IP Library Granted Patent US 6,977,292
Granted Patent B2
US 6,977,292 · App. 10/332,454 · Granted Dec 20, 2005

Nucleophile-stable thioester generating compounds, methods of production and use

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Quick Facts
Patent No.
US 6,977,292
App. No.
10/332,454
Granted
Dec 20, 2005
Kind
B2
Abstract

The invention is directed to nucleophile-stable thioester generating compounds comprising a carboxyester thiol. The compounds have wide applicability in organic synthesis, including the generation of peptide-, polypeptide- and other polymer-thioesters. The invention is particularly useful for generating activated-thioesters from precursors that are made under conditions in which strong nucleophiles are employed, such as peptides or polypeptides made using Fmoc SPPS, as well as multi-step ligation or conjugation schemes that require (or benefit from the use of) compatible selective approaches for directing a specific ligation or conjugation reaction of interest.

Claims (23)

1. A nucleophile-stable carboxyester thiol of the formula X—C(O)—O—CH(R″)—(CH 2 ) n —S—R′″, where X is a target molecule of interest comprising an amine protected with one or more nucleophile-labile protecting groups, R″ is hydrogen or a non-nucleophile stable group, n is 1 or 2, and R′″ is hydrogen, a protecting group, or an acid-, reductive-, or light-labile linker attached to a resin or protecting group that is removable under non-nucleophilic conditions.

2. The nucleophile-stable carboxyester thiol of claim 1 , wherein said amine is present on a moiety selected from the group consisting of an amino acid, peptide and polypeptide.

3. The nucleophile-stable carboxyester thiol of claim 1 , wherein said nucleophile-cleavable protecting group is Fmoc.

4. The nucleophile-stable carboxyester thiol of claim 1 , wherein R″ is selected from the group consisting of hydrogen, methyl, aliphatic, branched aliphatic, heteroatom, carbonyl, benzyl, substituted benzyl, nitrile, sulfoxy, and sulfone.

5. The nucleophile-stable carboxyester thiol of claim 1 , wherein R′″ is selected from the group consisting of hydrogen, aryl, benzyl, and alkyl.

6. The nucleophile-stable carboxyester thiol of claim 1 , wherein R″ or R′″ is covalently attached to a nucleophile-stable linker.

7. The nucleophile-stable carboxyester thiol of claim 6 , wherein said linker is covalently attached to a nucleophile-stable resin.

8. A nucleophile-stable thioester-generating resin comprising a carboxyester thiol.

9. The nucleophile-stable thioester-generating resin of claim 8 , which comprises the formula X—C(O)—O—CH(R″)—(CH 2 ) n —S-linker-resin or X—C(O)—O—CH(R″-linker-resin)-(CH 2 ) n —S—R′″, where X is a target molecule of interest comprising one or more nucleophile-labile protecting groups, R″ is hydrogen or a non-nucleophile stable group, n is 1 or 2, and R′″ is hydrogen, protecting group or an acid, reductive, or light labile linker attached to a resin or protecting group that is removable under non-nucleophilic conditions, and where said linker and resin are nucleophile-stable.

10. A nucleophile-stable carboxyester thiol of the formula X—C(O)—O—CH(R″)—(CH 2 ) n —S—R′″, where X is a target molecule of interest comprising one or more nucleophile-labile protecting groups, R″ is hydrogen or a non-nucleophile stable group, n is 1 or 2, and R′″ is hydrogen, a protecting group, or an acid-, reductive-, or light-labile linker attached to a resin or protecting group that is removable under non-nucleophilic conditions, wherein said nucleophile-labile protecting group is Fmoc.

11. The nucleophile-stable carboxyester thiol of claim 10 wherein the target molecule of interest X comprises an amine present on a moiety selected from the group consisting of an amino acid, peptide and polypeptide.

12. The nucleophile-stable carboxyester thiol of claim 10 , wherein R″ is selected from the group consisting of hydrogen, methyl, aliphatic, branched aliphatic, heteroatom, carbonyl, benzyl, substituted benzyl, nitrile, sulfoxy, and sulfone.

