Benzopyrazole compound

US12545648B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12545648-B2
Application numberUS-202017789662-A
CountryUS
Kind codeB2
Filing dateDec 30, 2020
Priority dateDec 31, 2019
Publication dateFeb 10, 2026
Grant dateFeb 10, 2026

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.

Disclosed is a benzopyrazole compound. Specifically disclosed are a compound as shown in formula (I) and a pharmaceutically acceptable salt thereof.

First claim

Opening claim text (preview).

The invention claimed is: 1 . A compound represented by formula (I) or a pharmaceutically acceptable salt thereof, wherein, X is selected from NH and O; ring A is selected from and the are optionally substituted by 1, 2 or 3 R a ; T 1 is selected from CH 2 and O; each of T 2 , T 3 and T 4 is independently selected from CH and N; T 5 is selected from NH and O; T 6 is selected from CH and N; ring B is selected from phenyl; R 1 is selected from H and C 1-3 alkoxy, and the C 1-3 alkoxy is optionally substituted by 1, 2 or 3 R b ; each of R 2 is independently selected from H, F, Cl, Br and CH 3 ; R 3 is selected from C 1-6 alkyl, and the C 1-6 alkyl is optionally substituted by 1, 2 or 3 R c ; m is selected from 0, 1 and 2; n is selected from 1 and 2; each of R a is independently selected from H and C 1-3 alkyl, and the C 1-3 alkyl is optionally substituted by 1, 2 or 3 R; each of R b is independently selected from H, F, Cl, Br and I; each of R c is independently selected from H, F, Cl, Br, I and OH; each of R is independently selected from F and OCH 3 . 2 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 1 , wherein the compound is selected from 3 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 1 , wherein each of R a is independently selected from H, CH 3 , CF 3 , CH 2 CH 3 , C(CH 3 ) 2 and CH 2 CH 2 OCH 3 . 4 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 1 , wherein ring A is selected from and the are optionally substituted by 1, 2 or 3R a . 5 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 4 , wherein ring A is selected from and are optionally substituted by 1, 2 or 3 R a . 6 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 5 , wherein ring A is selected from 7 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 1 , wherein the structural moiety is selected from 8 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 7 , wherein the structural moiety selected from 9 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 1 , wherein R 1 is selected from H and OCH 3 , and the OCH 3 is optionally substituted by 1, 2 or 3 R b . 10 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 9 , wherein R 1 is selected from H and OCH 3 . 11 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 1 , wherein R 3 is selected from C 1-3 alkyl, and the C 1-3 alkyl is optionally substituted by 1, 2 or 3 R. 12 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 11 , wherein R 3 is selected from CH 3 , CH 2 CH 3 and C(CH 3 ) 2 . 13 . The compound or the pharmaceutically acceptable salt thereof as claimed in claim 1 , wherein the compound is selected from 14 . A compound represented by the following formula or a pharmaceutically acceptable salt thereof, and the compound is selected from 15 . A method for treating diseases related to glucocorticoid receptors in a subject in need thereof, comprising: administering an effective amount of the compound or the pharmaceutically acceptable salt thereof as claimed in claim 1 to the subject. 16 . The method as claimed in claim 15 , wherein the diseases related to glucocorticoid receptors are rheumatoid arthritis.

Assignees

Inventors

Classifications

  • Ortho-condensed systems · CPC title

  • Ortho-condensed systems · CPC title

  • Ortho-condensed systems · CPC title

  • directly linked by a ring-member-to-ring-member bond · CPC title

  • directly linked by a ring-member-to-ring-member bond · CPC title

Patent family

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External sources

Frequently asked questions

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

What does patent US12545648B2 cover?
Disclosed is a benzopyrazole compound. Specifically disclosed are a compound as shown in formula (I) and a pharmaceutically acceptable salt thereof.
Who is the assignee on this patent?
Medshine Discovery Inc
What technology area does this patent fall under?
Primary CPC classification C07D231/56. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 10 2026 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).