Iodine → 2-Amino-5-chloro-3-iodopyridine

HRID 402594

Reaction equation

HRID 402594 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][N:3]=1.S(=O)(=O)(O)O.[I:14](O)(=O)(=O)=O.II.[OH-].[Na+]>C(O)(=O)C.O>[NH2:1][C:2]1[C:7]([I:14])=[CH:6][C:5]([Cl:8])=[CH:4][N:3]=1

Participants

7

Conditions

Temperature
80 °C

Procedure

To a mixed solution of 2-amino-5-chloropyridine (2.6 g, 0.020 mol) in acetic acid/water (7.8 mL/1.8 mL) that cooled with ice bath, conc.sulfuric acid (0.26 mL, 4.9 mmol) was added dropwise, and then periodic acid (0.95 g, 4.2 mmol) and iodine (2.0 g, 8.0 mmol) were added. The reaction mixture was stirred at 80° C. for 6 h. Cooled to ambient temperature, the reaction mixture was poured into ice water, and neutralized by aqueous 5M sodium hydroxide solution. After removal of the precipitate by filtration, the filtrate was extracted with ethyl acetate. The organic layer was washed with saturated sodium thiosulfate solution, aqueous 1M sodium hydroxide solution and brine then dried over sodium sulfate and concentrated to afford 2-amino-5-chloro-3-iodopyridine as solid (4.4 g, y. 85%).

Workup

  1. temperatureCooled to ambient temperature
  2. customAfter removal of the precipitate
  3. filtrationby filtration
  4. extractionthe filtrate was extracted with ethyl acetate
  5. washThe organic layer was washed with saturated sodium thiosulfate solution, aqueous 1M sodium hydroxide solution and brine
  6. dry with materialthen dried over sodium sulfate
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-b68ec7662cf94ca8a0c367402bd1b17a
Source dataset
uspto-grants-2014_06
Patent number
US08742113B2

Linked notes

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