WO2021228216A1 - BIARYL COMPOUND CAPABLE OF SERVING AS RORγ MODULATOR - Google Patents

BIARYL COMPOUND CAPABLE OF SERVING AS RORγ MODULATOR Download PDF

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WO2021228216A1
WO2021228216A1 PCT/CN2021/093788 CN2021093788W WO2021228216A1 WO 2021228216 A1 WO2021228216 A1 WO 2021228216A1 CN 2021093788 W CN2021093788 W CN 2021093788W WO 2021228216 A1 WO2021228216 A1 WO 2021228216A1
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alkyl
compound
halogen
pharmaceutically acceptable
reaction
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PCT/CN2021/093788
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Chinese (zh)
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程耀邦
黄亚飞
周娟
董志强
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上海辉启生物医药科技有限公司
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Definitions

  • the present invention belongs to the technical field of chemical medicine, and specifically relates to biaryl compounds with ROR ⁇ t inhibitory activity, pharmaceutical compositions containing the compounds, methods for preparing the compounds, and preparation of the compounds for prevention or treatment and ROR ⁇ t Use in medicine for related diseases.
  • RORs Retinoic acid receptor-related orphan receptors
  • NF1R nuclear receptor superfamily of ligand-dependent transcription factors.
  • the RORs subfamily mainly includes three subtypes: ROR ⁇ , ROR ⁇ and ROR ⁇ .
  • ROR ⁇ contains two members: ROR ⁇ 1 (also called ROR ⁇ ) and ROR ⁇ 2 (also called ROR ⁇ t).
  • ROR ⁇ 1 is distributed in skeletal muscle, thymus, testis, pancreas, prostate, heart and liver, etc., while ROR ⁇ t is only expressed in certain immune systems. In the cell.
  • Th17 cells are a type of helper T cells that produce IL-17 and other pro-inflammatory cytokines. Th17 cells play a key role in many mouse autoimmune disease models, such as experimental allergic encephalomyelitis (EAE) and collagen-induced arthritis (CIA) animal models. In addition, IL-17 levels can be detected in some human autoimmune diseases including rheumatoid arthritis (RA), multiple sclerosis (MS), psoriasis (Psoriasis) and inflammatory bowel disease (IBD) The improvement. The number of Th17 cells found in tissues and peripheral blood samples of patients with autoimmune diseases increased. Therefore, Th17 cells or the cytokine IL-17 produced by Th17 cells are closely related to the pathogenesis of inflammation and autoimmune diseases.
  • RA rheumatoid arthritis
  • MS multiple sclerosis
  • Psoriasis psoriasis
  • IBD inflammatory bowel disease
  • Cosentyx (Secukinumab/AIN457), a monoclonal antibody developed by Novartis to specifically block IL-17 to treat psoriasis, has been approved by the FDA for marketing. This is the first drug in the psoriasis treatment market. A drug that acts on IL-17. Subsequently, the monoclonal antibody ixekizumab, which targets the pro-inflammatory cytokine IL-17A, was approved for indications of psoriasis and psoriatic arthritis. The clinical success of these monoclonal antibodies proves the importance of the IL-17 signaling pathway in inflammatory and autoimmune diseases, and demonstrates that ROR ⁇ t inhibitors can affect the IL-17 signaling pathway to treat inflammatory and autoimmune diseases. The potential for disease.
  • ROR ⁇ t can be used as a new target of drugs for the treatment of autoimmune diseases. It will be of great significance to find ROR ⁇ t small molecule inhibitors and use them in the treatment of ROR ⁇ t-mediated diseases, such as inflammation and autoimmune diseases.
  • ROR ⁇ t inhibitors for the prevention and/or treatment of ROR ⁇ t-related diseases, such as inflammation and autoimmune diseases.
  • ROR ⁇ t-related diseases such as inflammation and autoimmune diseases.
  • such compounds are expected to have high selectivity for ROR subtypes and good or even improved druggability based on structural optimization, so as to provide more medications for patients with related diseases. The choice can also provide a better treatment effect.
  • the present invention relates to compounds that can be used to prevent or treat diseases related to ROR ⁇ t.
  • the compound of the present invention not only shows satisfactory ROR ⁇ t inhibitory activity, has the ability to regulate Th17 cell differentiation, thereby inhibiting the production of IL-17, but also shows good performance in in vivo pharmacokinetic experiments, which indicates With improved druggability and improved bioavailability; in addition, it also shows good safety and has a lower risk of drug interactions.
  • the compound of the present invention can not only achieve the purpose of preventing or treating diseases related to ROR ⁇ t, but also the prepared drug is expected to have improved absorption, improved curative effect at the same dose, or provide the same curative effect at a lower dose, and more Long half-life and/or reduced possible side effects. Therefore, the present invention also provides the use of the compound of the present invention in the preparation of a medicament for the prevention or treatment of diseases related to ROR ⁇ t, a pharmaceutical composition containing the compound, and the prevention and/or treatment of ROR ⁇ t by administering the compound. Methods of related diseases.
  • a compound of formula (I), its stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates are provided:
  • R 1 and R 2 are each independently selected from hydrogen, halogen, cyano, nitro, C 1 -C 6 alkyl, -OC 1 -C 6 alkyl, -SC 1 -C 6 alkyl, -NH-C 1 -C 6 alkyl, -N-(C 1 -C 6 alkyl) 2 , -C 1 -C 6 alkyl -OC 1 -C 6 alkyl, -C 1 -C 6 alkyl -SC 1- C 6 alkyl, -C 1 -C 6 alkyl-NH-C 1 -C 6 alkyl or -C 1 -C 6 alkyl-N(C 1 -C 6 alkyl) 2 , wherein the C 1 -C 6 alkyl is optionally substituted by halogen or cyano;
  • R 3 is selected from H, -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl, -NR a R a or -OR a, wherein C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally substituted with substituents independently selected from the group consisting of halogen, cyano, nitro, C 3 optionally substituted by halogen -C 7 -cycloalkyl, R a, -OR a, -SR a , or -NR a R a, R a is selected from H or an optionally halogen-substituted C 1 -C 6 alkyl, or connected to the same N two R a on the nitrogen atom may form a 4-7 membered heterocyclic group together with the N atom to which they are attached;
  • R 4 is selected from -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl or optionally C 1 -C 6 alkyl, C 3 -C 7 ring Alkyl or 4-7 membered heterocycloalkyl substituted amino, wherein the C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally selected independently of each other from the following substituents: halogen, cyano, nitro, R a, -OR a, -SR a, -NR a R a optionally substituted with halogen or C 3 -C 7 cycloalkyl group, wherein R a Two groups selected from H or C 1 -C 6 alkyl optionally substituted by halogen, or two groups attached to the same N atom can form 4-7 membered nitrogen-containing heterocycloalkanes together with the N
  • R 5 and R 6 are each independently selected from H, halogen, cyano or C 1 -C 6 alkyl optionally substituted by halogen or cyano;
  • n and p are each independently selected from 0, 1, or 2 and
  • n is selected from 0 or 1.
  • a compound of formula (I), its stereoisomers, tautomers, and stable isotopic variants which have ROR ⁇ t inhibitory activity and are used as drugs, especially as ROR ⁇ t inhibitors.
  • a pharmaceutically acceptable salt or solvate A pharmaceutically acceptable salt or solvate.
  • a pharmaceutical composition comprising the above-mentioned compound of the present invention and a pharmaceutically acceptable excipient.
  • the pharmaceutical composition of the present invention is provided for preventing or treating diseases related to ROR ⁇ t.
  • the pharmaceutical composition may additionally contain additional therapeutically active ingredients suitable for use in combination with the compounds of the present invention.
  • a pharmaceutical combination comprising the above-mentioned compound of the present invention and another active agent.
  • a method for preventing or treating diseases related to ROR ⁇ t in a mammal, especially a human comprising administering an effective amount of the compound of the present invention described herein or a drug containing the same combination.
  • alkyl as used herein means a straight or branched chain aliphatic hydrocarbon group having the specified number of carbon atoms. Specifically, the alkyl group may have 1 to 6, 1 to 5, 1 to 4, 1 to 3, or 1 to 2 carbon atoms.
  • suitable C 1-6 alkyl groups include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isoamyl Base, neopentyl, n-hexyl and isohexyl. Certain alkyl groups have 1 to 3 carbon atoms.
  • alkoxy refers to the group -O-alkyl, where alkyl has the meaning described herein. Specifically, the term refers to the group -OC 1-6 alkyl.
  • suitable alkoxy groups include, but are not limited to, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, tert-butoxy, sec-butoxy, n-pentoxy, n-hexyl Oxy and 1,2-dimethylbutoxy.
  • Specific alkoxy groups have 1 to 3 carbon atoms.
  • alkylthio refers to the group -S-alkyl, where alkyl has the meaning described herein. Specifically, the term refers to the group -SC 1-6 alkyl.
  • suitable alkylthio groups include, but are not limited to, methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, tert-butylthio, sec-butylthio, n-pentylthio, n-hexyl Sulfuryl and 1,2-dimethylbutylsulfanyl.
  • Specific alkylthio groups have 1 to 3 carbon atoms.
  • halogen-substituted C 1 -C 6 alkyl refers to the above-mentioned C 1 -C 6 alkyl, in which one or more (for example, 1, 2, 3, 4, or 5) hydrogen The atoms are replaced by halogens.
  • the halogens may be the same or different, and may be located on the same or different C atoms.
  • halogen-substituted C 1 -C 6 alkyl are, for example, -CH 2 F, -CHF 2 , -CF 3 , -CCl 3 , -C 2 F 5 , -C 2 Cl 5 , -CH 2 CF 3 , -CH 2 Cl, CH 2 CH 2 CF 3 or -CF(CF 3 ) 2 and so on.
  • halogen-substituted C 1 -C 6 alkoxy refers to the above-mentioned C 1 -C 6 alkoxy, wherein one or more (e.g., 1, 2, 3, 4 or 5 ) The hydrogen atom is replaced by a halogen.
  • the halogens may be the same or different, and may be located on the same or different C atoms.
  • halogen substituted C 1 -C 6 alkoxy group examples include, for example, -OCH 2 F, -OCHF 2 , -OCF 3 , -OCCl 3 , -OC 2 F 5 , -OC 2 Cl 5 , -OCH 2 CF 3. -OCH 2 Cl or -OCH 2 CH 2 CF 3 and so on.
  • halogen-substituted C 1 -C 6 alkylthio refers to the C 1 -C 6 alkylthio group described above, of which one or more (e.g., 1, 2, 3, 4 or 5 ) The hydrogen atom is replaced by a halogen.
  • the halogens may be the same or different, and may be located on the same or different C atoms.
  • halogen substituted C 1 -C 6 alkylthio group examples include, for example, -SCH 2 F, -SCHF 2 , -SCF 3 , -SCCl 3 , -SC 2 F 5 , -SC 2 Cl 5 , -SCH 2 CF 3. -SCH 2 Cl or -SCH 2 CH 2 CF 3 and so on.
  • cycloalkyl as used herein means a monocyclic, fused polycyclic, bridged polycyclic or spirocyclic non-aromatic saturated hydrocarbon ring structure having the specified number of ring atoms.
  • the cycloalkyl group may have 3 to 12 carbon atoms, specifically 3 to 10, and more specifically 3 to 7 carbon atoms, that is, C 3 -C 7 cycloalkyl.
  • suitable cycloalkyl groups include, but are not limited to, monocyclic C 3 -C 7 cycloalkyl groups such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cycloheptyl.
  • Specific cycloalkyl groups have 3 to 5 carbon atoms.
  • halogen-substituted C 3 -C 7 cycloalkyl refers to the above-mentioned C 3 -C 7 cycloalkyl, of which one or more (e.g. 1, 2, 3, 4 or 5 ) The hydrogen atom is replaced by a halogen.
  • the halogens may be the same or different, and may be located on the same or different C atoms.
  • Specific examples include, but are not limited to, 2-fluorocyclopropyl, 2,3-difluorocyclopropyl, 2,2,3,3-tetrafluorocyclopropyl, 2,3-difluorocyclobutyl, 2, 4-Difluorocyclobutyl and so on.
  • heterocycloalkyl means a monocyclic, fused polycyclic, spirocyclic, or bridged polycyclic heteroatom including one or more heteroatoms independently selected from O, N, and S and a specified number of ring atoms.
  • the heterocycloalkyl group may have 4 to 12 ring members, specifically 4 to 10 ring members, and more specifically 4 to 7 ring members.
  • the heterocycloalkyl group usually contains up to 4 heteroatoms, more usually up to 3 heteroatoms, more usually up to 2, such as a single heteroatom, such as a 4-7 membered monocyclic heterocycloalkyl group having one heteroatom such as N, That is, 4-7 membered nitrogen-containing heterocycloalkyl.
  • suitable heterocycloalkyl groups include, but are not limited to, azetidinyl, oxetanyl, thietanyl, pyrrolidinyl (e.g., 1-pyrrolidinyl, 2-pyrrolidinyl, and 3 -Pyrrolidinyl), tetrahydrofuranyl (e.g.
  • Tetrahydropyranyl Tetrahydrothiopyranyl (for example 4-tetrahydrothiopyranyl), morpholinyl, thiomorpholinyl, dioxanyl, piperazinyl, or azepanyl.
  • heterocyclic ring can have 1 to 4 heteroatoms, as long as the heterocyclic ring or heteroaromatic ring is chemically feasible and stable.
  • halo or halogen as used herein means fluorine (F), chlorine (Cl), bromine (Br), and iodine (I).
  • the specific halogen is fluorine or chlorine.
  • halogen substituted group as used herein is intended to include monohalogenated or polyhalogenated groups in which one or more identical or different halogens replace one or more hydrogens in the group.
  • cyano as used herein means the group -CN.
  • nitro as used herein means the group -NO 2 .
  • amino as used herein means the group -NH 2 ;
  • the term "optionally substituted by” means that the group may be unsubstituted or be substituted by one or more (e.g. 0, 1, 2, 3, 4 or 5 or more, or any of which can be derived Range) Substituting the listed substituents for this group, wherein the substituents may be the same or different.
  • the optionally substituted group has 1 substituent.
  • the optionally substituted group has 2 substituents.
  • the optionally substituted group has 3 substituents.
  • the optionally substituted group has 4 substituents.
  • the C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl, or 4-7 membered heterocycloalkyl used in the definition of compounds herein optionally carries one or more substituents.
  • halogens preferably F
  • pharmaceutically acceptable means approved by or can be approved by the corresponding agency of each country, or listed in the generally recognized pharmacopoeia for animals and more specifically humans, or when administered to animals such as humans in appropriate amounts Molecular entities and compositions that do not produce adverse, allergic or other adverse reactions.
  • pharmaceutically acceptable salt means a salt of the compound of the present invention that is pharmaceutically acceptable and has the desired pharmacological activity of the parent compound.
  • such salts are non-toxic, and can be inorganic acid addition salts, organic acid addition salts, and base addition salts.
  • such salts include: (1) acid addition salts formed with inorganic acids, such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, etc.; or acid addition salts formed with organic acids, Organic acids such as acetic acid, propionic acid, caproic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid Acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, 2-naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, glucoheptanoic acid, 3-phenylpropionic acid, trimethylacetic acid, tert-butyl Acetic acid, lauryl sulfuric acid, gluconic acid, glutacetate
  • prodrug means a compound that has a cleavable group and becomes a compound of the present invention that has pharmacological activity in the body through solvolysis or under physiological conditions, including derivatives of the compound of the present invention.
  • Prodrugs include acid derivatives well known in the art, such as esters prepared by reacting a parent acid with a suitable alcohol, or amides prepared by reacting a parent acid compound with a substituted or unsubstituted amine, or anhydrides or mixed anhydrides. Simple aliphatic or aromatic esters, amides, and anhydrides derived from acid groups pendant to the compounds of the present invention are particularly useful prodrugs. Specific such prodrugs are C 1-8 alkyl, C 2-8 alkenyl, optionally substituted C 6-10 aryl and (C 6-10 aryl)-(C 1- 4 alkyl) esters.
  • stereoisomer as used herein means an isomer formed due to at least one asymmetric center. In compounds with one or more (for example, 1, 2, 3, or 4) asymmetric centers, it can produce racemic mixtures, single enantiomers, diastereomeric mixtures, and Individual diastereomers. Specific molecules can also exist as geometric isomers (cis/trans). Similarly, the compounds of the present invention may exist as a mixture of two or more different structural forms in rapid equilibrium (commonly referred to as tautomers). Representative examples of tautomers include keto-enol tautomers, phenol-ketone tautomers, nitroso-oxime tautomers, imine-enamine tautomers Wait. For example, nitroso-oximes can exist in equilibrium in the following tautomeric forms in solution:
  • the compounds of the present invention may have one or more asymmetric centers, and therefore may be prepared in the form of (R)- or (S)-stereoisomers respectively or in the form of mixtures thereof.
  • R and S represent the relative configuration of the chiral center.
  • solvate refers to a solvent addition form containing stoichiometric or non-stoichiometric solvents, including, for example, solvates with water, such as hydrates, or with organic solvents, such as methanol, ethanol, or Solvates of acetonitrile, namely as methanolate, ethanolate or acetonitrile respectively; or in the form of any polymorph. It should be understood that such solvates of the compounds of the present invention also include solvates of pharmaceutically acceptable salts of the compounds of the present invention.
  • isotopic variant refers to a compound in which one or more of the atoms constituting the compound is replaced by an atom having an atomic mass or mass number that is different from the atomic mass or mass number commonly found in nature.
  • isotopes that can be incorporated into one or more atoms of the compounds of the present invention include, for example, 2 H, 3 H, 13 C, 14 C, 15 N, 17 O, 18 O, 31 P, 32 P, 35 S, 18 F and 36 Cl, thereby forming isotopic variants of the compounds of the present invention, whether they are radioactive or not, are intended to be encompassed within the scope of the present invention.
  • the incorporated isotope is 2H (deuterium); in other embodiments, the incorporated isotope is 3H (tritium).
  • disease related to ROR ⁇ t means that ROR ⁇ t promotes the occurrence and development of the disease, or inhibiting ROR ⁇ t will reduce the incidence of the disease and reduce or eliminate the disease symptoms.
  • "disease related to ROR ⁇ t” is especially selected from inflammation or autoimmune diseases, cancer, etc., including but not limited to psoriasis, rheumatoid arthritis, psoriatic arthritis, ankylosing spine Inflammation, multiple sclerosis, systemic lupus erythematosus, graft-versus-host disease, inflammatory bowel disease, Crohn's disease, ulcerative colitis, chronic obstructive pulmonary disease, asthma, glomerulonephritis, lupus nephritis, myocarditis, thyroid Inflammation, dry eye, uveitis, Behcet's disease, allergic dermatitis, acne, scleroderma, bronchitis, derm
  • the preferred indications of the present invention are selected from psoriasis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, multiple sclerosis, inflammatory bowel disease, dry eye, allergic dermatitis, chronic obstruction COPD, asthma, necrotizing enterocolitis, liver fibrosis, non-alcoholic steatohepatitis (NASH), new coronavirus pneumonia, triple negative breast cancer and prostate cancer.
  • subject or “individual” as used herein includes human or non-human animals.
  • exemplary human individuals include human individuals (referred to as patients) or normal individuals suffering from diseases such as those described herein.
  • non-human animals include all vertebrates, such as non-mammals (such as birds, amphibians, reptiles) and mammals, such as non-human primates, livestock and/or domesticated animals (such as sheep, dogs). , Cats, cows, pigs, etc.).
  • terapéuticaally effective amount means that when administered to a subject to treat a disease, it is sufficient to reduce or completely alleviate the symptoms or other harmful effects of the disorder; reverse, completely stop or slow the progression of the disorder; or reduce the deterioration of the disorder
  • the amount of risk, the "effective amount” may vary depending on the compound, the disease and its severity, and the age and weight of the subject to be treated.
  • prevention means to administer a subject suspected of suffering from or susceptible to ROR ⁇ t-related diseases as defined herein, especially inflammation or autoimmune diseases, such as mammals, such as humans. Or multiple compounds of the present invention, which reduce the risk of suffering from the defined disease.
  • prevention encompasses the use of the compounds of the present invention prior to the diagnosis or determination of any clinical and/or pathological symptoms.
  • treatment refers to the administration of one or more of the compounds of the invention described herein to a subject suffering from the disease or having symptoms of the disease, such as a mammal, such as a human, for Cure, alleviate, alleviate or affect the disease or the symptoms of the disease.
  • the disease is a disease related to ROR ⁇ t as defined herein, especially inflammation or an autoimmune disease.
  • pharmaceutical combination means that the compound of the present invention can be combined with other active agents to achieve the purpose of the present invention.
  • the other active agent may be one or more additional compounds of the present invention, or may be a second or additional (e.g., third ) Compound. Such active agents are suitably present in combination in an effective amount to achieve the intended purpose.
  • the other active agent may be co-administered with the compound of the present invention in a single pharmaceutical composition, or administered separately from the compound of the present invention in separate discrete units, and when administered separately, they may be administered simultaneously or sequentially. The sequential administration may be close or distant in time.
  • pharmaceutically acceptable excipient or carrier refers to one or more compatible solid or liquid fillers or gel substances, which are pharmacologically inactive and are compatible with other ingredients in the composition. It should be acceptable for administration to warm-blooded animals such as humans, and used as a carrier or medium for the compound of the present invention in the administration form. Examples include, but are not limited to, cellulose and its derivatives (such as carboxymethyl cellulose).
  • solid lubricants such as magnesium stearate
  • calcium sulfate such as calcium sulfate
  • vegetable oils such as propylene glycol, glycerin, mannitol, sorbitol, etc.
  • emulsifiers such as Tween Class
  • wetting agents such as sodium lauryl sulfate
  • coloring agents such as sodium lauryl sulfate
  • flavoring agents such as pepperminophen, etc.
  • stabilizers
  • C n-n+m or C n -C n+m in the definition of the compound of the present invention includes various cases of n to n+m carbon atoms, for example, C 1-6 includes C 1 , C 2 , C 3 , C 4 , C 5 and C 6 , and also include any range from n to n+m, for example, C 1-6 includes C 1-2 , C 1-3 , C 1-4 , and C 2- 6. C 3-6 etc.
  • n-membered to n+m-membered in the definition of the compound of the present invention means that the number of ring atoms is from n to n+m.
  • a 3-12-membered ring includes a 3-membered ring, a 4-membered ring, a 5-membered ring, and a 6-membered ring.
  • Rings, 12-membered rings, etc. also include any range from n to n+m.
  • 3-12-membered rings include 3-6-membered rings, 3-9-membered rings, 5-6-membered rings, and 5-7-membered rings , 6-7 membered ring, 6-8 membered ring and 6-10 membered ring, etc.
  • the compound of the present invention is the free form of the compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof; most preferably, the free form of the compound of formula (I) or a pharmaceutically acceptable salt thereof.
  • Certain compounds of the present invention may exist in polymorphic or amorphous forms, and they also fall within the scope of the present invention.
  • the compound of formula (I) may be in the form of a co-crystal with another chemical entity, and this specification includes all such co-crystals.
  • the compounds of the present invention may exist as individual enantiomers or as a mixture of enantiomers.
  • a compound of formula (I) or a pharmaceutically acceptable salt thereof which is a single enantiomer with an enantiomeric excess (%ee) >95, >98% or >99%.
  • a single enantiomer is present in an enantiomeric excess (%ee) of >99%.
  • the present invention provides a compound of formula (I), its stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates:
  • R 1 and R 2 are each independently selected from hydrogen, halogen, cyano, nitro, C 1 -C 6 alkyl, -OC 1 -C 6 alkyl, -SC 1 -C 6 alkyl, -NH-C 1 -C 6 alkyl, -N-(C 1 -C 6 alkyl) 2 , -C 1 -C 6 alkyl -OC 1 -C 6 alkyl, -C 1 -C 6 alkyl -SC 1- C 6 alkyl, -C 1 -C 6 alkyl-NH-C 1 -C 6 alkyl or -C 1 -C 6 alkyl-N(C 1 -C 6 alkyl) 2 , wherein the C 1 -C 6 alkyl is optionally substituted by halogen or cyano;
  • R 3 is selected from H, -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl, -NR a R a or -OR a, wherein C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally substituted with substituents independently selected from the group consisting of halogen, cyano, nitro, C 3 optionally substituted by halogen -C 7 -cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is selected from H or optionally halogen-substituted C 1 -C 6 alkyl, or connected to the same two R a may be formed on the N-atom together with the N atom to which they are attached, 4-7 membered nitrogen-containing heterocyclic group;
  • R 4 is selected from -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl or optionally C 1 -C 6 alkyl, C 3 -C 7 ring Alkyl or 4-7 membered heterocycloalkyl substituted amino, wherein the C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally selected independently of each other Substitution from the following substituents: halogen, cyano, nitro, R a , -OR a , -SR a , -NR a R a or C 3 -C 7 cycloalkyl optionally substituted by halogen, R a is selected A C 1 -C 6 alkyl group optionally substituted by H or halogen, or two groups attached to the same N atom can form a 4-7 membered nitrogen-containing heterocycloalkyl group
  • R 5 and R 6 are each independently selected from H, halogen, cyano or C 1 -C 6 alkyl optionally substituted by halogen or cyano;
  • n and p are each independently selected from 0, 1, or 2 and
  • n is selected from 0 or 1.
  • n is zero.
  • n 1
  • R 1 and R 2 are each independently H.
  • R 1 and R 2 are each independently halogen, such as F, Cl, Br or I; preferably F or Cl.
  • both R 1 and R 2 are H. In a specific embodiment, R 1 is H and R 2 is halogen. In a specific embodiment, R 1 is halogen and R 2 is H. In a specific embodiment, R 1 and R 2 are both halogen, and the two may be the same or different.
  • R 1 and R 2 are each independently selected from C 1 -C 6 alkyl, -OC 1 -C 6 alkyl, -SC 1 -C 6 alkyl,- NH-C 1 -C 6 alkyl or -N-(C 1 -C 6 alkyl) 2 , wherein the C 1 -C 6 alkyl group is optionally substituted by halogen (preferably F).
  • R 1 and R 2 are each independently selected from -C 1 -C 6 alkyl-OC 1 -C 6 alkyl, -C 1 -C 6 alkyl-SC 1- C 6 alkyl, -C 1 -C 6 alkyl-NH-C 1 -C 6 alkyl or -C 1 -C 6 alkyl-N(C 1 -C 6 alkyl) 2 , where C The 1- C 6 alkyl group is optionally substituted by halogen (preferably F).
  • Specific examples include but are not limited to -CH 2 OCH 3 , -CH 2 CH 2 OCH 3 , -CH 2 OCH 2 CH 3 , -CH 2 CH 2 OCH 2 CH 3 , -CH 2 NHCH 3 , -CH 2 N( CH 3 ) 2 , -CH 2 OCF 3 , -CH 2 CH 2 OCF 3 , -CH 2 OCH 2 CF 3 , -CH 2 NHCF 3 , -CH 2 N(CF 3 ) 2 and so on.
  • R 3 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, which is optionally selected by one or more groups independently selected from substituents: halogen, optionally halogen-substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or a plurality of halogen-substituted C 1 -C 6 alkyl, or are connected on the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • R 3 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted with F, Cl, Br, I, R a , or - substituted with OR a, wherein R a It is H or C 1 -C 3 alkyl optionally substituted with one or more halogens (preferably F).
  • R a It is H or C 1 -C 3 alkyl optionally substituted with one or more halogens (preferably F).
  • Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, trifluoromethyl, trifluoroethyl, hydroxymethyl, hydroxyethyl, methoxymethyl, methoxyethyl, Trifluoromethoxymethyl or trifluoromethoxyethyl, etc.
  • R 3 is C 1 -C 3 alkyl, such as methyl, ethyl, propyl or isopropyl.
  • R 3 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted by C 3 -C 7 cycloalkyl optionally substituted by halogen.
  • Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentyl Ethyl and so on.
  • R 3 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted with -NR a R a, wherein R a is independently selected from H or optionally with one or more halogen substituted C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, aminomethyl, aminoethyl, aminopropyl, methylaminomethyl, dimethylaminomethyl, methylethylamino Methyl, azetidinyl methyl, pyrrolidinyl methyl, piperidinyl methyl, etc.
  • R 3 is -C 3 -C 7 cycloalkyl, which is optionally substituted with one or more groups independently selected from: halogen, optionally halogen substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 - C 6 alkyl, or are connected on the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • R 3 is -C 3 -C 5 cycloalkyl, such as cyclopropyl, cyclobutyl or cyclopentyl.
  • R 3 is -C 3 -C 7 cycloalkyl, optionally substituted with one or more groups independently selected from the following groups: halogen, R a ,, - OR a or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 6 alkyl.
  • Specific examples include, but are not limited to, 2,3-difluorocyclopropyl, 2,2,3,3-tetrafluorocyclopropyl, 2,3-difluorocyclobutyl, methylcyclopropyl or cyclobutyl , Dimethylcyclopropyl or cyclobutyl, trifluoromethylcyclopropyl or cyclobutyl, hydroxycyclopropyl or cyclobutyl, trifluoromethoxycyclopropyl or cyclobutyl, methylamino ring Propyl, dimethylaminocyclopropyl, trifluoromethylaminocyclopropyl, etc.
  • R 3 is 4-7-membered heterocycloalkyl, optionally substituted with one or more substituents independently selected from the following radicals: halogen, R a, -OR a, -SR a, or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 6 alkyl, or are connected on the same two N atoms R a may form a 4-7 membered nitrogen-containing heterocyclic group together with the N atom to which they are attached.
  • R 3 is 4-7 membered heterocycloalkyl, such as azetidinyl, oxetanyl, thietane, pyrrolidinyl (e.g., 1-pyrrolidinyl , 2-pyrrolidinyl and 3-pyrrolidinyl), tetrahydrofuranyl (e.g. 1-tetrahydrofuranyl, 2-tetrahydrofuranyl and 3-tetrahydrofuranyl), tetrahydrothienyl (e.g. 1-tetrahydrothienyl, 2-tetrahydrofuranyl) Hydrothienyl and 3-tetrahydrothienyl), piperidinyl (e.g.
  • substituents independently selected from F, Cl, Br, I, R a, -OR a substituted with -NR a R a or a group, wherein R a is independently selected from H or any Select C 1 -C 3 alkyl substituted with one or more halogens.
  • R 3 is -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • Specific examples include but are not limited to -NH 2 , -NHCH 3 , -NCH 3 CH 3 , -N(CH 2 CH 3 )CH 3 , -N(CH 2 CH 3 )(CH 2 CH 3 )-, -NHCF 3 , -N(CH 3 )CF 3 , -N(CF 3 )CF 3 , -N(CH 2 CF 3 )CF 3 or -N(CH 2 CF 3 )(CH 2 CF 3 )-, -NH( CH 2 CH 2 CH 3 ), azetidinyl, pyrrolidinyl, piperidinyl, etc.
  • R 4 is selected from -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, which is optionally selected by one or more groups independently selected from group: halogen, optionally halogen-substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen substituted C 1 -C 6 alkyl, or are connected on the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • R 4 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted with F, Cl, Br, I, R a or -OR a, wherein R a It is H or C 1 -C 3 alkyl optionally substituted with one or more halogens (preferably F).
  • halogens preferably F.
  • Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, trifluoromethyl, trifluoroethyl, hydroxymethyl, hydroxyethyl, methoxymethyl, methoxyethyl, Trifluoromethoxymethyl or trifluoromethoxyethyl, etc.
  • R 4 is C 1 -C 3 alkyl, such as methyl, ethyl, propyl, or isopropyl.
  • R 4 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted by C 3 -C 7 cycloalkyl optionally substituted by halogen.
  • Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentyl Ethyl and so on.
  • R 4 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted with -NR a R a, wherein R a is independently selected from H or optionally with one or more halogen substituted C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, aminomethyl, aminoethyl, aminopropyl, methylaminomethyl, dimethylaminomethyl, methylethylamino Methyl, azetidinyl methyl, pyrrolidinyl methyl, piperidinyl methyl, etc.
  • R 4 is -C 3 -C 7 cycloalkyl, which is optionally substituted with one or more groups independently selected from: halogen, optionally halogen substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 - C 6 alkyl, or are connected on the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • R 4 is -C 3 -C 5 cycloalkyl, such as cyclopropyl, cyclobutyl or cyclopentyl.
  • R 4 is -C 3 -C 7 cycloalkyl, optionally substituted with one or more substituents independently selected from the following radicals: halogen, R a, -OR a or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 6 alkyl.
  • Specific examples include, but are not limited to, 2,3-difluorocyclopropyl, 2,2,3,3-tetrafluorocyclopropyl, 2,3-difluorocyclobutyl, methylcyclopropyl or cyclobutyl , Dimethylcyclopropyl or cyclobutyl, trifluoromethylcyclopropyl or cyclobutyl, hydroxycyclopropyl or cyclobutyl, trifluoromethoxycyclopropyl or cyclobutyl, methylamino ring Propyl, dimethylaminocyclopropyl, trifluoromethylaminocyclopropyl, etc.
  • R 4 is 4-7 membered heterocycloalkyl, optionally substituted with one or more substituents independently selected from the following radicals: halogen, R a, -OR a, -SR a, or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 6 alkyl, or are connected on the same two N atoms R a may form a 4-7 membered nitrogen-containing heterocyclic group together with the N atom to which they are attached.
  • R 4 is 4-7 membered heterocycloalkyl, such as azetidinyl, oxetanyl, thietane, pyrrolidinyl (e.g., 1-pyrrolidinyl , 2-pyrrolidinyl and 3-pyrrolidinyl), tetrahydrofuranyl (e.g. 1-tetrahydrofuranyl, 2-tetrahydrofuranyl and 3-tetrahydrofuranyl), tetrahydrothienyl (e.g. 1-tetrahydrothienyl, 2-tetrahydrofuranyl) Hydrothienyl and 3-tetrahydrothienyl), piperidinyl (e.g.
  • substituents independently selected from F, Cl, Br, I, R a, -OR a substituted with -NR a R a or a group, wherein R a is independently selected from H or any Select C 1 -C 3 alkyl substituted with one or more halogens.
  • R 4 is an amino group optionally substituted with C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl, or 4-7 membered heterocycloalkyl.
  • the substituted amino C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl having each of the above embodiments as R C 4 l -
  • R 4 is an amino group substituted with a C 1 -C 6 alkyl group optionally substituted by halogen.
  • Specific examples include, but are not limited to, -NH 2 , -NHCH 3 , -NCH 3 CH 3 , -N(CH 2 CH 3 )CH 3 , -N(CH 2 CH 3 )(CH 2 CH 3 )-, -NHCF 3 , -N(CH 3 )CF 3 , -N(CF 3 )CF 3 ,- N(CH 2 CF 3 )CF 3 or -N(CH 2 CF 3 )(CH 2 CF 3 )-, -NH(CH 2 CH 2 CH 3 ), azetidinyl, pyrrolidinyl, piperidinyl Wait.
  • R 5 and R 6 are each independently selected from halogens, such as F, Cl, Br, I.
  • R 5 and R 6 are each independently selected from C 1 -C 6 alkyl optionally substituted with halogen. In a specific embodiment, R 5 and R 6 are each independently selected from C 1 -C 3 alkyl substituted with at least three halogens. In a more specific embodiment, R 5 and R 6 are each independently selected from C 1 -C 3 alkyl substituted by three fluorines. Specific examples include, but are not limited to, trifluoromethyl, trifluoroethyl, penta Fluoroethyl and so on. In the most specific embodiment, both R 5 and R 6 are -CF 3 .
  • both m and p are zero.
  • m is 0 and p is 1.
  • m is 0 and p is 2.
  • m is 1 and p is 0.
  • m is 1 and p is 1.
  • m is 1 and p is 2.
  • m is 2 and p is 0.
  • m is 2 and p is 1.
  • m is 2 and p is 2.
  • the present invention provides a compound of formula (I), its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate:
  • R 1 and R 2 are each independently selected from hydrogen, halogen or C 1 -C 6 alkyl, wherein the C 1 -C 6 alkyl is optionally substituted by halogen;
  • R 3 is selected from H, -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl or -NR a R a, wherein C 1 -C 6 alkyl or C 3 -C 7 cycloalkyl optionally independently selected from the following substituents: halogen, optionally halogen-substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a;
  • R 4 is selected from -C 1 -C 6 alkyl or -NR a R a, wherein said C 1 -C 6 alkyl is optionally independently substituted with substituents selected from: R a, halogen or -NR a R a :
  • R a is selected from H or an optionally halogen-substituted C 1 -C 6 alkyl, or are connected on the same N atom may form two R a 4-7 membered nitrogen-containing together with the N atom to which they are attached, Cycloalkyl
  • R 5 and R 6 are each independently selected from halogen or C 1 -C 6 alkyl optionally substituted by halogen;
  • n and p are each independently selected from 0, 1, or 2 and
  • n is selected from 0 or 1.
  • R 1 and R 2 are each independently selected from hydrogen or halogen, such as F, Cl, Br, I. In a specific embodiment, both R 1 and R 2 are H. In a specific embodiment, R 1 is H and R 2 is halogen. In a specific embodiment, R 1 is halogen and R 2 is H. In a specific embodiment, R 1 and R 2 are both halogen, and the two may be the same or different.
  • R 3 is -C 1 -C 3 alkyl, optionally substituted with a substituent independently selected from: H, halogen or optionally substituted by halogen ⁇ C 3 -C 7 cycloalkyl.
  • substituents independently selected from: H, halogen or optionally substituted by halogen ⁇ C 3 -C 7 cycloalkyl.
  • Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, trifluoromethyl, trifluoroethyl, cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl Group, cyclopentylmethyl, cyclopentylethyl, etc.
  • R 3 is -C 1 -C 3 alkyl, such as methyl, ethyl, propyl or isopropyl.
  • R 3 is -C 1 -C 3 alkyl, substituted -NR a R a, wherein R a is selected from H or optionally halogen-substituted C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • Specific examples include, but are not limited to, aminomethyl, aminoethyl, aminopropyl, methylaminomethyl, dimethylaminomethyl, methylethylaminomethyl, azetidinylmethyl, pyrrolidinylmethyl , Piperidinyl methyl, etc.
  • a compound of formula (I) is, R 3 is -C 3 -C 7 cycloalkyl, which is optionally substituted independently selected from the following groups: halogen, R a, or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 3 alkyl.
