http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-119651-A1

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filingDate 2019-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2022-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-119651-A1
titleOfInvention HETEROCYCLIC AND HETEROARYL COMPOUNDS TO TREAT HUNTINGTON'S DISEASE
abstract Condensed pyridazine and pyrazine derivative heterocyclic compounds and pharmaceutical compositions comprising them all of which are used for the treatment of Huntington's disease (HD) are provided. Claim 1: A compound comprising, a compound of formula (1) or a form thereof, wherein: dashed lines represent one or more double bonds optionally present where permitted by available valences; W¹ is independently C-Rᵃ, CH-Rᵃ, N, N-Rᵇ, O or S where allowed by the available valences; W² is independently C-Rᵃ, CH-Rᵃ, N, or N-Rᵇ where allowed by available valences, and; W³ is independently C, CH or N where permitted by available valences; wherein at least one of W¹, W² or W³ is N or N-Rᵇ; W⁴ and W⁵ are independently C-Rᵃ or N, where when W¹ is S or O, W² is C-Rᵃ, and W³ is C; Rᵃ is in each case independently selected from hydrogen, cyano, halogen, hydroxy, C₁₋₆-alkyl, deutero-C₁₋₄-alkyl, halo-C₁₋₆-alkyl, C₁₋₆-alkoxy, halo-C₁₋₆-alkoxy, alkoxy C₁₋₆-C₁₋₆-alkyl, amino, C₁₋₆-alkylamino, (C₁₋₆-alkyl)₂-amino, amino-C₁₋₆-alkyl, and hydroxy-C₁₋₆-alkyl; Rᵇ is selected from hydrogen and C₁₋₆ alkyl; R¹ is selected from C₃₋₁₀ cycloalkyl and heterocyclyl, where heterocyclyl is a 3-7 membered monocyclic, 6-10 membered bicyclic or 13-16 membered polycyclic, saturated or partially unsaturated ring system having 1, 2 or 3 ring member heteroatoms independently selected from N, O or S, and wherein each occurrence of C₃₋₁₀ cycloalkyl and heterocyclyl is optionally substituted with one, two or three R³ substituents and optionally with an additional R⁴ substituent, or, wherein, alternatively, each occurrence of C₃₋₁₀ cycloalkyl and heterocyclyl is optionally substituted with one, two, three or four R³ substituents; R² is selected from phenyl, heterocyclyl and heteroaryl, wherein heterocyclyl is a 3-7 membered monocyclic, 6-10 membered bicyclic or 13-16 membered polycyclic, saturated or partially unsaturated ring system having 1, 2 or 3 membered heteroatoms in the ring independently selected from N, O or S, where heteroaryl is a 3-7 membered monocyclic or 6-10 membered bicyclic ring system having 1, 2, 3 or 4 membered heteroatoms in the ring independently selected from N, O or S, and wherein each occurrence of phenyl, heterocyclyl and heteroaryl is optionally substituted with one, two or three R⁵ substituents, and optionally with one additional R⁶ substituent; R³ is each independently selected from cyano, halogen, hydroxy, C₁₋₆-alkyl, deutero-C₁₋₄-alkyl, halo-C₁₋₆-alkyl, C₁₋₆-alkoxy, halo-C₁₋₆-alkoxy, C₁₋-alkoxy ₆-C₁₋₆-alkyl, amino, C₁₋₆-alkylamino, (C₁₋₆-alkyl)₂-amino, amino-C₁₋₆-alkyl, and hydroxy-C₁₋₆-alkyl; R⁴ is selected from C₃₋₁₀ cycloalkyl, phenyl, heteroaryl and heterocyclyl, wherein heterocyclyl is a 3-7 membered monocyclic, 6-10 membered bicyclic or 13-16 membered polycyclic, saturated or partially unsaturated ring system, which has 1, 2 or 3 membered heteroatoms in the ring independently selected from N, O or S, where heteroaryl is a 3-7 membered monocyclic or 6-10 membered bicyclic ring system having 1, 2, 3 or 4 heteroatom ring members independently selected from N, O or S, and wherein each occurrence of C₃₋₁₀ cycloalkyl, phenyl, heterocyclyl and heteroaryl is optionally substituted with one, two or three R⁷ substituents; R⁵ is in each case independently selected from halogen, hydroxy, cyano, nitro, C₁₋₆ alkyl, deutero-C₁₋₄ alkyl, halo-C₁₋₆ alkyl, C₁₋₆ alkoxy, halo-C₁₋₆ alkoxy, oxime , amino, C₁₋₆-alkylamino, (C₁₋₆-alkyl)₂-amino and C₁₋₆-alkyl-thio; R⁶ is selected from phenyl and heteroaryl, wherein heteroaryl is a 3-7 membered monocyclic or 6-10 membered bicyclic ring system having 1, 2, 3 or 4 membered heteroatoms in the ring independently selected from N, O or S, and wherein each occurrence of phenyl and heteroaryl is optionally substituted with one, two, three or four R⁸ substituents; R⁷ is each independently selected from cyano, halogen, hydroxy, C₁₋₆-alkyl, deutero-C₁₋₄-alkyl, halo-C₁₋₆-alkyl, C₁₋₆-alkoxy, halo-C₁₋₆-alkoxy, C₁₋-alkoxy ₆-C₁₋₆-alkyl, amino, C₁₋₆-alkylamino, (C₁₋₆-alkyl)₂-amino, amino-C₁₋₆-alkyl and C₃₋₁₀-cycloalkyl; and R⁸ is each independently selected from cyano, halogen, hydroxy, C₁₋₆ alkyl, deutero-C₁₋₄ alkyl, halo-C₁₋₆ alkyl, C₁₋₆ alkoxy, halo-C₁₋₆ alkoxy, C₁ alkoxy ₋₆-C₁₋₆-alkyl, amino, C₁₋₆-alkylamino, (C₁₋₆-alkyl)₂-amino, amino-C₁₋₆-alkyl and C₃₋₁₀-cycloalkyl; wherein a form of the compound is selected from the group consisting of salt, hydrate, solvate, racemate, enantiomer, diastereomer, stereoisomer, and tautomeric form thereof.
priorityDate 2018-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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