L-Proline → 1-[3-(3-pyridylcarbonyl)acryloyl]-L-proline

HRID 66539Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 66539
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]([CH:9]=[CH:10][C:11]([OH:13])=O)=[O:8])[CH:2]=1.[NH:14]1[CH2:21][CH2:20][CH2:19][C@H:15]1[C:16]([OH:18])=[O:17]>O1CCCC1>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]([CH:9]=[CH:10][C:11]([N:14]2[CH2:21][CH2:20][CH2:19][C@H:15]2[C:16]([OH:18])=[O:17])=[O:13])=[O:8])[CH:2]=1

Komponenten

4

Edukt 2

HCID 145742L-ProlineHCID 534274223-(3-Pyridylcarbonyl)acrylic acid

Produkt 1

HCID 537182731-[3-(3-pyridylcarbonyl)acryloyl]-L-proline

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

As for Example 27, 3-(3-pyridylcarbonyl)acrylic acid (0.01 mole) is reacted with N,N'-carbonyldiimidazole (0.011 mole) in tetrahydrofuran and to the mixture is added 0.011 mole of L-proline. The mixture is refluxed for 16 hours and the solvent removed under reduced pressure. The mixture is partitioned between dichloromethane and water containing acetic acid. The organic layer is separated, washed with water and dried over magnesium sulfate. The solvent is removed in vacuo to yield 1-[3-(3-pyridylcarbonyl)acryloyl]-L-proline. The preceding compound is dissolved in carbon tetrachloride and 0.03 mole of thioacetic acid is added. The mixture is heated 3 hours and the solvent is removed in vacuo to give the product of the Example as a glass.

Aufarbeitung

  1. temperatureThe mixture is refluxed for 16 hours
  2. customthe solvent removed under reduced pressure
  3. customThe mixture is partitioned between dichloromethane and water
  4. additioncontaining acetic acid
  5. customThe organic layer is separated
  6. washwashed with water
  7. dry with materialdried over magnesium sulfate
  8. customThe solvent is removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-be135ac334454be08754e24ed39db82b
Quelldatensatz
uspto-grants-1982_08
Patentnummer
US04342691

Notizen zur Reaktion

Wird geladen…