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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290527생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1290527

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) δ8.49(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 번호US05750754
출처 데이터셋uspto-grants-1998_05
ORD IDord-6a3d701db8254e6192a68951ad2aa912
출처 메모uspto-grants-1998_05