WO2021143822A1 - Dérivé imide bicyclique, son procédé de préparation et son application en médecine - Google Patents

Dérivé imide bicyclique, son procédé de préparation et son application en médecine Download PDF

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WO2021143822A1
WO2021143822A1 PCT/CN2021/072091 CN2021072091W WO2021143822A1 WO 2021143822 A1 WO2021143822 A1 WO 2021143822A1 CN 2021072091 W CN2021072091 W CN 2021072091W WO 2021143822 A1 WO2021143822 A1 WO 2021143822A1
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group
membered
compound
general formula
alkyl
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Chinese (zh)
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杨方龙
贾敏强
何卫明
陈刚
贺峰
陶维康
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江苏恒瑞医药股份有限公司
上海恒瑞医药有限公司
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Publication of WO2021143822A1 publication Critical patent/WO2021143822A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present disclosure belongs to the field of medicine, and relates to a novel cereblon E3 ubiquitin ligase protein-binding ligand compound and protein degradation targeting chimera (PROTACs) compound containing the same, and its preparation Method, and its application in medicine.
  • the present disclosure relates to a novel cyclic imide cerebellar protein E3 ubiquitin ligase protein-binding ligand compound represented by general formula (IM) and protein degradation targeting chimeras (PROTACs) containing the same Compound, its preparation method, and its application in medicine.
  • IM general formula
  • PROTACs protein degradation targeting chimeras
  • PROTACs PROteolysis TArgeting Chimeras
  • the PROTACs molecule is a bifunctional molecule. One end contains a ligand that binds to E3 ubiquitin ligase, and the other end contains a ligand that binds to the target protein. The two parts are connected by a connecting unit. The linking unit is pulled closer, so that the E3 ligase and the target protein are very close, which in turn causes the polyubiquitination of the target protein and the degradation of the proteasome.
  • PROTACs adopt a completely different mechanism of action and mechanism from small molecule inhibitors.
  • the ligand of E3 ubiquitin ligase recruits E3 ubiquitin ligase to the vicinity of the target protein, and then the target protein is labeled with ubiquitination by narrowing the distance with the target protein.
  • the labeled target protein will be degraded by the proteasome system in the body to inhibit the corresponding protein pathway (Cell Biochem Funct. 2019, 37, 21-30).
  • PROTACs Compared with traditional small molecule drugs, due to changes in the binding mechanism, PROTACs only need to instantaneously bind to the target protein to complete the process of ubiquitin transfer to achieve irreversible degradation of the target protein.
  • PROTACs have the following advantages: 1) stronger degradation and longer-lasting efficacy; 2) higher selectivity for the target protein; 3) can overcome the traditional small molecule inhibitors caused by the mutation of the target protein Drug resistance (Cell Chem. Biol. 2018, 25, 67-77).
  • the discovery process of CRBN type E3 ligase ligand is related to the study of thalidomide's mechanism of action.
  • cereblon is a binding protein of thalidomide (Science 2010, 327, 1345).
  • Cerebellar protein is part of the E3 ubiquitin ligase protein complex, which acts as a substrate receptor to select ubiquitinated proteins.
  • the study shows that thalidomide-cerebellar protein binding in vivo may be the cause of thalidomide teratogenicity.
  • the compound and related structures can be used as anti-inflammatory agents, anti-angiogenic agents and anti-cancer agents.
  • Lenalidomide and pomalidomide obtained by further modification of the structure of thalidomide have greatly improved their safety and significantly reduced their teratogenic effects.
  • Lenalidomide has been approved by the FDA in 2006 for marketing.
  • Two technological papers published in Science in 2014 pointed out that lenalidomide works by degrading two special B cell transcription factors, Ikaros family zinc finger structural proteins 1 and 3 (IKZF1 and IKZF3), which further reveals The structure of thalidomide may be combined with the E3 ubiquitin ligase protein complex of the cerebellar protein to further play a role in degrading the target protein (Science, 2014, 343, 301; Science, 2014, 343, 305).
  • CRBN ligands are widely used in protein degradation, and a series of PROTACs molecules based on CRBN ligands have been developed. Due to the influence of CRBN ligand itself on the target point, it may additionally degrade zinc finger domain protein. Therefore, the design and synthesis of new and highly selective CRBN ligands is also particularly important in the synthesis of PROTACs molecules.
  • the present disclosure has developed a new type of cyclic imide derivatives, which can be used as effective CRBN ligands, and can further synthesize corresponding PROTACs molecules. These molecules demonstrate their application as estrogen receptor degrading agents to treat estrogen receptor-mediated or dependent diseases.
  • CLM cerebellar protein E3 ubiquitin ligase protein binding ligand compound represented by general formula (IM);
  • R 1 and R 2 , R 2 and R 3 , R 3 and R 4 together with the carbon atoms to which they are connected form a four- to fourteen-membered heterocyclic group, wherein the heterocyclic group contains 1 to 2 heteroatoms selected from N atom, O atom and S atom, optionally selected from halogen, alkyl, heteroalkyl, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, One or more substituents of nitro, cycloalkyl, heterocyclyl, aryl and heteroaryl;
  • R 1 , R 2 , R 3 and R 4 are the same or different, and are each independently selected from covalent bond, hydrogen atom, deuterium atom, halogen, alkyl, deuterated alkyl, heteroalkyl, alkenyl, alkyne Group, alkoxy, haloalkyl, haloalkoxy, hydroxy, hydroxyalkyl, cyano, amino, cycloalkyl, heterocyclyl, aryl and heteroaryl; wherein the alkyl, heteroalkyl, Alkoxy, cycloalkyl, heterocyclyl, aryl and heteroaryl are each independently optionally selected from halogen, alkyl, heteroalkyl, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano , Amino, nitro, cycloalkyl, heterocyclyl, aryl and heteroaryl substituted by one or more substituents, provided that R 1 and R 2 , R 2 and R 3
  • L is a linking unit, one end of which can be arbitrarily connected to the heterocyclic group formed by R 1 , R 2 , R 3 , R 4 and R 1 and R 2 , R 2 and R 3 , R 3 and R 4 on the formula (IM)
  • the substitution site is connected by a covalent bond, and the other end is connected with PTM;
  • PTM is a small molecule compound ligand that binds to a target protein or polypeptide, which is connected to L by a covalent bond;
  • n 0, 1, or 2.
  • a compound having the structure of CLM-L-PTM, or its tautomer, meso, racemate, enantiomer, or diastereomer CLM is a cerebellar protein E3 ubiquitin ligase protein binding ligand compound represented by the general formula (IM);
  • R 1 and R 2 , R 2 and R 3 , R 3 and R 4 together with the carbon atoms to which they are connected form a four- to fourteen-membered heterocyclic group, wherein the heterocyclic group contains 1 to 2 heteroatoms selected from N atom, O atom and S atom, optionally selected from halogen, alkyl, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, ring Substituted by one or more substituents in the alkyl group, heterocyclic group, aryl group and heteroaryl group;
  • R 1 , R 2 , R 3 and R 4 are the same or different, and are each independently selected from covalent bond, hydrogen atom, deuterium atom, halogen, alkyl, deuterated alkyl, heteroalkyl, alkenyl, alkyne Group, alkoxy, haloalkyl, haloalkoxy, hydroxy, hydroxyalkyl, cyano, amino, cycloalkyl, heterocyclyl, aryl and heteroaryl; wherein the alkyl, heteroalkyl, Alkoxy, cycloalkyl, heterocyclyl, aryl and heteroaryl are each independently optionally selected from halogen, alkyl, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro Is substituted by one or more substituents in the group, cycloalkyl, heterocyclyl, aryl and heteroaryl, provided that at least one of R 1 and R 2 , R 2 and R 3
  • L is a linking unit, one end of which can be arbitrarily connected to the heterocyclic group formed by R 1 , R 2 , R 3 , R 4 and R 1 and R 2 , R 2 and R 3 , R 3 and R 4 on the formula (IM)
  • the substitution site is connected by a covalent bond, and the other end is connected with PTM;
  • PTM is a small molecule compound ligand that binds to a target protein or polypeptide, which is connected to L by a covalent bond;
  • n 0, 1, or 2.
  • Ring A, Ring B and Ring C are the same or different, and are each independently a four- to fourteen-membered heterocyclic group, wherein the heterocyclic group contains 1 to 2 atoms selected from the group consisting of N atoms, O atoms and S atoms Heteroatom
  • Ring E, ring D and ring M are the same or different, and are each independently a four- to fourteen-membered N-containing heterocyclic group, wherein the N-containing heterocyclic group contains 1 N atom and optionally Contain 1 heteroatom selected from N atom, O atom and S atom;
  • R 5a is selected from covalent bond, hydrogen atom, alkyl, heteroalkyl, haloalkyl, hydroxy, hydroxyalkyl, amino, cycloalkyl, heterocyclyl, aryl and heteroaryl;
  • R 5 are the same or different, and are each independently selected from covalent bonds, hydrogen atoms, halogens, alkyl groups, alkoxy groups, haloalkyl groups, hydroxyl groups, hydroxyalkyl groups, cyano groups, amino groups, nitro groups, cycloalkyl groups, Heterocyclic group, aryl group and heteroaryl group;
  • R f are the same or different, and are each independently selected from a hydrogen atom, a halogen, an alkyl group, an alkoxy group, a haloalkyl group, a hydroxyl group, a hydroxyalkyl group, a cyano group, an amino group, a nitro group, a cycloalkyl group, a heterocyclic group, Aryl and heteroaryl;
  • p is 0, 1, 2, 3 or 4;
  • p is 1, 2, 3 or 4;
  • f 0, 1, 2, 3 or 4;
  • R 1 , R 2 , R 3 , R 4 and any R 5 is connected to the connecting unit L through a covalent bond;
  • G 1 , G 2 , R 1 to R 4 and n are as defined in the compound of general formula (IM).
  • the shown cerebellar protein E3 ubiquitin ligase protein binding ligand compound is selected from the group consisting of general formula (IM-1aa), general formula (IM-2aa) and general formula (IM-3aa)
  • Ring B is a four- to fourteen-membered heterocyclic group, wherein the heterocyclic group contains 1 to 2 heteroatoms selected from N atoms, O atoms and S atoms;
  • Ring E, ring D and ring M are the same or different, and are each independently a four- to fourteen-membered N-containing heterocyclic group, wherein the N-containing heterocyclic group contains 1 N atom and optionally Contain 1 heteroatom selected from N atom, O atom and S atom;
  • R 5a is selected from covalent bond, hydrogen atom, alkyl, heteroalkyl, haloalkyl, hydroxy, hydroxyalkyl, amino, cycloalkyl, heterocyclyl, aryl and heteroaryl;
  • R 5 are the same or different, and are each independently selected from covalent bonds, hydrogen atoms, halogens, alkyl groups, alkoxy groups, haloalkyl groups, hydroxyl groups, hydroxyalkyl groups, cyano groups, amino groups, nitro groups, cycloalkyl groups, Heterocyclic group, aryl group and heteroaryl group;
  • R f are the same or different, and are each independently selected from a hydrogen atom, a halogen, an alkyl group, an alkoxy group, a haloalkyl group, a hydroxyl group, a hydroxyalkyl group, a cyano group, an amino group, a nitro group, a cycloalkyl group, a heterocyclic group, Aryl and heteroaryl;
  • p is 0, 1, 2, 3 or 4;
  • p is 1, 2, 3 or 4;
  • f 0, 1, 2, 3 or 4;
  • R 1 , R 3 , R 4 , R 5a and any R 5 is connected to the connecting unit L through a covalent bond;
  • G 1 , G 2 , R 1 to R 4 and n are as defined in the compound of general formula (IM).
