Method for preparing 5-amino-benzoyl-benzofuran derivatives

Patent metadata

Field	Value
Publication number	US-9499507-B2
Application number	US-201214361562-A
Country	US
Kind code	B2
Filing date	Nov 28, 2012
Priority date	Nov 29, 2011
Publication date	Nov 22, 2016
Grant date	Nov 22, 2016

Abstract

The invention relates to a method for preparing 5-amino-benzoyl-benzofuran derivatives having the general formula in which R 1 is hydrogen or an alkyl or aryl group and R 2 is hydrogen, an alkyl, alkoxy or dialkylaminoalkoxy group. According to the invention, the compounds having formula I are prepared by hydrogenating a 5-nitro-benzofuran derivative having the general formula in which R 1 and R 2 have the same meaning as above in the presence of palladized charcoal as a catalyst and in an ether or a mixture of ether as a solvent, thus forming the desired compounds.

First claim

The invention claimed is:

1. A process for the preparation of 5-amino-benzoyl-benzofuran compounds of formula:

in which R 1 represents hydrogen or an alkyl or aryl group and R 2 represents hydrogen or an alkyl, alkoxy or dialkylaminoalkoxy group, comprising hydrogenating a 5-nitrobenzofuran compound of formula:

in which R 1 and R 2 have the same meanings as above, in the presence of a palladium-on-charcoal catalyst and in a solvent comprising an ether or a mixture of ethers.

2. A process for the preparation of sulfonamidobenzofuran compounds of formula:

or a pharmaceutically acceptable salt thereof, in which R 1 represents hydrogen or an alkyl or aryl group, R 2 represents hydrogen or an alkyl, alkoxy or dialkylaminoalkoxy group and R 3 represents an alkyl or aryl group, comprising:
a) hydrogenating a 5-nitrobenzofuran compound of formula:

in which R 1 and R 2 have the same meanings as above, in the presence of a palladium-on-charcoal catalyst and in a solvent comprising an ether or a mixture of ethers to form a reaction medium comprising a 5-amino-benzoyl-benzofuran compound, in the free base form, of formula:

in which R 1 and R 2 have the same meanings as above,
b) treating said reaction medium with a halide of formula:
Hal-SO 2 R 3   IV

in which Hal represents a halogen and R 3 has the same meaning as above, in the presence of a basic agent, and forming the sulfonamidobenzofuran compound of formula III in the free base form, and optionally reacting the formed compound with an organic or inorganic acid in order to form a pharmaceutically acceptable salt thereof.

3. The process as claimed in claim 1 , wherein:
R 1 represents a linear or branched C 1 -C 8 alkyl group or a phenyl group, and
R 2 represents a linear or branched C 1 -C 8 alkyl group, a linear or branched C 1 -C 8 alkoxy group or a dialkylaminoalkoxy group in which each linear or branched alkyl group is a C 1 -C 8 alkyl group and the linear or branched alkoxy group is a C 1 -C 8 alkoxy group.

4. The process as claimed in claim 1 , wherein:
R 1 represents a linear or branched C 1 -C 4 alkyl group, and
R 2 represents a linear or branched C 1 -C 4 alkyl group, a linear or branched C 1 -C 4 alkoxy group or a dialkylaminoalkoxy group in which each linear or branched alkyl group is a C 1 -C 4 alkyl group and the linear or branched alkoxy group is a C 1 -C 4 alkoxy group.

5. The process as claimed in claim 1 wherein R 1 represents n-butyl, and R 2 represents 3-[di(n-butyl)amino]propoxy.

6. The process as claimed in claim 1 wherein the ether is a dialkyl ether, a cyclic ether or a mixture thereof.

7. The process as claimed in claim 6 , wherein the dialkyl ether is methyl tert-butyl ether and the cyclic ether is tetrahydrofuran.

8. The process as claimed in claim 1 wherein the catalyst, which consists of palladium-on-charcoal having a water content, is used in a proportion of from 1% to 10% by weight relative to the weight of compound of formula II.

9. The process as claimed in claim 8 , wherein the palladium-on-charcoal having a water content is used in the form of a suspension in water.

10. The process as claimed in claim 1 wherein the hydrogenation takes place at a temperature ranging from ambient temperature to 50-60° C.

