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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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8-(4-Nitrophenyl)imidazo[1,2-a]pyridine → Benzenamine,4-imidazo[1,2-a]pyridin-8-yl-

HRID 1982540
ノート
印刷プレビュー

反応式

HRID 1982540 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:11]3[N:12]([CH:16]=[CH:17][N:18]=3)[CH:13]=[CH:14][CH:15]=2)=[CH:6][CH:5]=1)([O-])=O>C(O)(=O)C.[Fe]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([C:10]2[C:11]3[N:12]([CH:16]=[CH:17][N:18]=3)[CH:13]=[CH:14][CH:15]=2)=[CH:8][CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 233169598-(4-Nitrophenyl)imidazo[1,2-a]pyridine

生成物 1

HCID 13810555Benzenamine,4-imidazo[1,2-a]pyridin-8-yl-

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 176Acetic Acid溶媒

実験手順

Add 45 g of iron powder to a solution of 15 g (62.7 mmol) of the product from Example 19 in 400 ml of 75% acetic acid. Heat to 60°-70° C. for 2 hr. Filter the reaction mixture over celite and concentrate the filtrate to approximately 50 ml under vacuum. Neutralize the residue with saturated sodium carbonate solution and extract with three 200 ml portions of methylene chloride. Dry the combined extracts over sodium sulfate, treat with charcoal and remove the solvent in vacuo. Crystallize the residue from ether to provide the title compound.

後処理

  1. temperatureHeat to 60°-70° C. for 2 hr
  2. filtrationFilter the reaction mixture over celite and
  3. concentrationconcentrate the filtrate to approximately 50 ml under vacuum
  4. extractionNeutralize the residue with saturated sodium carbonate solution and extract with three 200 ml portions of methylene chloride
  5. dry with materialDry the combined extracts over sodium sulfate
  6. additiontreat with charcoal
  7. customremove the solvent in vacuo
  8. customCrystallize the residue from ether

出典と根拠

ORDレコード
ord-9129e40b0db1457f91d0a0dff5c0082a
出典データセット
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04596872

反応ノート

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