  • Ring E is a four- to fourteen-membered N-containing heterocyclic group, wherein the N-containing heterocyclic group contains, in addition to one N atom, optionally one selected from the group consisting of N atom, O atom and S atom Heteroatom
  • R 5 are the same or different, and are each independently selected from covalent bonds, hydrogen atoms, halogens, alkyl groups, alkoxy groups, haloalkyl groups, hydroxyl groups, hydroxyalkyl groups, cyano groups, amino groups, nitro groups, cycloalkyl groups, Heterocyclic group, aryl group and heteroaryl group;
  • R 5a is selected from covalent bond, hydrogen atom, alkyl, heteroalkyl, haloalkyl, hydroxy, hydroxyalkyl, amino, cycloalkyl, heterocyclyl, aryl and heteroaryl;
  • R f are the same or different, and are each independently selected from a hydrogen atom, a halogen, an alkyl group, an alkoxy group, a haloalkyl group, a hydroxyl group, a hydroxyalkyl group, a cyano group, an amino group, a nitro group, a cycloalkyl group, a heterocyclic group, Aryl and heteroaryl;
  • R 1 , R 2 , R 3 , R 4 and R 5a is connected to the connecting unit L through a covalent bond;
  • r is 1 or 2;
  • s is 0 or 1;
  • t 0, 1 or 2;
  • g is 1, 2 or 3;
  • p 0, 1, 2 or 3;
  • f 0, 1, 2, 3 or 4;
  • G 1 , G 2 , R 1 to R 4 and n are as defined in the compound of general formula (IM).
  • G 1 , G 2 , R 1 , R 5 , R 5a , g and n are as defined in the compound of general formula (IM-13).
  • R 5a is selected from covalent bond, hydrogen atom, alkyl, heteroalkyl, haloalkyl, hydroxy, hydroxyalkyl, amino, cycloalkyl, heterocyclyl, aryl and heteroaryl;
  • R 1 , R 2 , R 3 , R 4 and R 5a is connected to the connecting unit L through a covalent bond;
  • R 1 to R 4 are as defined in the compound of general formula (IM).
  • -L 1 -and -L 2 - are the same or different, and are each independently selected from a covalent bond, -O-, -S-, -NR 6 -, -CR 7 R 8 -, -C(O)-, -S(O)-, -S(O) 2 -, -C(S)-, -C(O)O-, -C(O)NR 6 -and -NR 6 C(O)-;
  • R 1L and R 2L are the same or different, and are each independently selected from a covalent bond, an alkylene group, a heteroalkylene group, an alkenylene group and an alkynylene group, wherein the alkylene group, heteroalkylene group, and alkylene group Alkenyl and alkynylene groups are optionally selected from halogen, alkyl, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, oxo, cycloalkyl, heterocyclyl, aryl and heteroaryl Substituted by one or more substituents in the group;
  • Q 1 and Q 2 are the same or different, and are each independently selected from cycloalkyl, heterocyclyl, aryl and heteroaryl, wherein the cycloalkyl, heterocyclyl, aryl and heteroaryl are each independently Is optionally selected from one of halogen, alkyl, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, oxo, cycloalkyl, heterocyclyl, aryl and heteroaryl or Replaced by multiple substituents;
  • R 6 is selected from a hydrogen atom, an alkyl group, a heteroalkyl group, a halogenated alkyl group, a cycloalkyl group, a heterocyclic group, an aryl group and a heteroaryl group;
  • R 7 and R 8 are the same or different, and are each independently selected from hydrogen atom, halogen, alkyl, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, oxo, cycloalkyl, heterocycle Group, aryl and heteroaryl.
  • v is an integer from 1 to 10;
  • j is an integer from 0 to 10;
  • k is an integer from 0 to 10;
  • L is -(CH 2 ) v -or v is an integer from 1 to 10.
  • j is an integer from 0 to 10;
  • k is an integer from 0 to 10.
  • L is a connecting unit, preferably R 2L or Q 1 -R 2L ;
  • R 2L is selected from covalent bond, C 1-12 alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene, wherein the C 1-12 alkylene Alkyl, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene are optionally selected from halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, cyano, amino, oxo, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to 10 One or more substituents in the membered heteroaryl group; preferably, R 2L is a covalent bond or a C 1-12 alkylene group, wherein the C 1-12 alkylene group is optionally selected from halogen , C 1-6 alkyl, C 1-6 alkoxy, C 1-6
  • Q 1 is selected from 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to 10 membered heteroaryl, wherein the 3 to 8 membered cycloalkyl, 3 to 8
  • the membered heterocyclic group, the 6 to 10 membered aryl group and the 5 to 10 membered heteroaryl group are each independently optionally selected from halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl , Hydroxy, C 1-6 hydroxyalkyl, cyano, amino, oxo, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl group and 5 to 10 membered heteroaryl group Is substituted by one or more substituents; preferably, Q 1 is selected from 3 to 8 membered heterocyclic groups, wherein the 3 to 8 membered heterocyclic groups are optionally selected
  • PTM is a small molecule compound ligand that binds to a target protein or polypeptide
  • p is 0, 1, 2, 3 or 4;
  • p is 1, 2, 3 or 4;
  • Ring B, ring D, ring E, R 1 , R 3 -R 5 , R f , G 1 , G 2 , f and n are as defined in the general formula (IM-1aa) and the general formula (IM-2aa).
  • t 0, 1 or 2;
  • g is 1, 2 or 3;
  • p 0, 1, 2 or 3;
  • PTM, L, ring E, R 1 , R 3 -R 5 , R f , G 1 , G 2 , f and n are as defined in general formula (IM-9) or general formula (IM-13aa).
  • E is O atom or NH
  • Z is a covalent bond, or selected from O atom, NR m and CH 2 ;
  • M 1 , M 2 , M 3 , M 4 and M 5 are the same or different, and each independently is an N atom or CR n ;
  • R 1p are the same or different, and are each independently selected from a hydrogen atom, a deuterium atom, a halogen, an alkyl group, a deuterated alkyl group, a heteroalkyl group, an alkenyl group, an alkoxy group, a halogenated alkyl group, a halogenated alkoxy group, a hydroxyl group, a hydroxyalkyl group Group, cyano group, amino group, cycloalkyl group, heterocyclic group, aryl group and heteroaryl group;
  • R 2p , R 3p and R 4p are the same or different, and are each independently selected from a hydrogen atom, a deuterium atom, a halogen, an alkyl group, a deuterated alkyl group, a heteroalkyl group, an alkenyl group, an alkoxy group, a halogenated alkyl group, and a halogenated alkoxy group.
  • R 3p and R 4p together with the attached carbon atom form a cycloalkyl or heteroalkyl group
  • R 5p is selected from a hydrogen atom, a deuterium atom, an alkyl group, a deuterated alkyl group, a heteroalkyl group, an alkenyl group, a halogenated alkyl group, a hydroxyl group, a hydroxyalkyl group, an amino group, a cycloalkyl group, a heterocyclic group, an aryl group, and a heteroaryl group ;
  • R 6p are the same or different, and are each independently selected from a hydrogen atom, a deuterium atom, a halogen, an alkyl group, a deuterated alkyl group, a heteroalkyl group, an alkenyl group, an alkoxy group, a halogenated alkyl group, a halogenated alkoxy group, a hydroxyl group, and a hydroxyl group.
  • R 7p are the same or different, and are each independently selected from a hydrogen atom, a deuterium atom, a halogen, an alkyl group, a deuterated alkyl group, a heteroalkyl group, an alkenyl group, an alkoxy group, a halogenated alkyl group, a halogenated alkoxy group, a hydroxyl group, and a hydroxyl group.
  • R m is selected from a hydrogen atom, an alkyl group, a heteroalkyl group, a haloalkyl group, a cycloalkyl group, a heterocyclic group, an aryl group and a heteroaryl group;
  • R n is selected from hydrogen atom, halogen, alkyl, alkenyl, alkoxy, haloalkyl, haloalkoxy, hydroxy, hydroxyalkyl, cyano, amino, cycloalkyl, heterocyclic, aryl and heteroaryl base;
  • h 0, 1, 2, 3, 4 or 5;
  • q 0, 1, 2, 3, 4 or 5;
  • y is 0, 1, 2, 3, 4, or 5.
  • Z, M 1 -M 5 , R 1p -R 4p , R 6p , R 7p , h, q and y are as defined above.
  • Another aspect of the present disclosure provides a compound represented by general formula (IM), or a tautomer, meso, racemate, enantiomer, diastereomer, or isotope thereof Derivatives, or mixtures thereof or pharmaceutically acceptable salts thereof,
  • R 1 and R 2 , R 2 and R 3 , R 3 and R 4 together with the carbon atoms to which they are connected form a four- to fourteen-membered heterocyclic group, wherein the heterocyclic group contains 1 to 2 heteroatoms selected from N atom, O atom and S atom, optionally selected from halogen, alkyl, alkoxy, haloalkyl, hydroxyl, hydroxyalkyl, cyano, amino, nitro, R w , substituted by one or more substituents in cycloalkyl, heterocyclic, aryl and heteroaryl;
  • R 1 , R 2 , R 3 and R 4 are the same or different, and are each independently selected from a hydrogen atom, a deuterium atom, a halogen, an alkyl group, a deuterated alkyl group, a heteroalkyl group, an alkenyl group, an alkynyl group, and an alkoxy group.
  • R w is an amino protecting group, preferably tert-butoxycarbonyl
  • n 0, 1, or 2.
