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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1993346생성일: 2026년 10월 26일

Potassium Phosphate, Tribasic → 5-(3-fluoro-4-methoxyphenyl)-3-methyl-2-methylthio-3H-pyrimidin-4-one

https://huagongshe.com/reaction/1993346

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물3-Fluoro-4-methoxyphenylboronic acidHCID 2782194—
반응물5-Bromo-3-methyl-2-(methylthio)pyrimidin-4(3H)-oneHCID 3264666—
반응물2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물5-(3-fluoro-4-methoxyphenyl)-3-methyl-2-methylthio-3H-pyrimidin-4-oneHCID 58828891—

반응 조건

온도100 °C

반응 단계

5-Bromo-3-methyl-2-methylthio-4(3H)-pyrimidinone (Step 3, 14.77 g, 62.8 mmol), 3-fluoro-4-methoxyphenylboronic acid (20.11 g, 118.3 mmol), Pd2(dba)3 (1.869 g, 2.04 mmol), S-phos ligand (Strem Chemical, 3.45 g, 8.40 mmol) and K3PO4 (42.27 g, 199.1 mmol) were suspended in toluene (200 mL). Ar was bubbled through the solution for 5 min, and the reaction was placed in an oil bath (100° C.) and stirred for 6.25 h, at which time LCMS analysis indicated a complete reaction. The reaction was cooled to RT and allowed to stand overnight. It was diluted with CH2Cl2 (200 mL) and filtered through a 1-inch plug of silica gel which was washed exhaustively with MeOH, EtOAc, and CH2Cl2. (Some solid material stuck in the flask had to be taken up in water and extracted with EtOAc separately). The filtrate (and EtOAc extracts) were all combined and concentrated, resulting in an orange solid. This was treated with hexanes and filtered, and the resultant light yellow solid was washed repeatedly with hexanes and then put on the high vacuum overnight. The title compound was obtained as a light yellow solid. MS (ESI pos. ion) m/z: 281. Calc'd for C13H13FN2O2S: 280.07.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07652009B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-23150f509d7e4c9dbff5600ad6ec2017
출처 메모uspto-grants-2010_01