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Chemical Structure| 323591-23-7 Chemical Structure| 323591-23-7

Structure of 323591-23-7

Chemical Structure| 323591-23-7

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Product Details of [ 323591-23-7 ]

CAS No. :323591-23-7
Formula : C6H7BrN2S
M.W : 219.10
SMILES Code : CSC1=NC=C(CBr)C=N1
MDL No. :MFCD24465277

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Application In Synthesis of [ 323591-23-7 ]

* 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 [ 323591-23-7 ]

[ 323591-23-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19858-50-5 ]
  • [ 323591-23-7 ]
YieldReaction ConditionsOperation in experiment
63% With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20℃; for 16.0h; To a mixture of 113 (1.02 g, 653 mrnoi) and PPh3 (3.4g, 131 mmol)in DCM (50 mL) is added carbon tetrabromide (4.3 g, 13.1 rnrnoi). After stirring at room temperature for 16 hours, the mixture is diluted with DCM, washed with brine, dried over anhydrous sodium sulfate, filtered, concentrated, and purified by silica gel column chromatography (EA:PE 1:20) to give 137 as a pale yellow oil (900 mg, 63percent). (MS: [M÷H] 2190)
With dibromo sulfoxide; In dichloromethane; at 20℃; for 2.5h; To a solution of the above compound (0.19 g, 1.2 mmol) in 8.5 mL CH2CI2 was added thionyl bromide (0.1 1 mL, 1.5 mmol). The reaction was stirred at room temperature for 2.5 h and quenched with saturated aqueous ammonium chloride. The layers were separated, and the organic portion was washed with water and brine, dried over sodium sulfate, filtered, and concentrated to afford 5-(bromomethyl)-2-(methylsulfanyl)pyrimidine that gave a mass ion (ES+) of 221.1 (83/4Br) for M+H\\
With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 0℃; for 1.0h; To the solution of <strong>[19858-50-5](2-(methylthio)pyrimidin-5-yl)methanol</strong> (0.88 g, 5.6 mmol) in DCM (20 ml) at 0°C was added triphenylphosphine (2.1 g, 7.9 mmol) and carbon tetrabromide(2.6 g, 7.9 mmol). The resulting solution was stirred at 0°C for 1 hour. The reaction mixture was purified on silica gel column using EtOAc/hexane as eluting solvents to give 5- (bromomethyl)-2-(methylthio)pyrimidine. LC/MS: (M+ 1 ): 218.90; 220.90.
 

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