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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 516559생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/516559

반응식

참여 물질

역할이름HCID투입량
반응물Potassium FluorideHCID 522689—
반응물Tris(3-sulfonatophenyl) phosphineHCID 3675707—
반응물2-(4-(Difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 22032303—
반응물Methyl 6-amino-2-chloro-5-methoxypyrimidine-4-carboxylateHCID 52270701—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물Methyl 6-amino-2-(4-(difluoromethoxy)phenyl)-5-methoxypyrimidine-4-carboxylateHCID 9041074439.8%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09113629B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-4f6a3727b08b49e08055c2f63ee5073e
출처 메모uspto-grants-2015_08