Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1741275생성일: 2026년 10월 26일
Ethyl Acetate → 4-[3-(5-(1,2,4-Triazol-4-yl)-1H-indol-3-yl)propyl]-1-(alpha-methoxycarbonylbenzyl)piperidine
https://huagongshe.com/reaction/1741275
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Benzeneacetic acid, alpha-bromo-, methyl ester | HCID 137806 | — |
| 반응물 | 4-[3-(5-(1,2,4-Triazol-4-yl)-1H-indol-3-yl)propyl]piperidine | HCID 21835239 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-[3-(5-(1,2,4-Triazol-4-yl)-1H-indol-3-yl)propyl]-1-(alpha-methoxycarbonylbenzyl)piperidine | HCID 21835209 | — |
반응 단계
4-[3-(5-(1,2,4-Triazol-4-yl)-1H-indol-3-yl)propyl]piperidine (Description 2, 0.800 g, 0.0026 mol) was dissolved in anhydrous DMF (10 ml), under N2, and potassium carbonate (0.540 g, 0.0039 mol) added followed by (±)-methyl α-bromophenylacetate (Aldrich, 0.5 ml, 0.0031 mol). The reaction was stirred at 25° C. for 16 h, then poured into ethyl acetate (100 ml) and H2O (30 ml). The organic layer was collected, washed with H2O (3×30 ml), dried over MgSO4 and evaporated with 1-5% MeOH/CH2Cl2 to obtain the title compound as a colourless oil. 1H NMR 1.23-1.33 (6H, m), 1.66 (5H, m), 2.04 (1H, br m), 2.72 (2H, t, J=3 Hz), 2.96 (1H, bm), 3.69 (3H, s), 3.98 (1H, br s), 7.11 (1H, d, J=1 Hz), 7.14 (1H, d, J=2 Hz), 7.33 (3H, m), 7.43-7.48 (2H, m), 7.50 (1H, d, J=3 Hz), 7.51 (1H, d, J=1 Hz), 8.07 (br s, indole (NH)), 8.45 (2H, s, Ar (triazole)).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05973156 |
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| 출처 데이터셋 | uspto-grants-1999_10 |
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| ORD ID | ord-7643b46c4e9447ef9e96d0557779fd3c |
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| 출처 메모 | uspto-grants-1999_10 |
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