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HRID 41595作成日:2026年10月24日

Pyrazole → 2-methyl-4-(1H-pyrazol-1-yl)pyridine

https://huagongshe.com/ja/reaction/41595

反応式

関与物質

役割名称HCID仕込み量
反応物PyrazoleHCID 1048—
反応物1,10-PhenanthrolineHCID 1318—
反応物Potassium CarbonateHCID 11430—
反応物4-Bromo-2-methylpyridineHCID 2762835—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒TolueneHCID 1140—
生成物2-methyl-4-(1H-pyrazol-1-yl)pyridineHCID 6725318592%

反応条件

温度120 °C

反応手順

To a mixture of 4-bromo-2-methylpyridine [22282-99-1] (350 mg, 2.05 mmol), 1H-pyrazole (140 mg, 2.05 mmol), 1,10-phenanthroline (74 mg, 0.41 mmol) and K2CO3 (567 mg, 4.1 mmol) in toluene (2 mL), CuI (19 mg, 0.1 mmol) was added and the reaction mixture was heated at 120° C. for 70 h in a sealed tube. The reaction mixture was cooled to rt, quenched with water (50 mL) and extracted with dichloromethane (150 mL). The organic layer was washed with brine and dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified flash column chromatography (eluent: 30% ethyl acetate in hexane) to yield the title compound (300 mg, 92%). [1H NMR (300 MHz, CDCl3) ♀ ppm 8.53 (d, 1H), 8.02 (d, 1H), 7.77 (d, 1H), 7.55 (d, 1H), 7.44-7.40 (m, 1H), 6.52 (t, 1H), 2.62 (s, 3H); TLC Rf=0.28 (ethyl acetate/hexane 30:70)].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530648B2
出典データセットuspto-grants-2013_09
ORD IDord-ba31f049f5f24f55a3d18e92a376ae81
出典メモuspto-grants-2013_09