 1 N hydrochloric acid (5×25 mL). The pH of the combined aqueous layer was then adjusted to about 8 with solid sodium hydroxide. The aqueous layer was then extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate and concentrated to provide 7-amino-quinoline-3-carboxylic acid ethyl ester (155 mg, 68%) as a yellow solid. The crude solid can be further purified by flash column chromatography using silica gel (EM Science, Gibbstown, N.J., 230-400 mesh) in 60% ethyl acetate in hexanes if desired.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713489B2
出典データセットuspto-grants-2004_03
ORD IDord-194726897d924469839c471fea67f027
出典メモuspto-grants-2004_03