Reaktion #531898

ord-df13b387e7ea40b7a4e7d23944febddd

Reaktionsgleichung

NC(=O)[C@H](N)CCC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)O
H-D-iGlu-D-Trp-OH
NC(=O)[C@H](N)CCC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)O
D-isoglutamyl-D-tryptophan
Cl
HCl
COC(C)(C)C
tert-butyl methyl ether
Cl
HCl
NC(=O)[C@H](N)CCC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)O
D-isoglutamyl-D-tryptophan
Cl
HCl
ClCCl
dichloromethane
N[C@H](CCC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)O)C(=O)O
thymodepressin
NC(=O)[C@H](N)CCC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)O
H-D-iGlu-D-Trp-OH
NC(=O)[C@H](N)CCC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)O
D-isoglutamyl-D-tryptophan

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeH-D-Glu-(γ-D-Trp-OR2)-α-OR1 precipitates out of dichloromethane
  2. 2
    Sonstigecan be removed by filtration
  3. 3
    workup.ADDITIONTreatment of the acid addition salt with a metal hydroxide in an inert solvent such as methanol
  4. 4
    Sonstigefor one phase homogeneous hydrolysis
  5. 5
    Sonstigeaffords
  6. 6
    ExtraktionUpon extraction of the reaction mixture with a water immiscible solvent such as ethyl acetate or tert-butyl methyl ether
  7. 7
    Sonstigethe solution is evaporated
  8. 8
    workup.ADDITIONthe base addition salt (in mono carboxylate form) of H-D-iGlu-D-Trp-OH

Vorschrift

A solution of the base addition salt of D-isoglutamyl-D-tryptophan is prepared by the acid deprotection of the dipeptide Boc-D-Glu-(γ-D-Trp-OR2)-α-OR1, wherein each of R1 and R2 is independently selected from the group consisting of benzyl and C1-C4 alkyl. For example, HCl deprotection of Boc-D-Glu-(γ-D-Trp-OR2)-α-OR1 in an inert solvent such as dichloromethane, affords the HCl salt of H-D-Glu-(γ-D-Trp-OR2)-α-OR1. For the combination where R1 is benzyl and R2 is methyl, the product HCl.H-D-Glu-(γ-D-Trp-OR2)-α-OR1 precipitates out of dichloromethane and can be removed by filtration. Treatment of the acid addition salt with a metal hydroxide in an inert solvent such as methanol for one phase homogeneous hydrolysis or with tert-butyl methyl ether for two phase hydrolysis affords H-D-iGlu-D-Trp-OH base addition salt in solution. Upon extraction of the reaction mixture with a water immiscible solvent such as ethyl acetate or tert-butyl methyl ether, the aqueous phase is neutralized to pH of about 6 to about 7 and the solution is evaporated to reduced the volume to an estimated ratio of less than about 1 part solute:8 parts water. The solute, as predicted by the speciation calculations as shown in FIG. 8, is the base addition salt (in mono carboxylate form) of H-D-iGlu-D-Trp-OH. If sodium hydroxide is used as the metal hydroxide, the solute will be the mono sodium form of the H-D-iGlu-D-Trp-OH in water. Adjustment of this solution to pH of about 2.5 to about 3.0 will result in the precipitation of solid thymodepressin, H-D-iGlu-D-Trp-OH.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08476235B2uspto-grants-2013_07