US 11,884,619 B2
Reagents and methods for esterification
Ronald T. Raines, Madison, WI (US); and Nicholas McGrath, Fairmont, MN (US)
Assigned to Wisconsin Alumni Research Foundation, Madison, WI (US)
Filed by Wisconsin Alumni Research Foundation, Madison, WI (US)
Filed on Jul. 8, 2021, as Appl. No. 17/370,829.
Application 17/370,829 is a continuation of application No. 16/780,237, filed on Feb. 3, 2020, granted, now 11,091,423, issued on Aug. 17, 2021.
Application 16/780,237 is a continuation of application No. 14/212,381, filed on Mar. 14, 2014, granted, now 10,577,303, issued on Mar. 3, 2020.
Claims priority of provisional application 61/783,385, filed on Mar. 14, 2013.
Prior Publication US 2022/0055979 A1, Feb. 24, 2022
This patent is subject to a terminal disclaimer.
Int. Cl. C07C 67/18 (2006.01); C07C 245/12 (2006.01)
CPC C07C 67/18 (2013.01) [C07C 245/12 (2013.01)] 20 Claims
 
1. A method for esterification of one or more carboxylic acid groups in a compound containing one or more carboxylic acid groups which comprises the step of reacting the one or more compounds with a diazo-compound of formula:

OG Complex Work Unit Chemistry
wherein the R1 and R2 groups of the diazo compound are selected such that the corresponding organic compound of formula:

OG Complex Work Unit Chemistry
exhibits a —C—H pKa value between 18 and 29 as measured in DMSO;
wherein the one or more esters formed are bio-reversible;
wherein the reaction is carried out in buffered aqueous solvent at a pH between 5 and 7, in the absence of catalyst;
wherein the compound containing the one or more carboxylic acid groups is not an amino acid; and
wherein:
R1 comprises an electron withdrawing group selected from nitro, cyano, halogen, ammonium (—NR′3+), aryloxy, alkoxy, sulfonic ester (—SO2—R′), sulfonium (—S(R′)2+), phosphonium (—P(R′)3+), —COOR′, —COR′, —CON(R′)2, —OCOR′, alkylthio, arylthio, aryl, —C≡CR′, and —C═CR′2, where each R′ independently, is hydrogen, or an optionally substituted alky, alkenyl, alkynyl, aryl, alkylaryl, or arylalkyl, where two R′ on the same atom may together with that atom form a 5- to 8-member carbocyclic or heterocyclic ring in which one or more ring atoms can be replaced with —CO—, —O—, —CS—, —S— or —NR—, where R is hydrogen or an alkyl group having 1-3 carbon atoms; and
R2 is selected from the group consisting of an alkyl, aryl, alkyl aryl, heteroaryl, and heterocyclic group, each of which is optionally substituted.