Phosphorus oxychloride → 2-chloro-1-methyl-1H-imidazo[4,5-b]pyridine

HRID 1044203Notes

Reaction equation

HRID 1044203 reaction equation
[CH3:1][N:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[NH:4][C:3]1=O.P(Cl)(Cl)([Cl:14])=O.[Cl-].[Cl-].[Ca+2]>>[Cl:14][C:3]1[N:2]([CH3:1])[C:10]2[C:5]([N:4]=1)=[N:6][CH:7]=[CH:8][CH:9]=2

Participants

4

Reactant 3

HCID 24813Phosphorus oxychlorideHCID 8542361-Methyl-1h-imidazo[4,5-b]pyridin-2(3h)-oneHCID 5284359Calcium Chloride

Product 1

HCID 585772702-chloro-1-methyl-1H-imidazo[4,5-b]pyridine

Procedure

The mixture of 1-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (1.1 g) and phosphorus oxychloride (6.87 mL) was stirred at 100° C. under a dry atmosphere (CaCl2 tube) for 5 h. The mixture was neutralized with sat.NaHCO3 at 0° C. and extracted with EtOAc. The organic layer was separated, washed with water and brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by column chromatography (NH silica gel, eluted with 0%-50% EtOAc in hexane) to give 2-chloro-1-methyl-1H-imidazo[4,5-b]pyridine (600 mg) as a white solid.

Workup

  1. extractionNaHCO3 at 0° C. and extracted with EtOAc
  2. customThe organic layer was separated
  3. washwashed with water and brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by column chromatography (NH silica gel, eluted with 0%-50% EtOAc in hexane)

Sources & evidence

ORD record
ord-73fff1e9b0264e7aa2f731adbb4b08b1
Source dataset
uspto-grants-2013_10
Patent number
US08563575B2

Reaction notes

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