WO2016140879A1 - Riluzole prodrugs and their use - Google Patents

Riluzole prodrugs and their use Download PDF

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Publication number
WO2016140879A1
WO2016140879A1 PCT/US2016/019787 US2016019787W WO2016140879A1 WO 2016140879 A1 WO2016140879 A1 WO 2016140879A1 US 2016019787 W US2016019787 W US 2016019787W WO 2016140879 A1 WO2016140879 A1 WO 2016140879A1
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WO
WIPO (PCT)
Prior art keywords
benzo
amino
thiazol
oxo
trifluoromethoxy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
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PCT/US2016/019787
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English (en)
French (fr)
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WO2016140879A9 (en
Inventor
Jay Edward Wrobel
Allen B. Reitz
Jeffery Claude PELLETIER
Garry Robert Smith
Haiyan Bian
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Biohaven Pharmaceutical Holding Co Ltd
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Biohaven Pharmaceutical Holding Co Ltd
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Publication date
Priority to LTEPPCT/US2016/019787T priority Critical patent/LT3265448T/lt
Priority to HK18108642.5A priority patent/HK1248706B/en
Priority to ES16759303T priority patent/ES2905318T3/es
Priority to PL16759303T priority patent/PL3265448T3/pl
Priority to RS20220149A priority patent/RS62915B1/sr
Priority to PH1/2021/550250A priority patent/PH12021550250A1/en
Priority to EA201791951A priority patent/EA034759B1/ru
Priority to HRP20220208TT priority patent/HRP20220208T1/hr
Priority to CA2978158A priority patent/CA2978158C/en
Priority to SG11201706831RA priority patent/SG11201706831RA/en
Priority to EP21209037.7A priority patent/EP4011870A1/en
Priority to MX2017011196A priority patent/MX380828B/es
Priority to EP16759303.7A priority patent/EP3265448B1/en
Priority to SI201631457T priority patent/SI3265448T1/sl
Priority to US15/549,154 priority patent/US10485791B2/en
Priority to KR1020237034132A priority patent/KR20230147746A/ko
Priority to BR112017018832-5A priority patent/BR112017018832B1/pt
Priority to KR1020177027618A priority patent/KR102587894B1/ko
Priority to DK16759303.7T priority patent/DK3265448T3/da
Priority to JP2017546176A priority patent/JP6700293B2/ja
Priority to AU2016226463A priority patent/AU2016226463B2/en
Application filed by Biohaven Pharmaceutical Holding Co Ltd filed Critical Biohaven Pharmaceutical Holding Co Ltd
Priority to CN201680025374.6A priority patent/CN107567438B/zh
Publication of WO2016140879A1 publication Critical patent/WO2016140879A1/en
Publication of WO2016140879A9 publication Critical patent/WO2016140879A9/en
Priority to IL253989A priority patent/IL253989B/en
Priority to PH12017501576A priority patent/PH12017501576B1/en
Anticipated expiration legal-status Critical
Priority to US16/449,948 priority patent/US10905681B2/en
Priority to US16/689,150 priority patent/US11052070B2/en
Priority to AU2020233650A priority patent/AU2020233650B2/en
Priority to IL278080A priority patent/IL278080B/en
Priority to US17/151,585 priority patent/US12295942B2/en
Priority to US17/164,654 priority patent/US12005046B2/en
Priority to US17/367,484 priority patent/US12213965B2/en
Priority to CY20221100236T priority patent/CY1125112T1/el
Priority to AU2022202163A priority patent/AU2022202163B2/en
Priority to US18/361,837 priority patent/US12005047B2/en
Priority to US18/361,838 priority patent/US12472165B2/en
Priority to US18/361,836 priority patent/US20240091205A1/en
Priority to US19/196,629 priority patent/US20250332148A1/en
Ceased legal-status Critical Current

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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • A61K31/5375—1,4-Oxazines, e.g. morpholine
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    • C07D277/62—Benzothiazoles
    • C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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Definitions

  • the present invention describes compounds and methods useful as prodrug agents, useful for the treatment of cancers including melanoma through the release of riluzole.
  • riluzole A recently conducted Phase 0 human clinical trial of riluzole (Rilutek 1 M ) demonstrated dramatic efficacy in certain melanoma patients after only 14 days of treatment.
  • Riluzole the only FDA approved drug to treat amyotrophic lateral sclerosis (ALS), showed clinical or radiologic evidence of tumor response in four of 12 patients with Stage III and IV melanoma, cancer with a poor prognosis and severely limited treatment options.
  • riluzole (RILUTEK®) for cancers or other diseases is significantly constrained due to high levels of variability in hepatic metabolism of the drug, dose dependent effects on the liver, and a negative food effect associated with the drag when administered with meals.
  • the approved LFSPI notes that that riluzole tablets should be taken at least 1 hour before, or 2 hours after, a meal to avoid food-related decreases in bioavailability that may interfere with the ability to achieve or maintain therapeutic blood concentrations.
  • Such fasting requirements amount to six hours of fasting per day when administered twice daily.
  • Riluzole is also believed to be clinically relevant in additional disease states, including a variety of central nervous system ("CNS”) and depression/anxiety states.
  • CNS central nervous system
  • CNS central nervous system
  • Riluzole is also believed to be clinically relevant in additional disease states, including a variety of central nervous system ("CNS”) and depression/anxiety states.
  • CNS central nervous system
  • These include, but are not limited to, bipolar disorder, treatment resistant and major depression, obsessive-compulsive disorder, general anxiety disorder, panic disorder, social anxiety, mood disorders, cognitive disorders, dementia, agitation, apathy, psychoses, post-traumatic stress disorders, irritability, disinhibition, learning disorders, memory loss, personality disorders, bipolar disorders, Rett syndrome, eating disorders, conduct disorder, neurodegenerative disorders, pain disorders, supranuclear palsy, frontotemporal dementia, frontotemporal lobar degeneration, delirium, Alzheimer's disease, mild cognitive impairment, mild cognitive impairment due to Alzheimer's
  • riluzole can have issues in liver metabolism. Pro-drags of riluzole will provide more predictable pharmacokinetic properties and metabolic profiles for the parent compound, leading to an improved therapeutic effect in each of the aforementioned disease states.
  • Riluzole has been approved for 25 years without solutions to the pharmacokinetic and metabolic limitations of the drug. The intrinsic property of the drag itself teaches away from the sublingual administration of riluzole.
  • Riluzole has a very low solubility in water, poor oral palatabilit , pH dependent chemical stability, and intense as well as persistent numbness or burning sensation throughout the oral cavity. Techniques aimed at reducing these undesirable effects, such as use of chelating agents, would only facilitate the oral swallowing and gastric absorption rather than resulting in sublingual absorption.
  • riluzole is clinically relevant to generalized anxiety disorder (GAD) and is useful for the attenuation of presynaptic glutaniate release. Riluzole is also useful for the normalization, enhancement or potentiation of the uptake of glutamate by glia (Cork et ai. US 8,778,979).
  • the present i nvention addresses the need to indentify new treatments for melanoma by identifying novel prodrugs of riluzole which possess enhanced stability to hepatic metabolism and are delivered into systemic circulation by oral administration.
  • the present invention can also treat or prevent various neurological or CNS states as well as depression/anxiety states.
  • the riluzole prodrugs are cleaved to release riluzole in the plasma via either an enzymatic or general biophysical release process.
  • the present invention is directed toward riluzole derivatives of formula (I), including enantiomers, diasteroemers, hydrates, solvates, pharmaceutically acceptable salts, and complexes thereof, wherein: is selected from the group consisting of Ci-C 6 fluoroalkyl, OR 2 , (CR 6a R 6b ) m N a nd
  • R 2 is selected from the group consisting of CH 2 (CH 2 ) n NR 3 R c ,
  • R 3a and R 3c are independently selected from the group consisting of hydrogen, Q-Ce alkyi, C3-C7 branched alkyi, C3-C7 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, and C0 2 R 4 ;
  • R 3a and R 3b cannot both be C i-C 6 alkyi
  • R 3a and R 3B are taken together with the atom to which they are bound to form an optionally substituted three to six membered saturated heterocyclic ring consisting of two to five carbon atoms and a member selected from the group consisting of O, NR 5 , S, and S0 2 ;
  • n 1 or 2;
  • R 4 is selected from the group consisting of C
  • R 1 is selected from the group consisting of Q- e aikyl, C3-C7 branched alkyi, C3-C7 cycloalkyl, C 2 -C 6 alkenyl, and C 2 -C f , alkynyl;
  • R°* and R°" are at each occurrence independently selected from the group consisting of hydrogen, optionally substituted Cj-Ce alkyi, optionally substituted C3-O ? branched alkyi, optionally substituted C 3 -C 7 cycloalkyl, C 2 -C 6 alkenyl, and C 2 -C 6 alkynyl;
  • R°° and R 6u are taken together with the atom to which they are bound to form an optionally substituted 6 membered ring;
  • n 1, 2, or 3;
  • R' is selected from the group
  • R 8a and R 8 " are at each occurrence independently selected from the group consisting of hydrog CH 3 , CH(CH 3 ) 2 , CH 2 CH(CH 3 ) 2 , CH(CH 3 )CH 2 CH 3 , CH 2 OH, CH(OH)CH 3 , CH 2 Ph, CH 2 (4-OH- Ph), (CH 2 ) 4 NH 2 , (CH 2 ) 3 NHC(NH 2 )NH, CH 2 (3-indole), CH 2 (5-imidazole), CH 2 C0 2 H,
  • Ci -Ce alkyl is at each occurrence independently selected from the group consisting of hydrogen, Ci -Ce alkyl, C3-C7 branched alkyl, C3-C 7 cycloalkyl, C 2 -C6 alkenyl, and C 2 -Ce alkynyl;
  • Y is at each occurrence independently selected from the group consisting of H 2 or O;
  • R l0a and R l0t> are at each occurrence independently selected from the group consisting of hydrogen, CH 3 , CH 2 CH 3 , O hi Ti . CH 2 CH(CH 3 )2, CH(CH 3 )CH 2 CH 3 , CH OI !.
  • R l0a and R l0b are taken together with the atom to which they are bound to form an optionally substituted three to six membered saturated carbocyclic ring;
  • R' ' is at each occurrence independently selected from the group consisting of hydrogen, Ci- alkyl, C 3 -C 6 branched alkyl, C 3 -C 6 cycloalkyl, C CV, alkenyl, Ci-Ce haloalkyl, and C 2 -C 6 alkynyl; R lJa and R' !
  • R l is at each occurrence independently selected from the group consisting of hydrogen, Q-Q alkyl, COCR 13a R ,3b R !5a R 15b , COCR ,3a R i3b OR 14 , S0 2 CR !3a R 1 b NR i5a R !5b ,
  • R' 1 and R ' 3 are taken together with the atom to which they are bound to form an optionally substituted four to six membered saturated heterocyclic ring containing a nitrogen atom and optionally containing an additional heteroatom from the group consisting of N and O;
  • R' 3a and R 1Jb are at each occurrence independently selected from the group consisting hydrogen, ( ⁇ , CH 2 CH 3 , CH 2 CH 2 CH 3 .
