Crystal form, salt form, composition and preparation method of pyridazine compound

CN119677731APending Publication Date: 2025-03-21BRIXUN PHARMACEUTICAL (NANTONG) CO LTD
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Patent Information

Application Number
CN202380056182.1
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Priority Date
2022-08-05
Filing Date
2023-08-01
Publication Date
2025-03-21

AI Technical Summary

Technical Problem

Existing NLRP3 inhibitors are not yet on the market. The preclinical compound MCC950 has a significant inhibitory effect, but no drug has yet passed clinical verification. The development of NLRP3 inhibitors has broad application prospects, but there are problems with complex preparation methods and difficulty in industrialization.

Method used

Provides crystal forms A, B and C of pyridazine compounds and their preparation methods. The crystal forms are determined through specific X-ray powder diffraction patterns and thermal analysis data, and the crystal forms are prepared with high physical and chemical stability. Compounds for the preparation of NLRP3 inhibitors.

Benefits of technology

It can effectively inhibit the activity of NLRP3 inflammasome and the activation of downstream caspase-1, inhibit the maturation and secretion of IL-1β, has good pharmacokinetic properties, and is suitable for the treatment of Parkinson's disease and Alzheimer's disease. and other related diseases.

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Abstract

The invention discloses a crystal form, a salt form, a composition and a preparation method of a pyridazine compound, and particularly discloses a preparation method and application of a crystal form A and a composition of a compound shown as a formula (I), a crystal form B of a compound shown as a formula (II) and a crystal form C of a compound shown as a formula (III).
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