IP Library Patent Application 11578871
Patent Application
App. No. 11/578,871

Process of Preparing Esters and Ethers of Probucol and Derivatives Thereof

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
11/578,871
Abstract

The current patent application provides methods for manufacturing compounds of Formula I wherein all substituents are described herein.

Claims (109)

1 . A process of manufacturing a compound of Formula I or its ester or salt thereof,

wherein Z 1 , Z 2 , Z 3 , and Z 4 are independently selected from the group consisting of hydrogen and alkyl, said alkyl optionally substituted by hydroxy, alkyl, alkenyl, acyl, nitro, amino, halo, carboxy and cyano;

Z 5 and Z 6 are the same or different and independently selected from the group consisting of alkyl, alkenyl, and aryl all of which can be optionally substituted by hydroxy, alkyl, alkenyl, acyl, nitro, amino, halo, carboxy and cyano;

Z 5 and Z 6 can come together to form a carbocyclic ring;

M is selected from the group consisting of hydrogen, an optionally substituted unsaturated acyl having from 1 to 18 carbon atoms, and an optionally substituted saturated acyl having from 1 to 18 carbon atoms, said optionally substituted unsaturated acyl and optionally substituted saturated acyl optionally containing a polar or charged functionality; and

J is selected from the group consisting of an optionally substituted unsaturated acyl having from 1 to 18 carbon atoms and an optionally substituted saturated acyl having from 1 to 18 carbon atoms, said optionally substituted unsaturated acyl and optionally substituted saturated acyl optionally containing a polar or charged functionality;

the process comprising:

reacting a compound of Formula II

wherein Z 1 , Z 2 , Z 3 , Z 4 , Z 5 and Z 6 are as previously defined,

with a compound of Formula III,

wherein Y is R 2 or NR 2 % 5 ;

R 1 , R 2 , R 3 and R 4 and R 5 are independently selected from an optionally substituted C 1 -C 10 alkyl or an optionally substituted C 2 -C 10 alkenyl;

R 1 and R 2 can optionally come together to form a ring;

R 3 and R 4 can optionally come together to form a ring;

and a compound selected from the group consisting of a saturated or unsaturated acyl halide, saturated or unsaturated carboxylic acid anhydride and a saturated or unsaturated activated carboxylic acid ester, all of which may optionally be substituted by one or more substituents selected from the group consisting of protected hydroxy, alkyl, alkenyl, acyl, nitro, protected amino, amino, halo, protected carboxy and cyano; and

separating and isolating the compound of Formula I.

2 . The process of claim 1 to manufacture a compound of Formula IV or its ester or salt thereof,

wherein J is selected from the group consisting of an optionally substituted unsaturated acyl having from 1 to 18 carbon atoms and an optionally substituted saturated acyl having from 1 to 18 carbon atoms, said optionally substituted unsaturated acyl and optionally substituted saturated acyl optionally containing a polar or charged functionality;

the process comprising:

reacting a compound of Formula V

with a compound of Formula III,

wherein Y is R 2 or NR 2 R 5 ;

R 1 , R 2 , R 3 and R 4 and R 5 are independently selected from an optionally substituted C 1 -C 10 alkyl or an optionally substituted C 2 -C 10 alkenyl;

R 1 and R 2 can optionally come together to form a ring;

R 3 and R 4 can optionally come together to form a ring;

and a compound selected from the group consisting of a saturated or unsaturated acyl halide, saturated or unsaturated carboxylic acid anhydride and a saturated or unsaturated activated carboxylic acid ester, all of which may optionally be substituted by one or more substituents selected from the group consisting of protected hydroxy, alkyl, alkenyl, acyl, nitro, protected amino, amino, halo, protected carboxy and cyano; and

separating and isolating the compound of Formula IV.

