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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238277생성일: 2026년 10월 26일

Cesium carbonate → methyl 5-(1H-pyrazol-4-yl)thiophene-3-carboxylate

https://huagongshe.com/reaction/238277

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물tert-butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylateHCID 16217654—
반응물Methyl 5-bromothiophene-3-carboxylateHCID 45873035—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물methyl 5-(1H-pyrazol-4-yl)thiophene-3-carboxylateHCID 5811035853.5%

반응 조건

온도110 °C

반응 단계

5-Bromo-thiophene-3-carboxylic acid methyl ester (6 g, 27 mmol) was dissolved in a mixture of DME (75 mL), IMS (25 mL) and water (12.5 mL). Caesium carbonate (13.2 g, 40 mmol) and 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrazole-1-carboxylic acid tert-butyl ester (9.2 g, 31 mmol) were added and the mixture stirred under argon. Palladium tetrakis-(triphenylphosphine) (3.1 g, 2.7 mmol) was then added and the mixture heated at 110° C. for 6 hours. The mixture was allowed to cool to room temperature and then diluted with water. The product was extracted into DCM and washed with brine, then dried over sodium sulphate, filtered and the solvent removed by evaporation under vacuum. The residue was triturated with diethyl ether to give the title compound as a pale yellow solid (3.01 g). LCMS m/z 209.1 [M+H]+. R.T.=3.72 min (Analytical Method 4). 1H NMR (400 MHz, d6-DMSO): δ 8.2 (s, 1H), 8.15 (s, 1H), 7.85 (s, 1H), 7.5 (s, 1H), 3.8 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642621B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-7cb3435494504c13b0bb5791727fe208
출처 메모uspto-grants-2014_02