Triethylamine → 2-(Dimethylphosphonomethylamino)-3-(4-biphenylyl)-propionic acid

HRID 487222Notes

Reaction equation

HRID 487222 reaction equation
[C:1]1([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:6]=[CH:5][C:4]([CH2:7][C:8](=O)[C:9]([OH:11])=[O:10])=[CH:3][CH:2]=1.[CH3:19][O:20][P:21]([CH2:25][NH2:26])(=[O:24])[O:22][CH3:23].C(N(CC)CC)C.C([BH3-])#N.[Na+]>C1COCC1.CCO.C1COCC1>[CH3:19][O:20][P:21]([CH2:25][NH:26][CH:8]([CH2:7][C:4]1[CH:5]=[CH:6][C:1]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:2][CH:3]=1)[C:9]([OH:11])=[O:10])([O:22][CH3:23])=[O:24]

Participants

7

Procedure

To a stirred suspension of 4-biphenyl-pyruvic acid in anhydrous THF-EtOH (50 mL, 9:1) is added aminomethylphosphonic acid dimethyl ester (520 mg, 3.7 mmol) in THF-EtOH (5 mL, 9:1). The pH is then adjusted with triethylamine to 6.6. After 20 minutes, sodium cyanoborohydride (100 mg, 1.6 mmol) in THF (2.5 mL) is added over 30 minutes. The solution is stirred for 18 hours and then concentrated. Ether (20 mL) is added and the mixture is cooled and treated with 1N HCl (7 mL). After stirring at room temperature for 30 minutes, the solid is filtered off and washed with ether and water to yield 2-(dimethylphosphonomethylamino)-3-(4-biphenylyl)-propionic acid as a waxy solid.

Workup

  1. concentrationconcentrated
  2. additionEther (20 mL) is added
  3. temperaturethe mixture is cooled
  4. additiontreated with 1N HCl (7 mL)
  5. stirringAfter stirring at room temperature for 30 minutes
  6. filtrationthe solid is filtered off
  7. washwashed with ether and water

Sources & evidence

ORD record
ord-c5fc5633de0a4753bfdd5e7d70a9820e
Source dataset
uspto-grants-1994_03
Patent number
US05294632

Reaction notes

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