3 . The process of claim 1 to manufacture a compound of Formula IV or its ester or salt thereof,

wherein J is selected from the group consisting of an optionally substituted unsaturated acyl having from 1 to 18 carbon atoms and an optionally substituted saturated acyl having from 1 to 18 carbon atoms, said optionally substituted unsaturated acyl and optionally substituted saturated acyl optionally containing a polar or charged functionality;

the process comprising:

reacting a compound of Formula V

with a compound of Formula VI,

wherein R 6 is selected from an optionally substituted C 1 -C 10 alkyl or an optionally substituted C 2 -C 10 alkenyl;

m is an integer selected from 1 to 7;

n is an integer selected from 1 to 7;

and a compound selected from the group consisting of a saturated or unsaturated acyl halide, saturated or unsaturated carboxylic acid anhydride and a saturated or unsaturated activated carboxylic acid ester, all of which may optionally be substituted by one or more substituents selected from the group consisting of protected hydroxy, alkyl, alkenyl, acyl, nitro, protected amino, amino, halo, protected carboxy and cyano; and

separating and isolating said compound of Formula IV.

4 . The process of claim 1 to manufacture a compound of Formula IV or its ester or salt thereof,

wherein J is selected from the group consisting of an optionally substituted unsaturated acyl having from 1 to 18 carbon atoms and an optionally substituted saturated acyl having from 1 to 18 carbon atoms, said optionally substituted unsaturated acyl and optionally substituted saturated acyl optionally containing a polar or charged functionality;

the process comprising:

reacting a compound of Formula V

with a compound of Formula VII,

wherein m is an integer selected from 1 to 7;

n is an integer selected from 1 to 7;

and a compound selected from the group consisting of a saturated or unsaturated acyl halide, saturated or unsaturated carboxylic acid anhydride and a saturated or unsaturated activated carboxylic acid ester, all of which may optionally be substituted by one or more substituents selected from the group consisting of protected hydroxy, alkyl, alkenyl, acyl, nitro, protected amino, amino, halo, protected carboxy and cyano; and

separating and isolating said compound of Formula IV.

5 . The process of claim 1 to manufacture a compound of Formula IV or its ester or salt thereof,

wherein J is selected from the group consisting of an optionally substituted unsaturated acyl having from 1 to 18 carbon atoms and an optionally substituted saturated acyl having from 1 to 18 carbon atoms, said optionally substituted unsaturated acyl and optionally substituted saturated acyl optionally containing a polar or charged functionality;

the process comprising:

reacting a compound of Formula V

with a compound of Formula VII,

wherein m is an integer selected from 1 to 7;

n is an integer selected from 1 to 7;

and a compound selected from the group consisting of succinic acid anhydride, glutaric acid anhydride, adipic acid anhydride, suberic acid anhydride, sebacic acid anhydride, azelaic acid anhydride, phthalic acid anhydride, maleic acid anhydride, and acetic acid anhydride, all of which may optionally be substituted by one or more substituents selected from the group consisting of protected hydroxy, alkyl, alkenyl, acyl, nitro, protected amino, halo, protected carboxy and cyano; and

separating and isolating said compound of Formula IV.

6 . The process of claim 1 to manufacture a compound of Formula VIII, IX or X or its ester or salt thereof,

the process comprising:

reacting a compound of Formula V

with a compound of Formula VII,

wherein m is an integer selected from 1 to 7;

n is an integer selected from 1 to 7;

and a compound selected from the group consisting of succinice acid anhydride, glutaric acid anhydride, and acetic acid anhydride, all of which may optionally be substituted by one or more substituents selected from the group consisting of protected hydroxy, alkyl, alkenyl, acyl, nitro, protected amino, halo, protected carboxy and cyano; and

separating and isolating said compound of Formula VIII, IX or X.

7 . The process of claim 1 to manufacture a compound of Formula VIII, IX or X or its ester or salt thereof,

the process comprising:

reacting a compound of Formula V

with a compound of Formula DBU or DBN,

and a compound selected from the group consisting of succinic acid anhydride, glutaric acid anhydride, and acetic acid anhydride, all of which may optionally be substituted by one or more substituents selected from the group consisting of protected hydroxy, alkyl, alkenyl, acyl, nitro, protected amino, halo, protected carboxy and cyano; and

separating and isolating said compound of Formula VIII, IX or X.

8 . The process of claim 1 to manufacture a compound of Formula VIII or its ester or salt thereof,

the process comprising:

reacting a compound of Formula V

with a compound of Formula DBU,

and succinic acid anhydride; and

separating and isolating said compound of Formula VIII.

