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HRID 1468973作成日:2026年10月27日

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

https://huagongshe.com/reaction/1468973

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium fluorideHCID 25953—
反応物Methyl 6-amino-2-chloro-5-methoxypyrimidine-4-carboxylateHCID 52270701—
反応物5-Fluoro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]oxadiazoleHCID 90403859—
触媒HCID 178418476HCID 178418476—
溶媒Acetonitrile--water (1/1)HCID 18373917—
生成物Methyl 6-amino-2-(6-fluorobenzo[c][1,2,5]oxadiazol-5-yl)-5-methoxypyrimidine-4-carboxylateHCID 9040459640.9%

反応条件

温度115 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09006250B2
出典データセットuspto-grants-2015_04
ORD IDord-095fa5622b374946892d12364e65bc40
出典メモuspto-grants-2015_04