  • R l3a and R l3 ° are taken together with the atom to which they are bound to form an optionally substituted three to si membered saturated carbocyclic ring;
  • R l3a and R l3 ° are taken together with the atom to which they are bound to form an optionally substituted six membered saturated heterocyclic ring with one O atom within the ring;
  • R' " ' a and R l4 are taken together with the atoms to which they are bound to form an optionally substituted four to six membered ring containing one nitrogen atom;
  • R' " ' a and R 15 * are taken together with the atoms to which they are bound to form an optionally substituted four to six membered ring containing one nitrogen atom;
  • Y 1 is at each occurrence independently selected from the group consisting of 3 ⁇ 4, O, and ⁇ H/ ⁇ OC3 ⁇ 4Ph;
  • R' 4 is at each occurrence independently selected from the group consisting of hydrogen, Q-Ce alkyl, C 3 -C 6 branched alkyl, C 3 -C 6 cycioalkyl, C 2 -Ce alkenyl, and C 2 -Ce alkynyl;
  • R lia and R , 5b are at each occurrence independently selected from the group consisting of H, Q-Ce alkyl, C3-C7 branched alkyl, C 3 -C7 cycioalkyl, C 2 -Ce alkenyl, C 2 -Ce alkynyl Ci -Ce fiuoroalkyi, COR' 1 , CH 2 R 21 , S0 2 R 3 , an optionally substituted four to six membered saturated heterocyclic ring containing a heteroatom selected from the group consisting of NR 24 and O, COCHR i3 NH 2
  • R 1>a and R *jb are taken together with the atom to which they are bound to form an optionally substituted three to six membered saturated heterocyclic ring consisting of two to five carbon atoms and a member selected from the group consisting of O, NR 5 , S, and S0 2 ;
  • R" is ai each occurrence independently selected from the group consisting of hydrogen, C-. -C f , alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C 2 -Ce alkenyl, and C 2 -Ce alkynyl;
  • R l S is ai each occurrence independently selected from the group consisting of hydrogen, C-. -C f , alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C 2 ⁇ C-6 alkenyl, and C 2 -C 6 alkynyl;
  • R" and R l S are taken together with the atoms to which they are bound to form an optionally substituted five or six membered ring containing two nitrogen atoms;
  • R' 9a and R l9b are at each occurrence independently selected from the group consisting of hydrogen, optionally substituted Cj-Q alkyl, optionally substituted C3-C7 branched alkyl, optionally substituted C3-C7 cycloalkyl, optionally substituted CyQ alkenyl, and optionally substituted C Ce alkynyl;
  • R l9a and R l9 ° are taken together with the atom to which they are bound to form an optionally substituted 3 to 6 membered carbocyciic ring;
  • R 2J is at each occurrence independently selected from the group consisting of hydrogen, Ci-Ce alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C Ce alkenyl, and C 2 -Ce alkynyl;
  • q 1, or 2;
  • R 2 ' is at each occurrence independently selected from the group consisting of hydrogen, Ci- alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, Ci-C 6 fluoroalkyi, optionally substituted aryl, and optionally substituted heteroaryl;
  • R 2 is at each occurrence independently selected from the group consisting of C r C 6 alkyl, C3-C7 branched alkyl, C3 -C7 cycloalkyl, C 2 -Ce alkenyl, C 2 ⁇ C-6 alkynyl, optionally substituted aryl, opiionaily substituted heteroaryl;
  • R 23 is selected from the group consisting H, CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3 , CH 2 CCH, CH(CH 3 ) 2 , CH 2 CH(CH 3 ) 2 , CH(CH 3 )CH 2 CH 3 , CH 2 OH, CH 2 OCH 2 Ph, CH 2 CH 2 OCH 2 Ph, CH(OH)CH 3 , CH 2 Ph, CH 2 (cyclohexyl), CH 2 (4-OH-Ph), (CH 2 ) 4 NH 2 , (CH 2 ) 3 NHC(NH 2 )NH, CH 2 (3-indole), CH 2 (5-iniidazoie), CH 2 C0 2 H, CH 2 CH 2 CO 2 H, CH 2 CONH 2 , and CH 2 CH 2 CONH 2 ;
  • R *1 ⁇ 2 is at each occurrence independently selected from the group consisting of H, Cj-Q alkyl, C 3 - C 7 branched alkyl, C3-C7 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, optionally substituted aryl, optionally substituted heteroaryl, COR 23 , and S0 2 -Ci.. t ,alkyi;
  • R' " is at each occurrence independently selected from the group consisting of H, C Q alkyl, C3- C7 branched alkyl, C3-C7 cycloalkyl, Ci-C(, alkenyl, C Ce alkynyl, optionally substituted aryl, optionally substituted heteroaryl, Ci-Ce alkoxy, and Ci -Ce alkylamino.
  • the compounds of the present invention include compounds having formula (II):
  • the compounds of the present invention include compounds having formula (111):
  • the compounds of the present invention include compounds having formula (IV):
  • the compounds of the present invention include compounds having formula (V):
  • the compounds of the present invention include compounds having formula (VI):
  • the compounds of the present invenlion include compounds having formula (VII):
  • the compounds of the present invention include compounds having formula (VIII):
  • the compounds of the present invenlion include compounds having formula (IX):
  • the compounds of the present invention include compounds having formula (X):
  • the compounds of the present invention include compounds having formula (XI): including enantiomers, diasteroemers, hydrates, solvates, pharmaceutically acceptable salts, and complexes thereof.
  • the compounds of the present invention include compounds having formula (XII):
  • the compounds of the present invention include compounds having formula (XIII):
  • the compounds of the present invention include compounds having formula (XIV):
  • eoaotiomers including eoaotiomers, diasteroemers, hydrates, solvates, pharmaceutically acceptable salts, and complexes thereof.
  • the compounds of the present invention include compounds having formula (XV):
  • eoantiomers including eoantiomers, diasteroemers, hydrates, solvates, pharmaceutically acceptable salts, and complexes thereof.
  • the compounds of the present invention include compounds having formula (X VI):
  • the compounds of the present invention include compounds having formula (XVil):
  • Hie compounds of the present invention include compounds having formula (XVIII)
  • R 23 is selected from the group consisting H, CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3, CH 2 CCH, CH(CH 3 ) 2 , ( ⁇ . ⁇ ⁇ , CH(CH 3 )CH 2 CH 3 , CH 2 OH, CH 2 OCH 2 Ph, CH 2 CH 2 OCH 2 Ph, CH(OH)CH 3 , CH 2 Ph, CH 2 (cyclohexyl), CH 2 (4-OH-Ph), (CH 2 ) 4 NH 2 , (CH 2 ) 3 NHC(NH 2 )NH, CH 2 (3-indole), CH 2 (5-irnidazole), CH 2 C0 2 H, CH 2 CH 2 C0 2 H, CH 2 CONH 2 , and CH 2 CH 2 CONH 2 .
  • the present invention further relates to compositions comprising:
  • the present invention yet further relates to an effective amount of one or more compounds according to the present invention and an anticancer agent.
  • the present invention also relates to a method for treating or preventing cancer, particularly melanoma, said method comprising administering to a subject an effective amount of a compound or composition according to the present invention, possibly in conjunction with an excipient and/or an anticancer agent.
  • the present invention also relates to a method for treating or preventing disease or conditions associated with cancer, particularly melanoma.
  • Said methods comprise administering to a subject an effective amount of a compound or composition according to the present invention, possibly in conjunction with an excipient and/or an anticancer agent..
  • Cancers that may be treated or prevented by administering to a subject an effective amount of a compound or composition according to the present invention, or a pharmaceutically acceptable salt, solvate, anomer, enantiomer or hydrate thereof, possibly with an excipient or an anticancer agent, includi ovarian cancer, cervical cancer, breast cancer, prostate cancer, testicular cancer, lung cancer, renal cancer, colorectal cancer, skin cancer, brain cancer including glioma and glioblastoma, and leukemia.
  • the present invention also provides a sublingual or sustained release formulation which may comprise an effective amount of riluzole or a pharmaceutically acceptable salts, solvate, anomers, enantiomers, hydrate or prodrugs thereof to treat cancers in combination with immunotherapies (including alone or in combination with vaccines, anti-PDI , anti-PDLl , anti-CTLA4 or other immunotherapy or checkpoint inhibitor targets including: CTLA4, cytotoxic T-lymphocyte-associated antigen 4; Ig, immunoglobulin; LAG3, lymphocyte activation gene 3; mAbs, monoclonal antibodies; PDl, programmed cell death protein 1 ; PDL, PDl ligand; ⁇ 3, T cell membrane protein 3, CD40L, A2aR, adenosine A2a receptor; B7RP1 , B7-related protein 1; BTLA, B and T lymphocyte attenuator; GAL9, galectin 9; ⁇ ⁇ , herpesvirus entry mediator; ICOS, in
  • the present invention also relates to a method for treating or preventing various neurological or CNS states as well as depression anxiety states in which riluzole is clinically relevant including, but are not limited to, bipolar disorder, treatment resistant and major depression, general anxiety disorder, panic disorder, social anxiety, mood disorders, cognitive disorders, dementia, agitation, apathy, psychoses, post-traumatic stress disorders, irritability, disinhibition, learning disorders, memory loss, personality disorders, bipolar disorders, Rett syndrome, eating disorders, conduct disorder, neurodegenerative disorders, pain disorders, supranuclear palsy, frontotemporal dementia, frontotemporal lobar degeneration, delirium, Alzheimer's disease, mild cognitive impairment, mild cognitive impairment due to Alzheimer' s disease, drug addiction, tinnitus, mental retardation, obsessive-compulsive disorder, spinal muscular atrophy, radiation therapy, multiple sclerosis, chronic cerebellar ataxia, hereditary spinocerebellar ataxia, spinocerebellar ataxia, spor
  • the present invention yet further relates to a method of enhancing the activity of a serotonin reuptake inhibitor (SRI) in an individual in need thereof.
  • the methods comprise co-administering to the individual an effective amount of a compound or composition according to the present invention and a SRI.
  • the serotonin reuptake inhibitor can be citalopram, escitalopram, ilouxetine, fluvoxamine, paroxetine, sertraline, trazodone, venlafaxine, mirtazepine, clomipramine, or combinations with other psychottopic medications including an anti-psychotic, an anticonvulsant, a tricyclic antidepressant, a monoamine oxidase inhibitor, a selective serotonin reuptake inhibitor, a selective serotonin- norepinephrine reuptake inhibitor, a norepinephrine dopamine reuptake inhibitor, a serotortin-2 antagonist reuptake inhibitor, a benzodiazepine, a wakefulness promoting agent, anti-manic agent, or a combination of one or more of the foregoing.
  • the present invention further rel tes to a process for preparing the riluzole prodrugs of the present invention.
  • Figure 1 Time concentration curve for example 125 and released riluzole via both intravenous and oral administration.
  • Figure 3 Time-concentration curves for 2-Amino-N- ⁇ [methyl( ⁇ [6-(trifluoromethoxy)-l ,3-benzo thiazol-2-3'l]carbamoyl ⁇ methyl)carba]Tsoyl]meth)'l ⁇ acetamide (Example 204) and released riluzole via both intravenous and oral administration.
  • Figure 5 PK in fasted male mice for Example 204 , IV administration, 1 rng kg. and PO administration 5 mg/kg. Monitor disappearance of Prodrug and appearance of riluzole.
  • Figure 6 PK in Cynomolgus Monkey for Example 204 , IV administration, 1 mg/kg. and PO administration s mg kg. Monitor appearance of riluzole.
  • the prodrugs of the present invention are capable of treating and preventing cancers such as melanoma by releasing riluzole in vivo.
  • Prodrugs of riluzole have enhanced stability to hepatic metabolism and are delivered into systemic circulation by oral administration, and are then cleaved to release riluzole in the plasma via either an enzymatic or general biophysical release process.
  • Riluzole has dramatic anti-melanoma activity in vitro, in mice and in a Phase 0 human clinical trial.
  • the pro-drags of the present invention are also capable of treating and preventing other disease states in which riluzole is clinically relevant including, but are not limited to, amyotrophic lateral sclerosis (ALS) bipolar disorder, treatment resistant and major depression, general anxiety disorder, panic disorder, social anxiety, mood disorders, cognitive disorders, dementia, agitation, apathy, psychoses, post-traumatic stress disorders, irritability, disinhibition, learning disorders, memory loss, personality disorders, bipolar disorders, Rett syndrome, eating disorders, conduct disorder, neurodegenerative disorders, pain disorders, supranuclear palsy, frontotemporal dementia, frontotemporal lobar degeneration, delirium, Alzheimer's disease, mild cognitive impairment, mild cognitive impairment due to Alzheimer's disease, drug addiction, tinnitus, mental retardation, obsessive-compulsive disorder, spinal muscular atrophy, radiation therapy, multiple sclerosis, chronic cerebellar ataxia, hereditary spinocerebellar ataxia, spinocerebellar
  • compositions are described as having, including, or comprising specific components, or where processes are described as having, including, or comprising specific process steps, it is contemplated that compositions of the present teachings also consist essentially of, or consist of, the recited components, and that the processes of the present teachings also consist essentially of, or consist of, the recited processing steps.
  • an element or component is said to be included in and/or selected from a list of recited elements or components, it should be understood that the element or component can be any one of the recited elements or components and can be selected from the group consisting of two or more of the recited elements or components.
  • halogen shall mean chlorine, bromine, fluorine and iodine.
  • alkyl and “aliphatic” whether used alone or as part of a substituent group refers to straight and branched carbon chains having 1 to 20 carbon atoms or any number within this range, for example 1 to 6 carbon atoms or 1 to 4 carbon atoms.
  • Designated numbers of carbon atoms e.g. Q. ) shall refer independently to the number of carbon atoms in an alkyl moiety or to the alkyl portion of a larger alkyl-containing substituent.
  • Non-limiting examples of alkyl groups include methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec- butyl, iso-butyl, tert-butyl, and the like.
  • Alkyl groups can be optionally substituted.
  • Non-limiting examples of substituted alkyl groups include hydroxymethyl, chloromethyl, trifluoromethyl, aminomethyl, 1 -chloroethyl, 2-hydroxyethyl, 1,2-difluoroethyl, 3-carboxypropyi, and the like.
  • substituent groups with multiple alkyl groups such as (Ci.Ce alkyl ⁇ amino, the alkyl groups may be the same or different.
  • cycloalkyl refers to a non- aromatic carbon-containing ring including cyciized alkyl, alkenyl, and alkynyl groups, e.g., having from 3 to 14 ring carbon atoms, preferably from 3 to 7 or 3 to 6 ring carbon atoms, or even 3 to 4 ring carbon atoms, and optionally containing one or more (e.g., 1 , 2, or 3) double or triple bond.
