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Chemical Structure| 50339-06-5

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Product Details of [ 50339-06-5 ]

CAS No. :50339-06-5
Formula : C7H7N3O
M.W : 149.15
SMILES Code : O=C1NC2=NC=CC=C2N1C
MDL No. :MFCD00462572

Safety of [ 50339-06-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 50339-06-5 ]

* 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 [ 50339-06-5 ]

[ 50339-06-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 75-44-5 ]
  • [ 56291-51-1 ]
  • [ 50339-06-5 ]
  • 2
  • [ 56291-51-1 ]
  • [ 50339-06-5 ]
  • 3
  • [ 56291-51-1 ]
  • [ 530-62-1 ]
  • [ 50339-06-5 ]
YieldReaction ConditionsOperation in experiment
51% In tetrahydrofuran; at 23℃; for 15h;Inert atmosphere; In an oven dried round bottom flask, the above product 24 (213.7 mg, 1.7 mmol, 1 eq.) and 1,1’carbonyldiimidazole (422.0 mg, 2.6 mmol, 1.5 eq.) was added and flushed with argon three times. Dry THF (5.26 ml) was added and the reaction mixture was stirred overnight under argon. The crude mixture was partitioned between brine and EtOAc, and the product was extracted with EtOAc. The organic layer was separated, dried anhydrous Na2SO4 , filtered and evaporated to dryness under vacuum. The crude product was purified by column chromatography on silica gel using a solvent gradient from 50% EtOAc in hexanes to 100% EtOAc to give the desired intermediate 25a as yellow solid (131 mg, 51%)
In tetrahydrofuran; at 20℃; 85c) 1-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one CDI (2.251 g) was added to a solution of N3-methylpyridine-2,3-diamine (1.14 g) in THF (dry) (50 ml) at room temperature. The mixture was stirred at room temperature under a dry atmosphere (CaCl2 tube) over weekend. The reaction mixture was concentrated in vacuo. The residue was purified by column chromatography (silica gel, eluted with 0%-100% EtOAc in hexane) to give 1-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (1.1 g) as a white solid.MS (API+): [M+H]+ not detected.1H NMR (300 MHz, DMSO-d6) δ 3.29 (3H, s), 7.02 (1H, dd, J=7.9, 5.3 Hz), 7.40 (1H, dd, J=7.9, 1.5 Hz), 7.90 (1H, dd, J=5.3, 1.5 Hz), 11.51 (1H, brs).
 

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