  • Another aspect of the present disclosure provides a compound represented by general formula (IM), or a tautomer, meso, racemate, enantiomer, diastereomer, or isotope thereof Derivatives, or mixtures thereof or pharmaceutically acceptable salts thereof,
  • R 1 and R 2 , R 2 and R 3 , R 3 and R 4 together with the carbon atoms to which they are connected form a four- to fourteen-membered heterocyclic group, wherein the heterocyclic group contains 1 to 2 heteroatoms selected from N atom, O atom and S atom, optionally selected from halogen, alkyl, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, ring Substituted by one or more substituents in the alkyl group, heterocyclic group, aryl group and heteroaryl group;
  • R 1 , R 2 , R 3 and R 4 are the same or different, and are each independently selected from a hydrogen atom, a deuterium atom, a halogen, an alkyl group, a deuterated alkyl group, a heteroalkyl group, an alkenyl group, an alkynyl group, and an alkoxy group.
  • n 0, 1, or 2.
  • IM general formula
  • IM-1 general formula (IM-2), general formula (IM-3), general formula (IM-1aa)
  • IM-2aa The cerebellar protein E3 ubiquitin ligase protein binding ligand compound represented by general formula (IM-2aa) and general formula (IM-3aa):
  • Ring M is a four- to fourteen-membered N-containing heterocyclic group, wherein the N-containing heterocyclic group contains, in addition to one N atom, optionally one selected from the group consisting of N atom, O atom and S atom Heteroatom
  • R 1 , R 2 , R 3 and R 4 are the same or different, and are each independently selected from hydrogen atom, halogen, C 1-6 alkyl, C 1-6 deuterated alkyl, 1 to 6 membered heteroalkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 alkoxy, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxy, C 1-6 hydroxyalkyl, cyano, Amino, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to 10 membered heteroaryl; wherein the C 1-6 alkyl group, 1 to 6 membered heteroalkyl Group, C 1-6 alkoxy group, 3 to 8 membered cycloalkyl group, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl group and 5 to 10 membered heteroaryl group are each independently optionally selected from
  • R 5 are each the same or different, and are each independently selected from hydrogen atom, halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, Cyano, amino, nitro, R w , 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to 10 membered heteroaryl;
  • R 5a is selected from hydrogen atom, halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, cyano, amino, nitro, R w , 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl group and 5 to 10 membered heteroaryl group substituted by one or more substituents;
  • R w is an amino protecting group, preferably tert-butoxycarbonyl
  • Ring A, ring B, ring C, G 1 , G 2 , n and p are as defined in the general formulas (IM-1), (IM-2) and (IM-3) above; ring D, ring E, R f , p and f are as defined in the above general formulas (IM-1aa), (IM-2aa) and (IM-3aa).
  • IM general formula (IM)
  • IM-1aa the cerebellar protein E3 ubiquitin ligase represented by the general formula (IM-1aa), the general formula (IM-2aa) and the general formula (IM-3aa)
  • IM-1aa the cerebellar protein E3 ubiquitin ligase represented by the general formula (IM-1aa)
  • IM-2aa the general formula
  • IM-3aa Protein binding ligand compounds
  • R 1 , R 2 , R 3 and R 4 are the same or different, and are each independently selected from hydrogen atom, halogen, C 1-6 alkyl, C 1-6 deuterated alkyl, 1 to 6 membered heteroalkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 alkoxy, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxy, C 1-6 hydroxyalkyl, cyano, Amino group, 3 to 8 membered cycloalkyl group, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl group and 5 to 10 membered heteroaryl group; wherein said C 1-6 alkyl group, 1 to 6 membered heteroalkyl group Group, C 1-6 alkoxy group, 3 to 8 membered cycloalkyl group, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl group and 5 to 10 membered heteroaryl group are each independently
  • R 5 are each the same or different, and are each independently selected from hydrogen atom, halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, Cyano, amino, nitro, R w , 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to 10 membered heteroaryl;
  • R 5a is selected from hydrogen atom, halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, cyano, amino, nitro, R w , 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl group and 5 to 10 membered heteroaryl group substituted by one or more substituents;
  • R w is an amino protecting group, preferably tert-butoxycarbonyl
  • Ring B is a four- to fourteen-membered heterocyclic group, wherein the heterocyclic group contains 1 to 2 heteroatoms selected from N atoms, O atoms and S atoms;
  • Ring E, ring D and ring M are the same or different, and are each independently a four- to fourteen-membered N-containing heterocyclic group, wherein the N-containing heterocyclic group contains 1 N atom and optionally Contain 1 heteroatom selected from N atom, O atom and S atom;
  • R f are the same or different, and are each independently selected from a hydrogen atom, a halogen, an alkyl group, an alkoxy group, a haloalkyl group, a hydroxyl group, a hydroxyalkyl group, a cyano group, an amino group, a nitro group, a cycloalkyl group, a heterocyclic group, Aryl and heteroaryl;
  • f 0, 1, 2, 3 or 4;
  • p is 0, 1, 2, 3 or 4;
  • p is 1, 2, 3 or 4;
  • n 0, 1, or 2.
  • IM general formula (IM)
  • a tautomer meso, racemate, enantiomer, diastereomer, or isotope thereof
  • Derivatives, or mixtures thereof or pharmaceutically acceptable salts thereof which are selected from:
  • R 1 , R 2 , R 3 and R 4 are the same or different, and are each independently selected from covalent bond, hydrogen atom, halogen, C 1-6 alkyl, C 1-6 deuterated alkyl, 1 to 6 member Heteroalkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 alkoxy, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxy, C 1-6 hydroxyalkyl , Cyano, amino, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to 10 membered heteroaryl; wherein the C 1-6 alkyl, 1 to 6-membered heteroalkyl, C 1-6 alkoxy, 3- to 8-membered cycloalkyl, 3- to 8-membered heterocyclyl, 6- to 10-membered aryl, and 5- to 10-membered heteroaryl are each independently optionally Selected from
  • R 5a is selected from a hydrogen atom, an alkyl group, a heteroalkyl group, a haloalkyl group, a hydroxy group, a hydroxyalkyl group, an amino group, R w , a cycloalkyl group, a heterocyclic group, an aryl group and a heteroaryl group;
  • R w is an amino protecting group, preferably tert-butoxycarbonyl.
  • Typical compounds represented by the compounds of general formula (IM) in the present disclosure include but are not limited to:
  • Typical compounds of the compounds with the structure of CLM-L-PTM described in the present disclosure include but are not limited to:
  • PTM is a small molecule compound ligand that binds to a target protein, wherein the target protein is selected from B7.1 and B7, TNFR2, NADPH oxidase, BclIBax and other partners in the apoptosis pathway
  • Squalene cyclase inhibitor CXCR1, CXCR2, nitric oxide (NO) synthetase, cyclooxygenase 1, cyclooxygenase 2, 5HT receptor, dopamine receptor, G protein namely Gq, histamine Receptor, 5-lipoxygenase, tryptase serine protease, thymidylate synthase, purine nucleoside phosphorylase, GAPDH trypanosoma, glycogen phosphorylase, carbonic anhydrase, chemokine receptor, JAW STAT, RXR and analogs, HIV1 protease, HIV1 integrase, influenza neuraminidase, hepatitis B reverse transcriptase, sodium channels, multidrug resistance (MDR), protein P-glycoprotein, tyrosine kinase, CD23, CD124, tyrosinase p561ck, CD4, CD5, 1L-2 receptor,
  • Another aspect of the present disclosure relates to a method for preparing compounds of general formula (I-1) or general formula (I-2), or tautomers, mesosomes, racemates, enantiomers thereof , Diastereomers, isotopic derivatives, or mixtures thereof or pharmaceutically acceptable salts thereof, which include:
  • R 5a is a hydrogen atom
  • L is R 2L'- CH 2 or Q 1 -CH 2 ;
  • R 2L ' is selected from covalent bond, C 1-12 alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene, wherein the C 1-12 Alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene are optionally selected from halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, cyano, amino, oxo, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to One or more substituents in the 10-membered heteroaryl group; preferably, R 2L 'is a covalent bond or a C 1-12 alkylene group, wherein the C 1-12 alkylene group is optionally selected From halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6
  • p is 1, 2, 3 or 4;
  • PTM, Q 1 , ring B, ring D, ring E, G 1 , G 2 , R 1 , R 3 -R 5 , R f , f and n are as general formula (I-1) and general formula (I-2 ).
  • Another aspect of the present disclosure relates to a method for preparing compounds of general formula (I-3) or general formula (I-4), or tautomers, mesosomes, racemates, enantiomers thereof , Diastereomers, isotopic derivatives, or mixtures thereof or pharmaceutically acceptable salts thereof, which include:
  • R 5a is a hydrogen atom
  • L is R 2L'- CH 2 or Q 1 -CH 2 ;
  • R 2L ' is selected from covalent bond, C 1-12 alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene, wherein the C 1-12 Alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene are optionally selected from halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, cyano, amino, oxo, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to One or more substituents in the 10-membered heteroaryl group; preferably, R 2L 'is a covalent bond or a C 1-12 alkylene group, wherein the C 1-12 alkylene group is optionally selected From halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6
  • PTM, Q 1 , ring E, G 1 , G 2 , R 1 , R 3 -R 5 , R f , g, f, p, n and t are as general formula (I-3) and general formula (I-4 ).
  • Another aspect of the present disclosure relates to a method for preparing a compound of general formula (I-3), or its tautomer, meso, racemate, enantiomer, diastereomer,
  • the method of isotopic derivative, or its mixture form or its pharmaceutically acceptable salt which includes:
  • X is a leaving group, preferably but not limited to chlorine, bromine and iodine;
  • R 5a is a hydrogen atom
  • L is R 2L'- CH 2 or Q 1 -CH 2 ;
  • R 2L ' is selected from covalent bond, C 1-12 alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene, wherein the C 1-12 Alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene are optionally selected from halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, cyano, amino, oxo, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to One or more substituents in the 10-membered heteroaryl group; preferably, R 2L 'is a covalent bond or a C 1-12 alkylene group, wherein the C 1-12 alkylene group is optionally selected From halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6
  • R 5b , R 5c , R 5d and R 5e are each the same or different, and are each independently selected from a hydrogen atom, a halogen, an alkyl group, an alkoxy group, a haloalkyl group, a hydroxyl group, a hydroxyalkyl group, a cyano group, an amino group, and a nitro group , Cycloalkyl, heterocyclyl, aryl and heteroaryl;
  • t is 0, 1 or 2; preferably, t is 0 or 1;
  • PTM, Q 1 , G 1 , G 2 , R 3 -R 5 , p and n are as defined in the general formula (I-3).
  • Another aspect of the present disclosure relates to a pharmaceutical composition containing a compound represented by any of the above-mentioned general formulas of the present disclosure or its tautomer, mesosome, racemate, or enantiomer Conformers, diastereomers, isotopic derivatives, or mixtures thereof, or pharmaceutically acceptable salts thereof, and one or more pharmaceutically acceptable carriers, diluents or excipients.
  • the present disclosure further relates to compounds represented by any of the above general formulas or tautomers, mesoisomers, racemates, enantiomers, diastereomers, isotopic derivatives, or mixtures thereof.
