تفاعل #657296

ord-6106cadbdf3b4cf5ac9f726b44cc800f

معادلة التفاعل

CCN(CC)CC
Triethylamine
O=C1O[C@H](CO)[C@@H](O)[C@H]1O
D-(+)-Ribonic acid gamma-lactone
CO
methanol
NCCc1ccc(O)c(O)c1
3-Hydroxytyramine
NC(=O)[C@H](O)[C@H](O)[C@H](O)CO.NCCc1ccc(O)c(O)c1
dopamine ribonamide
المردود 188.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.DISSOLUTIONuntil dissolved
  2. 2
    أخرىan additional 5 min
  3. 3
    workup.DISSOLUTIONto dissolve
  4. 4
    workup.STIRRINGwith stirring, over the course of about 10 minutes
  5. 5
    درجة الحرارةthe reaction mixture refluxed for 4 hr
  6. 6
    أخرىSolvents were removed by rotary evaporation
  7. 7
    أخرىto remove any residual water
  8. 8
    أخرى(1 hr.)
  9. 9
    أخرىto give a white solid
  10. 10
    أخرىagain resulting in a white solid as a product
  11. 11
    ترشيحThe resultant solid was collected by filtration
  12. 12
    أخرىdried in vacuo for 6 hrs

الإجراء التجريبي

D-(+)-Ribonic acid gamma-lactone (2.0 gm, 13.5 mmol) was added to methanol (25 mL) in a 100 mL round bottom flask with stirring until dissolved, and then an additional 5 min. 3-Hydroxytyramine (2.6 gm, 13.5 mmol) was added slowly, allowing it to dissolve, with stirring, over the course of about 10 minutes. Triethylamine (1.4 gm, 13.5 mmol) was then added and the reaction mixture refluxed for 4 hr. in the dark, during which time the solution acquired a slight yellow color. Solvents were removed by rotary evaporation using anhydrous ethanol as an azeotrope to remove any residual water. The resultant dried product constituted a thick syrup which solidified upon standing (1 hr.) to give a white solid. The white solid product was stirred (1 hr.) with acetone (40 mL), again resulting in a white solid as a product. The resultant solid was collected by filtration and dried in vacuo for 6 hrs. yielding dopamine ribonamide (3.83 gm, 12.7 mmol, 94.1% yield.) 1H and 13C-NMR results and CHN analyses were consistent with structure. Melting point was 90-91° C. Predicted C13H19N1: (301.30): C, 51.82; H, 6.36; N, 4.65; Analysis results of synthesis product: C, 51.67; H, 6.40; N, 4.69.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09023818B2uspto-grants-2015_05