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Chemical Structure| 5834-04-8 Chemical Structure| 5834-04-8

Structure of 5834-04-8

Chemical Structure| 5834-04-8

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Product Details of [ 5834-04-8 ]

CAS No. :5834-04-8
Formula : C7H7ClOS
M.W : 174.65
SMILES Code : O=C(Cl)CCC1=CC=CS1

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Application In Synthesis of [ 5834-04-8 ]

* 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 [ 5834-04-8 ]

[ 5834-04-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5928-51-8 ]
  • [ 5834-04-8 ]
YieldReaction ConditionsOperation in experiment
90.9% With thionyl chloride; In chloroform; General procedure: The appropriate acetic acid (10 mmol) was brought to reflux with thionyl chloride (12 mmol) in chloroform (30 mL). The reaction was monitored by IR until absorption appeared between 1780 cm-1 and 1815 cm-1. The solvent was evaporated under reduced pressure.
With thionyl chloride; for 1h; To a solution of 2,5-diaminopyrimidine-4,6-diol hydrogen chloride (1.04 g, 5.8 mmol) in sodium hydroxide (17.8 mmol) solution (25 ml of H2O) was added 3-thiophen-2-ylpropionyl chloride (6.4 mmol). The latter was prepared by refluxing 3-thiophen-2-ylpropionic acid (6.4 mmol) in thionyl chloride (500 muL) for 1 hour whereupon the excess of thionyl chloride was removed by evaporation in vacuo. The reaction mixture was stirred at room temperature for 18 hours. The pH of the suspension was adjusted to approximately 6 and the solids were filtered off. The title compound (1.25 g) was characterized by its mass spectrum: MS m/z (%): 515 ([M+H]+, 100).
With thionyl chloride; for 1h;Reflux; Example 152 Synthesis of N-(2-amino-4,6-dihydroxypyrimidin-5-yl)-3-thiophen-2-yl-propionamide To a solution of 2,5-diaminopyrimidine-4,6-diol hydrogen chloride (1.04 g, 5.8 mmol) in sodium hydroxide (17.8 mmol) solution (25 ml of H2O) was added 3-thiophen-2-ylpropionyl chloride (6.4 mmol). The latter was prepared by refluxing 3-thiophen-2-ylpropionic acid (6.4 mmol) in thionyl chloride (500 muL) for 1 hour whereupon the excess of thionyl chloride was removed by evaporation in vacuo. The reaction mixture was stirred at room temperature for 18 hours. The pH of the suspension was adjusted to approximately 6 and the solids were filtered off. The title compound (1.25 g) was characterized by its mass spectrum: MS m/z (%): 515 ([M+H]+, 100).
  • 2
  • [ 5928-51-8 ]
  • [ 79-37-8 ]
  • [ 5834-04-8 ]
YieldReaction ConditionsOperation in experiment
In hexane; dichloromethane; N,N-dimethyl-formamide; A. 3-(2-Thienyl)propionyl chloride To a solution of 5.0 g (0.032 mol) of 3-(2-thienyl)propionic acid in 2 ml of methylene chloride and 25 ml of oxalyl chloride was added three drops of N,N-dimethylformamide slowly. Following evolution of the gas the reaction mixture was concentrated under vacuum and 20 ml of hexane was added to the residue. The resulting mixture was filtered and the filtrate was concentrated under vacuum. The resulting compound, 3-(2-thienyl)propionyl chloride, was used directly in the following reaction.
 

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