  • the present disclosure further relates to compounds represented by any of the above general formulas or tautomers, mesoisomers, racemates, enantiomers, diastereomers, isotopic derivatives, or mixtures thereof.
  • the present disclosure further relates to compounds represented by any of the above general formulas or tautomers, mesoisomers, racemates, enantiomers, diastereomers, isotopic derivatives, or mixtures thereof Use of the form, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing the same in the preparation of a medicament for the treatment or prevention of estrogen receptor-mediated or dependent diseases or disorders.
  • the present disclosure also relates to a method for treating or preventing a condition treated by degrading a target protein bound to a targeting ligand, which comprises administering to a patient a therapeutically effective amount of a compound represented by any of the above general formulas or a mutual variation thereof Conformers, mesosomes, racemates, enantiomers, diastereomers, isotopic derivatives, or mixtures thereof, or pharmaceutically acceptable salts thereof, or pharmaceutical compositions containing them .
  • the present disclosure also relates to a method for treating or preventing diseases treated by binding to cerebellar protein protein in the body, which comprises administering to a patient a therapeutically effective amount of a compound represented by any of the above general formulas or a tautomer, internal Racemates, racemates, enantiomers, diastereomers, isotopic derivatives, or mixtures thereof, or pharmaceutically acceptable salts thereof, or pharmaceutical compositions containing them.
  • the present disclosure also relates to a method for treating or preventing estrogen receptor-mediated or dependent diseases or disorders, which comprises administering to a patient a therapeutically effective amount of a compound represented by any of the above general formulas or its tautomers Isomers, mesosomes, racemates, enantiomers, diastereomers, isotopic derivatives, or mixtures thereof, or pharmaceutically acceptable salts thereof, or pharmaceutical compositions containing them.
  • the present disclosure further relates to a compound represented by any of the above general formulas or its tautomers, mesosomes, racemates, enantiomers, diastereomers, isotopic derivatives, or In the form of a mixture thereof, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing the same, it is used as a medicine.
  • the present disclosure further relates to compounds represented by any of the above general formulas or tautomers, mesoisomers, racemates, enantiomers, diastereomers, isotopic derivatives, or mixtures thereof
  • the present disclosure further relates to compounds represented by any of the above general formulas or tautomers, mesoisomers, racemates, enantiomers, diastereomers, isotopic derivatives, or mixtures thereof Form, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing the same, which is used for the treatment or prevention of conditions that are treated by binding to cerebellar protein in the body.
  • the present disclosure further relates to compounds represented by any of the above general formulas or tautomers, mesoisomers, racemates, enantiomers, diastereomers, isotopic derivatives, or mixtures thereof Form, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing the same, which is used to treat or prevent estrogen receptor-mediated or dependent diseases or disorders.
  • the diseases treated by degrading the target protein bound to the targeting ligand and the diseases treated by binding to the cerebellar protein protein in the body are preferably selected from abnormal cell proliferation, tumors, immune diseases, diabetes, and cardiovascular diseases. Diseases, infectious diseases and inflammatory diseases; more preferably tumors and infectious diseases.
  • the tumor is cancer; preferably selected from breast cancer, endometrial cancer, uterine cancer, testicular cancer, cervical cancer, prostate cancer, ovarian cancer, fallopian tube tumor, ovarian tumor, leukemia, skin cancer, squamous cell carcinoma, Basal cell carcinoma, adenocarcinoma, renal cell carcinoma, bladder cancer, bowel cancer, colon cancer, esophageal cancer, head cancer, kidney cancer, liver cancer, lung cancer, neck cancer, pancreatic cancer, stomach cancer, lymphoma, non-Hodgkin's lymph Tumor, melanoma, myeloproliferative disease, sarcoma, angiosarcoma, peripheral neuroepithelioma, glioma, astrocytoma, oligodendroglioma, ependymoma, glioblastoma, adult Neurocytoma, gangliocytoma, ganglion glioma, medulloblastoma, pineal
  • the infectious disease is selected from viral pneumonia, avian influenza, meningitis, gonorrhea or infection with HIV, HBV, HCV, HSV, HPV, RSV, CMV, Ebola virus, flavivirus, scar virus, rotavirus Virus, influenza, coronavirus, EBV, drug-resistant virus, RNA virus, DNA virus, adenovirus, poxvirus, picornavirus, togavirus, orthomyxovirus, retrovirus, hepatotropic DNA virus, Gram Negative bacteria, Gram-positive bacteria, atypical bacteria, Staphylococcus, Streptococcus, Escherichia coli, Salmonella, Helicobacter pylori, Chlamydiaceae, Mycoplasma, fungi, protozoa, intestinal worms, worms, prions or parasites.
  • the active compound can be formulated into a form suitable for administration by any appropriate route, and the active compound is preferably in a unit dose form, or in a form in which the patient can self-administer in a single dose.
  • the unit dose of the compound or composition of the present disclosure can be expressed in the form of a tablet, capsule, cachet, bottled syrup, powder, granule, lozenge, suppository, rejuvenated powder or liquid preparation.
  • the dosage of the compound or composition used in the treatment methods of the present disclosure will generally vary with the severity of the disease, the weight of the patient, and the relative efficacy of the compound.
  • a suitable unit dose may be 0.1-1000 mg.
  • the pharmaceutical composition of the present disclosure may contain one or more excipients selected from the following ingredients: fillers (diluents), binders, wetting agents, disintegrants or excipients Wait.
  • the composition may contain 0.1 to 99% by weight of the active compound.
  • the pharmaceutical composition containing the active ingredient may be in a form suitable for oral administration, such as tablets, dragees, lozenges, water or oil suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups or Elixirs.
  • Oral compositions can be prepared according to any method known in the art for preparing pharmaceutical compositions, and such compositions can contain one or more ingredients selected from the group consisting of sweeteners, flavoring agents, coloring agents and preservatives, To provide pleasing and delicious medicinal preparations.
  • the tablet contains the active ingredient and non-toxic pharmaceutically acceptable excipients suitable for the preparation of tablets for mixing.
  • excipients can be inert excipients, granulating agents, disintegrating agents, binders and lubricants. These tablets may be uncoated or may be coated by known techniques that mask the taste of the drug or delay disintegration and absorption in the gastrointestinal tract, thereby providing a sustained release effect over a longer period of time.
  • Oral preparations can also be provided in soft gelatin capsules in which the active ingredient is mixed with an inert solid diluent or the active ingredient is mixed with a water-soluble carrier or oil vehicle.
  • Aqueous suspensions contain the active substance and excipients suitable for the preparation of aqueous suspensions for mixing. Such excipients are suspending agents, dispersing agents or wetting agents. Aqueous suspensions may also contain one or more preservatives, one or more coloring agents, one or more flavoring agents, and one or more sweetening agents.
  • Oil suspensions can be formulated by suspending the active ingredients in vegetable oil or mineral oil.
  • the oil suspension may contain thickeners.
  • the above-mentioned sweeteners and flavoring agents can be added to provide a palatable preparation. These compositions can be preserved by adding antioxidants.
  • the pharmaceutical composition of the present disclosure may also be in the form of an oil-in-water emulsion.
  • the oil phase can be vegetable oil, mineral oil or a mixture thereof.
  • Suitable emulsifiers can be naturally occurring phospholipids, and the emulsions can also contain sweeteners, flavoring agents, preservatives and antioxidants.
  • Such preparations may also contain a demulcent, a preservative, a coloring agent and an antioxidant.
  • the pharmaceutical composition of the present disclosure may be in the form of a sterile injectable aqueous solution.
  • Acceptable solvents or solvents that can be used include water, Ringer's solution, and isotonic sodium chloride solution.
  • the sterile injection preparation can be a sterile oil-in-water injection microemulsion in which the active ingredient is dissolved in the oil phase, and the injection or microemulsion can be injected into the patient's bloodstream by local mass injection.
  • a continuous intravenous delivery device can be used.
  • An example of such a device is the Deltec CADD-PLUS.TM. 5400 intravenous pump.
  • the pharmaceutical composition of the present disclosure may be in the form of a sterile injection water or oil suspension for intramuscular and subcutaneous administration.
  • the suspension can be formulated according to known techniques using suitable dispersing or wetting agents and suspending agents.
  • the sterile injection preparation may also be a sterile injection solution or suspension prepared in a parenterally acceptable non-toxic diluent or solvent.
  • sterile fixed oil can be conveniently used as a solvent or suspending medium. For this purpose, any blended fixed oil can be used.
  • fatty acids can also be used to prepare injections.
  • the compounds of the present disclosure can be administered in the form of suppositories for rectal administration.
  • These pharmaceutical compositions can be prepared by mixing the drug with a suitable non-irritating excipient that is solid at ordinary temperatures but liquid in the rectum and thus will melt in the rectum to release the drug.
  • the dosage of the drug depends on many factors, including but not limited to the following factors: the activity of the specific compound used, the age of the patient, the weight of the patient, the health of the patient, and the behavior of the patient. , The patient’s diet, time of administration, mode of administration, rate of excretion, combination of drugs, etc.; in addition, the best treatment mode such as the mode of treatment, the daily dosage of the compound or the type of pharmaceutically acceptable salt can be based on the traditional The treatment plan to verify.
  • alkyl refers to a saturated aliphatic hydrocarbon group, which is a straight or branched chain group containing 1 to 20 carbon atoms, preferably containing 1 to 12 (e.g. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12) carbon atoms, more preferably alkyl groups containing 1 to 6 carbon atoms.
  • Non-limiting examples include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, sec-butyl, n-pentyl, 1,1-dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1-ethylpropyl, 2-methylbutyl, 3-methylbutyl, n-hexyl, 1-ethyl-2- Methylpropyl, 1,1,2-trimethylpropyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 2,2-dimethylbutyl, 1,3 -Dimethylbutyl, 2-ethylbutyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 2,3-dimethylbutyl, n-heptyl, 2 -Methylhexyl, 3-methylhexyl, 4-methylhe
  • lower alkyl groups containing 1 to 6 carbon atoms More preferred are lower alkyl groups containing 1 to 6 carbon atoms.
  • Non-limiting examples include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, and sec-butyl.
  • alkyl group 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, 2-methylbutyl, 3-methylbutyl, n-hexyl, 1-ethyl-2-methylpropyl, 1,1,2-trimethylpropyl, 1,1-dimethylbutyl, 1,2-dimethyl Butyl, 2,2-dimethylbutyl, 1,3-dimethylbutyl, 2-ethylbutyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl Group, 2,3-dimethylbutyl, etc.
  • the alkyl group may be substituted or unsubstituted.
  • the substituent When substituted, the substituent may be substituted at any available point of attachment.
