Nitric esters of derivatives of the 2-(2,6-di-halo-phenylamino) phenylacetic acid and process for their preparation

Claim 2

Derivatives of the 2-(2,6-di-halo-phenylamino)phenylacetic acid, characterized in that they lave the following general formula: ##STR9## wherein: A and B are selected among hydrogen, linear or branched, substituted or non substituted alkyl chains, X is halogen selected among chlorine and bromine, Y is selected among oxygen, NH, NR 1 , wherein R 1 is a linear or branched alkyl group, and n is comprised between 1 and 10.

Claim 3

A derivative of the 2-(2,6-di-halophenylamino)phenylacetic acid according to claim 1, characterized in that X is chlorine, A and B are hydrogen, Y is oxygen and n is equal to 4.

Claim 4

A derivative of the 2-(2,6-di-halophenylamino)phenylacetic acid according to claim 1, characterized in that X is chlorine, A and B are hydrogen, Y is oxygen and n is equal to 2.

Claim 5

A derivative of the 2-(2,6-di-halophenylamino)phenylacetic acid according to claim 1, characterized in that X is chlorine, A and B are hydrogen, Y is NH and n is equal to 4.

Claim 6

A process for the preparation of a derivative of 2-(2,6-di-halo-phenylamino) phenylacetic acid, having the following formula (I): ##STR10## wherein: A and B are selected among hydrogen, linear and branched, substituted and non-substituted alkyl chains, X is halogen selected among chlorine and bromine, Y is selected among oxygen, NH, NR 1 , wherein R 1 is a linear or branched alkyl group and n is comprised between 1 and 10, comprising: reaction between the sodium salt of the 2-(2,6-di-halo-phenylamino)phenylacetic acid or of the 2-(2,6-di-halo-phenylamino)phenylacetic acid functionalized to the carboxylic group, with a compound having the following formula (IV): ##STR11## wherein: R 4 is selected among chlorine, bromine, NHR in which R is hydrogen or linear or branched alkyl chain, A and B are selected among hydrogen, linear or branched, substituted or non-substituted alkyl chains, R 3 is selected among chlorine, bromine and iodine, and n is comprised between 1 and 10, the carboxylic group of the 2-(2,6-di-halo-phenylamino)phenylacetic acid being functionalized as acylic chloride, or anhydride, obtaining in this way the corresponding monomer ester or the corresponding amide; reaction of said monomer ester or said amide with a nitrating agent, obtaining in this way nitric esters of derivatives of the 2-(2,6-di-halo-phenylamino)phenylacetic acid (I).

Claim 7

A process for the preparation of a derivative of 2-(2,6-di-halo-phenylamino) phenylacetic acid, having the following formula (I): ##STR10## wherein: A and B are selected among hydrogen, linear and branched, substituted and non-substituted alkyl chains, X is halogen selected among chlorine and bromine, Y is selected among oxygen, NH, NR 1 , wherein R 1 is a linear or branched alkyl group and n is comprised between 1 and 10, comprising: reaction between the sodium salt of the 2-(2,6-di-halo-phenylamino)phenylacetic acid or of the 2-(2,6-di-halo-phenylamino)phenylacetic acid functionalized to the carboxylic group, with a compound having the following formula (IV): ##STR11## wherein: R 4 is selected among chlorine, bromine, NHR in which R is hydrogen or linear or branched alkyl chain, A and B are selected among hydrogen, linear or branched, substituted or non-substituted alkyl chains, R 3 is selected among chlorine, bromine and iodine, and n is comprised between 1 and 10, the carboxylic group of the 2-(2,6-di-halo-phenylamino)phenylacetic acid being functionalized as acylic chloride, or anhydride, obtaining in this way the corresponding monomer ester or the corresponding amide; reaction of said monomer ester or said amide with a nitrating agent, obtaining in this way nitric esters of derivatives of the 2-(2,6-di-halo-phenylamino)phenylacetic acid (I).

