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HRID 1827461作成日:2026年10月25日

4-Ethyl-2-methylpyridine → HCID 178436305、化合物

https://huagongshe.com/reaction/1827461

反応式

関与物質

役割名称HCID仕込み量
反応物4-Ethyl-2-methylpyridineHCID 68307—
反応物ButyllithiumHCID 178418339—
反応物HCID 178520036HCID 178520036—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178436305HCID 17843630532%

反応手順

To a stirred solution of 4-ethyl-2-methylpyridine (0.458 9, 3.79 mmol) in THF (4mL) at −50 degrees Celsius, add butyl lithium (1.5 mL, 2.5 M, 3.79 mmol) slowly and stir for 10 minutes. To the reaction, slowly add a solution of 6-Chloro-1H-indazole-3-carbaldehyde (0.5 g, 1.89 mmol) in THF (4 mL). After stirring for 10 minutes, the reaction was quenched with 1 N citric acid (10 mL). The mixture was diluted with EtOAc (50 mL), water (20 mL), and saturated NaCl (10 mL). The layers were separated, and the aqueous was extracted with EtOAc (3×15 mL). The organics were combined and washed with saturated NaCl (20 mL). After drying the organic layer over Na2SO4, the solids were removed by filtration and the liquid was concentrated to an oil by rotary evaporation. Chromatography (40 g silica gel, 60–100% EtOAc/hex) yields the desired product (142 mg, 32%) and recovered 6-Chloro-1H-indazole-3-carbaldehyde (348 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07053107B2
出典データセットuspto-grants-2006_05
ORD IDord-1cf3762e7edb43eba9e8b60d8675ebcc
出典メモuspto-grants-2006_05