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HRID 266739생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/266739

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물TriethylamineHCID 8471—
반응물1-(4-Pyridyl)piperazineHCID 70517—
반응물Methyl 2-(4-bromoacetylphenoxy)isobutyrateHCID 18918561—
용매AcetonitrileHCID 6342—
생성물Methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrateHCID 18918633—

반응 단계

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) δ 8.15 (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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05652242
출처 데이터셋uspto-grants-1997_07
ORD IDord-e684ea0586cb44a9b522ee99200f1e6d
출처 메모uspto-grants-1997_07