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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
ノート
印刷プレビュー

反応式

HRID 2108588 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

9

反応物 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、化合物

生成物 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
収率 12.4%

試薬・触媒・溶媒 3

HCID 702Ethanol溶媒HCID 962Water溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
60 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-df0f9546bcfa4fccb9ff06d1fd55069f
出典データセット
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07514441B2

反応ノート

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