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Ethylenediamine → 2,6-Diamino-N2-(2-aminoethyl)-5-nitropyridine

HRID 31847
ノート
印刷プレビュー

反応式

HRID 31847 の反応式
[NH2:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[C:4](Cl)[N:3]=1.[NH2:12][CH2:13][CH2:14][NH2:15].[OH-].[Na+]>O>[NH2:12][CH2:13][CH2:14][NH:15][C:4]1[CH:5]=[CH:6][C:7]([N+:8]([O-:10])=[O:9])=[C:2]([NH2:1])[N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3301EthylenediamineHCID 14798Sodium HydroxideHCID 27240356-Chloro-3-nitropyridin-2-ylamine

生成物 1

HCID 221423802,6-Diamino-N2-(2-aminoethyl)-5-nitropyridine

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

1 mmol of 2-amino-6-chloro-3-nitropyridine and 15 mmol of 1,2-diaminoethane were stirred at reflux for fourteen hours. The reaction mixture was concentrated in vacuo and solution of 1.5 mmol of NaOH in water was added. This solution was extracted twice with 95%/5% methylene chloride/methanol. The aqueous was then saturated with salt and extracted twice with 95%/5% acetonitrile/methanol and then finally extrated twice with 95%/5% ethylacetate/methanol. All organic fractions were combined and dried over sodium sulfate to obtain (2-aminoethyl)(6-amino-5-nitro(2-pyridyl))amine.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureat reflux for fourteen hours
  2. additionwas added
  3. extractionThis solution was extracted twice with 95%/5% methylene chloride/methanol
  4. extractionsaturated with salt and extracted twice with 95%/5% acetonitrile/methanol
  5. dry with materialdried over sodium sulfate

出典と根拠

ORDレコード
ord-92d0d0ce25ff48e1be007eecd5189581
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07425557B2

反応ノート

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