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Chemical Structure| 98298-63-6 Chemical Structure| 98298-63-6

Structure of 98298-63-6

Chemical Structure| 98298-63-6

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Product Details of [ 98298-63-6 ]

CAS No. :98298-63-6
Formula : C7H9ClN2O
M.W : 172.61
SMILES Code : O=C(Cl)C1=C(C)N(C)N=C1C
MDL No. :MFCD03421589

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Application In Synthesis of [ 98298-63-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 98298-63-6 ]

[ 98298-63-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 98298-63-6 ]
  • [ 1125-29-7 ]
  • 2
  • [ 1125-29-7 ]
  • [ 98298-63-6 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; at 79℃; for 3h; 1,3,5-Trimethyl-1H-pyrazole-4-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide was prepared from 3-nitrobenzoyl chloride using the following multiple step procedure: Step 1: 1,3,5-Trimethyl-1H-pyrazole-4-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide.; A dry flask was charged with 1,3,5-Trimethyl-1H-pyrazole-4-carboxylic acid (0.122 g, 0.791 mmol) and thionyl chloride (5 mL) and allowed to stir at 79° C. for 3 h. The thionyl chloride was then removed by concentration in vacuo. The crude acid chloride was cooled to room temperature, and then dissolved in THF (8 mL). 6-(3-Amino-benzoyl)-1,3-dihydro-indol-2-one (as prepared in Example 40, 0.200 g, 0.793 mmol) was added to the THF solution of the acid chloride, and the mixture was allowed to reflux overnight. The reaction mixture was then allowed to cool to room temperature and subsequently vacuum filtered. The solid was washed with 0° C. THF (5 mL) and collected to afford the 1,3,5-Trimethyl-1H-pyrazole-4-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide as a solid (0.169 g, 0.440 mmol, 56percent).
With thionyl chloride; for 2h;Heating / reflux; Example 1-2 Production of N-{2-(1,3-dimethylbutyl)-4-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl}-5-chloro-1-methyl-3-trifluoromethylpyrazole-4-carboxamide (compound No. 1-103) 5-Chloro-1-methyl-3-trifluoromethylpyrazole-4-carboxylic acid (230 mg, 1 mmol) was dissolved in thionyl chloride (2 ml), and the solution was stirred at reflux temperature for 2 hours.. After concentration under reduced pressure, the resulting acid chloride was added to a solution of 2-(1,3-dimethylbutyl)-4-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]aniline (330 mg, 1 mmol) and triethylamine (150 mg, 1.5 mmol) in tetrahydrofuran (10 ml) under ice-cooling, and the resulting mixture was stirred at room temperature for 2 hours.. The reaction mixture was diluted with ethyl acetate and then washed with water.. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, and the resulting residue was separated and purified by silica gel column chromatography (hexane: ethyl acetate = 3: 1) to obtain 233 mg of the desired compound. Physical property: melting point 102-104°C. Yield: 43percent.
 

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