  • Specific examples include, but are not limited to, 2,3-difluorocyclopropyl, 2,2,3,3-tetrafluorocyclopropyl, 2,3-difluorocyclobutyl, methylcyclopropyl or cyclobutyl , Dimethylcyclopropyl or cyclobutyl, trifluoromethylcyclopropyl or cyclobutyl, methylaminocyclopropyl, dimethylaminocyclopropyl, trifluoromethylaminocyclopropyl, etc.
  • R 3 is -C 3 -C 5 cycloalkyl, such as cyclopropyl, cyclobutyl, or cyclopentyl.
  • a compound of formula (I) is, R 3 is -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 3 alkyl or connected to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • Specific examples include but are not limited to -NH 2 , -NHCH 3 , -NCH 3 CH 3 , -N(CH 2 CH 3 )CH 3 , -N(CH 2 CH 3 )(CH 2 CH 3 )-, -NHCF 3 , -N(CH 3 )CF 3 , -N(CF 3 )CF 3 , -N(CH 2 CF 3 )CF 3 or -N(CH 2 CF 3 )(CH 2 CF 3 )-, -NH( CH 2 CH 2 CH 3 ), azetidinyl, pyrrolidinyl, piperidinyl, etc.
  • R 4 is -C 1 -C 3 alkyl, optionally substituted by halogen.
  • halogen include, but are not limited to, methyl, ethyl, propyl or isopropyl, trifluoromethyl, trifluoroethyl, pentafluoroethyl, and the like.
  • R 4 is -C 1 -C 3 alkyl, such as methyl, ethyl, propyl or isopropyl.
  • R 4 is -C 1 -C 3 alkyl, substituted -NR a R a, wherein R a is selected from H or optionally halogen-substituted C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
  • Specific examples include, but are not limited to, aminomethyl, aminoethyl, aminopropyl, methylaminomethyl, dimethylaminomethyl, methylethylaminomethyl, azetidinylmethyl, pyrrolidinylmethyl , Piperidinyl methyl, etc.
  • R 4 is is -NR a R a, wherein R a is selected from H or an optionally halogen-substituted C 1 -C 3 alkyl, or connected to the same the two R a N atom may form a 4-7 membered nitrogen-containing heterocyclic group together with the N atom to which they are attached.
  • Specific examples include but are not limited to -NH 2 , -NHCH 3 , -NCH 3 CH 3 , -N(CH 2 CH 3 )CH 3 , -N(CH 2 CH 3 )(CH 2 CH 3 )-, -NHCF 3 , -N(CH 3 )CF 3 , -N(CF 3 )CF 3 , -N(CH 2 CF 3 )CF 3 or -N(CH 2 CF 3 )(CH 2 CF 3 )-, -NH( CH 2 CH 2 CH 3 ), azetidinyl, pyrrolidinyl, piperidinyl, etc.
  • R 5 and R 6 are each independently selected from C 1 -C 3 alkyl substituted by halogen. In a more specific embodiment, R 5 and R 6 are each independently selected from C 1 -C 3 alkyl substituted with at least three halogens. In a more specific embodiment, R 5 and R 6 are each independently C 1 -C 3 alkyl substituted with at least three F. Specific examples include, but are not limited to, trifluoromethyl, trifluoroethyl, pentafluoroethyl, and the like. In the most specific embodiment, both R 5 and R 6 are -CF 3 .
  • Preferred embodiments of the compounds of the present invention include the following compounds, their stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates,
  • the present invention provides a class of biaryl compounds with the structure of general formula (I). It has been found through research that this class of compounds can effectively inhibit the ROR ⁇ t protein receptor, thereby regulating the differentiation of Th17 cells and inhibiting the production of IL-17. As an immunomodulator for the treatment of diseases related to Th17 cell differentiation.
  • the invention provides compounds of the invention for use as drugs, especially as ROR ⁇ t inhibitors.
  • the present invention provides compounds of the present invention for the treatment, especially for the treatment and/or prevention of diseases related to ROR ⁇ t.
  • the present invention provides the present invention for treating and/or preventing ROR ⁇ t to promote the occurrence and development of the disease or inhibiting ROR ⁇ t will reduce the incidence of the disease, reduce or eliminate the disease symptoms of the disease.
  • Compounds, the diseases such as inflammation or autoimmune diseases, cancer, etc., including but not limited to psoriasis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, multiple sclerosis, systemic lupus erythematosus , Graft versus host disease, inflammatory bowel disease, Crohn’s disease, ulcerative colitis, chronic obstructive pulmonary disease, asthma, glomerulonephritis, lupus nephritis, myocarditis, thyroiditis, dry eye, uveitis, Behcet's disease, allergic dermatitis, acne, scleroderma, bronchitis, dermatomuscular allergic rhinitis, nec
  • the compound of the present invention can be formulated into a pharmaceutical composition according to standard pharmaceutical practice.
  • drugs with better pharmacokinetic properties and higher bioavailability can be prepared from the compound of the present invention.
  • the present invention provides a pharmaceutical composition comprising the above-mentioned compound of the present invention and a pharmaceutically acceptable excipient.
  • the pharmaceutical composition of the present invention is provided for use in the prevention or treatment of diseases related to ROR ⁇ t in mammals such as human subjects.
  • the pharmaceutical composition of the present invention may additionally contain additional therapeutically active ingredients suitable for use in combination with the compound of the present invention.
  • the additional therapeutic agent is as defined herein for the drug combination.
  • the pharmaceutical composition of the present invention can be formulated by techniques known to those skilled in the art, such as the technique disclosed in Remington's Pharmaceutical Sciences 20th Edition.
  • the above-mentioned pharmaceutical composition of the present invention can be prepared by mixing the compound of the present invention with one or more pharmaceutically acceptable excipients.
  • the preparation may further include the step of mixing one or more other active ingredients with the compound of the present invention and one or more pharmaceutically acceptable excipients.
  • excipients included in a particular composition will depend on various factors, such as the mode of administration and the form of the provided composition. Suitable pharmaceutically acceptable excipients are well known to those skilled in the art and are described in, for example, Ansel, Howard C., etc., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems.
  • Diluents such as glucose, lactose or mannitol
  • carriers pH adjusters, buffers, sweeteners, fillers, stabilizers, surfactants, wetting agents, lubricants, emulsifiers, suspending agents, preservatives Agents, antioxidants, sunscreens, glidants, processing aids, coloring agents, flavoring agents, flavoring agents, and other known additives.
  • the pharmaceutical composition of the present invention can be administered in a standard manner.
  • suitable modes of administration include oral, intravenous, rectal, parenteral, topical, transdermal, ocular, nasal, buccal, or pulmonary (inhalation) administration, where parenteral infusion includes intramuscular, intravenous, intraarterial, and peritoneal Intra or subcutaneous administration.
  • the compounds of the present invention can be formulated into tablets, capsules, syrups, powders, granules, aqueous or oily solutions or suspensions, (lipid) emulsions, dispersible powders, suppositories, etc., by methods known in the art. Ointments, creams, drops, aerosols, dry powder preparations and sterile injectable aqueous or oily solutions or suspensions.
  • the size of the preventive or therapeutic dose of the compound of the present invention will vary according to a series of factors, including the individual being treated, the severity of the disorder or condition, the rate of administration, the treatment of the compound, and the judgment of the prescribing physician.
  • the effective dose is about 0.0001 to about 5000 mg per kg body weight per day, for example, about 0.01 to about 1000 mg/kg/day (single or divided administration). For a 70 kg person, this would add up to about 0.007 mg/day to about 7000 mg/day, for example, about 0.7 mg/day to about 1500 mg/day.
  • the content or amount of the compound of the present invention in the pharmaceutical composition may be about 0.01 mg to about 1000 mg, suitably 0.1-500 mg, preferably 0.5-300 mg, more preferably 1-150 mg, particularly preferably 1-50 mg, For example, 1.5 mg, 2 mg, 4 mg, 10 mg, 25 mg, etc.; correspondingly, the pharmaceutical composition of the present invention will contain 0.05 to 99% w/w (weight percentage), such as 0.05 to 80% w/w, such as 0.10 to 70% w/w, for example 0.10 to 50% w/w of the compound of the invention, all weight percentages are based on the total composition. It should be understood that it may be necessary in some cases to use dosages that exceed these limits.
  • the present invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of the present invention and one or more pharmaceutically acceptable excipients, the composition being formulated for oral administration.
  • the composition may be provided in unit dosage form, for example in the form of a tablet, capsule or oral liquid preparation.
  • Such a unit dosage form may contain 0.1 mg to 1 g, for example 5 mg to 250 mg, of the compound of the present invention as an active ingredient.
  • the present invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of the present invention and one or more pharmaceutically acceptable excipients, the composition being formulated for topical administration.
  • Topical application may be in the form of, for example, a cream, lotion, ointment, or transdermal patch.
  • the present invention provides a pharmaceutical composition comprising a compound of the present invention and one or more pharmaceutically acceptable excipients, the composition being formulated for inhalation administration.
  • the inhalation administration can be by oral inhalation or intranasal administration.
  • the compound of the present invention can be effectively used in the present invention in a daily dose, for example, up to 500 ⁇ g, such as 0.1-50 ⁇ g, 0.1-40 ⁇ g, 0.1-30 ⁇ g, 0.1-20 ⁇ g, or 0.1-10 ⁇ g of the present invention Compound.
  • the pharmaceutical composition of the present invention for oral inhalation can be formulated as a dry powder, suspension (in liquid or gas) or solution (in liquid), and can be in any suitable form and using any suitable inhaler device known in the art Administration includes, for example, metered-dose inhalers (MDI), dry powder inhalers (DPI), nebulizers, and soft mist inhalers. Multi-chamber devices can be used to deliver the compounds of the specification and one or more other active ingredients (when present).
  • MDI metered-dose inhalers
  • DPI dry powder inhalers
  • nebulizers nebulizers
  • soft mist inhalers soft mist inhalers.
  • Multi-chamber devices can be used to deliver the compounds of the specification and one or more other active ingredients (when present).
  • the compounds of the present invention can be used in methods for treating various diseases in animals, especially mammals such as humans.
  • the present invention provides a method of modulating, especially inhibiting ROR ⁇ t activity, which method comprises contacting a cell with a compound of the present invention as described above to modulate, especially inhibiting, the activity of ROR ⁇ t in the cell.
  • the present invention provides a method for preventing or treating diseases related to ROR ⁇ t (for example, diseases treatable or preventable by ROR ⁇ t inhibition), the method comprising administering to an individual in need thereof an effective amount of the above-mentioned present
  • diseases related to ROR ⁇ t for example, diseases treatable or preventable by ROR ⁇ t inhibition
  • the present invention provides the use of the compound of the present invention or a pharmaceutical composition containing the same as described above, for inhibiting ROR ⁇ t activity, or for treating and/or preventing diseases related to ROR ⁇ t, for example, by inhibiting ROR ⁇ t Treatable or preventable diseases.
  • the present invention also provides the use of the compound of the present invention or the pharmaceutical composition containing it in the preparation of medicines, especially the use of medicines with ROR ⁇ t receptor inhibitor activity.
  • the present invention provides the use of the compound of the present invention as described above or a pharmaceutical composition containing the same in the preparation of a medicament for the treatment or prevention of diseases related to ROR ⁇ t, for example, diseases that can be treated or prevented by ROR ⁇ t inhibition , wherein the compound or pharmaceutical composition is optionally combined with one or more chemotherapy or immunotherapy.
  • the compound of the present invention can be administered as the sole active ingredient, or can be administered in combination with another drug or therapy.
  • the additional drugs or therapies may have or produce the same or different pharmacological effects, provided that when used in combination with the compounds of the present invention, they do not cause undesirable activity reduction, adverse interactions, or side effects.
  • the present invention provides a drug combination comprising the compound of the present invention as described above and one or more other drugs or therapies that function through the same or different mechanisms of action, or a combination of both.
  • the drug combination is used to inhibit ROR ⁇ t activity, or to treat and/or prevent diseases related to ROR ⁇ t.
  • the compound of the present invention in the pharmaceutical combination of the present invention and other active agents used in the combination can be administered simultaneously, separately or sequentially through the same or different administration routes.
  • the other active agent may be co-administered with the compound of the present invention in a single pharmaceutical composition, or administered separately from the compound of the present invention in separate discrete units, such as a combination product, preferably in the form of a kit.
  • they are administered separately they can be carried out simultaneously or sequentially, and the successive administrations can be close or distant in time.
  • the compound of the present invention and the additional drug can be (i) before sending the combined product to the physician (for example, in the case of a kit containing the compound of the present invention and the additional drug); (ii) immediately before administration The physician himself (or under the guidance of the physician); (iii) the patient himself, for example, during the sequential administration of the compound of the present invention and another drug, are added to the combination therapy together.
  • the present invention also provides a kit comprising two or more separate pharmaceutical compositions, at least one of which contains the compound of the present invention, and the rest contains other active agents used in combination, And a device containing the composition respectively.
  • the kit of the present invention is particularly suitable for administering different dosage forms, such as oral dosage forms and parenteral dosage forms, or for administering different compositions at different dosage intervals.
  • the appropriate dosage of the compound of the present invention and other active agents in the combination can usually be determined by those skilled in the art, for example, from the dosage range of the compound described in this specification and the approved or published dosage range of other active compounds.
  • the doses of other co-administered drugs will of course vary according to factors such as the type of co-administered drugs, the specific drugs used, the disease to be treated, the patient's general health status, and the judgment of the physician or veterinarian.
  • the other active agent may be one or more second or additional (e.g. Three) compounds.
  • these active agents may be compounds known to modulate other biologically active pathways, or may be compounds that modulate different components in the biologically active pathways involved in the compounds of the present invention, or even biologically related to the compounds of the present invention. Compounds with overlapping targets.
  • the present invention provides a drug combination, for example as a drug for the treatment of one of the diseases listed herein, such as psoriasis, COPD, asthma, psoriatic arthritis or compulsive spine Inflammation, which contains the compound of the present invention, and at least one active ingredient selected from:
  • Glucocorticoid receptor agonists (steroidal or non-steroidal);
  • PDE4 Phosphodiesterase-4
  • the compounds of the present invention can also be combined with other therapies, including but not limited to surgery, radiation therapy, transplantation (for example, stem cell transplantation, bone marrow transplantation), tumor immunotherapy and the like.
  • other therapies including but not limited to surgery, radiation therapy, transplantation (for example, stem cell transplantation, bone marrow transplantation), tumor immunotherapy and the like.
  • the present invention provides a method for inhibiting ROR ⁇ t activity or for treating and/or preventing diseases related to ROR ⁇ t, including administering the pharmaceutical combination of the present invention to a subject in need.
  • the present invention also provides the use of the pharmaceutical combination of the present invention in the preparation of drugs for inhibiting ROR ⁇ t activity or for treating and/or preventing diseases related to ROR ⁇ t.
  • diseases related to ROR ⁇ t include inflammation or autoimmune diseases, cancer, etc., including but not limited to silver.
  • Preferred diseases associated with ROR ⁇ t are selected from the group consisting of psoriasis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, multiple sclerosis, inflammatory bowel disease, dry eye, allergic dermatitis, chronic Obstructive pulmonary disease (COPD), asthma, necrotizing enterocolitis, liver fibrosis, non-alcoholic steatohepatitis (NASH), new coronavirus pneumonia, triple negative breast cancer and prostate cancer.
  • COPD chronic Obstructive pulmonary disease
  • NASH non-alcoholic steatohepatitis
  • compositions, methods, uses, and pharmaceutical combinations of the present invention the preferred compounds of formula (I), their stereoisomers, tautomers, stable isotopic variants, Pharmaceutically acceptable salts or solvates; more preferred are the specific compounds listed above, such as compounds 1-13, or their pharmaceutically acceptable salts or solvates.
  • the administered dose of a compound or drug is described herein, it should be understood that the dose is based on the weight of the free base and does not include any derived components thereof, unless the instructions indicate otherwise.
  • the present invention also provides a method for preparing the compound of formula (I).
  • the following exemplifies a general synthetic scheme for synthesizing the compound of the present invention.
  • appropriate reaction conditions are known to those skilled in the art or can be routinely determined.
  • the raw materials and reagents used in the preparation of these compounds are generally commercially available, or can be prepared by the following methods, methods similar to those given below, or methods known in the art.
  • the raw materials and intermediates in the synthesis reaction process can be separated and purified using conventional techniques, including but not limited to filtration, distillation, crystallization, chromatography and the like.
  • the material can be characterized by conventional methods including physical constants and spectral data.
  • the method includes the following steps:
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , m and p are as defined above for general formula (I);
  • Prot is an amino protecting group, including but not limited to Boc, Cbz, Fmoc or PMB , Preferably Boc;
  • Step 1 The compound of formula (I-1) generates the compound of formula (I-2) in free or salt form; this reaction is preferably carried out under the action of hydrobromic acid (for example, 40% hydrobromic acid in water), preferably at a suitable temperature Carry out, for example, 50-200°C, 80-150°C, preferably 90-120°C; the salt form is, for example, the hydrobromide salt form;
  • hydrobromic acid for example, 40% hydrobromic acid in water
  • Step 2 The compound of formula (I-2) in free or salt form is cyclized with the compound of formula (I-3) to form the compound of formula (I-4) in free or salt form; this reaction is preferably carried out in a suitable solvent, and It is preferably carried out at a suitable temperature, the solvent can be selected from, for example, protic solvents, such as methanol, ethanol, propanol, etc., and the temperature is selected from, for example, 50-200°C, 80-150°C, preferably 90-120°C; Salt form such as hydrobromide salt form;
  • Step 3 The compound of formula (I-4) in free or salt form and the amino protecting agent to produce the compound of formula (I-5); wherein the amino protecting agent is well known in the art, including but not limited to di-tert-butyl dicarbonate (( Boc) 2 O), CbzCl, FmocCl or PMB-Cl, the reaction is preferably carried out in a suitable organic solvent, the organic solvent may be selected from tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, dichloromethane, 1,4-dioxane, dimethylsulfoxide and any combination thereof, preferably Tetrahydrofuran; the reaction is preferably carried out in the presence of a suitable base, the base may be selected from sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethy
  • Step 4 The compound of formula (I-5) reacts with the Tf reagent to produce the compound of formula (I-6);
  • the Tf reagent is a reagent that can react with a hydroxyl group to generate an OTf group, including but not limited to trifluoromethanesulfonic anhydride, trifluoromethanesulfonic anhydride, Fluoromethanesulfonyl chloride or N-phenylbis(trifluoromethanesulfonyl)imide;
  • the reaction is preferably carried out in the presence of a base, and the base can be selected from sodium carbonate, potassium carbonate, cesium carbonate, N,N- Diisopropylethylamine, triethylamine, HOBt or pyridine;
  • the reaction is preferably carried out in an organic solvent, the organic solvent may be selected from dichloromethane, tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl
  • Step 5 The compound of formula (I-6) and the compound of formula (I-7) are coupled under the action of a catalyst, such as a palladium catalyst, to obtain a compound of formula (I-8);
  • a catalyst such as a palladium catalyst
  • the palladium catalyst is a well-known palladium catalyst for coupling in the art, including but not limited to Pd 2 (dba) 3, etc.; the reaction is preferably carried out in a suitable organic solvent, and the organic solvent may be selected from tetrahydrofuran , Ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N,N dimethylacetamide, dichloromethane, 1,4-bis Oxane, dimethyl sulfoxide and any combination thereof, preferably 1,4-dioxane; the reaction is preferably carried out in the presence of a phosphine ligand, the phosphine ligand including but not limited to 4,5-bis Diphenylphosphine-9,9-dimethylxanthene; the reaction is preferably carried out in the presence of a suitable base, which can be selected from sodium carbonate, potassium carbonate, cesium carbon
  • Step 6 The compound of formula (I-8) generates the compound of formula (I-9) under the action of an oxidizing agent;
  • the oxidizing agent is selected from, for example, H 2 O 2 , mCPBA and peroxyacetic acid;
  • the reaction is preferably carried out in an organic solvent
  • the organic solvent can be selected from dichloromethane, tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N,N-di Methyl acetamide, 1,4-dioxane, dimethyl sulfoxide and any combination thereof, preferably dichloromethane;
  • the reaction is preferably carried out at a suitable temperature, for example -50°C to 200°C, -20 °C to 100 °C, for example -10 °C to 50 °C, for example -10 °C to 10 °C, preferably in an
  • Step 7 The compound of formula (I-9) is hydrolyzed to produce the compound of formula (I-10); the reaction is preferably carried out in the presence of a base, and the base can be selected from sodium hydroxide, potassium hydroxide, sodium carbonate, and potassium carbonate Or cesium carbonate, the base is preferably used in the form of an aqueous solution; the reaction is preferably carried out in an organic solvent, the organic solvent can be selected from alcohol solvents such as (methanol, ethanol or propanol), tetrahydrofuran, ethers (such as diethyl ether, Ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, 1,4-dioxane, dimethylsulfoxide and Any combination thereof, preferably methanol; the reaction is preferably carried out at a suitable temperature, such as -20°C to -200°C, 5-100°C, 10-50°C,
  • Step 8 The compound of formula (I-10) reacts with the compound of formula (I-11) under the action of a condensing agent to produce a compound of formula (I-12);
  • the condensing agent is a condensing agent for coupling carboxylic acid and amine well known in the art, including but not limited to 1-propyl phosphoric anhydride (T3P), EDC, DCC, HATU, etc.; the reaction is preferably in a suitable In an organic solvent, the organic solvent can be selected from dichloromethane, tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N , N-dimethylacetamide, 1,4-dioxane, dimethylsulfoxide and any combination thereof, preferably dichloromethane; the reaction is preferably carried out in the presence of a suitable base, and the base includes But not limited to sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, triethylamine, HOBt or pyridine,
  • Step 9 The amino protecting group of the compound of formula (I-12) is removed to produce the compound of formula (I-13); the reaction is carried out under the action of an acid (such as TFA or HCl), and the reaction is preferably carried out in a suitable organic In a solvent, the organic solvent can be selected from dichloromethane, tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N, N-dimethylacetamide, 1,4-dioxane, dimethylsulfoxide and any combination thereof, preferably dichloromethane; the reaction is preferably carried out at a suitable temperature, for example -50°C to 200°C , -20°C to 100°C, such as -10°C to 50°C, such as -10°C to 20°C; Step 10: Formula (I-13) compound and formula (I-14) or its activated form (such as the corresponding
  • the method includes the following steps:
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , m and p are as defined above for general formula (I);
  • Prot is an amino protecting group, including but not limited to Boc, Cbz, Fmoc or PMB , Preferably Boc;
  • Step 1 The compound of formula (II-1) is reacted with R 4 SH or its salt (such as sodium salt) to produce the compound of formula (II-2); the reaction is preferably carried out under an inert gas atmosphere, and the inert gas includes but not Limited to nitrogen, argon or helium, etc.;
  • Step 2 The compound of formula (II-2) is reacted with an amino protecting agent to produce a compound of formula (II-3); wherein the amino protecting agent is well known in the art, including but not limited to di-tert-butyl dicarbonate ((Boc) 2 O ), CbzCl, FmocCl or PMB-Cl; the reaction is preferably carried out in the presence of a suitable base, and the base can be selected from sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, three Ethylamine, HOBt, pyridine or 4-dimethylaminopyridine;
  • the amino protecting agent is well known in the art, including but not limited to di-tert-butyl dicarbonate ((Boc) 2 O ), CbzCl, FmocCl or PMB-Cl; the reaction is preferably carried out in the presence of a suitable base, and the base can be selected from sodium carbonate, potassium carbon
  • Step 3 The compound of formula (II-3) is oxidized to produce the compound of formula (II-4) under the action of an oxidizing agent;
  • the oxidizing agent is selected from, for example, H 2 O 2 , mCPBA and peroxyacetic acid;
  • Step 4 The compound of formula (II-4) is reduced under the action of a reducing agent to produce a compound of formula (II-5);
  • the reducing agent is, for example, selected from DABAL-H, lithium aluminum tetrahydrogen or sodium borohydride;
  • the reaction is preferably It is carried out under an inert gas atmosphere, and the inert gas includes but is not limited to nitrogen, argon or helium, etc.;
  • Step 5 The compound of formula (II-5) is reacted with methanol or its activated form (such as sodium methoxide) to produce the compound of formula (II-6); the reaction is preferably carried out in the presence of 4-methylbenzenesulfonic acid pyridine (PPTS) ;
  • PPTS 4-methylbenzenesulfonic acid pyridine
  • Step 6 The compound of formula (II-6) is reacted with alkyl cyanosilane (such as TMSCN) to produce the compound of formula (II-7); the reaction is preferably carried out in the presence of boron trifluoride ether; the reaction is preferably in an inert gas In an atmosphere, the inert gas includes, but is not limited to, nitrogen, argon, or helium, etc.;
  • Step 7 The amino protecting group of the compound of formula (II-7) is removed to produce the compound of formula (II-8); the reaction is carried out, for example, under the action of an acid (such as TFA or HCl);
  • Step 8 The compound of formula (II-8) is reacted with R 3 COOH or its activated form such as the corresponding acid chloride or acid anhydride to produce the compound of formula (II-9); the reaction is preferably carried out in the presence of a base, and the base may be optional From sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, triethylamine, HOBt or pyridine; the reaction can be carried out in the presence of a condensing agent such as the like, wherein the condensing agent is in the art Well-known condensing agents for the coupling of carboxylic acids and amines, including but not limited to 1-propyl phosphoric anhydride (T3P), EDC, DCC, HATU;
  • Step 9 The compound of formula (II-9) is hydrolyzed to produce the compound of formula (II-10); the reaction is preferably carried out in the presence of a base, and the base can be selected from sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate Or cesium carbonate;
  • Step 10 The compound of formula (II-10) reacts with the compound of formula (I-11) under the action of a condensing agent to produce the target compound of formula (I-b);
  • the condensing agent is a condensing agent for coupling carboxylic acid and amine well known in the art, including but not limited to T3P, EDC, DCC, HATU or N,N,N',N'-tetramethylchloroformamidine Hexafluorophosphate, etc.; the reaction is preferably carried out in the presence of a suitable base, including but not limited to sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, triethylamine, N-methylimidazole, HOBt or pyridine;
  • a suitable base including but not limited to sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, triethylamine, N-methylimidazole, HOBt or pyridine;
  • the reaction in the above steps is preferably carried out in an organic solvent
  • the organic solvent can be selected from alcohol solvents such as (methanol, ethanol or propanol), tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N- Methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, 1,4-dioxane, dichloromethane, dimethylsulfoxide and any combination thereof; for hydrolysis reaction A mixture of organic solvent and water can be used;
  • alcohol solvents such as (methanol, ethanol or propanol)
  • ethers such as diethyl ether, ethylene glycol monomethyl ether, etc.
  • N- Methylpyrrolidone N,N-dimethylformamide, N,N-dimethylacetamide, 1,4-dioxane, dichloromethane, dimethylsulfoxide and any combination thereof
  • the reaction in the above steps is preferably carried out at a suitable temperature, such as -100°C to 0°C, -80°C to -20°C, -50°C to 200°C, -20°C to 100°C, -20°C to 20°C, -10°C to 20°C, -10°C to 50°C, 0-200°C, 10-100°C, 20-50°C or room temperature (20-25°C).
  • a suitable temperature such as -100°C to 0°C, -80°C to -20°C, -50°C to 200°C, -20°C to 100°C, -20°C to 20°C, -10°C to 20°C, -10°C to 50°C, 0-200°C, 10-100°C, 20-50°C or room temperature (20-25°C).
  • the above synthesis scheme only lists the preparation methods of some of the compounds of the present invention.
  • the compound of the present invention or its stereoisomers, tautomers, stable isotope derivatives, pharmaceutically acceptable salts or solvates can be passed through a variety of methods, including the methods and examples given above
  • the given method or a similar method is prepared by a person of ordinary skill in the art on the basis of the above-mentioned synthesis scheme and combined with conventional techniques in the field.
  • experimental materials and reagents used in the following examples can be obtained from commercial channels, prepared according to the method of the prior art, or prepared according to a method similar to that disclosed in the present application unless otherwise specified.
  • PdCl 2 (dtbpf) 1,1'-Di-tert-butylphosphinoferrocene palladium dichloride
  • xantphos 4,5-bisdiphenylphosphine-9,9-dimethylxanthene
  • HATU 2-(7-Azobenzotriazole)-N,N,N’,N’,-Tetramethylurea hexafluorophosphate
  • PE Petroleum ether
  • column chromatography uses silica gel (300-400 mesh) produced by Rushan Sun Desiccant Co., Ltd.; thin layer chromatography uses GF254 (0.25 mm); nuclear magnetic resonance chromatography (NMR) uses Varian- 400 NMR measurement; liquid-mass spectrometry (LC/MS) uses Agilent TechnologiESI 6120 liquid-mass spectrometry.
  • Example 1 and Example 2 R-2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl )-[1,1'-Biphenyl]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide or S-2-acetyl-N-(2'-fluoro- 4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1,1'-biphenyl]-4-yl)-5-(methylsulfon Acyl) isoindoline-1-carboxamide
  • Step 2 Synthesis of ((2-(4-bromo-3-fluorophenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)trimethylsilane
  • Step 2 Synthesis of tert-butyl 5-(methylthio)-1-oxoisoindoline-2-carboxylate
  • Step 3 Synthesis of tert-butyl 5-(methylsulfonyl)-1-oxoisoindoline-2-carboxylate
  • Step 4 Synthesis of tert-butyl 1-hydroxy-5-(methylsulfonyl)isoindoline-2-carboxylate
  • Step 5 Synthesis of tert-butyl 1-methoxy-5-(methylsulfonyl)isoindoline-2-carboxylate
  • Step 6 Synthesis of tert-butyl 1-cyano-5-(methylsulfonyl)isoindoline-2-carboxylate
  • Step 7 Synthesis of methyl 5-methylsulfonylisoindoline-1-carboxylate hydrochloride
  • Step 8 Synthesis of methyl 2-acetyl-5-(methylsulfonyl)isoindoline-1-carboxylate
  • Step 10 Compound 2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1,1 Synthesis of'-Biphenyl]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide
  • Step 11 R-2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1, 1'-Biphenyl)-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide or S-2-acetyl-N-(2'-fluoro-4'-(1 ,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)-5-(methylsulfonyl)isoindole Synthesis of morpholin-1-carboxamide
  • Racemate 2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1,1 '-Biphenyl]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide (1.29g dissolved in about 250mL methanol, injection volume 8.0mL) was tested by Waters SFC 150 (room temperature, 100bar,214nm) and 250*25mm 10 ⁇ m (Supercritical carbon dioxide: methanol, 45:55, 3.0min, 70mL/min) separation to obtain R-2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3, 3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide or S- 2-Acetyl-N-(2
  • Step 2 Synthesis of ethyl 6-hydroxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylate hydrobromide
  • Step 3 Synthesis of 6-hydroxy-3,4-dihydroisoquinoline-1,2(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
  • Step 4 6-(((Trifluoromethyl)sulfonyl)oxy)-3,4-dihydroisoquinoline-1,2(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester Synthesis
  • Step 5 Synthesis of 6-(methylthio)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
  • Step 6 Synthesis of 6-(methylsulfonyl)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
  • Step 7 Synthesis of 2-(tert-butoxycarbonyl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid
  • Step 2 Synthesis of 2-(4'-amino-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3-hexafluoropropane-2-ol
  • Step 1 1-((4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl) Synthesis of tert-butyl carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
  • reaction mixture was stirred overnight at room temperature, and the reaction was complete as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with DCM (15mLx2), the organic phases were combined, and washed with saturated ammonium chloride (20mL), saturated sodium bicarbonate (20mL) and saturated brine (20mL) successively, and It was dried with sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to obtain the target compound (90.0 mg, crude product, brown oil).
  • LC-MS(ESI) m/z: 673.1 [M+H] + .
  • Step 2 N-(4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)- Synthesis of 6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
  • Step 3 2-Acetyl-N-(4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • LC-MS monitored the reaction to be complete.
  • the reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product.
  • Step 1 1-((2'-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl] Synthesis of -4-yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
  • Step 2 N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
  • Step 3 2-Acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1' -Biphenyl]-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (100 mg, 0.169 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, DIEA (0.084 mL, 0.508 mmol) and acetyl chloride (0.030 mL, 0.423 mmol) were sequentially added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted for 30 minutes at room temperature.
  • LC-MS monitored the reaction to be complete.
  • the reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product.
  • Example 5 and Example 6 R-2-acetyl-N-(2'-fluoro-4'-(1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)- [1,1'-Biphenyl]-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide or S-2-acetyl- N-(2'-Fluoro-4'-(1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)- 6-(Methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • Example 7 2-Acetyl-6-(ethylsulfonyl)-N-(2'-fluoro-4'-(1,1,1,3,3,3,3-hexafluoro-2-hydroxyl) Propan-2-yl)-[1,1'-biphenyl]-4-yl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • Step 1 Synthesis of 6-(ethylthio)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
  • Step 2 Synthesis of 6-(ethylsulfonyl)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
  • Step 3 Synthesis of 2-(tert-butoxycarbonyl)-6-(ethylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid
  • Step 4 6-(Ethylsulfonyl)-1-((2'-fluoro-4'-(1,1,1,3,3,3,3-hexafluoro-2-hydroxypropan-2-yl )-[1,1'-Biphenyl]-4-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
  • reaction mixture was stirred overnight at room temperature, and the reaction was complete as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with DCM (15mL ⁇ 2), the organic phases were combined, and washed with saturated ammonium chloride (20mL), saturated sodium bicarbonate (20mL) and saturated brine (20mL) in turn, It was dried with sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to obtain the target compound (100 mg, crude product, brown oil).
  • Step 5 6-(Ethylsulfonyl)-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[ Synthesis of 1,1'-biphenyl]-4-yl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
  • Step 6 2-Acetyl-6-(ethylsulfonyl)-N-(2'-fluoro-4'-(1,1,1,3,3,3,3-hexafluoro-2-hydroxypropane) -2-yl)-[1,1'-biphenyl]-4-yl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • LC-MS monitored the reaction to be complete.
  • the reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product.
  • Example 8 2-Acetyl-N-(4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropyl-2-yl)-[1,1'-biphenyl ]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide
  • Step 1 1,1,1,3,3,3-hexafluoro-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane- Synthesis of 2-yl)phenyl)propan-2-ol
  • Step 3 1-((2-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
  • reaction mixture was stirred at room temperature for 2 hours, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with DCM (15mL ⁇ 2), the organic phases were combined, washed with saturated sodium bicarbonate (20mL) and saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, The filtrate was concentrated under reduced pressure to obtain the target compound (80.0 mg, crude product, brown liquid).
  • LC-MS(ESI) m/z: 689.1 [MH] - .
  • Step 4 N-(2-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4 -Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
  • Step 5 2-Acetyl-N-(2-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'- Synthesis of biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • N-(2-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl )-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (70.0 mg, 0.119 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.049 mL, 0.356 mmol) and acetyl chloride (0.021 mL, 0.296 mmol) were sequentially added dropwise to the reaction solution.
  • reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product.
  • Example 10 2-Acetyl-N-(2-chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1' -Biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • Step 1 2-(4'-Amino-2'-chloro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3,3-hexafluoropropane-2 -Synthesis of alcohol
  • Step 2 1-((2-Chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
  • reaction mixture was stirred at room temperature for 2 hours, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with DCM (15mLx2), the organic phases were combined, washed with saturated sodium bicarbonate (20mL) and saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, and filtered The filtrate was concentrated under reduced pressure to obtain the target compound (150 mg, crude product, brown oil).
  • Step 3 N-(2-Chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4 -Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
  • Step 4 2-Acetyl-N-(2-chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'- Synthesis of biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • N-(2-chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl )-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (140 mg, 0.231 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.096 mL, 0.692 mmol) and acetyl chloride (0.041 mL, 0.577 mmol) were sequentially added dropwise to the reaction solution.
  • reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product.
  • Example 11 N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl] -4-yl)-6-(methylsulfonyl)-2-propionyl-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • Step 1 1-((2'-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl] Synthesis of -4-yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
  • reaction mixture was stirred at room temperature for 2 hours, and TLC monitored the reaction to be complete.
  • the reaction solution was poured into water (20mL), extracted with DCM (15mLx2), the organic phases were combined, washed with saturated sodium bicarbonate (20mL) and saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, The filtrate was concentrated under reduced pressure to obtain the target compound (1.00 g, crude product, light brown solid).
  • Step 2 N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
  • Step 3 N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)-6-(methylsulfonyl)-2-propionyl-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (100 mg, 0.169 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.071 mL, 0.508 mmol) and propionyl chloride (0.037 mL, 0.423 mmol) were sequentially added dropwise to the reaction solution.
  • reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product.
  • Example 12 2-(Cyclopropanecarbonyl)-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[ 1,1'-Biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
  • N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (100 mg, 0.169 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.071 mL, 0.508 mmol) and cyclopropylformyl chloride (0.0385 mL, 0.423 mmol) were sequentially added dropwise to the reaction solution.
  • reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product.
  • Example 13 N 1 -(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl ]-4-yl)-N 2 -methyl-6-(methylsulfonyl)-3,4-dihydroisoquinoline-1,2(1H)-dimethylamide
  • N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (100 mg, 0.169 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.071 mL, 0.508 mmol) and methylcarbamoyl chloride (39.6 mg, 0.423 mmol) were sequentially added to the reaction solution.
  • reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS.
  • the ROR ⁇ -LBD coding sequence was inserted into the pBIND plasmid (Promega, E1581).
  • the expression vector and the reporter vector (pGL4.35 carrying the luciferase reporter gene driven by the stably integrated GAL4 promoter) are co-expressed in HEK293T host cells.
  • the inhibitor binds to the corresponding chimeric receptor
  • the chimeric receptor binds to the GAL4 binding site on the reporter gene carrier and inhibits reporter gene expression. According to the strength of the chemiluminescence signal, the inhibitory activity of the compound on ROR ⁇ was judged.
  • test compounds were diluted with DMSO in a 3-fold gradient, 10 dilution gradients, and the starting concentration was 10 mM.
  • the positive control AZD-0284 was diluted with DMSO in a 3-fold gradient, 10 dilution gradients, and the initial concentration was 10mM.
  • step 2.2 Inoculate the cells (see step 2.2) into a 384 cell culture plate (6007680-50, PE), 15,000 cells per well, 25 ⁇ l FBS medium containing 5% carbon adsorption;
  • Example IC 50 (nM) Emax% 1 15.46 101.5 3 106 97.07 4 34.56 100.2 5 15.84 99.5 7 76.3 97.32 8 24.98 98.29 9 185.9 99.26 10 22.54 101.1 11 76.33 101.6 12 144.6 103.5 13 697.8 96.87 AZD-0284 34.81 99.79
  • Emax% is the relative maximum inhibition rate relative to AZD-0284 at 10 ⁇ M.
