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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl 4-bromoacetylphenoxyacetate | HCID 243438 | — |
| 반응물 | 4-Piperazin-1-yl-quinoline | HCID 1534386 | — |
| 반응물 | 4-(Piperazin-1-yl)-5,6,7,8-tetrahydroquinoline | HCID 18918426 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | Methyl 4-[2-[4-(5,6,7,8-tetrahydro-4-quinolinyl)piperazin-1-yl]-acetyl]phenoxyacetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05563141 |
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| 출처 데이터셋 | uspto-grants-1996_10 |
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| ORD ID | ord-434a6d501beb4a898364ec078ee92640 |
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| 출처 메모 | uspto-grants-1996_10 |
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