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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290490생성일: 2026년 10월 26일

Potassium hydride → Methyl 4-[2-[4-(4-pyridyl)piperazin-2-one-1-yl]acetyl]phenoxyacetate

https://huagongshe.com/reaction/1290490

반응식

참여 물질

역할이름HCID투입량
반응물Potassium hydrideHCID 82127—
반응물Methyl 4-bromoacetylphenoxyacetateHCID 243438—
반응물4-(Pyridin-4-YL)piperazin-2-oneHCID 18918356—
용매DimethylformamideHCID 6228—
생성물Methyl 4-[2-[4-(4-pyridyl)piperazin-2-one-1-yl]acetyl]phenoxyacetateHCID 18918332—

반응 단계

A dispersion of potassium hydride in mineral oil (35% w/w, 0.63 g) was added to a stirred suspension of 4-(4-pyridyl)piperazin-2-one (0.885 g) in DMF (10 ml) and the mixture was stirr-ed at room temperature for 2 hours. To the anion thus formed, was added methyl 4-bromoacetylphenoxyacetate (1.44 g) and the mixture was stirred at room temperature for 20 hours. Solvent was evaporated and the residue partitioned between dichloromethane (20 ml) and water (20 ml). The organic layer was dried (MgSO4) and evaporated. The residue was purified by flash column chromatography, the product being eluted with 1/9/0.1 v:v:v methanol/dichloromethane/0.88 S.G aqueous ammonia. Recrystallisation from ethyl acetate gave the title compound, m.p. 164°-165° C.; NMR (d6DMSO) δ 8.2(2H,d), 7.97(2H,d), 7.08(2H,d), 6.83(2H,d), 4.93(4H,d), 4.02(2H,s), 3.71(3H,s), 3.7(2H,m), 3.52(2H,m); m/e 384 (M+H)+ ; calculated for C20H21N3O5 : C, 62.7; H, 5.52; N, 11.0. Found: C, 62.6; H, 5.6; N, 10.9%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05750754
출처 데이터셋uspto-grants-1998_05
ORD IDord-34b62b3defd64b40ab61bffb4a64cd9e
출처 메모uspto-grants-1998_05