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Chemical Structure| 4894-26-2 Chemical Structure| 4894-26-2

Structure of 4894-26-2

Chemical Structure| 4894-26-2

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Product Details of [ 4894-26-2 ]

CAS No. :4894-26-2
Formula : C11H10N2
M.W : 170.21
SMILES Code : C(N1)(C=NCC2)=C2C3=C1C=CC=C3
MDL No. :MFCD00603181

Safety of [ 4894-26-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P362+P364-P332+P313

Application In Synthesis of [ 4894-26-2 ]

* 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 [ 4894-26-2 ]

[ 4894-26-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 4894-26-2 ]
  • [ 20197-92-6 ]
  • [ 20999-50-2 ]
YieldReaction ConditionsOperation in experiment
75% In N,N-dimethyl-formamide; at 95℃; for 20h;Inert atmosphere; General procedure: To a solution isotaic anhydride (usually 0.5 mmol) in anhydrous DMF (3 mL) was added 3,4-dihydroisoquinoline or 4,9-dihydro-3H-pyrido[3,4-b]indole (0.65mmol, 1.3 eq) and the reaction mixture was stirred at 95 °C for 20 hrs. To the cooled mixture were added 20 mL of water drop wise while stirring. The precipitated solid was collected by filtration, washed with water, dried in vacuo to give the target.
  • 2
  • [ 4894-26-2 ]
  • [ 320-72-9 ]
  • 1,3-dichloro-7,8,13,13b-tetrahydro-5H-benzo[5',6'][1,3]oxazino[3',2':1,2]pyrido[3,4-b]indol-5-one [ No CAS ]
  • 3
  • [ 4894-26-2 ]
  • [ 20332-16-5 ]
  • [ 38990-11-3 ]
  • 4
  • [ 271-34-1 ]
  • [ 4894-26-2 ]
  • 3-(1,2,3,4-tetrahydro-β-carboline-1-yl)-5-azaindole [ No CAS ]
YieldReaction ConditionsOperation in experiment
69% With toluene-4-sulfonic acid; In neat (no solvent); at 100℃; for 2h;Microwave irradiation; the mixture of the cyclic imine 3,4-dihydroisoquinoline (66 mg, 0.50 mmol);6,7-dihydrothieno[3,2-c]pyridine (51 mg, 0.38 mmol); 3,4-dihydro--carboline (63 mg, 0.38 mmol) or4,5-dihydro-3H-benz[c]azepine (55.3 mg, 0.38 mmol); and the electron-rich aromatic compound (7-, 6-,4-, or <strong>[271-34-1]5-azaindole</strong> (30 mg, 0.25 mmol)) were placed in a 10 mL pressurized reaction vial and heated ina microwave reactor, under the conditions given in Tables 1-3. In the case of <strong>[271-34-1]5-azaindole</strong>, 10 mol % ofp-TSA (4.3 mg, 0.025 mmol) as a catalyst was also added.
 

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