Claim 8

Process for the preparation of a derivative of a 2- ( 2,6-di-halophenylamino)phenylacetic acid, having the following formula (I): ##STR12## wherein: A and B are selected among hydrogen, linear and branched, substituted and non-substituted alkyl chains, X is a halogen selected among chlorine and bromine, Y is selected among oxygen, NH, NR 1 , wherein R 1 is a linear or branched alkyl group and n is comprised between 1 and 10, comprising: reaction between the sodium salt of the 2-(2,6-di-halo-phenylamino)phenylacetic acid or of the 2-(2,6-di-halo-phenylamino)phenylacetic acid functionalized carboxylic group, with a compound having the following formula (V): ##STR13## wherein: R 4 is selected among chlorine, bromine, NHR in which R is hydrogen or linear or branched alkyl chain, A and B are selected among hydrogen, linear or branched, substituted or non-substituted alkyl chains, and n is comprised between 1 and 10, the carboxylic group of the 2-(2,6-di-halo-phenylamino)phenylacetic acid being functionalized as acylic chloride, or anhydride, obtaining the corresponding monomer ester or the corresponding amide; reaction of said monomer ester or said amide with a halogenating compound, obtaining in this way said monomer ester or said amide, having a terminal halogen group; reaction of said monomer ester or said amide having a terminal halogen group with a nitrating agent, obtaining in this way nitric esters of derivatives of the 2-(2,6-di-halo-phenylamino)phenylacetic acid (I).

Claim 9

Process for the preparation of a derivative of a 2- ( 2,6-di-halophenylamino)phenylacetic acid, having the following formula (I): ##STR12## wherein: A and B are selected among hydrogen, linear and branched, substituted and non-substituted alkyl chains, X is a halogen selected among chlorine and bromine, Y is selected among oxygen, NH, NR 1 , wherein R 1 is a linear or branched alkyl group and n is comprised between 1 and 10, comprising: reaction between the sodium salt of the 2-(2,6-di-halo-phenylamino)phenylacetic acid or of the 2-(2,6-di-halo-phenylamino)phenylacetic acid functionalized carboxylic group, with a compound having the following formula (V): ##STR13## wherein: R 4 is selected among chlorine, bromine, NHR in which R is hydrogen or linear or branched alkyl chain, A and B are selected among hydrogen, linear or branched, substituted or non-substituted alkyl chains, and n is comprised between 1 and 10, the carboxylic group of the 2-(2,6-di-halo-phenylamino)phenylacetic acid being functionalized as acylic chloride, or anhydride, obtaining the corresponding monomer ester or the corresponding amide; reaction of said monomer ester or said amide with a halogenating compound, obtaining in this way said monomer ester or said amide, having a terminal halogen group; reaction of said monomer ester or said amide having a terminal halogen group with a nitrating agent, obtaining in this way nitric esters of derivatives of the 2-(2,6-di-halo-phenylamino)phenylacetic acid (I).

Claim 10

A pharmaceutical composition comprising an effective therapeutic amount of a derivative of a 2-(2,6-di-halo-phenylamino)phenylacetic acid according to claim 1; and an inert, non-toxic, pharmacologically acceptable carrier.

Claim 11

A therapeutic method for treating rheumatic diseases in a warm-blooded animal comprising administering to said warm-blooded animal an effective amount of a derivative of a 2-(2,6-di-halo-phenylamino) phenylacetic acid according to claim 1.

Claim 12

A therapeutic method for treating cardiovascular illnesses in a warm-blooded animal comprising administering to said warm-blooded animal an effective amount of a derivative of a 2-(2,6-di-halo-phenylamino) phenylacetic acid according to claim 1.

Claim 13

A therapeutic method for treating miocardial and brain ischemiae in a warm-blooded animal comprising administering to said warm-blooded animal an effective amount of a derivative of a 2-(2,6-di-halo-phenylamino) phenylacetic acid according to claim 1.

Claim 14

A therapeutic method for treating arterial thrombosis in a warm-blooded animal comprising administering to said warm-blooded animal an effective amount of a derivative of a 2-(2,6-di-halo-phenylamino) phenylacetic acid according to claim 1.

Claim 15

The process as claimed in claim 5, wherein said nitrating agent is AgNO 3 .

Claim 16

The process as claimed in claim 6, wherein said halogenating compound is PBr 3 .

Claim 17

The process as claimed in claim 6, wherein said nitrating agent is AgNO 3 .