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Chemical Structure| 1196473-61-6 Chemical Structure| 1196473-61-6

Structure of 1196473-61-6

Chemical Structure| 1196473-61-6

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Product Details of [ 1196473-61-6 ]

CAS No. :1196473-61-6
Formula : C14H13BN2O5
M.W : 300.07
SMILES Code : O=C(C1=CN=C(OC2=CC=C3C(B(O)OC3)=C2)N=C1)OCC

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* 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 [ 1196473-61-6 ]

[ 1196473-61-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1196473-37-6 ]
  • [ 287714-35-6 ]
  • [ 1196473-61-6 ]
YieldReaction ConditionsOperation in experiment
0.678 g With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; for 25h; To a solution of 20 (0.5 g, 3.33 mmol) in anhydrous DMF (15 mL) were added K2CO3 (1.382 g, 10.0 mmol) and 2-chloro-pyrimidine-5-carboxylic acid methyl ester (0.575 g, 3.33 mmol) at room temperature. After stirring at room temperature for 25 h, the reaction mixture was cooled to 0 °C diluted with water (20 mL) and acidified to pH 2 using diluted hydrochloric acid. The white precipitate was collected, washed with water and dried to give 0.678 g of 23; mp 117-118 °C.
With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; for 25h; To a solution of <strong>[1196473-37-6]3H-benzo[c][1,2]oxaborole-1,6-diol</strong> (0.5 g, 3.33 mmol) in anhydrous DMF (15 mL) were added K2CO3 (1.382 g, 10.0 mmol) and 2-chloro-pyrimidine-5-carboxylic acid methyl ester (0.575 g, 3.33 mmol) at room temperature. After stirring at room temperature for 25 h, the reaction mixture was cooled to 0° C. diluted with water (20 mL) and acidified to pH 2 using diluted hydrochloric acid. The white precipitate was collected, washed with water and dried to give 0.678 g of pure product. Mp 117-118° C. 1HNMR (400 MHz, DMSO-d6) delta 9.26 (s, 1H), 9.08 (s, 2H), 7.44-7.57 (m, 2H), 7.31-7.40 (m, 1H), 5.03 (s, 2H), 3.88 (s, 3H). MS (ESI) m/z=287 [M+H]+.
 

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