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HRID 1970076作成日:2026年10月26日

N-(3,4-Dichlorophenyl)thiourea → 8-[2-(3,4-dichlorophenylamino)-thiazol-4-yl]-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylate

https://huagongshe.com/reaction/1970076

反応式

関与物質

役割名称HCID仕込み量
反応物N-(3,4-Dichlorophenyl)thioureaHCID 710776—
反応物8-(2-bromo-acetyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylateHCID 86627583—
溶媒EthanolHCID 702—
生成物8-[2-(3,4-dichlorophenylamino)-thiazol-4-yl]-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylateHCID 8662758914%

反応条件

温度90 °C

反応手順

87 mg (1.2 mmol) of (3,4-dichlorophenyl)-thiourea is added to a suspension of 124 mg (0.33 mmol) of 8-(2-bromo-acetyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate in 3.5 mL of ethanol. The mixture is stirred at 90° C. for 6 hours then the mixture is cooled to room temperature. The solvent is evaporated, then the product is purified by preparative LCMS. After drying, 23 mg (14%) of 8-[2-(3,4-dichlorophenylamino)-thiazol-4-yl]-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate is obtained in the form of a beige solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08426437B2
出典データセットuspto-grants-2013_04
ORD IDord-92601354ced746f1a83e3b47dedad97f
出典メモuspto-grants-2013_04