Selenium Dioxide → HCID 86687800, compound

HRID 1427413Notes

Reaction equation

HRID 1427413 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH2:8])[C:3]=1[N+:9]([O-:11])=[O:10].[Se](=O)=[O:13]>O1CCOCC1.O>[NH2:8][C:4]1[C:3]([N+:9]([O-:11])=[O:10])=[C:2]([CH:7]=[CH:6][N:5]=1)[CH:1]=[O:13]

Participants

5

Conditions

Temperature
100 °C

Procedure

To a solution of 4-methyl-3-nitropyridin-2-amine (10.0 g, 65.0 mmol) in a mixture of dioxane (400 mL) and water (50 mL) was added selenium dioxide (29.0 g, 260 mmol) and the reaction mixture was heated to 100° C. for 16 hr and then cooled to RT and filtered through a pad of celite. The pad was washed with a mixture of EtOAc/THF (3:1 v/v, 100 mL) and the combined filtrate and washings were evaporated in vacuo. The residue was partitioned between EtOAc/THF (3:1 v/v, 100 mL) and sat aq. NaHCO3 (150 mL) diluted with water (150 mL). The aq layer was separated and was extracted with EtOAc/THF (3:1 v/v, 4×100 mL) and the combined organic extracts were dried and evaporated in vacuo to afford 2-amino-3-nitroisonicotinaldehyde as a brown solid (2.73 g, 25%); Rt 0.75 min (Method 2); m/z 168 (M+H)+, (ES+).

Workup

  1. temperaturecooled to RT
  2. filtrationfiltered through a pad of celite
  3. washThe pad was washed with a mixture of EtOAc/THF (3:1 v/v, 100 mL)
  4. customthe combined filtrate and washings were evaporated in vacuo
  5. customThe residue was partitioned between EtOAc/THF (3:1 v/v, 100 mL)
  6. additiondiluted with water (150 mL)
  7. customThe aq layer was separated
  8. extractionwas extracted with EtOAc/THF (3:1 v/v, 4×100 mL)
  9. customthe combined organic extracts were dried
  10. customevaporated in vacuo

Sources & evidence

ORD record
ord-116cac17c9c04e438cbdb0cf956da984
Source dataset
uspto-grants-2015_01
Patent number
US08933228B2

Reaction notes

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