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HRID 1742608作成日:2026年10月26日

Dimethylformamide → 4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)-methoxy]-2-pyrimidinecarbonitrile

https://huagongshe.com/reaction/1742608

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物PyrimidineHCID 9260—
反応物Oxalyl chlorideHCID 65578—
反応物4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-2-pyrimidinecarboxaldehyde oximeHCID 136378412—
溶媒AcetonitrileHCID 6342—
生成物4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)-methoxy]-2-pyrimidinecarbonitrileHCID 1992298622.3%

反応条件

温度0 °C

反応手順

Dimethylformamide (0.05 g, 0.6 mmoles) is cooled to 0° C. in 10 mL of acetonitrile under argon. Oxalyl chloride (0.1 g, 0.9 mmoles) is added and the reaction mixture is stirred at 0° C. for 10 minutes. 4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-2-pyrimidinecarboxaldehyde oxime (0.2 g, 0.6 mmoles) is dissolved in 10 mL of acetonitrile and cooled to 0° C. The vilsmier reagent prepared above is added to the pyrimidine solution at 0° C. After 3 hours at 0° C, the reaction is quenched by the addition of 10 mL of saturated sodium bicarbonate and extracted with ether (3×10 mL). The organic extract is washed with 50 mL of brine and dried over magnesium sulfate. Evaporation of the solvent gives a red oil which is purified by flash chromatography (silica, 10% ether/chloroform) to give 4,6-bis (1,1-dimethylethyl) -5-[(2-methoxyethoxy)methoxy]-2-pyrimidinecarbonitrile (43 mg, 22%) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05340815
出典データセットuspto-grants-1994_08
ORD IDord-1e6b7d209bd24b1fb2b70f7811b85fe9
出典メモuspto-grants-1994_08