  • Activity Example 2 The compound inhibits the differentiation of human PBMC Th17 cells
  • mice first resuscitate PBMC cells and plate them, and then stimulate PBMC cells with stimulating factors (anti-hCD28: 5 ⁇ g/mL; rhTGF- ⁇ 1: 5ng/mL; rhIL-6: 20ng/mL; rhIL-23: 10ng/Ml)
  • stimulating factors anti-hCD28: 5 ⁇ g/mL
  • rhTGF- ⁇ 1 5ng/mL
  • rhIL-6 20ng/mL
  • rhIL-23 10ng/Ml
  • the maximum concentration starts from 3 ⁇ M.
  • the supernatant is collected for IL-17 ELISA.
  • the inhibitory rate of the compound to inhibit the secretion of IL-17 from Th17 cells is determined by Graphad8.0 Fit the IC 50 value.
  • the assay results show that the compound of the present invention has a better ability to inhibit the differentiation and secretion of IL-17 from Th17 cells to human PBMC (as shown in Table 2).
  • Emax% is the maximum inhibition rate.
  • the incubation system contains 0.5 mg protein/mL microsomes, cofactors, and PBS, pre-incubated at 37°C for 3 minutes, and the substrate (ie, test compound) is added to initiate the reaction. Samples were taken at 0, 1, 5, 10, 15, 20, 30, 60 min at the beginning of the reaction, and appropriate terminator was added to terminate the reaction.
  • Sample processing add appropriate samples to each, vortex and centrifuge at high speed, take the supernatant, and use HPLC-MS/MS to detect the substrate.
  • the peak area at the time of 0 min is regarded as 100%.
  • the results are shown in Table 3.
  • the PK determination method of each compound is as follows: 6 C57BL/6 mice (from Shanghai Lingchang Biotechnology Co., Ltd.) were divided into two groups, 3 mice in each group. One group was administered intravenously (IV) with a dose of 1 mg/kg and the vehicle was 5% DMSO/95% (20% Captisol); one group was administered by oral (PO) intragastric administration with a dose of 5 mg/kg and the vehicle It is 0.5% CMC-Na/0.5% Tween 80. Blood was collected from the saphenous vein of the calf in each group at 0, 0.083, 0.25, 0.5, 1, 2, 4, 6, 8, and 24 hours after administration. Collect about 40 ⁇ L of blood into an anticoagulation tube containing EDTA-K2.
  • the blood collected at each time point was centrifuged at 4°C and 8000 rpm for 5 minutes to obtain plasma.
  • Another 1.5 mL centrifuge tube is labeled with the compound name, animal number, and time point, and the plasma is transferred to the tube.
  • the plasma was stored at -80°C until analysis.
  • the UPLC-MS/MS method was used to determine the concentration of the compound in the plasma, and the Phoenix WinNolin 6.4 pharmacokinetic software was used to calculate the pharmacokinetic parameters of the obtained data.
  • the specific experimental results are as follows, and the results show that the compound has better pharmacokinetic absorption and has pharmacokinetic advantages.
  • the AUC 0-last (ng/mL*hr) and bioavailability of the compound of the present invention are significantly improved, showing that it has better druggability

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Abstract

The present invention relates to a compound of formula (I), and a stereisomer, a tautomer, a stable isotopic variant, a pharmaceutically acceptable salt or a solvate thereof, a pharmaceutical composition comprising the compound, a method for treating or preventing RORγt-related diseases by using the compound, and use of the compound in the preparation of drugs for treating or preventing the RORγt-related diseases.

Description

可用作RORγ调节剂的联芳基类化合物Biaryl compounds that can be used as RORγ regulators
交叉引用cross reference
本申请要求2020年5月15日递交的中国专利申请202010411934.X的优先权。This application claims the priority of the Chinese patent application 202010411934.X filed on May 15, 2020.
技术领域Technical field
本发明属于化学医药技术领域，具体涉及具有RORγt抑制活性的联芳基类化合物、包含所述化合物的药物组合物、制备所述化合物的方法，以及所述化合物在制备用于预防或治疗与RORγt有关的疾病的药物中的用途。The present invention belongs to the technical field of chemical medicine, and specifically relates to biaryl compounds with RORγt inhibitory activity, pharmaceutical compositions containing the compounds, methods for preparing the compounds, and preparation of the compounds for prevention or treatment and RORγt Use in medicine for related diseases.
背景技术Background technique
视黄酸受体相关孤儿受体(retinoic acid recetor-related orphan receptors，RORs)，又称为NF1R，属于配体依赖的转录因子核受体超家族的一个亚家族。RORs亚家族主要包括RORα、RORβ和RORγ这三个亚型。RORγ含有两个成员：RORγ1(也称RORγ)和RORγ2(也称作RORγt)，其中RORγ1分布于骨骼肌、胸腺、睾丸、胰腺、前列腺、心脏和肝脏等处，而RORγt仅表达于某些免疫细胞中。Retinoic acid receptor-related orphan receptors (RORs), also known as NF1R, belong to a subfamily of the nuclear receptor superfamily of ligand-dependent transcription factors. The RORs subfamily mainly includes three subtypes: RORα, RORβ and RORγ. RORγ contains two members: RORγ1 (also called RORγ) and RORγ2 (also called RORγt). Among them, RORγ1 is distributed in skeletal muscle, thymus, testis, pancreas, prostate, heart and liver, etc., while RORγt is only expressed in certain immune systems. In the cell.
Littman等人最早报道RORγt对于初始CD4+T细胞分化成Th17细胞是必需的(Cell,2006126,1121–1133)。经抗原刺激的Thp细胞向Th17细胞分化过程中，在IL-6、IL-21和TGF-β等细胞因子作用下诱导表达RORγt。从RORγt缺失小鼠中分离出来的Thp细胞，向Th17细胞株分化的能力明显降低。这些都表明RORγt是促进Th17细胞分化的关键调节因子。Littman et al. first reported that RORγt is necessary for the differentiation of initial CD4+ T cells into Th17 cells (Cell, 2006126, 1121–1133). During the differentiation of Thp cells stimulated by antigens into Th17 cells, the expression of RORγt is induced under the action of cytokines such as IL-6, IL-21 and TGF-β. Thp cells isolated from RORγt-deficient mice have a significantly reduced ability to differentiate into Th17 cell lines. All these indicate that RORγt is a key regulator of Th17 cell differentiation.
Th17细胞是辅助性T细胞的一种，会产生IL-17及其他促炎性细胞因子。Th17细胞在许多小鼠自身免疫性疾病模型中均发挥了关键的作用，如实验性变态反应性脑脊髓炎(EAE)和胶原诱导性关节炎(CIA)动物模型。此外，在一些人类自身免疫性疾病包括类风湿性关节炎(RA)、多发性硬化(MS)、银屑病(Psoriasis)和炎症性肠病(IBD)中，均能检测到IL-17水平的提高。自身免疫性疾病患者的组织和外周血液样本中所发现的Th17细胞数量均增多。因此，Th17细胞或其产生的细胞因子IL-17与炎症及自身免疫性疾病的发病机制存在紧密联系。Th17 cells are a type of helper T cells that produce IL-17 and other pro-inflammatory cytokines. Th17 cells play a key role in many mouse autoimmune disease models, such as experimental allergic encephalomyelitis (EAE) and collagen-induced arthritis (CIA) animal models. In addition, IL-17 levels can be detected in some human autoimmune diseases including rheumatoid arthritis (RA), multiple sclerosis (MS), psoriasis (Psoriasis) and inflammatory bowel disease (IBD) The improvement. The number of Th17 cells found in tissues and peripheral blood samples of patients with autoimmune diseases increased. Therefore, Th17 cells or the cytokine IL-17 produced by Th17 cells are closely related to the pathogenesis of inflammation and autoimmune diseases.
2015年1月，由诺华公司开发的通过特异性阻断IL-17治疗银屑病的单克隆抗体Cosentyx(Secukinumab/AIN457)，已获FDA批准上市，这是治疗银屑病类药物市场中首个作用于IL-17的药物。随后，靶向促炎性细胞因子IL-17A的单克隆抗体ixekizumab，被批准应用于适应症银屑病、银屑病关节炎。这些单克隆抗体临床上的成功，证明了IL-17信号通路在炎性与自身免疫性疾病中的重要性，并且展示了通过RORγt抑制剂影响IL-17信号通路而治疗炎性与自身免疫性疾病的潜在可能性。In January 2015, Cosentyx (Secukinumab/AIN457), a monoclonal antibody developed by Novartis to specifically block IL-17 to treat psoriasis, has been approved by the FDA for marketing. This is the first drug in the psoriasis treatment market. A drug that acts on IL-17. Subsequently, the monoclonal antibody ixekizumab, which targets the pro-inflammatory cytokine IL-17A, was approved for indications of psoriasis and psoriatic arthritis. The clinical success of these monoclonal antibodies proves the importance of the IL-17 signaling pathway in inflammatory and autoimmune diseases, and demonstrates that RORγt inhibitors can affect the IL-17 signaling pathway to treat inflammatory and autoimmune diseases. The potential for disease.
因此，RORγt可作为治疗自身免疫性疾病药物的新靶点，寻找RORγt小分子抑制剂并将其用于RORγt介导的疾病、例如炎症和自身免疫性疾病的治疗将具有重要意义。Therefore, RORγt can be used as a new target of drugs for the treatment of autoimmune diseases. It will be of great significance to find RORγt small molecule inhibitors and use them in the treatment of RORγt-mediated diseases, such as inflammation and autoimmune diseases.
至今为止，共有4个RORγt抑制剂的小分子化合物在临床2期，7个RORγt抑制剂的小 分子在临床1期，还没有化合物进入临床3期。因此，仍然非常需要发现和开发新的RORγt抑制剂化合物以用于预防和/或治疗与RORγt有关的疾病，例如炎症和自身免疫性疾病。这样的化合物除了应具有令人满意的RORγt抑制活性外，还期望基于结构的优化而具备对ROR亚型具有高选择性和良好的、甚至改进的成药性，以便为相关疾病患者提供更多用药选择的同时还能提供更好的治疗效果。So far, there are a total of 4 small molecule compounds of RORγt inhibitors in clinical phase 2 and 7 small molecules of RORγt inhibitors in clinical phase 1, and no compound has entered clinical phase 3. Therefore, there is still a great need to discover and develop new RORγt inhibitor compounds for the prevention and/or treatment of RORγt-related diseases, such as inflammation and autoimmune diseases. In addition to having satisfactory RORγt inhibitory activity, such compounds are expected to have high selectivity for ROR subtypes and good or even improved druggability based on structural optimization, so as to provide more medications for patients with related diseases. The choice can also provide a better treatment effect.
发明简述Brief description of the invention
本发明涉及可用于预防或治疗与RORγt有关的疾病的化合物。特别地，已经鉴定，本发明的化合物不仅显示令人满意的RORγt抑制活性，具有调控Th17细胞分化、从而抑制IL-17产生的能力，而且在体内药代动力学实验中显示良好的性能，预示着改进的成药性和改进的生物利用度；此外还显示良好的安全性，具有较低的药物相互作用风险。因此，本发明化合物不仅可实现用于预防或治疗与RORγt有关的疾病的目的，而且所制备的药物有望具有改善的吸收、在同等剂量下疗效提高、或以更低的剂量提供相同疗效、更长的半衰期和/或降低可能的副作用。由此，本发明还提供了本发明化合物在制备用于预防或治疗与RORγt有关的疾病的药物中的用途、包含所述化合物的药物组合物和通过施用所述化合物预防和/或治疗与RORγt有关的疾病的方法。The present invention relates to compounds that can be used to prevent or treat diseases related to RORγt. In particular, it has been identified that the compound of the present invention not only shows satisfactory RORγt inhibitory activity, has the ability to regulate Th17 cell differentiation, thereby inhibiting the production of IL-17, but also shows good performance in in vivo pharmacokinetic experiments, which indicates With improved druggability and improved bioavailability; in addition, it also shows good safety and has a lower risk of drug interactions. Therefore, the compound of the present invention can not only achieve the purpose of preventing or treating diseases related to RORγt, but also the prepared drug is expected to have improved absorption, improved curative effect at the same dose, or provide the same curative effect at a lower dose, and more Long half-life and/or reduced possible side effects. Therefore, the present invention also provides the use of the compound of the present invention in the preparation of a medicament for the prevention or treatment of diseases related to RORγt, a pharmaceutical composition containing the compound, and the prevention and/or treatment of RORγt by administering the compound. Methods of related diseases.
因此，在本发明的一方面，提供了式(I)化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物：Therefore, in one aspect of the present invention, a compound of formula (I), its stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates are provided:
Figure PCTCN2021093788-appb-000001
Figure PCTCN2021093788-appb-000001
其中：in:
R 1和R 2各自独立地选自氢、卤素、氰基、硝基、C 1-C 6烷基、-O-C 1-C 6烷基、-S-C 1-C 6烷基、-NH-C 1-C 6烷基、-N-(C 1-C 6烷基) 2、-C 1-C 6烷基-O-C 1-C 6烷基、-C 1-C 6烷基-S-C 1-C 6烷基、-C 1-C 6烷基-NH-C 1-C 6烷基或-C 1-C 6烷基-N(C 1-C 6烷基) 2，其中所述C 1-C 6烷基任选被卤素或氰基取代； R 1 and R 2 are each independently selected from hydrogen, halogen, cyano, nitro, C 1 -C 6 alkyl, -OC 1 -C 6 alkyl, -SC 1 -C 6 alkyl, -NH-C 1 -C 6 alkyl, -N-(C 1 -C 6 alkyl) 2 , -C 1 -C 6 alkyl -OC 1 -C 6 alkyl, -C 1 -C 6 alkyl -SC 1- C 6 alkyl, -C 1 -C 6 alkyl-NH-C 1 -C 6 alkyl or -C 1 -C 6 alkyl-N(C 1 -C 6 alkyl) 2 , wherein the C 1 -C 6 alkyl is optionally substituted by halogen or cyano;
R 3选自H、-C 1-C 6烷基、-C 3-C 7环烷基、-4-7元杂环烷基、-NR aR a或-OR a，其中C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基任选被独立地选自以下的取代基取代：卤素、氰基、硝基、任选被卤素取代的C 3-C 7环烷基、R a、-OR a、-SR a或-NR aR a，R a选自H或任选被卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基； R 3 is selected from H, -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl, -NR a R a or -OR a, wherein C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally substituted with substituents independently selected from the group consisting of halogen, cyano, nitro, C 3 optionally substituted by halogen -C 7 -cycloalkyl, R a, -OR a, -SR a , or -NR a R a, R a is selected from H or an optionally halogen-substituted C 1 -C 6 alkyl, or connected to the same N two R a on the nitrogen atom may form a 4-7 membered heterocyclic group together with the N atom to which they are attached;
R 4选自-C 1-C 6烷基、-C 3-C 7环烷基、-4-7元杂环烷基或任选被C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基取代的氨基，其中所述C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基任选被各自独立地选自以下的取代基取代：卤素、氰基、硝基、R a、-OR a、-SR a、-NR aR a或任选被卤素取代的C 3-C 7环烷基，其中R a选自H或任选被卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个基团可以与它们所连接的N原子一起形成4-7元含氮杂环烷基； R 4 is selected from -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl or optionally C 1 -C 6 alkyl, C 3 -C 7 ring Alkyl or 4-7 membered heterocycloalkyl substituted amino, wherein the C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally selected independently of each other from the following substituents: halogen, cyano, nitro, R a, -OR a, -SR a, -NR a R a optionally substituted with halogen or C 3 -C 7 cycloalkyl group, wherein R a Two groups selected from H or C 1 -C 6 alkyl optionally substituted by halogen, or two groups attached to the same N atom can form 4-7 membered nitrogen-containing heterocycloalkanes together with the N atom to which they are attached base;
R 5和R 6各自独立地选自H、卤素、氰基或任选被卤素或氰基取代的C 1-C 6烷基； R 5 and R 6 are each independently selected from H, halogen, cyano or C 1 -C 6 alkyl optionally substituted by halogen or cyano;
m和p各自独立地选自0、1或2，且m and p are each independently selected from 0, 1, or 2, and
n选自0或1。n is selected from 0 or 1.
在本发明的另一方面，提供了具有RORγt抑制活性、用作药物、尤其是用作RORγt抑制剂的式(I)化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物。In another aspect of the present invention, there is provided a compound of formula (I), its stereoisomers, tautomers, and stable isotopic variants which have RORγt inhibitory activity and are used as drugs, especially as RORγt inhibitors. , A pharmaceutically acceptable salt or solvate.
在本发明的另一方面，提供了用于治疗、尤其是用于治疗或预防与RORγt有关的疾病的式(I)化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物。In another aspect of the present invention, there is provided a compound of formula (I), its stereoisomers, tautomers, stable isotopic variants for the treatment, especially for the treatment or prevention of diseases related to RORγt , A pharmaceutically acceptable salt or solvate.
在本发明的另一方面，提供了包含上述本发明化合物和可药用赋形剂的药物组合物。在一个具体的方面，提供了所述本发明的药物组合物，用于预防或治疗与RORγt有关的疾病。在一个具体的方面，药物组合物可以另外包含适合与本发明化合物组合使用的另外的治疗活性成分。In another aspect of the present invention, there is provided a pharmaceutical composition comprising the above-mentioned compound of the present invention and a pharmaceutically acceptable excipient. In a specific aspect, the pharmaceutical composition of the present invention is provided for preventing or treating diseases related to RORγt. In a specific aspect, the pharmaceutical composition may additionally contain additional therapeutically active ingredients suitable for use in combination with the compounds of the present invention.
在本发明的另一方面，提供了包含上述本发明化合物和另外的活性剂的药物组合。In another aspect of the present invention, there is provided a pharmaceutical combination comprising the above-mentioned compound of the present invention and another active agent.
在本发明的另一方面，提供了用于在哺乳动物、特别是人中预防或治疗与RORγt有关的疾病的方法，该方法包括施用有效量的本文所述的本发明化合物或包含其的药物组合物。In another aspect of the present invention, there is provided a method for preventing or treating diseases related to RORγt in a mammal, especially a human, the method comprising administering an effective amount of the compound of the present invention described herein or a drug containing the same combination.
在本发明的另一方面，提供了上述本发明的化合物或药物组合物用于预防或治疗与RORγt有关的疾病的用途。In another aspect of the present invention, the use of the above-mentioned compound or pharmaceutical composition of the present invention for preventing or treating diseases related to RORγt is provided.
在本发明的另一方面，提供了上述本发明的化合物或药物组合物在制备用于预防或治疗与RORγt有关的疾病的药物中的用途。In another aspect of the present invention, there is provided the use of the above-mentioned compound or pharmaceutical composition of the present invention in the preparation of a medicament for the prevention or treatment of diseases related to RORγt.
在另外的方面，提供了用于合成本发明化合物的方法，其中代表性的合成方案和途径在下文描述。In another aspect, methods for synthesizing the compounds of the present invention are provided, in which representative synthetic schemes and pathways are described below.
通过阅读随后的详细描述，本发明的其它目的和优点对于本领域技术人员将变得显而易见。By reading the detailed description that follows, other objects and advantages of the present invention will become apparent to those skilled in the art.
发明详述Detailed description of the invention
定义definition
除非另外指出，本说明书和权利要求书中使用的各个术语具有以下所示含义。在特定的 术语或短语没有特别定义的情况下，不应该被认为是不确定或不清楚的，而是应该按照本文上下文或者本领域的普通含义适当地理解。本文定义的许多基团都是任选被取代的，该定义部分所给出的取代基列表仅仅是示例性的，不意欲限制本说明书和权利要求书中其他部分所定义的取代基。Unless otherwise indicated, each term used in this specification and claims has the meaning shown below. In the case that a specific term or phrase is not specifically defined, it should not be regarded as uncertain or unclear, but should be properly understood in accordance with the context of the text or the ordinary meaning in the art. Many groups defined herein are optionally substituted. The list of substituents given in the definition section is only exemplary and is not intended to limit the substituents defined in other parts of this specification and claims.
本文所用的术语“烷基”意指具有指定碳原子数目的直链或支链脂族烃基。具体地，烷基可以具有1至6个、1至5个、1至4个、1至3个或1至2个碳原子。适合的C 1-6烷基的实例包括但不限于甲基、乙基、正丙基、异丙基、正丁基、异丁基、仲丁基、叔丁基、正戊基、异戊基、新戊基、正己基和异己基。特定的烷基具有1至3个碳原子。 The term "alkyl" as used herein means a straight or branched chain aliphatic hydrocarbon group having the specified number of carbon atoms. Specifically, the alkyl group may have 1 to 6, 1 to 5, 1 to 4, 1 to 3, or 1 to 2 carbon atoms. Examples of suitable C 1-6 alkyl groups include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isoamyl Base, neopentyl, n-hexyl and isohexyl. Certain alkyl groups have 1 to 3 carbon atoms.
本文所用的术语“烷氧基”意指基团-O-烷基，其中烷基具有本文所述的含义。具体地，该术语系指基团-O-C 1-6烷基。适合的烷氧基的实例包括但不限于甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、叔丁氧基、仲丁氧基、正戊氧基、正己氧基及1,2-二甲基丁氧基。特定的烷氧基具有1至3个碳原子。 The term "alkoxy" as used herein refers to the group -O-alkyl, where alkyl has the meaning described herein. Specifically, the term refers to the group -OC 1-6 alkyl. Examples of suitable alkoxy groups include, but are not limited to, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, tert-butoxy, sec-butoxy, n-pentoxy, n-hexyl Oxy and 1,2-dimethylbutoxy. Specific alkoxy groups have 1 to 3 carbon atoms.
本文所用的术语“烷硫基”意指基团-S-烷基，其中烷基具有本文所述的含义。具体地，该术语系指基团-S-C 1-6烷基。适合的烷硫基的实例包括但不限于甲硫基、乙硫基、正丙硫基、异丙硫基、正丁硫基、叔丁硫基、仲丁硫基、正戊硫基、正己硫基及1,2-二甲基丁硫基。特定的烷硫基具有1至3个碳原子。 The term "alkylthio" as used herein refers to the group -S-alkyl, where alkyl has the meaning described herein. Specifically, the term refers to the group -SC 1-6 alkyl. Examples of suitable alkylthio groups include, but are not limited to, methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, tert-butylthio, sec-butylthio, n-pentylthio, n-hexyl Sulfuryl and 1,2-dimethylbutylsulfanyl. Specific alkylthio groups have 1 to 3 carbon atoms.
本文中所用的术语“卤素取代的C 1-C 6烷基“指上文所述的C 1-C 6烷基，其中一个或多个(例如1、2、3、4或5个)氢原子被卤素代替。本领域技术人员应当理解，当卤素取代基多于一个时，卤素可以相同也可以不同，并且可以位于相同或不同的C原子上。“卤素取代的C 1-C 6烷基”的实例有例如-CH 2F、-CHF 2、-CF 3、-CCl 3、-C 2F 5、-C 2Cl 5、-CH 2CF 3、-CH 2Cl、CH 2CH 2CF 3或-CF(CF 3) 2等。 As used herein, the term "halogen-substituted C 1 -C 6 alkyl" refers to the above-mentioned C 1 -C 6 alkyl, in which one or more (for example, 1, 2, 3, 4, or 5) hydrogen The atoms are replaced by halogens. Those skilled in the art should understand that when there are more than one halogen substituents, the halogens may be the same or different, and may be located on the same or different C atoms. Examples of "halogen-substituted C 1 -C 6 alkyl" are, for example, -CH 2 F, -CHF 2 , -CF 3 , -CCl 3 , -C 2 F 5 , -C 2 Cl 5 , -CH 2 CF 3 , -CH 2 Cl, CH 2 CH 2 CF 3 or -CF(CF 3 ) 2 and so on.
本文中所用的术语“卤素取代的C 1-C 6烷氧基“指上文所述的C 1-C 6烷氧基，其中一个或多个(例如1、2、3、4或5个)氢原子被卤素代替。本领域技术人员应当理解，当卤素取代基多于一个时，卤素可以相同也可以不同，并且可以位于相同或不同的C原子上。“卤素取代的C 1-C 6烷氧基”的实例有例如-OCH 2F、-OCHF 2、-OCF 3、-OCCl 3、-OC 2F 5、-OC 2Cl 5、-OCH 2CF 3、-OCH 2Cl或-OCH 2CH 2CF 3等。 As used herein, the term "halogen-substituted C 1 -C 6 alkoxy" refers to the above-mentioned C 1 -C 6 alkoxy, wherein one or more (e.g., 1, 2, 3, 4 or 5 ) The hydrogen atom is replaced by a halogen. Those skilled in the art should understand that when there are more than one halogen substituents, the halogens may be the same or different, and may be located on the same or different C atoms. Examples of the "halogen substituted C 1 -C 6 alkoxy group" are, for example, -OCH 2 F, -OCHF 2 , -OCF 3 , -OCCl 3 , -OC 2 F 5 , -OC 2 Cl 5 , -OCH 2 CF 3. -OCH 2 Cl or -OCH 2 CH 2 CF 3 and so on.
本文中所用的术语“卤素取代的C 1-C 6烷硫基“指上文所述的C 1-C 6烷硫基，其中一个或多个(例如1、2、3、4或5个)氢原子被卤素代替。本领域技术人员应当理解，当卤素取代基多于一个时，卤素可以相同也可以不同，并且可以位于相同或不同的C原子上。“卤素取代的C 1-C 6烷硫基”的实例有例如-SCH 2F、-SCHF 2、-SCF 3、-SCCl 3、-SC 2F 5、-SC 2Cl 5、-SCH 2CF 3、-SCH 2Cl或-SCH 2CH 2CF 3等。 As used herein, the term "halogen-substituted C 1 -C 6 alkylthio" refers to the C 1 -C 6 alkylthio group described above, of which one or more (e.g., 1, 2, 3, 4 or 5 ) The hydrogen atom is replaced by a halogen. Those skilled in the art should understand that when there are more than one halogen substituents, the halogens may be the same or different, and may be located on the same or different C atoms. Examples of the "halogen substituted C 1 -C 6 alkylthio group" include, for example, -SCH 2 F, -SCHF 2 , -SCF 3 , -SCCl 3 , -SC 2 F 5 , -SC 2 Cl 5 , -SCH 2 CF 3. -SCH 2 Cl or -SCH 2 CH 2 CF 3 and so on.
本文所用的术语“环烷基”意指具有指定环原子数的单环、稠合多环、桥接多环或螺环非芳族饱和烃环结构。环烷基可具有3至12个碳原子，具体地3至10个，且更具体地3至7个碳原子，即C 3-C 7环烷基。适合的环烷基的实例包括但不限于单环C 3-C 7环烷基，如环丙 基、环丁基、环戊基、环己基和环庚基。特定的环烷基具有3至5个碳原子。 The term "cycloalkyl" as used herein means a monocyclic, fused polycyclic, bridged polycyclic or spirocyclic non-aromatic saturated hydrocarbon ring structure having the specified number of ring atoms. The cycloalkyl group may have 3 to 12 carbon atoms, specifically 3 to 10, and more specifically 3 to 7 carbon atoms, that is, C 3 -C 7 cycloalkyl. Examples of suitable cycloalkyl groups include, but are not limited to, monocyclic C 3 -C 7 cycloalkyl groups such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cycloheptyl. Specific cycloalkyl groups have 3 to 5 carbon atoms.
本文中所用的术语“卤素取代的C 3-C 7环烷基”指上文所述的C 3-C 7环烷基，其中一个或多个(例如1、2、3、4或5个)氢原子被卤素代替。本领域技术人员应当理解，当卤素取代基多于一个时，卤素可以相同也可以不同，并且可以位于相同或不同的C原子上。具体的实例包括但不限于2-氟环丙基、2,3-二氟环丙基、2,2,3,3-四氟环丙基、2,3-二氟环丁基、2,4-二氟环丁基等。 As used herein, the term "halogen-substituted C 3 -C 7 cycloalkyl" refers to the above-mentioned C 3 -C 7 cycloalkyl, of which one or more (e.g. 1, 2, 3, 4 or 5 ) The hydrogen atom is replaced by a halogen. Those skilled in the art should understand that when there are more than one halogen substituents, the halogens may be the same or different, and may be located on the same or different C atoms. Specific examples include, but are not limited to, 2-fluorocyclopropyl, 2,3-difluorocyclopropyl, 2,2,3,3-tetrafluorocyclopropyl, 2,3-difluorocyclobutyl, 2, 4-Difluorocyclobutyl and so on.
本文所用的术语“杂环烷基”意指包括一或多个独立地选自O、N及S的杂原子及指定环原子数的单环、稠合多环、螺环或桥接多环非芳族饱和环结构，或其N-氧化物，或其S-氧化物或S-二氧化物。杂环烷基可具有4至12个环成员，具体地4至10个环成员，且更具体地4至7个环成员。杂环烷基通常含有至多4个杂原子，更通常至多3个杂原子，更通常至多2个，例如单个杂原子，例如具有一个杂原子如N的4-7元单环杂环烷基，即4-7元含氮杂环烷基。适合的杂环烷基的实例包括但不限于氮杂环丁烷基、氧杂环丁烷基、硫杂环丁基、吡咯烷基(例如1-吡咯烷基、2-吡咯烷基及3-吡咯烷基)、四氢呋喃基(例如1-四氢呋喃基、2-四氢呋喃基及3-四氢呋喃基)、四氢噻吩基(例如1-四氢噻吩基、2-四氢噻吩基及3-四氢噻吩基)、哌啶基(例如1-哌啶基、2-哌啶基、3-哌啶基及4-哌啶基)、四氢吡喃基(例如4-四氢吡喃基)、四氢噻喃基(例如4-四氢噻喃基)、吗啉基、硫吗啉基、二噁烷基、哌嗪基或氮杂环庚烷基。As used herein, the term "heterocycloalkyl" means a monocyclic, fused polycyclic, spirocyclic, or bridged polycyclic heteroatom including one or more heteroatoms independently selected from O, N, and S and a specified number of ring atoms. Aromatic saturated ring structure, or its N-oxide, or its S-oxide or S-dioxide. The heterocycloalkyl group may have 4 to 12 ring members, specifically 4 to 10 ring members, and more specifically 4 to 7 ring members. The heterocycloalkyl group usually contains up to 4 heteroatoms, more usually up to 3 heteroatoms, more usually up to 2, such as a single heteroatom, such as a 4-7 membered monocyclic heterocycloalkyl group having one heteroatom such as N, That is, 4-7 membered nitrogen-containing heterocycloalkyl. Examples of suitable heterocycloalkyl groups include, but are not limited to, azetidinyl, oxetanyl, thietanyl, pyrrolidinyl (e.g., 1-pyrrolidinyl, 2-pyrrolidinyl, and 3 -Pyrrolidinyl), tetrahydrofuranyl (e.g. 1-tetrahydrofuranyl, 2-tetrahydrofuranyl and 3-tetrahydrofuranyl), tetrahydrothienyl (e.g. 1-tetrahydrothienyl, 2-tetrahydrothienyl and 3-tetrahydrothienyl) Thienyl), piperidinyl (e.g. 1-piperidinyl, 2-piperidinyl, 3-piperidinyl and 4-piperidinyl), tetrahydropyranyl (e.g. 4-tetrahydropyranyl), Tetrahydrothiopyranyl (for example 4-tetrahydrothiopyranyl), morpholinyl, thiomorpholinyl, dioxanyl, piperazinyl, or azepanyl.
有机合成领域普通技术人员均理解，稳定的化学可行的杂环，无论芳族还是非芳族，其中最大杂原子数或所含杂原子的类型由环大小、不饱和度及杂原子的价数决定。一般而言，杂环可具有1至4个杂原子，只要杂环或杂芳环在化学可行及稳定即可。Those of ordinary skill in the field of organic synthesis understand that stable chemically feasible heterocycles, whether aromatic or non-aromatic, in which the maximum number of heteroatoms or the type of heteroatoms contained are determined by the ring size, degree of unsaturation, and valence of the heteroatoms. Decide. Generally speaking, a heterocyclic ring can have 1 to 4 heteroatoms, as long as the heterocyclic ring or heteroaromatic ring is chemically feasible and stable.
本文所用的术语“卤代”或“卤素”意指氟(F)、氯(Cl)、溴(Br)及碘(I)。特定的卤代为氟或氯。本文所用的术语“被卤素取代的”基团旨在包括单卤代或多卤代基团，其中一个或多个相同或不同的卤素取代基团中的一个或多个氢。The term "halo" or "halogen" as used herein means fluorine (F), chlorine (Cl), bromine (Br), and iodine (I). The specific halogen is fluorine or chlorine. The term "halogen substituted" group as used herein is intended to include monohalogenated or polyhalogenated groups in which one or more identical or different halogens replace one or more hydrogens in the group.
本文所用的术语“氰基”意指基团-CN。The term "cyano" as used herein means the group -CN.
本文所用的术语“硝基”意指基团-NO 2。 The term "nitro" as used herein means the group -NO 2 .
本文所用的术语“氨基”意指基团-NH 2； The term "amino" as used herein means the group -NH 2 ;
本文所用的术语“任选被……取代“意指基团可以是未取代的或被一个或多个(例如0、1、2、3、4或5或更多，或其中可衍生的任何范围)对该基团所列的取代基取代，其中所述取代基可以相同或不同。在一个实施方案中，任选取代的基团具有1个取代基。在另一个实施方案中，任选取代的基团具有2个取代基。在另一个实施方案中，任选取代的基团具有3个取代基。在另一个实施方案中，任选取代的基团具有4个取代基。As used herein, the term "optionally substituted by" means that the group may be unsubstituted or be substituted by one or more (e.g. 0, 1, 2, 3, 4 or 5 or more, or any of which can be derived Range) Substituting the listed substituents for this group, wherein the substituents may be the same or different. In one embodiment, the optionally substituted group has 1 substituent. In another embodiment, the optionally substituted group has 2 substituents. In another embodiment, the optionally substituted group has 3 substituents. In another embodiment, the optionally substituted group has 4 substituents.
除非另外定义，本文化合物定义中使用的C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基任选地携带一个或多个取代基，所述取代基可选自H、F、Cl、Br、I、氰基、硝基、C 1-C 6烷基(例如甲基、乙基、丙基、异丙基、丁基、异丁基、仲丁基、叔丁基、戊基、新戊基、己基、 1,2-二甲基丁基等)、C 3-C 7环烷基(环丙基、环丁基、环戊基、环己基、环庚基)、-OH、-O-C 1-C 6烷基(例如甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、叔丁氧基、仲丁氧基、正戊氧基、正己氧基及1,2-二甲基丁氧基等)、-SH、-S-C 1-C 6烷基(例如甲硫基、乙硫基、正丙硫基、异丙硫基、正丁硫基、叔丁硫基、仲丁硫基、正戊硫基、正己硫基及1,2-二甲基丁硫基等)或-NH 2、-NH-C 1-C 6烷基(例如甲基氨基、乙基氨基、丙基氨基、异丙基氨基、正丁基氨基、叔丁基氨基、仲丁基氨基、正戊基氨基、正己基氨基及1,2-二甲基丁基氨基等)、-N(C 1-C 6烷基) 2(例如二甲基氨基、甲基乙基氨基、二乙基氨基等)，其中的C 1-C 6烷基或C 3-C 7环烷基任选被一个或多个卤素(优选F)取代。 Unless otherwise defined, the C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl, or 4-7 membered heterocycloalkyl used in the definition of compounds herein optionally carries one or more substituents. Can be selected from H, F, Cl, Br, I, cyano, nitro, C 1 -C 6 alkyl (e.g. methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl Group, tert-butyl, pentyl, neopentyl, hexyl, 1,2-dimethylbutyl, etc.), C 3 -C 7 cycloalkyl (cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl , Cycloheptyl), -OH, -OC 1 -C 6 alkyl (e.g. methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, tert-butoxy, sec-butoxy Group, n-pentyloxy, n-hexyloxy and 1,2-dimethylbutoxy, etc.), -SH, -SC 1 -C 6 alkyl (e.g. methylthio, ethylthio, n-propylthio, Isopropylthio, n-butylthio, tert-butylthio, sec-butylthio, n-pentylthio, n-hexylthio and 1,2-dimethylbutylthio, etc.) or -NH 2 , -NH-C 1- C 6 alkyl (e.g. methylamino, ethylamino, propylamino, isopropylamino, n-butylamino, tert-butylamino, sec-butylamino, n-pentylamino, n-hexylamino and 1 , 2-Dimethylbutylamino, etc.), -N(C 1 -C 6 alkyl) 2 (such as dimethylamino, methylethylamino, diethylamino, etc.), where C 1 -C The 6 alkyl group or C 3 -C 7 cycloalkyl group is optionally substituted with one or more halogens (preferably F).
本文所用的术语“本发明的化合物”意欲涵盖如本文所定义的通式(I)的化合物或其任一优选或具体的实施方案、它们的立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，以及前药。类似地，本文中对“中间体”的称谓，无论其本身是否被请求保护，若上下文允许，则均意欲涵盖其游离形式以及上述各衍生形式。The term "compounds of the present invention" as used herein is intended to encompass compounds of general formula (I) as defined herein or any preferred or specific embodiments thereof, their stereoisomers, tautomers, stable Isotopic variants, pharmaceutically acceptable salts or solvates, and prodrugs. Similarly, the term "intermediate" in this article, regardless of whether it is claimed for protection or not, if the context permits, it is intended to cover its free form as well as the above-mentioned derivative forms.
本文所用的术语“药学可接受的”意指由各个国家的相应机构批准的或可由其批准，或列于用于动物且更具体地人类的一般公认药典中，或当向动物例如人类适量施用时不会产生不利、过敏或其它不良反应的分子实体和组合物。The term "pharmaceutically acceptable" as used herein means approved by or can be approved by the corresponding agency of each country, or listed in the generally recognized pharmacopoeia for animals and more specifically humans, or when administered to animals such as humans in appropriate amounts Molecular entities and compositions that do not produce adverse, allergic or other adverse reactions.
