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HRID 14529作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/14529

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物2-MethylpiperidineHCID 7974—
反応物Potassium CarbonateHCID 11430—
反応物4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
溶媒Ethyl AcetateHCID 8857—
生成物4-(2-Butynyloxy)-6-(2-methylpiperidino)pyrimidineHCID 5781981827%

反応条件

温度120 °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 2-methylpiperidine was added therein, and the mixture was stirred for 4 hours at 80 and 3 hours at 120° 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 66 mg of 4-(2-butynyloxy)-6-(2-methylpiperidino)pyrimidine (hereinafter, referred to as Compound (20)).

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-0bf0dadf27e64875acc546a93a5645dc
出典メモuspto-grants-2010_06