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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1666491생성일: 2026년 10월 24일

HCID 54438385, 화합물 → 4-(fluoro(3-(5-(trifluoromethyl)pyridin-2-yloxy)phenyl)methylene)-N-(6-methylpyridin-3-yl)piperidine-1-carboxamide

https://huagongshe.com/ko/reaction/1666491

반응식

참여 물질

역할이름HCID투입량
반응물HCID 54438385HCID 54438385—
반응물2-(3-(Fluoro(piperidin-4-ylidene)methyl)phenoxy)-5-(trifluoromethyl)pyridineHCID 66876266—
촉매TriethylamineHCID 8471—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물4-(fluoro(3-(5-(trifluoromethyl)pyridin-2-yloxy)phenyl)methylene)-N-(6-methylpyridin-3-yl)piperidine-1-carboxamideHCID 6687612559.3%

반응 단계

To a solution of 2-(3-(fluoro(piperidin-4-ylidene)methyl)phenoxy)-5-(trifluoromethyl)pyridine (110 mg, 0.312 mmol) and phenyl 6-methylpyridin-3-ylcarbamate (71.2 mg, 0.312 mmol) in DMSO (5 mL) under a N2 atmosphere was added 5 drops of triethyl amine and the reaction mixture was stirred for 12 h. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with water several times to remove the excess DMSO. The title compound was crystallized from hexane and diethyl ether to give the pure title compound (90 mg). 1H NMR (500 MHz, CDCl3): δ 2.5 (brs, 2H), 2.6 (brs, 2H), 2.8 (s, 3H), 3.7 (brs, 2H), 3.8 (brs, 2H), 7.0 (d, 1H, J=7.5 Hz), 7.1-7.3 (m, 3H), 7.4 (m, 2H), 7.9 (d, 1H, J=7.5 Hz), 8.4 (s, 1H), 9.0 (d, 1H, J=8.5 Hz), 9.4 (s, 1H), 9.8 (s, 1H); 13C NMR (125 MHz, CDCl3): 22.6, 25.6, 27.8, 44.2, 44.4, 53.4, 111.6, 114.1, 114.3, 121.4, 122.0, 123.8, 125.3, 129.7, 130.0, 133.8, 134.7, 136.9, 138.7, 145.4, 151.8, 153.0, 154.6, 165.4; m/z (487.4 M+ H+); HPLC: 98.9%; MP: 158-160° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044052B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-97478792f5ae4ec4886a9ff577f71e1a
출처 메모uspto-grants-2011_10