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HRID 423390생성일: 2026년 10월 26일

N,N-Dimethylpiperidin-4-amine → 1-(5-bromopyridin-2-yl)-N,N-dimethylpiperidin-4-amine

https://huagongshe.com/reaction/423390

반응식

참여 물질

역할이름HCID투입량
반응물N,N-Dimethylpiperidin-4-amineHCID 417391—
반응물5-Bromo-2-fluoropyridineHCID 2783168—
생성물1-(5-bromopyridin-2-yl)-N,N-dimethylpiperidin-4-amineHCID 5829957692.3%

반응 조건

온도80 °C

반응 단계

Mix 5-bromo-2-fluoro-pyridine (1.00 g, 5.68 mmol) and N,N-dimethyl-piperidin-4-yl-amine (1.50 g, 11.70 mmol) together and heat to 80° C. for 64 h. Partition the reaction between CH2Cl2 (5 mL) and 1N NaOH (8 mL). Collect the organic phase and extract the aqueous phase with additional CH2Cl2 (2×20 mL). Combine the organic solutions, then dry, filter, and concentrate. Purify the crude material by flash chromatography using an eluent of 5% MeOH (2N NH3)/CH2Cl2 to give 1.49 g (92%) of the title compound as a white solid. 1H NMR (CDCl3) δ 1.46 (dq, 2H, J=4.0, 11.8 Hz), 1.86 (br d, 2H, J=12.8 Hz), 2.26 (s, 6H), 2.32 (m, 1H), 2.80 (dt, 2H, J=2.7, 12.8 Hz), 4.23 (br d, 2H, J=13.2 Hz), 6.53 (d, 1H, J=8.9 Hz), 7.46 (dd, 1H, J=2.8, 9.0 Hz), 8.13 (d, 1H, J=2.6 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101764B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-cbb2a61260084d44b4ea4684921d9062
출처 메모uspto-grants-2012_01