Synthesis and use of croconaine compounds

Patent metadata

Field	Value
Publication number	US-9353092-B2
Application number	US-201414311267-A
Country	US
Kind code	B2
Filing date	Jun 21, 2014
Priority date	Jun 27, 2013
Publication date	May 31, 2016
Grant date	May 31, 2016

Abstract

The present disclosure provides compositions and methods for the synthesis and use of croconaine compounds. The disclosed compounds are easily prepared from croconic acid. A halothiophene is reacted with an alkanolamine, the resulting aminothiophene is modified by appending a desired functional group to the hydroxyl group, and the modified aminothiophene is reacted with croconic acid to form the final compound. Applications of such croconaine compounds include photothermal imaging, photothermal therapy, light-activated drug release, and tissue welding.

First claim

What is claimed is:

1. A compound of formula (I):

wherein:
R 1 and R 2 are the same and are selected from selected from the group consisting of heteroaryl, alkoxy, aryloxy, and a first reactive group; and
R 3 and R 4 are the same and are selected from the group consisting of —H, alkyl, substituted alkyl, arylalkyl, aryl, substituted aryl, heteroaryl, and a second reactive group;
wherein the first reactive group and the second reactive group are each independently

wherein Q is alkyl, Y is aryl, X is halo, and the wavy line indicates the point of attachment to R 1 , R 2 , R 3 or R 4 ;
or wherein R 1 and R 3 taken together form a substituted 5- or 6-membered ring, wherein the ring is substituted with a first reactive group;
or wherein R 2 and R 4 taken together form a substituted 5- or 6-membered ring, wherein the ring is substituted with a first reactive group, and when R 1 and R 3 taken together form a substituted 5- or 6-membered ring, R 2 and R 4 are taken together form a substituted 5- or 6-membered ring, and R 1 and R 3 taken together and R 2 and R 4 taken together are the same;
or a pharmaceutically acceptable salt, optical isomer, geometric isomer or tautomer thereof.

2. The compound of claim 1 , wherein said first reactive group is —O—CH 2 —C≡CH.

3. The compound of claim 2 , wherein said second reactive group is —O—CH 2 —C≡CH.

4. A compound selected from the group consisting of:
compound (1)

or a pharmaceutically acceptable salt, optical isomer, geometric isomer or tautomer thereof.

5. The compound of claim 1 wherein R 1 is a first reactive group or tetrazole.

6. The compound of claim 5 wherein the first reactive group is —O—CH 2 —C≡CH.

7. The compound of claim 5 wherein R 2 is a first reactive group or tetrazole.

8. The compound of claim 7 ; wherein the first reactive group is —O—CH 2 —C≡CH.

9. The compound of claim 1 wherein R 1 and R 2 are both reactive groups.

10. The compound of claim 1 wherein R 3 and R 4 are both ethyl, benzyl, or second reactive groups.

11. The compound of claim 1 wherein the compound of formula (I) is compound (1):

or a pharmaceutically acceptable salt, geometric isomer, or tautomer thereof.

