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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 410669생성일: 2026년 10월 27일

Cesium carbonate → 1-[5-(3-Methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)-1,3-thiazol-2-yl]cyclohexanecarbonitrile

https://huagongshe.com/reaction/410669

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참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물N-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-(trifluoromethyl)pyrimidin-2-amineHCID 58456089—
반응물1-(5-Bromothiazol-2-yl)cyclohexanecarbonitrileHCID 67429713—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Ethyl AcetateHCID 8857—
생성물1-[5-(3-Methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)-1,3-thiazol-2-yl]cyclohexanecarbonitrileHCID 5845613582.6%

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온도100 °C

반응 단계

N-[3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4-(trifluoromethyl)pyrimidin-2-amine (INTERMEDIATE 3, 134 mg, 0.35 mmol), the compound from Step 2 (96 mg, 0.35 mmol), cesium carbonate (346 mg, 1.06 mmol), X-Phos (16.9 mg, 0.035 mmol) and Pd2(dba)3 (16.2 mg, 0.018 mmol) were placed in a flask and evacuated/purged with N2 for three times. Dioxane (1.5 mL) and water (0.15 mL) were degassed by undersurface N2 bubbling and added to the reaction vessel. The resulting reaction mixture was stirred at 100° C. for 5 hrs and then diluted with EtOAc (5 mL), washed with brine (5 mL), dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica (gradient elution 7% to 60% EtOAc in Hexanes) to give the title compound (128 mg, 0.289 mmol, 82% yield) as an off white foam. MS ESI: [M+H]+ m/z 444.1. 1H NMR (500 MHz, CD3-OD) δ 8.72 (d, J=5.0, 1H), 8.06 (bs, 1H), 8.00 (s, 1H), 7.48 (bs, 1H), 7.16 (bs, 1H), 7.14 (d, J=4.9, 1H), 2.41-2.37 (m, 5H), 2.06-2.00 (m, 2H), 1.94-1.89 (m, 2H), 1.85-1.73 (m, 3H), 1.40 (m, 1H). rhSYK activity=++.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759366B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-c5883e7a6a5f493e9afa6541b86f69b7
출처 메모uspto-grants-2014_06