  • the substituent is preferably independently selected from the group consisting of H atom, D atom, halogen, and alkane. Is substituted by one or more substituents in the group, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclyl, aryl, and heteroaryl.
  • heteroalkyl means an alkyl of one or more -CH 2 - is selected from NH, O and substituted with S or one or more selected -CH- substituted N atom; wherein said Alkyl groups are as defined above; heteroalkyl groups can be substituted or unsubstituted.
  • the substituents can be substituted at any available point of attachment, and the substituents are preferably independently optionally selected from the H atom
  • D atom halogen, alkyl, alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclic, aryl, heteroaryl Substituents are substituted.
  • alkoxy refers to -O- (alkyl) and -O- (unsubstituted cycloalkyl), where the definition of alkyl or cycloalkyl is described herein.
  • alkoxy groups include: methoxy, ethoxy, propoxy, butoxy, cyclopropoxy, cyclobutoxy, cyclopentyloxy, cyclohexyloxy.
  • the alkoxy group may be optionally substituted or unsubstituted.
  • the substituent is preferably one or more of the following groups, which are independently selected from H atom, D atom, halogen, alkyl group, alkoxy group , Haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclyl, aryl, heteroaryl substituted by one or more substituents.
  • alkylene refers to a saturated linear or branched aliphatic hydrocarbon group, which has two residues derived from the removal of two hydrogen atoms from the same carbon atom or two different carbon atoms of the parent alkane, which is A straight or branched chain group containing 1 to 20 carbon atoms, preferably containing 1 to 12 (for example, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12) carbons Atom, more preferably an alkylene group containing 1 to 6 carbon atoms.
  • Non-limiting examples of alkylene include, but are not limited to, methylene (-CH 2 -), 1,1-ethylene (-CH(CH 3 )-), 1,2-ethylene (-CH 2 -) CH 2 )-, 1,1-propylene (-CH(CH 2 CH 3 )-), 1,2-propylene (-CH 2 CH(CH 3 )-), 1,3-propylene (-CH 2 CH 2 CH 2 -), 1,4-butylene (-CH 2 CH 2 CH 2 CH 2 -), etc.
  • the alkylene group may be substituted or unsubstituted. When substituted, the substituent may be substituted at any available point of attachment.
  • the substituent is preferably independently optionally selected from alkyl, alkenyl, alkynyl , Alkoxy, alkylthio, alkylamino, halogen, thiol, hydroxyl, nitro, cyano, cycloalkyl, heterocyclyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy Substituted by one or more substituents in the group, cycloalkylthio group, heterocycloalkylthio group and oxo group.
  • heteroalkylene means that one or more -CH 2 -in an alkylene group is substituted by a heteroatom selected from N, O and S; wherein the alkylene group is as defined above; heteroalkylene It can be substituted or unsubstituted. When substituted, the substituents can be substituted at any available attachment point.
  • the substituents are preferably independently selected from H atom, D atom, halogen, alkyl, Alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclyl, aryl, and heteroaryl are substituted by one or more substituents.
  • alkenyl refers to an alkyl compound containing a carbon-carbon double bond in the molecule, wherein the definition of the alkyl group is as described above.
  • Alkenyl groups may be substituted or unsubstituted.
  • the substituents are preferably one or more of the following groups, which are independently selected from hydrogen atoms, alkyl groups, alkoxy groups, halogens, halogenated alkyl groups, hydroxyl groups, One or more substituents among hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclic, aryl and heteroaryl groups are substituted.
  • alkenylene refers to a residue having two residues derived from the same carbon atom or two different carbon atoms of the parent alkenyl group by removing two hydrogen atoms, wherein the definition of the alkenyl group is as described above.
  • alkynyl refers to an alkyl compound containing a carbon-carbon triple bond in the molecule, wherein the definition of the alkyl group is as described above.
  • the alkynyl group may be substituted or unsubstituted.
  • the substituent is preferably one or more of the following groups, which are independently selected from hydrogen atoms, alkyl groups, alkoxy groups, halogens, halogenated alkyl groups, hydroxyl groups, One or more substituents among hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclic, aryl and heteroaryl groups are substituted.
  • alkynylene refers to a residue having two residues derived from the same carbon atom or two different carbon atoms of the parent alkynyl group by removing two hydrogen atoms, wherein the alkynyl group is defined as described above.
  • cycloalkyl refers to a saturated or partially unsaturated monocyclic or polycyclic cyclic hydrocarbon substituent.
  • the cycloalkyl ring contains 3 to 20 carbon atoms, preferably 3 to 12 carbon atoms, more preferably 3 to 8 (E.g., 3, 4, 5, 6, 7, and 8) carbon atoms, more preferably 3 to 6 carbon atoms.
  • Non-limiting examples of monocyclic cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cyclohexadienyl, cycloheptyl, cycloheptatriene Groups, cyclooctyl, etc.; polycyclic cycloalkyls include spiro, fused, and bridged cycloalkyls.
  • spirocycloalkyl refers to a polycyclic group that shares one carbon atom (called a spiro atom) between 5- to 20-membered monocyclic rings, which may contain one or more double bonds. It is preferably 6 to 14 yuan, more preferably 7 to 10 yuan (for example, 7, 8, 9 or 10 yuan).
  • the spirocycloalkyl group is classified into a single spirocycloalkyl group, a bispirocycloalkyl group or a polyspirocycloalkyl group, preferably a single spirocycloalkyl group and a bispirocycloalkyl group. More preferably, it is a 4-membered/4-membered, 4-membered/5-membered, 4-membered/6-membered, 5-membered/5-membered, or 5-membered/6-membered monospirocycloalkyl.
  • spirocycloalkyl groups include:
  • fused cycloalkyl refers to a 5- to 20-membered all-carbon polycyclic group in which each ring in the system shares an adjacent pair of carbon atoms with other rings in the system, wherein one or more of the rings may contain one or Multiple double bonds. It is preferably 6 to 14 yuan, more preferably 7 to 10 yuan (for example, 7, 8, 9 or 10 yuan).
  • bicyclic, tricyclic, tetracyclic or polycyclic condensed cycloalkyl groups preferably bicyclic or tricyclic, more preferably 3-membered/4-membered, 3-membered/5-membered, 3-membered/6-membered , 4 yuan/4 yuan, 4 yuan/5 yuan, 4 yuan/6 yuan, 5 yuan/4 yuan, 5 yuan/5 yuan, 5 yuan/6 yuan, 6 yuan/3 yuan, 6 yuan/4 yuan, 6 5-membered and 6-membered/6-membered bicyclic alkyl groups.
  • fused cycloalkyl groups include:
  • bridged cycloalkyl refers to a 5- to 20-membered, all-carbon polycyclic group in which any two rings share two carbon atoms that are not directly connected, which may contain one or more double bonds. It is preferably 6 to 14 yuan, more preferably 7 to 10 yuan. According to the number of constituent rings, it can be classified into bicyclic, tricyclic, tetracyclic or polycyclic bridged cycloalkyls, preferably bicyclic, tricyclic or tetracyclic, and more preferably bicyclic or tricyclic.
  • bridged cycloalkyl groups include:
  • the cycloalkyl ring includes the cycloalkyl as described above (including monocyclic, spiro, fused and bridged rings) fused to an aryl, heteroaryl or heterocycloalkyl ring, wherein it is connected to the parent structure
  • the ring together is a cycloalkyl group, non-limiting examples include indanyl, tetrahydronaphthyl, benzocycloheptyl, etc.; preferably indanyl, tetrahydronaphthyl.
  • Cycloalkyl groups can be substituted or unsubstituted. When substituted, the substituents can be substituted at any available point of attachment.
  • the substituents are preferably independently optionally selected from hydrogen atoms, halogens, alkyl groups, Alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclyl, aryl, and heteroaryl are substituted by one or more substituents.
  • heterocyclyl refers to a saturated or partially unsaturated monocyclic or polycyclic cyclic hydrocarbon substituent containing 3 to 20 ring atoms, one or more of which is selected from nitrogen, oxygen or S(O) m (where m is an integer of 0 to 2) heteroatoms, but does not include the ring part of -OO-, -OS- or -SS-, and the remaining ring atoms are carbon.
  • It preferably contains 3 to 12 (for example, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12) ring atoms, of which 1 to 4 (for example, 1, 2, 3, and 4) are hetero Atom; more preferably contains 3 to 8 ring atoms, of which 1-3 are heteroatoms; more preferably contains 3 to 6 ring atoms, of which 1-3 are heteroatoms; most preferably contains 5 or 6 ring atoms, wherein 1-3 are heteroatoms.
  • Non-limiting examples of monocyclic heterocyclic groups include pyrrolidinyl, tetrahydropyranyl, 1,2.3.6-tetrahydropyridinyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, Homopiperazinyl and so on.
  • Polycyclic heterocyclic groups include spiro, condensed, and bridged heterocyclic groups.
  • spiroheterocyclic group refers to a polycyclic heterocyclic group that shares one atom (called a spiro atom) between 5- to 20-membered monocyclic rings, in which one or more ring atoms are selected from nitrogen, oxygen or S(O ) Heteroatoms of m (where m is an integer of 0 to 2), and the remaining ring atoms are carbon. It can contain one or more double bonds. It is preferably 6 to 14 yuan, more preferably 7 to 10 yuan.
  • the spiro heterocyclic group is classified into a single spiro heterocyclic group, a dispiro heterocyclic group or a polyspiro heterocyclic group, preferably a single spiro heterocyclic group and a dispiro heterocyclic group. More preferably, it is a 4-membered/4-membered, 4-membered/5-membered, 4-membered/6-membered, 5-membered/5-membered, or 5-membered/6-membered monospiro heterocyclic group.
  • Non-limiting examples of spiroheterocyclic groups include:
  • fused heterocyclic group refers to a 5- to 20-membered polycyclic heterocyclic group in which each ring in the system shares an adjacent pair of atoms with other rings in the system.
  • One or more rings may contain one or more Double bonds, one or more of the ring atoms are heteroatoms selected from nitrogen, oxygen or S(O) m (wherein m is an integer of 0 to 2), and the remaining ring atoms are carbon. It is preferably 6 to 14 yuan, more preferably 7 to 10 yuan (for example, 7, 8, 9 or 10 yuan).
  • bicyclic, tricyclic, tetracyclic or polycyclic fused heterocyclic groups preferably bicyclic or tricyclic, more preferably 3-membered/4-membered, 3-membered/5-membered, 3-membered/6-membered , 4 yuan/4 yuan, 4 yuan/5 yuan, 4 yuan/6 yuan, 5 yuan/4 yuan, 5 yuan/5 yuan, 5 yuan/6 yuan, 6 yuan/3 yuan, 6 yuan/4 yuan, 6 5-membered and 6-membered/6-membered bicyclic fused heterocyclic groups
  • fused heterocyclic groups include:
  • bridged heterocyclic group refers to a 5- to 14-membered polycyclic heterocyclic group with any two rings sharing two atoms that are not directly connected, which may contain one or more double bonds, one or more of the ring atoms It is a heteroatom selected from nitrogen, oxygen or S(O) m (where m is an integer of 0 to 2), and the remaining ring atoms are carbon. It is preferably 6 to 14 yuan, more preferably 7 to 10 yuan.