13. The nucleophile-stable carboxyester thiol of claim 10 wherein R′″ is selected from the group consisting of hydrogen, aryl, benzyl, and alkyl.

14. The nucleophile-stable carboxyester thiol of claim 10 , wherein R″ or R′″ is covalently attached to a nucleophile-stable linker.

15. The nucleophile-stable carboxyester thiol of claim 14 , wherein said linker is covalently attached to a nucleophile-stable resin.

16. A nucleophile-stable carboxyester thiol of the formula X—C(O)—O—CH(R″)—(CH 2 ) n —S—R′″, where X is a target molecule of interest comprising one or more nucleophile-labile protecting groups, R″ is hydrogen or a non-nucleophile stable group, n is 1 or 2, and R′″ is hydrogen, a protecting group, or an acid-, reductive-, or light-labile linker attached to a resin or protecting group that is removable under non-nucleophilic conditions, wherein R″ is covalently attached to a nucleophile-stable linker, and wherein the linker is covalently attached to a nucleophile-stable resin.

17. The nucleophile-stable carboxyester thiol of claim 16 wherein the target molecule of interest X comprises an amine present on a moiety selected from the group consisting of an amino acid, peptide and polypeptide.

18. The nucleophile-stable carboxyester thiol of claim 16 wherein R″ is selected from the group consisting of hydrogen, methyl, aliphatic, branched aliphatic, heteroatom, carbonyl, benzyl, substituted benzyl, nitrile, sulfoxy, and sulfone.

19. The nucleophile-stable carboxyester thiol of claim 16 , wherein R′″ is selected from the group consisting of hydrogen, aryl, benzyl, and alkyl.

20. A nucleophile-stable carboxyester thiol of the formula X—C(O)—O—CH(R″)—(CH 2 ) n —S—R′″, where X is a target molecule of interest comprising one or more nucleophile-labile protecting groups, R″ is hydrogen or a non-nucleophile stable group, n is 1 or 2, and R′″ is hydrogen, a protecting group, or an acid-, reductive-, or light-labile linker attached to a resin or protecting group that is removable under non-nucleophilic conditions, wherein R′″ is covalently attached to a nucleophile-stable linker, and wherein the linker is covalently attached to a nucleophile-stable resin.

21. The nucleophile-stable carboxyester thiol of claim 20 wherein the target molecule of interest X comprises an amine present on a moiety selected from the group consisting of an amino acid, peptide and polypeptide.

22. The nucleophile-stable carboxyester thiol of claim 20 , wherein R″ is selected from the group consisting of hydrogen, methyl, aliphatic, branched aliphatic, heteroatom, carbonyl, benzyl, substituted benzyl, nitrile, sulfoxy, and sulfone.

23. The nucleophile-stable carboxyester thiol of claim 20 , wherein R′″ is selected from the group consisting of hydrogen, aryl, benzyl, and alkyl.

Assignments (4)
AMYLIN PHARMACEUTICALS, LLC ASSIGNS AN EQUAL AND UNDIVIDED ONE-HALF OF ITS ENTIRE RIGHT, TITLE AND INTEREST TO ASTRAZENECA PHARMACEUTICALS LP Recorded Oct 26, 2012
From: AMYLIN PHARMACEUTICALS, LLC
To: ASTRAZENECA PHARMACEUTICALS LP
Reel/Frame 029195/0555 →
CHANGE OF NAME Recorded Oct 25, 2012
From: AMYLIN PHARMACEUTICALS, INC.
To: AMYLIN PHARMACEUTICALS, LLC
Reel/Frame 029198/0340 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 19, 2006
From: GRYPHON THERAPEUTICS, INC.
To: AMYLIN PHARMACEUTICALS, INC.
Reel/Frame 017038/0657 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2003
From: BOTTI, PAOLO; BRADBURNE, JAMES A.; KENT, STEPHEN B.H.
To: GRYPHON THERAPEUTICS, INC.
Reel/Frame 013996/0401 →