Granted Patent B2

US 12,509,416 · App. 18/409,063 · Granted Dec 30, 2025

Inventors: Salvatore Demartis (Milan, IT); Francesca Viti (Salorino, CH); Marie McNulty (Dublin, IE)

Assignee: Nogra Pharma Limited

C07C231/10C07C201/12C07C205/56C07C227/04C07C231/02C07C231/18C07C233/54C07C303/28

Abstract

Claims (36)

1 . A process for preparing a substantially optically pure compound of Formula (VII):

the process comprising:

reacting a compound of Formula (I):

with an activating agent, in the presence of an amine base, to form an intermediate of Formula (I-A):

wherein LG is a leaving group;

treating the intermediate of Formula (I-A) with a base solution in the presence of an alcohol solvent, to eliminate the leaving group and thereby forming an intermediate of Formula (I-B):

hydrolyzing the intermediate of Formula (I-B) to form a compound of Formula (IV):

hydrogenating the compound of Formula (IV) to form a compound of Formula (V):

resolving the compound of Formula (V) to form a substantially optically pure compound of Formula (VI):

and

acylating the compound of Formula (VI) to form the compound of Formula (VII), wherein the substantially optically pure compound of Formula (VII) is at least 95% of the enantiomer:

expressed as a percentage of both enantiomers.

2 . The process of claim 1 , wherein reacting a compound of Formula (I) with an activating agent comprises reacting in the presence of a solvent selected from the group consisting of toluene, dichloromethane, tetrahydrofuran, diethyl ether, 2-methyltetrahydrofuran, and acetonitrile.

3 . The process of claim 2 , wherein the solvent is toluene.

4 . The process of claim 1 , wherein the amine base is selected from the group consisting of triethylamine, N,N-diisopropylethylamine, and pyridine.

5 . The process of claim 4 , wherein the amine base is triethylamine.

6 . The process of claim 1 , wherein the activating agent is a sulfonylating agent, or a halogenating agent.

7 . The process of claim 1 , wherein the activating agent is selected from the group consisting of methanesulfonyl chloride, p-toluenesulfonyl chloride, p-bromobenzenesulfonyl chloride, phenyl triflimide, triflic anhydride, and nonafluorobutanesulfonic anhydride.

8 . The process of claim 1 , wherein the activating agent is methanesulfonyl chloride.

9 . The process of claim 1 , wherein the leaving group is selected from the group consisting of —OSO 2 -aryl, —OSO 2 —C 1-4 alkyl, chloro, bromo, and iodo; wherein C 1-4 alkyl and aryl may be optionally substituted with one or more substituents each independently selected, for each occurrence, from the group consisting of fluoro, bromo, and —CH 3 .

10 . The process of claim 9 , wherein the leaving group is —OSO 2 -phenyl or —OSO 2 —C 1-4 alkyl.

11 . The process of claim 1 , wherein the leaving group is —OSO 2 Me.

12 . The process of claim 1 , wherein the alcohol solvent comprises methanol.

13 . The process of claim 1 , wherein the base solution comprises sodium hydroxide.

14 . The process of claim 1 , wherein hydrolyzing the intermediate of Formula (I-B) to form a compound of Formula (IV) comprises:

(i) contacting the intermediate of Formula (I-B) with an alkali hydroxide and water; and

(ii) neutralizing to form the compound of Formula (IV).

15 . The process of claim 1 , wherein hydrogenating the compound of Formula (IV) to form a compound of Formula (V) comprises contacting the compound of Formula (IV) with hydrogen and a catalyst.

16 . The process of claim 1 , wherein resolving the compound of Formula (V) to form a substantially optically pure compound of Formula (VI) comprises:

(a) resolving a compound of Formula (V) in the presence of a chiral acid thereby forming a chiral salt of the compound of Formula (VI); and

(b) neutralizing the chiral salt of the compound of Formula (VI) thereby forming the compound of Formula (VI).

17 . The process of claim 16 , wherein the chiral salt of the compound of Formula (VI) is:

18 . The process of claim 16 , wherein neutralizing comprises contacting the chiral salt of the compound of Formula (VI), with (i) an aqueous base; and then (ii) acidifying the solution by adding an acid.

19 . The process of claim 1 , wherein acylating comprises contacting the compound of Formula (VI) with an acylating agent in the presence of an organic solvent selected from the group consisting of ethyl acetate, tetrahydrofuran, diethyl ether, dichloromethane, and toluene.

20 . The process of claim 1 , wherein the substantially optically pure compound of Formula (VII) is at least 98% of the enantiomer:

expressed as a percentage of both enantiomers.

Assignments (3)

Continuity (3)

References Cited (400)