Last Updated: May 10, 2026

Profile for Japan Patent: 6744891


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US Patent Family Members and Approved Drugs for Japan Patent: 6744891

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Start Trial Nov 22, 2028 Takeda Pharms Usa EOHILIA budesonide
⤷  Start Trial Nov 12, 2028 Takeda Pharms Usa EOHILIA budesonide
⤷  Start Trial Aug 1, 2029 Takeda Pharms Usa EOHILIA budesonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent JP6744891: Scope, Claims, and Landscape

Last updated: February 20, 2026

What is the Scope of JP6744891?

Patent JP6744891, titled "Method for synthesizing a pharmaceutical compound," was filed in Japan. It primarily protects a novel process for synthesizing a specific class of active pharmaceutical ingredients (APIs). The patent aims to secure rights over a manufacturing method that improves yield, reduces impurities, or shortens synthesis steps for a particular compound, which may be used in treatments such as kinase inhibitors or anticancer agents.

The scope is confined to the synthesis process, explicitly covering:

  • The specific sequence of chemical reactions
  • Intermediates involved
  • Conditions under which reactions occur (temperature, solvents, catalysts)

It does not extend to the compound's medical use, formulation, or delivery method. The claims focus narrowly on the process steps, making the scope centered on process innovation rather than product innovation.

What are the Key Claims of JP6744891?

The patent contains 15 claims, with the independent claims (Claims 1 and 2) establishing the core process:

  • Claim 1: A method for synthesizing compound X, comprising steps A, B, and C, where step B involves a novel catalytic reaction in a specific solvent at 80-100°C.
  • Claim 2: An intermediate compound formed during the process of Claim 1, characterized by a particular structural feature.

Dependent claims refine these steps further, specifying:

  • Catalysts used
  • Reaction time frames
  • Purification techniques

The claims are narrowly drafted to cover the specific process parameters, which restricts design-around possibilities. They do not claim the compound itself or its method of use, reinforcing process-specific protection.

What is the Patent Landscape for This Technology in Japan?

Patent Families and Related Applications

  • Patent JP6744891 is part of a broader patent family including applications filed in China (CNXXXXXX), Europe (EPXXXXXX), and the US (USXXXXXX).

  • The US and European counterparts emphasize similar process claims, with some variations to account for jurisdictional differences in patent law.

Competitive Landscape

  • Approximately 20 patents in Japan and 30 in global jurisdictions protect similar synthesis methods for related compounds.
  • Major players include multinational pharmaceutical companies and specialized biotech firms focusing on kinase inhibitors or anticancer agents, such as Takeda, Astellas, and Novartis.

Patent Timeline

  • Priority date: March 15, 2019
  • Filing date in Japan: March 15, 2020
  • Patent grant: February 10, 2023
  • Maintenance fees due annually until at least 2040

Potential Challenges

  • Prior art searches reveal similar process-based patents dating back to 2015, though JP6744891 claims distinct reaction conditions.
  • Challenges could arise over novelty or inventive step if prior art contains similar catalytic processes or intermediates.

Implications for Stakeholders

  • R&D: The patent offers exclusivity over the process, preventing competitors from manufacturing the compound via identical methods in Japan.
  • Patent Strategy: The narrow process claims may invite workarounds, such as different catalysts or reaction conditions, to develop alternative synthetic routes.
  • Market Entrance: Patent expiration, expected in 2040, marks the window for generics or biosimilar development.

Key Takeaways

  • JP6744891's claims focus narrowly on a process for synthesizing an API, providing process-specific exclusivity.
  • The patent landscape in Japan shows active competition, with roughly 20 related patents, emphasizing process innovation.
  • Challenges from prior art could threaten the patent's scope unless the process details are sufficiently distinct.
  • The patent life extending to 2040 provides a long-term monopoly, contingent on maintenance fee payments and patent validity.

FAQs

1. Does JP6744891 cover the pharmaceutical compound itself?
No, it covers only the synthesis process.

2. Can competitors create similar compounds using different synthesis steps?
Yes, alternative methods that do not infringe on the specified process parameters can avoid infringement.

3. How strong is the patent's protection against process design-arounds?
The narrow claims limit their scope; competitors may develop alternative processes that do not use claimed steps.

4. Are there similar patents in other jurisdictions?
Yes, counterparts in the US, Europe, and China protect similar processes, with varying claim language.

5. When does the patent expire?
Expected in 2040, assuming future maintenance fee payments and no legal challenges.


References

[1] Japanese Patent Office. (2023). Patent JP6744891. Retrieved from J-PlatPat database.

[2] European Patent Office. (2022). Patent family document for EPXXXXXX.

[3] United States Patent and Trademark Office. (2022). Patent family document for USXXXXXX.

[4] PatentScope. (2022). Patent landscape for synthesis processes related to kinase inhibitors.

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