Method for preparing apremilast

Patent metadata

Field	Value
Publication number	US-10781173-B2
Application number	US-201716313732-A
Country	US
Kind code	B2
Filing date	Jun 30, 2017
Priority date	Jun 30, 2016
Publication date	Sep 22, 2020
Grant date	Sep 22, 2020

Abstract

Provided is a method for preparing apremilast of formula I. Method one: (S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethylamine N-acetyl-L-leucine salt of formula II is reacted with 3-acetylaminophthalic anhydride of formula III in an aprotic solvent to produce the compound of formula I; method two: (S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethylamine N-acetyl-L-leucine salt of formula II is reacted with 3-acetylaminophthalic anhydride of formula III in an organic solvent in the presence of an organic alkali or an alkali metal hydride to produce the compound of formula I. The method for preparing apremilast requires inexpensive raw materials and reagents, is suitable for industrial production, and has great economic effects.

First claim

The invention claimed is:

1. A preparation method for apremilast represented by formula I, comprising the following methods:
method one: (S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethylamine N-acetyl-L-leucine salt of formula II is reacted with 3-acetylaminophthalic anhydride of formula III in an aprotic solvent to obtain the compound of formula I, wherein the aprotic solvent is selected from the group consisting of acetonitrile, tetrahydrofuran, 1,4-dioxane, N,N-dimethylformamide, N,N-dimethylacetamide, N-methylpyrrolidone, toluene, nitrobenzene, 1,2-dichlorobenzene and xylene or any combinations thereof;
method two: (S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethylamine N-acetyl-L-leucine salt of formula II is reacted with 3-acetylaminophthalic anhydride of formula III in an organic solvent in the presence of an organic alkali or an alkali metal hydride to obtain the compound of formula I, wherein the organic solvent is selected from the group consisting of acetonitrile, toluene, xylene, ethyl acetate, isopropyl acetate, N,N-dimethylformamide, N,N-dimethylacetamide or a mixture thereof;
wherein the reaction equation is as follows:

2. The preparation method according to claim 1 , wherein the aprotic solvent of the method one is selected from the group consisting of acetonitrile, toluene, xylene, N,N-dimethylformamide and N-methylpyrrolidone or any combinations thereof.

3. The preparation method according to claim 1 , wherein for the method one, the mass to volume ratio of the compound of formula II to the aprotic solvent is 1:(3-10) g/mL.

4. The preparation method according to claim 1 , wherein
the reaction of the method one is carried out within the temperature range of 40° C.-150° C.

5. The preparation method according to claim 1 , wherein
the reaction time of the method one is controlled within the range of 12-24 hours.

6. The preparation method according to claim 1 , wherein the organic solvent of the method two is selected from the group consisting of acetonitrile, ethyl acetate, toluene, isopropyl acetate and N,N-dimethylformamide or any combinations thereof.

7. The preparation method according to claim 1 , wherein the organic alkali of the method two is selected from the group consisting of triethylamine, sodium methoxide and sodium hydride.

8. The preparation method according to claim 1 , wherein for the method two, the molar ratio of the amount of the compound of formula II to the amount of the organic alkali is 1:(0.1-4), and the molar ratio of the amount of the compound of formula II to the amount of the alkali metal hydride is 1:(1-3).

9. The preparation method according to claim 1 , wherein the reaction of the method two is carried out within the temperature range of 40° C.-120° C.; the reaction time being controlled within the range of 2-24 hours.

10. The preparation method according to claim 2 , wherein the aprotic solvent of the method one is selected from the group consisting of acetonitrile.

11. The preparation according to claim 4 , wherein the reaction of the method one is carried out within the temperature range of 75° C.-80° C.

12. The preparation method according to claim 6 , wherein the organic solvent of the method two is selected from the group consisting of acetonitrile, ethyl acetate, toluene and N,N-dimethylformamide or any combinations thereof.

13. The preparation method according to claim 9 , wherein the reaction of the method two is carried out within the temperature range of 40° C.-90° C.; the reaction time being controlled within the range of 12-18 hours.

Assignees

• Zhejiang Huahai Pharm Co Ltd

Inventors

• Du Xiaoqiu
• Zhou Lianchao
• Liu Jiegen

Classifications

• C07C317/28

  with sulfone or sulfoxide groups bound to acyclic carbon atoms of the carbon skeleton · CPC title

• C07C315/04

  by reactions not involving the formation of sulfone or sulfoxide groups · CPC title

• C07D209/46

  with an oxygen atom in position 1 · CPC title

• C07C45/63

  by introduction of halogen; by substitution of halogen atoms by other halogen atoms · CPC title

• C07C49/84

  containing ether groups, [IMAGE cpc-sch-C07C-0958.gif] groups,[IMAGE cpc-sch-C07C-0959.gif] groups, or[IMAGE cpc-sch-C07C-0960.gif] groups · CPC title