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

HRID 1155034Notes

Reaction equation

HRID 1155034 reaction equation
[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

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

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 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.

Workup

  1. temperatureThe mixture is refluxed 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

Sources & evidence

ORD record
ord-5bab5dcd2b854f60857da669b4c9fbc2
Source dataset
uspto-grants-1981_11
Patent number
US04299769

Reaction notes

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