9 . The process of claim 1 to manufacture a compound of Formula VIII or its ester or salt thereof,

the process comprising:

reacting a compound of Formula V

with a compound of Formula DBU,

and succinic acid anhydride;

and further comprising the addition of an alkaline carbonate; and

separating and isolating said compound of Formula VIII.

10 . A process for manufacturing a compound of Formula I or its ester or salt thereof,

wherein Z 1 , Z 2 , Z 3 , and Z 4 are independently selected from the group consisting of hydrogen and alkyl, said alkyl optionally substituted by hydroxy, alkyl, alkenyl, acyl, nitro, amino, halo, carboxy and cyano;

Z 5 and Z 6 are the same or different and independently selected from the group consisting of alkyl, alkenyl, and aryl all of which can be optionally substituted by hydroxy, alkyl, alkenyl, acyl, nitro, amino, halo, carboxy and cyano;

Z 5 and Z 6 can come together to form a carbocyclic ring;

M is selected from the group consisting of hydrogen, an optionally substituted unsaturated alkyl having from 1 to 10 carbon atoms, and an optionally substituted saturated alkyl having from 1 to 10 carbon atoms, said optionally substituted unsaturated alkyl and optionally substituted saturated alkyl optionally containing a polar or charged functionality; and

J is selected from the group consisting of an optionally substituted unsaturated alkyl having from 1 to 10 carbon atoms, and an optionally substituted saturated alkyl having from 1 to 10 carbon atoms, said optionally substituted unsaturated alkyl and optionally substituted saturated alkyl optionally containing a polar or charged functionality;

the process comprising:

reacting a compound of Formula II

wherein Z 1 , Z 2 , Z 3 , Z 4 , Z 5 and Z 6 are as previously defined,

with a compound of Formula III,

wherein Y is R 2 or NR 2 R 5 ;

R 1 , R 2 , R 3 and R 4 and R 5 are independently selected from an optionally substituted C 1 -C 10 alkyl or an optionally substituted C 2 -C 10 alkenyl;

R 1 and R 2 can optionally come together to form a ring;

R 3 and R 4 can optionally come together to form a ring;

and a compound selected the group consisting of a saturated or unsaturated alkyl halide, saturated or unsaturated alkyl-O-sulfonyl alkyl, a saturated or unsaturated alkyl-O-sulfonyl aryl, a saturated or unsaturated alkyl-O-acyl, and a saturated or unsaturated epoxide, all of which may optionally be substituted by one or more substituents selected from the group consisting of protected hydroxy, alkyl, alkenyl, acyl, nitro, protected amino, halo, protected carboxy, epoxide and cyano; and

separating and isolating the compound of Formula I.

11 . The process of claim 10 to manufacture a compound of Formula IV or its ester or salt thereof,

wherein J is selected from the group consisting of an optionally substituted unsaturated alkyl having from 1 to 10 carbon atoms, and an optionally substituted saturated alkyl having from 1 to 10 carbon atoms, said optionally substituted unsaturated alkyl and optionally substituted saturated alkyl optionally containing a polar or charged functionality;

the process comprising:

reacting a compound of Formula V

with a compound of Formula III,

wherein Y is R 1 or NR 2 R 5 ;

R 1 , R 2 , R 3 and R 4 and R 5 are independently selected from an optionally substituted C 1 -C 10 alkyl or an optionally substituted C 2 -C 10 alkenyl;

R 1 and R 2 can optionally come together to form a ring;

R 3 and R 4 can optionally come together to form a ring;

and a compound selected from the group consisting of a saturated or unsaturated alkyl halide, saturated or unsaturated alkyl-O-sulfonyl alkyl, a saturated or unsaturated alkyl-O-sulfonyl aryl, a saturated or unsaturated alkyl-O-acyl, and a saturated or unsaturated epoxide, all of which may optionally be substituted by one or more substituents selected from the group consisting of protected hydroxy, alkyl, alkenyl, acyl, nitro, protected amino, halo, protected carboxy, epoxide and cyano; and

separating and isolating the compound of Formula IV.