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HRID 1082085作成日:2026年10月27日

Sodium hydride → 4-[2-(4-Diphenylmethylpiperazino)ethoxy]-2-(4-methoxyphenyl)-6-methylpyrimidine

https://huagongshe.com/reaction/1082085

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物4-(Diphenylmethyl)-1-piperazineethanolHCID 4742573—
反応物4-Chloro-2-(4-methoxyphenyl)-6-methylpyrimidineHCID 15383455—
溶媒TetrahydrofuranHCID 8028—
生成物4-[2-(4-Diphenylmethylpiperazino)ethoxy]-2-(4-methoxyphenyl)-6-methylpyrimidineHCID 1538344647.4%

反応手順

0.6 g of 4-chloro-2-(4-methoxyphenyl)-6-methylpyrimidine and 0.76 g of 1-diphenylmethyl-4-(2-hydroxyethyl)piperazine were dissolved in 20 ml of dried tetrahydrofuran. After addition of 0.1 g of 60% sodium hydride, the mixture was stirred for 20 hours at room temperature. The reaction mixture was poured into ice-water and was extracted with ethyl acetate. After the extract was washed with water and was dried with anhydrous magnesium sulfate, then was evaporated in vacuo. The resulting residue was purified with column chromatography with silica gel (Wako gel C-200, elution with chloroform and then chloroform:ethyl acetate=8:1). The desired fraction was crystallized by evaporating the solvent under reduced pressure. The crystals were recrystallized with the solvent mixed with chloroform and ether, resulting to obtain 0.6 g of crystals. Melting point is 132° to 133° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05589477
出典データセットuspto-grants-1996_12
ORD IDord-dbdb18525f4e49babad3f498d183d767
出典メモuspto-grants-1996_12