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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273040생성일: 2026년 10월 26일

Potassium Carbonate → N-({4-[4-(3-piperidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-yl}methyl)pyridin-2-amine

https://huagongshe.com/reaction/273040

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물N-(3-chloropropyl)piperidine hydrochlorideHCID 79624—
반응물4-{4-[(pyridin-2-ylamino)methyl]tetrahydro-2H-pyran-4-yl}phenolHCID 68577944—
용매DimethylformamideHCID 6228—
생성물N-({4-[4-(3-piperidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-yl}methyl)pyridin-2-amineHCID 5983751676.3%

반응 단계

4-{4-[(pyridin-2-ylamino)methyl]tetrahydro-2H-pyran-4-yl}phenol (200 mg, 0.704 mmol), 3-chloropropylpiperidine hydrochloride (152 mg, 0.775 mmol) and potassium carbonate (204 mg, 1.48 mmol) were stirred in DMF (1 ml) at 45° C. for 24 hours until complete. The reaction was then partitioned between ethyl acetate (40 ml) and water (40 ml). The organic layer was separated, dried over sodium sulphate and concentrated in vacuo to give a solid. The solid was purified by preparative HPLC to give the title compound (220 mg, 76%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 1.44-1.55 (m, 2H), 1.64-1.78 (m, 4H), 1.85-2.00 (m, 2H), 2.08-2.18 (m, 4H), 2.52-2.70 (m, 6H), 3.48 (d, 2H), 3.52-3.62 (m, 2H), 3.78-3.85 (m, 2H), 4.02 (t, 2H), 6.21 (d, 1H), 6.50 (t, 1H), 6.90 (d, 2H), 7.24 (d, 2H), 7.34 (t, 1H), 8.01 (d, 1H). LRMS APCI+ m/z 410 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456164B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-a2ec25f8de7b45628d549e1838557851
출처 메모uspto-grants-2008_11