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

HRID 735363노트

반응식

HRID 735363 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]=1

참가 물질

8

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

  1. customwas irradiated at 150° C. in a microwave reactor for 2.5 hours
  2. customThe two reaction mixtures
  3. extractionextracted with ethyl acetate (3×50 mL)
  4. washThe combined organic layers were washed with water (20 mL)
  5. dry with materialwith saturated sodium chloride solution (50 mL), dried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customThe crude product was purified by flash chromatography on silica gel
  8. washeluting with ethyl acetate

출처 및 근거

ORD 기록
ord-4419d7907f4c40be8385cea827892086
출처 데이터셋
uspto-grants-2009_09
특허 번호
US07592456B2

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