CYCLIC DIPEPTIDES AS FEED ADDITIVES

• US 20110295006A1
• Filed: 05/26/2011
• Published: 12/01/2011
• Est. Priority Date: 05/27/2010
• Status: Abandoned Application

• Current Assignee: Evonik Degussa GmbH
• Original Assignee: Evonik Degussa GmbH
• Inventors: HAEUSSNER, Thomas, KOBLER, Christoph, WECKBECKER, Christoph
• Application Number:
  US13/116,823
• Publication Number:
  US 20110295006A1
• Time in Patent Office: Days
• US Class Current: 544/357
• CPC Class Codes: A23K 20/105 Aliphatic or alicyclic compounds
• CPC Class Codes: A23K 20/147 Polymeric derivatives, e.g. peptides or proteins
• CPC Class Codes: A23K 50/10 for ruminants
• CPC Class Codes: A23K 50/80 for aquatic animals, e.g. fish, crustaceans or molluscs
• CPC Class Codes: A61P 1/00 Drugs for disorders of the alimentary tract or the digestive system
• CPC Class Codes: C07D 241/08 with oxygen atoms directly attached to ring carbon atoms

Abstract

Feed additives containing essential amino acids which are diketopiperazines of formulas (IV) or (V) or salts thereof are provided:

In formulas (IV) and (V), R¹ and R² may be an amino acid residue such as methionine, lysine, threonine, tryptophan, histidine, valine, leucine, isoleucine, phenylalanine, arginine, and cysteine, and may optionally be the same residue.

Additionally provided are the diketopiperazines of formulas (IV) and (V) and a method to for their production.

Claims

1. A feed additive, comprising:

at least one diketopiperazine of formula (IV) or a salt thereof;

2. The feed additive according to claim 1, wherein

R¹ or R² is a methionyl residue (R=—

(CH₂)₂SCH₃), and

a configuration of the structure is at least one selected from the group consisting of a DD-, a LL-, a LD- and a DL-configuration.

3. The feed additive according to claim 1, wherein

a configuration of the diketopiperazine of formula (IV) is at least one selected from the group consisting of a cyclo-D-EAA-D-EAA, a cyclo-L-EAA-D-EAA, a cyclo-D-EAA-L-EAA and a cyclo-L-EAA-L-EAA, and

EAA is an amino acid selected from the group consisting of methionine, lysine, threonine, tryptophan, histidine, valine, leucine, isoleucine, phenylalanine, arginine, cysteine and cystine.

4. The feed additive according to claim 3, wherein the diketopiperazine of formula (IV) is a diastereomeric mixture of cyclo-DL-EAA-DL-EAA.

5. The feed additive according to claim 1, wherein

R¹ and R² are both a methionyl residue (R=—

(CH₂)₂SCH₃), and

the diketopiperazine of formula (IV) is in the DD-, LL-, DL- or LD-configuration or a mixture thereof,

with the proviso that the diketopiperazine with the LL-configuration is only present in a mixture with at least one other configuration.

6. The feed additive according to claim 5, wherein

the diketopiperazine of formula (IV) is a diastereomeric mixture comprising DD/LL-cyclo-Met-Met and meso-cyclo-Met-Met, where Met is methionine.

7. A feed mixture, comprising at least one feed additive according to claim 1.

8. The feed mixture according to claim 7, further comprising:

at least one substance selected from the group consisting of DL-methionine, L-EAA, DL-EAA, DD/LL/DL/LD-methionyl-EAA, DD/LL/DL/LD-EAA-methionine, DD/LL-methionyl-EAA, DD/LL-EAA-methionine, D-methionyl-L-EAA, L-methionyl-L-EAA, D-methionyl-D-EAA, L-methionyl-D-EAA, D-EAA-L-methionine, L-EAA-L-methionine, D-EAA-D-methionine and L-EAA-D-methionine.

