Piperidinyl monocarboxylic acids as S1P1 receptor agonists

US9266867B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9266867-B2
Application numberUS-201214111438-A
CountryUS
Kind codeB2
Filing dateApr 10, 2012
Priority dateApr 12, 2011
Publication dateFeb 23, 2016
Grant dateFeb 23, 2016

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention relates to novel compounds acting as agonists at S1P (sphingosine-1-phosphate) receptors, compositions containing these compounds, use of these compounds in medicine and their process of preparation.

First claim

Opening claim text (preview).

The invention claimed is: 1. A compound of formula (I): wherein: Ar is a phenyl group optionally substituted by one or more identical or different group(s) selected from the group consisting of halogen, alkyl, cycloalkyl, —Oalkyl, and phenyl; R1 represents —X—(Y) n — where —X— is selected from the group consisting of -alkyl-, -alkenyl-, -alkynyl-, -aryl-, and -alkylaryl-, each Y, identical or different is selected from the group consisting of H, OH, halogen, —Oalkyl, —Oalkylaryl, —OalkylOalkyl, —Oaryl, heteroaryl, —Oaryl(Oalkyl), —Ocycloalkyl, -cycloalkyl, and heterocyclyl; n is 1 to 3; and where R1 is not —C(═O)OH; and R2 is H or alkyl; or one of its stereoisomers or salts thereof. 2. The compound according to claim 1 , wherein Ar is a phenyl group substituted with two identical or different groups in addition to the oxadiazole group. 3. The compound according to claim 1 of formula (II): wherein: R3 is selected from halogen, phenyl, cycloalkyl, alkyl, and —Oalkyl; Hal represents a halogen atom. 4. The compound according to claim 1 , wherein R1 is selected from: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, secondary butyl, tertiary butyl, n-pentyl, isopentyl, n-hexyl, isohexyl, hydroxymethyl, hydroxyethyl, hydroxypropyl, methoxymethyl, ethoxymethyl, methoxyethyl, vinyl, allyl, methoxyethoxymethyl, ethoxyethoxymethyl, ethoxyethoxyethyl, Phenyl, benzyl, benzyloxymethyl, benzyloxyethyl, —CH 2 -[Ph(o-F)], —CH 2 -[Ph(m-F)], —CH 2 -[Ph(p-F)], —CH 2 -[Ph(o-OMe)], —CH 2 -[Ph(m-OMe)], or —CH 2 -[Ph(p-OMe)], methoxybutyl, methoxyethoxymethyl, methoxyethoxyethyl, —CH 2 -[Ph(o,o-F 2 )], —CH 2 -[Ph(m-CF 3 )], —CH 2 -furyl, —CH 2 -pyridyl, (2-methoxy-phenoxy)-ethyl, 4-methoxy-benzyl, isopropoxy methyl, cyclopentyloxymethyl, thiophen-2-ylmethyl, cyclopropylmethyl, 2-morpholin-4-yl-ethyl, 3-piperidin-1-yl-propyl, 3-pyrrolidin-1-yl-propyl. 5. The compound according to claim 1 , wherein R2 is H. 6. The compound according to claim 3 , wherein R3 is selected from the group consisting of phenyl, cyclohexyl, cyclopentyl, isobutyl, and isopropoxy. 7. The compound according to claim 1 which is selected from the group consisting of: 1-{4-[5-(3-chloro-4-cyclohexylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-methylpiperidine-4-carboxylic acid 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-methylpiperidine-4-carboxylic acid 1-{4-[5-(3-chloro-4-cyclopentylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-methylpiperidine-4-carboxylic acid 1-{4-[5-(2-Chlorobiphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-methylpiperidine-4-carboxylic acid 1-{4-[5-(3-chloro-4-cyclopentylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-methoxymethylpiperidine-4-carboxylic acid 1-{4-[5-(3-chloro-4-cyclohexylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-methoxymethylpiperidine-4-carboxylic acid 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-ethylpiperidine-4-carboxylic acid 4-allyl-1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}piperidine-4-carboxylic acid 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-propylpiperidine-4-carboxylic acid 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-(2-methoxyethoxymethyl)piperidine-4-carboxylic acid 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-hydroxymethylpiperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutylphenyl)-[1,2,4]oxadiazol-3-yl]-benzyl}-4-methoxymethylpiperidine-4-carboxylic acid 4-Allyl-1-{4-[5-(2-chlorobiphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]-benzyl}piperidine-4-carboxylic acid 1-{4-[5-(2-Chlorobiphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-propylpiperidine-4-carboxylic