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HRID 586374作成日:2026年10月25日

2-(3-fluorophenyl)-1H-imidazole → 6-chloro-2-{[2-(3-fluorophenyl)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/586374

反応式

関与物質

役割名称HCID仕込み量
反応物2-(3-fluorophenyl)-1H-imidazoleHCID 316816—
反応物Dichloromethane methanolHCID 21226129—
反応物2-Chloromethyl-6-chloro-3-(1-propyl)-imidazolo[1,2-a]pyridineHCID 22335107—
溶媒Ethyl AcetateHCID 8857—
溶媒DimethylacetamideHCID 31374—
生成物6-chloro-2-{[2-(3-fluorophenyl)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridineHCID 22335084—

反応条件

温度60 °C

反応手順

Kt-BuO (0.69 mL of 1 M in THF, 0.69 mmol) is added to a solution of 3-fluoro-(1H-imidazol-2-yl)benzene (88 mg, 0.58 mmol) in anhydrous DMA (1 mL). After 15 minutes, 2-chloromethyl-6-chloro-3-(1-propyl)-imidazolo[1,2-a]pyridine (140 mg, 0.58 mmol) is added and the reaction mixture is stirred and heated at 60° C. for 15 minutes. The reaction mixture is diluted with EtOAc (10 mL), washed with water (3 mL), brine (3 mL), dried over Na2SO4, filtered and evaporated at reduced pressure to obtain a yellow solid. Sequential chromatography on silica gel eluting with EtOAc and then 5%MeOH/CH2Cl2 provides 6-chloro-2-{[2-(3-fluoropheny)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridine as a cream-colored yellow solid. TLC (10% MeOH/CH2Cl2) Rf=0.35.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06936617B2
出典データセットuspto-grants-2005_08
ORD IDord-8d638e36cfbd4aaab052ecb27541dd34
出典メモuspto-grants-2005_08