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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2217생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/2217

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 번호US05728701
출처 데이터셋uspto-grants-1998_03
ORD IDord-f693e1231b194064866be7bc3c6466fb
출처 메모uspto-grants-1998_03