Sodium hydride → 1-(3,4-Dichiorobenzyl)-2-pyridin-2-yl-1H-benzoimidazole

HRID 963444

反応式

HRID 963444 の反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[NH:11][C:10]2[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=2[N:8]=1.[H-].[Na+].[Cl:18][C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][C:26]=1[Cl:27])[CH2:22]Br>CN(C=O)C.O>[Cl:18][C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][C:26]=1[Cl:27])[CH2:22][N:11]1[C:10]2[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=2[N:8]=[C:7]1[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=1

参加物

6

反応物 3

HCID 24758Sodium hydrideHCID 708212-(2'-Pyridyl)benzimidazoleHCID 6397264-(Bromomethyl)-1,2-dichlorobenzene

生成物 1

HCID 153762251-(3,4-Dichiorobenzyl)-2-pyridin-2-yl-1H-benzoimidazole収率 36.7%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

2-Pyridin-2-yl-lH-benzoimidazole (1.95 g, 0.01 mol) was dissolved in DMF (50 mL) under an atmosphere of nitrogen. Sodium hydride (60% dispersion in oil, 0.48 g, 0.012 mol) was then added. The reaction mixture was stirred at ambient temperature for 0.5 hour. 3,4-Dichlorobenzyl bromide (2.4 g, 0.01 mol) was then added. The mixture was stirred at 80° C. for a period of 4 hours. The mixture was cooled and diluted with water. The mixture was then extracted with ethyl acetate. The organic extract was washed with water twice then evaporated. The residue was triturated with a small amount of ethyl acetate/hexane. The solid was collected and crystallized from ethanolic hydrogen chloride. The solid was collected to give the title compound (1.3 g, 36.7% yield) as a mono-hydrochloride, light brown solid, m.p. 227°-229° C. Anal. Calcd. for Cl9Hl3Cl2N3-HCl: C, 58.41; H, 3.61; N, 10.76.. Found: C, 58.21; H, 3.54; N, 10.80. Mass spectrum (+FAB; [M+H]+) 354/356/358. 1H-NMR (DMSO-d6 ; 400 MHz) 8 8.78 (d, 1H), 8.52 (d, 1H), 8.15 (t, 1H), 7.9 (d, 1H), 7.77 (d, 1H), 7.65 (d, 2H), 7.54 (d, 1H), 7.48-7.52 (m, 2H), 7.23 (d, 1H), and 6.22 ppm (s, 2H).

後処理

  1. stirringThe mixture was stirred at 80° C. for a period of 4 hours
  2. temperatureThe mixture was cooled
  3. extractionThe mixture was then extracted with ethyl acetate
  4. extractionThe organic extract
  5. washwas washed with water twice
  6. customevaporated
  7. customThe residue was triturated with a small amount of ethyl acetate/hexane
  8. customThe solid was collected
  9. customcrystallized from ethanolic hydrogen chloride
  10. customThe solid was collected

出典と根拠

ORDレコード
ord-66f230093170450a8e296d34fd904649
出典データセット
uspto-grants-1998_06
特許番号
US05763473

関連ノート

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