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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1082085생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1082085

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-(Diphenylmethyl)-1-piperazineethanolHCID 4742573—
반응물4-Chloro-2-(4-methoxyphenyl)-6-methylpyrimidineHCID 15383455—
용매TetrahydrofuranHCID 8028—
생성물4-[2-(4-Diphenylmethylpiperazino)ethoxy]-2-(4-methoxyphenyl)-6-methylpyrimidineHCID 1538344647.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05589477
출처 데이터셋uspto-grants-1996_12
ORD IDord-dbdb18525f4e49babad3f498d183d767
출처 메모uspto-grants-1996_12