RU2014121205A - Производные азолов - Google Patents
Производные азолов Download PDFInfo
- Publication number
- RU2014121205A RU2014121205A RU2014121205/04A RU2014121205A RU2014121205A RU 2014121205 A RU2014121205 A RU 2014121205A RU 2014121205/04 A RU2014121205/04 A RU 2014121205/04A RU 2014121205 A RU2014121205 A RU 2014121205A RU 2014121205 A RU2014121205 A RU 2014121205A
- Authority
- RU
- Russia
- Prior art keywords
- optionally substituted
- group
- alkyl
- membered saturated
- unsaturated heterocycle
- Prior art date
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- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 26
- 125000000217 alkyl group Chemical group 0.000 claims abstract 21
- 229920006395 saturated elastomer Polymers 0.000 claims abstract 21
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract 16
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 15
- 125000005843 halogen group Chemical group 0.000 claims abstract 15
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 12
- 150000007980 azole derivatives Chemical class 0.000 claims abstract 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 11
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 11
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract 9
- -1 hydroxy, difluoromethoxy Chemical group 0.000 claims abstract 8
- 125000001424 substituent group Chemical group 0.000 claims abstract 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract 7
- 125000004122 cyclic group Chemical group 0.000 claims abstract 7
- 239000012634 fragment Substances 0.000 claims abstract 7
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 7
- 239000001301 oxygen Substances 0.000 claims abstract 7
- 125000004434 sulfur atom Chemical group 0.000 claims abstract 7
- 125000003118 aryl group Chemical group 0.000 claims abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 12
- 150000003839 salts Chemical class 0.000 claims 11
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000001589 carboacyl group Chemical group 0.000 claims 5
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 4
- 125000002947 alkylene group Chemical group 0.000 claims 4
- 125000004043 oxo group Chemical group O=* 0.000 claims 4
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical group NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 239000004480 active ingredient Substances 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 150000003851 azoles Chemical class 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 206010008118 cerebral infarction Diseases 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 201000004384 Alopecia Diseases 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 208000019901 Anxiety disease Diseases 0.000 claims 1
- 201000006474 Brain Ischemia Diseases 0.000 claims 1
- 206010048962 Brain oedema Diseases 0.000 claims 1
- 206010008120 Cerebral ischaemia Diseases 0.000 claims 1
- 208000030814 Eating disease Diseases 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 208000019454 Feeding and Eating disease Diseases 0.000 claims 1
- 208000018522 Gastrointestinal disease Diseases 0.000 claims 1
- 208000023105 Huntington disease Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 claims 1
- 208000019022 Mood disease Diseases 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 208000027418 Wounds and injury Diseases 0.000 claims 1
- 125000005236 alkanoylamino group Chemical group 0.000 claims 1
- 208000006752 brain edema Diseases 0.000 claims 1
- 208000026106 cerebrovascular disease Diseases 0.000 claims 1
- 150000001924 cycloalkanes Chemical class 0.000 claims 1
- 230000006378 damage Effects 0.000 claims 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 1
- 235000014632 disordered eating Nutrition 0.000 claims 1
- 206010013663 drug dependence Diseases 0.000 claims 1
- 206010015037 epilepsy Diseases 0.000 claims 1
- 230000003676 hair loss Effects 0.000 claims 1
- 208000026278 immune system disease Diseases 0.000 claims 1
- 230000004054 inflammatory process Effects 0.000 claims 1
- 208000014674 injury Diseases 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 201000000980 schizophrenia Diseases 0.000 claims 1
- 208000011117 substance-related disease Diseases 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 0 CC(C)C(N)N(C)C(*)=C(C)C Chemical compound CC(C)C(N)N(C)C(*)=C(C)C 0.000 description 2
- WDKUQDLCGCWYGO-UHFFFAOYSA-N CC(C)N(C(C)=NN1C(C)C)C1=O Chemical compound CC(C)N(C(C)=NN1C(C)C)C1=O WDKUQDLCGCWYGO-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
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- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
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- A61K31/4196—1,2,4-Triazoles
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
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- 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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- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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Abstract