  • Cycloalkyl groups can be monocyclic (e.g., cyclohexyl) or polycyclic (e.g., containing fused, bridged, and/or spiro ring systeins), wherein the carbon atoms are located inside or outside of the ring system. Any suitable ring position of the cycloalkyl group can be covendinglv linked to the defined chemical structure. Cycloalkyl rings can be optionally substituted.
  • Nonlimiting examples of cycloalkyl groups include: cyclopropyl, 2-methyi-cyclopropyl, cyclopropenyl, cyclobutyl, 2,3-dihydroxycyclobutyl, cyclobutenyl, cyclopentyl, cyclopentenyl, cyclopentadienyl, cyclohexyl, cyclohexenyl, cycloheptyl, cyclooctanyl, decalinyl, 2,5- dimethylcyclopentyl, 3,5-dichiorocyclohexyl, 4-hydroxycyclohexyl, 3,3,5-trimethylcyclohex- 1-yl, octahydropentalenyl, octahydro- lH-indenyl, 3a,4,5,6,7,7a-hexahydro-3H-inden-4-yl, decahydroazulenyl; bicyclo[6.2.0]
  • cycloalkyl also includes carbocyclic rings which are bicyclic hydrocarbon rings, non-limiting examples of which include, bicyclo-[2.1 . I Jhexanyl, bicyclo[2.2.1]heptanyl, bicyclo[3.1.1]heptanyl, l,3-dimethyl[2.2. I]heptan-2-yl, bicyclo[2.2.2]octanyl, and bicyclo[3.3.3]undecanyl.
  • Haloalkyl is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, substituted with 1 or more halogen.
  • Haloalkyl groups include perhaloalkyl groups, wherein all hydrogens of an alkyl group have been replaced with halogens (e.g., -CF 3 , CF1CF 3 ).
  • Haloalkyl groups can optionally be substituted with one or more subslituents in addition to halogen.
  • haloalkyl groups include, but are not iimiled to, fluoromethyL dichioroetiiyl, trifluoromethyL trichloromelhyl, pentafluoroethyl, and pentachloroethyl groups.
  • alkoxy refers to the group -O-alkyl, wherein the alkyl group is as deiined above. Alkoxy groups optionally may be substituted.
  • v cyclic alkoxy refers to a ring containing 3 to 6 carbon atoms and at least one oxygen atom (e.g., tetrahydrofuran, tetrahydro-2H-pyran). C3.Ce cyclic alkoxy groups optionally may be substituted.
  • aryl wherein used alone or as part of another group, is defined herein as an unsaturated, aromatic monocyclic ring of 6 carbon members or to an unsaturated, aromatic polycyclic ring of from 10 to 14 carbon members.
  • Aryl rings can be, for example, phenyl or naphthyl ring each optionally substituted with one or more moieties capable of replacing one or more hydrogen atoms.
  • Non-limiting examples of aryl groups include: phenyl, naphthylen- I -yS, naphthylen-2-yl, 4-fluorophenyl, 2-hydroxyphenyl, 3 -methylphenyl, 2-amino-4-fluorophenyl, 2- (N,N-diethylamino phenyl, 2-cyanophenyl, 2,6-di-tert-butylphenyl, 3-methoxyphenyl, 8- hydroxynaphthylen-2-yl 4,5-dimethoxynaphthylen-l-yl, and 6-cyano-naphthylen-l-yl.
  • Aryl groups also include, for example, phenyl or naphthyl rings fused with one or more saturated or partially saturated carbon rings (e.g., bicyclo[4.2.0]octa-l,3,5-trienyl, indanyl), which can be subsliluled at one or more carbon atoms of the aromatic and/or saturated or partially saturated rings.
  • phenyl or naphthyl rings fused with one or more saturated or partially saturated carbon rings (e.g., bicyclo[4.2.0]octa-l,3,5-trienyl, indanyl), which can be subsliluled at one or more carbon atoms of the aromatic and/or saturated or partially saturated rings.
  • arylalkyl refers to the group -alkyl-aryl, where the alkyl and aryl groups are as defined herein.
  • Aralkyi groups of the present invention are optionally substituted. Examples of arylalkyl groups include, for example, benzyl, 1 -phenylethyl, 2-phenyieihyi, 3- phenylpropyl, 2-phenylpropyl, fluorenylmefhyl and the like.
  • heterocyclic and/or “heterocycle” and/or “heterocyiyi,” whether used alone or as pari of another group, are defined herein as one or more ring having from 3 to 20 atoms wherein at least one atom in at least one ring is a heteroatom selected from nitrogen (N), oxygen (O), or sulfur (S), and wherein further the ring that includes the heteroatom is non-aromatic.
  • the non-heteroatom bearing ring may be aryl (e.g., indolinyl, tetrahydroquinolinyl, chromanyl).
  • heterocycle groups have from 3 to 14 ring atoms of which from 1 to 5 are heteroatoms independently selected from nitrogen (N), oxygen (O), or sulfur (S).
  • N nitrogen
  • O oxygen
  • S sulfur
  • One or more N or S atoms in a heterocycle group can be oxidized.
  • Heterocycle groups can be optionally substituted.
  • Non-limiting examples of heterocyclic units having a single ring include: diazirinyl, aziridinyl, urazolyl, azetidinyl, pyrazolidinyl, imidazolidinyl, oxazolidinyl, isoxazolinyl, isoxazolyl, thiazolidinyi, isothiazoiyl, isothiazolinyl oxathiazolidinonyl, oxazolidinonyl, hydantoinyl, tetrahydrofuranyl, pyrrolidinyi, morpholinyi, piperazinyl, piperidinyi, dihydropyranyl, tetrahydropyranyi, piperidin-2-onyl (valerolactam), 2,3,4,5-tetrahydro-lH-azepinyl, 2,3-dihydro- lH-indole, and 1 ,2,3,4-
  • Non-limiting examples of heterocyclic units having 2 or more rings include: hexahydro-l H-pyrrolizinyl, 3a,4,5,6,7,7a-hexahydro-lH- benzo[d]imidazolyl, 3a,4,5,6,7,7a-hexahydro-lH-indolyl, 1,2,3,4-tetrahydroquinolinyl, chromanyl, isochromanyl, indolinyl, isoindolinyl, and decahydro-l.H-cycloocta[b]pyrrolyl.
  • heteroaryl is defined herein as one or more rings having from 5 to 20 atoms wherein at least one atom in at least one ring is a heteroatom chosen from nitrogen (N), oxygen (O), or sulfur (S), and wherein further at least one of the rings that includes a heteroatom is aromatic.
  • the non-heteroatom bearing ring may be a carbocycle (e.g., 6,7-Dihydro-5H- cyclopeiitapyrimidine) or aryl (e.g., benzofuranyl, benzothiophenyl, indolyl).
  • heteroaryl groups have from 5 to 14 ring atoms and contain from 1 to 5 ring heteroatoms independently selected from nitrogen (N), oxygen (Q), or sulfur (S).
  • N nitrogen
  • Q oxygen
  • S sulfur
  • One or more N or S atoms in a heieroaryl group can be oxidized.
  • Heieroaryl groups can be substituted.
  • Non-limiting examples of heteroaryl rings containing a single ring include: 1 ,2,3,4- tetrazolyl, [l,2,3]triazolyl, [l ,2,4]triazoiyi, triazinyl, ihiazolyl, 1 H-imidazolyi, oxazolyl, furanyl, thiopheneyl, pyrimidinyl, 2- phenylpyrimidinyl, pyridinyl, 3-methylpyridinyl, and 4-dimethylaminopyridinyl.
  • heteroaryl rings containing 2 or more fused rings include: benzofuranyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, cinnolinyl, naphthyridinyl, phenatithridinyl, 7H-puriny1, 9H-purinyi, 6-amino-9H-purinyl, 5H-pyrrolo[3,2-d]pyrimidinyl, 7H- pyrrolo[2,3-d]pyrimidinyl, pyrido[2,3-d]pyrimidinyl, benzo[d]thiazolyl, lH-indolyl, 4,5,6,7- tetrahydro- 1-H-indolyl, quinoxalinyl, 5-methylquinoxalinyl, quinazolinyl, quinolinyl, 8-hydroxy- quinolinyl, and isoquinolinyl.
  • the ring when two subsdtuents are taken together to form a ring having a specified number of ring atoms (e.g., R 2 and J taken together with the nitrogen (N) to which they are attached to form a ring having from 3 to 7 ring members), the ring can have carbon atoms and optionally one or more (e.g., 1 to 3) additional heteroatoms independently selected from nitrogen (N), oxygen (O), or sulfur (S).
  • the ring can be saturated or partially saturated and can be optionally substituted.
  • fused ring units as well as spiroeyclic rings, bieyclic rings and the like, which comprise a single heteroatom will be considered to belong to the cyclic family corresponding to the heteroatom containing ring.
  • 1,2,3,4- tetrahydroquinoline having the formula:
  • aryl ring When a fused ring unit contains heteroatoms in both a saturated and an aryl ring, the aryl ring will predominate and determine the type of category to which the ring is assigned. For example, 1,2,3,4-tetrahydro- [l ,8]naphthyridine having the formula:
  • substituted is used throughout the specification.
  • substituted is defined herein as a moiety, whether acyclic or cyclic, which has one or more hydrogen atoms replaced by a substituent or several (e.g., 1 to 10) substituents as defined herein below.
  • the substituents are capable of replacing one or two hydrogen atoms of a single moiety at a time.
  • these substituents can replace two hydrogen atoms on two adjacent carbons to form said substituent, new moiety or unit.
  • a substituted unit that requires a single hydrogen atom replacement includes halogen, hydroxy!, and the like.
  • a two hydrogen atom replacement includes carbonyl, oximino, and the like.
  • a two hydrogen atom replacement from adjacent carbon atoms includes epoxy, and the like.
  • substituted is used throughout the present specification to indicate that a moiety can have one or more of the hydrogen atoms replaced by a substituent. When a moiety is described as “substituted” any number of the hydrogen atoms may be replaced.
  • difluoromethyl is a substituted C] alkyl
  • trifl uoromethyl is a substituted Q alkyl
  • 4- hydroxyphenyl is a substituted aromatic ring
  • (N,N-dimethyl-5-amino)octanyl is a substituted Cg alkyl
  • 3-guanidinopropyl is a substituted C3 alkyl
  • 2-carboxypyridinyl is a substituted heteroaryl.
  • variable groups defined herein e.g., alkyl, cycloalkyl, alkoxy, aryloxy, aryl, heterocycle and heteroaryl groups defined herein, whether used alone or as part of another group, can be optionally substituted. Optionally substituted groups will be so indicated.
  • haloalkyl C,.. 6 alkoxy, C 2 . 8 alkenyl, C 2 .g alkynyl, C 3 .. I 4 cvcloalkyl, aryl, heterocycle, or heteroaryl, wherein each of the alkyl, haloalkyl, alkenyl, alkynyl, alkoxy, cycloalkyl, aryl, heterocycle, and heteroaryl groups is optionally substituted with 1- 10 (e.g., 1 -6 or 1 -4) groups selected independently from halogen, -CN, -N(1 ⁇ 2, oxo, and W '6 ; wherein
  • R ' at each occurrence, independently is hydrogen, -OR “' , -SR “ , ⁇ C(0)R ' ', ⁇ C(0)OR “ , ⁇ C(0)N(R 27 ) 2 , -S0 2 R 27 , -S(0) 2 OR 27 , -N(R 27 ) 2 , -NR 27 C(0)R 27 , ( ' ,. alkyl, C diligent haloalkyl, C 2 .
  • R 2 ' at each occurrence, independently is hydrogen, Cus alkyl, C [ acute6 haloalkyl, C 2 _8 alkenyl, C 2 .» alkynyl, cycloalkyl (e.g., cycloalkyl), aryl, heterocycle, or heteroaryi, or two R 7 units taken together with the atom(s) to which they are bound form an optionally substituted carbocycie or heterocycle wherein said carbocycie or heterocycle preferably has 3 to 7 ring atoms.
  • the substituents are selected from:
  • OR 28 for example, -OH, -OCH 3 , -OCH 2 CH 3 , -OCH 2 CH 2 CH 3 ;
  • -S0 2 R 28 for example, -SO -S i: ⁇ S0 2 CH 3 ; -S0 2 C 6 H 5 ;
  • each R 28 is independently hydrogen, optionally substituted Ci -Ce linear or branched alkyl (e.g., optionally substituted C 1 -C4 linear or branched alkyl), or optionally substituted C Ce cycloalkyl (e.g optionally substituted C3-C4 cycloalkyl); or two R 28 units can be taken together to form a ring comprising 3-7 ring atoms.
  • each R 2S is independently hydrogen, Ci-Ce linear or branched alkyl optionally substituted with halogen or Cj-Ch cycloalkyl or C3-C6 cycloalkyl.
  • C j.Ce alkyl is specifically intended to individually disclose C-, , C 3 ⁇ 4 C3, Q, C5, Q, Q.Ce, C1-C5, C1-C4, C 1 -C3, C r C 2 , C 2 -C 6 , C2-C5, C 2 -C4, C 2 -C3, C 3 -C 6 , C3-C5, C3-C4, C 4 -C 6 , -C5, and C 5 -C 6 , alkyl.
