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HRID 469449作成日:2026年10月26日

Sodium Hydroxide → 2-(2-Carbamoylthiophen-3-ylamino)-2-phenylacetic acid

https://huagongshe.com/reaction/469449

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Ethyl bromophenylacetateHCID 97780—
反応物3-Aminothiophene-2-carboxamideHCID 518993—
溶媒AcetonitrileHCID 6342—
生成物2-(2-Carbamoylthiophen-3-ylamino)-2-phenylacetic acidHCID 5855698970.4%

反応手順

A solution of ethyl 2-bromo-2-phenylacetate (349 μl, 2.00 mmol) and 3-aminothiophene-2-carboxamide (284 mg, 2.00 mmol) in acetonitrile (2 ml) was heated under microwave irradiation at 100° C. for 1 hour. Acetonitrile was evaporated, and the residue was dissolved in EtOH (2 ml). Sodium hydroxide (80 mg, 2.00 mmol) was added, and the reaction mixture was stirred at room temperature for 24 hours. Then ethanol was evaporated, and the residue was taken up with water and washed with EtOAc. The pH of the aqueous phase was adjusted to 3 with HCl, and product was extracted with EtOAc. The organic phase was dried over Na2SO4, filtered and evaporated to dryness to obtain 2-(2-carbamoylthiophen-3-ylamino)-2-phenylacetic acid (389 mg, 70% yield), which was used in the next step without any further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629160B2
出典データセットuspto-grants-2014_01
ORD IDord-e9f8c34ea1a948a480eff70d7cb1f441
出典メモuspto-grants-2014_01