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Chemical Structure| 394223-19-9 Chemical Structure| 394223-19-9

Structure of 394223-19-9

Chemical Structure| 394223-19-9

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Product Details of [ 394223-19-9 ]

CAS No. :394223-19-9
Formula : C9H8N2O2
M.W : 176.17
SMILES Code : O=C(C1=CC2=NC=CC=C2N1)OC
MDL No. :MFCD09743416

Safety of [ 394223-19-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 394223-19-9 ]

* 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 [ 394223-19-9 ]

[ 394223-19-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 67-56-1 ]
  • [ 17288-32-3 ]
  • [ 394223-19-9 ]
YieldReaction ConditionsOperation in experiment
90 - 100% With potassium carbonate; at 55℃; for 1h; Add to ethyl 4-azaindole-2-carboxylate 4a (42.3 mmol) in MeOH (50 mL), K2CO3 (1.20 equiv, 50.7 mmol) and stir the suspension with heating to 55° C. for 1 h. Monitor the reaction by tlc (Et2O/hept). When complete, concentrate the reaction in vacuo, dilute with H2O and stir for 15 min. Collect the solid by filtration and dry in a vacuum oven at 65° C. for 3 h to afford about 90percent to about 100percent of the desired methyl 4-azaindole-2-carboxylate 5a.
  • 2
  • 4-Amino-1-[2-(R)-hydroxy-2-(6-methoxyquinolin-4-yl)]ethylpiperidine [ No CAS ]
  • [ 394223-19-9 ]
  • [ 17288-52-7 ]
YieldReaction ConditionsOperation in experiment
(a) 1H-Pyrrolo[3,2-b]pyridin-2-carboxaldehyde This was prepared from methyl 1H-pyrrolo[3,2-b]pyridin-2-carboxylate (0.1 g) and amine (1d) by the method of Example 16c, (except that the alcohol was stirred with manganese (II) oxide overnight) and used without purification.
  • 3
  • [ 67-56-1 ]
  • [ 17288-32-3 ]
  • [ 394223-19-9 ]
  • [ 853685-35-5 ]
  • [ 17288-35-6 ]
 

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