9. The feed mixture according to claim 7, further comprising:

DL-methionine; and

at least one substance selected from the group consisting of L-EAA, DL-EAA, DD/LL/DL/LD-methionyl-EAA, DD/LL/DL/LD-EAA-methionine, DD/LL-methionyl-EAA, DD/LL-EAA-methionine, D-methionyl-L-EAA, L-methionyl-L-EAA, D-methionyl-D-EAA, L-methionyl-D-EAA, D-EAA-L-methionine, L-EAA-L-methionine, D-EAA-D-methionine and L-EAA-D-methionine;

wherein a proportion of DL-methionine is from 0.01 to 90 wt. %.

10. The feed mixture according to claim 7, further comprising:

DL-methionine;

a L-EAA and

at least one substance selected from the group consisting of DL-EAA, DD/LL/DL/LD-methionyl-EAA, DD/LL/DL/LD-EAA-methionine, DD/LL-methionyl-EAA, DD/LL-EAA-methionine, D-methionyl-L-EAA, L-methionyl-L-EAA, D-methionyl-D-EAA, L-methionyl-D-EAA, D-EAA-L-methionine, L-EAA-L-methionine, D-EAA-D-methionine and L-EAA-D-methionine;

wherein a proportion of the DL-methionine is from 0.01 to 90 wt. % and a proportion of the L-EAA is from 0.01 to 90 wt. %.

11. A diketopiperazine or a salt thereof, of formula (IV):

12. The diketopiperazine according to claim 11, wherein a configuration of the diketopiperazine of formula (IV) is at least one selected from the group consisting of cyclo-D-EAA-D-EAA, cyclo-L-EAA-D-EAA, cyclo-D-EAA-L-EAA, cyclo-L-EAA-L-EAA,

wherein EAA is an amino acid selected from the group consisting of methionine, lysine, threonine, tryptophan, histidine, valine, leucine, isoleucine, phenylalanine, arginine, cysteine and cystine.

13. The diketopiperazine according to claim 11, wherein a configuration of the diketopiperazine of formula (IV) is a diastereomeric mixture of cyclo-DL-EAA-DL-EAA.

14. The diketopiperazine according to claim 11, wherein R¹ and R² are both a methionyl residue (R=—

(CH₂)₂SCH₃), and

the diketopiperazine of formula (IV) is in the DD-, LL-, DL- or LD-configuration or a mixture thereof, with the proviso that the diketopiperazine with the LL configuration is only present mixed with other configurations.

15. The diketopiperazine according to claim 14, wherein the diketopiperazine of formula (IV) is a mixture of DD/LL-cyclo-Met-Met and meso-cyclo-Met-Met.

16. A feed additive for ruminants, fresh or salt water fishes and crustaceans comprising the diketopiperazine or salt thereof according to claim 11.

17. A method of production of a diketopiperazine of formula (IV) or a salt thereof:

18. The method according to claim 17, wherein the amino acid ester of formula (III) is obtained by esterification of an amino acid of formula (I):

19. The method according to claim 18, wherein the esterification is carried out in the presence of a strong acid.

20. The method according to claim 19, wherein the strong acid is HCl or H₂SO₄.

21. The method according to claim 17, wherein R′

is selected from the group consisting of methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, and benzyl.

22. The method according to claim 17, wherein a temperature of the reaction of the amino acid ester to form the diketopiperazine is from 30 to 220°

C.

23. The method according to claim 17, further comprising removing the compound of formula II by distillation.

24. The method according to claim 17, wherein the reaction of the amino acid ester to obtain the diketopiperazine takes place in absence of a transamidation catalyst.

25. The method according to claim 17, wherein a purity of the obtained diketopiperazine is greater than 50 wt. % as determined according to HPLC.

26. The method according to claim 17, further comprising:

recovering amino acid ester not reacted; and

recycling the recovered amino acid ester to the process.

27. The method according to claim 17, further comprising:

recovering the compound of formula (III); and

recycling the compound to a process for preparing the ester of formula (I).

28. Method according to claim 17, wherein a compound of formula R′

—

OH not completely converted in the esterification of the amino acid to the amino acid ester and/or obtained again in the conversion of the amino acid ester to the diketopiperazine is recovered and returned to the process.