Substituted 1,2-dihydro-3H-pyrazolo[3,4-D]pyrimidin-3-ones

US11261192B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11261192-B2
Application numberUS-201916971254-A
CountryUS
Kind codeB2
Filing dateFeb 26, 2019
Priority dateMar 9, 2018
Publication dateMar 1, 2022
Grant dateMar 1, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Compounds of Formula (I) are provided herein. Such compounds, as well as pharmaceutically acceptable salts and compositions thereof, are useful for treating diseases or conditions, including conditions characterized by excessive cellular proliferation, such as breast cancer.

First claim

Opening claim text (preview).

What is claimed is: 1. A compound of Formula (I), or a pharmaceutically acceptable salt thereof, having the structure: wherein: R 1 is selected from the group consisting of hydrogen, halogen and a substituted or unsubstituted C 1 -C 6 alkyl; Ring A is selected from the group consisting of a substituted or unsubstituted phenyl and a substituted or unsubstituted 5-6 membered monocyclic heteroaryl; Ring B is selected from the group consisting of a substituted or unsubstituted monocyclic 5-7 membered carbocyclyl and a substituted or unsubstituted 5-7 membered monocyclic heterocyclyl; R 2 is selected from the group consisting of m is 0, 1, 2 or 3; R 3 is selected from the group consisting of halogen and a substituted or unsubstituted C 1 -C 6 alkyl; X is selected from the group consisting of hydrogen, halogen, hydroxy, cyano, a substituted or unsubstituted 4-6 membered monocyclic heterocyclyl, a substituted or unsubstituted amine(C 1 -C 6 alkyl), a substituted or unsubstituted —NH—(CH 2 ) 1-6 -amine, a mono-substituted amine, a di-substituted amine, an amino, a substituted or unsubstituted C 1 -C 6 alkyl, a substituted or unsubstituted C 1 -C 6 alkoxy, a substituted or unsubstituted C 3 -C 6 cycloalkoxy, a substituted or unsubstituted (C 1 -C 6 alkyl)acyl, a substituted or unsubstituted C-amido, a substituted or unsubstituted N-amido, a substituted or unsubstituted C-carboxy, a substituted or unsubstituted O-carboxy, a substituted or unsubstituted O-carbamyl and a substituted or unsubstituted N-carbamyl; Y is CH or N; Y 1 is CR 4A or N; Y 2 is CR 4B or N; Ring C is selected from the group consisting of a substituted or unsubstituted C 6 -C 10 aryl, a substituted or unsubstituted monocyclic 5-10 membered heteroaryl, a substituted or unsubstituted monocyclic 5-7 membered carbocyclyl, a substituted or unsubstituted 5-7 membered monocyclic heterocyclyl and a substituted or unsubstituted 7-10 membered bicyclic heterocyclyl; R 4A and R 4B are independently selected from the group consisting of hydrogen, halogen and an unsubstituted C 1-4 alkyl; and R 5 is a substituted or unsubstituted 5-7 membered monocyclic heterocyclyl. 2. The compound of claim 1 , wherein R 1 is hydrogen. 3. The compound of claim 1 , wherein Ring A is a substituted or unsubstituted 5-6 membered monocyclic heteroaryl. 4. The compound of claim 3 , wherein is selected from the group consisting of: wherein each of the aforementioned groups are substituted or unsubstituted. 5. The compound of claim 3 , wherein Ring A is unsubstituted. 6. The compound of claim 1 , wherein Ring B is a substituted or unsubstituted monocyclic 5-7 membered carbocyclyl. 7. The compound of claim 6 , wherein Ring B is a substituted monocyclic 5 membered carbocyclyl. 8. The compound of claim 6 , wherein Ring B is substituted with 1, 2 or 3 substituents independently selected from the group consisting of fluoro, hydroxy, amino, an unsubstituted —NHC(O)C 1 -C 6 alkyl, an unsubstituted C 1 -C 6 haloalkyl and an unsubstituted C 1 -C 6 alkyl. 9. The compound of claim 1 , wherein R 2 is wherein Y is CH. 10. The compound of claim 9 , wherein X is a substituted or unsubstituted 4-6 membered monocyclic heterocyclyl. 11. The compound of claim 10 , wherein X is selected from the group consisting of a substituted or unsubstituted azetidine, a substituted or unsubstituted oxetane, a substituted or unsubstituted diazetidine, a substituted or unsubstituted azaoxetane, a substituted or unsubstituted pyrrolidine, a substituted or unsubstituted tetrahydrofuran, a substituted or unsubstituted imidazoline, a substituted or unsubstituted pyrazolidine, a substituted or unsubstituted piperidine, a substituted or unsubstituted tetrahydropyran, a substituted or unsubstituted piperazine, a substituted or unsubstituted morpholine and a substituted or unsubstituted dioxane. 12. The compound of claim 10 , wherein X is substituted. 13. The compound of claim 12 , wherein X is substituted with 1 or 2 substituents independently selected from the group consisting of fluorine, an unsubstituted C 1 -C 6 alkyl, an unsubstituted C 1 -C 6 hydroxyalkyl, an unsubstituted amine(C 1 -C 6 alkyl) and an unsubstituted (C 1 -C 6 alkyl)acyl. 14. The compound of claim 1 , wherein R 2 is 15. The compound of claim 9 , wherein m is 0. 16. The compound of claim 1 , wherein the compound is selected from the group consisting of: or a pharmaceutically acceptable salt of any of the foregoing. 17. The compound of claim 1 , wherein the compound is selected from the group consisting of: or a pharmaceutically acceptable salt of any of the foregoing. 18. A pharmaceutical composition comprising an effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent, excipient or combination thereof. 19. A method for ameliorating or treating a cancer comprising administering an effective amount of claim 1 , or a pharmaceutically acceptable salt thereof, to a subject having the cancer, wherein the cancer is selected from a brain cancer, a cervicocerebral cancer, an esop

Assignees

Inventors

Classifications

  • Ring systems of four or more rings · CPC title

  • Ortho- or peri-condensed ring systems · CPC title

  • A61P35/00Primary

    Antineoplastic agents · CPC title

  • ortho- or peri-condensed with heterocyclic rings · CPC title

  • C07D471/04Primary

    Ortho-condensed systems · CPC title

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Frequently asked questions

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What does patent US11261192B2 cover?
Compounds of Formula (I) are provided herein. Such compounds, as well as pharmaceutically acceptable salts and compositions thereof, are useful for treating diseases or conditions, including conditions characterized by excessive cellular proliferation, such as breast cancer.
Who is the assignee on this patent?
Recurium Ip Holdings Llc
What technology area does this patent fall under?
Primary CPC classification A61P35/00. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Mar 01 2022 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 7 related publications on this page (citations in our corpus or others sharing the same primary CPC).