acid 1-{4-[5-(2-Chlorobiphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-(2-methoxyethoxymethyl)piperidine-4-carboxylic acid 4-Benzyloxymethyl-1-{4-[5-(2-chlorobiphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]-benzyl}piperidine-4-carboxylic acid 4-Benzyloxymethyl-1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}piperidine-4-carboxylic acid 1-{4-[5-(2-Chlorobiphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-hydroxymethylpiperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-phenylpiperidine-4-carboxylic acid 4-Benzyl-1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]oxadiazol-3-yl]-benzyl}-4-(4-fluoro-benzyl)-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]oxadiazol-3-yl]-benzyl}-4-(2-fluoro-benzyl)-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]oxadiazol-3-yl]-benzyl}-4-(4-methoxy-benzyl)-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]oxadiazol-3-yl]-benzyl}-4-(2-methoxy-benzyl)-piperidine-4-carboxylic acid 1-{4-[5-(2-chlorobiphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-methoxymethylpiperidine-4-carboxylic acid 1-{4-[5-(2-Chlorobiphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-ethylpiperidine-4-carboxylic acid 1-{4-[5-(4-Isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methyl-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-(4-methoxy-butyl)-piperidine-4-carboxylic acid 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-(2-methoxyethoxymethyl)piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-(2-phenoxy-ethyl)-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-(2,6-difluoro-benzyl)-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-isobutyl-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-isopropyl-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-(3-trifluoro methyl-benzyl)-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]oxadiazol-3-yl]-benzyl}-4-furan-2-ylmethyl-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-pyridin-2-ylmethyl-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-[2-(2-methoxy-phenoxy)-ethyl]-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-pyridin-3-ylmethyl-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isobutyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-pyridin-4-ylmethyl-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isopropoxy-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methyl-piperidine-4-carboxylic acid 1-{4-[5-(4-tert-Butyl-3-chloro-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methyl-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-propyl-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methyl-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isopropoxy-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-(2-methoxy-ethoxymethyl)-piperidine-4-carboxylic acid 1-{4-[5-(3-Chloro-4-isopropoxy-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-ethyl-piperidine-4-carboxylic acid 4-Allyl-1-{4-[5-(3-chloro-4-isopropoxy-phenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-piperidine-4-carboxylic acid 1-{4-[5-(2-Chloro-biphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-pyridin-2-ylmethyl-piperidine-4-carboxylic acid 1-{4-[5-(2-Chloro-biphenyl-4-yl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-(4-methoxy-benzyl)-piperidine-4-carboxylic acid 1-{4-[5-(2-Chloro-biphenyl-4-yl)-[1,2,4]-

Assignees

Inventors

Classifications

  • Immunomodulators · CPC title

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • Drugs for disorders of the cardiovascular system · CPC title

  • for hyperglycaemia, e.g. antidiabetics · CPC title

  • Drugs for immunological or allergic disorders · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9266867B2 cover?
The present invention relates to novel compounds acting as agonists at S1P (sphingosine-1-phosphate) receptors, compositions containing these compounds, use of these compounds in medicine and their process of preparation.
Who is the assignee on this patent?
Capet Marc, Berrebi-Bertrand Isabelle, Robert Philippe, and 14 more
What technology area does this patent fall under?
Primary CPC classification C07D413/10. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 23 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).