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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 896786생성일: 2026년 10월 24일

Potassium Carbonate → 4-[5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-N-phenyl-2-pyrimidinamine

https://huagongshe.com/ko/reaction/896786

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-[5-Chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-2-butyn-1-oneHCID 21992233—
반응물HCID 178418691HCID 178418691—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4-[5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-N-phenyl-2-pyrimidinamineHCID 1124702736%

반응 조건

온도150 °C

반응 단계

To a solution of 1-[5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-2-butyn-1-one (1.0 g, 3.36 mmol) in 1-methyl-2-pyrrolidinone (4 mL) was added N-phenylguanidine nitrate (1.0 g, 5.0 mmol) and anhydrous potassium carbonate (0.7 g, 5.0 mmol). The resulting mixture was heated at 150° C. for 12 hours and concentrated in vacuo to a syrup. Ethyl acetate and water were added and the phases separated. The organic phase was dried (magnesium sulfate), filtered and concentrated to a solid. This solid was crystallized from acetonitrile to give 500 mg (36%) of 4-[5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-N-phenyl-2-pyrimidinamine as a yellow solid. 1H-NMR (CDCl3): δ 8.48 (d, 1H), 8.45 (d, 1H), 8.23 (d, 1H), 7.64 (m, 4H), 7.42 (t, 2H), 7.1-7.25 (m, 4H), 6.93 (dd, 1H), 6.52 (d, 1H); 19F-NMR (CDCl3): δ −112.29; MS m/z 416 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06919352B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-49d153cf5b9a47d88c7d679a5cb9d3d4
출처 메모uspto-grants-2005_07