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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2110725생성일: 2026년 10월 27일

Cesium carbonate → 3-{6-[2-(2-Fluoro-4-trifluoromethyl-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenol

https://huagongshe.com/reaction/2110725

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물(3-hydroxyphenyl)boronic AcidHCID 2734359—
반응물(6-Chloro-2-methoxy-pyrimidin-4-yl)-[2-(2-fluoro-4-trifluoromethyl-phenyl)-ethyl]-amineHCID 57636111—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물3-{6-[2-(2-Fluoro-4-trifluoromethyl-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenolHCID 69069566116.9%

반응 단계

A mixture of (6-chloro-2-methoxy-pyrimidin-4-yl)-[2-(2-fluoro-4-trifluoromethyl-phenyl)-ethyl]-amine [1.47 g, 4.2 mmol, see Example 52, step 1], (3-hydroxy-phenyl)-boronic acid, (637 mg, 4.62 mmol), and Cs2CO3 (3.4 g, 10.5 mmol) in ethylene glycol dimethyl ether (20 mL) and water (4 mL) is degassed by bubbling with Argon gas for 5 minutes, and treated with tetrakis(triphenylphosphine)palladium (0) (243 mg, 0.21 mmol) at room temperature. After 15 h at 85° C., the mixture is diluted with water (50 mL), and extracted with EtOAc (2×50 mL). The extracts are dried (MgSO4), filtered through a pad of SiO2, and concentrated to afford 3-{6-[2-(2-fluoro-4-trifluoromethyl-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenol (2 g). LCMS: RT=2.32 minutes; MS: 408 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07517889B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-e596076e7c034ee8af268d285bf2fe7d
출처 메모uspto-grants-2009_04