本文所用的术语“药学可接受的盐“意指药学上可接受且具有母体化合物所需药理学活性的本发明化合物的盐。具体地，此类盐无毒，可为无机酸加成盐或有机酸加成盐及碱加成盐。具体地，此类盐包括：(1)与无机酸形成的酸加成盐，该无机酸如盐酸、氢溴酸、硫酸、硝酸、磷酸等；或与有机酸形成的酸加成盐，该有机酸如乙酸、丙酸、己酸、乙醇酸、丙酮酸、乳酸、丙二酸、丁二酸、苹果酸、马来酸、富马酸、酒石酸、柠檬酸、苯甲酸、肉桂酸、扁桃酸、甲磺酸、乙磺酸、苯磺酸、2-萘磺酸、4-甲苯磺酸、樟脑磺酸、葡糖庚酸、3-苯基丙酸、三甲基乙酸、叔丁基乙酸、月桂基硫酸、葡萄糖酸、谷氨酸、羟基萘甲酸、水杨酸、硬脂酸、黏康酸等；或(2)当存在于母体化合物中的酸性质子经金属离子如碱金属离子、碱土金属离子或铝离子置换时、或与有机碱如乙醇胺、二乙醇胺、三乙醇胺、N-甲基葡糖胺等配位时形成的盐。本领域技术人员了解制备药用盐的一般原理和技术，例如Berge等，Pharm ScL，66，1-19.(1977)中所述的那些。The term "pharmaceutically acceptable salt" as used herein means a salt of the compound of the present invention that is pharmaceutically acceptable and has the desired pharmacological activity of the parent compound. Specifically, such salts are non-toxic, and can be inorganic acid addition salts, organic acid addition salts, and base addition salts. Specifically, such salts include: (1) acid addition salts formed with inorganic acids, such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, etc.; or acid addition salts formed with organic acids, Organic acids such as acetic acid, propionic acid, caproic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid Acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, 2-naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, glucoheptanoic acid, 3-phenylpropionic acid, trimethylacetic acid, tert-butyl Acetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid, etc.; or (2) when the acidic protons present in the parent compound pass through metal ions such as alkali metal ions , Alkaline earth metal ion or aluminum ion replacement, or coordination with organic bases such as ethanolamine, diethanolamine, triethanolamine, N-methylglucamine and other salts. Those skilled in the art understand the general principles and techniques for preparing pharmaceutical salts, such as those described in Berge et al., Pharma ScL, 66, 1-19. (1977).
本文所用的术语“前药”意指具有可裂解基团且通过溶剂分解或在生理条件下变成在体内具有药学活性的本发明化合物的化合物，包括本发明化合物的衍生物。前药包括本领域熟知的酸衍生物，如通过母体酸与适合醇反应制备的酯，或通过母体酸化合物与取代或未取代的胺反应制备的酰胺，或酸酐或混合酸酐。衍生自本发明化合物侧接的酸基的简单脂族或芳族酯、酰胺及酸酐为尤其适用的前药。特定的此类前药为本发明化合物的C 1-8烷基、C 2-8烯基、任选被取代的C 6-10芳基及(C 6-10芳基)-(C 1-4烷基)酯。 The term "prodrug" as used herein means a compound that has a cleavable group and becomes a compound of the present invention that has pharmacological activity in the body through solvolysis or under physiological conditions, including derivatives of the compound of the present invention. Prodrugs include acid derivatives well known in the art, such as esters prepared by reacting a parent acid with a suitable alcohol, or amides prepared by reacting a parent acid compound with a substituted or unsubstituted amine, or anhydrides or mixed anhydrides. Simple aliphatic or aromatic esters, amides, and anhydrides derived from acid groups pendant to the compounds of the present invention are particularly useful prodrugs. Specific such prodrugs are C 1-8 alkyl, C 2-8 alkenyl, optionally substituted C 6-10 aryl and (C 6-10 aryl)-(C 1- 4 alkyl) esters.
本文中所用的术语“立体异构体“表示由于至少一个不对称中心形成的异构体。在具有一个或多个(例如1个、2个、3个或4个)不对称中心的化合物中，其可产生外消旋混合物、单一对映异构体、非对映异构体混合物和单独的非对映异构体。特定分子也可以以几何异构 体(顺式/反式)存在。类似地，本发明的化合物可以以两种或更多种处于快速平衡的不同结构形式的混合物(通常称作互变异构体)存在。互变异构体的代表性实例包括酮-烯醇互变异构体、苯酚-酮互变异构体、亚硝基-肟互变异构体、亚胺-烯胺互变异构体等。例如，亚硝基-肟在溶液中可以下列互变异构形式平衡存在：The term "stereoisomer" as used herein means an isomer formed due to at least one asymmetric center. In compounds with one or more (for example, 1, 2, 3, or 4) asymmetric centers, it can produce racemic mixtures, single enantiomers, diastereomeric mixtures, and Individual diastereomers. Specific molecules can also exist as geometric isomers (cis/trans). Similarly, the compounds of the present invention may exist as a mixture of two or more different structural forms in rapid equilibrium (commonly referred to as tautomers). Representative examples of tautomers include keto-enol tautomers, phenol-ketone tautomers, nitroso-oxime tautomers, imine-enamine tautomers Wait. For example, nitroso-oximes can exist in equilibrium in the following tautomeric forms in solution:
Figure PCTCN2021093788-appb-000002
Figure PCTCN2021093788-appb-000002
需要理解的是，本申请的范围涵盖所有这样的以任意比例(例如60％、65％、70％、75％、80％、85％、90％、95％、96％、97％、98％、99％)的异构体或其混合物。It should be understood that the scope of this application covers all such items in arbitrary proportions (for example, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%). , 99%) isomers or mixtures thereof.
本发明化合物可具有一或多个不对称中心，因此可以分别以(R)-或(S)-立体异构体形式制备或以其混合物形式制备。本文化合物结构式或结构片段中使用的
Figure PCTCN2021093788-appb-000003
或
Figure PCTCN2021093788-appb-000004
表示不对称中心即手性中心的相对构型。相应地，在本发明所提供的化合物或中间体的命名中以R和S表示关于该手性中心的相对构型。 The compounds of the present invention may have one or more asymmetric centers, and therefore may be prepared in the form of (R)- or (S)-stereoisomers respectively or in the form of mixtures thereof. Used in the structural formulas or structural fragments of the compounds in this article
Figure PCTCN2021093788-appb-000003
or
Figure PCTCN2021093788-appb-000004
Indicates the relative configuration of the asymmetric center, that is, the chiral center. Correspondingly, in the naming of the compounds or intermediates provided by the present invention, R and S represent the relative configuration of the chiral center.
本文所用的术语“溶剂合物”是指包含化学计量的或非化学计量的溶剂的溶剂加成形式，包括例如与水的溶剂合物，例如水合物，或与有机溶剂、例如甲醇、乙醇或乙腈的溶剂合物，即分别作为甲醇化物、乙醇化物或乙腈化物；或为任何多晶型物的形式。应当理解的是，本发明化合物的这类溶剂合物还包括本发明化合物的药学可接受盐的溶剂合物。The term "solvate" as used herein refers to a solvent addition form containing stoichiometric or non-stoichiometric solvents, including, for example, solvates with water, such as hydrates, or with organic solvents, such as methanol, ethanol, or Solvates of acetonitrile, namely as methanolate, ethanolate or acetonitrile respectively; or in the form of any polymorph. It should be understood that such solvates of the compounds of the present invention also include solvates of pharmaceutically acceptable salts of the compounds of the present invention.
本文所使用的术语“同位素变体”是指构成该化合物的一或多个原子被具有与自然界中通常发现的原子质量或质量数不同的原子质量或质量数的原子所取代的化合物。可以掺入本发明化合物的一个或多个原子上的同位素的实例包括例如 2H、 3H、 13C、 14C、 15N、 17O、 18O、 31P、 32P、 35S、 18F和 36Cl，从而形成本发明化合物的同位素变化形式，其无论是否具有放射性，都旨在涵盖在本发明的范围内。在一些实施方案中，所掺入的同位素是2H(氘)；在另一些实施方案中，所掺入的同位素是3H(氚)。 The term "isotopic variant" as used herein refers to a compound in which one or more of the atoms constituting the compound is replaced by an atom having an atomic mass or mass number that is different from the atomic mass or mass number commonly found in nature. Examples of isotopes that can be incorporated into one or more atoms of the compounds of the present invention include, for example, 2 H, 3 H, 13 C, 14 C, 15 N, 17 O, 18 O, 31 P, 32 P, 35 S, 18 F and 36 Cl, thereby forming isotopic variants of the compounds of the present invention, whether they are radioactive or not, are intended to be encompassed within the scope of the present invention. In some embodiments, the incorporated isotope is 2H (deuterium); in other embodiments, the incorporated isotope is 3H (tritium).
本文所用的术语“与RORγt有关的疾病”意指RORγt对所述疾病的发生和发展起到促进作用，或抑制RORγt将降低疾病的发生率、减少或消除疾病病状的疾病。对于本发明而言，“与RORγt有关的疾病”尤其选自炎症或自身免疫性疾病、癌症等，包括但不限于银屑病、类风湿性关节炎、银屑病性关节炎、强直性脊柱炎、多发性硬化、系统性红斑狼疮、移植物抗宿主疾病、炎症性肠病、克隆氏病、溃疡性结肠炎、慢性阻塞性肺病、哮喘、血管球性肾炎、狼疮性肾炎、心肌炎、甲状腺炎、干眼症、葡萄膜炎、白塞病、过敏性皮肤炎、粉刺、硬皮病、支气管炎、皮肌过敏性鼻炎、坏死性小肠结肠炎(NEC,Necrotizing Enterocolitis)、肝纤维化、非酒精性脂肪性肝炎(NASH)、新冠病毒肺炎(New coronavirus pneumonia)、胰岛素依赖性I型糖尿病、三阴乳腺癌和前列腺癌等。本发明优选的适应症选自银屑病、类风湿性关节炎、银屑病性关节炎、强直性脊柱炎、多发性硬化、炎症性肠病、干眼症、过敏性皮肤炎、慢性阻塞性肺病(COPD)、哮喘、坏死性小肠结肠炎、肝纤维化、非酒精性脂肪性肝炎(NASH)、新冠病毒肺炎、三阴乳腺癌和前列腺癌。As used herein, the term "disease related to RORγt" means that RORγt promotes the occurrence and development of the disease, or inhibiting RORγt will reduce the incidence of the disease and reduce or eliminate the disease symptoms. For the present invention, "disease related to RORγt" is especially selected from inflammation or autoimmune diseases, cancer, etc., including but not limited to psoriasis, rheumatoid arthritis, psoriatic arthritis, ankylosing spine Inflammation, multiple sclerosis, systemic lupus erythematosus, graft-versus-host disease, inflammatory bowel disease, Crohn's disease, ulcerative colitis, chronic obstructive pulmonary disease, asthma, glomerulonephritis, lupus nephritis, myocarditis, thyroid Inflammation, dry eye, uveitis, Behcet's disease, allergic dermatitis, acne, scleroderma, bronchitis, dermatomuscular allergic rhinitis, necrotizing enterocolitis (NEC, Necrotizing Enterocolitis), liver fibrosis, Non-alcoholic steatohepatitis (NASH), new coronavirus pneumonia (New coronavirus pneumonia), insulin-dependent type I diabetes, triple negative breast cancer and prostate cancer. The preferred indications of the present invention are selected from psoriasis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, multiple sclerosis, inflammatory bowel disease, dry eye, allergic dermatitis, chronic obstruction COPD, asthma, necrotizing enterocolitis, liver fibrosis, non-alcoholic steatohepatitis (NASH), new coronavirus pneumonia, triple negative breast cancer and prostate cancer.
本文所用的术语“受试者”或“个体”包括人或非人动物。示例性人个体包括患有疾病(例如本文所述的疾病)的人个体(称为患者)或正常个体。本发明中“非人动物”包括所有脊椎动物，例如非哺乳动物(例如鸟类、两栖动物、爬行动物)和哺乳动物，例如非人灵长类、家畜和/或驯化动物(例如绵羊、犬、猫、奶牛、猪等)。The term "subject" or "individual" as used herein includes human or non-human animals. Exemplary human individuals include human individuals (referred to as patients) or normal individuals suffering from diseases such as those described herein. In the present invention, "non-human animals" include all vertebrates, such as non-mammals (such as birds, amphibians, reptiles) and mammals, such as non-human primates, livestock and/or domesticated animals (such as sheep, dogs). , Cats, cows, pigs, etc.).
本文所使用的术语“治疗有效量”意指当向受试者施用以治疗疾病时足以减轻或完全缓解病症的症状或其它有害作用；逆转、完全停止或减缓病症的进展；或降低病症恶化的风险的量，“有效量”可视化合物、疾病及其严重程度及待治疗的受试者的年龄、体重等而变化。The term "therapeutically effective amount" as used herein means that when administered to a subject to treat a disease, it is sufficient to reduce or completely alleviate the symptoms or other harmful effects of the disorder; reverse, completely stop or slow the progression of the disorder; or reduce the deterioration of the disorder The amount of risk, the "effective amount" may vary depending on the compound, the disease and its severity, and the age and weight of the subject to be treated.
本文所使用的术语“预防”意指给怀疑患上或易感于如本文所定义的与RORγt有关的疾病、尤其是炎症或自身免疫疾病的受试者、例如哺乳动物、例如人施用一种或多种本发明的化合物，使得罹患所定义疾病的风险降低。术语“预防”包含在诊断或确定任何临床和/或病理症状以前使用本发明的化合物。As used herein, the term "prevention" means to administer a subject suspected of suffering from or susceptible to RORγt-related diseases as defined herein, especially inflammation or autoimmune diseases, such as mammals, such as humans. Or multiple compounds of the present invention, which reduce the risk of suffering from the defined disease. The term "prevention" encompasses the use of the compounds of the present invention prior to the diagnosis or determination of any clinical and/or pathological symptoms.
本文所用的术语“治疗”是指给患有所述疾病、或者具有所述疾病的症状的受试者、例如哺乳动物、例如人施用一种或多种本文所述的本发明化合物，用以治愈、缓解、减轻或影响所述疾病或所述疾病的症状。在本发明具体的实施方案中，所述疾病是本文所定义的与RORγt有关的疾病、尤其是炎症或自身免疫疾病。The term "treatment" as used herein refers to the administration of one or more of the compounds of the invention described herein to a subject suffering from the disease or having symptoms of the disease, such as a mammal, such as a human, for Cure, alleviate, alleviate or affect the disease or the symptoms of the disease. In a specific embodiment of the present invention, the disease is a disease related to RORγt as defined herein, especially inflammation or an autoimmune disease.
本文所用的术语“药物组合”是指本发明化合物可与其它活性剂组合用于实现本发明的目的。所述其他活性剂可以是一种或多种另外的本发明化合物，或可以是与本发明化合物相容即不会相互不利影响、或具有互补活性的第二种或另外的(例如第三种)化合物。这类活性剂以达到预期目的的有效量适宜地组合存在。所述其他活性剂可以与本发明化合物在单一药物组合物中共同施用，或与本发明化合物处于不同的离散单元中分别施用，当分别施用时可以同时或相继进行。所述相继施用在时间上可以是接近或隔远的。The term "pharmaceutical combination" as used herein means that the compound of the present invention can be combined with other active agents to achieve the purpose of the present invention. The other active agent may be one or more additional compounds of the present invention, or may be a second or additional (e.g., third ) Compound. Such active agents are suitably present in combination in an effective amount to achieve the intended purpose. The other active agent may be co-administered with the compound of the present invention in a single pharmaceutical composition, or administered separately from the compound of the present invention in separate discrete units, and when administered separately, they may be administered simultaneously or sequentially. The sequential administration may be close or distant in time.
本文所用的术语“药学上可接受的赋形剂或载体”是指一种或多种相容性固体或液体填料或凝胶物质，其药理学上无活性，与组合物中的其它成分相容，并且应是对温血动物如人给药可接受的，用作本发明化合物在施用形式中的载体或介质，其实例包括但不限于纤维素及其衍生物(如羧甲基纤维素钠、醋酸纤维素等)、明胶、滑石、固体润滑剂(如硬脂酸镁)、硫酸钙、植物油、多元醇(如丙二醇、甘油、甘露醇、山梨醇等)、乳化剂(如吐温类)、润湿剂(如十二烷基硫酸钠)、着色剂、调味剂、稳定剂、抗氧化剂、防腐剂等。The term "pharmaceutically acceptable excipient or carrier" as used herein refers to one or more compatible solid or liquid fillers or gel substances, which are pharmacologically inactive and are compatible with other ingredients in the composition. It should be acceptable for administration to warm-blooded animals such as humans, and used as a carrier or medium for the compound of the present invention in the administration form. Examples include, but are not limited to, cellulose and its derivatives (such as carboxymethyl cellulose). Sodium, cellulose acetate, etc.), gelatin, talc, solid lubricants (such as magnesium stearate), calcium sulfate, vegetable oils, polyols (such as propylene glycol, glycerin, mannitol, sorbitol, etc.), emulsifiers (such as Tween) Class), wetting agents (such as sodium lauryl sulfate), coloring agents, flavoring agents, stabilizers, antioxidants, preservatives, etc.
除非另有规定，本发明化合物定义中的C n-n+m或C n-C n+m包括n至n+m个碳原子的各种情况，例如C 1-6包括C 1、C 2、C 3、C 4、C 5和C 6，也包括n至n+m中的任何一个范围，例如C 1-6包括C 1-2、C 1-3、C 1-4、C 2-6、C 3-6等。同理，本发明化合物定义中的n元至n+m元表示环原子数为n至n+m个，例如3-12元环包括3元环、4元环、、5元环、6元环、12元环等，也包括n至n+m元的任何一个范围，例如3-12元环包括3-6元环、3-9元环、5-6元环、5-7元环、6-7元环、6-8元环和6-10元环等。 Unless otherwise specified, C n-n+m or C n -C n+m in the definition of the compound of the present invention includes various cases of n to n+m carbon atoms, for example, C 1-6 includes C 1 , C 2 , C 3 , C 4 , C 5 and C 6 , and also include any range from n to n+m, for example, C 1-6 includes C 1-2 , C 1-3 , C 1-4 , and C 2- 6. C 3-6 etc. In the same way, n-membered to n+m-membered in the definition of the compound of the present invention means that the number of ring atoms is from n to n+m. For example, a 3-12-membered ring includes a 3-membered ring, a 4-membered ring, a 5-membered ring, and a 6-membered ring. Rings, 12-membered rings, etc., also include any range from n to n+m. For example, 3-12-membered rings include 3-6-membered rings, 3-9-membered rings, 5-6-membered rings, and 5-7-membered rings , 6-7 membered ring, 6-8 membered ring and 6-10 membered ring, etc.
应理解，当本文描述本发明化合物、包含其的药物组合物、药物组合以及相关的用途和 方法时所涉及的剂量，是基于游离形式的重量，而非基于其任何盐、水合物或溶剂化物等，除非说明书中另外定义。It should be understood that when describing the compounds of the present invention, pharmaceutical compositions, pharmaceutical combinations and related uses and methods, the dosages involved are based on the weight of the free form, rather than on any salt, hydrate or solvate thereof. Etc., unless otherwise defined in the specification.
本发明化合物Compound of the invention
本申请通篇使用的术语“发明的化合物”和“本发明的化合物”等，除非另外指出，涵盖本文各个实施方案及其具体或优选实施方式中定义的式(I)化合物、它们的立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，以及前药。所述立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物以及前药如上文定义部分所描述。优选地，本发明化合物为式(I)化合物的游离形式或其药学上可接受的盐或溶剂合物；最优选为式(I)化合物的游离形式或其药学上可接受的盐。The terms "compounds of the invention" and "compounds of the invention", etc. used throughout this application, unless otherwise specified, encompass the compounds of formula (I) defined in the various embodiments herein and their specific or preferred embodiments, and their stereoisomers. Constructs, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates, and prodrugs. The stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates, and prodrugs are as described in the definition section above. Preferably, the compound of the present invention is the free form of the compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof; most preferably, the free form of the compound of formula (I) or a pharmaceutically acceptable salt thereof.
本发明的某些化合物可以以多晶型或无定形形式存在，它们也落入本发明的范围内。当为固体结晶形式时，式(I)化合物可以是与另一种化学实体的共晶体形式，并且本说明书包括所有这些共晶体。Certain compounds of the present invention may exist in polymorphic or amorphous forms, and they also fall within the scope of the present invention. When in a solid crystalline form, the compound of formula (I) may be in the form of a co-crystal with another chemical entity, and this specification includes all such co-crystals.
在存在手性中心时，本发明的化合物可以以单独的对映异构体或对映体混合物形式存在。根据一个实施方案，提供了式(I)化合物或其药学上可接受的盐，其是对映体过量(％ee)＞95、＞98％或＞99％的单一对映体。优选地，单一对映异构体以＞99％的对映异构体过量(％ee)存在。In the presence of a chiral center, the compounds of the present invention may exist as individual enantiomers or as a mixture of enantiomers. According to one embodiment, there is provided a compound of formula (I) or a pharmaceutically acceptable salt thereof, which is a single enantiomer with an enantiomeric excess (%ee) >95, >98% or >99%. Preferably, a single enantiomer is present in an enantiomeric excess (%ee) of >99%.
具体地，一方面，本发明提供式(I)化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物：Specifically, in one aspect, the present invention provides a compound of formula (I), its stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates:
Figure PCTCN2021093788-appb-000005
Figure PCTCN2021093788-appb-000005
其中：in:
R 1和R 2各自独立地选自氢、卤素、氰基、硝基、C 1-C 6烷基、-O-C 1-C 6烷基、-S-C 1-C 6烷基、-NH-C 1-C 6烷基、-N-(C 1-C 6烷基) 2、-C 1-C 6烷基-O-C 1-C 6烷基、-C 1-C 6烷基-S-C 1-C 6烷基、-C 1-C 6烷基-NH-C 1-C 6烷基或-C 1-C 6烷基-N(C 1-C 6烷基) 2，其中所述C 1-C 6烷基任选被卤素或氰基取代； R 1 and R 2 are each independently selected from hydrogen, halogen, cyano, nitro, C 1 -C 6 alkyl, -OC 1 -C 6 alkyl, -SC 1 -C 6 alkyl, -NH-C 1 -C 6 alkyl, -N-(C 1 -C 6 alkyl) 2 , -C 1 -C 6 alkyl -OC 1 -C 6 alkyl, -C 1 -C 6 alkyl -SC 1- C 6 alkyl, -C 1 -C 6 alkyl-NH-C 1 -C 6 alkyl or -C 1 -C 6 alkyl-N(C 1 -C 6 alkyl) 2 , wherein the C 1 -C 6 alkyl is optionally substituted by halogen or cyano;
R 3选自H、-C 1-C 6烷基、-C 3-C 7环烷基、-4-7元杂环烷基、-NR aR a或-OR a，其中C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基任选被独立地选自以下的取代基取代：卤素、氰基、硝基、任选被卤素取代的C 3-C 7环烷基、R a、-OR a、-SR a或-NR aR a，其中R a选自H或任选被卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基； R 3 is selected from H, -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl, -NR a R a or -OR a, wherein C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally substituted with substituents independently selected from the group consisting of halogen, cyano, nitro, C 3 optionally substituted by halogen -C 7 -cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is selected from H or optionally halogen-substituted C 1 -C 6 alkyl, or connected to the same two R a may be formed on the N-atom together with the N atom to which they are attached, 4-7 membered nitrogen-containing heterocyclic group;
R 4选自-C 1-C 6烷基、-C 3-C 7环烷基、-4-7元杂环烷基或任选被C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基取代的氨基，其中所述C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基任选被各自独立地选自以下的取代基取代：卤素、氰基、硝基、R a、-OR a、-SR a、-NR aR a或任选被卤素取代的C 3-C 7环烷基，R a选自H或任选被卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个基团可以与它们所连接的N原子一起形成4-7元含氮杂环烷基； R 4 is selected from -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl or optionally C 1 -C 6 alkyl, C 3 -C 7 ring Alkyl or 4-7 membered heterocycloalkyl substituted amino, wherein the C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally selected independently of each other Substitution from the following substituents: halogen, cyano, nitro, R a , -OR a , -SR a , -NR a R a or C 3 -C 7 cycloalkyl optionally substituted by halogen, R a is selected A C 1 -C 6 alkyl group optionally substituted by H or halogen, or two groups attached to the same N atom can form a 4-7 membered nitrogen-containing heterocycloalkyl group together with the N atom to which they are attached ；
R 5和R 6各自独立地选自H、卤素、氰基或任选被卤素或氰基取代的C 1-C 6烷基； R 5 and R 6 are each independently selected from H, halogen, cyano or C 1 -C 6 alkyl optionally substituted by halogen or cyano;
m和p各自独立地选自0、1或2，且m and p are each independently selected from 0, 1, or 2, and
n选自0或1。n is selected from 0 or 1.
在一种式(I)化合物的实施方式中，n为0。In one embodiment of the compound of formula (I), n is zero.
在一种式(I)化合物的实施方式中，n为1。In one embodiment of the compound of formula (I), n is 1.
在一种式(I)化合物的实施方式中，R 1和R 2各自独立地为H。 In one embodiment of the compound of formula (I), R 1 and R 2 are each independently H.
在一种式(I)化合物的实施方式中，R 1和R 2各自独立地为卤素，例如F、Cl、Br或I；优选F或Cl。 In one embodiment of the compound of formula (I), R 1 and R 2 are each independently halogen, such as F, Cl, Br or I; preferably F or Cl.
在一个具体的实施方式中，R 1和R 2均为H。在一个具体的实施方式中，R 1为H且R 2为卤素。在一个具体的实施方式中，R 1为卤素且R 2为H。在一个具体的实施方式中，R 1和R 2均为卤素，二者可以相同或不同。 In a specific embodiment, both R 1 and R 2 are H. In a specific embodiment, R 1 is H and R 2 is halogen. In a specific embodiment, R 1 is halogen and R 2 is H. In a specific embodiment, R 1 and R 2 are both halogen, and the two may be the same or different.
在一种式(I)化合物的实施方式中，R 1和R 2各自独立地选自C 1-C 6烷基、-O-C 1-C 6烷基、-S-C 1-C 6烷基、-NH-C 1-C 6烷基或-N-(C 1-C 6烷基) 2，其中的C 1-C 6烷基任选被卤素(优选F)取代。具体的实例包括但不限于甲基、乙基、丙基、异丙基、丁基、异丁基、叔丁基、-CF 3、-CHF 2、-CH 2CF 3、-CF 2CF 3、-CH 2CH 2CF 3、-CH(CF 3) 2、-OCH 3、-OCF 3、-OCHF 2、-OCH 2CH 3、-OCH 2CF 3、-OCH 2CH 2CH 3、-OCH 2CH 2CF 3、-OCH(CF 3) 2、-SCH 3、-SCF 3、-SCH 2CH 3、-NH 2、-NHCH 3、-N(CH 3) 2、-NH-CH 2CH 3、-N(CH 3)(CH 2CH 3)、-NHCF 3、-N(CH 3)(CF 3)等。 In one embodiment of the compound of formula (I), R 1 and R 2 are each independently selected from C 1 -C 6 alkyl, -OC 1 -C 6 alkyl, -SC 1 -C 6 alkyl,- NH-C 1 -C 6 alkyl or -N-(C 1 -C 6 alkyl) 2 , wherein the C 1 -C 6 alkyl group is optionally substituted by halogen (preferably F). Specific examples include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, -CF 3 , -CHF 2 , -CH 2 CF 3 , -CF 2 CF 3 , -CH 2 CH 2 CF 3 , -CH(CF 3 ) 2 , -OCH 3 , -OCF 3 , -OCHF 2 , -OCH 2 CH 3 , -OCH 2 CF 3 , -OCH 2 CH 2 CH 3 ,- OCH 2 CH 2 CF 3 , -OCH(CF 3 ) 2 , -SCH 3 , -SCF 3 , -SCH 2 CH 3 , -NH 2 , -NHCH 3 , -N(CH 3 ) 2 , -NH-CH 2 CH 3 , -N(CH 3 )(CH 2 CH 3 ), -NHCF 3 , -N(CH 3 )(CF 3 ), etc.
在一种式(I)化合物的实施方式中，R 1和R 2各自独立地选自-C 1-C 6烷基-O-C 1-C 6烷基、-C 1-C 6烷基-S-C 1-C 6烷基、-C 1-C 6烷基-NH-C 1-C 6烷基或-C 1-C 6烷基-N(C 1-C 6烷基) 2，其中的C 1-C 6烷基任选被卤素(优选F)取代。具体的实例包括但不限于-CH 2OCH 3、-CH 2CH 2OCH 3、-CH 2OCH 2CH 3、-CH 2CH 2OCH 2CH 3、-CH 2NHCH 3、-CH 2N(CH 3) 2、-CH 2OCF 3、-CH 2CH 2OCF 3、-CH 2OCH 2CF 3、-CH 2NHCF 3、-CH 2N(CF 3) 2等。 In one embodiment of the compound of formula (I), R 1 and R 2 are each independently selected from -C 1 -C 6 alkyl-OC 1 -C 6 alkyl, -C 1 -C 6 alkyl-SC 1- C 6 alkyl, -C 1 -C 6 alkyl-NH-C 1 -C 6 alkyl or -C 1 -C 6 alkyl-N(C 1 -C 6 alkyl) 2 , where C The 1- C 6 alkyl group is optionally substituted by halogen (preferably F). Specific examples include but are not limited to -CH 2 OCH 3 , -CH 2 CH 2 OCH 3 , -CH 2 OCH 2 CH 3 , -CH 2 CH 2 OCH 2 CH 3 , -CH 2 NHCH 3 , -CH 2 N( CH 3 ) 2 , -CH 2 OCF 3 , -CH 2 CH 2 OCF 3 , -CH 2 OCH 2 CF 3 , -CH 2 NHCF 3 , -CH 2 N(CF 3 ) 2 and so on.
在一种式(I)化合物的实施方式中，R 3为-C 1-C 6烷基，优选C 1-C 3烷基，其任选被一个或多个独立地选自以下的基团取代：卤素、任选被卤素取代的C 3-C 7环烷基、R a、-OR a、-SR a或-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。 In one embodiment of the compound of formula (I), R 3 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, which is optionally selected by one or more groups independently selected from substituents: halogen, optionally halogen-substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or a plurality of halogen-substituted C 1 -C 6 alkyl, or are connected on the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
在具体的实施方式中，R 3为-C 1-C 6烷基，优选C 1-C 3烷基，任选被F、Cl、Br、I、R a或- OR a取代，其中R a为H或任选被一个或多个卤素(优选F)取代的C 1-C 3烷基。具体的实例包括但不限于甲基、乙基、丙基或异丙基、三氟甲基、三氟乙基、羟基甲基、羟基乙基、甲氧基甲基、甲氧基乙基、三氟甲氧基甲基或三氟甲氧基乙基等。在更具体的实施方案中，R 3为C 1-C 3烷基，例如甲基、乙基、丙基或异丙基。 In a specific embodiment, R 3 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted with F, Cl, Br, I, R a , or - substituted with OR a, wherein R a It is H or C 1 -C 3 alkyl optionally substituted with one or more halogens (preferably F). Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, trifluoromethyl, trifluoroethyl, hydroxymethyl, hydroxyethyl, methoxymethyl, methoxyethyl, Trifluoromethoxymethyl or trifluoromethoxyethyl, etc. In a more specific embodiment, R 3 is C 1 -C 3 alkyl, such as methyl, ethyl, propyl or isopropyl.
在具体的实施方式中，R 3为-C 1-C 6烷基，优选C 1-C 3烷基，任选被任选被卤素取代的C 3-C 7环烷基取代。具体的实例包括但不限于甲基、乙基、丙基或异丙基、环丙基甲基、环丙基乙基、环丁基甲基、环丁基乙基、环戊基甲基、环戊基乙基等。 In a specific embodiment, R 3 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted by C 3 -C 7 cycloalkyl optionally substituted by halogen. Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentyl Ethyl and so on.
在具体的实施方案中，R 3为-C 1-C 6烷基，优选C 1-C 3烷基，任选被-NR aR a取代，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 3烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。具体的实例包括但不限于甲基、乙基、丙基或异丙基、氨基甲基、氨基乙基、氨基丙基、甲基氨基甲基、二甲基氨基甲基、甲基乙基氨基甲基、氮杂环丁基甲基、吡咯烷基甲基、哌啶基甲基等。 In a specific embodiment, R 3 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted with -NR a R a, wherein R a is independently selected from H or optionally with one or more halogen substituted C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached. Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, aminomethyl, aminoethyl, aminopropyl, methylaminomethyl, dimethylaminomethyl, methylethylamino Methyl, azetidinyl methyl, pyrrolidinyl methyl, piperidinyl methyl, etc.
在一种式(I)化合物的实施方式中，R 3为-C 3-C 7环烷基，其任选被一个或多个独立地选自以下的基团取代：卤素、任选被卤素取代的C 3-C 7环烷基、R a、-OR a、-SR a或-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。在具体的实施方案中，R 3为-C 3-C 5环烷基，例如环丙基、环丁基或环戊基。 In one embodiment of the compound of formula (I), R 3 is -C 3 -C 7 cycloalkyl, which is optionally substituted with one or more groups independently selected from: halogen, optionally halogen substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 - C 6 alkyl, or are connected on the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached. In a specific embodiment, R 3 is -C 3 -C 5 cycloalkyl, such as cyclopropyl, cyclobutyl or cyclopentyl.
在具体的实施方式中，R 3为-C 3-C 7环烷基，任选被一个或多个独立地选自以下的基团取代：卤素、R a、、-OR a或-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 6烷基。具体的实例包括但不限于2,3-二氟环丙基、2,2,3,3-四氟环丙基、2,3-二氟环丁基、甲基环丙基或环丁基、二甲基环丙基或环丁基、三氟甲基环丙基或环丁基、羟基环丙基或环丁基、三氟甲氧基环丙基或环丁基、甲基氨基环丙基、二甲基氨基环丙基、三氟甲基氨基环丙基等。 In a specific embodiment, R 3 is -C 3 -C 7 cycloalkyl, optionally substituted with one or more groups independently selected from the following groups: halogen, R a ,, - OR a or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 6 alkyl. Specific examples include, but are not limited to, 2,3-difluorocyclopropyl, 2,2,3,3-tetrafluorocyclopropyl, 2,3-difluorocyclobutyl, methylcyclopropyl or cyclobutyl , Dimethylcyclopropyl or cyclobutyl, trifluoromethylcyclopropyl or cyclobutyl, hydroxycyclopropyl or cyclobutyl, trifluoromethoxycyclopropyl or cyclobutyl, methylamino ring Propyl, dimethylaminocyclopropyl, trifluoromethylaminocyclopropyl, etc.
在一种式(I)化合物的实施方式中，R 3为4-7元杂环烷基，其任选被一个或多个独立地选自以下的基团取代：卤素、R a、-OR a、-SR a或-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。在具体的实施方案中，R 3为4-7元杂环烷基，例如氮杂环丁烷基、氧杂环丁烷基、硫杂环丁基、吡咯烷基(例如1-吡咯烷基、2-吡咯烷基及3-吡咯烷基)、四氢呋喃基(例如1-四氢呋喃基、2-四氢呋喃基及3-四氢呋喃基)、四氢噻吩基(例如1-四氢噻吩基、2-四氢噻吩基及3-四氢噻吩基)、哌啶基(例如1-哌啶基、2-哌啶基、3-哌啶基及4-哌啶基)、四氢吡喃基(例如4-四氢吡喃基)、四氢噻喃基(例如4-四氢噻喃基)、吗啉基、硫吗啉基、二噁烷基或哌嗪基，其各自任选被一个或多个、例如1个、2个或3个独立地选自F、Cl、Br、I、R a、-OR a或-NR aR a的基团取代，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 3烷基。 In embodiments of the compounds (I) of formula, R 3 is 4-7-membered heterocycloalkyl, optionally substituted with one or more substituents independently selected from the following radicals: halogen, R a, -OR a, -SR a, or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 6 alkyl, or are connected on the same two N atoms R a may form a 4-7 membered nitrogen-containing heterocyclic group together with the N atom to which they are attached. In a specific embodiment, R 3 is 4-7 membered heterocycloalkyl, such as azetidinyl, oxetanyl, thietane, pyrrolidinyl (e.g., 1-pyrrolidinyl , 2-pyrrolidinyl and 3-pyrrolidinyl), tetrahydrofuranyl (e.g. 1-tetrahydrofuranyl, 2-tetrahydrofuranyl and 3-tetrahydrofuranyl), tetrahydrothienyl (e.g. 1-tetrahydrothienyl, 2-tetrahydrofuranyl) Hydrothienyl and 3-tetrahydrothienyl), piperidinyl (e.g. 1-piperidinyl, 2-piperidinyl, 3-piperidinyl and 4-piperidinyl), tetrahydropyranyl (e.g. 4 -Tetrahydropyranyl), tetrahydrothiopyranyl (for example 4-tetrahydrothiopyranyl), morpholinyl, thiomorpholinyl, dioxanyl or piperazinyl, each of which is optionally substituted by one or more one, e.g. 1, 2 or 3 substituents independently selected from F, Cl, Br, I, R a, -OR a substituted with -NR a R a or a group, wherein R a is independently selected from H or any Select C 1 -C 3 alkyl substituted with one or more halogens.
在一种式(I)化合物的实施方式中，R 3为-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 3烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。具体的实例包括但不限于-NH 2、-NHCH 3、-NCH 3CH 3、-N(CH 2CH 3)CH 3、-N(CH 2CH 3)(CH 2CH 3)-、-NHCF 3、-N(CH 3)CF 3、-N(CF 3)CF 3、-N(CH 2CF 3)CF 3或-N(CH 2CF 3)(CH 2CF 3)-、-NH(CH 2CH 2CH 3)、氮杂环丁基、吡咯烷基、哌啶基等。 In embodiments of the compounds (I) of formula in, R 3 is -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached. Specific examples include but are not limited to -NH 2 , -NHCH 3 , -NCH 3 CH 3 , -N(CH 2 CH 3 )CH 3 , -N(CH 2 CH 3 )(CH 2 CH 3 )-, -NHCF 3 , -N(CH 3 )CF 3 , -N(CF 3 )CF 3 , -N(CH 2 CF 3 )CF 3 or -N(CH 2 CF 3 )(CH 2 CF 3 )-, -NH( CH 2 CH 2 CH 3 ), azetidinyl, pyrrolidinyl, piperidinyl, etc.
在一种式(I)化合物的实施方式中，R 4选自-C 1-C 6烷基，优选C 1-C 3烷基，其任选被一个或多个独立地选自以下的基团取代：卤素、任选被卤素取代的C 3-C 7环烷基、R a、-OR a、-SR a或-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。 In one embodiment of the compound of formula (I), R 4 is selected from -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, which is optionally selected by one or more groups independently selected from group: halogen, optionally halogen-substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen substituted C 1 -C 6 alkyl, or are connected on the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached.
