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HRID 1993346作成日:2026年10月27日

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

https://huagongshe.com/reaction/1993346

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物3-Fluoro-4-methoxyphenylboronic acidHCID 2782194—
反応物5-Bromo-3-methyl-2-(methylthio)pyrimidin-4(3H)-oneHCID 3264666—
反応物2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物5-(3-fluoro-4-methoxyphenyl)-3-methyl-2-methylthio-3H-pyrimidin-4-oneHCID 58828891—

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07652009B2
出典データセットuspto-grants-2010_01
ORD IDord-23150f509d7e4c9dbff5600ad6ec2017
出典メモuspto-grants-2010_01