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HRID 981484作成日:2026年10月26日

Tetrahydrofuran → 2-(N-ethoxymethylanilino)-4-methyl-6-(1-propynyl) pyrimidine

https://huagongshe.com/reaction/981484

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Sodium hydrideHCID 24758—
反応物MepanipyrimHCID 86296—
溶媒Dimethyl SulfoxideHCID 679—
生成物2-(N-ethoxymethylanilino)-4-methyl-6-(1-propynyl) pyrimidineHCID 1432755962%

反応条件

温度50 °C

反応手順

A solution of 2-anilino-4-methyl-6-(1-propynyl)-pyrimidine (2.5 g) in dimethyl sulfoxide (2.5 ml) were added to a suspension in 50 ml of tetrahydrofuran of 0.5 g of sodium hydride (60%) of which oily component was removed, and the mixture was stirred at 50° C. for 1 hour. After cooling to room temperature, 1.5 g of chloromethyl ethyl ether was added thereto and the resulting mixture was stirred for 5 hours. The reaction mixture was poured into water and extracted with 150 ml of toluene. The toluene layer was washed wit water, dried over magnesium sulfate and concentrated by evaporation under reduced pressure. The rsidue was purified by silica gel column chromatography to obtain 1.6 g (yield: 62%) of 2-(N-ethoxymethylanilino)-4-methyl-6-(1-propynyl) pyrimidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04992438
出典データセットuspto-grants-1991_02
ORD IDord-cf1ffae5a76a4e4ca0f2cd1d6f4ff506
出典メモuspto-grants-1991_02