在具体的实施方式中，R 4为-C 1-C 6烷基，优选C 1-C 3烷基，任选被F、Cl、Br、I、R a或-OR a取代，其中R a为H或任选被一个或多个卤素(优选F)取代的C 1-C 3烷基。具体的实例包括但不限于甲基、乙基、丙基或异丙基、三氟甲基、三氟乙基、羟基甲基、羟基乙基、甲氧基甲基、甲氧基乙基、三氟甲氧基甲基或三氟甲氧基乙基等。在更具体的实施方案中，R 4为C 1-C 3烷基，例如甲基、乙基、丙基或异丙基。 In a particular embodiment, R 4 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted with F, Cl, Br, I, R a or -OR a, wherein R a It is H or C 1 -C 3 alkyl optionally substituted with one or more halogens (preferably F). Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, trifluoromethyl, trifluoroethyl, hydroxymethyl, hydroxyethyl, methoxymethyl, methoxyethyl, Trifluoromethoxymethyl or trifluoromethoxyethyl, etc. In a more specific embodiment, R 4 is C 1 -C 3 alkyl, such as methyl, ethyl, propyl, or isopropyl.
在具体的实施方式中，R 4为-C 1-C 6烷基，优选C 1-C 3烷基，任选被任选被卤素取代的C 3-C 7环烷基取代。具体的实例包括但不限于甲基、乙基、丙基或异丙基、环丙基甲基、环丙基乙基、环丁基甲基、环丁基乙基、环戊基甲基、环戊基乙基等。 In a specific embodiment, R 4 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted by C 3 -C 7 cycloalkyl optionally substituted by halogen. Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentyl Ethyl and so on.
在具体的实施方案中，R 4为-C 1-C 6烷基，优选C 1-C 3烷基，任选被-NR aR a取代，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 3烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。具体的实例包括但不限于甲基、乙基、丙基或异丙基、氨基甲基、氨基乙基、氨基丙基、甲基氨基甲基、二甲基氨基甲基、甲基乙基氨基甲基、氮杂环丁基甲基、吡咯烷基甲基、哌啶基甲基等。 In specific embodiments, R 4 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl, optionally substituted with -NR a R a, wherein R a is independently selected from H or optionally with one or more halogen substituted C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached. Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, aminomethyl, aminoethyl, aminopropyl, methylaminomethyl, dimethylaminomethyl, methylethylamino Methyl, azetidinyl methyl, pyrrolidinyl methyl, piperidinyl methyl, etc.
在一种式(I)化合物的实施方式中，R 4为-C 3-C 7环烷基，其任选被一个或多个独立地选自以下的基团取代：卤素、任选被卤素取代的C 3-C 7环烷基、R a、-OR a、-SR a或-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。在具体的实施方案中，R 4为-C 3-C 5环烷基，例如环丙基、环丁基或环戊基。 In one embodiment of the compound of formula (I), R 4 is -C 3 -C 7 cycloalkyl, which is optionally substituted with one or more groups independently selected from: halogen, optionally halogen substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 - C 6 alkyl, or are connected on the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached. In a specific embodiment, R 4 is -C 3 -C 5 cycloalkyl, such as cyclopropyl, cyclobutyl or cyclopentyl.
在具体的实施方式中，R 4为-C 3-C 7环烷基，任选被一个或多个独立地选自以下的基团取代：卤素、R a、-OR a或-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 6烷基。具体的实例包括但不限于2,3-二氟环丙基、2,2,3,3-四氟环丙基、2,3-二氟环丁基、甲基环丙基或环丁基、二甲基环丙基或环丁基、三氟甲基环丙基或环丁基、羟基环丙基或环丁基、三氟甲氧基环丙基或环丁基、甲基氨基环丙基、二甲基氨基环丙基、三氟甲基氨基环丙基等。 In a particular embodiment, R 4 is -C 3 -C 7 cycloalkyl, optionally substituted with one or more substituents independently selected from the following radicals: halogen, R a, -OR a or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 6 alkyl. Specific examples include, but are not limited to, 2,3-difluorocyclopropyl, 2,2,3,3-tetrafluorocyclopropyl, 2,3-difluorocyclobutyl, methylcyclopropyl or cyclobutyl , Dimethylcyclopropyl or cyclobutyl, trifluoromethylcyclopropyl or cyclobutyl, hydroxycyclopropyl or cyclobutyl, trifluoromethoxycyclopropyl or cyclobutyl, methylamino ring Propyl, dimethylaminocyclopropyl, trifluoromethylaminocyclopropyl, etc.
在一种式(I)化合物的实施方式中，R 4为4-7元杂环烷基，其任选被一个或多个独立地选自以下的基团取代：卤素、R a、-OR a、-SR a或-NR aR a，其中R a独立地选自H或任选被一个或 多个卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。在具体的实施方案中，R 4为4-7元杂环烷基，例如氮杂环丁烷基、氧杂环丁烷基、硫杂环丁基、吡咯烷基(例如1-吡咯烷基、2-吡咯烷基及3-吡咯烷基)、四氢呋喃基(例如1-四氢呋喃基、2-四氢呋喃基及3-四氢呋喃基)、四氢噻吩基(例如1-四氢噻吩基、2-四氢噻吩基及3-四氢噻吩基)、哌啶基(例如1-哌啶基、2-哌啶基、3-哌啶基及4-哌啶基)、四氢吡喃基(例如4-四氢吡喃基)、四氢噻喃基(例如4-四氢噻喃基)、吗啉基、硫吗啉基、二噁烷基或哌嗪基，其各自任选被一个或多个、例如1个、2个或3个独立地选自F、Cl、Br、I、R a、-OR a或-NR aR a的基团取代，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 3烷基。 In embodiments of the compounds (I) of formula, R 4 is 4-7 membered heterocycloalkyl, optionally substituted with one or more substituents independently selected from the following radicals: halogen, R a, -OR a, -SR a, or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 6 alkyl, or are connected on the same two N atoms R a may form a 4-7 membered nitrogen-containing heterocyclic group together with the N atom to which they are attached. In specific embodiments, R 4 is 4-7 membered heterocycloalkyl, such as azetidinyl, oxetanyl, thietane, pyrrolidinyl (e.g., 1-pyrrolidinyl , 2-pyrrolidinyl and 3-pyrrolidinyl), tetrahydrofuranyl (e.g. 1-tetrahydrofuranyl, 2-tetrahydrofuranyl and 3-tetrahydrofuranyl), tetrahydrothienyl (e.g. 1-tetrahydrothienyl, 2-tetrahydrofuranyl) Hydrothienyl and 3-tetrahydrothienyl), piperidinyl (e.g. 1-piperidinyl, 2-piperidinyl, 3-piperidinyl and 4-piperidinyl), tetrahydropyranyl (e.g. 4 -Tetrahydropyranyl), tetrahydrothiopyranyl (for example 4-tetrahydrothiopyranyl), morpholinyl, thiomorpholinyl, dioxanyl or piperazinyl, each of which is optionally substituted by one or more one, e.g. 1, 2 or 3 substituents independently selected from F, Cl, Br, I, R a, -OR a substituted with -NR a R a or a group, wherein R a is independently selected from H or any Select C 1 -C 3 alkyl substituted with one or more halogens.
在一种式(I)化合物的实施方式中，R 4为任选被C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基取代的氨基。在具体的实施方案中，氨基上取代的C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基各自具有以上实施方式中对作为R 4的C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基所定义的各具体实施方式或具体的实例。在最具体的实施方式中，R 4为被任选被卤素取代的C 1-C 6烷基取代的氨基，具体的实例包括但不限于-NH 2、-NHCH 3、-NCH 3CH 3、-N(CH 2CH 3)CH 3、-N(CH 2CH 3)(CH 2CH 3)-、-NHCF 3、-N(CH 3)CF 3、-N(CF 3)CF 3、-N(CH 2CF 3)CF 3或-N(CH 2CF 3)(CH 2CF 3)-、-NH(CH 2CH 2CH 3)、氮杂环丁基、吡咯烷基、哌啶基等。 In one embodiment of the compound of formula (I), R 4 is an amino group optionally substituted with C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl, or 4-7 membered heterocycloalkyl. In a specific embodiment, the substituted amino C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl having each of the above embodiments as R C 4 l - Each specific embodiment or specific example defined by C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl. In the most specific embodiment, R 4 is an amino group substituted with a C 1 -C 6 alkyl group optionally substituted by halogen. Specific examples include, but are not limited to, -NH 2 , -NHCH 3 , -NCH 3 CH 3 , -N(CH 2 CH 3 )CH 3 , -N(CH 2 CH 3 )(CH 2 CH 3 )-, -NHCF 3 , -N(CH 3 )CF 3 , -N(CF 3 )CF 3 ,- N(CH 2 CF 3 )CF 3 or -N(CH 2 CF 3 )(CH 2 CF 3 )-, -NH(CH 2 CH 2 CH 3 ), azetidinyl, pyrrolidinyl, piperidinyl Wait.
在一种式(I)化合物的实施方式中，R 5和R 6各自独立地选自卤素，例如F、Cl、Br、I。 In one embodiment of the compound of formula (I), R 5 and R 6 are each independently selected from halogens, such as F, Cl, Br, I.
在一种式(I)化合物的实施方式中，R 5和R 6各自独立地选自任选被卤素取代的C 1-C 6烷基。在具体的实施方式中，R 5和R 6各自独立地选自被至少三个卤素取代的C 1-C 3烷基。在更具体的实施方式中，R 5和R 6各自独立地选自被三个氟取代的C 1-C 3烷基，具体的实例包括但不限于三氟甲基、三氟乙基、五氟乙基等。在最具体的实施方式中，R 5和R 6均为-CF 3。 In one embodiment of the compound of formula (I), R 5 and R 6 are each independently selected from C 1 -C 6 alkyl optionally substituted with halogen. In a specific embodiment, R 5 and R 6 are each independently selected from C 1 -C 3 alkyl substituted with at least three halogens. In a more specific embodiment, R 5 and R 6 are each independently selected from C 1 -C 3 alkyl substituted by three fluorines. Specific examples include, but are not limited to, trifluoromethyl, trifluoroethyl, penta Fluoroethyl and so on. In the most specific embodiment, both R 5 and R 6 are -CF 3 .
在一种式(I)化合物的实施方式中，m和p均为0。在具体的实施方式中，m为0且p为1。在另一个具体的实施方式中，m为0且p为2。在另一个具体的实施方式中，m为1且p为0。在另一个具体的实施方式中，m为1且p为1。在另一个具体的实施方式中，m为1且p为2。在另一个具体的实施方式中，m为2且p为0。在另一个具体的实施方式中，m为2且p为1。在另一个具体的实施方式中，m为2且p为2。In one embodiment of the compound of formula (I), both m and p are zero. In a specific embodiment, m is 0 and p is 1. In another specific embodiment, m is 0 and p is 2. In another specific embodiment, m is 1 and p is 0. In another specific embodiment, m is 1 and p is 1. In another specific embodiment, m is 1 and p is 2. In another specific embodiment, m is 2 and p is 0. In another specific embodiment, m is 2 and p is 1. In another specific embodiment, m is 2 and p is 2.
需要说明的是，本发明的式(I)化合物涵盖以上各个独立的实施方式或各个具体实施方式，还涵盖上述各个实施方式或具体实施方式的任何组合或亚组合构成的实施方式，也涵盖以上任何优选或例举的任何组合所构成的实施方式。It should be noted that the compound of formula (I) of the present invention covers each of the above independent embodiments or each specific embodiment, as well as any combination or sub-combination of each of the above embodiments or specific embodiments, and also encompasses the above An embodiment constituted by any preferred or exemplified combination.
优选地，本发明提供式(I)化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物：Preferably, the present invention provides a compound of formula (I), its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate:
Figure PCTCN2021093788-appb-000006
Figure PCTCN2021093788-appb-000006
其中：in:
R 1和R 2各自独立地选自氢、卤素或C 1-C 6烷基，其中所述C 1-C 6烷基任选被卤素取代； R 1 and R 2 are each independently selected from hydrogen, halogen or C 1 -C 6 alkyl, wherein the C 1 -C 6 alkyl is optionally substituted by halogen;
R 3选自H、-C 1-C 6烷基、-C 3-C 7环烷基或-NR aR a，其中C 1-C 6烷基或C 3-C 7环烷基任选被独立地选自以下的取代基取代：卤素、任选被卤素取代的C 3-C 7环烷基、R a、-OR a、-SR a或-NR aR a； R 3 is selected from H, -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl or -NR a R a, wherein C 1 -C 6 alkyl or C 3 -C 7 cycloalkyl optionally independently selected from the following substituents: halogen, optionally halogen-substituted C 3 -C 7 cycloalkyl, R a, -OR a, -SR a , or -NR a R a;
R 4选自-C 1-C 6烷基或-NR aR a，其中所述C 1-C 6烷基任选被各自独立地选自以下的取代基取代：R a、卤素或-NR aR a： R 4 is selected from -C 1 -C 6 alkyl or -NR a R a, wherein said C 1 -C 6 alkyl is optionally independently substituted with substituents selected from: R a, halogen or -NR a R a :
R a选自H或任选被卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基； R a is selected from H or an optionally halogen-substituted C 1 -C 6 alkyl, or are connected on the same N atom may form two R a 4-7 membered nitrogen-containing together with the N atom to which they are attached, Cycloalkyl
R 5和R 6各自独立地选自卤素或任选被卤素取代的C 1-C 6烷基； R 5 and R 6 are each independently selected from halogen or C 1 -C 6 alkyl optionally substituted by halogen;
m和p各自独立地选自0、1或2，且m and p are each independently selected from 0, 1, or 2, and
n选自0或1。n is selected from 0 or 1.
在一种上述优选式(I)化合物的具体实施方式中，R 1和R 2各自独立地选自氢或卤素，例如F、Cl、Br、I。在一个具体的实施方式中，R 1和R 2均为H。在一个具体的实施方式中，R 1为H且R 2为卤素。在一个具体的实施方式中，R 1为卤素且R 2为H。在一个具体的实施方式中，R 1和R 2均为卤素，二者可以相同或不同。 In a specific embodiment of the above-mentioned preferred compound of formula (I), R 1 and R 2 are each independently selected from hydrogen or halogen, such as F, Cl, Br, I. In a specific embodiment, both R 1 and R 2 are H. In a specific embodiment, R 1 is H and R 2 is halogen. In a specific embodiment, R 1 is halogen and R 2 is H. In a specific embodiment, R 1 and R 2 are both halogen, and the two may be the same or different.
在一种上述优选式(I)化合物的具体实施方式中，R 3为-C 1-C 3烷基，任选被独立地选自以下的取代基取代：H、卤素或任选被卤素取代的C 3-C 7环烷基。具体的实例包括但不限于甲基、乙基、丙基或异丙基、三氟甲基、三氟乙基、环丙基甲基、环丙基乙基、环丁基甲基、环丁基乙基、环戊基甲基、环戊基乙基等。 In a specific embodiment of the above-mentioned preferred compound of formula (I), R 3 is -C 1 -C 3 alkyl, optionally substituted with a substituent independently selected from: H, halogen or optionally substituted by halogen的C 3 -C 7 cycloalkyl. Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, trifluoromethyl, trifluoroethyl, cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl Group, cyclopentylmethyl, cyclopentylethyl, etc.
在更具体的实施方式中，R 3为-C 1-C 3烷基，例如甲基、乙基、丙基或异丙基。 In a more specific embodiment, R 3 is -C 1 -C 3 alkyl, such as methyl, ethyl, propyl or isopropyl.
在更具体的实施方式中，R 3为-C 1-C 3烷基，被-NR aR a取代，其中R a选自H或任选被卤素取代的C 1-C 3烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。具体的实例包括但不限于氨基甲基、氨基乙基、氨基丙基、甲基氨基甲基、二甲基氨基甲基、甲基乙基氨基甲基、氮杂环丁基甲基、吡咯烷基甲基、哌啶基甲基等。 In a more specific embodiment, R 3 is -C 1 -C 3 alkyl, substituted -NR a R a, wherein R a is selected from H or optionally halogen-substituted C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached. Specific examples include, but are not limited to, aminomethyl, aminoethyl, aminopropyl, methylaminomethyl, dimethylaminomethyl, methylethylaminomethyl, azetidinylmethyl, pyrrolidinylmethyl , Piperidinyl methyl, etc.
在一种上述优选式(I)化合物的实施方式中，R 3为-C 3-C 7环烷基，其任选被独立地选自以下的基团取代：卤素、R a或-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 3烷基。具体的实例包括但不限于2,3-二氟环丙基、2,2,3,3-四氟环丙基、2,3-二氟环丁基、甲基环丙基或环丁基、二甲基环丙基或环丁基、三氟甲基环丙基或环丁基、甲基氨基环丙基、二甲基氨基环丙基、三氟甲基氨基环丙基等。 In the embodiment above preferred embodiment a compound of formula (I) is, R 3 is -C 3 -C 7 cycloalkyl, which is optionally substituted independently selected from the following groups: halogen, R a, or -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 3 alkyl. Specific examples include, but are not limited to, 2,3-difluorocyclopropyl, 2,2,3,3-tetrafluorocyclopropyl, 2,3-difluorocyclobutyl, methylcyclopropyl or cyclobutyl , Dimethylcyclopropyl or cyclobutyl, trifluoromethylcyclopropyl or cyclobutyl, methylaminocyclopropyl, dimethylaminocyclopropyl, trifluoromethylaminocyclopropyl, etc.
在更具体的实施方案中，R 3为-C 3-C 5环烷基，例如环丙基、环丁基或环戊基。 In a more specific embodiment, R 3 is -C 3 -C 5 cycloalkyl, such as cyclopropyl, cyclobutyl, or cyclopentyl.
在一种上述优选式(I)化合物的实施方式中，R 3为-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 3烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。具体的实例包括但不限于-NH 2、-NHCH 3、-NCH 3CH 3、-N(CH 2CH 3)CH 3、-N(CH 2CH 3)(CH 2CH 3)-、-NHCF 3、-N(CH 3)CF 3、-N(CF 3)CF 3、-N(CH 2CF 3)CF 3或-N(CH 2CF 3)(CH 2CF 3)-、-NH(CH 2CH 2CH 3)、氮杂环丁基、吡咯烷基、哌啶基等。 In the embodiment above preferred embodiment a compound of formula (I) is, R 3 is -NR a R a, wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 3 alkyl or connected to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached. Specific examples include but are not limited to -NH 2 , -NHCH 3 , -NCH 3 CH 3 , -N(CH 2 CH 3 )CH 3 , -N(CH 2 CH 3 )(CH 2 CH 3 )-, -NHCF 3 , -N(CH 3 )CF 3 , -N(CF 3 )CF 3 , -N(CH 2 CF 3 )CF 3 or -N(CH 2 CF 3 )(CH 2 CF 3 )-, -NH( CH 2 CH 2 CH 3 ), azetidinyl, pyrrolidinyl, piperidinyl, etc.
在一种上述优选式(I)化合物的实施方式中，R 4为-C 1-C 3烷基，任选被卤素取代。具体的实例包括但不限于甲基、乙基、丙基或异丙基、三氟甲基、三氟乙基、五氟乙基等。 In one of the above embodiments of the preferred compound of formula (I), R 4 is -C 1 -C 3 alkyl, optionally substituted by halogen. Specific examples include, but are not limited to, methyl, ethyl, propyl or isopropyl, trifluoromethyl, trifluoroethyl, pentafluoroethyl, and the like.
在更具体的实施方式中，R 4为-C 1-C 3烷基，例如甲基、乙基、丙基或异丙基。 In a more specific embodiment, R 4 is -C 1 -C 3 alkyl, such as methyl, ethyl, propyl or isopropyl.
在更具体的实施方式中，R 4为-C 1-C 3烷基，被-NR aR a取代，其中R a选自H或任选被卤素取代的C 1-C 3烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。具体的实例包括但不限于氨基甲基、氨基乙基、氨基丙基、甲基氨基甲基、二甲基氨基甲基、甲基乙基氨基甲基、氮杂环丁基甲基、吡咯烷基甲基、哌啶基甲基等。 In a more specific embodiment, R 4 is -C 1 -C 3 alkyl, substituted -NR a R a, wherein R a is selected from H or optionally halogen-substituted C 1 -C 3 alkyl, or attached to the same N atom may be two R a 4-7 membered nitrogen-containing heterocyclic group formed together with the N atom to which they are attached. Specific examples include, but are not limited to, aminomethyl, aminoethyl, aminopropyl, methylaminomethyl, dimethylaminomethyl, methylethylaminomethyl, azetidinylmethyl, pyrrolidinylmethyl , Piperidinyl methyl, etc.
在一种上述优选式(I)化合物的实施方式中，R 4为-NR aR a，其中R a选自H或任选被卤素取代的C 1-C 3烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基。具体的实例包括但不限于-NH 2、-NHCH 3、-NCH 3CH 3、-N(CH 2CH 3)CH 3、-N(CH 2CH 3)(CH 2CH 3)-、-NHCF 3、-N(CH 3)CF 3、-N(CF 3)CF 3、-N(CH 2CF 3)CF 3或-N(CH 2CF 3)(CH 2CF 3)-、-NH(CH 2CH 2CH 3)、氮杂环丁基、吡咯烷基、哌啶基等。 In the embodiment above preferred embodiment a compound of formula (I), R 4 is is -NR a R a, wherein R a is selected from H or an optionally halogen-substituted C 1 -C 3 alkyl, or connected to the same the two R a N atom may form a 4-7 membered nitrogen-containing heterocyclic group together with the N atom to which they are attached. Specific examples include but are not limited to -NH 2 , -NHCH 3 , -NCH 3 CH 3 , -N(CH 2 CH 3 )CH 3 , -N(CH 2 CH 3 )(CH 2 CH 3 )-, -NHCF 3 , -N(CH 3 )CF 3 , -N(CF 3 )CF 3 , -N(CH 2 CF 3 )CF 3 or -N(CH 2 CF 3 )(CH 2 CF 3 )-, -NH( CH 2 CH 2 CH 3 ), azetidinyl, pyrrolidinyl, piperidinyl, etc.
在一种上述优选式(I)化合物的实施方式中，R 5和R 6各自独立地选自被卤素取代的C 1-C 3烷基。在更具体的实施方式中，R 5和R 6各自独立地选自被至少三个卤素取代的C 1-C 3烷基。在更具体的实施方式中，R 5和R 6各自独立地被至少三个F取代的C 1-C 3烷基。具体的实例包括但不限于三氟甲基、三氟乙基、五氟乙基等。在最具体的实施方式中，R 5和R 6均为-CF 3。 In one embodiment of the above-mentioned preferred compound of formula (I), R 5 and R 6 are each independently selected from C 1 -C 3 alkyl substituted by halogen. In a more specific embodiment, R 5 and R 6 are each independently selected from C 1 -C 3 alkyl substituted with at least three halogens. In a more specific embodiment, R 5 and R 6 are each independently C 1 -C 3 alkyl substituted with at least three F. Specific examples include, but are not limited to, trifluoromethyl, trifluoroethyl, pentafluoroethyl, and the like. In the most specific embodiment, both R 5 and R 6 are -CF 3 .
需要说明的是，上述优选式(I)化合物涵盖各个独立的实施方式或各个具体实施方式，还涵盖其上述各个实施方式或具体实施方式的任何组合或亚组合构成的实施方式。It should be noted that the above-mentioned preferred compounds of formula (I) cover each independent embodiment or each specific embodiment, as well as any combination or sub-combination of each of the above-mentioned embodiments or specific embodiments.
本发明化合物的优选具体实施方式包括以下化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，Preferred embodiments of the compounds of the present invention include the following compounds, their stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates,
Figure PCTCN2021093788-appb-000007
Figure PCTCN2021093788-appb-000007
本发明的有益效果The beneficial effects of the present invention
本发明提供了一类具有通式(I)结构的联芳基类化合物，经研究发现，该类化合物可有效抑制RORγt蛋白受体，从而调控Th17细胞的分化，抑制IL-17的产生，可作为免疫调节剂用于Th17细胞分化相关类疾病的治疗药物。The present invention provides a class of biaryl compounds with the structure of general formula (I). It has been found through research that this class of compounds can effectively inhibit the RORγt protein receptor, thereby regulating the differentiation of Th17 cells and inhibiting the production of IL-17. As an immunomodulator for the treatment of diseases related to Th17 cell differentiation.
本发明的化合物具有下列有益效果：The compound of the present invention has the following beneficial effects:
对RORγt受体有高的抑制活性；It has high inhibitory activity on RORγt receptor;
调控Th17细胞的分化，抑制IL-17的产生；和/或Regulate the differentiation of Th17 cells and inhibit the production of IL-17; and/or
具有良好的药物代谢动力学性质，例如具有更长的t 1/2，从而例如可以加大给药间隔，更长的半衰期，使患者具有更好的依从性； It has good pharmacokinetic properties, such as a longer t 1/2 , so that, for example, the dosing interval can be increased, the half-life is longer, and the patient has better compliance;
具有改善的AUC0-last数据，具有更好的成药性，更高的生物利用度；和/或Have improved AUC0-last data, better druggability, and higher bioavailability; and/or
良好的安全性，如透膜性、P450(减少的药物相互作用风险)、溶解性等优异的性质。Good safety, such as membrane permeability, P450 (reduced risk of drug interaction), solubility and other excellent properties.
用于治疗或用作药物的本发明化合物Compounds of the invention for treatment or as medicine
一方面，本发明提供用作药物、尤其是用作RORγt抑制剂的本发明化合物。In one aspect, the invention provides compounds of the invention for use as drugs, especially as RORγt inhibitors.
另一方面，本发明提供用于治疗、尤其是用于治疗和/或预防与RORγt有关疾病的本发明化合物。In another aspect, the present invention provides compounds of the present invention for the treatment, especially for the treatment and/or prevention of diseases related to RORγt.
在具体的实施方式中，本发明提供用于治疗和/或预防RORγt对所述疾病的发生和发展起到促进作用或抑制RORγt将降低疾病的发生率、减少或消除疾病病状的疾病的本发明化合物，所述疾病例如炎症或自身免疫性疾病、癌症等，包括但不限于银屑病、类风湿性关节炎、银屑病性关节炎、强直性脊柱炎、多发性硬化、系统性红斑狼疮、移植物抗宿主疾病、炎症性肠病、克隆氏病、溃疡性结肠炎、慢性阻塞性肺病、哮喘、血管球性肾炎、狼疮性肾炎、心肌炎、甲状腺炎、干眼症、葡萄膜炎、白塞病、过敏性皮肤炎、粉刺、硬皮病、支气管炎、皮肌过敏性鼻炎、坏死性小肠结肠炎、肝纤维化、非酒精性脂肪性肝炎(NASH)、新冠病毒肺炎、胰岛素依赖性I型糖尿病、三阴乳腺癌和前列腺癌等。In a specific embodiment, the present invention provides the present invention for treating and/or preventing RORγt to promote the occurrence and development of the disease or inhibiting RORγt will reduce the incidence of the disease, reduce or eliminate the disease symptoms of the disease. Compounds, the diseases such as inflammation or autoimmune diseases, cancer, etc., including but not limited to psoriasis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, multiple sclerosis, systemic lupus erythematosus , Graft versus host disease, inflammatory bowel disease, Crohn’s disease, ulcerative colitis, chronic obstructive pulmonary disease, asthma, glomerulonephritis, lupus nephritis, myocarditis, thyroiditis, dry eye, uveitis, Behcet's disease, allergic dermatitis, acne, scleroderma, bronchitis, dermatomuscular allergic rhinitis, necrotizing enterocolitis, liver fibrosis, non-alcoholic steatohepatitis (NASH), new coronavirus pneumonia, insulin dependence Type I diabetes, triple-negative breast cancer and prostate cancer.
药物组合物及其施用Pharmaceutical composition and its administration
另一方面，为了使用本说明书的化合物用于治疗或预防目的，可以将本发明化合物根据标准药学实践配制为药物组合物。同时，基于本发明化合物良好的药物代谢动力学性质、改善的AUC0-last、良好的成药性，由本发明化合物可制备具有更好的药动学性质、更高生物利用度的药物。On the other hand, in order to use the compound of the present specification for therapeutic or preventive purposes, the compound of the present invention can be formulated into a pharmaceutical composition according to standard pharmaceutical practice. At the same time, based on the good pharmacokinetic properties, improved AUC0-last, and good druggability of the compound of the present invention, drugs with better pharmacokinetic properties and higher bioavailability can be prepared from the compound of the present invention.
因此，本发明提供一种药物组合物，其包含上述本发明化合物和药学可接受的赋形剂。Therefore, the present invention provides a pharmaceutical composition comprising the above-mentioned compound of the present invention and a pharmaceutically acceptable excipient.
在一个具体的实施方式中，提供了所述本发明的药物组合物，用于在哺乳动物如人受试者中预防或治疗与RORγt有关的疾病。In a specific embodiment, the pharmaceutical composition of the present invention is provided for use in the prevention or treatment of diseases related to RORγt in mammals such as human subjects.
在一个具体的实施方式中，本发明的药物组合物可以另外包含适合与本发明化合物组合使用的另外的治疗活性成分。在另一个具体的实施方式中，所述另外的治疗剂如本文对药物组合所定义。In a specific embodiment, the pharmaceutical composition of the present invention may additionally contain additional therapeutically active ingredients suitable for use in combination with the compound of the present invention. In another specific embodiment, the additional therapeutic agent is as defined herein for the drug combination.
本发明的药物组合物可以通过本领域技术人员已知的技术来配制，如在Remington’s Pharmaceutical Sciences第20版中公开的技术。例如，上述本发明的药物组合物，可以通过将本发明化合物与一种或多种药学可接受的赋形剂混合来制备。制备可进一步包括将一种或多种其它活性成分与本发明化合物和一种或多种药学可接受的赋形剂混合的步骤。The pharmaceutical composition of the present invention can be formulated by techniques known to those skilled in the art, such as the technique disclosed in Remington's Pharmaceutical Sciences 20th Edition. For example, the above-mentioned pharmaceutical composition of the present invention can be prepared by mixing the compound of the present invention with one or more pharmaceutically acceptable excipients. The preparation may further include the step of mixing one or more other active ingredients with the compound of the present invention and one or more pharmaceutically acceptable excipients.
选择包含在特定组合物中的赋形剂将取决于多种因素、例如给药方式和所提供的组合物的形式。合适的药学可接受的赋形剂是本领域技术人员熟知的且描述于例如Ansel,Howard C.,等,Ansel’s Pharmaceutical Dosage Forms and Drug Delivery Systems.Philadelphia:Lippincott,Williams&Wilkins,2004中，包括例如佐剂、稀释剂(例如葡萄糖、乳糖或甘露醇)、载体、pH 调节剂、缓冲剂、甜味剂、填充剂、稳定剂、表面活性剂、润湿剂、润滑剂、乳化剂、悬浮剂、防腐剂、抗氧化剂、遮光剂、助流剂、加工助剂、着色剂、加香剂、调味剂、其它已知添加剂。The choice of excipients included in a particular composition will depend on various factors, such as the mode of administration and the form of the provided composition. Suitable pharmaceutically acceptable excipients are well known to those skilled in the art and are described in, for example, Ansel, Howard C., etc., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems. Philadelphia: Lippincott, Williams & Wilkins, 2004, including, for example, adjuvants , Diluents (such as glucose, lactose or mannitol), carriers, pH adjusters, buffers, sweeteners, fillers, stabilizers, surfactants, wetting agents, lubricants, emulsifiers, suspending agents, preservatives Agents, antioxidants, sunscreens, glidants, processing aids, coloring agents, flavoring agents, flavoring agents, and other known additives.
本发明的药物组合物可以以标准方式施用。例如，合适的施用方式包括口服、静脉内、直肠、肠胃外、局部、经皮、眼、鼻、颊或肺(吸入)给药，其中肠胃外输注包括肌肉、静脉内、动脉内、腹膜内或皮下施用。为了这些目的，本发明的化合物可以通过本领域已知的方法配制成例如片剂、胶囊、糖浆、粉末、颗粒、水性或油性溶液或悬浮液、(脂质)乳剂、可分散粉末、栓剂、软膏、乳膏、滴剂、气溶胶、干粉制剂和无菌可注射水性或油性溶液或悬浮液的形式。The pharmaceutical composition of the present invention can be administered in a standard manner. For example, suitable modes of administration include oral, intravenous, rectal, parenteral, topical, transdermal, ocular, nasal, buccal, or pulmonary (inhalation) administration, where parenteral infusion includes intramuscular, intravenous, intraarterial, and peritoneal Intra or subcutaneous administration. For these purposes, the compounds of the present invention can be formulated into tablets, capsules, syrups, powders, granules, aqueous or oily solutions or suspensions, (lipid) emulsions, dispersible powders, suppositories, etc., by methods known in the art. Ointments, creams, drops, aerosols, dry powder preparations and sterile injectable aqueous or oily solutions or suspensions.
本发明化合物的预防或治疗剂量的大小将根据一系列因素而变化，包括所治疗的个体、病症或病况的严重性、给药的速率、化合物的处置及处方医师的判断。一般而言，有效剂量在每日每kg体重约0.0001至约5000mg，例如约0.01至约1000mg/kg/日(单次或分次给药)。对70kg的人而言，这会合计为约0.007mg/日至约7000mg/日，例如约0.7mg/日至约1500mg/日。根据给药模式，本发明化合物在药物组合物中的含量或用量可以是约0.01mg至约1000mg，适合地是0.1-500mg，优选0.5-300mg，更优选1-150mg，特别优选1-50mg，例如1.5mg、2mg、4mg、10mg、25mg等；相应地，本发明的药物组合物将包含0.05至99％w/w(重量百分比)，例如0.05至80％w/w，例如0.10至70％w/w，例如0.10至50％w/w的本发明化合物，所有重量百分比均基于总组合物。应当理解，可能有必要在某些情况下使用超出这些限制的剂量。The size of the preventive or therapeutic dose of the compound of the present invention will vary according to a series of factors, including the individual being treated, the severity of the disorder or condition, the rate of administration, the treatment of the compound, and the judgment of the prescribing physician. Generally, the effective dose is about 0.0001 to about 5000 mg per kg body weight per day, for example, about 0.01 to about 1000 mg/kg/day (single or divided administration). For a 70 kg person, this would add up to about 0.007 mg/day to about 7000 mg/day, for example, about 0.7 mg/day to about 1500 mg/day. Depending on the mode of administration, the content or amount of the compound of the present invention in the pharmaceutical composition may be about 0.01 mg to about 1000 mg, suitably 0.1-500 mg, preferably 0.5-300 mg, more preferably 1-150 mg, particularly preferably 1-50 mg, For example, 1.5 mg, 2 mg, 4 mg, 10 mg, 25 mg, etc.; correspondingly, the pharmaceutical composition of the present invention will contain 0.05 to 99% w/w (weight percentage), such as 0.05 to 80% w/w, such as 0.10 to 70% w/w, for example 0.10 to 50% w/w of the compound of the invention, all weight percentages are based on the total composition. It should be understood that it may be necessary in some cases to use dosages that exceed these limits.
在一种具体实施方式中，本发明提供了一种药物组合物，其包含本发明化合物和一种或多种药学可接受的赋形剂，该组合物被配制用于口服施用。该组合物可以以单位剂型提供，例如以片剂、胶囊或口服液体制剂的形式。这样的单位剂型可以含有0.1mg至1g，例如5mg至250mg的本发明化合物作为活性成分。In a specific embodiment, the present invention provides a pharmaceutical composition comprising a compound of the present invention and one or more pharmaceutically acceptable excipients, the composition being formulated for oral administration. The composition may be provided in unit dosage form, for example in the form of a tablet, capsule or oral liquid preparation. Such a unit dosage form may contain 0.1 mg to 1 g, for example 5 mg to 250 mg, of the compound of the present invention as an active ingredient.
在一种具体实施方式中，本发明提供了一种药物组合物，其包含本发明化合物和一种或多种药学可接受的赋形剂，该组合物被配制用于局部施用。局部施用可以是以例如乳膏剂、洗剂、软膏剂或透皮贴剂的形式。In a specific embodiment, the present invention provides a pharmaceutical composition comprising a compound of the present invention and one or more pharmaceutically acceptable excipients, the composition being formulated for topical administration. Topical application may be in the form of, for example, a cream, lotion, ointment, or transdermal patch.
在一种具体实施方式中，本发明提供了一种药物组合物，其包含本发明化合物和一种或多种药学可接受的赋形剂，该组合物被配制用于吸入施用。吸入施用可以通过口服吸入，也可以通过鼻内施用。当通过口服吸入施用时，本发明的化合物可以以每日剂量有效地用于本发明，例如至多500μg，如0.1-50μg、0.1-40μg、0.1-30μg、0.1-20μg或0.1-10μg的本发明化合物。口服吸入的本发明药物组合物可以配制成干粉、悬浮液(在液体或气体中)或溶液(在液体中)，且可以以任何合适的形式和使用任何本领域已知的合适的吸入器装置施用，包括例如定量吸入器(MDI)、干粉吸入器(DPI)、喷雾器和软雾吸入器。多室装置可用于递送本说明书的化合物和一种或多种其它活性成分(当存在时)。In a specific embodiment, the present invention provides a pharmaceutical composition comprising a compound of the present invention and one or more pharmaceutically acceptable excipients, the composition being formulated for inhalation administration. The inhalation administration can be by oral inhalation or intranasal administration. When administered by oral inhalation, the compound of the present invention can be effectively used in the present invention in a daily dose, for example, up to 500 μg, such as 0.1-50 μg, 0.1-40 μg, 0.1-30 μg, 0.1-20 μg, or 0.1-10 μg of the present invention Compound. The pharmaceutical composition of the present invention for oral inhalation can be formulated as a dry powder, suspension (in liquid or gas) or solution (in liquid), and can be in any suitable form and using any suitable inhaler device known in the art Administration includes, for example, metered-dose inhalers (MDI), dry powder inhalers (DPI), nebulizers, and soft mist inhalers. Multi-chamber devices can be used to deliver the compounds of the specification and one or more other active ingredients (when present).
治疗方法和用途Treatment methods and uses
基于上述本发明化合物具有的有益效果，本发明化合物可用于治疗动物，特别是哺乳动物例如人的各种病症的方法中。Based on the aforementioned beneficial effects of the compounds of the present invention, the compounds of the present invention can be used in methods for treating various diseases in animals, especially mammals such as humans.
