Iodine → 2-Iodo-6-(trifluoromethyl)pyridin-3-amine

HRID 2063288Notes

Reaction equation

HRID 2063288 reaction equation
[I:1]I.[NH2:3][C:4]1[CH:5]=[N:6][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:8][CH:9]=1>C(O)C.S([O-])([O-])(=O)=O.[Ag+2]>[NH2:3][C:4]1[C:5]([I:1])=[N:6][C:7]([C:10]([F:13])([F:11])[F:12])=[CH:8][CH:9]=1

Participants

5

Reactant 2

HCID 807IodineHCID 27377445-Amino-2-(trifluoromethyl)pyridine

Product 1

HCID 534254792-Iodo-6-(trifluoromethyl)pyridin-3-amineYield 65.8%

Reagents, catalysts & solvents 2

HCID 178418844HCID 178418844, compoundCatalystHCID 702EthanolSolvent

Procedure

1.56 g (6.17 mmol) of iodine are added, portionwise, to a mixture, stirred under argon at 20° C., of 1 g (6.17 mmol) of 3-amino-6-(trifluoromethyl)pyridine and 1.25 g (6.17 mmol) of silver sulphate in 40 ml of ethanol. The stirring is maintained for 18 hours. The insoluble material is removed by filtration and is washed with ethanol, the filtrate is concentrated under reduced pressure, and the residue is taken up in 100 ml of dichloromethane. The organic phase is washed successively with 20 ml of a 5% aqueous solution of sodium hydroxide, 40 ml of water and 20 ml of a saturated aqueous solution of sodium chloride, dried over sodium sulphate, concentrated under reduced pressure and then purified by silica column chromatography (eluents:heptane-ethyl acetate). 1.17 g of the expected product are thus isolated, which product is used as it is in the subsequent synthesis.

Workup

  1. temperatureThe stirring is maintained for 18 hours
  2. customThe insoluble material is removed by filtration
  3. washis washed with ethanol
  4. concentrationthe filtrate is concentrated under reduced pressure
  5. washThe organic phase is washed successively with 20 ml of a 5% aqueous solution of sodium hydroxide, 40 ml of water and 20 ml of a saturated aqueous solution of sodium chloride
  6. dry with materialdried over sodium sulphate
  7. concentrationconcentrated under reduced pressure
  8. custompurified by silica column chromatography (eluents:heptane-ethyl acetate)

Sources & evidence

ORD record
ord-e3eb5955a7894c68812bb734fc012c81
Source dataset
uspto-grants-2012_10
Patent number
US08288376B2

Reaction notes

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