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HRID 57091作成日:2026年10月25日

Ethyl Acetate → 3-(3-chloro-1H-pyrazol-1-yl)pyridine

https://huagongshe.com/reaction/57091

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物3-Chloro-1-(pyridine-3-yl)-1H-pyrazole-5-carboxylic acid hydrochlorideHCID 118021782—
触媒Copper oxideHCID 14829—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ammonium HydroxideHCID 14923—
生成物3-(3-chloro-1H-pyrazol-1-yl)pyridineHCID 6749954073.4%

反応条件

温度120 °C

反応手順

3-Chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acid hydrochloride (1.00 g, 3.65 mmol) was stirred in N,N-dimethylformamide (10 mL). Copper(II) oxide (58.0 mg, 0.730 mmol) was added and the reaction was heated at 120° C. for 16 hours, at which point the reaction was ˜20% complete. Additional copper(II) oxide (112 mg, 1.46 mmol) was added and the reaction was stirred for 5 hours, at which point the reaction was complete by thin layer chromatography (TLC) [Eluent: ethyl acetate]. The mixture was diluted with ammonium hydroxide (NH4OH) and water and extracted with ethyl acetate. The organic layer was washed with 15% lithium chloride and concentrated to provide an orange solid. The residue was purified by flash column chromatography using ethyl acetate as eluent and the pure fractions were concentrated to afford the desired product as a white solid (481 mg, 69.7%). The spectral characterization was in agreement with the product prepared previously.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434712B2
出典データセットuspto-grants-2016_09
ORD IDord-e057a9d09fff4e41a0af34e569f9968e
出典メモuspto-grants-2016_09