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HRID 861105作成日:2026年10月26日

Boron trifluoride → 1-[7-(Chloro)-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridin-3-yl]ethanone

https://huagongshe.com/reaction/861105

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluorideHCID 6356—
反応物Acetic AnhydrideHCID 7918—
反応物7-Chloro-2-(4-methoxyphenyl)pyrazolo[1,5-A]pyridineHCID 22350045—
溶媒TolueneHCID 1140—
生成物1-[7-(Chloro)-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridin-3-yl]ethanoneHCID 2235005165.2%

反応手順

To a solution of 7-chloro-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridine (18.7 g, 72.4 mmol) in toluene (300 mL) at room temperature was added acetic anhydride (8.2 mL, 86.9 mmol). Boron trifluoride diethyletherate (10.1 mL, 79.6 mmol) was then added dropwise and the resulting solution was heated at reflux for 4 hours. The reaction mixture was cooled to room temperature and quenched by the dropwise addition of saturated aqueous sodium bicarbonate. The reaction was extracted with ethyl acetate, and the ethyl acetate phase washed with brine, dried (magnesium sulfate), filtered and concentrated. The residue was purified by recrystallization from ethyl acetate-hexanes to give 1-[7-(chloro)-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridin-3-yl]ethanone (14.2 g, 65%) as reddish needles. 1H NMR (CDCl3): δ 8.37 (dd, 1H), 7.49 (dd, 2H), 7.39 (dd, 1H), 7.10 (dd, 1H), 6.98 (dd, 2H), 3.84 (s, 3H), 2.13 (s, 3H); MS m/z 301 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07153855B2
出典データセットuspto-grants-2006_12
ORD IDord-62a819332458421c8759b30165ad8d56
出典メモuspto-grants-2006_12