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Chemical Structure| 209853-24-7 Chemical Structure| 209853-24-7

Structure of 209853-24-7

Chemical Structure| 209853-24-7

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Product Details of [ 209853-24-7 ]

CAS No. :209853-24-7
Formula : C12H8N2OS
M.W : 228.27
SMILES Code : O=C1C2=C(C=C(C3=CC=CC=C3)S2)N=CN1
MDL No. :MFCD00499617

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Application In Synthesis of [ 209853-24-7 ]

* 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 [ 209853-24-7 ]

[ 209853-24-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64-18-6 ]
  • [ 100063-22-7 ]
  • [ 209853-24-7 ]
YieldReaction ConditionsOperation in experiment
6-Phenyl-3H-thieno[3, 2-d]pyrimidin-4-one VIIb21.4 g of ammonium acetate are added to a solution of 50 g of methyl 3-amino- 5-phenylthiophene-2-carboxylate IX in 168 ml of formic acid and the mixture is then heated under reflux for 6 hours. After cooling to 25C, the mixture is filtered and the crystals obtained are washed with water and then dried under reduced pressure. 62.3 g of the resulting formate are added to 56.2 ml of formamide and admixed with 45.1 g of ammonium formate. The mixture is stirred at 1400C for 10 hours and cooled to 25C, water is added and the precipitate formed is filtered off with suction. The precipitate is washed with water and dried under reduced pressure. In this way, 37.2 g of compound VIIb are obtained. NMR (300 MHz, DMSO-d6): δ = 7.38-7.52 (3H), 7.78-7.86 (3H), 8.13 (1 H).
6-Phenyl-3H-thieno[3, 2-d]pyrimidin-4-one VIIb21.4 g of ammonium acetate are added to a solution of 50 g of methyl 3-amino- 5-phenylthiophene-2-carboxylate IX in 168 ml of formic acid and the mixture is then heated under reflux for 6 hours. After cooling to 25C, the mixture is filtered and the crystals obtained are washed with water and then dried under reduced pressure. 62.3 g of the resulting formate are added to 56.2 ml of formamide and admixed with 45.1 g of ammonium formate. The mixture is stirred at 1400C for 10 hours and cooled to 25C, water is added and the precipitate formed is filtered off with suction. The precipitate is washed with water and dried under reduced pressure. In this way, 37.2 g of compound VIIb are obtained. NMR (300 MHz, DMSO-d6): δ = 7.38-7.52 (3H), 7.78-7.86 (3H), 8.13 (1 H)
 

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