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HRID 14528作成日:2026年10月23日

Dimethylformamide → 4-(2-Butynyloxy)-6-(3-methylpiperidino) pyrimidine

https://huagongshe.com/ja/reaction/14528

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物3-MethylpiperidineHCID 79081—
反応物4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
溶媒Ethyl AcetateHCID 8857—
生成物4-(2-Butynyloxy)-6-(3-methylpiperidino) pyrimidineHCID 5934114673.9%

反応条件

温度80 °C

反応手順

Into 2 ml of N,N-dimethylformamide was resolved 183 mg of 4-chloro-6-(2-butynyloxy)pyrimidine, 166 mg of potassium carbonate and 99 mg of 3-methylpiperidine was added therein, and the mixture was stirred for 4 hours at 80° C. The reaction mixture was cooled to near room temperature, ethyl acetate was added therein, and the mixture was washed with a saturated sodium chloride aqueous solution three times. The organic layers were dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 181 mg of 4-(2-butynyloxy)-6-(3-methylpiperidino) pyrimidine (hereinafter, referred to as Compound (19)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732448B2
出典データセットuspto-grants-2010_06
ORD IDord-b866f9dd667045cc8fad966c4332066d
出典メモuspto-grants-2010_06