  • composition of matter stand equally well for the prodrug agent described herein, including all enantiomeric forms, diastereomeric forms, salts, and the like, and the terms “compound,” “analog,” and “composition of matter” are used interchangeably throughout the present specification.
  • asymmetric atom also referred as a chirai center
  • some of the compounds can contain one or more asymmetric atoms or centers, which can thus give rise to optical isomers (enantiomers) and diastereomers.
  • the present teachings and compounds disclosed herein include such enantiomers and diastereomers, as well as the racemic and resolved, enaniiomericaiiy pure R and S stereoisomers, as well as other mixtures of the R and S stereoisomers and pharmaceutically acceptable salts thereof.
  • Optical isomers can be obtained in pure form by standard procedures known to those skilled in the art, which include, but are not limited to, diastereomeric salt formation, kinetic resolution, and asymmetric synthesis.
  • the present teachings also encompass cis and trans isomers of compounds containing alkenyl moieties (e.g., alkenes and irnines). It is also understood that the present teachings encompass all possible regioisomers, and mixtures thereof, which can be obtained in pure form by standard separation procedures known to those skilled in the art, and include, but are not limited to, column chromatography, thin-layer chromatography, and high-performance liquid chromatography.
  • Pharmaceutically acceptable salts of compounds of the present teachings, which can have an acidic moiety can be formed using organic and inorganic bases. Both mono and polyanionic salts are contemplated, depending on the number of acidic hydrogens available for deprotonation.
  • Suitable salts formed with bases include metal salts, such as alkali metal or alkaline earth metal salts, for example sodium, potassium, or magnesium salts; ammonia salts and organic amine salts, such as those formed with morpholine, thiomorpholine, piperidine, pyrrolidine, a mono-, di- or tri-lower alkylamine (e.g., ethyl-tert-butyl-, diethyl-, diisopropyS-, triethyl-, tributyl- or dimethylpropylamine), or a mono-, di-, or trihydroxy lower alkylamine (e.g., mono-, di- or triethanolamine).
  • metal salts such as alkali metal or alkaline earth metal salts, for example sodium, potassium, or magnesium salts
  • ammonia salts and organic amine salts such as those formed with morpholine, thiomorpholine, piperidine, pyrrolidine, a mono-,
  • inorganic bases include NaHCC>3, Na 2 COs, KHCO 3 , K 2 C0 3 , Cs 2 COj, LiOH, NaOH, KOH, NaH 2 P0 4 , Na 2 HP0 4 , and Na 3 P0 4 .
  • Internal sails also can be formed.
  • salts can be formed using organic and inorganic acids.
  • salts can be formed from the following acids: acetic, propionic, lactic, benzenesulfonic, benzoic, earnphorsuifonic, citric, tartaric, succinic, dichloroacetic, ethenesulfonic, formic, fumaric, gluconic, glutamic, hippuric, hydrobromic, hydrochloric, isethionic, lactic, rnaieic, malic, malonic, mandelic, methanesulfonic, mucic, napthalenesulfonic, nitric, oxalic, pamoic, pantothenic, phosphoric, phthalic, propionic, succinic, sulfuric, tartaric, toluenesulfonic, and earnphorsuifonic as well as other known pharmaceutically acceptable acids.
  • neuropsychiatric disorder is a mental or neurologic disorder which is associated with the nervous system.
  • the neuropsychiatric disorder may include anxiety disorders, mood disorders, neurodegenerative disorders, neurodevelopmental disorders, autism, pervasive developmental disorder, pain disorders, neuropathic pain, ALS, cognitive disorders, Huntington's disease, Parkinson's disease, supranuclear palsy, frontal temporal dementia, schizophrenia, delirium, Alzheimer's disease, depression, mania, attention deficit disorders, drug addiction, dementia, agitation, apathy, anxiety, psychoses, post-traumatic stress disorders, irritability, and disinhibition, learning disorders, memory loss, mental retardation, dementia, personality disorders, bipolar disorders, bipolar depression, generalized anxiety disorder, panic disorder, obsessive-compulsive disorders, trichotillomania, eating disorders, and the like.
  • neuropsychiatric disorders includes those listed in the Diagnostic and Statistical Manual of Mental Disorders (American Psychiatric Association, 5th Edition): Neurodevelopmental disorders.
  • Intellectual disabilities Intellectual disability (intellectual developmental disorder), Global developmental delay, Unspecified intellectual disability (Intellectual developmental disorder), Communication disorders, Language disorder, Speech sound disorder, Childhood-onset fluency disorder (stuttering), Social (pragmatic) communication disorder, Unspecified communication disorder.
  • Autism spectrum disorder Rett Syndrome, Attention deficit hyperactivity disorder (ADHD), Unspecified attention-deficit Hyperactivity disorder, Specific learning disorder, Motor disorders, Developmental coordination disorder, Stereotypic movement disorder, Tic disorders, Tourette's disorder, Persistent (Chronic) motor or vocal tic disorder, Provisional tic disorder, Other specified tic disorder, Unspecified tic disorder, Other neurodevelopmental disorders, Unspecified neurodevelopmental disorder, Schizophrenia spectrum and other psychotic disorders, Delusional disorder, Brief psychotic disorder, Schizophreniform disorder, Schizophrenia, Schizoaffective disorder, Major depressive or manic mood disorder concurrent with primary symptoms of schizophrenia, Substance/Medication- induced psychotic disorder, Psychotic disorder due to another medical condition, Catatonia, Other specified schizophrenia spectrum and other psychotic disorder, Unspecified schizophrenia spectrum and other psychotic disorder, Bipolar and related disorders, Anxiety disorders, Obsessive-compulsive and related disorders, Trauma- and stressor- elated disorders, Reactive attachment disorder, Disin
  • Unspecified trauma- and stressor-related disorder Dissociative disorders, Dissociative identity disorder, Dissociative amnesia, Depersonalization/Derealization disorder, Somatic symptom disorders, Encopresis, other elimination disorder, Disruptive, impulse-control and conduct disorders in DSM-5, Oppositional defiant disorder.
  • Intermittent explosive disorder Conduct disorder, Other specified disruptive, conduct disorder, unspecified disruptive, and conduct disorder, Substance-Related and Addictive Disorders, Substance-Related Disorders, Alcohol- Related Disorders, Alcohol Use Disorder, Alcohol Withdrawal, Cannabis-Related Disorders, Cannabis Use Disorder, Gambling Disorder, Cluster A personality disorders.
  • Paranoid personality disorder Schizoid personality disorder, Schizotypal personality disorder, Cluster B personality disorders, Antisocial personality disorder, Borderline personality disorder, Histrionic personality disorder, Narcissistic personality disorder, Cluster C personality disorders, Avoidant personality disorder, Dependent personality disorder, Obsessive-compulsive personality disorder, Paraphilic disorders.
  • DSM refers to a Diagnostic and Statistical Manual of Menial Disorders as provided by American Psychiatric Association's (APA) classification and diagnostic tool. Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5 or DSM-V) is updated in 2013 and exemplary disorders in DSM-V are listed in Appendix A. In addition, the DSM-V has a structure that includes broad categories and subdiagnoses indicating disorders, conditions and problems.
  • Neurodegenerative disorders could also include neurodegenerative or neurologic disorders including: Alzheimer's disease, dementia, vascular dementia, mixed dementia, Parkinson ' s disease, Huntington's disease, Amyotrophic lateral sclerosis (ALS), pseudobulbar affect, agitation in Alzheimer's disease, dementia, cerebellar ataxia, hereditary ataxias, multiple sclerosis, Progressive Supranuclear Palsy, pain disorders, neuropathic pain, neuropathies, stroke, seizure, Fragile X, etc.
  • ALS Amyotrophic lateral sclerosis
  • the neuropsychiatric symptoms may include anxiety, depression, stress, fatigue, feelings of panic, fear, uneasiness, problems in sleeping, cold or sweaty hands and/or feet, shortness of breath, heart palpitations, social phobia, fear of public speaking, an inability to be still and calm, dry mouth, numbness or tingling in the hands or feet, nausea, muscle tension, dizziness apathy, elation, disinhibition, irritability, wandering, and the like.
  • neuropsychiatric symptoms could include: delusions, hallucinations, disorganized thinking or speech, derailment of focal topic or loose associations, incoherence, grossly disorganized or abnormal motor behavior (including catatonia), negative symptoms - reduced emotional expression, avoliiion, alogia, anhedonia, asociality, dyskinesias (including tardive dyskinesia), anhedonia and dysphoria, anger and aggression, or symptoms of dissociation, or some combination of these.
  • cancer including Acute Lymphoblastic Leukemia (ALL), Acute Myeloid Leukemia (AML), Adrenocortical Carcinoms, Childhood cancers, AIDS-Related Cancers, Kaposi Sarcoma, AIDS-Related Lymphoma, Primary CNS Lymphoma, Anal Cancer, Astrocytomas, Atypical Teratoid/Rhabdoid Tumor, Basal Cell Carcinoma, Skin Cancer (Nonmelanoma), Bile Duct Cancer, Bladder Cancer, Bone Cancer, Ewing Sarcoma Family of Tumors, Osteosarcoma and Malignant Fibrous Histiocytoma, Brain Stem Glioma, Atypical Teratoid/Rhabdoid Tumor, Embryonal Tumors, Germ Cell Tumors, Craniopharyngioma, Ependymoma, Breast Cancer, Bronchial Tumors, Burkitt Lymphoma, Non-Hodgkin Lymp
  • treatment includes any treatment of a condition or disease in a subject, or particularly a human, and may include: (i) preventing the disease or condition from occurring in the subject which may be predisposed to the disease but has not yet been diagnosed as having it; (ii) inhibiting the disease or condition, i.e., arresting its development; relieving the disease or condition, i.e., causing regression of the condition; or (iii) ameliorating or relieving the conditions caused by the disease, i.e., symptoms of the disease. "Treatment" could be in combination with other standard therapies or alone.
  • terapéuticaally effective and “effective dose” refer to a substance or an amount that elicits a desirable biological activity or effect.
  • riluzole prodrug shall mean a compound that are cleaved to release riluzole in the plasma via either an enzymatic or general biophysical release process.
  • prodrug agent shall mean a compound mat are cleaved to release riluzole in the plasma via either an enzymatic or general biophysical release process.
  • the term "anticancer agent” shall mean a compound that is useful for the treatment or prevention of cancer, including but not limited to melanoma, ovarian cancer, cervical cancer, breast cancer, prostate cancer, testicular cancer, lung cancer, renal cancer, colorectal cancer, skin cancer, brain cancer, and leukemia. Except when noted, the terms “subject” or “patient” are used interchangeably and refer to mammals such as human patients and non-human primates, as well as experimental animals such as rabbits, rats, and mice, and other animals. Accordingly, the term “subject” or “patient” as used herein means any mammalian patient or subject to which the compounds of the invention can be administered.
  • accepted screening methods are employed to determine risk factors associated with a targeted or suspected disease or condition or to determine die status of an existing disease or condition in a subject.
  • These screening methods include, for example, conventional work-ups to determine risk factors that may be associated with the targeted or suspected disease or condition.