1. Производное азола формулы (I):,где в формуле (I)Rпредставляет собой атом водорода, Cалкил (где Cалкил необязательно замещен одним-тремя фрагментами, выбранными из группы, состоящей из гидрокси, атомов галогена, циано, Cциклоалкила и Cалкокси), Сциклоалкил или 4-8-членный насыщенный гетероцикл;Rпредставляет собой атом водорода или Cалкил;Rозначает арил или гетероарил (где арил или гетероарил необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей из Cалкокси, Cалкила, атомов галогена, трифторметила, трифторметокси, циано, гидрокси, дифторметокси и Cалкилсульфонила);каждый из заместителей Rи R, которые могут быть одинаковыми или различными, представляет собой атом водорода, Cалкил (где Cалкил необязательно замещен одним-тремя фрагментами, выбранными из группы, состоящей из гидрокси, атомов галогена, циано, Cциклоалкила и Cалкокси), Сциклоалкил или 4-8-членный насыщенный или ненасыщенный гетероцикл, содержащий один или несколько циклических атомов азота, кислорода или серы (где этот 4-8-членный насыщенный или ненасыщенный гетероцикл необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей из гидрокси, Cалкила, Cалкокси, атомов галогена, циано, Салканоила и трифторметила), или же заместители Rи Rс участием соединяющего их атома азота образуют 4-8-членный насыщенный или ненасыщенный гетероцикл, необязательно содержащий один или несколько циклических атомов азота, кислорода или серы, помимо указанного выше соединяющего атома азота (где этот 4-8-членный насыщенный или ненасыщенный гетероцикл необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей и�
Claims (11)
1. Производное азола формулы (I):
где в формуле (I)
R1 представляет собой атом водорода, C1-5 алкил (где C1-5алкил необязательно замещен одним-тремя фрагментами, выбранными из группы, состоящей из гидрокси, атомов галогена, циано, C3-7 циклоалкила и C1-5 алкокси), С3-7циклоалкил или 4-8-членный насыщенный гетероцикл;
R2 представляет собой атом водорода или C1-5 алкил;
R3 означает арил или гетероарил (где арил или гетероарил необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей из C1-5 алкокси, C1-5алкила, атомов галогена, трифторметила, трифторметокси, циано, гидрокси, дифторметокси и C1-5алкилсульфонила);
каждый из заместителей R4 и R5, которые могут быть одинаковыми или различными, представляет собой атом водорода, C1-5 алкил (где C1-5 алкил необязательно замещен одним-тремя фрагментами, выбранными из группы, состоящей из гидрокси, атомов галогена, циано, C3-7 циклоалкила и C1-5 алкокси), С3-7 циклоалкил или 4-8-членный насыщенный или ненасыщенный гетероцикл, содержащий один или несколько циклических атомов азота, кислорода или серы (где этот 4-8-членный насыщенный или ненасыщенный гетероцикл необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей из гидрокси, C1-5 алкила, C1-5 алкокси, атомов галогена, циано, С2-5 алканоила и трифторметила), или же заместители R4 и R5 с участием соединяющего их атома азота образуют 4-8-членный насыщенный или ненасыщенный гетероцикл, необязательно содержащий один или несколько циклических атомов азота, кислорода или серы, помимо указанного выше соединяющего атома азота (где этот 4-8-членный насыщенный или ненасыщенный гетероцикл необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей из гидрокси, C1-5алкила (где этот C1-5 алкил в свою очередь необязательно замещен одной или двумя гидроксильными группами), C1-5 алкокси, атомов галогена, циано, С2-5 алканоила, оксо, аминокарбонила, моно-C1-5 алкиламинокарбонила, ди-C1-5 алкиламинокарбонила, трифторметила, амино, моно-C1-5 алкиламино, ди-C1-5 алкиламино и С2-5 алканоиламино, причем в указанном 4-8-членном насыщенном или ненасыщенном гетероцикле необязательно имеется C1-5 алкиленовый фрагмент, соединяющий два различных циклических атома углерода), или образуют 2-окса-6-азаспиро[3.3]гепт-6-ил или 7-окса-2-азаспиро[3.5]нон-2-ил;
необязательно замещенный азольный цикл, который представлен приведенной ниже формулой (α):
имеет любую из структур, представленных приведенными ниже формулами группы (II):
где
Ry означает атом водорода или C1-5 алкил;
фрагменты X1 и X2 являются такими, что:
i) если X1 означает простую связь или фрагмент -CO-, X2 означает -C1-5алкилен- или -O-C1-5 алкилен-; и
ii) если X1 означает фрагмент -CONRx1-, X2 означает простую связь;
Rx1 представляет собой атом водорода или C1-5 алкил; и
цикл A представляет собой бензольный цикл, 6-членный ароматический гетероцикл (где бензольный цикл и 6-членный ароматический гетероцикл необязательно замещены одним или двумя фрагментами, выбранными из группы, состоящей из атомов галогена и C1-5 алкокси), 4-8-членный насыщенный или частично ненасыщенный гетероцикл, содержащий один или два атома азота (где 4-8-членный насыщенный или ненасыщенный гетероцикл необязательно замещен оксо группой) или С3-7 циклоалкан;
или фармацевтически приемлемая соль описанного производного азола.
