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HRID 1592213作成日:2026年10月24日

Potassium Carbonate → 4-(2-Butynyloxy)-6-(2,6-dichloro-4-fluorophenoxy)pyrimidine

https://huagongshe.com/ja/reaction/1592213

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Ammonium ChlorideHCID 25517—
反応物Phenol, 2,6-dichloro-4-fluoro-HCID 94950—
反応物4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
溶媒DimethylformamideHCID 6228—
生成物4-(2-Butynyloxy)-6-(2,6-dichloro-4-fluorophenoxy)pyrimidineHCID 2259982561.4%

反応条件

温度80 °C

反応手順

To 2 ml of N,N-dimethylformamide were added 0.2 g of 4-chloro-6-(2-butynyloxy)pyrimidine, 0.23 g of potassium carbonate, and 0.20 g of 2,6-dichloro-4-fluorophenol, followed by stirring at 80° C. for 7 hours. The reaction mixture was then left for cooling to room temperature and poured into a saturated aqueous ammonium chloride solution, which was extracted three times with chloroform. The chloroform layers were combined, washed with diluted hydrochloric acid and then with water, and dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography to give 0.22 g of 4-(2-butynyloxy)-6-(2,6-dichloro-4-fluorophenoxy)pyrimidine (the present compound (160)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07291730B2
出典データセットuspto-grants-2007_11
ORD IDord-c47668dd6bc14b65bc4e28ebedbff020
出典メモuspto-grants-2007_11