Acetic Acid → HCID 178489372, 화합물

HRID 1171123

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HRID 1171123 반응식
[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

참가 물질

6

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온도
70 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c59327663e77453189bd64494105215f
출처 데이터셋
uspto-grants-2010_11
특허 번호
US07829558B2

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