  • bridged heterocyclic groups include:
  • the heterocyclyl ring includes the heterocyclic group as described above (including monocyclic, spiro heterocyclic, fused heterocyclic and bridged heterocyclic ring) fused on an aryl, heteroaryl or cycloalkyl ring, wherein it is combined with the parent
  • the rings linked together in the structure are heterocyclic groups, non-limiting examples of which include:
  • the heterocyclic group may be substituted or unsubstituted. When substituted, the substituent may be substituted at any available point of attachment.
  • the substituents are preferably independently optionally selected from hydrogen atoms, halogens, alkyl groups, Alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclyl, aryl, and heteroaryl are substituted by one or more substituents.
  • aryl refers to a 6 to 14-membered all-carbon monocyclic or fused polycyclic (fused polycyclic ring is a ring that shares adjacent pairs of carbon atoms) with a conjugated ⁇ -electron system, preferably 6 to 10 membered , Such as phenyl and naphthyl.
  • the aryl ring includes the aryl ring as described above fused to a heteroaryl, heterocyclic or cycloalkyl ring, wherein the ring connected to the parent structure is an aryl ring, and non-limiting examples thereof include :
  • Aryl groups can be substituted or unsubstituted. When substituted, the substituents can be substituted at any available attachment point.
  • the substituents are preferably independently optionally selected from hydrogen atoms, halogens, alkyl groups, and alkyl groups.
  • One or more substituents of oxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclyl, aryl, and heteroaryl are substituted.
  • heteroaryl refers to a heteroaromatic system containing 1 to 4 (e.g. 1, 2, 3, and 4) heteroatoms, 5 to 14 ring atoms, where the heteroatoms are selected from oxygen, sulfur, and nitrogen.
  • Heteroaryl groups are preferably 5 to 10 members (for example, 5, 6, 7, 8, 9 or 10 members), more preferably 5 or 6 members, such as furyl, thienyl, pyridyl, pyrrolyl, N-alkane Pyrrolyl, pyrimidinyl, pyrazinyl, pyridazinyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl and the like.
  • the heteroaryl ring includes the above-mentioned heteroaryl group fused on an aryl, heterocyclic or cycloalkyl ring, wherein the ring connected with the parent structure is a heteroaryl ring, and non-limiting examples thereof include :
  • Heteroaryl groups can be substituted or unsubstituted. When substituted, the substituents can be substituted at any available point of attachment.
  • the substituents are preferably independently optionally selected from hydrogen atoms, halogens, alkyl groups, Alkoxy, haloalkyl, hydroxy, hydroxyalkyl, cyano, amino, nitro, cycloalkyl, heterocyclyl, aryl, and heteroaryl are substituted by one or more substituents.
  • cycloalkyl, heterocyclyl, aryl and heteroaryl groups have one residue derived by removing one hydrogen atom from the parent ring atom, or two residues derived from the same or two different ring atoms of the parent. Residues derived from three hydrogen atoms, namely "divalent cycloalkyl", “divalent heterocyclic group", “arylene”, and "heteroarylene".
  • amino protecting group is to keep the amino group unchanged when other parts of the molecule react, and to protect the amino group with a group that is easy to remove.
  • Non-limiting examples include tetrahydropyranyl, tert-butoxycarbonyl, acetyl, benzyl, allyl, p-methoxybenzyl, and the like. These groups may be optionally substituted with 1-3 substituents selected from halogen, alkoxy or nitro.
  • the amino protecting group is preferably tetrahydropyranyl.
  • cycloalkyloxy refers to cycloalkyl-O-, where cycloalkyl is as defined above.
  • haloalkyl refers to an alkyl group substituted with one or more halogens, where the alkyl group is as defined above.
  • deuterated alkyl refers to an alkyl group substituted with one or more deuterium atoms, where the alkyl group is as defined above.
  • hydroxy refers to the -OH group.
  • hydroxyalkyl refers to an alkyl group substituted with one or more hydroxy groups, where the alkyl group is as defined above.
  • halogen refers to fluorine, chlorine, bromine or iodine.
  • amino refers to -NH 2 .
  • cyano refers to -CN.
  • nitro refers to -NO 2 .
  • carboxylate group refers to -C(O)O(alkyl), -C(O)O(cycloalkyl), (alkyl)C(O)O- or (cycloalkyl)C(O ) O-, wherein alkyl and cycloalkyl are as defined above.
  • ubiquitin ligase refers to a family of proteins that promote the transfer of ubiquitin to a specific substrate protein and target the substrate protein for degradation.
  • cerebellar protein is an E3 ubiquitin ligase protein that alone or in combination with E2 ubiquitin ligase causes ubiquitin to attach to lysine on a target protein and then target a specific protein substrate for degradation by the proteasome. Therefore, E3 ubiquitin ligase alone or in combination with E2 ubiquitin conjugating enzyme is the reason for the transfer of ubiquitin to the target protein.
  • ubiquitin ligase participates in polyubiquitination so that the second ubiquitin is linked to the first ubiquitin, the third ubiquitin is linked to the second ubiquitin, and so on.
  • Polyubiquitinated labeled proteins are used for degradation by the proteasome.
  • Monoubiquitinated proteins are not targeted to the proteasome for degradation, but may instead change in their cellular location or function, for example via binding to other proteins that have domains capable of binding ubiquitin.
  • Lys48 on the ubiquitin chain. This is the lysine used to make polyubiquitin, which is recognized by the proteasome.
  • target protein refers to proteins and peptides that have any biological function or activity (including structure, regulation, hormones, enzymatic, genetic, immune, contraction, storage, transportation, and signal transduction).
  • the target protein includes structural proteins, receptors, enzymes, cell surface proteins, and proteins related to the integrated functions of cells, including proteins involved in each of the following: catalytic activity, aromatase activity, locomotor activity, helix Enzyme activity, metabolic process (anabolism and catabolism), antioxidant activity, proteolysis, biosynthesis, protein with kinase activity, oxidoreductase activity, transferase activity, hydrolase activity, lyase activity, isomerase activity , Ligase activity, enzyme regulator activity, signal transducer activity, structural molecule activity, binding activity (protein, lipid carbohydrate), receptor activity, cell motility, membrane fusion, cell communication, biological process regulation, development , Cell differentiation, stimulus, behavioral proteins, cell adhesion proteins, white matter involved in cell death, proteins involved
  • the protein includes proteins from eukaryotes and prokaryotes, including microorganisms, viruses, fungi, and parasites, as well as many others, including humans, microorganisms, viruses, fungi, and others that are targets of drug therapy.
  • Parasites, other animals include domestic animals, microorganisms and other antimicrobials and plants and even viruses used to determine antibiotic targets and many others.
  • isotopic derivative refers to a compound that differs in structure only in the presence of one or more isotopically enriched atoms.
  • isotopically enriched atoms For example, with the structure of the present disclosure, except for replacing hydrogen with "deuterium” or “tritium”, or replacing fluorine with 18 F-fluorine label ( 18 F isotope), or enriching with 11 C-, 13 C- or 14 C- Compounds in which carbon atoms ( 11 C-, 13 C-, or 14 C-carbon labels; 11 C-, 13 C- or 14 C- isotopes) replace carbon atoms are within the scope of the present disclosure. Such compounds can be used, for example, as analytical tools or probes in biological assays, or as tracers for in vivo diagnostic imaging of diseases, or as tracers for pharmacodynamics, pharmacokinetics, or receptor studies.
  • the present disclosure also includes compounds of general formula in various deuterated forms. Each available hydrogen atom connected to a carbon atom can be independently replaced by a deuterium atom. Those skilled in the art can refer to relevant literature to synthesize deuterated compounds of the general formula. Commercially available deuterated starting materials can be used when preparing the deuterated form of the general formula compound, or they can be synthesized using conventional techniques using deuterated reagents. Deuterated reagents include but are not limited to deuterated borane and tri-deuterated borane. Tetrahydrofuran solution, deuterated lithium aluminum hydride, deuterated ethyl iodide and deuterated methyl iodide, etc.
  • heterocyclic group optionally substituted by an alkyl group means that an alkyl group may but does not have to be present, and the description includes the case where the heterocyclic group is substituted by an alkyl group and the case where the heterocyclic group is not substituted by an alkyl group.
  • Substituted refers to one or more hydrogen atoms in the group, preferably up to 5, more preferably 1 to 3 hydrogen atoms, independently of each other, substituted with a corresponding number of substituents. It goes without saying that the substituents are only in their possible chemical positions, and those skilled in the art can determine possible or impossible substitutions (by experiment or theory) without too much effort. For example, an amino group or a hydroxyl group having free hydrogen may be unstable when combined with a carbon atom having an unsaturated (e.g., olefinic) bond.
  • “Pharmaceutical composition” means a mixture containing one or more of the compounds described herein or their physiologically/pharmaceutically acceptable salts or prodrugs and other chemical components, as well as other components such as physiological/pharmaceutically acceptable carriers And excipients.
  • the purpose of the pharmaceutical composition is to promote the administration to the organism, which is beneficial to the absorption of the active ingredient and thus the biological activity.
  • “Pharmaceutically acceptable salt” refers to the salt of the compound of the present disclosure, which is safe and effective when used in mammals, and has due biological activity.
  • the term "therapeutically effective amount” refers to a sufficient amount of a drug or agent that is non-toxic but can achieve the desired effect.
  • the determination of the effective amount varies from person to person, and depends on the age and general conditions of the recipient, as well as the specific active substance. The appropriate effective amount in each case can be determined by those skilled in the art according to routine experiments.
  • Another aspect of the present disclosure relates to a method for preparing a compound of general formula (I-1) or general formula (I-2), or a pharmaceutically acceptable salt thereof, which comprises:
  • R 5a is a hydrogen atom
  • L is R 2L'- CH 2 or Q 1 -CH 2 ;
  • R 2L ' is selected from covalent bond, C 1-12 alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene, wherein the C 1-12 Alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene are optionally selected from halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, cyano, amino, oxo, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to One or more substituents in the 10-membered heteroaryl group; preferably, R 2L 'is a covalent bond or a C 1-12 alkylene group, wherein the C 1-12 alkylene group is optionally selected From halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6
  • p is 1, 2, 3 or 4;
  • PTM, Q 1 , ring B, ring D, ring E, G 1 , G 2 , R 1 , R 3 -R 5 , R f , f, and n are as general formula (I-1) and general formula (I- 2) as defined in.
