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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469449생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/469449

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Ethyl bromophenylacetateHCID 97780—
반응물3-Aminothiophene-2-carboxamideHCID 518993—
용매AcetonitrileHCID 6342—
생성물2-(2-Carbamoylthiophen-3-ylamino)-2-phenylacetic acidHCID 5855698970.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629160B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-e9f8c34ea1a948a480eff70d7cb1f441
출처 메모uspto-grants-2014_01