Acetic Acid → HCID 178489372、化合物

HRID 1171123ノート

反応式

HRID 1171123 の反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[O:17][CH3:18])=[N:9][N:8](COCC[Si](C)(C)C)[C:5]2=[N:6][CH:7]=1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC.C(O)(=O)C>C1COCC1.CO>[Br:1][C:2]1[CH:3]=[C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[O:17][CH3:18])=[N:9][NH:8][C:5]2=[N:6][CH:7]=1

参加物

6

反応条件

温度
70 °C

実験手順

To a solution of 5-bromo-3-(2-methoxy-phenyl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-b]pyridine (260 mg, 0.60 mmol) in THF (3 mL) was added tetrabutylammonium fluoride (6 mL of 1 M in THF solution, 6.00 mmol) and molecular sieves. The solution was heated under reflux (70° C.) for 4 hours without stirring. The solution was cooled to ambient temperature and acidified to pH=5 by adding dropwise a dilute solution of acetic acid in MeOH. The solution was filtered and the filtrate was concentrated via rotary evaporation. The material was extracted into EtOAc and washed 3×H2O. The organic layer was dried over Na2SO4 and concentrated down to afford 5-bromo-3-(2-methoxy-phenyl)-1H-pyrazolo[3,4-b]pyridine as an orange solid (177 mg, 97% yield). MS: m/z 303.9, 305.9 [M+H+]. The material was used directly in step 2 without further purification.

後処理

  1. temperatureThe solution was heated
  2. temperatureThe solution was cooled to ambient temperature
  3. filtrationThe solution was filtered
  4. concentrationthe filtrate was concentrated via rotary evaporation
  5. extractionThe material was extracted into EtOAc
  6. washwashed 3×H2O
  7. dry with materialThe organic layer was dried over Na2SO4
  8. concentrationconcentrated down

出典と根拠

ORDレコード
ord-c59327663e77453189bd64494105215f
出典データセット
uspto-grants-2010_11
特許番号
US07829558B2

反応ノート

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