  • the prodrug agents are selected from:
  • the prodrug agents of the present invention are N-substituted riluzole analogs, and include all enantiomeric and diastereomeric forms and pharmaceutically accepted salts thereof having the formula (I):
  • R J R Ja and R J " are independently seiected from the groisp consisting of hydrogen, C-. -Cf, alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyi, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, and C0 2 R 4 ;
  • R Ja and R c cannot both be Ci-Ce alkyi
  • R J* and R J" are taken together with the atom to which they are bound to form an optionally substituted three to six membered saturated heterocyclic ring consisting of two to five carbon atoms and a member selected from the group consisting of O, NR 3 , S, and S0 2 ;
  • n ⁇ or 2
  • R 4 is selected from the group consisting of Cj -Cg alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyi, C2-C6 alkenyl, C2- alkynyl, optionally substituted phenyl, and optionally substituted benzyl;
  • R 3 is selected from the group consisting of Cj -Cg alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyi, C2-C6 alkenyl, and C2-C6 alkynyl;
  • R 6a and R 6 " are at each occurrence independently selected from the group consisting of hydrogen, optionally substituted C alkyl, optionally substituted C3-C7 branched alkyl, optionally substituted C2-Q alkenyl, optionally substituted C2-Q alkynyl, and optionally substituted C3-O ? cycloalkyi,;
  • R 6a and R 6n are taken together with the atom to which they are bound to form an optionally substituted 6 membered ring;
  • n I, 2, or 3;
  • R 7 is seiected from the group consisting of COC R 8a R sb (NHR 9 ), ⁇ -- ⁇ and
  • R "a and R iu are at each occurrence independently selected from the group consisting of hydrogen, ( ⁇ 1 ⁇ .. CH(CH 3 ) 2 , CH 2 CH(CH 3 ) 2 , ⁇ 1 ⁇ ⁇ 1 ; ⁇ ( ⁇ ⁇ . ⁇ ( ⁇ ⁇ : . CH 2 OH, CH(OH)CH 3 , CH 2 Ph, CH 2 (4-OH- Ph), (CH 2 ) 4 NH 2 , (CH2) 3 NHC(NH 2 )NH, CH 2 (3 -indole), CH 2 (5-imidazole), CH 2 C0 2 H,
  • R 9 is at each occurrence independently selected from the group consisting of hydrogen, C, -C 6 alkyi, C3-C7 branched alkyl, C3-C7 cycloalkyi, C 2 -C 6 alkenyl, and C 2 -C 6 alkynyl;
  • Y is at each occurrence independently selected from the group consisting of H 2 or O;
  • R' Ja and R l0i> are at each occurrence independently seiected from the group consisting of hydrogen, CH 3 , CH 2 CH 3 , CH(CH 3 ) 2 , CH 2 CH(CH 3 ) 2 , CH(CH 3 )CH 2 CH 3 , CH 2 OH, CH 2 OCH 2 Ph, CH(OH)CH 3 , CH 2 Ph, CH 2 (4-OH-Ph), (CH 2 ) 4 H 2 , (CH 2 ) 3 HC(NH 2 )NH, CH 2 (3-indole), CH 2 (5- imidazole), CH 2 (CCH), CH 2 (cyclohexyl), ⁇ i i - ⁇ ⁇ - ⁇ . CH 2 CH 2 C0 2 H, CH 2 CONH 2 , and
  • R' Ja and R l0b are taken together with the atom to which they are bound to form an optionaily substituted three to six membered saturated carbocyciic ring;
  • R' 1 is at each occurrence independently selected from the group consisting of hydrogen, Cj-C 6 alkyl, C 3 -C 7 branched alkyl, C 3 -C 7 cycloalkyl, C 2 -C 6 alkenyl, C C 6 haloalkyl, and C 2 -C 6 alkynyl
  • R l0a and R 11 are taken together with the atoms to which they are bound to form an optionally substituted four to six membered ring containing one nitrogen atom, and R l is not hydrogen
  • R l0 ° and R n are taken together with the atoms to which they are bound to form an optionally substituted four to six membered ring containing one nitrogen atom, and R l is not hydrogen
  • R" is at each occurrence independently selected from the group consisting of hydrogen, Ci- I 3 3 ⁇ 4 ,3b R i5a R I5b , COCR l3a R 13b QR 14 , S0 2 CR i3
  • R' ! and R' 2 are taken together with the atom to which they are bound to form an optionally substituted four to six membered saturated heterocyclic ring containing a nitrogen atom and optionally containing an additional heteroatom from the group consisting of N and O;
  • R' j and R l3b are at each occurrence independently selected from the group consisting hydrogen, CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3 , CH 2 CCH, CH(CH 3 ) 2 , CH 2 CH(CH 3 ) 2 , CH(CH 3 )CH 2 CH 3 , CH 2 OH, CH 2 OCH 2 Ph, CH 2 CH 2 OCH 2 Ph, CH(OH)CH 3 , CH 2 Ph, CH 2 (cyclohexyl), CH 2 (4-OH-Ph), (CH 2 ) 4 NH 2 , (CH 2 ) 3 NHC(NH 2 )NH, CH 2 (3-indole), CH 2 (5-imidazole), CH 2 C0 2 H, CH 2 CH 2 C0 2 H, CH 2 CONH 2 , and CH 2 CH 2 CONH 2 ;
  • R l3a and R l3 ° are taken together with the atom to which they are bound to form an optionally substituted three to six membered saturated carbocyciic ring;
  • R' 3a and R' 3b are taken together with the atom to which they are bound to form an optionally substituted six membered saturated heterocyclic ring with one O atom within the ring;
  • R' 3a and R" * are taken together with the atoms to which they are bound to form an optionally substituted four to six membered ring containing one nitrogen atom;
  • R l3a and R. 15a are taken together with the atoms to which they are bound to form an optionally substituted four to six membered ring containing one nitrogen atom;
  • Y 1 is at each occurrence independently selected from the group consisting of H 2 , O, and -H/- OCH 2 Ph;
  • R l4 is at each occurrence independently seiected from the group consisting of hydrogen, Cj -Ce alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C2-Q alkenyl, and Ci-Ce alkynyl;
  • R 1>a and R l5b are at each occurrence independently selected from the group consisting of H, Cj-Q alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C2- alkenyl, C2-Q alkynyl, Q- fluoroalkyl, COR" 1 , CH 2 R 2 ', SOijR 2* , an optionally substituted four to six membered saturated heterocyclic ring containing a heteroatom selected from the group consisting of NR 24 and O, COCHR" J NH 2
  • R l5a and R l5 ° are taken together with the atom to which they are bound to form an optionally substituted four to six membered saturated heterocyclic ring optionally containing one O atom within the ring;
  • R" is at each occurrence independently seiected from the group consisting of hydrogen, Q- , alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C2-Q alkenyl, and Ci-Ce alkynyl;
  • R' s is at each occurrence independently seiected from the group consisting of hydrogen, Q-C 6 alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C 2 -C 6 alkenyl, and C2-Q alkynyl;
  • R 1 ' and R' 8 are taken together with the atoms to which they are bound to form an optionally substituted five or six membered ring containing two nitrogen atoms;
  • R' 9a and R l b are ai each occurrence independently selected from the group consisting of hydrogen, optionally substituted Q-Ce alkyl, optionally substituted C3-C7 branched alkyl, optionally substituted C3-C7 cycloalkyl, optionally substitoted C 2 -C6 alkenyl, and optionally substituted C 2 -C6 alkynyl;
  • R l9a and R l9 ° are taken together with the atom to which they are bound to form an optionally substituted 3 to 6 membered carbocyclic ring;
  • R 20 is at each occurrence independently selected from the group consisting of hydrogen, Ci -C ' e alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C2-Q alkenyl, and Ci-Ce alkynyl;
  • q 1, or 2;
  • R 2 ' is at each occurrence independently selected from the group consisting of hydrogen, Cj -Ce alkyl, C3-C7 branched alkyl, C3-C7 cycloalkyl, C2- alkenyl, C2-Q alkynyl, Q- fluoroalkyl, optionally substituted aryl, and optionally substituted heteroaryl;
  • R 2 is at each occurrence independently selected from the group consisting of Q-Q alkyl, C3-C7 branched alkyl, C3 cycloalkyl, , C2-Q alkenyl, C2-Q alkynyl optionally substituted aryl, optionally substituted heteroaryl;
  • R 23 is selected from the group consisting H, CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3 , CH 2 CCH, CH(CH 3 ) 2 , CH 2 CH(CH 3 )2, ( ⁇ ! ⁇ ( 1 ! : ⁇ ( ⁇ ⁇ ( ' ! ! :. CH 2 OH, CH 2 OCH 2 Ph, ⁇ ⁇ ⁇ ⁇ ⁇ .- ⁇ .
  • R 24 is ai each occurrence independently selected from the group consisting of H, Q-Q alkyl, C 3 - C 7 branched alkyl, C3-C7 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, optionally substituted aryl, opiionaily substituted heteroaryl, COR ⁇ and S0 2 -Ci_ 5 alkyl;
  • R 25 is at each occurrence independently selected from the group consisting of H, Q-Q alkyl, C3- C 7 branched alkyl, C3-C7 cycloalkyl, C 2 -Cs alkenyl, C 2 -Q alkynyl, opiionaily substituted aryl, optionally substituted heteroaryl, Ci-Cealkoxy, and Ci-Q alkylarnino.
  • the compounds of the present invention include compounds having formula (II): including enantiomers, diasteroemers, hydrates, solvates, pharmaceutically acceptable salts, and complexes thereof.
  • the compounds of the present invention include compounds having formula (III):
  • the compounds of the present invention include compounds having formula (IV):
  • the compounds of the present invention include compounds having formula (V): including enantiomers, diasteroemers, hydrates, solvates, pharmaceutically acceptable salts, and complexes thereof.
  • the compounds of the present invention include compounds having formula (VI):
  • the compounds of the present invention include compounds having formula (VII):
  • the compounds of the present invention include compounds having formula (VIII):
  • the compounds of the present invention include compounds having formula (IX):
  • the compounds of the present invention include compounds having formula (X):
  • Hie compounds of the present invention include compounds having formula including enantiomers, diasteroemers, hydrates, solvates, pharmaceutically acceptable salts, and complexes thereof.
  • the compounds of the present invention include compounds having formula (XII):
  • the compounds of the present invention include compounds having formula (XIII):
  • the compounds of the present invention include compounds having formula (XIV):
  • the compounds of the present invention include compounds having formula (X V):
  • the compounds of the present invention include compounds having formula (XVI):
  • the compounds of the present invention include compounds having formula (XVII):
  • the compounds of the present invention include compounds having formula (XVIII)
  • R 23 is selected from the group consisting H, CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3> CH 2 CCH, CH(CH 3 ) 2 ,
  • CH 2 (5-irnidazoie), CH 2 C0 2 H, CH 2 CH 2 C0 2 H, CH 2 CONH 2 , and CH 2 CH 2 CONH 2 .
  • R 1 is Cj -Ce fluoroalkyl.
  • R 1 is OR 2 .
  • R 1 is (CR 6a R 6b ) m NHR 7 .
  • R 2 is CH 2 (CH 2 ) n NR a R :'
  • R Jd is hydrogen
  • R 3a is Ci-CV, aikyl.
  • R 3a is C3-C7 cycioalkyi.
  • R 3a is C3-C7 branched aikyl
  • R 3a is C Ce aikenyi.
  • R 3a is C 2 -C 6 alkynyl.
  • R 3 is COjR 4 .
  • R hydrogen
  • R 3 s CrC 6 aikyl In some embodiments R 3 s CrC 6 aikyl.
  • R 3 s C3-C7 cycioalkyi.
  • R 3 s Ca-Ce alkenyl.
  • R 3 s C2-C6 alkynyl.
  • R is C0 2 .R 1 ⁇ 2 .
  • R 3a and R jb are taken together with the atom to which they are bound to form an optionally substituted three to six membered saturated heterocyclic ring consisting of two to five carbon atoms and a member selected from the group consisting of O, NR 5 , S, and S ⁇ 3 ⁇ 4;
  • R is Ci-C 6 aikyl.
  • R is C3 branched aikyl.
  • R is C3-C7 cycioalkyi.
  • K is C2-C6 aikenyi.
  • R 4 is C2-C6 aikynyl.
  • R 4 is optionally substituted ph
  • R 4 is benzyl
  • R 5 is Ci-C 6 alkyl
  • R 5 is C3-C7 branched alkyl
  • R 5 is C3-C7 cycloalkyl.
  • R 5 is C2-C6 aikenyi.
  • R 5 is C2-C6 aikynyl.
  • R oa is hydrogen
  • R oa is optionaliy substituted Q-Ce alkyl.
  • R oa is optionaliy substituted C3-C7 branched alkyl.
  • R oa is optionaliy substituted C3-C7 cycloalkyl.
  • R°° is optionaliy substituted V, aikenyi.
  • R na is optionaliy substituted C CV, aikynyl.
  • R nb is hydrogen
  • R ob is optionally substituted C-. -Ce alkyl.
  • R ob is optionally substituted C3-C7 branched alkyl.
  • R ob is optionally substituted C3-C7 cycloalkyl.
  • R ob is optionally substituted C Ce aikenyi.
  • R ob is optionally substituted C 2 -C 6 aikynyl.
  • R ua and R 6b are taken together with the atom to which they are bound to form an optionally substituted 6 inembered ring.
  • n 1
  • n 2 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 + (0.05 * (1 +
  • m is 3.
  • R 7 is COC R a R 8b (NHR 9 ).
  • R 7 is In some enibodimenls R' is
  • R "'a is hydrogen
  • R 8 " is CH 3 .
  • R "a is ⁇ ⁇ ( ⁇ ⁇ . ⁇ ). ⁇ .
  • R "a is CH 2 CH(CH 3 ) 2 .
  • R 8a is CH(CH 3 )CH 2 CH 3 .
  • R"" is CHjOH.
  • R ;!a is CH(OH)CH> In some embodiments R "a is CH 2 Ph.
  • R* a is CH 2 (4-OH-Ph).
  • R M is (CH 2 ) H 2 .
  • R Sa is (CH 2 ) 3 NHC(NH 2 )NH.
  • R &a is CH 2 (3 -indole).
  • R ba is CH 2 (5-imtdazole).
  • R 8a is CH 2 C0 2 H.
  • R Sa is CH 2 CH 2 C0 2 H.
  • R &a is CH 2 CONH .
  • R a is CH 2 CH 2 CONH 2 . In some embodiments R b is hydrogen.
  • R 8b is CH 3 .
  • R 8b is CH(CH 3 ) 2 .
  • R Sb is CH 2 CH(CH ; ) .
  • R 8b is CH(CH 3 )CH,CH 3 . In some embodiments R 8b is CH 2 OH.
  • R 8b is CH(OH)CH 3 .
  • R 8b is CH 2 Ph.
  • R 8b is CH 2 (4-OH-Ph).