因此，另一方面，本发明提供了调节、尤其是抑制RORγt活性的方法，所述方法包括使细胞与如前所述的本发明化合物相接触以调节、尤其是抑制细胞中RORγt的活性。Therefore, in another aspect, the present invention provides a method of modulating, especially inhibiting RORγt activity, which method comprises contacting a cell with a compound of the present invention as described above to modulate, especially inhibiting, the activity of RORγt in the cell.
另一方面，本发明提供了预防或治疗与RORγt相关的疾病(例如通过RORγt抑制可治疗或预防的疾病)的方法，所述方法包括向需要其的个体施用有效量的如前所述的本发明化合物或包含其的本发明药物组合物。In another aspect, the present invention provides a method for preventing or treating diseases related to RORγt (for example, diseases treatable or preventable by RORγt inhibition), the method comprising administering to an individual in need thereof an effective amount of the above-mentioned present The compound of the invention or the pharmaceutical composition of the invention containing it.
另一方面，本发明提供了如前所述的本发明化合物或包含其的药物组合物的用途，用于抑制RORγt活性，或者用于治疗和/或预防与RORγt相关的疾病、例如通过RORγt抑制可治疗或预防的疾病。On the other hand, the present invention provides the use of the compound of the present invention or a pharmaceutical composition containing the same as described above, for inhibiting RORγt activity, or for treating and/or preventing diseases related to RORγt, for example, by inhibiting RORγt Treatable or preventable diseases.
另一方面，本发明还提供了如前所述的本发明化合物或包含其的药物组合物在制备药物中的用途，尤其是具有RORγt受体抑制剂活性的药物中的应用。On the other hand, the present invention also provides the use of the compound of the present invention or the pharmaceutical composition containing it in the preparation of medicines, especially the use of medicines with RORγt receptor inhibitor activity.
另一方面，本发明提供如前所述的本发明化合物或包含其的药物组合物在制备用于治疗或预防与RORγt相关的疾病、例如通过RORγt抑制可治疗或预防的疾病的药物中的用途，其中所述化合物或药物组合物任选地与一种或多种化学治疗或免疫治疗联合。In another aspect, the present invention provides the use of the compound of the present invention as described above or a pharmaceutical composition containing the same in the preparation of a medicament for the treatment or prevention of diseases related to RORγt, for example, diseases that can be treated or prevented by RORγt inhibition , Wherein the compound or pharmaceutical composition is optionally combined with one or more chemotherapy or immunotherapy.
药物组合Drug combination
本发明的化合物可以作为唯一的活性成分施用，也可以与另外的药物或疗法组合进行施用。所述另外的药物或疗法可以具有或产生相同或不同的药理学功效，但条件是在与本发明化合物联合使用时不会导致不期望的活性降低、不良相互作用或副作用。The compound of the present invention can be administered as the sole active ingredient, or can be administered in combination with another drug or therapy. The additional drugs or therapies may have or produce the same or different pharmacological effects, provided that when used in combination with the compounds of the present invention, they do not cause undesirable activity reduction, adverse interactions, or side effects.
因此，另一方面，本发明提供药物组合，包含如前所述的本发明化合物以及一种或多种通过相同或不同作用机制发挥作用的其他药物或疗法，或由二者组成。在具体的实施方式中，该药物组合用于抑制RORγt活性，或用于治疗和/或预防与RORγt相关的疾病。Therefore, in another aspect, the present invention provides a drug combination comprising the compound of the present invention as described above and one or more other drugs or therapies that function through the same or different mechanisms of action, or a combination of both. In a specific embodiment, the drug combination is used to inhibit RORγt activity, or to treat and/or prevent diseases related to RORγt.
本发明的药物组合中的本发明化合物和组合使用的其他活性剂可以通过相同或不同的施用途径同时、分别或依次施用。所述其他活性剂可以与本发明化合物在单一药物组合物中共同施用，或与本发明化合物处于不同的离散单元中分别施用，例如组合产品,优选为药盒形式。当分别施用时可以同时或相继进行，所述相继施用在时间上可以是接近或隔远的。而且，本发明的化合物和另外的药物可以(i)在将组合产品发送给医师之前(例如在包含本发明的化合物和另外的药物的药盒的情形中)；(ii)在临施用前由医师自身(或在医师指导下)；(iii)由患者自身、例如在本发明的化合物和另外药物的依次施用期间，一起加入组合治疗中。The compound of the present invention in the pharmaceutical combination of the present invention and other active agents used in the combination can be administered simultaneously, separately or sequentially through the same or different administration routes. The other active agent may be co-administered with the compound of the present invention in a single pharmaceutical composition, or administered separately from the compound of the present invention in separate discrete units, such as a combination product, preferably in the form of a kit. When they are administered separately, they can be carried out simultaneously or sequentially, and the successive administrations can be close or distant in time. Furthermore, the compound of the present invention and the additional drug can be (i) before sending the combined product to the physician (for example, in the case of a kit containing the compound of the present invention and the additional drug); (ii) immediately before administration The physician himself (or under the guidance of the physician); (iii) the patient himself, for example, during the sequential administration of the compound of the present invention and another drug, are added to the combination therapy together.
因此，在具体的实施方式中，本发明还提供了药盒，其包含两种或多种单独的药物组合物，其中至少一种包含本发明的化合物，其余的包含组合使用的其他活性剂，以及分别容纳所述组合物的装置。本发明的药盒特别适用于施用不同的剂型，如口服剂型和胃肠外剂型，或者适合于以不同的剂量间隔施用不同的组合物。Therefore, in a specific embodiment, the present invention also provides a kit comprising two or more separate pharmaceutical compositions, at least one of which contains the compound of the present invention, and the rest contains other active agents used in combination, And a device containing the composition respectively. The kit of the present invention is particularly suitable for administering different dosage forms, such as oral dosage forms and parenteral dosage forms, or for administering different compositions at different dosage intervals.
在本发明的药物组合中，本发明化合物和其他活性剂在组合时的适合用量通常可由本领域技术人员通过例如从本说明书中描述的化合物的剂量范围和其它活性化合物的批准或公布的剂量范围开始来确定，共施用的其它药物的剂量当然将根据所用的共用药物的类型、所用具体药物、待治疗的病症、患者的一般健康状况、医师或兽医的判断等因素而变化。In the pharmaceutical combination of the present invention, the appropriate dosage of the compound of the present invention and other active agents in the combination can usually be determined by those skilled in the art, for example, from the dosage range of the compound described in this specification and the approved or published dosage range of other active compounds. To determine at the beginning, the doses of other co-administered drugs will of course vary according to factors such as the type of co-administered drugs, the specific drugs used, the disease to be treated, the patient's general health status, and the judgment of the physician or veterinarian.
就本发明的药物组合物和药物组合而言，所述其他活性剂可以是一种或多种与本发明化合物不会相互不利影响、具有增强、互补活性的第二种或另外的(例如第三种)化合物，例如这些活性剂可以是已知调节其他生物活性通路的化合物，或者可以是调节本发明化合物所涉及生物活性通路中的不同组分的化合物，或甚至是与本发明化合物的生物靶点相重叠的化合物。With regard to the pharmaceutical composition and pharmaceutical combination of the present invention, the other active agent may be one or more second or additional (e.g. Three) compounds. For example, these active agents may be compounds known to modulate other biologically active pathways, or may be compounds that modulate different components in the biologically active pathways involved in the compounds of the present invention, or even biologically related to the compounds of the present invention. Compounds with overlapping targets.
在一个具体的实施方式中，本发明提供了药物组合，例如用作用于治疗本文所列疾病之一的药物，所述疾病例如银屑病、COPD、哮喘、银屑病关节炎或强制性脊柱炎，其包含本发明化合物，和至少一种选自以下的活性成分：In a specific embodiment, the present invention provides a drug combination, for example as a drug for the treatment of one of the diseases listed herein, such as psoriasis, COPD, asthma, psoriatic arthritis or compulsive spine Inflammation, which contains the compound of the present invention, and at least one active ingredient selected from:
a)β-肾上腺素受体激动剂；a) β-adrenergic receptor agonists;
b)毒蕈碱性受体拮抗剂；b) Muscarinic receptor antagonists;
c)关节毒蕈碱受体拮抗剂和β-肾上腺素受体激动剂；以及c) Joint muscarinic receptor antagonists and β-adrenergic receptor agonists; and
d)糖皮质激素受体激动剂(甾族或非甾族)；d) Glucocorticoid receptor agonists (steroidal or non-steroidal);
e)磷酸二酯酶-4(PDE4)抑制剂。e) Phosphodiesterase-4 (PDE4) inhibitor.
本发明化合物还可以与其他疗法组合，所述其他疗法包括但不限于手术、辐射治疗、移植(例如干细胞移植、骨髓移植)、肿瘤免疫疗法等。The compounds of the present invention can also be combined with other therapies, including but not limited to surgery, radiation therapy, transplantation (for example, stem cell transplantation, bone marrow transplantation), tumor immunotherapy and the like.
相应地，本发明提供了用于抑制RORγt活性或用于治疗和/或预防与RORγt相关疾病的方法，包括向有需要的受试者施用本发明的药物组合。本发明还提供了所述本发明药物组合在制备用于抑制RORγt活性或用于治疗和/或预防与RORγt相关疾病的药物中的用途。Accordingly, the present invention provides a method for inhibiting RORγt activity or for treating and/or preventing diseases related to RORγt, including administering the pharmaceutical combination of the present invention to a subject in need. The present invention also provides the use of the pharmaceutical combination of the present invention in the preparation of drugs for inhibiting RORγt activity or for treating and/or preventing diseases related to RORγt.
对于上述涉及药物组合物、治疗方法和用途以及药物组合的各个方面，与RORγt相关的疾病(例如通过RORγt抑制可治疗或预防的疾病)包括炎症或自身免疫疾病、癌症等，包括但不限于银屑病、类风湿性关节炎、银屑病性关节炎、强直性脊柱炎、多发性硬化、系统性红斑狼疮、移植物抗宿主疾病、炎症性肠病、克隆氏病、溃疡性结肠炎、慢性阻塞性肺病、哮喘、血管球性肾炎、狼疮性肾炎、心肌炎、甲状腺炎、干眼症、葡萄膜炎、白塞病、过敏性皮肤炎、粉刺、硬皮病、支气管炎、皮肌过敏性鼻炎、坏死性小肠结肠炎、肝纤维化、非酒精性脂肪性肝炎(NASH)、新冠病毒肺炎、胰岛素依赖性I型糖尿病、三阴乳腺癌和前列腺癌等。优选的与RORγt相关的疾病选自银屑病、类风湿性关节炎、银屑病性关节炎、强直性脊柱炎、多发性硬化、炎症性肠病、干眼症、过敏性皮肤炎、慢性阻塞性肺病(COPD)、哮喘、坏死性小肠结肠炎、肝纤维化、非酒精性脂肪性肝炎(NASH)、新冠病毒肺炎、三阴乳腺癌和前列腺癌。Regarding the foregoing aspects related to pharmaceutical compositions, treatment methods and uses, and drug combinations, diseases related to RORγt (for example, diseases that can be treated or prevented by RORγt inhibition) include inflammation or autoimmune diseases, cancer, etc., including but not limited to silver. Scoria, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, multiple sclerosis, systemic lupus erythematosus, graft versus host disease, inflammatory bowel disease, Crohn's disease, ulcerative colitis, Chronic obstructive pulmonary disease, asthma, glomerulonephritis, lupus nephritis, myocarditis, thyroiditis, dry eye, uveitis, Behcet's disease, allergic dermatitis, acne, scleroderma, bronchitis, dermatomuscular hypersensitivity Rhinitis, necrotizing enterocolitis, liver fibrosis, non-alcoholic steatohepatitis (NASH), new coronavirus pneumonia, insulin-dependent type I diabetes, triple negative breast cancer and prostate cancer. Preferred diseases associated with RORγt are selected from the group consisting of psoriasis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, multiple sclerosis, inflammatory bowel disease, dry eye, allergic dermatitis, chronic Obstructive pulmonary disease (COPD), asthma, necrotizing enterocolitis, liver fibrosis, non-alcoholic steatohepatitis (NASH), new coronavirus pneumonia, triple negative breast cancer and prostate cancer.
对于上述本发明化合物、药物组合物、方法、用途、药物组合而言，优选上文所述优选的式(I)化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物；更优选上文所列的具体化合物、例如化合物1-13，或它们药学可接受的盐或溶剂合物。For the above-mentioned compounds, pharmaceutical compositions, methods, uses, and pharmaceutical combinations of the present invention, the preferred compounds of formula (I), their stereoisomers, tautomers, stable isotopic variants, Pharmaceutically acceptable salts or solvates; more preferred are the specific compounds listed above, such as compounds 1-13, or their pharmaceutically acceptable salts or solvates.
当本文描述化合物或药物的施用剂量时，应理解，该剂量基于游离碱的重量，不包括其任何衍生成份，除非说明书另外指出。When the administered dose of a compound or drug is described herein, it should be understood that the dose is based on the weight of the free base and does not include any derived components thereof, unless the instructions indicate otherwise.
本发明化合物的合成Synthesis of the compounds of the invention
另一方面，本发明还提供了一种制备式(I)化合物的方法，下文举例说明了合成本发明化合物的通用合成方案。对于各反应步骤而言，适当的反应条件是本领域技术人员已知的或可以常规确定的。如果没有特别说明，在制备这些化合物中使用的原料和试剂通常可商购获得，或者可以通过下文的方法、与下文给出的方法类似的方法或本领域已知的方法制得。如果需要，合成反应流程中的原料和中间体可以采用常规技术进行分离和纯化，所述技术包括但不限于过滤、蒸馏、结晶、色谱法等。所述材料可以采用包括物理常数和波谱数据在内的常规方法表征。On the other hand, the present invention also provides a method for preparing the compound of formula (I). The following exemplifies a general synthetic scheme for synthesizing the compound of the present invention. For each reaction step, appropriate reaction conditions are known to those skilled in the art or can be routinely determined. Unless otherwise specified, the raw materials and reagents used in the preparation of these compounds are generally commercially available, or can be prepared by the following methods, methods similar to those given below, or methods known in the art. If necessary, the raw materials and intermediates in the synthesis reaction process can be separated and purified using conventional techniques, including but not limited to filtration, distillation, crystallization, chromatography and the like. The material can be characterized by conventional methods including physical constants and spectral data.
在一个实施方案中，所述方法包括以下步骤：In one embodiment, the method includes the following steps:
流程1：Process 1:
Figure PCTCN2021093788-appb-000008
Figure PCTCN2021093788-appb-000008
其中R 1、R 2、R 3、R 4、R 5、R 6、m和p如上面对通式(I)所定义；Prot是氨基保护基，包括但不限于Boc、Cbz、Fmoc或PMB，优选Boc； Wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , m and p are as defined above for general formula (I); Prot is an amino protecting group, including but not limited to Boc, Cbz, Fmoc or PMB , Preferably Boc;
步骤1：式(I-1)化合物生成游离或盐形式的式(I-2)化合物；该反应优选在氢溴酸(例如40％氢溴酸水溶液)的作用下进行，优选在适合的温度进行，例如50-200℃、80-150℃，优选90-120℃；所述盐形式例如氢溴酸盐形式；Step 1: The compound of formula (I-1) generates the compound of formula (I-2) in free or salt form; this reaction is preferably carried out under the action of hydrobromic acid (for example, 40% hydrobromic acid in water), preferably at a suitable temperature Carry out, for example, 50-200°C, 80-150°C, preferably 90-120°C; the salt form is, for example, the hydrobromide salt form;
步骤2：游离或盐形式的式(I-2)化合物跟式(I-3)化合物环合生成游离或盐形式的式(I-4)化合物；该反应优选在适当的溶剂中进行，且优选在适当的温度进行，所述溶剂可选自例如质子溶剂，例如甲醇、乙醇、丙醇等，所述温度选自例如50-200℃、80-150℃，优选90-120℃；所述盐形式例如氢溴酸盐形式；Step 2: The compound of formula (I-2) in free or salt form is cyclized with the compound of formula (I-3) to form the compound of formula (I-4) in free or salt form; this reaction is preferably carried out in a suitable solvent, and It is preferably carried out at a suitable temperature, the solvent can be selected from, for example, protic solvents, such as methanol, ethanol, propanol, etc., and the temperature is selected from, for example, 50-200°C, 80-150°C, preferably 90-120°C; Salt form such as hydrobromide salt form;
步骤3：游离或盐形式的式(I-4)化合物与氨基保护剂生成式(I-5)化合物；其中氨基保护剂是本领域众所周知的，包括但不限于二碳酸二叔丁酯((Boc) 2O)、CbzCl、FmocCl或PMB-Cl，所述反应优选在适合的有机溶剂中进行，所述有机溶剂可选自四氢呋喃、醚类(例如乙醚、乙二醇单甲醚等)、N-甲基吡咯烷酮、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、二氯甲烷、1,4-二氧六环、二甲基亚砜及其任意组合，优选四氢呋喃；所述反应优选在适合的碱存在下进行，所述的碱可选自碳酸钠、碳酸钾、碳酸铯、N,N-二异丙基乙胺、三乙胺、HOBt或吡啶，优选地，所述的碱是三乙胺；所述反应优选在适合的温度进行，例如0-200℃、5-100℃、10-50℃，优选室温； Step 3: The compound of formula (I-4) in free or salt form and the amino protecting agent to produce the compound of formula (I-5); wherein the amino protecting agent is well known in the art, including but not limited to di-tert-butyl dicarbonate (( Boc) 2 O), CbzCl, FmocCl or PMB-Cl, the reaction is preferably carried out in a suitable organic solvent, the organic solvent may be selected from tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, dichloromethane, 1,4-dioxane, dimethylsulfoxide and any combination thereof, preferably Tetrahydrofuran; the reaction is preferably carried out in the presence of a suitable base, the base may be selected from sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, triethylamine, HOBt or pyridine, preferably Preferably, the base is triethylamine; the reaction is preferably carried out at a suitable temperature, such as 0-200°C, 5-100°C, 10-50°C, preferably room temperature;
步骤4：式(I-5)化合物跟Tf试剂反应生成式(I-6)化合物；所述Tf试剂是能与羟基反应生成OTf基团的试剂，包括但不限于三氟甲磺酸酐、三氟甲磺酰氯或N-苯基双(三氟甲磺酰)亚胺；所述反应优选在碱存在下进行，所述的碱可选自碳酸钠、碳酸钾、碳酸铯、N,N-二异丙基乙胺、三乙胺、HOBt或吡啶；所述反应优选在有机溶剂中进行，所述有机溶剂可选自二氯甲烷、四氢呋喃、醚类(例如乙醚、乙二醇单甲醚等)、N-甲基吡咯烷酮、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、1,4-二氧六环、二甲基亚砜及其任意组合，优选二氯甲烷；所述反应优选在适合的温度下进行，例如-50℃至200℃、-20℃至100℃、例如-10℃至50℃，例如-10℃至10℃，优选在冰浴中；所述反应优选在惰性气体气氛下进行，所述惰性气体包括但不限于氮气、氩气或氦气等；Step 4: The compound of formula (I-5) reacts with the Tf reagent to produce the compound of formula (I-6); the Tf reagent is a reagent that can react with a hydroxyl group to generate an OTf group, including but not limited to trifluoromethanesulfonic anhydride, trifluoromethanesulfonic anhydride, Fluoromethanesulfonyl chloride or N-phenylbis(trifluoromethanesulfonyl)imide; the reaction is preferably carried out in the presence of a base, and the base can be selected from sodium carbonate, potassium carbonate, cesium carbonate, N,N- Diisopropylethylamine, triethylamine, HOBt or pyridine; the reaction is preferably carried out in an organic solvent, the organic solvent may be selected from dichloromethane, tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether) Etc.), N-methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, 1,4-dioxane, dimethylsulfoxide and any combination thereof, preferably two Methyl chloride; the reaction is preferably carried out at a suitable temperature, such as -50°C to 200°C, -20°C to 100°C, such as -10°C to 50°C, such as -10°C to 10°C, preferably in an ice bath ; The reaction is preferably carried out under an inert gas atmosphere, the inert gas including but not limited to nitrogen, argon or helium, etc.;
步骤5：式(I-6)化合物跟式(I-7)的化合物在催化剂、如钯催化剂的作用下通过偶联得到式(I-8)化合物；Step 5: The compound of formula (I-6) and the compound of formula (I-7) are coupled under the action of a catalyst, such as a palladium catalyst, to obtain a compound of formula (I-8);
其中所述钯催化剂是本领域众所周知的用于偶联的钯催化剂，包括但不限于Pd 2(dba) 3等；所述反应优选在适合的有机溶剂中进行，所述有机溶剂可选自四氢呋喃、醚类(例如乙醚、乙二醇单甲醚等)、N-甲基吡咯烷酮、N,N-二甲基甲酰胺、N,N二甲基乙酰胺、二氯甲烷、1,4-二氧六环、二甲基亚砜及其任意组合，优选1,4-二氧六环；所述反应优选在膦配体存在下进行，所述膦配体包括但不限于4,5-双二苯基膦-9,9-二甲基氧杂蒽；所述反应优选在适合的碱存在下进行，所述的碱可选自碳酸钠、碳酸钾、碳酸铯、N,N-二异丙基乙胺、三乙胺、HOBt或吡啶，优选地，所述的碱是N,N-二异丙基乙胺；所述反应优选在适合的温度下进行，例如50-200℃、80-150℃，优选90-120℃； The palladium catalyst is a well-known palladium catalyst for coupling in the art, including but not limited to Pd 2 (dba) 3, etc.; the reaction is preferably carried out in a suitable organic solvent, and the organic solvent may be selected from tetrahydrofuran , Ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N,N dimethylacetamide, dichloromethane, 1,4-bis Oxane, dimethyl sulfoxide and any combination thereof, preferably 1,4-dioxane; the reaction is preferably carried out in the presence of a phosphine ligand, the phosphine ligand including but not limited to 4,5-bis Diphenylphosphine-9,9-dimethylxanthene; the reaction is preferably carried out in the presence of a suitable base, which can be selected from sodium carbonate, potassium carbonate, cesium carbonate, N,N-diiso Propylethylamine, triethylamine, HOBt or pyridine, preferably, the base is N,N-diisopropylethylamine; the reaction is preferably carried out at a suitable temperature, such as 50-200°C, 80°C -150°C, preferably 90-120°C;
步骤6：式(I-8)化合物在氧化剂的作用下生成式(I-9)化合物；所述氧化剂选自例如H 2O 2、 mCPBA和过氧乙酸；所述反应优选在有机溶剂中进行，所述有机溶剂可选自二氯甲烷、四氢呋喃、醚类(例如乙醚、乙二醇单甲醚等)、N-甲基吡咯烷酮、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、1,4-二氧六环、二甲基亚砜及其任意组合，优选二氯甲烷；所述反应优选在适合的温度下进行，例如-50℃至200℃、-20℃至100℃、例如-10℃至50℃，例如-10℃至10℃，优选在冰浴中； Step 6: The compound of formula (I-8) generates the compound of formula (I-9) under the action of an oxidizing agent; the oxidizing agent is selected from, for example, H 2 O 2 , mCPBA and peroxyacetic acid; the reaction is preferably carried out in an organic solvent The organic solvent can be selected from dichloromethane, tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N,N-di Methyl acetamide, 1,4-dioxane, dimethyl sulfoxide and any combination thereof, preferably dichloromethane; the reaction is preferably carried out at a suitable temperature, for example -50°C to 200°C, -20 °C to 100 °C, for example -10 °C to 50 °C, for example -10 °C to 10 °C, preferably in an ice bath;
步骤7：式(I-9)化合物水解生成式(I-10)化合物；所述反应优选在碱存在下进行，所述的碱可选自氢氧化钠、氢氧化钾、碳酸钠、碳酸钾或碳酸铯，所述碱优选以水溶液形式应用；所述反应优选在有机溶剂中进行，所述有机溶剂可选自醇溶剂例如(甲醇、乙醇或丙醇)、四氢呋喃、醚类(例如乙醚、乙二醇单甲醚等)、N-甲基吡咯烷酮、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、1,4-二氧六环、二甲基亚砜及其任意组合，优选甲醇；所述反应优选在适合的温度下进行，例如-20℃至-200℃、5-100℃、10-50℃，优选室温；Step 7: The compound of formula (I-9) is hydrolyzed to produce the compound of formula (I-10); the reaction is preferably carried out in the presence of a base, and the base can be selected from sodium hydroxide, potassium hydroxide, sodium carbonate, and potassium carbonate Or cesium carbonate, the base is preferably used in the form of an aqueous solution; the reaction is preferably carried out in an organic solvent, the organic solvent can be selected from alcohol solvents such as (methanol, ethanol or propanol), tetrahydrofuran, ethers (such as diethyl ether, Ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, 1,4-dioxane, dimethylsulfoxide and Any combination thereof, preferably methanol; the reaction is preferably carried out at a suitable temperature, such as -20°C to -200°C, 5-100°C, 10-50°C, preferably room temperature;
步骤8：式(I-10)化合物在缩合剂的作用下跟式(I-11)化合物反应生成式(I-12)化合物；Step 8: The compound of formula (I-10) reacts with the compound of formula (I-11) under the action of a condensing agent to produce a compound of formula (I-12);
其中所述缩合剂是本领域众所周知的用于羧酸与胺偶联的缩合剂，包括但不限于1-丙基磷酸酐(T3P)、EDC、DCC、HATU等；所述反应优选在适合的有机溶剂中进行，所述有机溶剂可选自二氯甲烷、四氢呋喃、醚类(例如乙醚、乙二醇单甲醚等)、N-甲基吡咯烷酮、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、1,4-二氧六环、二甲基亚砜及其任意组合，优选二氯甲烷；所述反应优选在适合的碱存在下进行，所述的碱包括但不限于碳酸钠、碳酸钾、碳酸铯、N,N-二异丙基乙胺、三乙胺、HOBt或吡啶，优选地，所述的碱是N,N-二异丙基乙胺；所述反应优选在适合的温度下进行，例如0-200℃、10-100℃或20-50℃，优选室温(20-25℃)。Wherein the condensing agent is a condensing agent for coupling carboxylic acid and amine well known in the art, including but not limited to 1-propyl phosphoric anhydride (T3P), EDC, DCC, HATU, etc.; the reaction is preferably in a suitable In an organic solvent, the organic solvent can be selected from dichloromethane, tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N , N-dimethylacetamide, 1,4-dioxane, dimethylsulfoxide and any combination thereof, preferably dichloromethane; the reaction is preferably carried out in the presence of a suitable base, and the base includes But not limited to sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, triethylamine, HOBt or pyridine, preferably, the base is N,N-diisopropylethylamine; The reaction is preferably carried out at a suitable temperature, such as 0-200°C, 10-100°C or 20-50°C, preferably room temperature (20-25°C).
步骤9：式(I-12)化合物脱除氨基保护基生成式(I-13)的化合物；所述反应例如在酸(如TFA或者HCl)的作用下进行，所述反应优选在适合的有机溶剂中进行，所述有机溶剂可选自二氯甲烷、四氢呋喃、醚类(例如乙醚、乙二醇单甲醚等)、N-甲基吡咯烷酮、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、1,4-二氧六环、二甲基亚砜及其任意组合，优选二氯甲烷；所述反应优选在适合的温度下进行，例如-50℃至200℃、-20℃至100℃、例如-10℃至50℃，例如-10℃至20℃；步骤10：式(I-13)化合物与式(I-14)或其活化形式(例如相应的酰氯(式(I-15)或酸酐)反应生成目标化合物I-a；所述反应优选在碱存在下进行，所述的碱可选自碳酸钠、碳酸钾、碳酸铯、N,N-二异丙基乙胺、三乙胺、HOBt或吡啶；所述反应优选在有机溶剂中进行，所述有机溶剂可选自二氯甲烷、四氢呋喃、醚类(例如乙醚、乙二醇单甲醚等)、N-甲基吡咯烷酮、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、1,4-二氧六环、二甲基亚砜及其任意组合，优选二氯甲烷；所述反应可在缩合剂例如等存在下进行，其中所述缩合剂是本领域众所周知的用于羧酸与胺偶联的缩合剂，包括但不限于1-丙基磷酸酐(T3P)、EDC、DCC、HATU；所述反应优选在适合的温度下进行，例如0-200℃、10-100℃或20-50℃，优选室温(20-25℃)。Step 9: The amino protecting group of the compound of formula (I-12) is removed to produce the compound of formula (I-13); the reaction is carried out under the action of an acid (such as TFA or HCl), and the reaction is preferably carried out in a suitable organic In a solvent, the organic solvent can be selected from dichloromethane, tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N-methylpyrrolidone, N,N-dimethylformamide, N, N-dimethylacetamide, 1,4-dioxane, dimethylsulfoxide and any combination thereof, preferably dichloromethane; the reaction is preferably carried out at a suitable temperature, for example -50°C to 200°C , -20°C to 100°C, such as -10°C to 50°C, such as -10°C to 20°C; Step 10: Formula (I-13) compound and formula (I-14) or its activated form (such as the corresponding acid chloride (Formula (I-15) or acid anhydride) react to produce the target compound Ia; the reaction is preferably carried out in the presence of a base, and the base can be selected from sodium carbonate, potassium carbonate, cesium carbonate, and N,N-diisopropyl Ethylamine, triethylamine, HOBt or pyridine; the reaction is preferably carried out in an organic solvent, and the organic solvent can be selected from dichloromethane, tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N -Methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, 1,4-dioxane, dimethylsulfoxide and any combination thereof, preferably dichloromethane; The reaction can be carried out in the presence of a condensing agent such as the like, wherein the condensing agent is a condensing agent for coupling carboxylic acid and amine well known in the art, including but not limited to 1-propyl phosphoric anhydride (T3P), EDC, DCC, HATU; the reaction is preferably carried out at a suitable temperature, such as 0-200°C, 10-100°C or 20-50°C, preferably room temperature (20-25°C).
在一个实施方案中，所述方法包括以下步骤：In one embodiment, the method includes the following steps:
流程2：Process 2:
Figure PCTCN2021093788-appb-000009
Figure PCTCN2021093788-appb-000009
其中R 1、R 2、R 3、R 4、R 5、R 6、m和p如上面对通式(I)所定义；Prot是氨基保护基，包括但不限于Boc、Cbz、Fmoc或PMB，优选Boc； Wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , m and p are as defined above for general formula (I); Prot is an amino protecting group, including but not limited to Boc, Cbz, Fmoc or PMB , Preferably Boc;
步骤1：式(II-1)化合物与R 4SH或其盐(例如钠盐)反应生成式(II-2)化合物；所述反应优选在惰性气体气氛下进行，所述惰性气体包括但不限于氮气、氩气或氦气等； Step 1: The compound of formula (II-1) is reacted with R 4 SH or its salt (such as sodium salt) to produce the compound of formula (II-2); the reaction is preferably carried out under an inert gas atmosphere, and the inert gas includes but not Limited to nitrogen, argon or helium, etc.;
步骤2：式(II-2)化合物与氨基保护剂反应生成式(II-3)化合物；其中氨基保护剂是本领域众所周知的，包括但不限于二碳酸二叔丁酯((Boc) 2O)、CbzCl、FmocCl或PMB-Cl；所述反应优选在适合的碱存在下进行，所述的碱可选自碳酸钠、碳酸钾、碳酸铯、N,N-二异丙基乙胺、三乙胺、HOBt、吡啶或4-二甲氨基吡啶； Step 2: The compound of formula (II-2) is reacted with an amino protecting agent to produce a compound of formula (II-3); wherein the amino protecting agent is well known in the art, including but not limited to di-tert-butyl dicarbonate ((Boc) 2 O ), CbzCl, FmocCl or PMB-Cl; the reaction is preferably carried out in the presence of a suitable base, and the base can be selected from sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, three Ethylamine, HOBt, pyridine or 4-dimethylaminopyridine;
步骤3：式(II-3)化合物氧化剂的作用下氧化生成式(II-4)化合物；所述氧化剂选自例如H 2O 2、mCPBA和过氧乙酸； Step 3: The compound of formula (II-3) is oxidized to produce the compound of formula (II-4) under the action of an oxidizing agent; the oxidizing agent is selected from, for example, H 2 O 2 , mCPBA and peroxyacetic acid;
步骤4：式(II-4)化合物在还原剂的作用下还原生成式(II-5)化合物；所述还原剂例如选自DABAL-H、四氢铝锂或硼氢化钠；所述反应优选在惰性气体气氛下进行，所述惰性气体包括但不限于氮气、氩气或氦气等；Step 4: The compound of formula (II-4) is reduced under the action of a reducing agent to produce a compound of formula (II-5); the reducing agent is, for example, selected from DABAL-H, lithium aluminum tetrahydrogen or sodium borohydride; the reaction is preferably It is carried out under an inert gas atmosphere, and the inert gas includes but is not limited to nitrogen, argon or helium, etc.;
步骤5：式(II-5)化合物与甲醇或其活化形式(例如甲醇钠)反应生成式(II-6)化合物；所述反应优选在4-甲基苯磺酸吡啶(PPTS)存在下进行；Step 5: The compound of formula (II-5) is reacted with methanol or its activated form (such as sodium methoxide) to produce the compound of formula (II-6); the reaction is preferably carried out in the presence of 4-methylbenzenesulfonic acid pyridine (PPTS) ；
步骤6：式(II-6)化合物跟烷基氰硅烷(例如TMSCN)反应生成式(II-7)化合物；所述反应优选在 三氟化硼乙醚存在下进行；所述反应优选在惰性气体气氛下进行，所述惰性气体包括但不限于氮气、氩气或氦气等；Step 6: The compound of formula (II-6) is reacted with alkyl cyanosilane (such as TMSCN) to produce the compound of formula (II-7); the reaction is preferably carried out in the presence of boron trifluoride ether; the reaction is preferably in an inert gas In an atmosphere, the inert gas includes, but is not limited to, nitrogen, argon, or helium, etc.;
步骤7：式(II-7)化合物脱除氨基保护基生成式(II-8)化合物；所述反应例如在酸(如TFA或者HCl)的作用下进行；Step 7: The amino protecting group of the compound of formula (II-7) is removed to produce the compound of formula (II-8); the reaction is carried out, for example, under the action of an acid (such as TFA or HCl);
步骤8：式(II-8)化合物与R 3COOH或其活化形式例如相应的酰氯或酸酐反应生成式(II-9)化合物；所述反应优选在碱存在下进行，所述的碱可选自碳酸钠、碳酸钾、碳酸铯、N,N-二异丙基乙胺、三乙胺、HOBt或吡啶；所述反应可在缩合剂例如等存在下进行，其中所述缩合剂是本领域众所周知的用于羧酸与胺偶联的缩合剂，包括但不限于1-丙基磷酸酐(T3P)、EDC、DCC、HATU； Step 8: The compound of formula (II-8) is reacted with R 3 COOH or its activated form such as the corresponding acid chloride or acid anhydride to produce the compound of formula (II-9); the reaction is preferably carried out in the presence of a base, and the base may be optional From sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, triethylamine, HOBt or pyridine; the reaction can be carried out in the presence of a condensing agent such as the like, wherein the condensing agent is in the art Well-known condensing agents for the coupling of carboxylic acids and amines, including but not limited to 1-propyl phosphoric anhydride (T3P), EDC, DCC, HATU;
步骤9：式(II-9)化合物水解生成式(II-10)化合物；所述反应优选在碱存在下进行，所述的碱可选自氢氧化钠、氢氧化钾、碳酸钠、碳酸钾或碳酸铯；Step 9: The compound of formula (II-9) is hydrolyzed to produce the compound of formula (II-10); the reaction is preferably carried out in the presence of a base, and the base can be selected from sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate Or cesium carbonate;
步骤10：式(II-10)化合物在缩合剂的作用下跟式(I-11)化合物反应生成目标化合物式(I-b)化合物；Step 10: The compound of formula (II-10) reacts with the compound of formula (I-11) under the action of a condensing agent to produce the target compound of formula (I-b);
其中所述缩合剂是本领域众所周知的用于羧酸与胺偶联的缩合剂，包括但不限于T3P、EDC、DCC、HATU或N,N,N',N'-四甲基氯甲脒六氟磷酸盐等；所述反应优选在适合的碱存在下进行，所述的碱包括但不限于碳酸钠、碳酸钾、碳酸铯、N,N-二异丙基乙胺、三乙胺、N-甲基咪唑、HOBt或吡啶；Wherein the condensing agent is a condensing agent for coupling carboxylic acid and amine well known in the art, including but not limited to T3P, EDC, DCC, HATU or N,N,N',N'-tetramethylchloroformamidine Hexafluorophosphate, etc.; the reaction is preferably carried out in the presence of a suitable base, including but not limited to sodium carbonate, potassium carbonate, cesium carbonate, N,N-diisopropylethylamine, triethylamine, N-methylimidazole, HOBt or pyridine;
上述步骤中的反应优选在有机溶剂中进行，所述有机溶剂可选自醇溶剂例如(甲醇、乙醇或丙醇)、四氢呋喃、醚类(例如乙醚、乙二醇单甲醚等)、N-甲基吡咯烷酮、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、1,4-二氧六环、二氯甲烷、二甲基亚砜及其任意组合；对于水解反应可以使用有机溶剂与水的混合物；The reaction in the above steps is preferably carried out in an organic solvent, and the organic solvent can be selected from alcohol solvents such as (methanol, ethanol or propanol), tetrahydrofuran, ethers (such as diethyl ether, ethylene glycol monomethyl ether, etc.), N- Methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, 1,4-dioxane, dichloromethane, dimethylsulfoxide and any combination thereof; for hydrolysis reaction A mixture of organic solvent and water can be used;
上述步骤中的反应优选在适合的温度下进行，例如-100℃至0℃、-80℃至-20℃、-50℃至200℃、-20℃至100℃、-20℃至20℃、-10℃至20℃、-10℃至50℃、0-200℃、10-100℃、20-50℃或室温(20-25℃)。The reaction in the above steps is preferably carried out at a suitable temperature, such as -100°C to 0°C, -80°C to -20°C, -50°C to 200°C, -20°C to 100°C, -20°C to 20°C, -10°C to 20°C, -10°C to 50°C, 0-200°C, 10-100°C, 20-50°C or room temperature (20-25°C).
