Cesium carbonate → HCID 86696663, compound

HRID 2365810Notes

Reaction equation

HRID 2365810 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4](F)[CH:3]=1.[O:9]1[CH2:14][CH2:13][CH:12]([NH2:15])[CH2:11][CH2:10]1.C(=O)([O-])[O-].[Cs+].[Cs+]>CS(C)=O.C(OCC)(=O)C>[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH:15][CH:12]2[CH2:13][CH2:14][O:9][CH2:10][CH2:11]2)[CH:3]=1

Participants

6

Reactant 3

HCID 10796Cesium carbonateHCID 4192234-AminotetrahydropyranHCID 27628514-Bromo-2-fluoropyridine

Product 1

HCID 86696663HCID 86696663, compoundYield 55.6%

Reagents, catalysts & solvents 2

HCID 679Dimethyl SulfoxideSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
90 °C

Procedure

4-Bromo-2-fluoropyridine (1.38 g, 7.84 mmol) was dissolved in DMSO (20 mL), and (tetrahydro-pyran-4-yl)amine (0.912 g, 9.02 mmol) was added, followed by cesium carbonate (5.11 g, 15.7 mmol). The mixture was heated to 90° C. and agitated 3 hours. After cooling, the mixture was diluted with ethyl acetate (200 mL) and washed with water (5×), brine, dried and evaporated to give 4-bromo-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine (1.12 g, 4.36 mmol, 55.5% yield) as an oil.

Workup

  1. temperatureAfter cooling
  2. washwashed with water (5×), brine
  3. customdried
  4. customevaporated

Sources & evidence

ORD record
ord-ce28222cf5364c50a372ee75bbec49b3
Source dataset
uspto-grants-2014_04
Patent number
US08697715B2

Reaction notes

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