  • Another aspect of the present disclosure relates to a method for preparing a compound of general formula (I-3) or general formula (I-4), or a pharmaceutically acceptable salt thereof, which comprises:
  • R 5a is a hydrogen atom
  • L is R 2L'- CH 2 or Q 1 -CH 2 ;
  • R 2L ' is selected from covalent bond, C 1-12 alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene, wherein the C 1-12 Alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene are optionally selected from halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, cyano, amino, oxo, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to One or more substituents in the 10-membered heteroaryl group; preferably, R 2L 'is a covalent bond or a C 1-12 alkylene group, wherein the C 1-12 alkylene group is optionally selected From halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6
  • PTM, Q 1 , ring E, G 1 , G 2 , R 1 , R 3 -R 5 , R f , g, f, p, n and t are as general formula (I-3) and general formula (I-4 ).
  • Another aspect of the present disclosure relates to a method for preparing a compound of general formula (I-3), or a pharmaceutically acceptable salt thereof, which comprises:
  • X is a leaving group, preferably but not limited to chlorine, bromine and iodine;
  • R 5a is a hydrogen atom
  • L is R 2L' -CH 2 or Q 1 -CH 2 ;
  • R 2L ' is selected from covalent bond, C 1-12 alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene, wherein the C 1-12 Alkylene, 1 to 12 membered heteroalkylene, C 2-12 alkenylene and C 2-12 alkynylene are optionally selected from halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, hydroxy, C 1-6 hydroxyalkyl, cyano, amino, oxo, 3 to 8 membered cycloalkyl, 3 to 8 membered heterocyclic group, 6 to 10 membered aryl and 5 to One or more substituents in the 10-membered heteroaryl group; preferably, R 2L 'is a covalent bond or a C 1-12 alkylene group, wherein the C 1-12 alkylene group is optionally selected From halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6
  • R 5b , R 5c , R 5d and R 5e are each the same or different, and are each independently selected from a hydrogen atom, a halogen, an alkyl group, an alkoxy group, a haloalkyl group, a hydroxyl group, a hydroxyalkyl group, a cyano group, an amino group, and a nitro group , Cycloalkyl, heterocyclyl, aryl and heteroaryl;
  • t is 0, 1 or 2; preferably, t is 0 or 1;
  • PTM, Q 1 , G 1 , G 2 , R 3 -R 5 , p and n are as defined in the general formula (I-3).
  • providing acidic conditions can be organic or inorganic acids, including but not limited to acetic acid, trifluoroacetic acid, phosphoric acid, benzenesulfonic acid, preferably acetic acid; it can also be strong acid salts including but not limited to hydrochloride, Sulfate, nitrate, benzenesulfonate, trifluoromethanesulfonate, trifluoroacetate, etc., preferably hydrochloride or trifluoroacetate;
  • the reagents that provide alkaline conditions include organic bases and inorganic bases.
  • the organic bases include but are not limited to triethylamine, N,N-diisopropylethylamine, n-butyllithium, and Lithium isopropylamide, potassium acetate, sodium acetate, sodium ethoxide, sodium tert-butoxide or potassium tert-butoxide
  • the inorganic bases include but are not limited to sodium hydride, potassium phosphate, sodium carbonate, potassium carbonate, cesium carbonate, Sodium hydroxide, lithium hydroxide monohydrate, lithium hydroxide and potassium hydroxide; preferably sodium acetate or potassium carbonate.
  • the reducing agent includes, but is not limited to, sodium triacetoxyborohydride, sodium borohydride, lithium borohydride, sodium cyanoborohydride, sodium acetylborohydride, etc., preferably sodium triacetoxyborohydride .
  • the above synthesis scheme is preferably carried out in a solvent.
  • the solvents used include but are not limited to: ethylene glycol dimethyl ether, acetic acid, methanol, ethanol, acetonitrile, n-butanol, toluene, tetrahydrofuran, dichloromethane, petroleum ether, ethyl acetate, N-hexane, dimethyl sulfoxide, 1,4-dioxane, water, N,N-dimethylformamide, N,N-dimethylacetamide and mixtures thereof.
  • the structure of the compound is determined by nuclear magnetic resonance (NMR) or/and mass spectrometry (MS).
  • NMR shift ( ⁇ ) is given in units of 10 -6 (ppm).
  • NMR was measured with Bruker AVANCE-400 nuclear magnetic instrument, and the solvent was deuterated dimethyl sulfoxide (DMSO-d 6 ), deuterated chloroform (CDCl 3 ), deuterated methanol (CD 3 OD), and the internal standard was four Methylsilane (TMS).
  • HPLC High performance liquid chromatography analysis uses Agilent HPLC 1200DAD, Agilent HPLC 1200VWD and Waters HPLC e2695-2489 high pressure liquid chromatograph.
  • HPLC preparation uses Waters 2545-2767, Waters 2767-SQ Detecor2, Shimadzu LC-20AP and Gilson GX-281 preparative chromatographs.
  • CombiFlash rapid preparation instrument uses Combiflash Rf200 (TELEDYNE ISCO).
  • the thin layer chromatography silica gel plate uses Yantai Huanghai HSGF254 or Qingdao GF254 silica gel plate, the size of the silica gel plate used for thin layer chromatography (TLC) is 0.15mm ⁇ 0.2mm, and the size of the thin layer chromatography separation and purification product is 0.4mm. ⁇ 0.5mm.
  • Silica gel thin-layer chromatography generally uses Yantai Huanghai silica gel 200-300 mesh silica gel as the carrier.
  • the known starting materials of the present disclosure can be synthesized by or according to methods known in the art, or can be purchased from ABCR GmbH & Co. KG, Acros Organics, Aldrich Chemical Company, Accela ChemBio Inc, Shanghai Bi Get Pharmaceuticals, Darui Chemicals, Adamas Reagents, Aladdin Reagents, Tichiai (Shanghai) Chemical Industry Development Co., Ltd. and other companies
  • reaction can all be carried out under an argon atmosphere or a nitrogen atmosphere.
  • the argon atmosphere or nitrogen atmosphere means that the reaction flask is connected to an argon or nitrogen balloon with a volume of about 1L.
  • the hydrogen atmosphere means that the reaction flask is connected to a hydrogen balloon with a volume of about 1L.
  • the pressure hydrogenation reaction uses Parr 3916EKX hydrogenator and Qinglan QL-500 hydrogen generator or HC2-SS hydrogenator.
  • the hydrogenation reaction is usually evacuated and filled with hydrogen, and the operation is repeated 3 times.
  • the microwave reaction uses the CEM Discover-S 908860 microwave reactor.
  • the solution refers to an aqueous solution.
  • reaction temperature is room temperature, which is 20°C to 30°C.
  • the monitoring of the reaction progress in the examples adopts thin layer chromatography (TLC), the developing solvent used in the reaction, the eluent system of column chromatography used in the purification of the compound, and the developing reagent system of thin layer chromatography include: A: Dichloromethane/methanol system; B: n-hexane/ethyl acetate system.
  • A Dichloromethane/methanol system
  • B n-hexane/ethyl acetate system.
  • the volume ratio of the solvent is adjusted according to the polarity of the compound, and it can also be adjusted by adding a small amount of basic or acidic reagents such as triethylamine and acetic acid.
  • the compound 5-hydroxy-2-methylbenzoic acid 4a (5.0g, 32.86mmol, Shanghai Bi De Pharmaceutical) was dissolved in 30mL of acetic acid, and nitric acid (2.96g, 32.86mmol, 70% Wt) was slowly added dropwise at room temperature, and stirred The reaction was carried out for 30 minutes, and then the reaction was heated to 50° C., and the reaction was stirred for 1 hour.
  • the reaction was diluted with water, extracted with ethyl acetate (50mL ⁇ 3), washed with saturated sodium chloride solution (50mL), dried with anhydrous sodium sulfate, filtered, the filtrate was concentrated under reduced pressure, and the silica gel column chromatography was used to develop solvent system A The resulting residue was purified to obtain the title compound 4b (4.0 g) with a yield of 61%.
  • reaction solution was spread over Celite and filtered, concentrated under reduced pressure, and the residue obtained was purified by silica gel column chromatography with a developing solvent system A to obtain a mixture of title compounds 6b and 6b' (7.4g).
  • the crude product 14a (668mg, 2.54mmol) was dissolved in methanol (10mL), thionyl chloride (300mg, 2.54mmol) was added dropwise, and the reaction was carried out at 80°C for 16 hours.
  • the reaction solution was concentrated under reduced pressure, and purified by thin-layer chromatography with the developing solvent system A to obtain the title compound 14b (570 mg). Yield: 81%.
  • Test Example 1 The binding activity of the compound of the present disclosure and E3 ubiquitin ligase cerebellar protein (CRBN)
  • the binding activity of the compound of the present disclosure and E3 ubiquitin ligase CRBN is reflected by the activity of the compound of the present disclosure to inhibit the binding of NanoLuc-CRBN expressed in HEK293 cells (ATCC, CRL-1573) and the CRBN tracer in NanoBRET TM cells.
  • HEK293 cells were transfected with NanoLuc-CRBN plasmid in NanoBRET TM TE In-Cell CRBN kit (Promega, Cat#CS1810C135). Each well of a 6-well plate was inoculated with 1 ⁇ 10 6 HEK293 cells and cultured with DMEM/High Glucose (GE Healthcare, Cat#SH30243.01) complete medium containing 10% fetal bovine serum.
  • the transfected HEK293 cells were trypsinized and washed with phenol red-free Opti-MEM medium (Gibco, Cat#11058021). Then, the cell density was adjusted to 2.2 ⁇ 10 5 cells/mL with phenol red-free Opti-MEM medium, and 45 ⁇ L, namely 10,000 cells, were added to each well of a white flat-bottomed 384-well plate (Corning, Cat#3574).
  • the Bravo automatic liquid dispensing system was used to formulate the test compound in DMSO to 10 concentration points with the initial concentration of 2mM and 3-fold dilutions.
  • the compound was further diluted 10-fold with phenol red-free Opti-MEM medium, and 5 ⁇ L of the diluted compound was added to each well of a 384-well plate to mix with the cells, and then incubated in a 37° C. incubator for 1 hour.
  • Luminescence dual emission module of PHERAstar FS to read the fluorescence values of 450nm (Donor emission) and 610nm (Acceptor emission), according to the formula [(Acceptor emission signal sample /Donor emission) of the signal sample) - (acceptor emission control signal has no tracer / donor emission signal without tracer calculated according to the BRET ratio value)] ⁇ 1000.
  • the BRET ratio value of the negative control well without tracer was set to 100% inhibition, and the BRET ratio value of the compound-free well was set to 0% inhibition. Calculating inhibition ratio of each compound concentration with the tracer CRBN binding protein, plotted using GraphPad Prism software compound dose-response curve and IC50 values are calculated IC.
