Diethyl (4-chloro-3-nitropyridine-2,6-diyl)bis(hydrogen carbonimidate) → (7-chloro-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl)-carbamic acid ethyl ester

HRID 252058Notes

Reaction equation

HRID 252058 reaction equation
[Cl:1][C:2]1[C:7]([N+:8]([O-])=O)=[C:6]([NH:11][C:12](OCC)=[O:13])[N:5]=[C:4]([NH:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])[CH:3]=1>[Ni]>[CH2:21]([O:20][C:18](=[O:19])[NH:17][C:4]1[N:5]=[C:6]2[NH:11][C:12](=[O:13])[NH:8][C:7]2=[C:2]([Cl:1])[CH:3]=1)[CH3:22]

Participants

3

Reactant 1

HCID 272578Diethyl (4-chloro-3-nitropyridine-2,6-diyl)bis(hydrogen carbonimidate)

Product 1

HCID 5358566(7-chloro-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl)-carbamic acid ethyl ester

Reagents, catalysts & solvents 1

HCID 935NickelCatalyst

Procedure

To a solution of diethyl 4-chloro-5-nitro-2,6-pyridinedicarbamate (intermediate for the preparation of 1) (500 mg) in ETOH (50 mL) was added Raney Ni (1 g) and stirred for 12 h under hydrogen atmosphere at room temperature. Reaction mixture was filtered on celite and filtrate was concentrated under reduced pressure. Residue was dissolved in 2-propanol (10 mL) and stirred for 60 h under reflux. The reaction mixture was cooled to room temperature and precipitate was filtered. The filtrate was concentrated to give 250 mg of (7-chloro-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl)-carbamic acid ethyl ester as a gray solid. 1H NMR confirmed the structure.

Workup

  1. customReaction mixture
  2. filtrationwas filtered on celite and filtrate
  3. concentrationwas concentrated under reduced pressure
  4. dissolutionResidue was dissolved in 2-propanol (10 mL)
  5. stirringstirred for 60 h
  6. temperatureunder reflux
  7. temperatureThe reaction mixture was cooled to room temperature
  8. filtrationprecipitate was filtered
  9. concentrationThe filtrate was concentrated

Sources & evidence

ORD record
ord-45f8c238ff6a421fa317b5e88c5a91a9
Source dataset
uspto-grants-2011_01
Patent number
US07868002B2

Reaction notes

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