Allyl bromide → HCID 10773123, compound

HRID 2262514Notes

Reaction equation

HRID 2262514 reaction equation
[NH2:1][C:2]1[C:6]([C:7]#[N:8])=[CH:5][NH:4][N:3]=1.[CH2:9](Br)[CH:10]=[CH2:11].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[CH2:11]([N:3]1[C:2]([NH2:1])=[C:6]([C:7]#[N:8])[CH:5]=[N:4]1)[CH:10]=[CH2:9]

Participants

5

Conditions

Temperature
80 °C

Procedure

3-Amino-4-pyrazolecarbonitrile 1 (Acros, 1.08 g, 10.0 mmol), allylbromide (Acros, 1.45 g, 12 mmol) and anhydrous potassium carbonate (Fisher, 1.65 g, 12 mmol) were suspended in 10 mL anhydrous DMF and heated at 80° C. under argon overnight. The solution was concentrated. Water was added (100 mL) and the organics were extracted with dichloromethane (3×100 mL). The combined dichloromethane fractions were washed with water (50 mL) and brine (50 mL) and were dried (magnesium sulfate). Concentration of the organics afforded a solid which was subjected to flash chromatography on silica gel (gradient elution 2:1 to 3:2 hexane: ethyl acetate). 589 mg (40%) of a white solid was obtained which was seen by NMR to contain an inseparable mixture of 5 and 6 in a 2.1:1 ratio. This mixture was used without further purification.

Workup

  1. concentrationThe solution was concentrated
  2. additionWater was added (100 mL)
  3. extractionthe organics were extracted with dichloromethane (3×100 mL)
  4. washThe combined dichloromethane fractions were washed with water (50 mL) and brine (50 mL)
  5. dry with materialwere dried (magnesium sulfate)
  6. customConcentration of the organics afforded a solid which

Sources & evidence

ORD record
ord-106de23393f9449a959ca2eacfd8058e
Source dataset
uspto-grants-2010_12
Patent number
US07851468B2

Reaction notes

Loading…