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HRID 25493作成日:2026年10月27日

Ethyl Acetate → 4-{3-[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-thioureido}-benzoic acid

https://huagongshe.com/reaction/25493

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物4-Isothiocyanatobenzoic acidHCID 242946—
反応物5-(5,6-difluoro1H-indol-2-yl)-2-methoxy-phenylamineHCID 9943439—
溶媒TetrahydrofuranHCID 8028—
生成物4-{3-[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-thioureido}-benzoic acidHCID 10115026—

反応条件

温度50 °C

反応手順

The product from Example 3, 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine, (0.274 g, 1.0 mmol) was mixed with 4-carboxyphenyl isothiocyanate (0.183 g, 1.0 mmol) in tetrahydrofuran (10 mL) and was heated briefly to 50° C. and then allowed to stand overnight at room temperature. The tetrahydrofuran was boiled off on the rotary evaporator (no vacuum) to give a solid. Ethyl acetate (5 mL) was added, and the mixture was allowed to stand overnight at room temperature. The insoluble material was collected by filtration and was a mixture. All material from the reaction mixture was taken up in tetrahydrofuran/ethyl acetate and more 4-carboxyphenyl isothiocyanate (0.020 g, 0.11 mmol) was added and the solvent was boiled off on the rotary evaporator. Ethyl acetate was added to the solid and the mixture allowed to stand overnight at room temperature. The insoluble material was collected by filtration (0.191 g), mp 201-203° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858739B2
出典データセットuspto-grants-2005_02
ORD IDord-0bb20bfbad2d47d092416d18cf09c6c3
出典メモuspto-grants-2005_02