# US 10,118,924 B2 · Process for the preparation of Apixaban and intermediates thereof

> Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt

- Number: US 10,118,924 B2
- Document ID: US10118924B2
- Status: Granted
- Kind: B2
- Application number: 15/696,758
- Filed: 2017-09-06
- Published: 2018-04-12
- Granted: 2018-11-06
- Earliest claimed: 2014-09-05
- Assignees: Unichem Laboratories Ltd
- Applicants: Unichem Laboratories Limited
- Inventors: Dhananjay G. Sathe; Arijit Das; Yashwant Surve; Ramdas N. Ahire
- Web page: https://patentgrep.com/patent/US10118924B2

## CPC

- C07D 471/04: Ortho-condensed systems
- C07D 211/86: Oxygen atoms
- C07D: HETEROCYCLIC COMPOUNDS (macromolecular compounds C08)

## Abstract

The present invention refers to novel process for the preparation of Apixaban. Further, the invention also related to a process for the preparation of intermediate of Apixaban from very basic and cheap row material i.e. Aniline which is widely commercially available. The present invention provides process for preparation of Apixaban using a different sequence of synthetic steps and does not involve use of Ullmann reaction.

## Claims

### Claim 1

A process for preparation of compound of formula (21) comprising steps of;
a. reacting aniline with a compound of formula (22) in presence of an inorganic base or aqueous solution of inorganic base or absence of any base optionally in presence of a phase transfer catalyst to obtain a compound of formula (24), wherein X is a leaving group;
b. optionally isolating the compound of formula (24);
c. cyclizing the compound of formula (24) in presence of an inorganic base or aqueous solution of the inorganic base optionally in presence of a phase transfer catalyst to obtain compound of formula (21)

### Claim 2 (depends on 1)

The process according to claim 1, wherein the inorganic base is selected from the group consisting of sodium carbonate, potassium carbonate, lithium carbonate, lithium hydroxide, sodium hydroxide, potassium hydroxide, ammonium hydroxide, lithium hydrate, potassium hydrate, sodium hydrate, lithium hydrogen carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, and mixture(s) thereof.

### Claim 3 (depends on 1)

The process according to claim 1, wherein step (a) and step (c) are carried out in presence of a solvent selected from the group consisting of methylene dichloride (MDC), toluene, ethyl acetate, methyl acetate, CHCl3, chlorobenzene, dimethylformamide (DMF), dimethylacetamide, N-methylpyrrolidone, acetonitrile, dimethyl sulfoxide, tetrahydrofuran (THF), dioxane and mixture(s) thereof.

### Claim 4 (depends on 1)

The process according to claim 1, wherein the phase transfer catalyst is selected from the group consisting of methyltridecyl ammonium chloride, trimethyl ammonium chloride, tetrabutyl ammonium bromide, dimethylethylhexadecyl ammonium bromide, ethyltripentyl ammonium iodide, benzyltrimethylammonium chloride, and hexadecyltributylphosphonium bromide.

### Claim 5 (depends on 1)

The process according to claim 1, wherein the leaving group is selected from the group consisting of Cl, Br, I, F, mesylate, triflate, tosylate and tert-butyldimethylsilyloxy group.

### Claim 6

A process for preparation of compound of formula (10) comprising steps of;
a. reacting aniline with a compound of formula (22) in presence of an inorganic base or aqueous solution of the inorganic base or absence of any base optionally in presence of a phase transfer catalyst to obtain a compound of formula (24), wherein X is a leaving group;
b. optionally isolating the compound of formula (24);
c. cyclizing the compound of formula (24) in presence of an inorganic base or aqueous solution of the inorganic base optionally in presence of a phase transfer catalyst to obtain a compound of formula (21);
d. optionally isolating compound of formula (21);
e. nitrating the compound of formula (21) with nitric acid in sulphuric acid or acetic acid to obtain compound of formula (10)

### Claim 7 (depends on 6)

The process according to claim 6, wherein the inorganic base is selected from the group consisting of sodium carbonate, potassium carbonate, lithium carbonate, lithium hydroxide, sodium hydroxide, potassium hydroxide, ammonium hydroxide, lithium hydrate, potassium hydrate, sodium hydrate, lithium hydrogen carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, and mixture(s) thereof.

### Claim 8 (depends on 6)

The process according to claim 6, step (a) and step (c) are carried out in presence of a solvent selected from the group consisting of methylene dichloride (MDC), toluene, ethyl acetate, methyl acetate, CHCl3, chlorobenzene, dimethylformamide (DMF), dimethylacetamide, N-methylpyrrolidone, acetonitrile, dimethyl sulfoxide, tetrahydrofuran (THF), dioxane and mixture(s) thereof.

### Claim 9 (depends on 6)

The process according to claim 6, wherein the phase transfer catalyst is selected from the group consisting of methyltridecyl ammonium chloride, trimethyl ammonium chloride, tetrabutyl ammonium bromide, dimethylethylhexadecyl ammonium bromide, ethyltripentyl ammonium iodide, benzyltrimethylammonium chloride, and hexadecyltributylphosphonium bromide.

### Claim 10 (depends on 6)

The process according to claim 6, wherein the leaving group is selected from the group consisting of Cl, Br, I, F, mesylate, triflate, tosylate and tert-butyldimethylsilyloxy group.