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HRID 1290490作成日:2026年10月27日

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

https://huagongshe.com/reaction/1290490

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium hydrideHCID 82127—
反応物Methyl 4-bromoacetylphenoxyacetateHCID 243438—
反応物4-(Pyridin-4-YL)piperazin-2-oneHCID 18918356—
溶媒DimethylformamideHCID 6228—
生成物Methyl 4-[2-[4-(4-pyridyl)piperazin-2-one-1-yl]acetyl]phenoxyacetateHCID 18918332—

反応手順

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%.

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-34b62b3defd64b40ab61bffb4a64cd9e
出典メモuspto-grants-1998_05