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Potassium Cyanide → HCID 68445800、化合物

HRID 2233169
ノート
印刷プレビュー

反応式

HRID 2233169 の反応式
Br[CH2:2][C:3]1[C:4]([F:15])=[CH:5][CH:6]=[C:7]2[C:12]=1[N:11]=[C:10]([O:13][CH3:14])[CH:9]=[N:8]2.[C-:16]#[N:17].[K+]>CN(C)C=O>[F:15][C:4]1[C:3]([CH2:2][C:16]#[N:17])=[C:12]2[C:7](=[CH:6][CH:5]=1)[N:8]=[CH:9][C:10]([O:13][CH3:14])=[N:11]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 9032Potassium Cyanide2 回HCID 67548259HCID 67548259、化合物

生成物 1

HCID 68445800HCID 68445800、化合物収率 57%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
50 °C

実験手順

A mixture of 8-bromomethyl-7-fluoro-2-(methyloxy)quinoxaline (5.89 g, 20 mmol) and potassium cyanide (3.2 g, 49 mmol) in dimethylformamide (125 ml) was heated at 50° C. for approx. 40 h. More potassium cyanide (0.8 g) was added and heating continued at 60° C. for ˜8 h. The mixture was then evaporated and the residue was dissolved in dichloromethane and washed with water. The aqueous phase was extracted twice with dichloromethane and the combined organic fractions were dried and evaporated. Chromatography on silica (300 g), eluting with 0-25% ethyl acetate/hexane gave product (2.47 g, 57%).

後処理

  1. temperatureheating
  2. customThe mixture was then evaporated
  3. dissolutionthe residue was dissolved in dichloromethane
  4. washwashed with water
  5. extractionThe aqueous phase was extracted twice with dichloromethane
  6. customthe combined organic fractions were dried
  7. customevaporated
  8. washChromatography on silica (300 g), eluting with 0-25% ethyl acetate/hexane

出典と根拠

ORDレコード
ord-79db6c8e988e4ce6baa59c7506a734dd
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07709483B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート