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Imidazole → 2-(3-Bromobenzoyl)-1H-imidazole

HRID 272654
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HRID 272654 반응식
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.C(N(CC)CC)C.[Br:13][C:14]1[CH:15]=[C:16]([CH:20]=[CH:21][CH:22]=1)[C:17](Cl)=[O:18].[OH-].[Na+]>N1C=CC=CC=1.O>[Br:13][C:14]1[CH:15]=[C:16]([CH:20]=[CH:21][CH:22]=1)[C:17]([C:2]1[NH:1][CH:5]=[CH:4][N:3]=1)=[O:18]
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참가 물질

7

반응물 4

HCID 795ImidazoleHCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 74377Benzoyl chloride, 3-bromo-

생성물 1

HCID 34184292-(3-Bromobenzoyl)-1H-imidazole수율 50%

시약·촉매·용매 2

HCID 962Water용매
HCID 1049
Pyridine
용매

실험 절차

A solution of imidazole (2.66 g, 39.1 mmol) and triethylamine (Et3N) 8.03 g, 79.4 mmol) in pyridine at 0° C. is treated with 3-bromobenzoyl chloride (17.5 g, 79.9 mmol), stirred for 5 min, allowed to warm to room temperature for 45 min, treated with an aqueous sodium hydroxide solution (7.5 N, 20 mL, 150 mmol), heated at reflux temperature for 2 h, cooled to room temperature, diluted with water, further cooled with an ice bath for 1 h and filtered. The filtercake is washed with water and dried under vacuum at 50° C. overnight to afford the title compound as a light tan solid, 4.89 g (50% yield), identified by NMR and mass spectral analyses. 1H NMR (500 MHz, CDCl3) δ 10.58 (br s, 1H), 8.73 (t, J=1.8 Hz, 1H), 8.61 (dt, J=7.8, 1.2 Hz, 1H), 7.75-7.72 (m, 1H), 7.42-7.38 (m, 2H), 7.32 (s, 1H); ESI MS m/z 250 [C10H7BrN2O+H]+.

후처리

  1. temperatureheated
  2. temperatureat reflux temperature for 2 h
  3. temperaturecooled to room temperature
  4. temperaturefurther cooled with an ice bath for 1 h
  5. filtrationfiltered
  6. washThe filtercake is washed with water
  7. customdried under vacuum at 50° C. overnight

출처 및 근거

ORD 기록
ord-a3362c9b49314105acb1741a2cb14a8b
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07456186B2

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