2-Bromopyridine → HCID 18794864, compound

HRID 1157831Notes

Reaction equation

HRID 1157831 reaction equation
[NH:1]1[CH:5]=[CH:4][N:3]=[N:2]1.Br[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>CN(C=O)C.[Cu](I)I>[N:1]1([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[CH:5]=[CH:4][N:3]=[N:2]1

Participants

6

Reactant 3

HCID 79732-BromopyridineHCID 62657Potassium Phosphate, TribasicHCID 178418936HCID 178418936, compound

Product 1

HCID 18794864HCID 18794864, compound

Reagents, catalysts & solvents 2

HCID 83717Copper iodideCatalystHCID 6228DimethylformamideSolvent

Conditions

Temperature
110 °C

Procedure

1,2,3-Triazole (5 g), 2-bromo pyridine (8.5 ml) and copper iodide (0.68 g) was taken in dry DMF under Nitrogen atmosphere. 1,2-(N,N-dimethyl)cyclohexyl diamine (1.02 g) and potassium phosphate (30.73 g) was added into above mixture. The reaction mixture was reflux at 110° C. for over night. TLC was checked no starting material and the reaction mixture was filtered through celite. The filtrate was diluted with water and product was extracted with dichloromethane. The organic layer was evaporated and the crude product was purified by column chromatography using 60-120 silica gel and pet ether\ethyl acetate as eluent to give compound 2-(1H-1,2,3-triazol-1-yl)pyridine as white solid.

Workup

  1. filtrationthe reaction mixture was filtered through celite
  2. additionThe filtrate was diluted with water and product
  3. extractionwas extracted with dichloromethane
  4. customThe organic layer was evaporated
  5. customthe crude product was purified by column chromatography

Sources & evidence

ORD record
ord-91275159aa1d46589fce4325470859b4
Source dataset
uspto-grants-2010_10
Patent number
US07807676B2

Reaction notes

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