2. Производное азола или его фармацевтически приемлемая соль по п. 1, где в приведенной выше формуле (I):
каждый из заместителей R4 и R5, которые могут быть одинаковыми или различными, представляет собой атом водорода, C1-5 алкил (где C1-5 алкил необязательно замещен одним-тремя фрагментами, выбранными из группы, состоящей из гидрокси, атомов галогена, циано, C3-7 циклоалкила и C1-5 алкокси), С3-7 циклоалкил или 4-8-членный насыщенный или ненасыщенный гетероцикл, содержащий один или несколько циклических атомов азота, кислорода или серы (где этот 4-8-членный насыщенный или ненасыщенный гетероцикл необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей из гидрокси, C1-5 алкила, C1-5 алкокси, атомов галогена, циано, С2-5 алканоила и трифторметила), или же заместители R4 и R5 с участием соединяющего их атома азота образуют 4-8-членный насыщенный или ненасыщенный гетероцикл, необязательно содержащий один или несколько циклических атомов азота, кислорода или серы, помимо указанного выше соединяющего атома азота (где этот 4-8-членный насыщенный или ненасыщенный гетероцикл необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей из гидрокси, C1-5алкила (где этот C1-5 алкил в свою очередь необязательно замещен одной или двумя гидроксильными группами), C1-5 алкокси, атомов галогена, циано, С2-5 алканоила, оксо, аминокарбонила, моно-C1-5 алкиламинокарбонила, ди-C1-5 алкиламинокарбонила и трифторметила, причем в указанном 4-8-членном насыщенном или ненасыщенном гетероцикле необязательно имеется C1-5 алкиленовый фрагмент, соединяющий два различных циклических атома углерода), или образуют 2-окса-6-азаспиро[3.3]гепт-6-ил или 7-окса-2-азаспиро[3.5]нон-2-ил.
3. Производное азола или его фармацевтически приемлемая соль по п. 1 или 2, где в приведенной выше формуле (I):
X1 означает простую связь;
X2 означает -C1-5 алкилен- или -O-C1-5 алкилен-; и
цикл A представляет собой бензольный цикл, 6-членный ароматический гетероцикл (где бензольный цикл и 6-членный ароматический гетероцикл необязательно замещены одним или двумя фрагментами, выбранными из группы, состоящей из атомов галогена и C1-5 алкокси) или 4-8-членный насыщенный или ненасыщенный гетероцикл, содержащий один или два атома азота (где 4-8-членный насыщенный или ненасыщенный гетероцикл необязательно замещен оксо группой).
4. Производное азола или его фармацевтически приемлемая соль по п. 1, где в приведенной выше формуле (I):
цикл A представляет собой бензольный цикл или 6-членный ароматический гетероцикл (где бензольный цикл и 6-членный ароматический гетероцикл необязательно замещены одним или двумя фрагментами, выбранными из группы, состоящей из атомов галогена и C1-5 алкокси).
5. Производное азола или его фармацевтически приемлемая соль по п. 1, где в приведенной выше формуле (I):
цикл A представляет собой бензольный цикл или пиридиновый цикл (где бензольный цикл и пиридиновый цикл необязательно замещены одним или двумя фрагментами, выбранными из группы, состоящей из атомов галогена и C1-5 алкокси).
6. Производное азола или его фармацевтически приемлемая соль по п. 1, где в приведенной выше формуле (I):
R1 означает C1-5 алкил;
R2 означает атом водорода; и
R3 означает фенил или пиридил (где фенил и пиридил необязательно замещены одним или двумя фрагментами, выбранными из группы, состоящей из C1-5 алкила, C1-5алкокси, атомов галогена, циано, трифторметила, дифторметокси, трифторметокси и C1-5 алкилсульфонила).
7. Производное азола или его фармацевтически приемлемая соль по п. 1, где в приведенной выше формуле (I):
необязательно замещенный азольный цикл приведенной ниже формулы (α):
имеет любую из структур в приведенной ниже группе формул (III):
где
Ry представляет собой атом водорода или метильную группу.
