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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1640459생성일: 2026년 10월 25일

Diisopropylethylamine → 1-{4-[4-(2,4-Dichlorobenzyl)piperazin-1-yl]butyl}-5-methyl-1H-pyrimidine-2,4-dione

https://huagongshe.com/reaction/1640459

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Sodium BromideHCID 253881—
반응물1-(2,4-Dichlorobenzyl)piperazineHCID 411179—
반응물1-(4-chlorobutyl)-5-methylpyrimidine-2,4(1H,3H)-dioneHCID 59337587—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물1-{4-[4-(2,4-Dichlorobenzyl)piperazin-1-yl]butyl}-5-methyl-1H-pyrimidine-2,4-dioneHCID 1171881033.4%

반응 단계

1-(4-Chlorobutyl)-5-methyl-1H-pyrimidine-2,4-dione (0.69 mmol, 0.15 g), 1-(2,4-dichlorobenzyl)piperazine (0.62 mmol, 0.15 g), sodium bromide (3.46 mmol, 0.36 g) and diisopropylethylamine (6.92 mmol, 0.89 g) were heated in N-methylpyrrolidinone (0.6 ml) at 120° C. for 5 hours. The reaction mixture was then allowed to cool, the suspension was filtered with suction, and the filtrate was concentrated. The residue was then then taken up in ethyl acetate and washed with saturated brine. The organic layer was dried, filtered to remove the desiccant and evaporated in vacuo. The resulting residue was purified by chromatography on silica gel (eluent: methyl tert-butyl ether/methanol (0-100%), resulting in 88.0 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08114875B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-85ba6cec0af0423ba4949588bab461f4
출처 메모uspto-grants-2012_02