  • R 8b is (CH 2 ) 4 NH 2 . In some embodiments R 8b is (CH 2 ) 3 NHC(NH 2 )NH.
  • R 8b is CH 2 (3-indole).
  • R 8b is CH 2 (5-imidazole).
  • R 8b is CH 2 C0 2 H.
  • R 8b is CH 2 CH 2 C0 2 H.
  • R 8b is CH 2 CONH 2 .
  • R 8b is CH 2 CH 2 CONH 2 .
  • R 9 is hydrogen
  • R 9 is C [-Ce aikyl.
  • R 9 is C3-C7 branched alkyl.
  • R 9 is C3-C7 cyeioaikyi.
  • R 9 is C 2 -Ce aikenyl.
  • R 9 is C 2 -Ce aikynyi.
  • Y is H 2 .
  • Y is O.
  • R' 0a is hydrogen
  • R' 0a is CH 3 .
  • R i 0a is CH 2 CH 3 .
  • R i 0a is CH(CH 3 ) 2 .
  • R i 0a is CH 2 CH(CH 3 ) 2 .
  • R i 0a is CH(CH 3 )CH 2 CH 3 .
  • R , 0a is CH 2 OH.
  • R 10a is CH 2 OCH 2 Ph.
  • R 10a is CH(OH)CH 3 .
  • R l0a is CH 2 Ph.
  • R 10a is CH 2 (4-OH-Ph).
  • R l0a is (CH 2 ) 4 NH 2 .
  • R 10a is (CH 2 ) 3 NHC(NH 2 )NH.
  • R l0a is CH 2 ( 3 -indole).
  • R l0a is CH 2 (5 -imidazole). In some embodiments R l0a is CH 2 (CCH).
  • R l0a is CH 2 (cyclohexyl)
  • R i0a is CH 2 C ) 2 H.
  • R ] Ua is CH 2 CH 2 C0 2 H.
  • R : 0a is CH CO H : .
  • R 10 ° is CH 2 CH 2 CO H 2 .
  • R :0c is hydrogen
  • R l0c is Cll;
  • R i0 " is CH 2 C3 ⁇ 4.
  • R i0 " is CH(C3 ⁇ 4) 2 .
  • R i0 " is CH ? CH(C3 ⁇ 4) 2 .
  • R l 0 is CH( €3 ⁇ 4) €3 ⁇ 4(3 ⁇ 4.
  • R l 0 is CH 2 OH.
  • R' UlJ is CH,QCH 2 Ph.
  • R ! 0 " is CH(QH)CH 3 .
  • R' 0u is CH 2 Ph.
  • R i 0b is CH 2 (4-OH-Ph).
  • R' 0b is (CH 2 ) 4 NH 2 .
  • R i 0b is (CH 2 ) 3 NHC(NH 2 )NH.
  • R' 0u is CH 2 (3-indole).
  • R' 0u is CH 2 (5-irntdazoie).
  • R ' 0b is CH 2 (CCH).
  • R'°* is CH 2 (cyclohexyl)
  • R l0 ° is CH 2 C0 2 H.
  • R l0 ° is CH 2 CH 2 C0 2 H.
  • R l0 ° is CH 2 CONH 2 .
  • R'° " is CH 2 CH 2 CONH 2 .
  • R ! ° a and R ,0b are taken together with the atom to which they are bound to form an optionally substituted three to six membered saturated carbocyclic ring.
  • R ! ' is hydrogen. In some embodiments R 1 is of C Ce alkyl.
  • R 1 is C3-C7 branched alkyl.
  • R 1 is C3-C7 cycloalkyl.
  • R 1 is C 2 -C6 alkenyl.
  • R 1 is Ci -C 6 haloalkyl.
  • R is C 2 -C 6 alkynyl.
  • R l0a and R' 1 are taken together with the atoms to which they are bound to form an optiotially substituted four to six rnembered ring containing one nitrogen atom, and R 12 is not hydrogen.
  • R i0 " and R 1 ' are taken together with the atoms to which they are bound to form an optionally substituted four to six rnembered ring containing one nitrogen atom, and R 12 is not hydrogen.
  • R' ⁇ is hydrogen
  • R 1 2 is Cj -Q, alkyl.
  • R i 2 is COCR ! 3a R ,3b NR LSa R !3 ⁇ 4 .
  • R i 2 is ( OCR : R " OR ⁇
  • 12 is COCR 13a R !3b NHSO->R i a .
  • R'" is 4 NH
  • R 1 is(CR i9a R ,9 ⁇ T HR 20 .
  • R 1 1 and R are taken together with the atom to which they are bound to form an optionally substituted four to six membered saturated heterocyclic ring containing a nitrogen atom and optionally containing an additional heteroatom from the group consisting of N and O.
  • R' ⁇ ' a is hydrogen
  • R' ja is CH- 5 .
  • R' ja s CH 2 CH 3 in some embodiments R' ja s CH 2 CH 3 .
  • R ja s CH 2 CCH.
  • R" a s en ( ⁇ ⁇ ⁇ ⁇ .
  • R 1 a s en on.
  • R ! ' a s CH 2 OCH 2 Ph.
  • R" a s CH 2 CH 2 OCH,Pb.
  • R ! a s CH(OH)C3 ⁇ 4.
  • R" a is CH 2 Ph.
  • R l3a s CH 2 (cyclohexyl).
  • R ' a s CH 2 (4-OH-Ph).
  • R ja s ⁇ CH 2 ) 4 NH 2 .
  • R ja s (CH 2 ) 3 NHC(NH, )NH.
  • R" a is CH 2 (3-indole).
  • R :3a is CH 2 (5-imidazole). in some embodiments R i3a is CH 2 C ) 2 H.
  • R i3a is CH 2 CH 2 C0 2 H. In some embodiments R 13a is CH 2 CONH 2 .
  • R 13a is CH 2 CH 2 CO H,.
  • R l c is hydrogen
  • R' 3 ° is C3 ⁇ 4.
  • R 13b is CH 2 C3 ⁇ 4.
  • R i 3b is CH 2 CH 2 CH 3 .
  • R i 3s is CH 2 CCH.
  • R i3B is CH(C3 ⁇ 4 ; .
  • R i3b is CH 2 CH( ( 3 ⁇ 4): . .
  • R " is CH(CH 3 )CH 2 CJ3 ⁇ 4. In some embodiments R ! 3b is CH 2 OH.
  • R ! 3b is CH 2 OCH 2 Ph.
  • R ! 3b is CH 2 CH 2 OCH 2 Ph.
  • R ! 3b is CH(OH)CH 3 .
  • R' " J is CH 2 Pb.
  • R , 3b is CH 2 (eyciohexyi).
  • R !3b is CH 2 (4-OH-Ph).
  • R ' jb is CH 2 > 4 NH 2 .
  • R l3b is (CH 2 ) 3 NHC(NH 2 )NH. in some embodiments R' "3 is CH 2 ( 3 -indole).
  • R ! ' D is CH 2 ( 5 -imidazole).
  • R ! is CH 2 C0 2 H.
  • R ! is CH 2 CH 2 C0 2 H.
  • R !jn is CH 2 CONH 2 .
  • R !jn is CH 2 CH 2 CQNH > .
  • R 1Ja and R 1 c are taken together with the atom to which they are bound to form an optionally substituted three to six mernbered saturated carbocyclic ring.
  • R 1Ja and R 1 c are taken together with the atom to which they are bound to form an optionally siibstituted six mernbered saturated heterocyclic ring with one O atom within the ring.
  • R 13a and R' 4 are taken together with the atoms to which they are bound to form an optionally siibstituted four to six mernbered ring containing one nitrogen atom.
  • R lja and R l5a are taken together with the atoms to which they are bound to form an optionally substituted four to six mernbered ring containing one nitrogen atom.
  • Y 1 is
  • Y 1 is H 2 .
  • Y 1 is O.
  • Y 1 is -H/-OCH 2 Ph.
  • R " is hydrogen
  • R " is Cj -Q, alkyl.
  • R'" is C3-C7 branched alkyl.
  • R' 4 is C3-C7 cycioalkyl.
  • R' 4 is C 2 -C6 alkenyi.
  • R' 4 is C 2 -C6 alkynyi.
  • R a is hydrogen
  • R a is C , -C 6 alkyl .
  • R a is C3-C7 branched
  • R a is C3-C7 cycioalkyl.
  • R a is C 2 -C6 alkenyi.
  • R l5a is C 2 -C alkynyi.
  • R l5a is Cj- s fluoroalkyl.
  • R l5a is COR 2 '.
  • R l5a is CH 2 R 21 .
  • R l5a is SO ? R 2 .
  • R l3 ° is an optionally substituted four to six membered saturated heterocyclic ring containing a heteroatom selected from the group consisti ng of NR 24 and O,
  • R i 5a is COCHR 23 NH 2 .
  • R' a is 3 ⁇ 4 ⁇ r 3 .
  • R i5a is ' ⁇ - CHF2
  • i 5a is CH2F
  • R i 5a is
  • R ] :,b is hydrogen.
  • R ! * is C C 6 alkyi.
  • R ! * is C3-C7 branched alkyl
  • R : * is C3-C7 cycloalkyl.
  • R , 3b is C 2 -C 6 alkenyl.
  • R l>b is C 2 --C b alkynyl. In some embodiments R : 3 ⁇ 4 is C C 6 fluoroalkyl.
  • R : 5n is COR 2 1 .
  • R : 5n is CH 2 R'.
  • R' 5 ° is SCbR " .
  • R l3 ° is an optionally substituted four to six membered saturai heterocyclic: ring containing a heteroatom selected from the group consisting of NR 24 and O, In some embodiments R i 5b is COCHR 23 NH 2 .
  • R°" is in some embodiirments R°° i ' 3 ⁇ 4 ⁇ CH F 2
  • R i 5t> is H 2' In some embodiments R°° some embodiments R 1
  • i 4
  • R° n is in some embodiments R
  • R : c is
  • R : a and R 15B ar taken together with the atom to which they are bound to form an optionally substituted four to six membered saturated heterocyclic ring optionally containing one O atom within the ring.
  • R l 6 is CH 2 .
  • R l 6 is O.
  • R l 6 is NH
  • R 1 ' is hydrogen
  • R 1 ' is Ci -C 6 alkyl.
  • R' ' is C3-C7 branched alkyl.
  • R 1 ' is C3-C7 cycloaikyl.
  • R' ' is C- alkenyl
  • R' ' is C- alkynyl
  • R i 8 is hydrogen
  • R i 8 is Cj -Cg alkyl.
  • R i 8 is C3-C7 branched alkyl.
  • R * 8 is C3-C7 cycloaikyl.
  • R' 8 is C 2 ⁇ C t , alkenyl.
  • R' 8 is C 2 -C6 alkynyl.
  • R * ' and R 18 are taken together with the atoms to which they are bound to form an optionally substituted five or six membered ring containing two nitrogen atoms.
  • R , 9a is hydrogen.
  • R , 9a is optionally substituted Ci -Ce alkyl.
  • R , 9a is optionally substituted C 3 -C 7 branched alkyl.
  • R , 9a is optionally substituted C3-C7 cycloaikyl.
  • R l 9a is optionally substituted C 2 -C 6 alkenyl.
  • R l 9a is optionally substituted C 2 -Ce alkynyl.
  • R l 9 ° is hydrogen
  • R l9 ° is optionally substituted Cj- alkyl.
  • R l 9 ° is optionally substituted C3-C7 branched alkyl.
  • R l9 ° is optionally substituted C3-C7 cycloaikyl.
  • R l9 ° is optionally substituted C 2 -C 6 alkenyl.
  • R l 9 ° is optionally substituted C2-Q alkynyl.
  • R l 9a and R' 9b are taken together with the atom to which they are bound to form an optionally substituted 3 rnembered carbocyciic ring.
  • R l 9a and R' 9b are taken together with the atom to which they are bound to form an optionally siibstituted 4 rnembered carbocyciic ring.
  • R l 9a and R l9b are taken together with the atom to which they are bound to form an optionally siibstituted .5 rnembered carbocyciic ring.
  • R l 9a and R l9b are taken together with the atom to which they are bound to form an optionally substituted 6 rnembered carbocyciic ring.
  • R 20 is hydrogen
  • R 20 is Cj -Cg alkyl.
  • R 20 is C3-C7 branched alkyl.
  • R 20 is C3-C7 cycloalkyl.
  • R 20 is C-rC alkenyl.
  • R " ° is C 2 ⁇ C t , alkynyl.
  • q is 1.
  • q is 2.
  • R 21 is hydrogen
  • R 21 is Ci -Ce alkyl.
  • R 21 is C3-C7 branched alkyl.
  • R 21 is C3-C7 cycloalkyl.
  • R 21 is C 2 ⁇ C 6 alkenyl.
  • R 21 is C alkynyl.
  • R 21 is Ci -C fluoroalkyl.
  • R 21 is optionally substituted aryl.
  • R 21 is optionally substituted heteroaryl.
  • R 22 is Ci -Ce alkyl.
