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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 266752생성일: 2026년 10월 24일

1-(4-Pyridyl)piperazine → Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]-2,2-dimethylacetyl]phenoxyacetate

https://huagongshe.com/ko/reaction/266752

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Pyridyl)piperazineHCID 70517—
반응물Methyl 4-(2,2-dimethylbromoacetyl)phenoxyacetateHCID 18918473—
용매AcetonitrileHCID 6342—
생성물Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]-2,2-dimethylacetyl]phenoxyacetateHCID 18918600—

반응 단계

Methyl 4-(2,2-dimethylbromoacetyl)phenoxyacetate (1.58 g) was added to a stirred solution of 1-(4-pyridyl)piperazine (1.63 g) in acetonitrile (40 ml). After 34 days, the solid formed was removed by filtration and the filtrate evaporated to give an oil. Purification by flash chromatography on silica, eluting with 0.5 to 4.0% v/v methanol/dichloromethane gave the title compound, 240 mg, as a white foam: NMR (d6DMSO) δ 8.49 (2H, d), 8.12 (2H, d), 6.96 (2H, d), 6.77 (2H, d), 4.87 (2H, s), 3.69 (3H, s), 3.28 (4H, t), 2.58 (4H, t), 1.25 (6H, s); m/e 398 (M+H)+ ; calculated for C22H27N3O4.0.25H2O: C, 65.7; H, 6.8; N, 10.4. found: C, 65.3; H, 6.9; N, 10.4%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05652242
출처 데이터셋uspto-grants-1997_07
ORD IDord-0c6b920ba89d439a8459f8ce52d93d10
출처 메모uspto-grants-1997_07