上述合成方案只是列举了本发明中部分化合物的制备方法。本发明的化合物或者其立体异构体、互变异构体、稳定的同位素衍生物、药学上可接受的盐或溶剂合物可以通过多种方法、包括上文给出的方法、实施例中给出的方法或与之类似的方法、由本领域普通技术人员在上述合成方案的基础上、结合本领域的常规技术而制备得到。The above synthesis scheme only lists the preparation methods of some of the compounds of the present invention. The compound of the present invention or its stereoisomers, tautomers, stable isotope derivatives, pharmaceutically acceptable salts or solvates can be passed through a variety of methods, including the methods and examples given above The given method or a similar method is prepared by a person of ordinary skill in the art on the basis of the above-mentioned synthesis scheme and combined with conventional techniques in the field.
本说明书中描述的化合物在以下实施例中进一步举例说明。这些实施例仅作为说明给出，而非限制性的。The compounds described in this specification are further exemplified in the following examples. These examples are given as illustrations only, and are not restrictive.
具体实施方式Detailed ways
以下结合具体实施例，对本发明的技术方案做进一步的描述，但是本发明的保护范围并不限于这些实施例。凡是不背离本发明构思的改变或等同替代均包括在本发明的保护范围之内。The technical solutions of the present invention will be further described below in conjunction with specific embodiments, but the protection scope of the present invention is not limited to these embodiments. Any changes or equivalent substitutions that do not deviate from the concept of the present invention are included in the protection scope of the present invention.
下列实施例中未注明具体条件的实验方法，通常按照这类反应的常规条件，或按照制造厂商所建议的条件。除非另外说明，否则百分比和份数是重量百分比和重量份数。除非另外说明，否则液体的比为体积比。The experimental methods that do not indicate specific conditions in the following examples usually follow the conventional conditions of this type of reaction or the conditions recommended by the manufacturer. Unless otherwise specified, percentages and parts are weight percentages and parts by weight. Unless otherwise specified, the ratio of the liquid is the volume ratio.
以下实施例中所用的实验材料和试剂如无特别说明均可从市售渠道获得、依据现有技术的方法制得或根据与本申请公开的类似的方法制得。The experimental materials and reagents used in the following examples can be obtained from commercial channels, prepared according to the method of the prior art, or prepared according to a method similar to that disclosed in the present application unless otherwise specified.
本申请使用化学名称是IUPAC名称,所用的缩写具有本领域通常理解的含义，除非说明书中另外清楚定义。在下面列出说明书中使用的缩写的含义：The chemical name used in this application is the IUPAC name, and the abbreviations used have the meaning commonly understood in the art, unless clearly defined otherwise in the specification. List the meanings of the abbreviations used in the instructions below:
PdCl 2(dtbpf)：1,1'-二叔丁基膦基二茂铁二氯化钯 PdCl 2 (dtbpf): 1,1'-Di-tert-butylphosphinoferrocene palladium dichloride
Pd(dppf)Cl 2：[1,1'-双(二苯基膦基)二茂铁]二氯化钯 Pd(dppf)Cl 2 : [1,1'-bis(diphenylphosphino)ferrocene]palladium dichloride
xantphos:4,5-双二苯基膦-9,9-二甲基氧杂蒽xantphos: 4,5-bisdiphenylphosphine-9,9-dimethylxanthene
Pd 2(dba) 3:三(二亚苄基丙酮)二钯 Pd 2 (dba) 3 : Tris (dibenzylideneacetone) two palladium
HATU：2-(7-偶氮苯并三氮唑)-N,N,N’,N’,-四甲基脲六氟磷酸盐HATU: 2-(7-Azobenzotriazole)-N,N,N’,N’,-Tetramethylurea hexafluorophosphate
DIEA：N,N-二异丙基乙胺DIEA: N,N-Diisopropylethylamine
DMF：N,N-二甲基甲酰胺DMF: N,N-Dimethylformamide
DMSO：二甲亚砜DMSO: Dimethyl sulfoxide
DCM：二氯甲烷DCM: Dichloromethane
EA:乙酸乙酯EA: ethyl acetate
PE：石油醚PE: Petroleum ether
rt:室温rt: room temperature
LC-MS：液相色谱质谱联用LC-MS: combined with liquid chromatography and mass spectrometry
ESI电喷雾离子化ESI electrospray ionization
m/z：质荷比m/z: Mass-to-charge ratio
TLC:薄层色谱TLC: Thin Layer Chromatography
TCFH:N,N,N',N'-四甲基氯甲脒六氟磷酸盐TCFH: N,N,N',N'-Tetramethylchloroformamidine hexafluorophosphate
Ret.time：保留时间Ret.time: retention time
合成实施例Synthesis Example
本发明提供的目标化合物制备方法中，柱层析色谱采用乳山太阳干燥剂有限公司生产的硅胶(300-400目)；薄层色谱采用GF254(0.25毫米)；核磁共振色谱(NMR)使用Varian-400核磁共振仪测定；液质联用(LC/MS)使用Agilent TechnologiESI 6120液质联用仪。In the method for preparing the target compound provided by the present invention, column chromatography uses silica gel (300-400 mesh) produced by Rushan Sun Desiccant Co., Ltd.; thin layer chromatography uses GF254 (0.25 mm); nuclear magnetic resonance chromatography (NMR) uses Varian- 400 NMR measurement; liquid-mass spectrometry (LC/MS) uses Agilent TechnologiESI 6120 liquid-mass spectrometry.
此外，凡涉及易氧化或易水解的原料的所有操作都在氮气保护下进行。除非另有说明，本发明使用的原料都是市售原料、无需进一步纯化可以直接使用，本发明使用的温度均为摄氏度℃。In addition, all operations involving raw materials that are easily oxidized or easily hydrolyzed are carried out under the protection of nitrogen. Unless otherwise specified, the raw materials used in the present invention are all commercially available raw materials and can be used directly without further purification. The temperatures used in the present invention are all in degrees Celsius.
当本发明化合物结构与化合物名称不一致时，通常以结构式所示为准，除非通过上下文可 以确定化合物名称正确。When the structure of the compound of the present invention is inconsistent with the name of the compound, the structure shown in the formula usually prevails, unless the correctness of the compound name can be determined by the context.
实施例1和实施例2：R-2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺或S-2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺Example 1 and Example 2: R-2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl )-[1,1'-Biphenyl]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide or S-2-acetyl-N-(2'-fluoro- 4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1,1'-biphenyl]-4-yl)-5-(methylsulfon Acyl) isoindoline-1-carboxamide
Figure PCTCN2021093788-appb-000010
Figure PCTCN2021093788-appb-000010
中间体2-(4'-氨基-2-氟-[1,1'-联苯]-4-基)-1,1,1,3,3,3-六氟丙-2-醇的合成Synthesis of intermediate 2-(4'-amino-2-fluoro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3-hexafluoropropan-2-ol
步骤1：全氟苯基4-溴-3-氟苯甲酸酯的合成Step 1: Synthesis of perfluorophenyl 4-bromo-3-fluorobenzoate
Figure PCTCN2021093788-appb-000011
Figure PCTCN2021093788-appb-000011
依次将4-溴-3-氟苯甲酸(30.0g，137mmol)，五氟苯酚(28.2g，153mmol)和二环己基碳二亚胺(31.9g，155mmol)溶于无水四氢呋喃(900mL)中。反应混合物在室温下搅拌过夜，TLC监测反应完全。将反应液过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝10:1)，得到目标化合物(56.0g，粗品，白色固体)。Dissolve 4-bromo-3-fluorobenzoic acid (30.0g, 137mmol), pentafluorophenol (28.2g, 153mmol) and dicyclohexylcarbodiimide (31.9g, 155mmol) in anhydrous tetrahydrofuran (900mL) in sequence . The reaction mixture was stirred at room temperature overnight, and TLC monitored the reaction to be complete. The reaction solution was filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product, which was separated and purified by a silica gel column (PE:EA=10:1) to obtain the target compound (56.0 g, crude product, white solid).
步骤2：((2-(4-溴-3-氟苯基)-1,1,1,3,3,3-六氟丙烷-2-基)氧基)三甲基硅烷的合成Step 2: Synthesis of ((2-(4-bromo-3-fluorophenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)trimethylsilane
Figure PCTCN2021093788-appb-000012
Figure PCTCN2021093788-appb-000012
将全氟苯基4-溴-3-氟苯甲酸酯(56.0g，145mmol)溶于甲苯(725mL)中。在冰浴下，依次将(三氟甲基)三甲基硅烷(131mL，873mmol)和1mol/L四丁基氟化铵四氢呋喃溶液(50.9mL，50.9mmol)滴加到反应液中。加完后，不撤掉冰浴，让反应液缓慢升到室温搅拌反应过夜，TLC监测反应完全。将反应液倒入冰的1mol/L稀盐酸(1.5L)中，用甲基叔丁基醚(700mLx2)萃取，合并有机相，用饱和食盐水(1.5L)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩，得到目标化合物(60.0g，粗品，棕色油状物)。Perfluorophenyl 4-bromo-3-fluorobenzoate (56.0 g, 145 mmol) was dissolved in toluene (725 mL). In an ice bath, (trifluoromethyl)trimethylsilane (131 mL, 873 mmol) and 1 mol/L tetrabutylammonium fluoride tetrahydrofuran solution (50.9 mL, 50.9 mmol) were sequentially added dropwise to the reaction solution. After the addition, without removing the ice bath, the reaction solution was allowed to slowly rise to room temperature and the reaction was stirred overnight. TLC monitored the completion of the reaction. Pour the reaction solution into ice 1mol/L dilute hydrochloric acid (1.5L), extract with methyl tert-butyl ether (700mLx2), combine the organic phases, wash with saturated brine (1.5L), and dry with anhydrous sodium sulfate , Filtered, and the filtrate was concentrated under reduced pressure to obtain the target compound (60.0 g, crude product, brown oil).
步骤3：2-(4-溴-3-氟苯基)-1,1,1,3,3,3-六氟丙烷-2-醇的合成Step 3: Synthesis of 2-(4-bromo-3-fluorophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol
Figure PCTCN2021093788-appb-000013
Figure PCTCN2021093788-appb-000013
将((2-(4-溴-3-氟苯基)-1,1,1,3,3,3-六氟丙烷-2-基)氧基)三甲基硅烷(70.0g，169mmol)溶于四氢呋喃(700mL)中，在室温下，将6mol/L稀盐酸(350mL)缓慢滴加到反应液中。加完后，在室温下继续搅拌反应过夜，LC-MS监测反应完全。将反应液倒入水(500mL)中，用甲基叔丁基醚(500mLx2)萃取，合并有机相，用饱和食盐水(1L)洗涤，用无水硫酸钠干燥，将反应液过滤，滤液减压浓缩，得到目标化合物(46.2g，粗品，黄色油状物)。LC-MS(ESI)m/z:338.9[M-H] -。 ((2-(4-Bromo-3-fluorophenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)trimethylsilane (70.0g, 169mmol) Dissolve in tetrahydrofuran (700 mL), and slowly add 6 mol/L dilute hydrochloric acid (350 mL) dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred overnight at room temperature, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (500mL), extracted with methyl tert-butyl ether (500mLx2), the organic phases were combined, washed with saturated brine (1L), dried with anhydrous sodium sulfate, the reaction solution was filtered, and the filtrate was reduced Concentrate under pressure to obtain the target compound (46.2 g, crude product, yellow oil). LC-MS(ESI) m/z: 338.9 [MH] - .
步骤4：2-(4'-氨基-2-氟-[1,1'-联苯]-4-基)-1,1,1,3,3,3,3-六氟丙烷-2-醇的合成Step 4: 2-(4'-Amino-2-fluoro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3,3-hexafluoropropane-2- Synthesis of alcohol
Figure PCTCN2021093788-appb-000014
Figure PCTCN2021093788-appb-000014
依次将2-(4-溴-3-氟苯基)-1,1,1,3,3,3-六氟丙烷-2-醇(46.2g,135mmol)，4-(4,4,5,5-四甲基-1,3,2-二氧杂硼烷-2-基)苯胺(23.7g,108mmol)，碳酸钾(37.4g,271mmol)和Pd(dppf)Cl 2(4.96g,6.77mmol)溶于1,4-二氧六环(500mL)和水(50mL)的混合溶剂中。在氮气保护下，反应混合物在100℃下搅拌反应2小时，LC-MS监测反应完全。将反应液过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝10:1-6:1)得到粗品，再经二氯甲烷打浆，得到目标化合物(20.0g，收率，白色固体)。LC-MS(ESI)m/z:395.0[M+ACN+H] +。 Sequentially mix 2-(4-bromo-3-fluorophenyl)-1,1,1,3,3,3-hexafluoropropane-2-ol (46.2g, 135mmol), 4-(4,4,5 ,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (23.7g, 108mmol), potassium carbonate (37.4g, 271mmol) and Pd(dppf)Cl 2 (4.96g, 6.77mmol) was dissolved in a mixed solvent of 1,4-dioxane (500mL) and water (50mL). Under the protection of nitrogen, the reaction mixture was stirred and reacted at 100°C for 2 hours. LC-MS monitored that the reaction was complete. The reaction solution was filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product. The crude product was separated and purified by silica gel column (PE:EA=10:1-6:1), and then slurried with dichloromethane to obtain the target compound (20.0g, yield, White solid). LC-MS(ESI) m/z: 395.0 [M+ACN+H] + .
中间体：2-乙酰基-5-(甲磺酰基)异吲哚啉-1-甲酸的合成Intermediate: Synthesis of 2-acetyl-5-(methylsulfonyl)isoindoline-1-carboxylic acid
步骤1：5-甲硫基异吲哚啉-1-酮的合成Step 1: Synthesis of 5-methylthioisoindolin-1-one
Figure PCTCN2021093788-appb-000015
Figure PCTCN2021093788-appb-000015
向5-溴异吲哚啉-1-酮(200g,943mmol)的DMF(2.00L)溶液中加入甲硫醇钠(50％,264g,1886mmol)。氩气保护，将反应混合物在110℃下搅拌1小时，停止反应。将反应液冷却至室温后倒入冰水(6.00L)中，得到黄色悬浊液。悬浊液过滤后用清水(1.50L)洗涤，得到滤渣。将滤渣溶于DCM(5.00L)中得到黄色溶液。将溶液用无水硫酸钠干燥、过滤，滤液减压浓缩，所得残留物经真空干燥后，得到目标化合物(140g，收率82.9％，黄色固体)。LC-MS(ESI)m/z 180.1[M+H] +。 To a solution of 5-bromoisoindolin-1-one (200 g, 943 mmol) in DMF (2.00 L) was added sodium methyl mercaptan (50%, 264 g, 1886 mmol). Under argon protection, the reaction mixture was stirred at 110°C for 1 hour to stop the reaction. The reaction solution was cooled to room temperature and poured into ice water (6.00 L) to obtain a yellow suspension. The suspension was filtered and washed with water (1.50L) to obtain a filter residue. The filter residue was dissolved in DCM (5.00 L) to obtain a yellow solution. The solution was dried with anhydrous sodium sulfate and filtered, the filtrate was concentrated under reduced pressure, and the residue obtained was vacuum dried to obtain the target compound (140 g, yield 82.9%, yellow solid). LC-MS (ESI) m/z 180.1 [M+H] + .
步骤2：5-(甲硫基)-1-氧代异吲哚啉-2-甲酸叔丁酯的合成Step 2: Synthesis of tert-butyl 5-(methylthio)-1-oxoisoindoline-2-carboxylate
Figure PCTCN2021093788-appb-000016
Figure PCTCN2021093788-appb-000016
向5-甲硫基异吲哚啉-1-酮(140g,782mmol)的DMF(1.40L)溶液中加入二碳酸二叔丁酯(222g,1016mmol)、4-二甲氨基吡啶(124g,1016mmol)。将反应混合液在室温下搅拌反应1小时，停止反应。将反应液倒入冰水(6.00L)中，得到黄色悬浊液。悬浊液在室温下搅拌30分钟后过滤，再用清水(1.00L)洗涤，得到滤渣。将滤渣溶于EA(3.00L)中得到黄色溶液。溶液分别用0.1N稀盐酸(800mL×2)、清水(800mL)洗涤后，用无水硫酸钠干燥、过滤，滤液减压浓 缩，所得残留物经真空干燥后，得到目标化合物(210g，收率96.2％，黄色固体)。LC-MS(ESI)m/z302.1[M+Na] +。 To 5-methylthio isoindolin-1-one (140g, 782mmol) in DMF (1.40L) solution was added di-tert-butyl dicarbonate (222g, 1016mmol), 4-dimethylaminopyridine (124g, 1016mmol) ). The reaction mixture was stirred and reacted at room temperature for 1 hour to stop the reaction. The reaction solution was poured into ice water (6.00 L) to obtain a yellow suspension. The suspension was stirred at room temperature for 30 minutes, filtered, and washed with water (1.00 L) to obtain a filter residue. The filter residue was dissolved in EA (3.00L) to obtain a yellow solution. The solution was washed with 0.1N dilute hydrochloric acid (800mL×2) and water (800mL), dried with anhydrous sodium sulfate, filtered, the filtrate was concentrated under reduced pressure, and the residue was vacuum dried to obtain the target compound (210g, yield 96.2%, yellow solid). LC-MS(ESI) m/z 302.1 [M+Na] + .
步骤3：5-(甲磺酰基)-1-氧代异吲哚啉-2-甲酸叔丁酯的合成Step 3: Synthesis of tert-butyl 5-(methylsulfonyl)-1-oxoisoindoline-2-carboxylate
Figure PCTCN2021093788-appb-000017
Figure PCTCN2021093788-appb-000017
0℃下，向5-(甲硫基)-1-氧代异吲哚啉-2-甲酸叔丁酯(210g,752mmol)的DCM(2.00L)溶液中加入间氯过氧苯甲酸(85％,382g,1879mmol)。反应混合液继续在室温下搅拌反应2小时，停止反应。将反应液用DCM(1.50L)稀释后，分别用氢氧化钠溶液(1.00L×2)、清水(1.00L)洗涤、无水硫酸钠干燥、过滤，滤液减压浓缩，所得残留物经真空干燥后，得到目标化合物(215g，收率91.9％，黄色固体)。LC-MS(ESI)m/z 334.0[M+Na] +。 At 0℃, to 5-(methylthio)-1-oxoisoindoline-2-carboxylate tert-butyl ester (210g, 752mmol) in DCM (2.00L) was added m-chloroperoxybenzoic acid (85 %, 382g, 1879mmol). The reaction mixture was stirred and reacted at room temperature for 2 hours to stop the reaction. The reaction solution was diluted with DCM (1.50L), washed with sodium hydroxide solution (1.00L×2), water (1.00L), dried with anhydrous sodium sulfate, filtered, the filtrate was concentrated under reduced pressure, and the residue was vacuumed. After drying, the target compound (215 g, yield 91.9%, yellow solid) was obtained. LC-MS (ESI) m/z 334.0 [M+Na] + .
步骤4：1-羟基-5-(甲磺酰基)异吲哚啉-2-甲酸叔丁酯的合成Step 4: Synthesis of tert-butyl 1-hydroxy-5-(methylsulfonyl)isoindoline-2-carboxylate
Figure PCTCN2021093788-appb-000018
Figure PCTCN2021093788-appb-000018
-20℃和氩气保护下，向5-(甲磺酰基)-1-氧异吲哚啉-2-甲酸叔丁酯(50.0g,161mmol)的DCM(1.00L)溶液中滴加(时间超过40分钟)二异丁基氢化铝的甲苯溶液(214mL,321mmol,1.50M)，滴加完成后，氩气保护下-20℃继续搅拌1小时。向反应液中加入饱和酒石酸钾钠溶液(800mL)，搅拌20分钟后，升温至室温。向混合液加入DCM(1.50L)后分离有机相。水相继续用DCM萃取(1.00L×2)。有机相合并后减压浓缩，所得残留物经真空干燥后，得到目标化合物，4批次共得(33.75g，收率64.7％，粉色固体)。LC-MS(ESI)m/z 335.9[M+Na] +。 Under protection of argon at -20℃, add 5-(methylsulfonyl)-1-oxoisoindoline-2-carboxylate tert-butyl ester (50.0g, 161mmol) in DCM (1.00L) solution dropwise (time More than 40 minutes) diisobutylaluminum hydride in toluene solution (214mL, 321mmol, 1.50M), after completion of the dropwise addition, continue stirring at -20°C for 1 hour under the protection of argon. A saturated potassium sodium tartrate solution (800 mL) was added to the reaction solution, and after stirring for 20 minutes, the temperature was raised to room temperature. After adding DCM (1.50 L) to the mixed solution, the organic phase was separated. The aqueous phase was continuously extracted with DCM (1.00L×2). The organic phases were combined and concentrated under reduced pressure. The residue obtained was vacuum dried to obtain the target compound, which was obtained in 4 batches (33.75 g, yield 64.7%, pink solid). LC-MS (ESI) m/z 335.9 [M+Na] + .
步骤5：1-甲氧基-5-(甲磺酰基)异吲哚啉-2-甲酸叔丁酯的合成Step 5: Synthesis of tert-butyl 1-methoxy-5-(methylsulfonyl)isoindoline-2-carboxylate
Figure PCTCN2021093788-appb-000019
Figure PCTCN2021093788-appb-000019
向1-羟基-5-(甲磺酰基)异吲哚啉-2-甲酸叔丁酯(15.0g,47.9mmol)的甲醇(200mL)溶液中加入4-甲基苯磺酸吡啶(1.20g,4.79mmol)。反应混合液在室温下搅拌反应1小时，停止反应。向反应液中加入三乙胺(33.3mL)淬灭，然后减压浓缩，所得残留物经真空干燥后，得到目标化合物(16.1g，粗品，紫黑色固体)。MS(ESI)m/z 349.9[M+Na] +。 To 1-hydroxy-5-(methylsulfonyl) isoindoline-2-carboxylic acid tert-butyl ester (15.0g, 47.9mmol) in methanol (200mL) was added 4-methylbenzenesulfonic acid pyridine (1.20g, 4.79mmol). The reaction mixture was stirred and reacted at room temperature for 1 hour to stop the reaction. Triethylamine (33.3 mL) was added to the reaction solution for quenching, and then concentrated under reduced pressure. After vacuum drying of the resulting residue, the target compound (16.1 g, crude product, purple black solid) was obtained. MS (ESI) m/z 349.9 [M+Na] + .
步骤6：1-氰基-5-(甲磺酰基)异吲哚啉-2-甲酸叔丁酯的合成Step 6: Synthesis of tert-butyl 1-cyano-5-(methylsulfonyl)isoindoline-2-carboxylate
Figure PCTCN2021093788-appb-000020
Figure PCTCN2021093788-appb-000020
-70℃和氩气保护下，向1-甲氧基-5-(甲磺酰基)异吲哚啉-2-甲酸叔丁酯(16.0g,48.9mmol)的DCM(300mL)溶液中依次加入三甲基氰硅烷(9.17mL,73.3mmol)和三氟化硼乙醚(9.25mL, 73.3mmol)。反应混合物在-70℃和氩气保护下继续搅拌1小时，停止反应。向反应液中加入饱和碳酸氢钠(50.0mL)溶液和DCM(200mL)后升温至室温。有机相分离后，水相继续用DCM(100mL×2)萃取。有机相合并后，用无水硫酸钠干燥、过滤，滤液减压浓缩，所得残留物经柱层析分离纯化(PE：EA＝5/1-3/1)，得到目标化合物(7.g，两步收率49.3％，白色固体)。LC-MS(ESI)m/z 323.0[M+H] +。 Under the protection of argon at -70℃, add 1-methoxy-5-(methylsulfonyl)isoindoline-2-carboxylic acid tert-butyl ester (16.0g, 48.9mmol) in DCM (300mL) solution successively Trimethylsilyl cyanide (9.17mL, 73.3mmol) and boron trifluoride ether (9.25mL, 73.3mmol). The reaction mixture was stirred at -70°C under the protection of argon for 1 hour to stop the reaction. A saturated sodium bicarbonate (50.0 mL) solution and DCM (200 mL) were added to the reaction solution, and the temperature was raised to room temperature. After the organic phase was separated, the aqueous phase was continuously extracted with DCM (100 mL×2). After the organic phases were combined, dried with anhydrous sodium sulfate and filtered, the filtrate was concentrated under reduced pressure, and the resulting residue was separated and purified by column chromatography (PE:EA=5/1-3/1) to obtain the target compound (7.g, The two-step yield is 49.3%, white solid). LC-MS(ESI) m/z 323.0 [M+H] + .
步骤7：5-甲基磺酰基异吲哚啉-1-甲酸甲酯盐酸盐的合成Step 7: Synthesis of methyl 5-methylsulfonylisoindoline-1-carboxylate hydrochloride
Figure PCTCN2021093788-appb-000021
Figure PCTCN2021093788-appb-000021
将1-氰基-5-(甲磺酰基)异吲哚啉-2-甲酸叔丁酯(22.5g,322mmol)加入盐酸甲醇(3M,225mL)，反应混合物在80℃下搅拌5小时，停止反应。将反应液减压浓缩，所得残留物经真空干燥后，得到目标化合物(20.4g，粗品，黑色固体)。LC-MS(ESI)m/z 255.9[M+H] +。 Add tert-butyl 1-cyano-5-(methylsulfonyl)isoindoline-2-carboxylate (22.5g, 322mmol) to methanol hydrochloride (3M, 225mL), and the reaction mixture was stirred at 80°C for 5 hours, and stopped reaction. The reaction solution was concentrated under reduced pressure, and the resulting residue was vacuum dried to obtain the target compound (20.4 g, crude product, black solid). LC-MS (ESI) m/z 255.9 [M+H] + .
步骤8：2-乙酰基-5-(甲磺酰基)异吲哚啉-1-甲酸甲酯的合成Step 8: Synthesis of methyl 2-acetyl-5-(methylsulfonyl)isoindoline-1-carboxylate
Figure PCTCN2021093788-appb-000022
Figure PCTCN2021093788-appb-000022
0℃和氩气保护下，向5-甲基磺酰异吲哚啉-1-甲酸甲酯盐酸(20.0g,68.6mmol)的DCM(250mL)溶液中依次加三乙胺(34.7g,343mmol)和滴加乙酰氯(10.8g,137mmol)。反应混合物在0℃和氩气保护下继续搅拌3小时，停止反应。向反应液中加入水(250mL)，有机相分离后，水相继续用DCM(200mL×2)萃取。有机相合并后减压浓缩，所得残留物经柱层析分离纯化(PE：EA＝1/1-0/1)，得到目标化合物(12.17g，两步收率58.6％，白色固体)。LC-MS(ESI)m/z298.0[M+H] +。 1H NMR(400MHz,CDCl 3)δ7.97–7.85(m,2H),7.70–7.62(m,1H),5.78–5.64(m,1H),5.09–4.99(m,1H),4.96–4.83(m,1H),3.85–3.73(m,3H),3.07(s,3H),2.25,2.10(s,3H)。 Under the protection of argon at 0℃, add triethylamine (34.7g, 343mmol) to a solution of methyl 5-methylsulfonylisoindoline-1-carboxylate hydrochloric acid (20.0g, 68.6mmol) in DCM (250mL). ) And acetyl chloride (10.8g, 137mmol) was added dropwise. The reaction mixture was stirred at 0°C under the protection of argon for 3 hours to stop the reaction. Water (250 mL) was added to the reaction solution, and after the organic phase was separated, the aqueous phase was continuously extracted with DCM (200 mL×2). The organic phases were combined and concentrated under reduced pressure, and the resulting residue was separated and purified by column chromatography (PE:EA=1/1-0/1) to obtain the target compound (12.17g, two-step yield 58.6%, white solid). LC-MS (ESI) m/z 298.0 [M+H] + . 1 H NMR (400MHz, CDCl 3 ) δ 7.97-7.85 (m, 2H), 7.70-7.62 (m, 1H), 5.78-5.64 (m, 1H), 5.09-4.99 (m, 1H), 4.96-4.83 (m, 1H), 3.85–3.73 (m, 3H), 3.07 (s, 3H), 2.25, 2.10 (s, 3H).
步骤9：2-乙酰基-5-(甲磺酰基)异吲哚啉-1-甲酸的合成Step 9: Synthesis of 2-acetyl-5-(methylsulfonyl)isoindoline-1-carboxylic acid
Figure PCTCN2021093788-appb-000023
Figure PCTCN2021093788-appb-000023
向2-乙酰基-5-(甲磺酰基)异吲哚啉-1-甲酸甲酯(11.8g,39.7mmol)的四氢呋喃/甲醇/水(V:V:V＝1:1:1,120mL)溶液中加入氢氧化钠(3.18g,79.4mmol)。反应混合物在室温继续搅拌2小时，停止反应。将反应液减压浓缩，向所得残留物中加入水(100mL)，用盐酸(3M)调pH～4,所得溶液搅拌16小时，过滤，滤饼水洗(10.0mL×2)，经真空干燥后，得到目标化合物(8.80g，78.2％，类白色固体)。LC-MS(ESI)m/z 284.1[M+H] +。 1H NMR(400MHz,DMSO-d 6)δ8.05–7.87(m,2H),7.76–7.58(m,1H),5.94,5.53(s,1H),5.05–4.92,4.90–4.82,4.69–4.60(m,2H),3.24(s,3H),2.13,2.00(s,3H)。 To methyl 2-acetyl-5-(methylsulfonyl)isoindoline-1-carboxylate (11.8g, 39.7mmol) in tetrahydrofuran/methanol/water (V:V:V=1:1:1, 120mL) Sodium hydroxide (3.18g, 79.4mmol) was added to the solution. The reaction mixture was continuously stirred at room temperature for 2 hours to stop the reaction. The reaction solution was concentrated under reduced pressure, water (100 mL) was added to the residue obtained, and the pH was adjusted to 4 with hydrochloric acid (3M). The resulting solution was stirred for 16 hours, filtered, and the filter cake was washed with water (10.0 mL×2) and dried under vacuum. , The target compound (8.80 g, 78.2%, off-white solid) was obtained. LC-MS (ESI) m/z 284.1 [M+H] + . 1 H NMR (400MHz, DMSO-d 6 ) δ8.05--7.87 (m, 2H), 7.76-7.58 (m, 1H), 5.94, 5.53 (s, 1H), 5.05--4.92, 4.90-4.82, 4.69- 4.60 (m, 2H), 3.24 (s, 3H), 2.13, 2.00 (s, 3H).
步骤10：化合物2-乙酰基-N-(2’-氟-4’-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1’-联苯]-4-基)-5-(甲磺酰基)异吲哚啉-1-甲酰胺的合成Step 10: Compound 2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1,1 Synthesis of'-Biphenyl]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide
Figure PCTCN2021093788-appb-000024
Figure PCTCN2021093788-appb-000024
向2-乙酰基-5-(甲磺酰)异吲哚啉-1-甲酸(4.00g,14.1mmol)和2-(4'-氨基-2-氟-[1,1'-联苯]-4-基)-1,1,1,3,3,3-六氟丙烷-2-醇(4.17g，11.8mmol)的乙腈(80.0mL)溶液中依次加入TCFH(9.90g，35.3mmol)和N-甲基咪唑(4.83g，58.8mmol)，反应液室温搅拌2小时后，停止反应。将反应液减压浓缩，所得残留物再经中压液相制备(乙腈/水＝0-45％)，得到目标化合物(3.10g，收率42.5％，白色固体)。MS(ESI)m/z 619.1[M+H] +。 1H NMR(400MHz,DMSO-d 6)δ10.88,10.64(s,1H),9.01(s,1H),8.05–8.00(m,1H),7.95–7.89(m,1H),7.78–7.67(m,4H),7.62–7.52(m,4H),5.94,5.74(s,1H),5.05–4.77(m,2H),3.23,3.22(s,3H),2.16,2.01(s,3H)。 To 2-acetyl-5-(methylsulfonyl)isoindoline-1-carboxylic acid (4.00g, 14.1mmol) and 2-(4'-amino-2-fluoro-[1,1'-biphenyl] -4-yl)-1,1,1,3,3,3-hexafluoropropan-2-ol (4.17g, 11.8mmol) in acetonitrile (80.0mL) was added TCFH (9.90g, 35.3mmol) And N-methylimidazole (4.83g, 58.8mmol), the reaction solution was stirred at room temperature for 2 hours, then the reaction was stopped. The reaction solution was concentrated under reduced pressure, and the residue obtained was prepared by a medium pressure liquid phase (acetonitrile/water=0-45%) to obtain the target compound (3.10 g, yield 42.5%, white solid). MS (ESI) m/z 619.1 [M+H] + . 1 H NMR (400MHz, DMSO-d 6 ) δ 10.88, 10.64 (s, 1H), 9.01 (s, 1H), 8.05-8.00 (m, 1H), 7.95-7.89 (m, 1H), 7.78-7.67 (m,4H),7.62-7.52(m,4H),5.94,5.74(s,1H),5.05-4.77(m,2H),3.23,3.22(s,3H),2.16,2.01(s,3H) .
步骤11：R-2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺或S-2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺的合成Step 11: R-2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1, 1'-Biphenyl)-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide or S-2-acetyl-N-(2'-fluoro-4'-(1 ,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)-5-(methylsulfonyl)isoindole Synthesis of morpholin-1-carboxamide
Figure PCTCN2021093788-appb-000025
Figure PCTCN2021093788-appb-000025
外消旋体2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺(1.29g溶于约250mL甲醇，进样体积8.0mL)经Waters SFC 150(室温,100bar,214nm)和250*25mm 10μm
Figure PCTCN2021093788-appb-000026
(超临界二氧化碳：甲醇，45:55,3.0min,70mL/min)分离，得到R-2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺或S-2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺(500mg，白色固体，Ret.time＝1.276min,e.e.99％)。LC-MS(ESI)m/z 619.2[M+H] +。 1H NMR(400MHz,DMSO-d 6)δ10.88,10.65(s,1H),9.01(s,1H),8.05–7.99(m,1H),7.95–7.89(m,1H),7.81–7.67(m,4H),7.63–7.50(m,4H),5.94,5.75(s,1H),5.12–4.99,4.95–4.77(m,2H),3.23-3.21(m,3H),2.17,2.01(s,3H). Racemate 2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1,1 '-Biphenyl]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide (1.29g dissolved in about 250mL methanol, injection volume 8.0mL) was tested by Waters SFC 150 (room temperature, 100bar,214nm) and 250*25mm 10μm
Figure PCTCN2021093788-appb-000026
(Supercritical carbon dioxide: methanol, 45:55, 3.0min, 70mL/min) separation to obtain R-2-acetyl-N-(2'-fluoro-4'-(1,1,1,3,3, 3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide or S- 2-Acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1,1'-biphenyl ]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide (500mg, white solid, Ret.time=1.276min, ee99%). LC-MS (ESI) m/z 619.2 [M+H] + . 1 H NMR (400MHz, DMSO-d 6 ) δ 10.88, 10.65 (s, 1H), 9.01 (s, 1H), 8.05-7.99 (m, 1H), 7.95-7.89 (m, 1H), 7.81-7.67 (m, 4H), 7.63 - 7.50 (m, 4H), 5.94, 5.75 (s, 1H), 5.12 - 4.99, 4.95 - 4.77 (m, 2H), 3.23-3.21 (m, 3H), 2.17, 2.01 ( s, 3H).
S-2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺或R-2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺(516mg，白色固体，Ret.time＝2.610min,e.e.98％)。LC-MS(ESI)m/z 619.2[M+H] +。 1H NMR(400MHz,DMSO-d 6)δ10.88,10.65(s,1H),9.01(s,1H),8.06 –7.99(m,1H),7.95–7.89(m,1H),7.82–7.67(m,4H),7.64–7.50(m,4H),5.94,5.75(s,1H),5.11–4.99,4.93–4.75(m,2H),3.23-3.21(m,3H),2.17,2.01(s,3H). S-2-Acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1,1'- Biphenyl)-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide or R-2-acetyl-N-(2'-fluoro-4'-(1,1, 1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)-5-(methylsulfonyl)isoindoline-1 -Formamide (516mg, white solid, Ret.time=2.610min, ee98%). LC-MS (ESI) m/z 619.2 [M+H] + . 1 H NMR (400MHz, DMSO-d 6 ) δ 10.88, 10.65 (s, 1H), 9.01 (s, 1H), 8.06 -7.99 (m, 1H), 7.95-7.89 (m, 1H), 7.82-7.67 (m,4H),7.64-7.50(m,4H),5.94,5.75(s,1H),5.11-4.99,4.93-4.75(m,2H),3.23-3.21(m,3H),2.17,2.01( s, 3H).
实施例3：2-乙酰基-N-(4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺Example 3: 2-Acetyl-N-(4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl] -4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000027
Figure PCTCN2021093788-appb-000027
中间体2-(叔丁氧基羰基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酸的合成Synthesis of intermediate 2-(tert-butoxycarbonyl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid
步骤1：3-(2-氨基乙基)苯酚氢溴酸盐的合成Step 1: Synthesis of 3-(2-aminoethyl)phenol hydrobromide
Figure PCTCN2021093788-appb-000028
Figure PCTCN2021093788-appb-000028
将2-(3-甲氧基苯基)乙胺(9.00g，59.5mmol)溶于40％氢溴酸水溶液(120g，595mmol)中。反应液在110℃下搅拌反应6小时，LC-MS监测反应完全。将反应液减压浓缩，得到目标化合物(9.00g，粗品，浅棕色固体)。LC-MS(ESI)m/z:179.1[M+ACN+H] +。 2-(3-Methoxyphenyl)ethylamine (9.00 g, 59.5 mmol) was dissolved in 40% aqueous hydrobromic acid (120 g, 595 mmol). The reaction solution was stirred and reacted at 110°C for 6 hours, and the reaction was completed as monitored by LC-MS. The reaction solution was concentrated under reduced pressure to obtain the target compound (9.00 g, crude product, light brown solid). LC-MS(ESI) m/z: 179.1 [M+ACN+H] + .
步骤2:6-羟基-1,2,3,4-四氢异喹啉-1-甲酸乙酯氢溴酸盐的合成Step 2: Synthesis of ethyl 6-hydroxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylate hydrobromide
Figure PCTCN2021093788-appb-000029
Figure PCTCN2021093788-appb-000029
将3-(2-氨基乙基)苯酚氢溴酸盐(9.00g，65.6mmol)溶于乙醇(90mL)中。在室温下，将50％乙醛酸乙酯甲苯溶液(14.7g，72.2mmol)滴加到反应液中。加完后，反应混合物在100℃下搅拌反应过夜，LC-MS监测反应完全。将反应液减压浓缩，得到目标化合物(20.0g，粗品，棕色油状物)。LC-MS(ESI)m/z:222.0[M+H] +。 3-(2-Aminoethyl)phenol hydrobromide (9.00 g, 65.6 mmol) was dissolved in ethanol (90 mL). At room temperature, a 50% ethyl glyoxylate toluene solution (14.7 g, 72.2 mmol) was added dropwise to the reaction solution. After the addition, the reaction mixture was stirred overnight at 100° C., and the reaction was completed as monitored by LC-MS. The reaction solution was concentrated under reduced pressure to obtain the target compound (20.0 g, crude product, brown oil). LC-MS(ESI) m/z: 222.0 [M+H] + .
