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HRID 735363作成日:2026年10月27日

N,N'-Dimethylethylenediamine → 4-Iodo-1H-benzimidazole

https://huagongshe.com/reaction/735363

反応式

関与物質

役割名称HCID仕込み量
反応物N,N'-DimethylethylenediamineHCID 8070—
反応物4-Bromo-1H-benzimidazoleHCID 11252584—
反応物Sodium iodide dihydrateHCID 23685997—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒AmmoniaHCID 222—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物4-Iodo-1H-benzimidazoleHCID 21099512155.9%

反応手順

Two reactions were set up as follows: A mixture of 4-bromo-1H-benzimidazole (725 mg, 3.68 mmol), sodium iodide dihydrate (1.37 g, 7.36 mmol), copper(I) iodide (70 mg, 0.37 mmol) and N,N′-dimethylethylenediamine (78 μL, 65 mg, 0.74 mmol) in dioxane (8 mL) was irradiated at 150° C. in a microwave reactor for 2.5 hours. The two reaction mixtures were combined, diluted with water (90 mL) and conc. ammonia (20 mL), then extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with water (20 mL), then with saturated sodium chloride solution (50 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel, eluting with ethyl acetate, yielding the product as a yellow-white solid (1.40 g, 78%). 1H NMR (400 MHz, d6-DMSO): δ 12.72 (1H, s), 8.28 (1H, s), 7.61-7.53 (2H, m), 7.01 (1H, t, J=7.8 Hz); m/z (ES+) 245 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07592456B2
出典データセットuspto-grants-2009_09
ORD IDord-4419d7907f4c40be8385cea827892086
出典メモuspto-grants-2009_09