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HRID 14525作成日:2026年10月24日

Dimethylformamide → 4-(2-Butynyloxy)-6-piperidinopyrimidine

https://huagongshe.com/ja/reaction/14525

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物PiperidineHCID 8082—
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-piperidinopyrimidineHCID 5934111677.1%

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 85 mg of piperidine was added therein, and the mixture was stirred for 5 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 178 mg of 4-(2-butynyloxy)-6-piperidinopyrimidine (hereinafter, referred to as Compound (16)).

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-f5009c6f621b42c18ff9760b3dfadcbd
出典メモuspto-grants-2010_06