Potassium Carbonate → HCID 9951467、化合物

HRID 1488493ノート

反応式

HRID 1488493 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][N:11]2[CH:15]=[N:14][N:13]=[CH:12]2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[Br:16][C:17]1[CH:24]=[CH:23][C:20]([CH2:21]Br)=[CH:19][CH:18]=1.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[Br:16][C:17]1[CH:24]=[CH:23][C:20]([CH2:21][N:10]([N:11]2[CH:15]=[N:14][N:13]=[CH:12]2)[C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=2)=[CH:19][CH:18]=1

参加物

5

実験手順

8 Milliliters of acetonitrile was added to 0.63 g of 4-[N-(4-nitrophenyl)amino]-4H-1,2,4-triazole, 0.82 g of 4-bromobenzyl bromide and 0.62 g of anhydrous potassium carbonate and the mixture was stirred for 3 hours at room temperature. The solvent was removed by distillation under reduced pressure, and water was added to the residue obtained, which was then extracted with chloroform. The chloroform layer separated was washed with water and dried over anhydrous magnesium sulfate, and the solvent was removed by distillation. The residue was purified by silica gel column chromatography to give crude crystals from the chloroform/methanol (100/1) eluate. The crude crystals were recrystallized from acetone to give 0.71 g of 4-[N-(4-bromobenzyl)-N-(4-nitrophenyl)amino]-4H-1,2,4-triazole.

後処理

  1. customThe solvent was removed by distillation under reduced pressure, and water
  2. additionwas added to the residue
  3. customobtained
  4. extractionwhich was then extracted with chloroform
  5. customThe chloroform layer separated
  6. washwas washed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customthe solvent was removed by distillation
  9. customThe residue was purified by silica gel column chromatography
  10. customto give crude crystals from the chloroform/methanol (100/1) eluate
  11. customThe crude crystals were recrystallized from acetone

出典と根拠

ORDレコード
ord-1a6bf35e835e4c4390528c86befa43bd
出典データセット
uspto-grants-1997_10
特許番号
US05674886

反応ノート

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