IP Library Granted Patent US 9,382,193
Granted Patent B2
US 9,382,193 · App. 14/583,850 · Granted Jul 5, 2016

Processes for forming amide bonds and compositions related thereto

Inventors: Lanny S. Liebeskind (Atlanta, GA); Wenting Wu (Decatur, GA); Zhihui Zhang (New Berlin, WI); Hao Li (Decatur, GA); Angus A. Lamar (Atlanta, GA)
Assignee: Emory University
C07C231/02C07C233/07C07C233/65C07C233/69C07D213/82C07D233/90C07D295/192C07D307/52C07F7/1852C07F7/1856C07H1/00C07H21/02C07K1/003C07K1/02C07K5/0606C07K5/06026C07K5/06034C07K5/06078C07K5/06086C07K5/06104C07K5/0812
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Quick Facts
Patent No.
US 9,382,193
App. No.
14/583,850
Granted
Jul 5, 2016
Kind
B2
Abstract

The disclosure relates to methods for producing amide bonds and reagents related thereto. In some embodiments, the disclosure relates to methods of producing an amide comprising mixing an O-silylated thionoester and an amine under conditions such that an amide is formed. In another embodiment, the disclosure relates to mixing a thiolacid, a silylating agent, and an amine under conditions such that an amide is formed.

Claims (10)

1. A method of making a compound with an amide bond comprising mixing an O-silylated thionoester and a primary or secondary amine under conditions such that an amide is formed.

2. The method of claim 1 , wherein the method further comprises the step of providing the O-silylated thionoester by mixing a compound with a thiolacid group, and a silylating agent under conditions such that an O-silylated thionoester is formed.

3. The method of claim 2 , wherein the silylating agent is selected from the group consisting of trimethylsilanecarbonitrile, bis(trimethylsilyl)acetamide, and phenylchlorosilane.

4. The method of claim 2 , wherein the method further comprises the step of providing a compound with a thiolacid group by i) mixing a compound with a carboxylic acid group and a coupling reagent providing an activated carboxylic acid and ii) mixing the activated carboxylic acid and a thiol nucleophile providing a compound with at thiolacid group.

5. The method of claim 4 , wherein the coupling reagent is selected from the group consisting of dicyclohexylcarbodiimide or isopropyl chlorocarbonate.

6. The method of claim 4 , wherein the thiol nucleophile is selected from the group consisting of sodium hydrogen sulfide and trimethylsilyl thiol.

7. The method of claim 4 , wherein the compound with a carboxylic acid group is an amino acid.

8. The method of claim 1 , wherein the method further comprises the step of providing the O-silylated thionoester by mixing a compound with a carboxylic acid group, disulfide, and a phosphine under conditions such that an O-silylated thionoester is formed.

9. The method of claim 8 , wherein the disulfide is bis trimethylsilyl disulfide.

10. The method of claim 8 , wherein the compound with a carboxylic acid group is an amino acid.

Assignments (1)
CONFIRMATORY LICENSE Recorded Apr 6, 2015
From: EMORY UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 035367/0549 →
Continuity (3)
Division 13280991 · Oct 25, 2011
Provisional Application 61407089 · Oct 27, 2010
Related Publication 20150315129A1 · Nov 5, 2015