  • Table 1 The IC 50 value of the compounds of the present disclosure inhibiting the binding of E3 ubiquitin ligase CRBN in HEK293 cells
  • the compound of the present disclosure can bind E3 ubiquitin ligase cerebellar protein (CRBN) well.
  • CRBN E3 ubiquitin ligase cerebellar protein
  • Test Example 2 The degrading activity of the compound of the present disclosure on ER ⁇ in MCF7 cells
  • ERa-positive breast cancer cell line MCF7 cells were cultured with DMEM/F12 medium (HyClone, SH30023.01) containing 10% fetal bovine serum (Corning, 35-010-CV). On the first day of the experiment, after the cells were digested, the cells were washed with phenol red-free DMEM/F12 medium (ThermoFisher, 11039-021) containing 5% activated charcoal-treated fetal bovine serum (BIOSUN, BS-0004-500) The cells were suspended and counted, and the cell density was adjusted to 1.79 ⁇ 10 5 cells/mL.
  • a 48-well plate (Corning, 3548), 280 ⁇ L of cell suspension was added to each well, and the cells were placed in a 37° C., 5% CO 2 incubator and cultured overnight.
  • the compound was serially diluted with DMSO, and further diluted with phenol red-free DMEM/F12 medium containing 5% activated charcoal-treated fetal bovine serum.
  • the cell lysate was PBS containing 6M urea, 1mM EDTA, 0.5% TritonX-100, 1mM PMSF and protease inhibitor (Roche, 04693159001).
  • the cells were lysed on ice for 15 minutes, and then 300 ⁇ L of PBS containing 1 mM EDTA and 0.5% TritonX-100 per well was added to dilute the urea to 1M.
  • the blocking solution in the blocked 96-well plate was discarded, 100 ⁇ L of diluted cell lysate was added to each well, placed in a 37° C. incubator and incubated for 2 hours, and the plate was washed five times with PBS containing 0.1% Tween.
  • the compound of the present disclosure can degrade estrogen receptor (ER ⁇ ) well.
  • Test Example 3 The inhibitory activity of the compound of the present disclosure on MCF7 cell proliferation
  • MCF7 cells (ATCC, HTB-22) were cultured with MEM (GE Healthcare, SH30024.01) complete medium containing 10% fetal bovine serum.
  • MEM GE Healthcare, SH30024.01
  • MEM medium containing 2% fetal bovine serum
  • test compounds of different concentrations prepared with culture medium to each well.
  • the final concentration of the compound is 9 concentration points starting from 100 nM in a 4-fold gradient dilution.
  • a blank control containing 0.5% DMSO is set and placed 37.
  • the compound of the present disclosure can well inhibit the proliferation of MCF7 cells.
  • Test Example 4 The inhibitory activity of the compounds of the present disclosure on the proliferation of MCF7 cells expressing ER ⁇ mutants
  • MCF7 cells expressing ERaY537S mutant were constructed by lentiviral infection.
  • MCF7/ER ⁇ Y537S cells were cultured in MEM (GE Healthcare, SH30024.01) complete medium containing 10% fetal bovine serum.
  • MEM GE Healthcare, SH30024.01
  • MEM medium containing 2% fetal bovine serum On the first day of the experiment, use MEM medium containing 2% fetal bovine serum to seed cells in a 96-well plate at a density of 3,000 cells/well, with 135 ⁇ L of cell suspension per well, and place in a 37°C, 5% CO 2 cell incubator Cultivate overnight.
  • a blank control containing 0.5% DMSO is set and placed 37. Incubate for 144 hours in a 5% CO 2 cell incubator. On the eighth day, take out the 96-well cell culture plate and add 75 ⁇ L to each well Luminescent Cell Viability Assay (Promega, G7573), placed at room temperature for 10 minutes, use a multi-label microplate microplate reader (PerkinElmer, VICTOR 3) to read the luminescence signal value, and use Graphpad Prism software to calculate according to the compound concentration and luminescence signal value The IC 50 value of the compound's inhibitory activity.
  • inhibitory IC 50 values of the compounds of the present disclosure on the proliferation of MCF7 cells expressing ERa mutants are shown in Table 4 below.
  • the compound of the present disclosure can well inhibit the proliferation of MCF7/ER ⁇ Y537S cells.

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Abstract

La présente invention concerne un dérivé imide bicyclique, son procédé de préparation et son application en médecine. La présente invention concerne plus particulièrement un nouveau composé ligand d'imide bicyclique représenté par la formule générale (IM) se liant à une protéine céréblon d'ubiquitine ligase E3. La présente invention concerne également une chimère ciblant la protéolyse (PROTAC) contenant celui-ci, son procédé de préparation et son application en médecine. La définition de chaque groupe dans la formule générale (IM) est identique à celle donnée dans la description.
PCT/CN2021/072091 2020-01-16 2021-01-15 Dérivé imide bicyclique, son procédé de préparation et son application en médecine WO2021143822A1 (fr)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022187423A1 (fr) * 2021-03-03 2022-09-09 The Regents Of The University Of Michigan Ligands de céréblon
WO2023143589A1 (fr) * 2022-01-29 2023-08-03 甘李药业股份有限公司 Inhibiteur de l'ubiquitine ligase e3 céréblon
WO2023241598A1 (fr) * 2022-06-14 2023-12-21 海创药业股份有限公司 Composé aromatique, son procédé de préparation et son utilisation dans la préparation d'un agent de dégradation du récepteur des œstrogènes
WO2024015406A1 (fr) * 2022-07-12 2024-01-18 Regents Of The University Of Michigan Dérivés d'indole utilises comme agents de dégradation du récepteur des œstrogènes
WO2024015412A1 (fr) * 2022-07-12 2024-01-18 Regents Of The University Of Michigan Dérivés de tétrahydronaphtalène en tant que agents de dégradation du récepteur des oestrogènes
WO2024054832A1 (fr) 2022-09-09 2024-03-14 Innovo Therapeutics, Inc. COMPOSÉS DE DÉGRADATION CK1α ET DOUBLE CK1α/GSPT1
WO2024067792A1 (fr) * 2022-09-29 2024-04-04 海南先声再明医药股份有限公司 Composé cyclique fusionné, composition pharmaceutique et leur utilisation
WO2024086644A1 (fr) * 2022-10-18 2024-04-25 Oncopia Therapeutics, Inc. D/B/A/ Sk Life Science Labs Ligands de céréblon et leurs utilisations

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116099004B (zh) * 2022-12-30 2024-01-30 深圳开悦生命科技有限公司 Rna解旋酶dhx33抑制剂在制备用于治疗膀胱癌的药物中的应用

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996003375A1 (fr) * 1994-07-27 1996-02-08 Schering Aktiengesellschaft 2-phenylindoles utilises comme medicaments antiestrogenes
WO2005028436A2 (fr) * 2003-09-17 2005-03-31 The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services Analogues du thalidomide
CN1741995A (zh) * 2002-11-26 2006-03-01 丸石制药株式会社 异吲哚啉衍生物
WO2016097072A1 (fr) * 2014-12-18 2016-06-23 F. Hoffmann-La Roche Ag Modulateurs des récepteurs des oestrogènes tétrahydro-pyrido[3,4-b]indole et utilisations associées
WO2018144649A1 (fr) * 2017-01-31 2018-08-09 Arvinas, Inc. Ligands de céréblon et composés bifonctionnels les contenant
WO2019223715A1 (fr) * 2018-05-23 2019-11-28 江苏恒瑞医药股份有限公司 Dérivé de benzopipéridine ou d'hétéroarylpipéridine, son procédé de préparation et son utilisation médicale
WO2020160196A1 (fr) * 2019-01-29 2020-08-06 Foghorn Therapeutics Inc. Composés et leurs utilisations
WO2021041664A1 (fr) * 2019-08-27 2021-03-04 The Regents Of The University Of Michigan Inhibiteurs de ligase e3 cereblon

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996003375A1 (fr) * 1994-07-27 1996-02-08 Schering Aktiengesellschaft 2-phenylindoles utilises comme medicaments antiestrogenes
CN1741995A (zh) * 2002-11-26 2006-03-01 丸石制药株式会社 异吲哚啉衍生物
WO2005028436A2 (fr) * 2003-09-17 2005-03-31 The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services Analogues du thalidomide
WO2016097072A1 (fr) * 2014-12-18 2016-06-23 F. Hoffmann-La Roche Ag Modulateurs des récepteurs des oestrogènes tétrahydro-pyrido[3,4-b]indole et utilisations associées
WO2018144649A1 (fr) * 2017-01-31 2018-08-09 Arvinas, Inc. Ligands de céréblon et composés bifonctionnels les contenant
WO2019223715A1 (fr) * 2018-05-23 2019-11-28 江苏恒瑞医药股份有限公司 Dérivé de benzopipéridine ou d'hétéroarylpipéridine, son procédé de préparation et son utilisation médicale
WO2020160196A1 (fr) * 2019-01-29 2020-08-06 Foghorn Therapeutics Inc. Composés et leurs utilisations
WO2021041664A1 (fr) * 2019-08-27 2021-03-04 The Regents Of The University Of Michigan Inhibiteurs de ligase e3 cereblon

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022187423A1 (fr) * 2021-03-03 2022-09-09 The Regents Of The University Of Michigan Ligands de céréblon
WO2023143589A1 (fr) * 2022-01-29 2023-08-03 甘李药业股份有限公司 Inhibiteur de l'ubiquitine ligase e3 céréblon
WO2023241598A1 (fr) * 2022-06-14 2023-12-21 海创药业股份有限公司 Composé aromatique, son procédé de préparation et son utilisation dans la préparation d'un agent de dégradation du récepteur des œstrogènes
WO2024015406A1 (fr) * 2022-07-12 2024-01-18 Regents Of The University Of Michigan Dérivés d'indole utilises comme agents de dégradation du récepteur des œstrogènes
WO2024015412A1 (fr) * 2022-07-12 2024-01-18 Regents Of The University Of Michigan Dérivés de tétrahydronaphtalène en tant que agents de dégradation du récepteur des oestrogènes
WO2024054832A1 (fr) 2022-09-09 2024-03-14 Innovo Therapeutics, Inc. COMPOSÉS DE DÉGRADATION CK1α ET DOUBLE CK1α/GSPT1
WO2024067792A1 (fr) * 2022-09-29 2024-04-04 海南先声再明医药股份有限公司 Composé cyclique fusionné, composition pharmaceutique et leur utilisation
WO2024086644A1 (fr) * 2022-10-18 2024-04-25 Oncopia Therapeutics, Inc. D/B/A/ Sk Life Science Labs Ligands de céréblon et leurs utilisations

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