Substituted pyrazolo[3,4-d]pyrimidines as PDE9 inhibitors

US11028092B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11028092-B2
Application numberUS-201916670093-A
CountryUS
Kind codeB2
Filing dateOct 31, 2019
Priority dateJun 8, 2017
Publication dateJun 8, 2021
Grant dateJun 8, 2021

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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.

The present invention is directed to pyrazolopyrimidine compounds of the general structural formula I:which may be useful as therapeutic agents for the treatment of disorders associated with phosphodiesterase 9 (PDE9). The present invention also relates to the use of such compounds for treating cardiovascular and cerebrovascular diseases, such as hypertension, chronic kidney disease and heart failure, and neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.

First claim

Opening claim text (preview).

What is claimed is: 1. A compound selected from the group consisting of: or a pharmaceutically acceptable salt thereof. 2. The compound of claim 1 , wherein the compound is: or a pharmaceutically acceptable salt thereof. 3. The compound of claim 2 , wherein the compound is: 4. The compound of claim 2 , wherein the compound is a pharmaceutically acceptable salt of: 5. The compound of claim 1 , wherein the compound is: or a pharmaceutically acceptable salt thereof. 6. The compound of claim 5 , wherein the compound is: 7. The compound of claim 5 , wherein the compound is a pharmaceutically acceptable salt of: 8. The compound of claim 1 , wherein the compound is: or a pharmaceutically acceptable salt thereof. 9. The compound of claim 8 , wherein the compound is: 10. The compound of claim 8 , wherein the compound is a pharmaceutically acceptable salt of: 11. The compound of claim 1 , wherein the compound is: or a pharmaceutically acceptable salt thereof. 12. The compound of claim 11 , wherein the compound is: 13. The compound of claim 11 , wherein the compound is a pharmaceutically acceptable salt of: 14. The compound of claim 1 , wherein the compound is: or a pharmaceutically acceptable salt thereof. 15. The compound of claim 14 , wherein the compound is: 16. The compound of claim 14 , wherein the compound is a pharmaceutically acceptable salt of: 17. The compound of claim 1 , wherein the compound is: or a pharmaceutically acceptable salt thereof. 18. The compound of claim 17 , wherein the compound is: 19. The compound of claim 17 , wherein the compound is a pharmaceutically acceptable salt of: 20. A pharmaceutical composition comprising an inert carrier and a compound of claim 1 , or a pharmaceutically acceptable salt thereof. 21. A method for inhibiting phosphodiesterase 9 activity in a mammalian patient, comprising administering to the mammalian patient a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof. 22. The method of claim 21 , wherein the mammalian patient has a disease or disorder associated with phosphodiesterase 9 dysfunction. 23. The method of claim 22 , wherein the disease or disorder associated with phosphodiesterase 9 dysfunction is selected from the group consisting of heart failure, hypertension, a cardiovascular disease, a cerebrovascular disease, and a chronic kidney disease. 24. The method of claim 22 , wherein the disease or disorder associated with phosphodiesterase 9 dysfunction is selected from the group consisting of drug induced psychosis, an anxiety disorder, a delusional disorder, a movement disorder, a neurological disorder, and a psychotic disorder.

Assignees

Inventors

Classifications

  • Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia · CPC title

  • of the kidneys · CPC title

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

  • Drugs for disorders of the nervous system · CPC title

  • C07D487/04Primary

    Ortho-condensed systems · CPC title

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What does patent US11028092B2 cover?
The present invention is directed to pyrazolopyrimidine compounds of the general structural formula I:which may be useful as therapeutic agents for the treatment of disorders associated with phosphodiesterase 9 (PDE9). The present invention also relates to the use of such compounds for treating cardiovascular and cerebrovascular diseases, such as hypertension, chronic kidney disease and heart f…
Who is the assignee on this patent?
Merck Sharp & Dohme
What technology area does this patent fall under?
Primary CPC classification C07D487/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 08 2021 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 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).