  • R 22 is C3-C7 branched alkyl.
  • R 22 is C3-C7 cycloalkyl.
  • R 22 is C 2 -C 6 alkenyl.
  • R 22 is Ci-Ce alkynyl. In some embodiments is optionally substituted aryl.
  • In some embodiments is CH 3 .
  • Ci -Ce alkyl In some embodiments is Ci -Ce alkyl.
  • In some embodiments is C3-C7 branched alkyl.
  • C3-C7 cycloalkyl In some embodiments is C3-C7 cycloalkyl.
  • Ci-Ce alkenyl In some embodiments is Ci-Ce alkenyl. In some embodiments R 24 is C Ce aikynyl.
  • R 24 is optionally substituted aryl.
  • R 24 is optionally substituted heteroaryl.
  • R 24 is COR "5 .
  • R 24 is SOi-Ci.ealkyi.
  • R 25 is hydrogen
  • R 25 is Ci -C 6 alkyl.
  • R 25 is C3-C7 branched alkyl.
  • R *J is C3-C7 cycloalkyl.
  • R "J is C- alkenyl
  • R" J is C- aikynyl.
  • R" J is optionally substituted aryl.
  • R" J is optionally substituted heteroaryl.
  • R "J is Ci -Q, alkoxy.
  • R' 'J is Ci -Q, alkylamino.
  • Exemplary embodiments include compounds having the formula (I) through (XVI) or a pharmaceutically acceptable salt form thereof, in combination with an anticancer agent.
  • anticancer agents include but are not limited to Vemurafenib, Ipiiimumab, Masitinib, Sorafenib, Lenalidomide, Obiimersen, Trametinib, Dabrafenib, R05185426, Veliparib, Bosetitan, YM 1.55, CNTO 95, CROl l-vcMMAE, CY503, Lenvatinib, Avastin, Tasidotin, Ramucirismab, IPI-504, Tasisuiam, W2871 , MPC-6827, RAF265, Dovitinib, Everolimus, MEK I 62, B M120, Nilotinib, Reolysin, 825A, Tremelimumab, ⁇ -88, Elesclomol, STA90
  • a compound depicted by the racemic formula will stand equally well for either of the two enantiomers or mixtures thereof, or in the case where a second chiral center is present, all diastereomers.
  • a compound depicted by the racemic formula will stand equally well for either of the two enantiomers or mixtures thereof, or in the case where a second chiral center is present, all diastereomers.
  • product formation can be monitored by spectroscopic means, such as nuclear magnetic resonance spectroscopy (e.g., ⁇ or l3 C), infrared spectroscopy, spectrophotometry (e.g., IJV-visibie), mass spectrometry, or by chromatography such as high pressure liquid chromatography (HPLC), gas chromatography (GC), gel-permeation chromatography (GPC), or thin layer chromatography (TLC).
  • spectroscopic means such as nuclear magnetic resonance spectroscopy (e.g., ⁇ or l3 C), infrared spectroscopy, spectrophotometry (e.g., IJV-visibie), mass spectrometry, or by chromatography such as high pressure liquid chromatography (HPLC), gas chromatography (GC), gel-permeation chromatography (GPC), or thin layer chromatography (TLC).
  • HPLC high pressure liquid chromatography
  • GC gas chromatography
  • GPC gel-permeation
  • Preparation of the compounds can involve protection and deprotection of various chemical groups.
  • the need for protection and deprotection and ihe selection of appropriate protecting groups can be readily determined by one skilled in the art.
  • the chemistry of protecting groups can be found, for example, in Greene et al.. Protective Groups in Organic Synthesis, 2d. Ed. (Wiley & Sons, 1991), the entire disclosure of which is incorporated by reference herein for all purposes.
  • Suitable solvents typically are substantially nonreactive with the reactants, intermediates, and/or products at the temperatures at which the reactions are carried out, i.e., temperatures that can range from the solvent's freezing temperature to the solvent's boiling temperature.
  • a given reaction can be carried out in one solvent or a mixture of more than one solvent.
  • suitable solvents for a particular reaction step can be selected.
  • the compounds of these teachings can be prepared by methods known in the art of organic chemistry.
  • the reagents used in ihe preparation of the compounds of these teachings can be either commercially obtained or can be prepared by standard procedures described in the literature.
  • compounds of the present invention can be prepared according to the method illustrated in the General Synthetic Schemes:
  • reagents used in the preparation of the compounds of this invention can be either commercially obtained or can be prepared by standard procedures described in the literature.
  • compounds in the genus may be produced by one of the following reaction schemes.
  • RiiuzoSe (1) a known compound
  • a compound of the formula (2) a known compound or a compound made by known methods
  • a coupling agent such as
  • 1- hydroxy-7-azabenzotriazole and the like optionally in the presence of a base such as triethyl mine, diisopropyiethylamine, N-methyiniorpholine and the like, in a solvent such as N,N- dimethylfonnamide, 1,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (3).
  • a base such as triethyl mine, diisopropyiethylamine, N-methyiniorpholine and the like
  • a solvent such as N,N- dimethylfonnamide, 1,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (3).
  • a compound of the formula (3) is reacted with an acid such as trifluoroacetie acid, hydrochloric acid, and the like in a solvent such as methyiene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (4).
  • an acid such as trifluoroacetie acid, hydrochloric acid, and the like
  • a solvent such as methyiene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (4).
  • a compound of the formula (4) is reacted with a compound of the formula (5), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0- (benzotriazol-l -yl)-N,N,N',N'-tetramethyluroniuni hexafluorophosphate, ⁇ , ⁇ '- dicyclohexylcarbodiimide, l-e hyl-3-(3-dimethylaminopropyl) carbodiimide, I - [Bis(dime hylamino)methylene]- 1.H- l,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate,
  • a coupling agent such as 0- (benzotriazol-l -yl)-N,N,N',N'-tetramethyluroniuni hexafluorophosphate, ⁇ , ⁇ '- dicyclohexy
  • 1- hydroxy-7-azabenzotriazole and the like optionally in the presence of a base such as triethyl amine, diisopropySeihylamine, N-methylmorpholine and the like, in a solvent such as N,N- dimethylformamide, 1,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (6), A compound of the formula (6) is reacted with an acid such as trifluoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (7).
  • a base such as triethyl amine, diisopropySeihylamine, N-methylmorpholine and the like
  • a solvent
  • a compound of the formula (4) is reacted with a compound of (8), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- l-yi)-N,N,N',N'-tetramethyl ronium hexafluorophosphate, N,N' ⁇ dicyclohexylcarbodiimide, 1 - ethy 1-3 -( 3 -d imethylaminopropyl) carbodiimide, l-[Bis( dimemylamino)methylene ] -1H-1,2,3- triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate, l-hydroxy-7-azabenzotriazole and the like, optionally in the presence of a base such as triethylamine, diisopropylemylarnine, N- methylmorpholine and the like, in a solvent such as N,N-
  • a compound of the formula (4) is reacted with a compound of (10), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(henzotriazoi- l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, ⁇ , ⁇ '-dicyclohexylcarbodiimide, 1 - ethyl-3-(3-dimethylaminopropyl) carbodiimide, l-[Bis(dimethyiamino)methy3ene]-lH- 1,2,3- triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate, l-hydroxy-7-azabenzotriazole and the like, optionally in the presence of a base such as txiethylamine, diisopropylefhylamine, N- meihyimorpholine and the like, in
  • a compound of the formula (11) is reacted with an acid such as trifluoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1 ,4-dioxane, and the like to provide a compound of the formula (12).
  • an acid such as trifluoroacetic acid, hydrochloric acid, and the like
  • a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1 ,4-dioxane, and the like to provide a compound of the formula (12).
  • a compound of the formula (4) is reacted with a compound of (13), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, ⁇ , ⁇ '-dicyclohexylcarbodiimide, 1- e yl-3-(3-dimethylaminopropyl) carbodiimide, l-[Bis(dimethylamino)methylene]-lH- 1,2,3- triazoio[4,5-b]pyridinium 3-oxid hexafluorophosphate, i-hydroxy-7-azabenzotriazole and the like, optionally in the presence of a base such as triethylamine, diisopropylethylamine, N- meihyimorpholine and the like, in a solvent such as ⁇ , ⁇ -di
  • a compound of the formula (4) is reacted with a compound of (15), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- l-yl)-N,N,N',N'-tetramethyluronium hexafiuorophosphate, ⁇ , ⁇ '-dicyclohexylcarbodiimide, 1- ethyl-3-(3-dimethylaminopropyl) carbodiimide, l -[Bis(dimethylamino)methylene]-lH- 1,2,3- triazolo[4,5-b]pyridinium 3-oxid hexafiuorophosphate, i-hydroxy-7-azabenzotriazole and the like, optionally in the presence of a base such as triethylamine, diisopropylethylamine, N- methyiniorphoiine and the like, in a solvent such as ⁇
  • a compound of the formula (16) is reacted with an acid such as trifluoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (17).
  • an acid such as trifluoroacetic acid, hydrochloric acid, and the like
  • a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (17).
  • Riluzole (1) a known compound, is reacted with a compound of the formula (18), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- 1 ⁇ yI)-N , ⁇ , ⁇ ', ⁇ '-tetramethyluronium hexafluorophosphate, ⁇ , ⁇ '- dicyclohexylcarbodiimide, l-ethyi-3-(3-dimethySaminopropyl) carbodiimide, 1-
  • a coupling agent such as 0-(benzotriazol- 1 ⁇ yI)-N , ⁇ , ⁇ ', ⁇ '-tetramethyluronium hexafluorophosphate, ⁇ , ⁇ '- dicyclohexylcarbodiimide, l-ethyi-3-(3-dimethySaminopropyl) carbodiimide, 1-
  • a compound of the formula (19) is reacted with an acid such as trifluoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of die formula (20).
  • an acid such as trifluoroacetic acid, hydrochloric acid, and the like
  • a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of die formula (20).
  • a compound of the formula (20) is reacted with a compound of (21), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- l-yl)-N,N,N',N'-tetramethyiuronium hexafluorophosphate, ⁇ , ⁇ '-dicyclohexyicarbodiirnide, 1- ethyl-3-(3-dimethylaminopropyl) carbodiimide, l- Bis(dimethylamino)methylene3-iH-l,2,3- triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate, l-hydroxy-7-azabenzotxiazole and the like, optionally in the presence of a base such as triethylamine, diisopropylethyiamine, N- meihylmorphoSine and the like, in a solvent such as N
  • a compound of the formula (20) is reacted with a compound of (23), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- l-yi)-N,N,N',N'-tetramethyluronium hexafluorophosphate, ⁇ , ⁇ '-dicyclohexylcarbodiimide, 1- ethyl-3-(3-dirnethylaminopropyl) carbodiimide, l-[Bis(dimethylamino)methylene]-lH- 1,2,3- triazoio[4,5-b]pyridinium 3-oxid hexafluorophosphate, l-hydroxy-7-azabenzotriazole and the like, optionally in the presence of a base such as triethylamine, diisopropylethyiamine, N- methyimorpholine and the like, in a solvent such as ⁇ , ⁇ -di
  • a compound of the formula (24) is reacted with an acid such as trifluoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1 ,4-dioxane, and the like to provide a compound of the formula (25).
  • an acid such as trifluoroacetic acid, hydrochloric acid, and the like
  • a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1 ,4-dioxane, and the like to provide a compound of the formula (25).
  • a compound of the formula (20) is reacted with a compound of (26), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- 1 -yl)-N,N,N',N'-tetxaniethyluronium hexafluorophosphate, ⁇ , ⁇ '-dicyclohexylcarbodiimide, I - ethyl-3-(3 ⁇ dimethylammopropyi) carbodiimide, l-[Bis(dimethylamino)methyleoe]-lH- l,2,3- triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate, l-hydroxy-7-azabenzotxiazole and the like, optionally in the presence of a base such as triethylamine, diisopropylethyiamine, N- methylmorphoiine and the like, in a
  • a compound of the formula (20) is reacted with a compound of (28), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- l-yi)-N,N,N',N'-tetramethyl ronium hexafluorophosphate, ⁇ , ⁇ '-dicyclohexylcarbodiimide, 1 - ethyl-3-(3 ⁇ dimethylammopropyi) carbodiijiiide, l-[Bis(dimethylamino)methyleoe]-lH- l,2,3- triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate, l-hydroxy-7-azabenzotriazole and the like, optionally in the presence of a base such as triethylamine, diisopropylethyiamine, N- methylmorpholine and the like, in a solvent such as N,N
  • a compound of the formula (29) is reacted with an acid such as trifluoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (30).
  • an acid such as trifluoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (30).
