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Chemical Structure| 1059191-49-9 Chemical Structure| 1059191-49-9

Structure of 1059191-49-9

Chemical Structure| 1059191-49-9

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Product Details of [ 1059191-49-9 ]

CAS No. :1059191-49-9
Formula : C8H7Cl2N3S
M.W : 248.13
SMILES Code : ClCC1=CN2C(SC)=NC(Cl)=CC2=N1
MDL No. :MFCD31697612

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Application In Synthesis of [ 1059191-49-9 ]

* 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 [ 1059191-49-9 ]

[ 1059191-49-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1005-38-5 ]
  • [ 534-07-6 ]
  • [ 1059191-49-9 ]
YieldReaction ConditionsOperation in experiment
49% With acetic acid; at 105℃; for 16h; Example 26A; 7-Chloro-2-(chloromethyl)-5-(methylthio)imidazo[1,2-c]pyrimidine 8 g (45.5 mmol) of 6-chloro-2-(methylthio)pyrimidine-4-amine and 5.78 g (45.55 mmol) of 1,3-dichloroacetone are dissolved in 53 ml of glacial acetic acid and heated at 105° C. for 16 h. After the reaction is complete, water is added and the precipitate is filtered off with suction. The crude product is further purified by silica gel chromatography. Drying under high vacuum results in 5.53 g (49percent of theory) of product.LCMS (method 4): Rt=3.33 min. (m/z=248 (M+H)+)1H-NMR (400 MHz, DMSO-d6): delta=7.99 (s, 1H), 7.58 (s, 1H), 4.85 (s, 2H), 2.76 (s, 3H).
44% With acetic acid; at 110℃; for 16h; 1,3-Dichloroacetone (2.89 g, 22.77 mmol) was added to a solution 6-chloro-2- methylsulfanyl-pyrimidin-4-ylamine (4 g, 22.77 mmol) in AcOH (15 mL) and the mixture was stirred at 110 °C for 16 hours. Then H20 was added and the solid formed was filtered off and dried in vacuo to yield 7-chloro-2-chloromethyl-5-methylsulfanyl-imidazo[l,2- c]pyrimidine (2.5 g, 44percent yield) as a pale brown solid that was used in the next step without further purification.
With acetic acid; at 110℃; for 16h; 1,3-Dichloroacetone (2.89 g, 22.77 mmol) was added to a solution 6-chloro-2-methylsulfanyl-pyrimidin-4-ylamine (4 g, 22.77 mmol) in AcOH (15 mL) and the mixture was stirred at 110° C. for 16 hours. Then H2O was added and the solid formed was filtered off and dried in vacuo to yield 7-chloro-2-chloromethyl-5-methylsulfanyl-imidazo[1,2-c]pyrimidine (2.5 g, 44percent yield) as a pale brown solid that was used in the next step without further purification.
 

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