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Chemical Structure| 1223432-03-8 Chemical Structure| 1223432-03-8

Structure of 1223432-03-8

Chemical Structure| 1223432-03-8

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Product Details of [ 1223432-03-8 ]

CAS No. :1223432-03-8
Formula : C14H19Br2N3O2
M.W : 421.13
SMILES Code : O=C(N1CCN(C2=NC=C(Br)C=C2Br)CC1)OC(C)(C)C
MDL No. :MFCD20921612

Safety of [ 1223432-03-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H317-H319
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 1223432-03-8 ]

* 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 [ 1223432-03-8 ]

[ 1223432-03-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75806-85-8 ]
  • [ 57260-71-6 ]
  • [ 1223432-03-8 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In butanone; for 8h;Reflux; To a mixture of <strong>[75806-85-8]2,3,5-tribromopyridine</strong> (10 g), 1-Boc-piperazine (6 g) and potassium carbonate (20 g) was added 2-butanone (80 mL), and the mixture was refluxed for 8 hr. After cooling, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated to give 4-(3,5-dibromopyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (13 g). To a mixture of 4-(3,5-dibromopyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (13 g), bis(tricyclohexylphosphine)palladium (II) dichloride (1.3 g), tripotassium phosphate (38 g) and cyclopropylboronic acid (8.4 g) were added toluene (100 mL) and water (5 mL), and the mixture was refluxed for 8 hr. After cooling, the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The residue was purified by column chromatography (hexane:ethyl acetate) to give 4-(3,5-dicyclopropylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (7 g). 4-(3,5-Dicyclopropylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (7 g) was dissolved in chloroform (25 mL), 4N hydrogen chloride/ethyl acetate (25 mL) was added, and the mixture was stirred at room temperature overnight. To the reaction mixture was added 1N aqueous sodium hydroxide solution (100 mL), and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, and the solvent was evaporated. The residue was dissolved in ethyl acetate (50 mL), 4N hydrogen chloride/ethyl acetate (8 mL) was added, and the mixture was filtered to give the title compound (3.2 g).
13 g With potassium carbonate; In butanone; for 8h;Reflux; [0399] Preparation Example 87: Preparation of 1-(3,5-dicyclopropylpyridin-2-yl)piperazine hydrochloride[0400][0401] To a mixture of <strong>[75806-85-8]2,3,5-tribromopyridine</strong> (10 g), 1-Boc-piperazine (6 g) and potassium carbonate (20 g) was added2-butanone (80 mL), and the mixture was stirred with heating under reflux for 8 hr. The reaction mixture was cooled,water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine,and the solvent was evaporated to give 4-(3,5-dibromopyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (13 g).To a mixture of the obtained 4-(3,5-dibromopyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (13 g), bis(tricyclohexylphosphine)palladium(II)dichloride (1.3 g), tripotassium phosphate (38 g) and cyclopropylboronic acid (8.4 g)were added toluene (100 mL) and water (5 mL), and the mixture was stirred with heating under reflux for 8 hr. Thereaction mixture was cooled, water was added, and the mixture was extracted with ethyl acetate. The organic layer waswashed with saturated brine, and the solvent was evaporated. The obtained residue was purified by column chromatography(hexane:ethyl acetate) to give 4-(3,5-dicyclopropylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (7g). The obtained 4-(3,5-dicyclopropylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (7 g) was dissolved in chloroform(25 mL), 4N hydrogen chloride/ethyl acetate (25 mL) was added, and the mixture was stirred at room temperatureovernight. To the reaction mixture was added 1N aqueous sodium hydroxide solution (100 mL), and the mixture wasextracted with chloroform. The organic layer was washed with saturated brine, and the solvent was evaporated. Theobtained residue was dissolved in ethyl acetate (50 mL), 4N hydrogen chloride/ethyl acetate (8 mL) was added, and theprecipitate was collected by filtration to give the title compound (3.2 g).
 

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