Sodium Hydroxide → HCID 136397847, compound

HRID 2068690Notes

Reaction equation

HRID 2068690 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]#[N:9])=[N:6][CH:7]=1.[OH-:10].[Na+].[NH2:12]O.Cl>CCO>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8](=[N:12][OH:10])[NH2:9])=[N:6][CH:7]=1

Participants

5

Conditions

Temperature
62.5 °C

Procedure

To a solution of 5-bromo-2-cyanopyridine (1.0 g, 5.50 mmol) in EtOH (100.0 mL) was added a solution of NaOH (0.22 g, 5.50 mmol dissolved in 2.0 ml H2O) followed by addition of NH2OH.HCl (0.38 g, 5.50 mmol). The resulting solution was heated to 60-65° C. for 16 h. After the completion of reaction (TLC monitoring), the solvent was evaporated and the residue was acidified with 3% HCl solution (20.0 mL) and heated to 100° C. till a clear solution was obtained. The reaction mixture was then cooled to room temperature and extracted with DCM (2×50 mL) that was later on discarded. The aqueous layer was basified with aqueous NH3 till pH 8 and extracted with EtOAc (3×50 mL). The combined organics was dried (Na2SO4), filtered and concentrated to obtain the desired product (0.75 g, 64%). MS: 216.01 (M+H)+.

Workup

  1. customAfter the completion of reaction (TLC monitoring)
  2. customthe solvent was evaporated
  3. temperatureheated to 100° C. till a clear solution
  4. customwas obtained
  5. temperatureThe reaction mixture was then cooled to room temperature
  6. extractionextracted with DCM (2×50 mL) that
  7. extractionextracted with EtOAc (3×50 mL)
  8. dry with materialThe combined organics was dried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-4689e43dab37442a8390dcd350eca187
Source dataset
uspto-grants-2012_10
Patent number
US08299065B2

Reaction notes

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