تفاعل #60614

ord-cc2db437f6ba4274b59e4b03fd5aa038

معادلة التفاعل

C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
COc1ccc2cc([C@H](C)C(=O)O)ccc2c1
Naproxen
O=C1CCC(=O)N1O
N-hydroxysuccinimide
COc1ccc2cc([C@H](C)C(=O)O)ccc2c1.O=C1CCC(=O)N1
Naproxen Succinimide

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
4°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe insoluble dicyclohexylurea removed by filtration
  2. 2
    أخرىThe solvent was removed by rotary evaporation
  3. 3
    workup.DISSOLUTIONthe residue dissolved in 30-40 mL CH2Cl2
  4. 4
    workup.ADDITIONApproximately 10 mL hexane was added
  5. 5
    workup.ADDITIONAdditional hexane was added dropwise until small planar white crystals
  6. 6
    أخرىto form
  7. 7
    workup.WAITthe solution was refrigerated overnight
  8. 8
    غسيلwashed with hexane
  9. 9
    أخرىdried in vacuum (2.30 g, 70.0%)

الإجراء التجريبي

To Naproxen (2.303 g, 10 mmol) in 5 mL of dioxane was added N-hydroxysuccinimide (1.16 g, 10 mmol) dissolved in 15 mL of dioxane and dicyclohexylcarbodiimide (2.27 g, 11 mmol) in 25 mL of dioxane. The reaction was stirred overnight and the insoluble dicyclohexylurea removed by filtration. The solvent was removed by rotary evaporation and the residue dissolved in 30-40 mL CH2Cl2. Approximately 10 mL hexane was added and the mixture was chilled to 4° C. for 2 hr. Additional hexane was added dropwise until small planar white crystals began to form and the solution was refrigerated overnight. The activated ester was harvested, washed with hexane and dried in vacuum (2.30 g, 70.0%)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07427600B2uspto-grants-2008_09