Synthesis of 1:1:1 co-crystal of 1-cyano-2-(4-cyclopropyl-benzyl)-4-(β-D-glucopyranos-1-yl)-benzene, L-proline and water

Patent metadata

Field	Value
Publication number	US-11225500-B2
Application number	US-201816771717-A
Country	US
Kind code	B2
Filing date	Dec 17, 2018
Priority date	Dec 19, 2017
Publication date	Jan 18, 2022
Grant date	Jan 18, 2022

Abstract

The invention relates to a process for the manufacture of the crystalline compound according to formula (I) comprising the steps (a) deacetylating the final intermediate (FI), (b) forming the crystalline compound according to formula (I) by reacting the deacetylated final intermediate of step (a) with L-proline and water and isolating the final reaction product; processes of manufacturing intermediates thereof; process intermediates and their uses in the processes according to the present invention.

First claim

The invention claimed is:

1. A process for the manufacture of final intermediate (FI) comprising the steps:
(a) reacting intermediate I1, wherein X is I, with at least one metalation agent, and subsequently adding the reaction product of such metalation to intermediate I2, wherein PG is a protection group, to yield intermediate I3;
(b) methylating intermediate I3 to yield intermediate I4;
(c) reducing intermediate I4 with a reduction agent to yield intermediate I5; and
(d) acetylating intermediate I5 to yield final intermediate FI;
wherein the intermediates I3, I4 and I5 are not isolated and/or purified before performing steps (b), (c) and/or (d), respectively:

2. The process according to claim 1 , wherein PG is trimethylsilyl (TMS).

3. The process according to claim 1 , wherein the at least one metalation agent comprises Turbo-Grignard (iPrMgCl*LiCl).

4. The process according to claim 1 , wherein the reduction agent comprises trimethylsilane.

5. A process for the manufacture of final intermediate (FI) comprising the steps:
(a) reacting intermediate I1, wherein X is I, with at least one metalation agent, and subsequently adding the reaction product of such metalation to intermediate I2, wherein PG is a protection group, to yield intermediate I3;
(b) methylating intermediate I3 to yield intermediate I4;
(c) acetylating intermediate I4 to yield intermediate I6;
(d) reducing intermediate I6 with a reduction agent to yield final intermediate FI;
wherein all of the intermediates I3, I4 and I6 are not isolated and/or purified before performing steps (b), (c) and/or (d), respectively:

6. The process according to claim 5 , wherein PG is trimethylsilyl (TMS).

7. The process according to claim 5 , where the at least one metalation agent comprises Turbo-Grignard (iPrMgCl*LiCl).

8. The process according to claim 5 , wherein the reduction agent comprises trimethylsilane.

9. A process for the manufacture of the crystalline compound 1-cyano-2-(4-cyclopropyl-benzyl)-4-(β-D-glucopyranos-1-yl)-benzene L-proline monohydrate according to formula (I)

comprising the following steps:
(a) 2-fluoro-4-bromobenzonitrile is reacted with isopropylmagnesium chloride and iodine to yield 2-fluoro-4-iodobenzonitrile;
(b) 2-fluoro-4-iodobenzonitrile is then coupled with ethyl-4-bromophenylacetate and subsequently decarboxylated to yield 2-(4-bromobenzyl)-4-iodo-benzonitrile;
(c) 2-(4-bromobenzyl)-4-iodo-benzonitrile is then reacted with intermediate “I2” [PG=trimethylsilyl (TMS)] and reduced and acetylated in a chemical synthesis sequence of halogen-metal exchange/lactone addition/acidic reduction/acetylation according to claim 4 , steps (b) and (c), with involved intermediates I3, I4 and I5 carrying a bromo substitution instead of the displayed cyclopropyl substitution at the distal benzyl moiety, wherein the intermediates I3, I4 and I5 are not isolated and/or purified before further processing;
(d) subsequently the cyclopropyl moiety is installed in the corresponding bromo analogue of final intermediate (FI) by means of a transition metal catalyzed reaction with a cyclopropyl species to obtain final intermediate (FI);
(e) final intermediate (FI) is then subjected to the process for the manufacture of the crystalline compound 1-cyano-2-(4-cyclopropyl-benzyl)-4-(β-D-glucopyranos-1-yl)-benzene L-proline monohydrate according to formula (I) according to the following steps:
(e.1) deacetylating the final intermediate (FI); and

(e.2) forming the crystalline compound according to formula (I) by reacting the deacetylated final intermediate of step (e.1) with L-proline and water to enable isolation of the final reaction product

10. The process according to claim 9 comprising the steps according to the following synthesis route:

wherein the above abbreviations have the following meanings:
iPrMgCl=isopropylmagnesium chloride; I2=iodine; THF=tetrahydrofuran; MeTHF=2-methyl tetrahydrofuran; tBuOK=potassium tert-butoxide; DMF=dimethylformamide; NaOH=sodium hydroxide; iPrMgCl.LiCl=isopropylmagnesium chloride lithium chloride; TMS=trimethylsilyl; MeSO 3 H=methanesulfonic acid; MeOH=methanol; Et 3 SiH=triethylsilane; BF 3 .OEt=boron trifluoride etherate; Ac 2 O=acetic anhydride; NMM=N-methylmorpholine; DMAP=4-dimethylaminopyridine; Ac=Acetyl; PdOAc2=palladium(II) acetate; PCy3=tricyclohexylphosphine; PhMe=toluene; iPrOH=isopropanol.

11. The process according to claim 9 , wherein the cyclopropyl species comprises cyclopropylboronic acid.

Assignees

• Boehringer Ingelheim Vetmedica Gmbh

Inventors

• Eckhardt Matthias
• Brink Monika
• Himmelsbach Frank
• Sahli Stefan
• Shu Chutian
• Wang Xiao-Jun
• Weber Beat Theodor
• Yang Bing-Shiou

Classifications

• C07D309/10 Primary

  Oxygen atoms · CPC title

• C07C291/00

  Compounds containing carbon and nitrogen and having functional groups not covered by groups C07C201/00 - C07C281/00 · CPC title

• C07H7/04

  Carbocyclic radicals · CPC title

• C07H15/26 Primary

  Acyclic or carbocyclic radicals, substituted by hetero rings · CPC title

• C07H1/00 Primary

  Processes for the preparation of sugar derivatives · CPC title