Reaktion #571827

ord-c109cfa40f434f979d6bd36cba4e61e0

Reaktionsgleichung

N[C@H](CCC(=O)O)C(=O)O
D-glutamic acid
NC(=O)C[C@@H](N)C(=O)O
D-asparagine
N[C@H](CC(=O)O)C(=O)O
D-aspartic acid
N[C@H](CS)C(=O)O
D-cysteine
NC(=O)CC[C@@H](N)C(=O)O
D-glutamine
C[C@@H](O)[C@H](N)C(=O)O
threonine
O=C(O)CNc1ccc(O)cc1
p-hydroxyphenylglycine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigebrings about a preferred crystallization of the threonine in its L-form
  2. 2
    SonstigeSimilarly, inclusion of the L-forms of the above additives leads to preferred crystallization of D-threonine
  3. 3
    workup.ADDITIONFurther, we have found that from a supersaturated aqueous solution of D,L-asparagine, on addition of D-aspartic acid, D-glutamic acid of D-glutamine, there
  4. 4
    Sonstigeresults
  5. 5
    Sonstigea preferred crystallization of L-asparagine monohydrate
  6. 6
    Sonstigeinclusion of the L-additives leads to preferred crystallization of D-asparagine monohydrate
  7. 7
    workup.ADDITIONFurther, we have found that addition of L-tyrosine (TYR), L-tyrosine-p-toluene sulfonate (TpTS), L-dopa, L-dopa-p-toluene sulfonate (DpTS), L-α-methyl dopa, L-α-methyl dopa-p-toluene sulfonate (MDpTS), L-phenylalanine (PHE), L-phenylalanine-p-toluene sulfonate (PpTS), L-phenyl glycine (PG), L-phenyl glycine p-toluene sulfonate (PGpTS), L-p-methoxy phenyl glycine (pMPG) or L-p-methoxy phenyl glycine p-toluene sulfonate (pMPGpTS) to a supersaturated solution of pHPGpTS in an 0.5N aqueous solution of p-toluene sulfonic acid
  8. 8
    Sonstigeprecipitation of the D-form of pHPGpTS

Vorschrift

We have found that addition of D-glutamic acid (D-GLU), D-asparagine (D-ASN), D-aspartic acid (D-ASP), or D-cysteine (D-CYS), or D-glutamine (D-GLN) in small amounts to a supersaturated solution of threonine in water brings about a preferred crystallization of the threonine in its L-form. Similarly, inclusion of the L-forms of the above additives leads to preferred crystallization of D-threonine. Further, we have found that from a supersaturated aqueous solution of D,L-asparagine, on addition of D-aspartic acid, D-glutamic acid of D-glutamine, there results a preferred crystallization of L-asparagine monohydrate; inclusion of the L-additives leads to preferred crystallization of D-asparagine monohydrate. Further, we have found that addition of L-tyrosine (TYR), L-tyrosine-p-toluene sulfonate (TpTS), L-dopa, L-dopa-p-toluene sulfonate (DpTS), L-α-methyl dopa, L-α-methyl dopa-p-toluene sulfonate (MDpTS), L-phenylalanine (PHE), L-phenylalanine-p-toluene sulfonate (PpTS), L-phenyl glycine (PG), L-phenyl glycine p-toluene sulfonate (PGpTS), L-p-methoxy phenyl glycine (pMPG) or L-p-methoxy phenyl glycine p-toluene sulfonate (pMPGpTS) to a supersaturated solution of pHPGpTS in an 0.5N aqueous solution of p-toluene sulfonic acid causes preferred precipitation of the D-form of pHPGpTS. On acidification the corresponding enantiomer of p-hydroxyphenylglycine can be obtained. Inclusion of the D-additives causes preferred precipitation of the L-form of pHPGpTS.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04533506uspto-grants-1985_08