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Chemical Structure| 10522-47-1 Chemical Structure| 10522-47-1

Structure of 10522-47-1

Chemical Structure| 10522-47-1

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Product Details of [ 10522-47-1 ]

CAS No. :10522-47-1
Formula : C10H8BrNO
M.W : 238.08
SMILES Code : COC1=C2N=CC=CC2=C(Br)C=C1
MDL No. :MFCD04966996
InChI Key :ZRQISUREPLHYIG-UHFFFAOYSA-N
Pubchem ID :4715023

Safety of [ 10522-47-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 10522-47-1 ]

* 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 [ 10522-47-1 ]

[ 10522-47-1 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 1198-14-7 ]
  • [ 77-78-1 ]
  • [ 10522-47-1 ]
  • 2
  • [ 1198-14-7 ]
  • [ 74-88-4 ]
  • [ 10522-47-1 ]
YieldReaction ConditionsOperation in experiment
70% With potassium carbonate; In acetone; for 8h;Reflux; 4-bromo-8-methoxyquinoline (112 mg, 0.5 mmol), K2C03 (207 mg, 1.25 mmol), CH3I (124 yL) And acetone (10 ml). The reaction mixture was heated to reflux for 8 h. After the completion of the reaction, the solvent was removed, and then extracted with CH2C12 and H2, and the organic phase was combined, washed with saturated brine, dried Na2SO4, filtered and concentrated.
General procedure: The K2CO3 (2.7 g, 0.02 mol) or KOH (1.6 g, 0.03 mol) was addedto a solution of 5-substituted 8-hydroxy quinoline 4a?c (0.01 mol)in acetone or THF (200 mL) at ambient temperature and the mixturewas stirred for 30 min. Then the methyl iodide (CH3I) (2.8 g,0.02 mol) was added dropwise and stirred overnight. The mixturesolution was concentrated to dryness, added water and extractedwith CH2Cl2 (150 mL 3). Finally, the organic layers were combined,washed with brine, dried with Na2SO4, filtered and evaporated.5a?c were obtained as brown oil, which could be usedwithout further purification.
  • 3
  • [ 10522-47-1 ]
  • [ 4151-80-8 ]
  • [ 910231-05-9 ]
  • 4
  • [ 103862-55-1 ]
  • [ 10522-47-1 ]
  • 5
  • [ 67-56-1 ]
  • [ 1198-14-7 ]
  • [ 10522-47-1 ]
YieldReaction ConditionsOperation in experiment
64% With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; for 5h; Example I-XIIPreparation of Compound 315General Procedure I-DBCH3I (5.68 g, 0.04 mol) was added to the mixture of <strong>[1198-14-7]5-bromoquinolin-8-ol</strong> (8 g, 0.036 mol), potassium carbonate (5.68 g, 0.04 mol) in 50 mL of DMF. The reaction mixture was stirred for 5 h at r.t, then water was added, and the precipitate was collected by filtration to afford compound I-XIIa (5.5 g, 64percent). MS (ESI) m/z (M+H)+ 238.
 

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