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HRID 516559作成日:2026年10月26日

Potassium Fluoride → Methyl 6-amino-2-(4-(difluoromethoxy)phenyl)-5-methoxypyrimidine-4-carboxylate

https://huagongshe.com/reaction/516559

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium FluorideHCID 522689—
反応物Tris(3-sulfonatophenyl) phosphineHCID 3675707—
反応物2-(4-(Difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 22032303—
反応物Methyl 6-amino-2-chloro-5-methoxypyrimidine-4-carboxylateHCID 52270701—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 6-amino-2-(4-(difluoromethoxy)phenyl)-5-methoxypyrimidine-4-carboxylateHCID 9041074439.8%

反応手順

To a 5-mL microwave safe vial was added potassium fluoride (0.151 g, 2.59 mmol), palladium (II) acetate (0.012 g, 0.052 mmol), 2-(4-(difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.28 g, 1.037 mmol), methyl 6-amino-2-chloro-5-methoxypyrimidine-4-carboxylate (0.226 g, 1.037 mmol), and 3,3′,3″-phosphinetriyltribenzenesulfonate (0.052 g, 0.104 mmol). A mixture of water (1 mL) and acetonitrile (2 mL) was added and the reaction was capped and placed in a Biotage Initiator™ microwave reactor for 6 min at 160° C., with external IR-sensor temperature monitoring from the side of the vessel. Upon cooling to room temperature, the reaction mixture was diluted with EtOAc (50 mL) and water (50 mL). An additional extraction using CH2Cl2 (50 mL) was combined with the EtOAc and dried over of Na2SO4 (50 g) after the CH2Cl2 layer was filtered through cotton plug. The combined organics were concentrated on a rotary evaporator and the residue was purified using a Teledyne ISCO purification system with a gradient eluent system of CH2Cl2 and EtOAc to yield the title compound as a tan solid (134.4 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09113629B2
出典データセットuspto-grants-2015_08
ORD IDord-4f6a3727b08b49e08055c2f63ee5073e
出典メモuspto-grants-2015_08