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HRID 1869170作成日:2026年10月26日

Potassium Carbonate → Methyl 1-(6-methoxyquinolin-4-yl)-1H-indole-3-carboxylate

https://huagongshe.com/reaction/1869170

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-Chloro-6-methoxyquinolineHCID 228348—
反応物Methyl indole-3-carboxylateHCID 589098—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒DimethylacetamideHCID 31374—
生成物Methyl 1-(6-methoxyquinolin-4-yl)-1H-indole-3-carboxylateHCID 68970220—

反応条件

温度140 °C

反応手順

1.73 g (12.5 mmol) of potassium carbonate and 0.968 g (5 mmol) of 4-chloro-6-methoxyquinoline are added to 0.876 g (5 mmol) of 3-methoxycarbonyl-1H-indole in 20 cm3 of dimethylacetamide under an argon atmosphere. After stirring at a temperature in the region of 140° C. for 20 hours, the reaction mixture is cooled and diluted with 200 cm3 of ethyl acetate and 200 cm3 of water. The organic phase is separated off by settling and washed with three times 200 cm3 of water and 200 cm3 of saturated aqueous sodium chloride solution and then it is dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (2.7 kPa). The residue obtained is purified by flash chromatography [eluent: cyclohexane/ethyl acetate (8/2 and then 7/3 by volume)]. Concentrating these fractions to dryness under reduced pressure (2.7 kPa) results in 0.7 g of 3-methoxycarbonyl-1-(6-methoxyquinol-4-yl)-1H-indole in the form of a white powder. Mass spectrum (EI): m/e 332 (M+•), m/e 301.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07638521B2
出典データセットuspto-grants-2009_12
ORD IDord-a644d3714b874741bd73fd5fe5905fa4
出典メモuspto-grants-2009_12