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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1174118생성일: 2026년 10월 27일

Ethyl bromopyruvate → Ethyl 2-pyridin-2-yl-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1174118

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromopyruvateHCID 66144—
반응물Pyridine-2-carbothioamideHCID 1549499—
용매EthanolHCID 702—
생성물Ethyl 2-pyridin-2-yl-1,3-thiazole-4-carboxylateHCID 1008276135.4%

반응 조건

온도25 °C

반응 단계

A solution of the product of Example 3H (25.4 mmol) in ethanol (50 mL) was treated with ethyl bromopyruvate (3 mL, 23.9 mmol) and molecular sieves (10 g, 3 Å), heated at reflux for 16 hours, cooled to 25° C., filtered and concentrated. The concentrate was partitioned between ethyl acetate and saturated NaHCO3, and the organic phase was washed with brine, dried over MgSO4, filtered and concentrated. The residue was chromatographed on silica gel eluting with 0-25% ethyl acetate in dichloromethane to give the title compound (1.98 g, 33% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07834043B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-7a125277526f45339d6f7ae805fcaa7b
출처 메모uspto-grants-2010_11