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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1468973생성일: 2026년 10월 26일

Cesium fluoride → Methyl 6-amino-2-(6-fluorobenzo[c][1,2,5]oxadiazol-5-yl)-5-methoxypyrimidine-4-carboxylate

https://huagongshe.com/reaction/1468973

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물Methyl 6-amino-2-chloro-5-methoxypyrimidine-4-carboxylateHCID 52270701—
반응물5-Fluoro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]oxadiazoleHCID 90403859—
촉매HCID 178418476HCID 178418476—
용매Acetonitrile--water (1/1)HCID 18373917—
생성물Methyl 6-amino-2-(6-fluorobenzo[c][1,2,5]oxadiazol-5-yl)-5-methoxypyrimidine-4-carboxylateHCID 9040459640.9%

반응 조건

온도115 °C

반응 단계

Methyl 6-amino-2-chloro-5-methoxypyrimidine-4-carboxylate (400 mg, 1.838 mmol), 5-fluoro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]oxadiazole (789 mg, 2.390 mmol), bis(triphenylphosphine)palladium(II) chloride (129 mg, 0.184 mmol), and cesium fluoride (558 mg, 3.68 mmol) were combined in 4 mL 1:1 ACN-water and heated at 115° C. for 30 min in a microwave reactor. The cooled reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with saturated NaCl, dried, and evaporated. The product was purified by flash chromatography (SiO2, eluting with 5-30% ethyl acetate in dichloromethane) to provide the title compound (240 mg, 39%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006250B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-095fa5622b374946892d12364e65bc40
출처 메모uspto-grants-2015_04