反应 #992707

ord-ed5ddc3afd484ac0885b0ae1a621f9f3

反应方程式

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

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  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
    温度to warm to room temperature (25° C.)
  4. 4
    workup.STIRRINGstirred for 18 hours
  5. 5
    其他The resulting precipitate was isolated by filtration and suction
  6. 6
    其他dried
  7. 7
    其他The precipitate was recrystallized from 300 milliliters of refluxing ethanol
  8. 8
    其他isolated by filtration
  9. 9
    洗涤rinsed with ethanol, suction
  10. 10
    其他dried
  11. 11
    其他vacuum dried in an oven overnight

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08012541B2uspto-grants-2011_09