4-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-1-pyridiniumolate → 3-(4-phenoxyphenyl)-1-(4-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

HRID 897863ノート

反応式

HRID 897863 の反応式
[NH2:1][C:2]1[N:7]=[CH:6][N:5]=[C:4]2[N:8]([C:24]3[CH:29]=[CH:28][N+:27]([O-])=[CH:26][CH:25]=3)[N:9]=[C:10]([C:11]3[CH:16]=[CH:15][C:14]([O:17][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)=[CH:13][CH:12]=3)[C:3]=12.O.[PH2]([O-])=O.[Na+]>[Pd].C(O)(=O)C>[O:17]([C:14]1[CH:13]=[CH:12][C:11]([C:10]2[C:3]3[C:4](=[N:5][CH:6]=[N:7][C:2]=3[NH2:1])[N:8]([C:24]3[CH:29]=[CH:28][N:27]=[CH:26][CH:25]=3)[N:9]=2)=[CH:16][CH:15]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1

参加物

5

反応物 2

HCID 223472784-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-1-pyridiniumolateHCID 178418950HCID 178418950、化合物2 回

生成物 1

HCID 223472473-(4-phenoxyphenyl)-1-(4-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine収率 20%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒3 回HCID 176Acetic Acid溶媒

実験手順

A suspension of 4-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-1-pyridiniumolate (0.100 g, 0.00025 mol) and 10% palladium on carbon (0.016 g, 0.00002 mol) in acetic acid (3 mL) was reacted with sodium hypophosphite monohydrate (0.033 g, 0.00038 mol) at 60° C. After 2 hours, an additional 10% palladium on carbon (0.016 g, 0.00002 mol) was added. The mixture was stirred 18 hours after which time additional 10% palladium on carbon (0.016 g, 0.00002 mol) and sodium hypophosphite monohydrate (0.033 g, 0.00038 mol) was added. The mixture was stirred for an additional 24 hours. The mixture was filtered through Celite® 521, washing with acetic acid. The solvent was removed in vacuo, and the residue was purified by preparative RP-HPLC (Rainin C18, 8 mm, 300 A, 25 cm; 40% isocratic for five minutes, then 40%-100% acetonitrile-0.1M ammonium acetate over 30 min, 21 ml/min). The acetonitrile was removed in vacuo and the aqueous mixture was lyopholyzed to give 3-(4-phenoxyphenyl)-1-(4-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.020 g, 0.00005 mol) as a white solid:

後処理

  1. additionwas added
  2. filtrationThe mixture was filtered through Celite® 521
  3. washwashing with acetic acid
  4. customThe solvent was removed in vacuo
  5. customthe residue was purified by preparative RP-HPLC (Rainin C18, 8 mm, 300 A, 25 cm
  6. wait40% isocratic for five minutes
  7. wait40%-100% acetonitrile-0.1M ammonium acetate over 30 min
  8. customThe acetonitrile was removed in vacuo

出典と根拠

ORDレコード
ord-f90a7b899ed64c1b90eba3c9863c4ded
出典データセット
uspto-grants-2005_07
特許番号
US06921763B2

反応ノート

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