Claims for Patent: 11,564,926

Summary for Patent: 11,564,926

Title:	Methods of synthesizing thyroid hormone analogs and polymorphs thereof
Abstract:	The disclosure describes methods of synthesis of pyridazinone compounds as thyroid hormone analogs and their prodrugs. Preferred methods according to the disclosure allow for large-scale preparation of pyridazinone compounds having high purity. In some embodiments, preferred methods according to the disclosure also allow for the preparation of pyridazinone compounds in better yield than previously used methods for preparing such compounds. Also disclosed are morphic forms of a pyridazinone compound. Further disclosed is a method for treating resistance to thyroid hormone in a subject having at least one TRβ mutation.
Inventor(s):	II D. Keith Hester, Robert J. Duguid, Martha J. Kelly, Anna Chasnoff, Gang Dong, Edwin L. Crow, Lianhe Shu, Ping Wang, Duk Soon Choi
Assignee:	Hoffmann La Roche Inc , Madrigal Pharmaceuticals Inc
Application Number:	US17/118,706
Patent Claims:	1. A morphic form of 2-(3,5-dichloro-4-((5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yl)oxy)phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carbonitrile, characterized by an onset melting temperature of about 321° C. and a differential scanning calorimetry (DSC) diagram that includes an endothermic peak at about 329° C. 2. The morphic form of claim 1, wherein the DSC diagram is substantially the same as that shown in FIG. 2 . 3. The morphic form of claim 1, having a purity of greater than 85%. 4. The morphic form of claim 1, having a purity of greater than 90%. 5. The morphic form of claim 1, having a purity of greater than 95%. 6. A pharmaceutical composition comprising the morphic form of claim 1 and a pharmaceutically acceptable carrier. 7. A method for treating nonalcoholic steatohepatitis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the morphic form of claim 5. 8. The method of claim 7, wherein the morphic form is administered orally. 9. A method for treating hypercholesterolemia in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the morphic form of claim 1. 10. The method of claim 9, wherein the morphic form is administered orally. 11. A method for treating fatty liver disease in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the morphic form of claim 1. 12. The method of claim 11, wherein the morphic form is administered orally. 13. A method for treating a resistance to thyroid hormone (RTH) syndrome in a subject having at least one TRβ mutation, the method comprising administering to the subject a therapeutically effective amount of the morphic form of claim 1. 14. The method of claim 13, wherein the morphic form is administered orally. 15. A dimethylacetamide (DMAC) solvate of 2-(3,5-dichloro-4-((5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yl)oxy)phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carbonitrile. 16. A methyl isobutyl ketone (MIBK) solvate of 2-(3,5-dichloro-4-((5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yl)oxy)phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carbonitrile. 17. A method of treating a subject having a resistance to thyroid hormone (RTH) syndrome, the method comprising: performing an assay to determine a presence of a TRβ mutation in a sample obtained from the subject; and administering a therapeutically effective amount of a compound of Formula (IV), if the TRβ mutation is present in the sample, wherein the compound of Formula (IV) has the following structure: wherein R3 is H or CH2Ra, in which Ra is hydroxyl, O-linked amino acid, —OP(O)(OH)2 or —OC(O)—Rb, Rb being lower alkyl, alkoxy, alkyl acid, or cycloalkyl; and R4 and R5 together are —N═C(Rc)—C(O)—NH—C(O)—, in which Rc is H or cyano. 18. The method of claim 17, wherein the TRβ mutation is selected from the group consisting of a substitution of threonine (T) for the wild type residue alanine (A) at amino acid position 234 of SEQ ID NO: 1 (A234T); a substitution of glutamine (Q) for the wild type residue arginine (R) at amino acid position 243 of SEQ ID NO: 1 (R243Q); a substitution of histidine (H) for the wild type residue arginine (R) at amino acid position 316 of SEQ ID NO: 1 (R316H); and a substitution of threonine (T) for the wild type residue alanine (A) at amino acid position 317 of SEQ ID NO: 1 (A317T). 19. The method of claim 17, wherein the TRβ mutation is a gene mutation or a mutation in the ligand-binding domain of a TRβ polypeptide. 20. The method of claim 19, wherein the TRβ polypeptide has a sequence of SEQ ID NO.: 1. 21. The method of claim 17, wherein the assay comprises: amplifying a nucleic acid in the sample with a primer that is complementary to a mutant TRβ polynucleotide; and determining the presence of the amplified nucleic acid. 22. The method of claim 21, wherein the mutant TRβ polynucleotide has a sequence of SEQ ID NO.: 2. 23. The method of claim 17, wherein the compound of Formula (IV) is 2-(3,5-dichloro-4-((5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yl)oxy)phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carbonitrile (“Compound A”). 24. The method of claim 23, wherein Compound A is in a morphic form characterized by an onset melting temperature of about 321° C. and a differential scanning calorimetry (DSC) diagram that includes an endothermic peak at about 329° C.