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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1455218생성일: 2026년 10월 27일

Water → 1-[5-(6-Ethoxy-2-methylsulfanyl-pyrimidin-4-yl)-thiophen-2-yl]-ethanone

https://huagongshe.com/reaction/1455218

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Carbonate IonHCID 19660—
반응물(5-Acetylthiophen-2-yl)boronic acidHCID 4143377—
반응물4-Chloro-6-ethoxy-2-(methylthio)pyrimidineHCID 53385553—
용매DimethylformamideHCID 6228—
생성물1-[5-(6-Ethoxy-2-methylsulfanyl-pyrimidin-4-yl)-thiophen-2-yl]-ethanoneHCID 6738955728%

반응 조건

온도80 °C

반응 단계

The crude product of Preparation 27, 4-chloro-6-ethoxy-2-methylsulfanylpyrimidine, (525 mg, 2.56 mmol) was dissolved in DMF (4 mL). To this solution was added 5-acetyl-2-thiopheneboronic acid (523 mg, 3.08 mmol), PdCl2dppf (209 mg, 0.26 mmol), potassim carbonate (1.06 g, 7.69 mmol) and water (0.4 mL). The reaction mixture was heated at 80° C. under nitrogen atmosphere for overnight. The reaction mixture was cooled and poured into 30 mL of water and was then extracted with diethyl ether (20 mL×3) three times. The ether layer was separated and dried with anhydrous MgSO4 and concentrated in vacuo. The resulting crude product was purified by flash silica column chromatography (20% ethyl acetate in hexane) to give product 1-[5-(6-ethoxy-2-methylsulfanyl-pyrimidin-4-yl)-thiophen-2-yl]-ethanone (210 mg, 28% yield over two steps). 1H-NMR (CDCl3): δ 7.67 (m, 2 H), 6.68 (s, 1 H), 4.46 (q, J=7.1 Hz, 2 H), 2.60 (s, 3 H), 2.59 (s, 3 H), 1.40 (t, J=7.1 Hz, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07482366B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-2406d409fd394826b21b37ae97d49c9a
출처 메모uspto-grants-2009_01