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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 864786생성일: 2026년 10월 26일

Methyl 4-bromoacetylphenoxyacetate → Methyl 4-[2-[4-(5,6,7,8-tetrahydro-4-quinolinyl)piperazin-1-yl]-acetyl]phenoxyacetate

https://huagongshe.com/reaction/864786

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 4-bromoacetylphenoxyacetateHCID 243438—
반응물4-Piperazin-1-yl-quinolineHCID 1534386—
반응물4-(Piperazin-1-yl)-5,6,7,8-tetrahydroquinolineHCID 18918426—
용매AcetonitrileHCID 6342—
생성물Methyl 4-[2-[4-(5,6,7,8-tetrahydro-4-quinolinyl)piperazin-1-yl]-acetyl]phenoxyacetateHCID 18924099—

반응 단계

In a similar manner to Example 1, methyl 4-bromoacetylphenoxyacetate (1.23 g), a 1:1 mixture containing 4-(1-piperazinyl)quinoline and 4-(1-piperazinyl)-5,6,7,8-tetrahydroquinoline (1.84 g) and acetonitrile (56 ml) yielded, after stirring at room temperature overnight, filtration and evaporation of the filtrate, an orange/brown oily residue which was purified by flash chromatography, first on neutral alumina by elution with 5% v/v methanol/dichloromethane, then on silica by elution with methanol/dichloromethane (0.5% v/v to 5% v/v), and finally by crystallisation of the lower Rf material from methanol/water, to yield the title compound (298 mg) as a cream solid: NMR (CDCl3) δ1.76 (2H, m), 1.89 (2H, m), 2.64 (2H, m), 2.76 (4H, m), 2.95 (2H, m), 3.07 (4H, m), 3.80 (2H, s), 3.81 (3H, s), 4.71 (2H, s), 6.68 (1H, d), 6.95 (2H, d), 8.03 (2H, d) 8.28 (1H, d); m/Z 424 (M+H)+ ; calculated for C24H29N3O4. 1.0 H2O: C, 65.3%; H, 7.08%; N, 9.52%; found: C, 65.6%; H, 6.7%; N, 9.3%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05563141
출처 데이터셋uspto-grants-1996_10
ORD IDord-434a6d501beb4a898364ec078ee92640
출처 메모uspto-grants-1996_10