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p-Toluenesulfonic acid → 6-Chloro-8-propylpurine

HRID 466680
ノート
印刷プレビュー

反応式

HRID 466680 の反応式
[NH2:1][C:2]1[C:7]([NH2:8])=[C:6]([Cl:9])[N:5]=[CH:4][N:3]=1.CO[C:12](OC)(OC)[CH2:13][CH2:14][CH3:15].C1(C)C=CC(S(O)(=O)=O)=CC=1>COCCO>[Cl:9][C:6]1[N:5]=[CH:4][N:3]=[C:2]2[C:7]=1[NH:8][C:12]([CH2:13][CH2:14][CH3:15])=[N:1]2
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 6101p-Toluenesulfonic acidHCID 780104,5-Pyrimidinediamine, 6-chloro-HCID 1235121,1,1-Trimethoxybutane

生成物 1

HCID 190122236-Chloro-8-propylpurine

試薬・触媒・溶媒 1

HCID 80192-Methoxyethanol溶媒

実験手順

To a solution of 4,5-diamino-6-chloropyrimidine (0.289 g, 2 mmol) in 2-methoxyethanol (10 ml) were added trimethylorthobutyrate (0.5 ml, 3 mmol) and p-toluenesulfonic acid (0.03 g), and the mixture was refluxed for 18 hours and then concentrated in vacuo. The residue was partitioned between water and and ethylacetate. The organic phase was then washed with brine and dried (MgSO4). The crude product obtained after evaporation of the solvent was purified by flash column chromatography on silica-gel using ethylacetate/hexane (1:1). The fractions containing pure product were pooled and concentrated in vacuo, and then allowed to stand at room temperature overnight. The crystalline product was filtered and dried.

後処理

  1. temperaturethe mixture was refluxed for 18 hours
  2. concentrationconcentrated in vacuo
  3. customThe residue was partitioned between water and and ethylacetate
  4. washThe organic phase was then washed with brine
  5. dry with materialdried (MgSO4)

出典と根拠

ORDレコード
ord-8e2f8f548bd0487ba0c22f452c391f51
出典データセット
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05157026

反応ノート

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