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HRID 864824作成日:2026年10月27日

Diethyl Ether → Methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrate

https://huagongshe.com/reaction/864824

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物TriethylamineHCID 8471—
反応物1-(4-Pyridyl)piperazineHCID 70517—
反応物Methyl 2-(4-bromoacetylphenoxy)isobutyrateHCID 18918561—
溶媒AcetonitrileHCID 6342—
生成物Methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrateHCID 18918633—

反応手順

The product from step (i) above (2.00 g) in acetonitrile (10 ml) was added dropwise over 15 minutes to a stirred solution of 1-(4-pyridyl)piperazine (1.04 g) and triethylamine (0.89 ml) in acetonitrile (15 ml) and the mixture stirred overnight. The precipitated solid was removed by filtration and the filtrate evaporated. Purification of the residue by flash chromatography on silica, eluting with 0 to 5% v/v methanol/dichloromethane, gave a yellow gum. Trituration of this gum with diethyl ether gave methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrate, 170 mg, as a white solid: m.p. 88°-90° C.; NMR (d6DMSO) δ8.15 (2H, d), 7.96 (2H, d), 6.82 (4H, m), 3.92 (2H, s), 3.70 (3H, s), 3.33 (4H, t), 2.63 (4H t) 1.60 (6H, s); m/e 398 (M+H)+ ; calculated for C22H27N3O4.0.25H2O: C, 65.8; H, 6.8; N, 10.5 found: C, 65.8; H, 7.1; N, 10.4%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05563141
出典データセットuspto-grants-1996_10
ORD IDord-5b0eb29b7df941ebac4b0927aa3c6acc
出典メモuspto-grants-1996_10