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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606668생성일: 2026년 10월 26일

Ethanol → (3-{[3-(2-Isopropoxy-phenoxy)-propylamino]-methyl}-phenyl)-piperidin-1-yl-methanone

https://huagongshe.com/reaction/606668

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참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물HydrazineHCID 9321—
반응물2-[3-(2-Isopropoxy-phenoxy)-propyl]-isoindole-1,3-dioneHCID 67045923—
반응물3-(2-Isopropoxy-phenoxy)-propylamineHCID 67046060—
생성물(3-{[3-(2-Isopropoxy-phenoxy)-propylamino]-methyl}-phenyl)-piperidin-1-yl-methanoneHCID 1125838845%

반응 조건

온도50 °C

반응 단계

3-(2-Isopropoxy-phenoxy)-propylamine. To a solution of 2-[3-(2-isopropoxy-phenoxy)-propyl]-isoindole-1,3-dione in EtOH (6 mL) was added hydrazine (0.448 g, 14.0 mmol), and the reaction mixture was heated to 50° C. for 30 min. The solvent was removed under reduced pressure, and the crude residue was partitioned between CH2Cl2 (50 mL) and H2O (50 mL). The aqueous layer was extracted with CH2Cl2 (3×50 mL), and the combined organic layers were washed with brine, dried (MgSO4), filtered, and concentrated under reduced pressure. The resulting residue was purified by column chromatography (20-50% EtOAc/hexanes) to provide the desired product (0.267 g, 45%). MS (ESI): mass calculated for C12H19NO2, 209.29; m/z found, 210.2 [M+H]+. 1H NMR (400 MHz, CDCl3): 6.91-6.83 (m, 4H), 4.46 (hept, J=6.1 Hz, 1H), 4.07 (t, J=5.9 Hz, 2H), 2.97 (t, J=6.5 Hz, 2H), 1.99 (quint, J=6.2 Hz, 2H), 1.32 (d, J=6.1 Hz, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915420B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-f909443f7586477887865841278719f7
출처 메모uspto-grants-2011_03