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Potassium Hydroxide → 3-Methyl-2-phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid [1-ethyl-1-(4-trifluoromethyl-phenyl)-propyl]-amide

HRID 2108588
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HRID 2108588 반응식
C(O[C:4]([C:6]1[CH:10]=[N:9][N:8]2[CH:11]([CH3:20])[CH:12]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[NH:13][C:7]=12)=[O:5])C.[OH-].[K+].[CH2:23]([C:25]([NH2:38])([C:28]1[CH:33]=[CH:32][C:31]([C:34]([F:37])([F:36])[F:35])=[CH:30][CH:29]=1)[CH2:26][CH3:27])[CH3:24].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CCO.CCOC(C)=O.O>[CH2:23]([C:25]([NH:38][C:4]([C:6]1[CH:10]=[N:9][N:8]2[CH:11]([CH3:20])[CH:12]([C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=3)[NH:13][C:7]=12)=[O:5])([C:28]1[CH:33]=[CH:32][C:31]([C:34]([F:36])([F:37])[F:35])=[CH:30][CH:29]=1)[CH2:26][CH3:27])[CH3:24]
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참가 물질

9

반응물 5

HCID 14797Potassium HydroxideHCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 576315553-[4-(Trifluoromethyl)phenyl]pentan-3-amineHCID 136071815HCID 136071815, 화합물

생성물 1

HCID 136071858
3-Methyl-2-phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid [1-ethyl-1-(4-trifluoromethyl-phenyl)-propyl]-amide
수율 12.4%

시약·촉매·용매 3

HCID 702Ethanol용매HCID 962Water용매HCID 8857Ethyl Acetate용매

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온도
60 °C

실험 절차

Compound 3 (0.085 g, 0.3 mmol) was dissolved in EtOH (3 mL). KOH (6M in water, 0.9 mL, 1.78 mmol) was added. The reaction stirred at 60° C. for 3 h. The solution was cooled, diluted with AcOEt (10 mL) and water (10 mL) and shaken vigorously. The Aqueous layer was separated and acidified to pH=3. This acidic layer was then extracted with AcOEt (3 times). The combined AcOEt layers were washed with brine, dried (Na2SO4) and concentrated. The residue was then dissolved in NMP (1 mL) and 1-ethyl-1-(4-trifluoromethyl-phenyl)-propylamine (0.087 g, 0.37 mmol), HATU (0.14 g, 0.37 mmol), and DIEA (0.14 mL, 0.78 mmol) were added. The reaction was heated to 80° C. for 2 days. The solution was then cooled, washed with water, dried (MgSO4), and concentrated. Flash chromatography (20% AcOEt/hexanes) gave 0.017 g (12% yield) of amide 5.

후처리

  1. temperatureThe solution was cooled
  2. stirringshaken vigorously
  3. customThe Aqueous layer was separated
  4. extractionThis acidic layer was then extracted with AcOEt (3 times)
  5. washThe combined AcOEt layers were washed with brine
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated
  8. dissolutionThe residue was then dissolved in NMP (1 mL)
  9. temperatureThe reaction was heated to 80° C. for 2 days
  10. temperatureThe solution was then cooled
  11. washwashed with water
  12. dry with materialdried (MgSO4)
  13. concentrationconcentrated

출처 및 근거

ORD 기록
ord-df0f9546bcfa4fccb9ff06d1fd55069f
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07514441B2

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