N,N'-Dimethylethylenediamine → 4-Iodo-1H-benzimidazole
반응식
Br[C:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.O.O.[I-:13].[Na+].CNCCNC>O1CCOCC1.O.N.[Cu]I>[I:13][C:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 4
실험 절차
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+].
후처리
- customwas irradiated at 150° C. in a microwave reactor for 2.5 hours
- customThe two reaction mixtures
- extractionextracted with ethyl acetate (3×50 mL)
- washThe combined organic layers were washed with water (20 mL)
- dry with materialwith saturated sodium chloride solution (50 mL), dried (MgSO4)
- concentrationconcentrated in vacuo
- customThe crude product was purified by flash chromatography on silica gel
- washeluting with ethyl acetate
출처 및 근거
- ORD 기록
- ord-4419d7907f4c40be8385cea827892086
- 출처 데이터셋
- uspto-grants-2009_09
- 특허 번호
- US07592456B2
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