Hydrochloric Acid → HCID 59394182, compound

HRID 1887643Notes

Reaction equation

HRID 1887643 reaction equation
[CH3:1][C:2]1([C:5](=O)[CH2:6][C:7]#[N:8])[CH2:4][CH2:3]1.Cl.[CH3:11][NH:12][NH2:13]>CCO.O1CCOCC1>[CH3:11][N:12]1[C:5]([C:2]2([CH3:1])[CH2:4][CH2:3]2)=[CH:6][C:7]([NH2:8])=[N:13]1

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 6061MethylhydrazineHCID 133930463-(1-Methylcyclopropyl)-3-oxopropanenitrile

Product 1

HCID 59394182HCID 59394182, compound

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 312751,4-DioxaneSolvent

Procedure

To a solution of 3-(1-methyl-cyclopropyl)-3-oxo-propionitrile (1.0 g, 8.1 mmol) in EtOH (10 mL) is added 4N HCl in Dioxane (10 mL). The mixture is stirred at room temperature for 16 hour. Concentrated under reduced pressure, the residue is dissolved in MeOH (40 mL) and treated with methylhydrazine (0.56 g, 12.2 mmol). The mixture is heated at 80° C. for 16 h. The solution is then concentrated in vacuo and the residue is purified by HPLC give product. MS (ESI) m/z 152.3 (M+1).

Workup

  1. concentrationConcentrated under reduced pressure
  2. dissolutionthe residue is dissolved in MeOH (40 mL)
  3. temperatureThe mixture is heated at 80° C. for 16 h
  4. concentrationThe solution is then concentrated in vacuo
  5. customthe residue is purified by HPLC
  6. customgive product

Sources & evidence

ORD record
ord-f42cbb4970494bd781ded3e42e3dabbc
Source dataset
uspto-grants-2013_08
Patent number
US08501756B2

Reaction notes

Loading…