IP Library Granted Patent US 10,252,999
Granted Patent B2
US 10,252,999 · App. 15/844,889 · Granted Apr 9, 2019

Process for preparing alkyl esters of 4-(5-(bis(2-hydroxyethyl)amino-1-methyl-1H-benzo[D]imidazol-2-yl)butyric acid

View Patent ↗
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 10,252,999
App. No.
15/844,889
Granted
Apr 9, 2019
Kind
B2
Abstract

An alkyl ester of 4-(5-(bis(2-hydroxyethyl)amino)-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid, such as ethyl 4-(5-(bis(2-hydroxyethyl)amino)-1-methyl-1H-benzo[d]imidazol-2-yl)butanoate, is obtained by reacting an alkyl ester of 4-(5-amino-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid with 2-hydroxyacetaldehyde under reducing conditions.

Claims (10)

1. A method of producing an alkyl ester of 4-(5-(bis(2-hydroxyethyl)amino)-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid, comprising reacting an alkyl ester of 4-(5-amino-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid with glycolaldehyde dimer under acidic reducing conditions.

2. A method of producing an alkyl ester of 4-(5-(bis(2-hydroxyethyl)amino)-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid, comprising reacting an alkyl ester of 4-(5-amino-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid with glycolaldehyde dimer in a reaction medium comprised of organic solvent, a glycolaldehyde dimer dissociation catalyst and a reducing agent, wherein the glycolaldehyde dimer dissociation catalyst is selected from the group consisting of 2-hydroxypyridine and an acid, wherein the acid is selected from the group consisting of acetic acid, trifluoroacetic acid, formic acid, propionic acid, butyric acid, benzoic acid, and glutaric acid, and a combination of the acids.

3. The method of claim 2 , wherein the solvent is dichloromethane.

4. The method of claim 2 , wherein the glycolaldehyde dimer dissociation catalyst is an acid, wherein the acid is selected from the group consisting of acetic acid, trifluoroacetic acid, formic acid, propionic acid, butyric acid, benzoic acid, and glutaric acid, and a combination of the acids.

5. The method of claim 2 , wherein the reducing agent is a borohydride or combination of borohydrides.

6. The method of claim 2 , wherein the reducing agent is sodium cyanoborohydride or sodium triacetoxyborohydride.

7. The method of claim 2 , wherein the reaction is carried out by the glycolaldehyde dimer being added incrementally to the reaction medium.

8. The method of claim 2 , wherein the reaction is carried out by the glycolaldehyde dimer and the reducing agent being added incrementally to the reaction medium.

9. The method of claim 2 , wherein the alkyl ester of 4-(5-amino-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid is a C1 to C6 branched or straight chain alkyl ester of 4-(5-amino-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid.

10. The method of claim 2 , wherein the alkyl ester of 4-(5-amino-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid is an ethyl or isopropyl ester of 4-(5-amino-1-methyl-1H-benzo[d]imidazol-2-yl)butyric acid.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2022
From: JOHNSON MATTHEY PUBLIC LIMITED COMPANY
To: MACFARLAN SMITH LIMITED
Reel/Frame 061888/0166 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2022
From: FU, XING; MATHARU, SAROOP SINGH
To: JOHNSON MATTHEY PUBLIC LIMITED COMPANY
Reel/Frame 059377/0661 →