Heterocyclic modulators of lipid synthesis
US-2024400552-A1 · Dec 5, 2024 · US
US9988382B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9988382-B2 |
| Application number | US-201715627145-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 19, 2017 |
| Priority date | Feb 6, 2015 |
| Publication date | Jun 5, 2018 |
| Grant date | Jun 5, 2018 |
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Compounds having a structure of formula (I), including stereoisomers and pharmaceutically acceptable salts and solvates thereof: wherein R 1 is as defined herein. Such compounds are inhibitors of the vesicular monoamine transporter 2 (VMAT2) and have utility for treating, for example, hyperkinetic disorders. Also disclosed are compositions containing these compounds in combination with a pharmaceutically acceptable carrier or diluent, as well as methods relating to the use in a subject in need thereof.
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We claim the following: 1. A compound having structure (I): or a stereoisomer or pharmaceutically acceptable salt or solvate thereof, wherein: R 1 is b) —P(═O)(OR 3 ) 2 ; c) —C(═O)alkyl, wherein alkyl is optionally substituted with R 10 and/or R 20 ; d) —C(═O)heterocyclyl, wherein heterocyclyl is optionally substituted with R 10 and/or R 20 ; e) —C(═O)carbocyclyl, wherein carbocyclyl is optionally substituted with R 10 and/or R 20 ; f) —C(═O)N(R 3 )alkyl, wherein alkyl is optionally substituted with R 10 and/or R 20 ; g) —C(═O)N(R 3 )carbocyclyl, wherein carbocyclyl is optionally substituted with R 10 and/or R 20 ; h) —C(═O)Oalkyl, wherein alkyl is optionally substituted with R 10 and/or R 20 ; or i) alkyl, wherein alkyl is optionally substituted with R 10 and/or R 20 ; and wherein, each R 3 is independently hydrogen or alkyl; each R 10 is independently halo, haloalkyl, cyano, nitro, trimethylsilanyl, —OR 30 , —SR 30 , —OC(O)—R 30 , —N(R 30 ) 2 , —C(O)R 30 , —C(O)OR 30 , —C(O)N(R 30 ) 2 , —N(R 30 )C(O)OR 31 , —N(R 30 )C(O)R 31 , —N(R 30 )C(═NR 31 )N(R 32 ) 2 , —N(R 30 )S(O) t R 31 (where t is 1 to 2), —S(O) t OR 30 (where t is 1 to 2), —S(O) p R 30 (where p is 0 to 2) or —S(O) t N(R 30 ) 2 (where t is 1 to 2), —OP(═O)(OR 30 ) 2 , or when a single atom bears two R 10 groups such two R 10 groups may be taken together to form oxo; each R 20 is independently alkyl, alkenyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heterocyclyl, heterocyclalkyl, heteroaryl or heteroarylalkyl, or when a single atom bears two R 20 groups such two R 20 groups may be taken together to form cycloalkyl, wherein each of said alkyl, alkenyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heterocyclyl, heterocyclalkyl, heteroaryl and heteroarylalkyl groups is optionally substituted with R 10 and/or R 22 ; each R 22 is independently alkyl, alkenyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heterocyclyl, heterocyclalkyl, heteroaryl or heteroarylalkyl, wherein each of said alkyl, alkenyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heterocyclyl, heterocyclalkyl, heteroaryl and heteroarylalkyl groups is optionally substituted with R 10 ; and each R 30 , R 31 and R 32 is independently hydrogen or alkyl. 2. The compound of claim 1 , wherein R 1 is —P(═O)(OR 3 ) 2 . 3. The compound of claim 1 , wherein R 1 is —C(═O)alkyl, and wherein alkyl is optionally substituted with R 10 and/or R 20 . 4. The compound of claim 3 , wherein the compound is selected from one of the following: Cpd. O—R 1 2-1 2-2 2-3 2-4 2-5 2-7 2-8 2-9 2-10 2-13 2-14 2-15 2-16 2-17
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Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00 · CPC title
Ortho-condensed systems · CPC title
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