تفاعل #420242

ord-e5ccd4e16c13406981c436d0490597cd

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    ترشيحthe mixture was filtered
  3. 3
    أخرىthe filtrate was evaporated to dryness under reduced pressure
  4. 4
    أخرىThe residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile)
  5. 5
    أخرىto yield 20.2 mg (0.077 mmol, 39%)

الإجراء التجريبي

(E)-4-Hex-2-enoic acid (23 mg, 0.2 mmol) and HBTU (76 mg, 0.2 mmol) were dissolved in a 1:1 mixture of anhydrous DMF and anhydrous acetonitrile (2 ml), after 5 minutes triethylamine (82 μl, 0.6 mmol) and N-(2-Methyl-4-pyridyl)propane-1,3-diamine hydrochloride (40 mg, 0.2 mmol) was added. To the mixture basic aluminium oxide was added, stirring was continued for one hour, the mixture was filtered and the filtrate was evaporated to dryness under reduced pressure. The residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 20.2 mg (0.077 mmol, 39%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08877934B2uspto-grants-2014_11