# US 11,299,558 B2 · Process for the preparation of low molecular weight heparin

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- Number: US 11,299,558 B2
- Document ID: US11299558B2
- Status: Granted
- Kind: B2
- Application number: 16/771,098
- Filed: 2018-12-11
- Published: 2021-06-24
- Granted: 2022-04-12
- Earliest claimed: 2017-12-11
- Assignees: Biological E Limited
- Applicants: Biological E Limited
- Inventors: Manohar Sarma Vedula; Sreedhar Kosgi; Narender Dev Mantena; Ratnakar Aryasomayajula
- Web page: https://patentgrep.com/patent/US11299558B2

## CPC

- C08B 37/0078: {Degradation products}
- C08B: POLYSACCHARIDES; DERIVATIVES THEREOF (polysaccharides containing less than six saccharide radicals attached to each other by glycosidic linkages C07H; fermentation or enzyme-using processes C12P19/00; sugar industry C13; production of cellulose D21)

## Abstract

The present invention provides an improved process for the preparation of Enoxaparin sodium. The process is simple, commercially viable and industrially advantageous.

## Claims

### Claim 1

A process for the preparation of Enoxaparin sodium, comprising the steps of:
a) salifying heparin sodium with benzethonium chloride to form benzethonium heparinate,
b) reacting the benzethonium heparinate obtained in step (a) with benzyl chloride in an inert solvent to form a crude heparin benzyl ester,
c) adding water to the reaction mixture containing the crude heparin benzyl ester obtained in step (b) at a temperature of 0° C. to room temperature to obtain a precipitate of heparin benzyl ester,
d) adding an alcoholic solution of sodium acetate to the reaction mixture containing the precipitate of heparin benzyl ester obtained in step (c) to isolate the heparin benzyl ester sodium salt,
e) depolymerizing the heparin benzyl ester sodium salt obtained in step (d) with sodium hydroxide to produce crude Enoxaparin sodium,
f) bleaching the crude Enoxaparin sodium obtained in step (e) at a pH of about 9-10 to obtain a decolorized Enoxaparin sodium, and
g) purifying the decolorized Enoxaparin sodium.

### Claim 2 (depends on 1)

The process as claimed in claim 1, wherein the inert solvent is selected from N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMA) and methylene chloride.

### Claim 3 (depends on 1)

The process as claimed in claim 1, wherein the ratio of benzethonium heparinate, inert solvent and benzyl chloride ranges from 1:2:1 to 1:6:1 by weight.

### Claim 4 (depends on 1)

The process as claimed in claim 1, wherein the addition of water to the reaction mixture containing the crude heparin benzyl ester obtained in step (b) is carried out at a temperature of 10° C. to 25° C. for 15 minutes to 4 hours.

### Claim 5 (depends on 1)

The process as claimed in claim 1, wherein the depolymerization is carried out by treating the heparin benzyl ester sodium salt with an aqueous solution of the sodium hydroxide at a temperature of 50° C. to 70° C. for 30 minutes to 3 hours.

### Claim 6 (depends on 5)

The process as claimed in claim 5, wherein the ratio of sodium hydroxide to heparin benzyl ester sodium salt is from 0.05 to 0.2 by weight.

### Claim 7 (depends on 1)

The process as claimed in claim 1, wherein the bleaching is carried out using 30% hydrogen peroxide.

### Claim 8 (depends on 1)

The process as claimed in claim 1, wherein the decolorized Enoxaparin sodium is purified by dissolving it in water, adding sodium chloride, and precipitating with alcohol.

### Claim 9 (depends on 8)

The process as claimed in claim 8, wherein the purified Enoxaparin sodium is subjected to lyophilization to obtain Enoxaparin sodium in powder form.

### Claim 10 (depends on 9)

The process as claimed in claim 9, wherein the lyophilization is carried out by dissolving the pure Enoxaparin sodium in a mixture of water and alcohol.

### Claim 11 (depends on 10)

The process as claimed in claim 10, wherein the alcohol is selected from a group comprising methanol, ethanol, isopropanol and a mixture thereof.

### Claim 12 (depends on 9)

The process as claimed in claim 9, wherein the lyophilization is carried out in a mixture of water and ethanol.

### Claim 13 (depends on 10)

The process as claimed in claim 10, wherein water and alcohol are present at a concentration of 85 to 95% (v/v) and 5 to 15% (v/v) respectively.