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Sodium Bicarbonate → 3-Cyanomethyl-2-methyl-8-(phenylpropoxy)-imidazo[1,2-a]pyridine

HRID 544453
ノート
印刷プレビュー

反応式

HRID 544453 の反応式
[NH2:1][C:2]1[C:7]([O:8][CH2:9][CH2:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:6][CH:5]=[CH:4][N:3]=1.Cl[CH:19]([C:23](=O)[CH3:24])[CH2:20][C:21]#[N:22].C(=O)(O)[O-].[Na+]>C(COC)OC>[C:21]([CH2:20][C:19]1[N:3]2[CH:4]=[CH:5][CH:6]=[C:7]([O:8][CH2:9][CH2:10][CH2:11][C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:2]2=[N:1][C:23]=1[CH3:24])#[N:22]
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 516892Sodium BicarbonateHCID 127582783-(3-Phenylpropoxy)pyridin-2-amineHCID 139002363-Chloro-4-oxopentanenitrile

生成物 1

HCID 204590053-Cyanomethyl-2-methyl-8-(phenylpropoxy)-imidazo[1,2-a]pyridine

試薬・触媒・溶媒 1

HCID 80711,2-Dimethoxyethane溶媒

実験手順

A mixture of 5.3 g of 2-amino-3-(3-phenylpropoxy)pyridine, 3.2 g of 3-chloro-4-oxopentanonitrile, 2.0 g sodium bicarbonate, and 50 ml dimethoxyethane was heated at reflux for 24 hrs., then stirred at room temperature 66 hrs. the solvent was removed in vacuo, the brown residue was taken up in 100 ml methylene chloride, filtered, dried over potassium carbonate and evaporated in vacuo to leave a brown gum residue. The residue was chromatographed on silica gel using first chloroform, then switching to 1:1 chloroform/ethyl acetate. The early eluates were combinedand evaporated and the resultant residue crystallized from isopropyl/ether to give the title compound (m.p. 143°-145° C.).

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 24 hrs
  3. customthe solvent was removed in vacuo
  4. filtrationfiltered
  5. dry with materialdried over potassium carbonate
  6. customevaporated in vacuo
  7. customto leave a brown gum residue
  8. customThe residue was chromatographed on silica gel using first chloroform
  9. customThe early eluates were combinedand evaporated
  10. customthe resultant residue crystallized from isopropyl/ether

出典と根拠

ORDレコード
ord-06372511cbfa412da2d65ad8471dc434
出典データセット
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04450164

反応ノート

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