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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1822004생성일: 2026년 10월 26일

2,6-Dichloropyridine → 2-Chloro-6-(1-cyclopropylmethyl-piperidin-4-yloxy)-pyridine

https://huagongshe.com/reaction/1822004

반응식

참여 물질

역할이름HCID투입량
반응물2,6-DichloropyridineHCID 16989—
반응물Sodium hydrideHCID 24758—
반응물1-(Cyclopropylmethyl)piperidin-4-olHCID 21428752—
용매DimethylformamideHCID 6228—
생성물2-Chloro-6-(1-cyclopropylmethyl-piperidin-4-yloxy)-pyridineHCID 5789372061%

반응 단계

Add NaH (60% dispersion in oil, 130 mg, 3.25 mmol) to a solution of 1-cyclopropylmethyl-piperidin-4-ol (preparation 11, 458 mg, 2.95 mmol) in DMF (8 mL) and stir for 20 min. Then add 2,6-dichloropyridine to the mixture and heat at 120° C. overnight. Quench the reaction with saturated NaHCO3, extract with methylene dichloride three times. Combine the organic layers, wash with saturated NaCl solution, dry over Na2SO4, filter and concentrate to give a residue. Chromatography (silica gel) eluting with 4% 2M NH3-methanol in methylene dichloride provides 480 mg (61%) of the title compound: mass spectrum (ion spray): m/z=267.2 (M+1); 1H NMR (CDCl3, ppm): 7.39 (t, 1H), 6.75 (d, 1H), 6.52 (d, 1H), 4.96 (m, 1H), 2.75 (m, 2H), 2.30 (m, 2H), 2.19 (d, 2H), 1.97 (m, 2H), 1.75 (m, 2H), 0.76 (m, 1H), 0.43 (m, 2H), 0.00 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07608629B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-9cef1e8696f9412d89afe1c9b59298c5
출처 메모uspto-grants-2009_10