11. The process as claimed in claim 1 wherein the hydrogenation takes place under a pressure of from 0.1 to 5 bar.

12. The process as claimed in claim 1 wherein 2-(n-butyl)-3-(4-{3-[di(n-butyl)amino]propoxy}benzoyl)-5-nitrobenzofuran is hydrogenated in the presence of palladium-on-charcoal as catalyst and in methyl tert-butyl ether, tetrahydrofuran or a mixture of methyl tert-butyl ether and tetrahydrofuran as solvent, to form 2-(n-butyl)-3-(4-{3-[di(n-butyl)amino]propoxy}benzoyl)-5-aminobenzofuran in the free base form.

13. A reaction medium, comprising:
a) a 5-nitrobenzofuran compound of formula:

in which R 1 represents hydrogen or an alkyl or aryl group and R 2 represents hydrogen or an alkyl, alkoxy or dialkylaminoalkoxy group,
b) palladium-on-charcoal, and
c) an ether or a mixture of ethers, as solvent.

14. The reaction medium as claimed in claim 13 , wherein R 1 represents n-butyl and R 2 represents 3-[di(n-butyl)amino]propoxy.

15. The process as claimed in claim 2 , wherein:
R 1 represents a linear or branched C 1 -C 8 alkyl group or a phenyl group,
R 2 represents a linear or branched C 1 -C 8 alkyl group, a linear or branched C 1 -C 8 alkoxy group or a dialkylaminoalkoxy group in which each linear or branched alkyl group is a C 1 -C 8 alkyl group and the linear or branched alkoxy group is a C 1 -C 8 alkoxy group, and
R 3 represents a linear or branched C 1 -C 8 alkyl group or a phenyl group.

16. The process as claimed in claim 2 wherein:
R 1 represents a linear or branched C 1 -C 4 alkyl group,
R 2 represents a linear or branched C 1 -C 4 alkyl group, a linear or branched C 1 -C 4 alkoxy group or a dialkylaminoalkoxy group in which each linear or branched alkyl group is a C 1 -C 4 alkyl group and the linear or branched alkoxy group is a C 1 -C 4 alkoxy group, and
R 3 represents a linear or branched C 1 -C 4 alkyl group.

17. The process as claimed in claim 2 , wherein R 1 represents n-butyl, R 2 represents 3-[di(n-butyl)amino]propoxy and R 3 represents methyl.

18. The process as claimed in claim 2 wherein the ether is a dialkyl ether, a cyclic ether or a mixture thereof.

19. The process as claimed in claim 18 , wherein the dialkyl ether is methyl tert-butyl ether and the cyclic ether is tetrahydrofuran.

20. The process as claimed in claim 2 wherein the catalyst, which consists of palladium-on-charcoal having a water content, is used in a proportion of from 1% to 10% by weight relative to the weight of compound of formula II.

21. The process as claimed in claim 20 , wherein the palladium-on-charcoal having a water content is used in the form of a suspension in water.

22. The process as claimed in claim 2 wherein the hydrogenation takes place at a temperature ranging from ambient temperature to 50-60° C.

23. The process as claimed in claim 2 wherein the hydrogenation takes place under a pressure of from 0.1 to 5 bar.

24. The process as claimed in claim 2 wherein 2-(n-butyl)-3-(4-{3-[di(n-butyl)amino]propoxy}benzoyl)-5-nitrobenzofuran is hydrogenated in the presence of palladium-on-charcoal as catalyst and in methyl tert-butyl ether, tetrahydrofuran or a mixture of methyl tert-butyl ether and tetrahydrofuran as solvent, to form 2-(n-butyl)-3-(4-{3-[di(n-butyl)amino]propoxy}benzoyl)-5-aminobenzofuran in the free base form.

25. The process as claimed in claim 2 wherein said sulfonamidobenzofuran compound is 2-(n-butyl)-3-(4-{3-[di(n-butyl)amino]propo

Assignees

• Sanofi Sa

Inventors

• Bon Xavier
• Delepine Jean-Louis
• Jourdin Laure
• Largeau Denis
• Vayron Philippe

Classifications

• C07D307/82

  with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring · CPC title

• C07D307/80 Primary

  Radicals substituted by oxygen atoms · CPC title