Reaction #992707

ord-ed5ddc3afd484ac0885b0ae1a621f9f3

Reaction equation

Nc1cccc(N)n1
2,6-Diaminopyridine
O=C(Cl)c1ccc(F)cc1
4-fluorobenzoyl chloride
O=C(Nc1cccc(NC(=O)c2ccc(F)cc2)n1)c1ccc(F)cc1
2,6-bis(4-fluorobenzoylamino)pyridine

Conditions

Temperature
0°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.ADDITIONtrietbylamine (28.0 milliliters, 20.2 grams, 0.2 mole) was added
  2. 2
    workup.ADDITIONwas added drop-wise over the course of 30 minutes
  3. 3
    Temperatureto warm to room temperature (25° C.)
  4. 4
    workup.STIRRINGstirred for 18 hours
  5. 5
    OtherThe resulting precipitate was isolated by filtration and suction
  6. 6
    Otherdried
  7. 7
    OtherThe precipitate was recrystallized from 300 milliliters of refluxing ethanol
  8. 8
    Otherisolated by filtration
  9. 9
    Washrinsed with ethanol, suction
  10. 10
    Otherdried
  11. 11
    Othervacuum dried in an oven overnight

Procedure

2,6-Diaminopyridine (10.9 grams, 0.1 mole) was dissolved in 500 milliliters dichloromethane and trietbylamine (28.0 milliliters, 20.2 grams, 0.2 mole) was added. The solution was chilled to 0° C. before 4-fluorobenzoyl chloride (24.0 milliliters, 31.7 grams, 0.2 mole) was added drop-wise over the course of 30 minutes. After stirring for 2 hours at 0° C., the solution was allowed to warm to room temperature (25° C.) and stirred for 18 hours. The resulting precipitate was isolated by filtration and suction dried. The precipitate was recrystallized from 300 milliliters of refluxing ethanol, isolated by filtration, rinsed with ethanol, suction dried, and vacuum dried in an oven overnight. The yield was 34.0 grams of white crystals.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08012541B2uspto-grants-2011_09