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HRID 1290527作成日:2026年10月27日

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

https://huagongshe.com/reaction/1290527

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Pyridyl)piperazineHCID 70517—
反応物Methyl 4-(2,2-dimethylbromoacetyl)phenoxyacetateHCID 18918473—
溶媒AcetonitrileHCID 6342—
生成物Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]-2,2-dimethylacetyl]phenoxyacetateHCID 18918600—

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05750754
出典データセットuspto-grants-1998_05
ORD IDord-6a3d701db8254e6192a68951ad2aa912
出典メモuspto-grants-1998_05