12. A process of making a compound of formula (I):

wherein:
R 1 and R 2 are the same and are selected from the group consisting of —H, alkyl, substituted alkyl, arylalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, carboxylic acid, alkoxy, aryloxy, amino, dialkylamino, triazole, alkyl hydroxysuccinimide ester, alkyl maleimide, alkyl isothiocyanate, alkyl azide, alkyl alkyne, alkyl haloacetamido, aryl ester, aryl hydroxysuccinimide ester, aryl maleimide, aryl isothiocyanate, aryl azide, aryl alkyne, aryl haloacetamido, alkoxy hydroxysuccinimide ester, alkoxy maleimide, alkoxy isothiocyanate, alkoxy azide, —O—CH 2 —C≡CH, alkoxy haloacetamido, aryloxy ester, aryloxy hydroxysuccinimide ester, aryloxy maleimide, aryloxy isothiocyanate, aryloxy azide, aryloxy alkyne, and aryloxy haloacetamido;
R 3 and R 4 are the same and are selected from the group consisting of —H, alkyl, substituted alkyl, arylalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, carboxylic acid, alkyl hydroxysuccinimide ester, alkyl maleimide, alkyl isothiocyanate, alkyl azide, alkyl alkyne, alkyl haloacetamido, aryl ester, aryl hyroxysuccinimide ester, aryl maleimide, aryl isothiocyanate, aryl azide, aryl alkyne, and aryl haloacetamido;
or wherein R 1 and R 3 taken together form an optionally substituted 5- or 6-membered ring;
or wherein R 2 and R 4 taken together form an optionally substituted 5- or 6-membered ring;
or a pharmaceutically acceptable salt, optical isomer, geometric isomer or tautomers thereof,
comprising contacting croconic acid with a compound of formula (II),

under conditions suitable for producing the photothermal compound of formula (I),
wherein:
R 1 , R 2 , R 3 , and R 4 are as defined for formula (I).

13. The process as in claim 12 , wherein said conditions suitable for producing the croconaine compound include heating to 120-130° C.

14. The process as in claim 12 , wherein said conditions suitable for producing the croconaine compound include heating for 45-75 minutes.

15. The process as in claim 12 , further comprising the steps of contacting a compound of formula (III),

wherein:
R 3 and R 4 are each independently selected from the group consisting of —H, alkyl, substituted alkyl, arylalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, carboxylic acid, alkyl hydroxysuccinimide ester, alkyl maleimide, alkyl isothiocyanate, alkyl azide, alkyl alkyne, alkyl haloacetamido, aryl ester, aryl hydroxysuccinimide ester, aryl maleimide, aryl isothiocyanate, aryl azide, aryl alkyne, and aryl haloacetamido;
with a compound of formula (IV),
Cl—R 1 or 2   (IV)

wherein:
R 1 and R 2 are each independently selected from the group consisting of —H, alkyl, substituted alkyl, arylalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, carboxylic acid, alkoxy, aryloxy, amino, dialkylamino, triazole, alkyl hydroxysuccinimide ester, alkyl maleimide, alkyl isothiocyanate, alkyl azide, alkyl alkyne, alkyl haloacetamido, aryl ester, aryl hydroxysuccinimide ester, aryl maleimide, aryl isothiocyanate, aryl azide, aryl alkyne, aryl haloacetamido, alkoxy hydroxysuccinimide ester, alkoxy maleimide, alkoxy isothiocyanate, alkoxy azide, alkoxy alkyne, alkoxy haloacetamido, aryloxy ester, aryloxy hydroxysuccinimide ester, aryloxy maleimide, aryloxy isothiocyanate, aryloxy azide, aryloxy alkyne, and aryloxy haloacetamido;
under conditions suitable to form a compound of formula (II),

wherein:

R 1 , R 2 , R 3 , and R 4 are defined for formulas (III) and (IV).

16. The process as in claim 15 , wherein the conditions suitable to form a compound of formula (II) include stirring at room temperature for 24-48 hours.

17. The process as in claim 15 , further comprising the steps characterized by contacting a compound of formula (V),

wherein:
X is a halogen atom,

with a compound of formula (VI),

wherein:
R 3 , and R 4 are each independently selected from the group consisting of —H, alkyl, substituted alkyl, arylalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, carboxylic acid, alkyl hydroxysuccinimide ester, alkyl maleimide, alkyl isothiocyanate, alkyl azide, alkyl alkyne, alkyl haloacetamido, aryl ester, aryl hydroxysuccinimide ester, aryl maleimide,

Assignees

• Univ Notre Dame Du Lac

Inventors

• Smith Bradley

Classifications

• C07D409/08

  linked by a carbon chain containing alicyclic rings · CPC title

• C07D409/14 Primary

  containing three or more hetero rings · CPC title