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HRID 861104作成日:2026年10月25日

Water → 7-Chloro-2-(4-methoxyphenyl)pyrazolo[1,5-A]pyridine

https://huagongshe.com/reaction/861104

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物Trifluoroacetic anhydrideHCID 9845—
反応物2-(6-Chloro-2-pyridinyl)-1-(4-methoxyphenyl)ethanone oximeHCID 73858320—
触媒Ferrous ChlorideHCID 24458—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物7-Chloro-2-(4-methoxyphenyl)pyrazolo[1,5-A]pyridineHCID 2235004552%

反応条件

温度15 °C

反応手順

To a solution of 2-(6-chloro-2-pyridinyl)-1-(4-methoxyphenyl)ethanone oxime (38.7 g, 140 mmol) in 1,2-dimethoxyethane (150 mL) at 0° C. was added trifluoroacetic anhydride (20 mL, 140 mmol), keeping the temperature below 10° C. during the addition. After the addition was complete, the reaction was warmed to 15° C. The solution was then cooled to 4° C. and a solution of triethylamine (39 mL, 280 mmol) in 1,2-dimethoxyethane (15 mL) was added over a period of 0.5 hours. The mixture was allowed to warm to room temperature and was stirred at room temperature for 1.5 hours. To this mixture was added iron(II) chloride (0.18 g, 1.4 mmol) and the reaction was heated at 75° C. for 15 hours. The reaction mixture was poured into water (300 mL). The resulting suspension was extracted with ethyl acetate. The organic phase was dried (magnesium sulfate), filtered and concentrated to a solid. This solid was recrystallized from methanol to give 7-chloro-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridine (18.7 g, 52%) as pale yellow needles. 1H NMR (CDCl3): δ 7.91 (d, 2H), 7.43 (d, 1H), 7.01 (t,1H), 6.95 (d, 2H), 6.81 (d, 1H), 6.80 (s, 1H), 3.83 (s, 3H); MS m/z 259 (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-51191a1c4e8d4b1b87bce5a1d24ac385
出典メモuspto-grants-2006_12