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

HRID 751636Notes

Reaction equation

HRID 751636 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][N:3]=1.[I:9]I>C(O)C.S([O-])([O-])(=O)=O.[Ag+2]>[Cl:8][C:5]1[CH:6]=[C:7]([I:9])[C:2]([NH2:1])=[N:3][CH:4]=1

Participants

5

Procedure

Silver sulfate (3.40 g, 10.9 mmol) and 2-amino-5-chloropyridine (1 g, 7.8 mmol) was added to a solution of iodine (2.76 g, 10.9 mmol) in ethanol (50 ml) and the reaction mixture stiffed at rt for 72 h. The mixture was filtered, washed with methanol and the filtrate concentrated in vacuo. The residue was partitioned between saturated Na2S2O3 solution (50 ml) and DCM (2×50 ml). The combined organics were dried (MgSO4), concentrated in vacuo and purified by chromatography on silica gel eluting with DCM to give the title compound as a beige solid. δH (CDCl3): 4.95 (2H, br s), 7.84 (1H, d), 7.98 (1H, d).

Workup

  1. filtrationThe mixture was filtered
  2. washwashed with methanol
  3. concentrationthe filtrate concentrated in vacuo
  4. customThe residue was partitioned between saturated Na2S2O3 solution (50 ml) and DCM (2×50 ml)
  5. dry with materialThe combined organics were dried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. custompurified by chromatography on silica gel eluting with DCM

Sources & evidence

ORD record
ord-b7364d2018184c679c9ebbd058519a76
Source dataset
uspto-grants-2008_07
Patent number
US07405210B2

Reaction notes

Loading…