Water → 3-Iodopyridine-2,6-diamine

HRID 1891553Notes

Reaction equation

HRID 1891553 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH2:8])[N:3]=1.[I:9]N1C(=O)CCC1=O.O>CS(C)=O>[I:9][C:7]1[C:2]([NH2:1])=[N:3][C:4]([NH2:8])=[CH:5][CH:6]=1

Participants

5

Procedure

2,6-Diaminopyridine (100 g, 916 mmol) was dissolved in dimethyl sulfoxide (400 mL), and N-iodosuccinimide (100 g, 445 mmol) was added in one portion while stirring at room temperature. The reaction solution was stirring for 10 minutes at room temperature. Water (3.5 L) was added to the reaction solution, and the precipitated solids were filtered out. The resulting aqueous layer was extracted with ethyl acetate (1.3 L) 3 times. The ethyl acetate layers were combined and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel chromatography (heptane:ethyl acetate=2:3) to obtain the title compound (23.8 g, 22.8%).

Workup

  1. stirringThe reaction solution was stirring for 10 minutes at room temperature
  2. filtrationthe precipitated solids were filtered out
  3. extractionThe resulting aqueous layer was extracted with ethyl acetate (1.3 L) 3 times
  4. customthe solvent was evaporated under a reduced pressure
  5. customThe residue was purified by silica gel chromatography (heptane:ethyl acetate=2:3)

Sources & evidence

ORD record
ord-7ae995bb39774df4be73e279af4c90a2
Source dataset
uspto-grants-2013_08
Patent number
US08507530B2

Reaction notes

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