IP Library Granted Patent US 8,524,892
Granted Patent B2
US 8,524,892 · App. 13/488,658 · Granted Sep 3, 2013

Methods and intermediates for the synthesis of porphyrins

Inventors: Jonathan S. Lindsey (Raleigh, NC); Masahiko Taniguchi (Raleigh, NC); Dazhong Fan (Raleigh, NC)
Assignee: North Carolina State University
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Quick Facts
Patent No.
US 8,524,892
App. No.
13/488,658
Granted
Sep 3, 2013
Kind
B2
Abstract

A method of making a porphyrin is carried out by: (a) condensing (i) a 1,9-bis(N,N-)dialkylaminomethyl)dipyrromethane of Formula II: with (ii) a dipyrromethane to produce a reaction product; then (b) oxidizing the reaction product; and then (c) optionally demetallating said reaction product to produce the porphyrin. The reaction is particularly useful for making substituted porphyrins with a wide range of substituents at the A and/or B (the 5 and/or 15) positions.

Claims (14)

1. A method of making a compound of Formula II:

wherein:

R a and R b are each independently loweralkyl;

R 1 is H, alkyl or aryl;

R 2 , R 3 , R 4 , and R 5 are each independently selected from the group consisting of H, halo, loweralkoxy, and loweralkylthio; and

A is selected from the group consisting of H, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloalkylalkenyl, cycloalkylalkynyl, aryl, arylalkyl, arylalkenyl, arylalkynyl, alkoxy, halo, mercapto, azido, cyano, hydroxyl, nitro, acyl, alkoxy, alkylthio, amino, alkylamino, arylalkylamino, disubstituted amino, acylamino, acyloxy, amide, sulfonamide, urea, alkoxylacylamino, aminoacyloxy, hydrophilic groups, surface attachment groups, cross-coupling groups and bioconjugatable groups; said method comprising:

reacting a dipyrromethane of Formula IV:

wherein A, R 2 , R 3 , R 4 and R 5 are as given above with an N,N-dialkylmethylammonium halide of Formula V:

wherein R a , R b and R 1 are as given above, and X is halo;

in a polar or nonpolar aprotic solvent selected from the group consisting of methylene chloride, chloroform, tetrahydrofuran, nitromethane, toluene, acetonitrile, and mixtures thereof at a temperature of from room temperature to 100° C. to produce said compound of Formula II.

2. The method of claim 1 , wherein A is a surface attachment group, cross-coupling group or bioconjugatable group.

3. The method of claim 2 , wherein A is an alkene, alkyne, alcohol, thiol, selenyl, phosphono, carboxylic acid, formyl, halo or amine group.

4. The method of claim 1 , wherein R 1 , R 3 , R 4 , and R 5 are each independently selected from the group consisting of H and halo.

5. The method of claim 1 , wherein R 2 , R 3 , R 4 , and R 5 are each H.

Assignments (1)
CONFIRMATORY LICENSE Recorded Sep 4, 2015
From: NORTH CAROLINA STATE UNIVERSITY RALEIGH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036556/0303 →
Continuity (4)
Division 13014914 · Jan 27, 2011
Division 12361715 · Jan 29, 2009
Division 11192934 · Jul 29, 2005
Related Publication 20120253052A1 · Oct 4, 2012