Water → 2-(3,3-Difluoroazetidin-1-yl)-5-nitropyridine

HRID 1019540Notes

Reaction equation

HRID 1019540 reaction equation
Cl.[F:2][C:3]1([F:7])[CH2:6][NH:5][CH2:4]1.Cl[C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][N:10]=1.C(N(CC)CC)C.O>CN(C)C=O.C(OCC)(=O)C>[F:2][C:3]1([F:7])[CH2:6][N:5]([C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][N:10]=2)[CH2:4]1

Participants

7

Reactant 4

HCID 962WaterHCID 8471TriethylamineHCID 783082-Chloro-5-nitropyridineHCID 27582473,3-Difluoroazetidine hydrochloride

Product 1

HCID 529372622-(3,3-Difluoroazetidin-1-yl)-5-nitropyridine

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
100 °C

Procedure

A mixture of 0.367 g (2.84 mmol) of 3,3-difluoroazetidine hydrochloride, 0.3 g (1.89 mmol) of 2-chloro-5-nitropyridine and 0.41 mL (2.84 mmol) of triethylamine in 10 mL of dimethylformamide is heated overnight at 100° C. After this time, the suspension is poured into a mixture of 30 mL of water and 30 mL of ethyl acetate. The aqueous phase is separated, and then extracted with 20 mL of ethyl acetate. The organic phases are combined, washed three times with 25 mL of water, then dried over sodium sulfate and concentrated at reduced pressure. The resultant product is purified by chromatography on a silica column, eluting with dichloromethane. We thus obtain 0.34 g of the expected product in the form of a yellow solid.

Workup

  1. customThe aqueous phase is separated
  2. extractionextracted with 20 mL of ethyl acetate
  3. washwashed three times with 25 mL of water
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated at reduced pressure
  6. customThe resultant product is purified by chromatography on a silica column
  7. washeluting with dichloromethane

Sources & evidence

ORD record
ord-c146d0c428a742448a45c35e750cee91
Source dataset
uspto-grants-2014_05
Patent number
US08716272B2

Reaction notes

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