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Iodine chloride → HCID 178494242、化合物

HRID 1062820
ノート
印刷プレビュー

反応式

HRID 1062820 の反応式
[CH3:1][O:2][C:3]1[N:8]=[C:7]([NH2:9])[N:6]=[C:5]2[NH:10][N:11]=[CH:12][C:4]=12.C([O-])(=O)C.[Na+].[I:18]Cl.S(S([O-])=O)([O-])(=O)=O.[Na+].[Na+]>O>[I:18][C:12]1[C:4]2[C:5](=[N:6][C:7]([NH2:9])=[N:8][C:3]=2[O:2][CH3:1])[NH:10][N:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 24640Iodine chlorideHCID 517045Sodium AcetateHCID 656671Sodium PyrosulfiteHCID 112521974-Methoxy-1H-pyrazolo[3,4-d]pyrimidin-6-amine

生成物 1

HCID 178494242HCID 178494242、化合物収率 78%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of compound 4 (105 g, 0.636 mol), sodium acetate (263 g) and iodine monochloride (140 g) was mechanically stirred in 1.3 L of water at a temperature between 92-98° C. for 5 h. The mixture was cooled to room temperature and a solution of sodium metabisulfite (139 g in 500 ml of water) was added. The mixture was stirred for 10 minutes and then filtered. The solid was rinsed with water and dried. The resulting dried solid was dissolved in 840 ml of hot DMF and precipitate by addition of 800 ml of water. The mixture was cooled in an ice-bath and the solid was filtered and dried to provide 144 g (78% yield) of 3-iodo-4-methoxy-6-aminopyrazolo[3,4-d]pyrimidine (5).

後処理

  1. filtrationfiltered
  2. washThe solid was rinsed with water
  3. customdried
  4. customThe resulting dried solid
  5. dissolutionwas dissolved in 840 ml of hot DMF
  6. additionprecipitate by addition of 800 ml of water
  7. temperatureThe mixture was cooled in an ice-bath
  8. filtrationthe solid was filtered
  9. customdried

出典と根拠

ORDレコード
ord-6979ae1963834190b21c9e89590d9238
出典データセット
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06962991B2

反応ノート

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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