8. Производное азола или его фармацевтически приемлемая соль по п. 1, где в приведенной выше формуле (I):
X1 означает простую связь;
X2 означает этилен или метилэтилен; и
заместители R4 и R5 с участием соединяющего их атома азота образуют 4-8-членный насыщенный или ненасыщенный гетероцикл, необязательно содержащий один или несколько циклических атомов азота, кислорода или серы, помимо указанного выше соединяющего атома азота (где этот 4-8-членный насыщенный или ненасыщенный гетероцикл необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей из гидрокси, C1-5алкила (где этот C1-5 алкил в свою очередь необязательно замещен одной или двумя гидроксильными группами), C1-5 алкокси, атомов галогена, циано, С2-5алканоила и трифторметила, причем в указанном 4-8-членном насыщенном или ненасыщенном гетероцикле необязательно имеется C1-5 алкиленовый фрагмент, соединяющий два различных циклических атома углерода), или образуют 2-окса-6-азаспиро[3.3]гепт-6-ил.
9. Производное азола или его фармацевтически приемлемая соль по п.1, где в приведенной выше формуле (I):
заместители R4 и R5 с участием соединяющего их атома азота образуют 5- или 6-членный насыщенный гетероцикл, необязательно содержащий один или несколько циклических атомов кислорода, помимо указанного выше соединяющего атома азота (где 6-членный насыщенный гетероцикл необязательно замещен одним или двумя фрагментами, выбранными из группы, состоящей из гидроксила и C1-5алкила, причем в указанном 6-членном насыщенном гетероцикле необязательно имеется C1-5 алкиленовый фрагмент, соединяющий два различных циклических атома углерода), или образуют 2-окса-6-азаспиро[3.3]гепт-6-ил.
10. Фармацевтическая композиция, включающая производное азола или его фармацевтически приемлемую соль по любому из пп. 1-9 в качестве действующего ингредиента.
11. Средство для лечения или профилактики расстройств настроения, тревожных расстройств, шизофрении, болезни Альцгеймера, болезни Паркинсона, хореи Хантингтона, расстройств пищевого поведения, гипертензии, желудочно-кишечных заболеваний, наркотической зависимости, эпилепсии, инфаркта мозга, ишемии мозга, отека мозга, травм головы, воспаления, иммунных заболеваний или облысения, включающее производное азола или его фармацевтически приемлемую соль по любому из пп. 1-9 в качестве действующего ингредиента.
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| US9663457B2 (en) * | 2014-04-09 | 2017-05-30 | Allergan, Inc. | Carbamoyl hydrazine derivatives as formyl peptide modulators |
| HRP20190853T1 (hr) | 2015-07-06 | 2019-06-28 | Gilead Sciences, Inc. | Cot modulatori i postupci za njihovu upotrebu |
| MX2019000512A (es) | 2016-07-12 | 2019-05-02 | Bayer Cropscience Ag | Compuestos biciclicos como plaguicidas. |
| CN106831713B (zh) * | 2017-01-13 | 2019-04-02 | 深圳大学 | 一种多靶点Aβ寡聚化抑制剂的合成方法及应用 |
| CN106831712B (zh) * | 2017-01-13 | 2019-04-02 | 深圳大学 | 一种多靶点Aβ寡聚化抑制剂 |
| CN107434778A (zh) * | 2017-05-23 | 2017-12-05 | 重庆文理学院 | 一种4‑羟基‑2h‑吡咯‑2‑酮衍生物的制备方法 |
| CN107857729B (zh) * | 2017-12-25 | 2019-10-15 | 福州大学 | 一种4-碘化-n-芳基化的吡唑类化合物的合成方法 |
| US10039749B1 (en) | 2018-01-15 | 2018-08-07 | King Saud University | Substituted pyrazole derivatives |
| EP3886854A4 (en) | 2018-11-30 | 2022-07-06 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| TWI770527B (zh) | 2019-06-14 | 2022-07-11 | 美商基利科學股份有限公司 | Cot 調節劑及其使用方法 |
| RU2730492C1 (ru) * | 2019-12-27 | 2020-08-24 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Российский химико-технологический университет имени Д.И. Менделеева" | Способ получения алкил 2-[([1,1'-бифенил]-4-карбонил)амино]-3-(1н-азол-1-ил) пропаноатов |
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| US11655237B2 (en) | 2020-03-30 | 2023-05-23 | Gilead Sciences, Inc. | Solid forms of a Cot inhibitor compound |
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| CN101528703B (zh) | 2006-09-11 | 2011-09-07 | 欧加农股份有限公司 | 2-(1-氧代-1h-异喹啉-2-基)乙酰胺衍生物 |
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