  • a compound of the formula (20) is reacted with a compound of (31), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- l-yl)-N,N,N',N'-tetramethylurotiium hexafluorophosphate, ⁇ , ⁇ '-dicyclohexylcarbodiimide, 1- efhyl-3-(3-dimethylaminopropyl) carbodiimide, l -[Bis(dimethylamino)methylene]-lH- 1,2,3- triazolo[4,5-b]pyriditiium 3-oxid hexafluorophosphate, l -hydroxy-7-azabenzotriazole and the like, optionally in the presence of a base such as triethyiamine, diisopropylethylamine, N- meihylmorpholine and the like, in a solvent such as N
  • a compound of the formula (32) is reacted with an acid such as trifluoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (33),
  • a compound of the formula (20) is reacted with a compound of (34), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, N,N'-dicyclohexylcarbodiimide, 1- ethyl-3-(3-dimethylaminopropyl) carbodiimide, l-[Bis(dimethylarnino)methy1ene]- l H- 1 ,2,3- triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate, l-hydroxy-7-azabenzotxiazole and the like, optionally in the presence of a base such as trietJiylamine, diisopropylethyiamine, N- methyltnorphoiine and the like, in a solvent
  • a compound of the formula (35) is reacted with an acid such as trifiuoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (36).
  • an acid such as trifiuoroacetic acid, hydrochloric acid, and the like
  • a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (36).
  • a compound of the formula (20) is reacted with a compound of (37), a known compound or a compound made by known methods, in the presence of a coupling agent such as 0-(benzotriazol- l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, ⁇ , ⁇ '-dicyclohexyScarbodiimide, l- eihyl-3-(3-dimethylaminopropyl) carbodiimide, l-[Bis(dimethylamino)methyleneJ-lH- 1,2,3- triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate, 1 -hydroxy-7-azabenzotriazole and the like, optionally in the presence of a base such as triethylamine, diisopropylethyiamine, N- methylmorpholine and the like, in a solvent such as ⁇ , ⁇ -di
  • a compound of the formula (38) is reacted with an acid such as trifiuoroacetic acid, hydrochloric acid, and the like in a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (39).
  • an acid such as trifiuoroacetic acid, hydrochloric acid, and the like
  • a solvent such as methylene chloride, 1,2-dichloroethane, tetrahydrofuran, 1,4-dioxane, and the like to provide a compound of the formula (39).
  • a compound of the formula (25) is reacted with a compound of (40), a known compound or a compound made by known methods, in the presence of a base such as triethylamine, diisopropylethylamine, N-methylmorpholine and the like, in a solvent such as N, N- dimethylformamide, 1 ,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (41).
  • a base such as triethylamine, diisopropylethylamine, N-methylmorpholine and the like
  • a solvent such as N, N- dimethylformamide, 1 ,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (41).
  • a compound of the formula (42), a known compound or a comopounds prepared by known methods, is reacted with triphosgene in the presence of a solvent such as as N,N- dimethylformamide, 1,4-dioxane, tetrahydrofuran, methylene chloride, chloroform, and the like.
  • the resulting product is then reacted with a compound of the formula (1) in the presence of a base such as triethylamine, diisopropylethylamine, N-methylmorpholine and the like, in the presence of a solvent such as N, N-dimethylformamide, 1,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (43).
  • a base such as triethylamine, diisopropylethylamine, N-methylmorpholine and the like
  • a solvent such as N, N-dimethylformamide, 1,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (43).
  • a compound of the formula (44) is reacted with hydrogen bromide in the presence of acetic acid, optionally in the presence of a solvent such as N, N- dimefhylformamide, 1 ,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (44).
  • acetic acid optionally in the presence of a solvent such as N, N- dimefhylformamide, 1 ,4-dioxane, tetrahydrofuran, methylene chloride and the like
  • heating optionally with microwave irradiation
  • a solvent such as as N,N- dimefhylformamide, 1 ,4-dioxane, tetrahydrofuran, methylene chloride, chloroform, and the like to provide a compound of the formula (46).
  • a compound of the formula (46) is reacted with a compound of the formula ( 1 ) in the presence of a base such as triethylamine, diisopropylethylamine, N-methylmorpholine, and the like, in the presence of a solvent such as N, N-dimethyiformamide, 1 ,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (43).
  • a base such as triethylamine, diisopropylethylamine, N-methylmorpholine, and the like
  • a solvent such as N, N-dimethyiformamide, 1 ,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (43).
  • a compound of the formula (48), a known compound or a comopounds prepared by known methods, is reacted with a compound of the formula (49), a known compound or a compounds prepared using known methods, in the presence of a solvent such as as N, N-dirnethyiforraarmde, 1,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (50).
  • a solvent such as as N, N-dirnethyiforraarmde, 1,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (50).
  • a solvent such as as N, N-dimethylformamide, 1 ,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (53).
  • a compoimd of the formula (54), a known compound or a comopounds prepared by known methods, is reacted with a compound of the formula (55), a known compound or a compounds prepared using known methods, in the presence of a base such as triethylamine, diisopropylethyiamine, N-methylmorpholioe and the like, in the presence of a solvent such as as N, N-dimethylformamide, 1,4-dioxane, tetrahydrofuran, methylene chioride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (56).
  • a base such as triethylamine, diisopropylethyiamine, N-methylmorpholioe and the like
  • a solvent such as as N, N-dimethylformamide, 1,4-dioxane, tetrahydrofuran, methylene chioride and the like, optionally with
  • a compound of the formula (56) is reacted with a compound of the formula (57), a known compound or a comopounds prepared by known methods, in the presence of a solvent such as N, N-dimethylfoimamide, dimethylsulfoxide, 1,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (58).
  • a solvent such as N, N-dimethylfoimamide, dimethylsulfoxide, 1,4-dioxane, tetrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (58).
  • a compound of the formula (56) is reacted with a compound of the formula (59), a known compound or a comopounds prepared by known methods wherein M is a counter ion such as sodium, potassium, tetrabutyl ammonium, and the like, in the presence of a solvent such as N, N- dimefhylformamide, dimethylsulfoxide, 1 ,4-dioxane, letrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (60).
  • a solvent such as N, N- dimefhylformamide, dimethylsulfoxide, 1 ,4-dioxane, letrahydrofuran, methylene chloride and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (60).
  • a compound of the formula (60) is reacted with hydrogen in the presence of a catalyst such as palladium on carbon, palladium on barium sulfate, palladium (II) acetate, tetraIds(triphenylphosphine)palladium(0), dichlorobis (triphenylphosphine)palladium(II), palladium on carbon, bis(acetonitrile)dichloropaUadium(II), and the like, in an organic solvent such as methanol, ethanol, ethyl acetate, tetrahydrofuran, 1,4-dioxane, dichloromethane, chloroform, 1,2-dichloroethane, ⁇ , ⁇ -dimet ylformamide, and the like, to provide a compound of the formula (61).
  • a catalyst such as palladium on carbon, palladium on barium sulfate, palladium (II) acetate, te
  • a compound of the formula (61) is reacted with a compound of the formula (62), a known compound or a compound prepared by known methods, in the presence of a hydride source such as sodium borohydride, sodium cyanoborohydride, sodium triacetoxy borohydride, and the like, optionally in the presence of an acid such as acetic acid, trifluoroacetic acid, formic acid, and the like, in an organic solvent such as methanol, ethanol, ethyl acetate, tetrahydrofuran, 1,4-dioxane, dichloromethane, chloroform, 1,2-dichloroethane, N,N- dimethylformamide, and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (63).
  • a hydride source such as sodium borohydride, sodium cyanoborohydride, sodium triacetoxy borohydride, and the like
  • an acid such as acetic acid, triflu
  • a compound of the formula (63) is reacted with a compound of the formula (62), a known compound or a compound prepared by known methods, in the presence of a hydride source such as sodium borohydride, sodium cyanoborohydride, sodium triacetoxy borohydride, and the like, optionally in the presence of an acid such as acetic acid, trifluoroacetic acid, formic acid, and the like, in an organic solvent such as methanol, eihanoS, ethyl acetate, tetrahydrofuran, 1,4-dioxane, dichloromethane, chloroform, 1 ,2- dichloroefhane, ⁇ , ⁇ -dimethylformamide, and the like, optionally with heating, optionally with microwave irradiation to provide a compound of the formula (64).
  • a hydride source such as sodium borohydride, sodium cyanoborohydride, sodium triacetoxy borohydride, and the like
  • an acid such
  • Schemes 1-21 describe the preparation of compounds containing chirai centers. Those skilled in the art of organic synthesis will recognize that the chemistry described in schemes 1-21 can be applied to prepare the enantiorner of the compounds described employing starting material containing the opposite stereochemistry. In the case of compounds with multiple chirai centers (hose skiiled in the art of organic synthesis will recognize that the chemistry described in schemes 1-21 can be employed to prepare compounds of the disclosure from starting materials containing the desired chirality and each chirai center.
  • Example 1-267 provides methods for preparing representative compounds of formula (I). The skilled practitioner will know how to substitute the appropriate reagents, starting materials and purification methods known to those skilled in the art, in order to prepare additional compounds of the present invention.
  • Method A LC/MS data were determined with a Waters Alliance 2695 HPLC/MS (Waters Symmetry C18, 4.6 x 75 mm, 3.5 um) with a 2996 diode array detector from 210-400 ram; the solvent system is 5-95% acetonitrile in water (with 0.1 % TFA) over nine minutes using a linear gradient, and retention times are in minutes. Mass spectrometry was performed on a Waters ZQ using electrospray in positive mode.
  • Method B Preparative reversed phase HPLC was performed on a Waters Sunfire column (19 x 50 mm, C18, 5 ⁇ ) with a 10 min mobile phase gradient of 10% acetonitrile/water to 90% acetonitrile/ water with 0.1% TFA as buffer using 214 and 254 nm as detection wavelengths. Injection and fraction collection were performed with a Giison 215 liquid handling apparatus using Trilution LC software.
  • Method C LC/MS data were determined on a Shimadzu LC 20AD instrument with a Phenomenex Luna C18 (3 Um) 50 X 3.0 mm column. Mobile phase consisted of water and acetonitrile with 0.3 % formic acid buffer.
  • Example 10 Synthesis of (R)-N-(6-(trifluoromethoxy)benzo[d]thiazol-2-yl)azetidine-2- carboxamide was prepared according to the procedure of example 5 from 2-amino-6-(trifluoromethoxy) benzimidazoie (0.50 g, 2.1 mmol) and N-i-butyloxycarbonyl-D-azetidine-2-carboxyIic acid (0.64 g, 3.2 mmol). Yield for Boc protected intermediate 0.60 g (69%).
  • Example 15 Synthesis of l-amino-N-(6-(trifluoromethoxy)benzo[d]thiazol-2- yl)cyc1obutanecarboxamide 1 -amino-N-(6-(txifluoromeftoxy)benzo[3 ⁇ 4 was prepared according io the procedure of example I from 2-amino-6-(trifluoromethoxy) benzimidazole (234 rog, 1.0 mmol) and V-t-butyloxycarbonyl-l -aniinocyclobutanecarboxylic acid (280 nig, 1.3 mmol). Yield for Boc protected intermediate 281 mg (65%).
  • carboxamide was prepared according to the procedures of example 16 from 2-amino-N-(6- (txifluoromethoxy)benzo[d]thiazol-2-yl)acetamide hydrochloride (60 nig, 0.25 mmol) and N-(t- butyloxycarbonyl)proline (89 mg, 0.32 mmol). Yield for Boc protected intermediate 62 rng (51%).
  • LC/MS method A: R, 4.13 min., (M+H) +

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AU2016226463A AU2016226463B2 (en) 2015-03-03 2016-02-26 Riluzole prodrugs and their use
CN201680025374.6A CN107567438B (zh) 2015-03-03 2016-02-26 利鲁唑前药及其用途
PL16759303T PL3265448T3 (pl) 2015-03-03 2016-02-26 Proleki riluzolu i ich zastosowanie
RS20220149A RS62915B1 (sr) 2015-03-03 2016-02-26 Prolekovi riluzola i njihova primena
PH1/2021/550250A PH12021550250A1 (en) 2015-03-03 2016-02-26 Riluzole prodrugs and their use
EA201791951A EA034759B1 (ru) 2015-03-03 2016-02-26 Пролекарства рилузола и их применение
HRP20220208TT HRP20220208T1 (hr) 2015-03-03 2016-02-26 Prolijekovi riluzola i njihova primjena
CA2978158A CA2978158C (en) 2015-03-03 2016-02-26 Riluzole prodrugs and their use
SG11201706831RA SG11201706831RA (en) 2015-03-03 2016-02-26 Riluzole prodrugs and their use
EP21209037.7A EP4011870A1 (en) 2015-03-03 2016-02-26 Pharmaceutical compositions comprising riluzole prodrugs
MX2017011196A MX380828B (es) 2015-03-03 2016-02-26 Fármacos precursores de riluzol y sus usos.
EP16759303.7A EP3265448B1 (en) 2015-03-03 2016-02-26 Riluzole prodrugs and their use
SI201631457T SI3265448T1 (sl) 2015-03-03 2016-02-26 Predzdravila riluzola in njihova uporaba
US15/549,154 US10485791B2 (en) 2015-03-03 2016-02-26 Riluzole prodrugs and their use
KR1020237034132A KR20230147746A (ko) 2015-03-03 2016-02-26 릴루졸 전구약물 및 그의 용도
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