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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 723985생성일: 2026년 10월 25일

Dimethylformamide → 5-Chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine-3-carbaldehyde

https://huagongshe.com/reaction/723985

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Ammonium HydroxideHCID 14923—
반응물Phosphorus oxychlorideHCID 24813—
반응물5-Chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridineHCID 22174845—
생성물5-Chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine-3-carbaldehydeHCID 21948682—

반응 단계

Phosphorous oxychloride (0.6 mL, 6.4 mmol) was added to N,N-dimethylformamide (10 mL) and the resulting mixture stirred at room temperature for 10 minutes. 5-Chloro-2-(4-fluorophenyl)pyrazolo[1,5-α]pyridine (1.0 g, 4.1 mmol) was added and the reaction mixture was stirred at room temperature for 12 hours. The reaction mixture was poured into ice-water and neutralized to pH 7 with aquous ammonium hydroxide. The resulting slurry was extracted with dichloromethane (3×40 mL). The combined organics were washed with brine, dried (magnesium sulfate), filtered and concentrated to give, after recrystallization from acetonitrile, 5-chloro-2-(4-fluorophenyl)pyrazolo [1,5-α]pyridine-3-carbaldehyde (0.95 g, 85%) as a white solid. 1H-NMR (CDCl3): δ10.07 (s, 1H), 8.49 (d, 1H), 8.44 (d, 1H), 7.78 (q, 2H), 7.22 (t, 2H), 7.07 (dd, 1H); MS m/z 275 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141569B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-abeb20bb17ef464c83c4fdbb356eda45
출처 메모uspto-grants-2006_11