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Chemical Structure| 1379218-75-3 Chemical Structure| 1379218-75-3

Structure of 1379218-75-3

Chemical Structure| 1379218-75-3

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Product Details of [ 1379218-75-3 ]

CAS No. :1379218-75-3
Formula : C8H6FN3O
M.W : 179.15
SMILES Code : O=C1NC(N)=NC2=C1C=CC=C2F

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Application In Synthesis of [ 1379218-75-3 ]

* 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 [ 1379218-75-3 ]

[ 1379218-75-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 420-04-2 ]
  • [ 144851-82-1 ]
  • [ 1379218-75-3 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In ethanol; water; at 100℃; Into a 500mL round bottom flask equipped with a magnetic stir bar was placed methyl 2-amino-6-methoxybenzoate (25 g, 149.6 mmol), ethanol (200 mL), cyanamide (9.43 g, 224 mmol), and concentrated HCl (6 mL). The mixture was allowed to stir at reflux for 6 hours. At one hour intervals, concentrated HCl (0.5 mL) was added. The reaction mixture was allowed to cool to room temperature and the solid, 7i, was isolated via filtration and washed with ethanol. 1H NMR (400 MHz, DMSO-d6) delta ppm 3.88 (s, 3 H), 6.96 (dd, J=8.2, 3.1 Hz, 2 H), 7.69 (t, J=8.3 Hz, 1 H), 8.28 (br. s., 2 H), 12.67 (br. s., 1 H)
With hydrogenchloride; In ethanol; water; at 80℃; for 18h; <strong>[144851-82-1]2-amino-3-fluoro-benzoic acid methyl ester</strong> (15g, 88.68 mmol) was dissolved in EtOH (100 ml_) in a 250ml_ pressure tube, then cyanamide (5.59 g, 133 mmol) and HCI (37% in H2O) were added and the reaction mixture stirred 18h at 80C. Upon cooling, a precipitate formed and isolated by filtration, washed with EtOH and dried in vacuo to afford the title compound as a white powder. Rt: 0.44min., m/z - 180 [M+H], method B.
 

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