步骤3：6-羟基-3,4-二氢异喹啉-1,2(1H)-二甲酸1-乙基酯2-叔丁基酯的合成Step 3: Synthesis of 6-hydroxy-3,4-dihydroisoquinoline-1,2(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
Figure PCTCN2021093788-appb-000030
Figure PCTCN2021093788-appb-000030
将6-羟基-1,2,3,4-四氢异喹啉-1-甲酸乙酯氢溴酸盐(20.0g，66.2mmol)溶于四氢呋喃(200mL)和水(40mL)的混合溶剂中，在室温下，依次将三乙胺(11.0mL,79.4mmol)和二碳酸二叔丁酯(16.7mL,72.8mmol)加到反应液中。加完后，反应液在室温下继续搅拌反应1小时，LC- MS监测反应完全。将反应液倒入水(150mL)中，用EA(50mL x 2)萃取，合并有机相，用饱和氯化铵水溶液(100mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝4:1-2:1)，得到目标化合物(12.3g，三步收率64.4％，黄色油状物)。LC-MS(ESI)m/z:320.1[M-H] -。 Dissolve 6-hydroxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid ethyl ester hydrobromide (20.0g, 66.2mmol) in a mixed solvent of tetrahydrofuran (200mL) and water (40mL) At room temperature, add triethylamine (11.0 mL, 79.4 mmol) and di-tert-butyl dicarbonate (16.7 mL, 72.8 mmol) to the reaction solution in sequence. After the addition, the reaction solution was stirred and reacted at room temperature for 1 hour. LC-MS monitored that the reaction was complete. The reaction solution was poured into water (150mL), extracted with EA (50mL x 2), the organic phases were combined, washed with saturated aqueous ammonium chloride (100mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product After separation and purification by silica gel column (PE:EA=4:1-2:1), the target compound (12.3g, three-step yield 64.4%, yellow oil) was obtained. LC-MS(ESI) m/z: 320.1 [MH] - .
步骤4：6-(((三氟甲基)磺酰基)氧基)-3,4-二氢异喹啉-1,2(1H)-二甲酸1-乙基酯2-叔丁基酯的合成Step 4: 6-(((Trifluoromethyl)sulfonyl)oxy)-3,4-dihydroisoquinoline-1,2(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester Synthesis
Figure PCTCN2021093788-appb-000031
Figure PCTCN2021093788-appb-000031
将6-羟基-3,4-二氢异喹啉-1,2(1H)-二甲酸1-乙基酯2-叔丁基酯(11.0g,34.2mmol)溶于无水DCM(200mL)中，在冰浴和氮气保护下，依次将N-苯基双(三氟甲磺酰)亚胺(14.7g,41.1mmol)和DIEA(11.3mL，68.5mmol)加入到反应液中。加完后，撤掉冰浴，反应混合物在室温下搅拌反应3小时，LC-MS监测反应完全。将反应液减压浓缩，得到目标化合物(37.0g，粗品，棕色油状物)。LC-MS(ESI)m/z:353.9[M-BOC+H] +。 Dissolve 6-hydroxy-3,4-dihydroisoquinoline-1,2(1H)-dicarboxylic acid 1-ethyl 2-tert-butyl ester (11.0g, 34.2mmol) in anhydrous DCM (200mL) Under the protection of ice bath and nitrogen, N-phenylbis(trifluoromethanesulfonyl)imide (14.7g, 41.1mmol) and DIEA (11.3mL, 68.5mmol) were added to the reaction solution in sequence. After the addition was completed, the ice bath was removed, and the reaction mixture was stirred at room temperature for 3 hours. LC-MS monitored that the reaction was complete. The reaction solution was concentrated under reduced pressure to obtain the target compound (37.0 g, crude product, brown oil). LC-MS(ESI) m/z: 353.9 [M-BOC+H] + .
步骤5：6-(甲硫基)-3,4-二氢异喹啉-1,2-(1H)-二甲酸1-乙基酯2-叔丁基酯的合成Step 5: Synthesis of 6-(methylthio)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
Figure PCTCN2021093788-appb-000032
Figure PCTCN2021093788-appb-000032
依次将6-(((三氟甲基)磺酰基)氧基)-3,4-二氢异喹啉-1,2(1H)-二甲酸1-乙基酯2-叔丁基酯(10.2g，12.4mmol)、Pd 2(dba) 3(1.13g，1.24mmol)、xantphos(1.43g，2.47mmol)、DIEA(4.09mL，24.7mmol)、甲硫醇(11.9g，24.7mmol)和1,4-二氧六环(50mL)加入到闷罐中。向闷罐中吹氮气，快速密封罐子，反应混合物在100℃下搅拌反应过夜，LC-MS监测反应。将反应液冷却至室温，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝20:1-15:1)，得到目标化合物(6.20g，粗品，黄色油状物)。LC-MS(ESI)m/z:252.0[M-BOC+H] +。 6-(((trifluoromethyl)sulfonyl)oxy)-3,4-dihydroisoquinoline-1,2(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester ( 10.2g, 12.4mmol), Pd 2 (dba) 3 (1.13g, 1.24mmol), xantphos (1.43g, 2.47mmol), DIEA (4.09mL, 24.7mmol), methyl mercaptan (11.9g, 24.7mmol) and 1,4-Dioxane (50mL) was added to the stuffy pot. Nitrogen was blown into the stuffy pot, the pot was quickly sealed, the reaction mixture was stirred at 100°C for overnight reaction, and the reaction was monitored by LC-MS. The reaction solution was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product, which was separated and purified by silica gel column (PE:EA=20:1-15:1) to obtain the target compound (6.20 g, crude product, yellow oil). LC-MS(ESI) m/z: 252.0 [M-BOC+H] + .
步骤6:6-(甲基磺酰基)-3,4-二氢异喹啉-1,2-(1H)-二甲酸1-乙基酯2-叔丁基酯的合成Step 6: Synthesis of 6-(methylsulfonyl)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
Figure PCTCN2021093788-appb-000033
Figure PCTCN2021093788-appb-000033
将6-(甲硫基)-3,4-二氢异喹啉-1,2-(1H)-二甲酸1-乙基酯2-叔丁基酯(6.20g，17.6mmol)溶于DCM(100mL)中。在冰浴下，将间氯过氧苯甲酸(8.95g，44.1mmol,85％含量)缓慢加到反应 液中。加完后，撤掉冰浴，反应混合物在室温下搅拌反应2小时，LC-MS监测反应完全。将反应液过滤，滤液依次用饱和碳酸氢钠(100mL)和饱和食盐水(100mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝10:1-2:1)，得到目标化合物(1.38g，两步收率：29.0％，黄色油状物)。LC-MS(ESI)m/z:382.1[M-H] -。 Dissolve 6-(methylthio)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester (6.20g, 17.6mmol) in DCM (100mL). Under an ice bath, m-chloroperoxybenzoic acid (8.95 g, 44.1 mmol, 85% content) was slowly added to the reaction solution. After the addition was completed, the ice bath was removed, and the reaction mixture was stirred at room temperature for 2 hours. LC-MS monitored that the reaction was complete. The reaction solution was filtered, and the filtrate was washed with saturated sodium bicarbonate (100mL) and saturated brine (100mL) in turn, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product, which was separated and purified by silica gel column (PE:EA= 10:1-2:1) to obtain the target compound (1.38g, two-step yield: 29.0%, yellow oil). LC-MS(ESI) m/z: 382.1[MH] - .
步骤7：2-(叔丁氧基羰基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酸合成Step 7: Synthesis of 2-(tert-butoxycarbonyl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid
Figure PCTCN2021093788-appb-000034
Figure PCTCN2021093788-appb-000034
将6-(甲基磺酰基)-3,4-二氢异喹啉-1,2-(1H)-二甲酸1-乙基酯2-叔丁基酯(1.38g，3.60mmol)溶于甲醇(20mL)中，在室温下，将1mol/L氢氧化钠水溶液(10.8mL，10.8mmol)滴加到反应液中。加完后，反应液在室温下继续搅拌反应2小时，LC-MS监测反应完全。将反应液倒入冰水(30mL)中，用1mol/L稀盐酸调pH到3左右，用EA(20mLx2)萃取，合并有机相，用无水硫酸钠干燥，过滤，滤液减压浓缩，得到目标化合物(1.12g，收率87.6％，黄色固体)。LC-MS(ESI)m/z:709.1[2M-H] -。 Dissolve 6-(methylsulfonyl)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester (1.38g, 3.60mmol) In methanol (20 mL), at room temperature, a 1 mol/L sodium hydroxide aqueous solution (10.8 mL, 10.8 mmol) was added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted at room temperature for 2 hours. LC-MS monitored that the reaction was complete. Pour the reaction solution into ice water (30mL), adjust the pH to about 3 with 1mol/L dilute hydrochloric acid, extract with EA (20mLx2), combine the organic phases, dry with anhydrous sodium sulfate, filter, and concentrate the filtrate under reduced pressure to obtain Target compound (1.12 g, yield 87.6%, yellow solid). LC-MS(ESI) m/z: 709.1 [2M-H] - .
中间体2-(4'-氨基-[1,1'-联苯]-4-基)-1,1,1,3,3,3-六氟丙烷-2-醇的合成Synthesis of intermediate 2-(4'-amino-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3-hexafluoropropane-2-ol
步骤1：2-(4-溴苯基)-1,1,1,3,3,3-六氟丙烷-2-醇的合成Step 1: Synthesis of 2-(4-bromophenyl)-1,1,1,3,3,3-hexafluoropropane-2-ol
Figure PCTCN2021093788-appb-000035
Figure PCTCN2021093788-appb-000035
将溴化铜(474mg，2.12mmol)溶于乙腈(20mL)中，在氮气保护下，冰浴下，将亚硝酸叔丁酯(0.347mL，2.89mmol)滴加到反应液中。加完后，将2-(4-氨基苯基)-1,1,1,3,3,3-六氟丙烷-2-醇(500mg，1.93mmol)溶于乙腈(5mL)中并滴加到反应液中，加完后，反应混合物在冰浴下继续搅拌反应1小时，LC-MS监测反应完全。将反应液倒入冰水(50mL)中，用甲基叔丁基醚(20mLx2)萃取，合并有机相，用饱和食盐水(50mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩，得到目标化合物(630mg，粗品，棕色油状)。LC-MS(ESI)m/z:320.9[M-H] -。 Copper bromide (474 mg, 2.12 mmol) was dissolved in acetonitrile (20 mL), and tert-butyl nitrite (0.347 mL, 2.89 mmol) was added dropwise to the reaction solution under the protection of nitrogen and ice bath. After the addition, dissolve 2-(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (500mg, 1.93mmol) in acetonitrile (5mL) and add dropwise Into the reaction solution, after the addition, the reaction mixture was stirred and reacted in an ice bath for 1 hour. LC-MS monitored that the reaction was complete. The reaction solution was poured into ice water (50mL), extracted with methyl tert-butyl ether (20mLx2), the organic phases were combined, washed with saturated brine (50mL), dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure To obtain the target compound (630 mg, crude product, brown oil). LC-MS(ESI) m/z: 320.9 [MH] - .
步骤2：2-(4'-氨基-[1,1'-联苯]-4-基)-1,1,1,3,3,3-六氟丙烷-2-醇的合成Step 2: Synthesis of 2-(4'-amino-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3-hexafluoropropane-2-ol
Figure PCTCN2021093788-appb-000036
Figure PCTCN2021093788-appb-000036
将2-(4-溴苯基)-1,1,1,3,3,3-六氟丙烷-2-醇(630mg，1.95mmol)、4-氨基苯硼酸频哪醇酯(427mg，1.95mmol)、碳酸钾(539mg，3.90mmol)和PdCl 2(dtbpf)(143mg，0.195mmol)加入到1,4-二氧六环(10mL)和水(1mL)的混合溶剂中。在氮气保护下，反应混合物在100℃下搅拌反应2小时，LC-MS监测反应完全。将反应混合物冷却至室温，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE:EA＝10:1-6:1)，得到目标化合物(299mg，两步收率46.2％，淡黄色固体)。LC-MS(ESI)m/z:334.0[M-H] -。 The 2-(4-bromophenyl)-1,1,1,3,3,3-hexafluoropropane-2-ol (630mg, 1.95mmol), 4-aminophenylboronic acid pinacol ester (427mg, 1.95 mmol), potassium carbonate (539 mg, 3.90 mmol) and PdCl 2 (dtbpf) (143 mg, 0.195 mmol) were added to a mixed solvent of 1,4-dioxane (10 mL) and water (1 mL). Under the protection of nitrogen, the reaction mixture was stirred and reacted at 100°C for 2 hours. LC-MS monitored that the reaction was complete. The reaction mixture was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain the crude product, which was separated and purified by silica gel column (PE:EA=10:1-6:1) to obtain the target compound (299mg, the two-step yield was 46.2%, pale yellow solid). LC-MS(ESI) m/z: 334.0 [MH] - .
2-乙酰基-N-(4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺的合成2-Acetyl-N-(4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl )-6-(Methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
步骤1：1-((4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲基磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁酯的合成Step 1: 1-((4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl) Synthesis of tert-butyl carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
Figure PCTCN2021093788-appb-000037
Figure PCTCN2021093788-appb-000037
将2-(叔丁氧基羰基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酸(42.4mg，0.119mmol)和2-(4'-氨基-[1,1'-联苯]-4-基)-1,1,1,3,3,3-六氟丙烷-2-醇(40.0mg，0.119mmol)溶于无水DCM(3mL)中。在室温下，依次将HATU(68.1mg，0.179mmol)和DIEA(0.0592mL，0.358mmol)加到反应液中。加完后，反应混合物在室温下搅拌反应过夜，LC-MS监测反应完全。将反应液倒入水(20mL)中，用DCM(15mLx2)萃取，合并有机相，依次用饱和氯化铵(20mL)，饱和碳酸氢钠(20mL)和饱和食盐水(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩，得到目标化合物(90.0mg，粗品，棕色油状)。LC-MS(ESI)m/z:673.1[M+H] +。 Combine 2-(tert-butoxycarbonyl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid (42.4mg, 0.119mmol) and 2-(4'-Amino-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3-hexafluoropropane-2-ol (40.0mg, 0.119mmol) dissolved in anhydrous DCM ( 3mL). At room temperature, HATU (68.1 mg, 0.179 mmol) and DIEA (0.0592 mL, 0.358 mmol) were sequentially added to the reaction solution. After the addition, the reaction mixture was stirred overnight at room temperature, and the reaction was complete as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with DCM (15mLx2), the organic phases were combined, and washed with saturated ammonium chloride (20mL), saturated sodium bicarbonate (20mL) and saturated brine (20mL) successively, and It was dried with sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to obtain the target compound (90.0 mg, crude product, brown oil). LC-MS(ESI) m/z: 673.1 [M+H] + .
步骤2：N-(4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐的合成Step 2: N-(4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)- Synthesis of 6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
Figure PCTCN2021093788-appb-000038
Figure PCTCN2021093788-appb-000038
将1-((4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲基磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁酯(90.0mg)溶于DCM(2mL)中。在冰浴下，将6mol/L盐酸二氧六环溶液(1mL)滴加到反应液中。加完后，撤掉冰浴，反应混合物在室温下继续搅拌反应2小时。将反应液减压浓缩，得到目标化合物(90.0mg，粗品，棕色油状)。LC-MS(ESI)m/z:573.0[M+H] +。 Add 1-((4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)aminomethyl Acyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (90.0 mg) was dissolved in DCM (2 mL). Under an ice bath, 6 mol/L hydrochloric acid dioxane solution (1 mL) was added dropwise to the reaction solution. After the addition, the ice bath was removed, and the reaction mixture was stirred and reacted at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure to obtain the target compound (90.0 mg, crude product, brown oil). LC-MS(ESI) m/z: 573.0 [M+H] + .
步骤3：2-乙酰基-N-(4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺的合成Step 3: 2-Acetyl-N-(4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000039
Figure PCTCN2021093788-appb-000039
将N-(4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐(90.0mg，0.157mmol)溶于无水DCM(3mL)中。在室温下，依次将DIEA(0.078mL，0.472mmol)和乙酰氯(0.028mL，0.393mmol)滴加到反应液中。加完后，反应液在室温下继续搅拌反应30分钟。LC-MS监测反应完全。将反应液直接浓缩并溶于甲醇(3mL)中，在室温下，将1mol/L氢氧化钠水溶液(2mL)滴加到反应液中。加完后，在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液倒入水(20mL)中，用EA(15mLx2)萃取，合并有机相，用饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝1:1-0:1)，得到粗品，再经反向柱分离纯化(乙腈：水＝7：3)，得到目标化合物(15.0mg，三步收率20.5％，白色固体)。LC-MS(ESI)m/z:615.0[M+H] +。 1H NMR(400MHz,CDCl 3)δ7.88–7.79(m,2H),7.72–7.61(m,3H),7.52–7.28(m,6H),6.27(s,1H),4.06–3.93(m,1H),3.86–3.74(m,1H),3.41–3.24(m,1H),3.10–2.99(m,4H),2.37(s,3H). N-(4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)-6- (Methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (90.0 mg, 0.157 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, DIEA (0.078 mL, 0.472 mmol) and acetyl chloride (0.028 mL, 0.393 mmol) were sequentially added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted for 30 minutes at room temperature. LC-MS monitored the reaction to be complete. The reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product. Column separation and purification (PE:EA=1:1-0:1) to obtain the crude product, and then reverse column separation and purification (acetonitrile:water=7:3) to obtain the target compound (15.0mg, three-step yield 20.5% , White solid). LC-MS(ESI) m/z: 615.0 [M+H] + . 1 H NMR (400MHz, CDCl 3 ) δ 7.88-7.79 (m, 2H), 7.72-7.61 (m, 3H), 7.52-7.28 (m, 6H), 6.27 (s, 1H), 4.06-3.93 (m ,1H), 3.86–3.74(m,1H), 3.41–3.24(m,1H), 3.10–2.99(m,4H), 2.37(s,3H).
实施例4：2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺Example 4: 2-Acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropane-2-yl)-[1,1 '-Biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000040
Figure PCTCN2021093788-appb-000040
步骤1：1-((2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁酯的合成Step 1: 1-((2'-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl] Synthesis of -4-yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
Figure PCTCN2021093788-appb-000041
Figure PCTCN2021093788-appb-000041
将2-(叔丁氧基羰基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酸(50.0mg，0.141mmol)和2-(4'-氨基-2-氟-[1,1'-联苯]-4-基)-1,1,1,3,3,3-六氟丙烷-2-醇(49.7mg，0.141mmol)溶于无水DCM(3mL)中。在室温下，依次将HATU(80.3mg，0.211mmol)和DIEA(0.070mL，0.422mmol)加到反应液中。加完后，反应混合物在室温下搅拌反应过夜，LC-MS监测反应完全。将反应液倒入水(20mL)中，用DCM(15mLx2)萃取，合并有机相，依次用饱和氯化铵(20mL)，饱和碳酸氢钠(20mL)和饱和食盐水(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩，得到目标化合物(100mg，粗品，棕色油状)。LC-MS(ESI)m/z:691.1[M+H] +。 Combine 2-(tert-butoxycarbonyl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid (50.0mg, 0.141mmol) and 2-(4'-Amino-2-fluoro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3-hexafluoropropane-2-ol (49.7mg, 0.141mmol) dissolved in Anhydrous DCM (3mL). At room temperature, HATU (80.3 mg, 0.211 mmol) and DIEA (0.070 mL, 0.422 mmol) were sequentially added to the reaction solution. After the addition, the reaction mixture was stirred overnight at room temperature, and the reaction was complete as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with DCM (15mLx2), the organic phases were combined, and washed with saturated ammonium chloride (20mL), saturated sodium bicarbonate (20mL) and saturated brine (20mL) successively, and After drying with sodium sulfate and filtering, the filtrate was concentrated under reduced pressure to obtain the target compound (100 mg, crude product, brown oil). LC-MS(ESI) m/z: 691.1 [M+H] + .
步骤2：N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐的合成Step 2: N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
Figure PCTCN2021093788-appb-000042
Figure PCTCN2021093788-appb-000042
将1-((2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁酯(100mg)溶于DCM(2mL)中。在冰浴下，将6mol/L盐酸二氧六环溶液(1mL)滴加到反应液中。加完后，撤掉冰浴，反应混合物在室温下继续搅拌反应2小时。将反应液减压浓缩，得到目标化合物(100mg，粗品，棕色油状)。LC-MS(ESI)m/z:591.0[M+H] +。 Add 1-((2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4 -Yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (100 mg) was dissolved in DCM (2 mL). Under an ice bath, 6 mol/L hydrochloric acid dioxane solution (1 mL) was added dropwise to the reaction solution. After the addition, the ice bath was removed, and the reaction mixture was stirred and reacted at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure to obtain the target compound (100 mg, crude product, brown oil). LC-MS(ESI) m/z: 591.0 [M+H] + .
步骤3：2-乙酰基-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺的合成Step 3: 2-Acetyl-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1' -Biphenyl]-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000043
Figure PCTCN2021093788-appb-000043
将N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐(100mg，0.169mmol)溶于无水DCM(3mL)中。在室温下，依次将DIEA(0.084mL，0.508mmol)和乙酰氯(0.030mL，0.423mmol)滴加到反应液中。加完后，反应液在室温下继续搅拌反应30分钟。LC-MS监测反应完全。将反应液直接浓缩并溶于甲醇(3mL)中，在室温下，将1mol/L氢氧化钠水溶液(2mL)滴加到反应液中。加完后，在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液倒入水(20mL)中，用EA(15mLx2)萃取，合并有机相，用饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝1:1-0:1)，得到粗品，再经反向硅胶柱分离纯化(乙腈：水＝7：3)，得到目标化合物(23.0mg，三步收率：25.8％，白色固体)。LC-MS(ESI)m/z:633.0[M+H] +. 1H NMR(400MHz,CDCl 3)δ7.87–7.81(m,2H),7.62–7.44(m,5H),7.42–7.27(m,3H),6.26(s,1H),3.97–3.87(m,1H),3.85–3.76(m,1H),3.31–3.19(m,1H),3.10–3.00(m,4H),2.35(s,3H). N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (100 mg, 0.169 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, DIEA (0.084 mL, 0.508 mmol) and acetyl chloride (0.030 mL, 0.423 mmol) were sequentially added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted for 30 minutes at room temperature. LC-MS monitored the reaction to be complete. The reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product. Column separation and purification (PE:EA=1:1-0:1) to obtain the crude product, and then reverse silica gel column separation and purification (acetonitrile:water=7:3) to obtain the target compound (23.0mg, three-step yield: 25.8%, white solid). LC-MS(ESI)m/z: 633.0[M+H] + . 1 H NMR(400MHz,CDCl 3 )δ7.87–7.81(m,2H), 7.62–7.44(m,5H), 7.42–7.27 (m,3H), 6.26(s,1H), 3.97--3.87(m,1H), 3.85--3.76(m,1H), 3.31--3.19(m,1H), 3.10--3.00(m,4H), 2.35 (s,3H).
实施例5和实施例6：R-2-乙酰基-N-(2'-氟-4'-(1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺或S-2-乙酰基-N-(2'-氟-4'-(1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺Example 5 and Example 6: R-2-acetyl-N-(2'-fluoro-4'-(1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)- [1,1'-Biphenyl]-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide or S-2-acetyl- N-(2'-Fluoro-4'-(1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)- 6-(Methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000044
Figure PCTCN2021093788-appb-000044
外消旋体2-乙酰基-N-(2'-氟-4'-(1,1,3,3,3-六氟-2-羟基丙-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺(1.60g溶于约150mL甲醇，进样体积3.0mL)经Waters SFC150(室温,100bar,214nm)和250*25mm 10μm Dr.maish Reprosil Chiral-OM(类似于
Figure PCTCN2021093788-appb-000045
)(超临界二氧化碳：甲醇，50:50,2.3min,70mL/min)分离，得到R-2-乙酰基-N-(2'-氟-4'-(1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺或S-2-乙酰基-N-(2'-氟-4'-(1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺(676mg，黄色固体，Ret.time＝0.778min,e.e.99.74％)。LC-MS(ESI)m/z 633.1[M+H] +。 1H NMR(400MHz,DMSO-d 6)δ10.78,10.73(s,1H),9.00(s,1H),7.87–7.80(m,3H),7.75–7.65(m,3H),7.61–7.50(m,4H),5.96,5.85(s,1H),4.14–4.06(m,1H),3.74–3.66(m,1H),3.30–3.22(m,1H),3.22–3.19(m,3H),3.09–3.00(m,1H),2.18,2.15(s,3H)。 Racemate 2-acetyl-N-(2'-fluoro-4'-(1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)-[1,1'- Biphenyl]-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide (1.60g dissolved in about 150mL methanol, injection volume 3.0mL ) After Waters SFC150 (room temperature, 100bar, 214nm) and 250*25mm 10μm Dr. maish Reprosil Chiral-OM (similar to
Figure PCTCN2021093788-appb-000045
) (Supercritical carbon dioxide: methanol, 50:50, 2.3min, 70mL/min) separation to obtain R-2-acetyl-N-(2'-fluoro-4'-(1,1,3,3,3) -Hexafluoro-2-hydroxypropane-2-yl)-[1,1'-biphenyl]-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquine Lin-1-carboxamide or S-2-acetyl-N-(2'-fluoro-4'-(1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[ 1,1'-Biphenyl]-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide (676mg, yellow solid, Ret.time =0.778min, ee99.74%). LC-MS (ESI) m/z 633.1 [M+H] + . 1 H NMR (400MHz, DMSO-d 6 ) δ 10.78, 10.73 (s, 1H), 9.00 (s, 1H), 7.87 - 7.80 (m, 3H), 7.75 - 7.65 (m, 3H), 7.61 - 7.50 (m, 4H), 5.96, 5.85 (s, 1H), 4.14-4.06 (m, 1H), 3.74-3.66 (m, 1H), 3.30-3.22 (m, 1H), 3.22-3.19 (m, 3H) ,3.09–3.00(m,1H), 2.18, 2.15(s,3H).
S-2-乙酰基-N-(2'-氟-4'-(1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺或R-2-乙酰基-N-(2'-氟-4'-(1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺(683mg，黄色固体，Ret.time＝1.107min,e.e.98.58％)。 1H NMR(400MHz,DMSO-d 6)δ10.78,10.73(s,1H),9.00(s,1H),7.87–7.80(m,3H),7.75–7.66(m,3H),7.61–7.51(m,4H),5.96,5.85(s,1H),4.14–4.06(m,1H),3.75–3.65(m,1H),3.30–3.22(m,1H),3.22–3.19(m,3H),3.09–3.01(m,1H),2.18,2.15(s,3H)。 S-2-acetyl-N-(2'-fluoro-4'-(1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl ]-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide or R-2-acetyl-N-(2'-fluoro- 4'-(1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl)-6-(methylsulfonyl) -1,2,3,4-Tetrahydroisoquinoline-1-carboxamide (683mg, yellow solid, Ret.time=1.107min, ee98.58%). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.78, 10.73 (s, 1H), 9.00 (s, 1H), 7.87-7.80 (m, 3H), 7.75-7.66 (m, 3H), 7.61-7.51 (m, 4H), 5.96, 5.85 (s, 1H), 4.14-4.06 (m, 1H), 3.75-3.65 (m, 1H), 3.30-3.22 (m, 1H), 3.22-3.19 (m, 3H) ,3.09–3.01(m,1H),2.18,2.15(s,3H).
实施例7：2-乙酰基-6-(乙基磺酰基)-N-(2'-氟-4'-(1,1,1,3,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯基]-4-基)-1,2,3,4-四氢异喹啉-1-甲酰胺Example 7: 2-Acetyl-6-(ethylsulfonyl)-N-(2'-fluoro-4'-(1,1,1,3,3,3,3-hexafluoro-2-hydroxyl) Propan-2-yl)-[1,1'-biphenyl]-4-yl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000046
Figure PCTCN2021093788-appb-000046
步骤1：6-(乙硫基)-3,4-二氢异喹啉-1,2-(1H)-二甲酸1-乙基酯2-叔丁基酯的合成Step 1: Synthesis of 6-(ethylthio)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
Figure PCTCN2021093788-appb-000047
Figure PCTCN2021093788-appb-000047
依次将6-(((三氟甲基)磺酰基)氧基)-3,4-二氢异喹啉-1,2(1H)-二甲酸1-乙基酯2-叔丁基酯(3.70g，8.16mmol)、Pd 2(dba) 3(747mg，0.816mmol)、xantphos(944mg，1.63mmol)、DIEA(2.70mL，16.3mmol)、乙硫醇(1.22mL，16.3mmol)和1,4-二氧六环(20mL)加入到封管中。向封管中吹氮气，快速密封管子，反应混合物在100℃下搅拌反应过夜，LC-MS监测反应完全。将反应液冷却至室温，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝20:1-15:1)，得到目标化合物(1.80g，粗品，黄色油状物)。LC-MS(ESI)m/z:266.0[M-BOC+H] +。 6-(((trifluoromethyl)sulfonyl)oxy)-3,4-dihydroisoquinoline-1,2(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester ( 3.70g, 8.16mmol), Pd 2 (dba) 3 (747mg, 0.816mmol), xantphos (944mg, 1.63mmol), DIEA (2.70mL, 16.3mmol), ethanethiol (1.22mL, 16.3mmol) and 1, 4-Dioxane (20 mL) was added to the sealed tube. Nitrogen was blown into the sealed tube and the tube was quickly sealed. The reaction mixture was stirred at 100°C for overnight reaction. LC-MS monitored that the reaction was complete. The reaction solution was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product, which was separated and purified by silica gel column (PE:EA=20:1-15:1) to obtain the target compound (1.80 g, crude product, yellow oil). LC-MS(ESI) m/z: 266.0 [M-BOC+H] + .
步骤2：6-(乙基磺酰基)-3,4-二氢异喹啉-1,2-(1H)-二甲酸1-乙基酯2-叔丁基酯的合成Step 2: Synthesis of 6-(ethylsulfonyl)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester
Figure PCTCN2021093788-appb-000048
Figure PCTCN2021093788-appb-000048
将6-(乙硫基)-3,4-二氢异喹啉-1,2-(1H)-二甲酸1-乙基酯2-叔丁基酯(1.80g，4.92mmol)溶于DCM(30mL)中。在冰浴下，将85％间氯过氧苯甲酸(2.50g，12.3mmol)缓慢加到反应液中。加完后，撤掉冰浴，反应混合物在室温下搅拌反应2小时，LC-MS监测反应完全。将反应液过滤，滤液依次用饱和碳酸氢钠(20mL)和饱和食盐水(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝15:1-5:1)，得到目标化合物(1.10g，三步收率：81.0％，黄色油状物)。LC-MS(ESI)m/z:396.1[M-H] -。 Dissolve 6-(ethylthio)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester (1.80g, 4.92mmol) in DCM (30mL). Under an ice bath, 85% m-chloroperoxybenzoic acid (2.50 g, 12.3 mmol) was slowly added to the reaction solution. After the addition was completed, the ice bath was removed, and the reaction mixture was stirred at room temperature for 2 hours. LC-MS monitored that the reaction was complete. The reaction solution was filtered, and the filtrate was washed with saturated sodium bicarbonate (20mL) and saturated brine (20mL) in turn, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product, which was separated and purified by silica gel column (PE:EA= 15:1-5:1) to obtain the target compound (1.10g, three-step yield: 81.0%, yellow oil). LC-MS(ESI) m/z: 396.1 [MH] - .
步骤3：2-(叔丁氧基羰基)-6-(乙基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酸的合成Step 3: Synthesis of 2-(tert-butoxycarbonyl)-6-(ethylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid
Figure PCTCN2021093788-appb-000049
Figure PCTCN2021093788-appb-000049
将6-(乙基磺酰基)-3,4-二氢异喹啉-1,2-(1H)-二甲酸1-乙基酯2-叔丁基酯(460mg，1.16mmol)溶于甲醇(5mL)中，在室温下，将1mol/L氢氧化钠水溶液(3.47mL，3.47mmol)滴加到反应液中。加完后，反应液在室温下继续搅拌反应2小时，LC-MS监测反应完全。将反应液倒入冰水(20mL)中，用1mol/L稀盐酸调pH到3左右，用EA(10mLx2)萃取，合并有机相，用无水硫酸钠干燥，过滤，滤液减压浓缩，得到目标化合物(362mg，收率84.7％，黄色固体)。LC-MS(ESI)m/z:737.1[2M-H] -。 Dissolve 6-(ethylsulfonyl)-3,4-dihydroisoquinoline-1,2-(1H)-dicarboxylic acid 1-ethyl ester 2-tert-butyl ester (460mg, 1.16mmol) in methanol (5mL), at room temperature, 1mol/L sodium hydroxide aqueous solution (3.47mL, 3.47mmol) was added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted at room temperature for 2 hours. LC-MS monitored that the reaction was complete. Pour the reaction solution into ice water (20mL), adjust the pH to about 3 with 1mol/L dilute hydrochloric acid, extract with EA (10mLx2), combine the organic phases, dry with anhydrous sodium sulfate, filter, and concentrate the filtrate under reduced pressure to obtain Target compound (362 mg, yield 84.7%, yellow solid). LC-MS(ESI) m/z: 737.1 [2M-H] - .
步骤4：6-(乙基磺酰基)-1-((2'-氟-4'-(1,1,1,3,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯基]-4-基)氨基甲酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁酯的合成Step 4: 6-(Ethylsulfonyl)-1-((2'-fluoro-4'-(1,1,1,3,3,3,3-hexafluoro-2-hydroxypropan-2-yl )-[1,1'-Biphenyl]-4-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
Figure PCTCN2021093788-appb-000050
Figure PCTCN2021093788-appb-000050
将2-(叔丁氧基羰基)-6-(乙基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酸(50.0mg，0.135mmol)和2-(4'-氨基-2-氟-[1,1'-联苯]-4-基)-1,1,1,3,3,3-六氟丙烷-2-醇(47.8mg，0.203mmol)溶于无水DCM(3mL)中。在室温下，依次将HATU(77.2mg，0.203mmol)和DIEA(0.067mL，0.406mmol)加到反应液中。加完后，反应混合物在室温下搅拌反应过夜，LC-MS监测反应完全。将反应液倒入水(20mL)中，用DCM(15mLx2)萃取，合并有机相，依次用饱和氯化铵(20mL)、饱和碳酸氢钠(20mL)和饱和食盐水(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到目标化合物(100mg，粗品，棕色油状)。LC-MS(ESI)m/z:705.1[M+H] +。 Combine 2-(tert-butoxycarbonyl)-6-(ethylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid (50.0mg, 0.135mmol) and 2-(4'-Amino-2-fluoro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3-hexafluoropropane-2-ol (47.8mg, 0.203mmol) dissolved in Anhydrous DCM (3mL). At room temperature, HATU (77.2 mg, 0.203 mmol) and DIEA (0.067 mL, 0.406 mmol) were sequentially added to the reaction solution. After the addition, the reaction mixture was stirred overnight at room temperature, and the reaction was complete as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with DCM (15mL×2), the organic phases were combined, and washed with saturated ammonium chloride (20mL), saturated sodium bicarbonate (20mL) and saturated brine (20mL) in turn, It was dried with sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to obtain the target compound (100 mg, crude product, brown oil). LC-MS(ESI) m/z: 705.1 [M+H] + .
步骤5：6-(乙基磺酰基)-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐的合成Step 5: 6-(Ethylsulfonyl)-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[ Synthesis of 1,1'-biphenyl]-4-yl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
Figure PCTCN2021093788-appb-000051
Figure PCTCN2021093788-appb-000051
将6-(乙基磺酰基)-1-((2'-氟-4'-(1,1,1,3,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯基]-4-基)氨基甲酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁基酯(100mg，0.142mmol)溶于DCM(2mL)中。在冰浴下，将6mol/L盐酸二氧六环溶液(1mL)滴加到反应液中。加完后，撤掉冰浴，反应混合物在室温下继续搅拌反应2小时。将反应液减压浓缩，得到目标化合物(100mg，粗品，棕色油状)。LC-MS(ESI)m/z:605.0[M+H] +。 Add 6-(ethylsulfonyl)-1-((2'-fluoro-4'-(1,1,1,3,3,3,3-hexafluoro-2-hydroxypropan-2-yl)- [1,1'-Biphenyl]-4-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (100mg, 0.142mmol) dissolved in DCM ( 2mL). Under an ice bath, 6 mol/L hydrochloric acid dioxane solution (1 mL) was added dropwise to the reaction solution. After the addition, the ice bath was removed, and the reaction mixture was stirred and reacted at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure to obtain the target compound (100 mg, crude product, brown oil). LC-MS(ESI) m/z: 605.0 [M+H] + .
步骤6：2-乙酰基-6-(乙基磺酰基)-N-(2'-氟-4'-(1,1,1,3,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯基]-4-基)-1,2,3,4-四氢异喹啉-1-甲酰胺的合成Step 6: 2-Acetyl-6-(ethylsulfonyl)-N-(2'-fluoro-4'-(1,1,1,3,3,3,3-hexafluoro-2-hydroxypropane) -2-yl)-[1,1'-biphenyl]-4-yl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000052
Figure PCTCN2021093788-appb-000052
将6-(乙基磺酰基)-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐(100mg，0.165mmol)溶于无水DCM(3mL)中。在室温下，依次将DIEA(0.082mL，0.496mmol)和乙酰氯(0.024mL，0.331mmol)滴加到反应液中。加完后，反应液在室温下继续搅拌反应30分钟。LC-MS监测反应完全。将反应液直接浓缩并溶于甲醇(3mL) 中，在室温下，将1mol/L氢氧化钠水溶液(2mL)滴加到反应液中。加完后，在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液倒入水(20mL)中，用EA(15mLx2)萃取，合并有机相，用饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝1：1-0：1)得到粗品，再经反向硅胶柱分离纯化(乙腈：水＝7：3)得到目标化合物(25.0mg，三步收率：34.5％，白色固体)。LC-MS(ESI)m/z:647.0[M+H] +； 1H NMR(400MHz,CDCl 3)δ7.83–7.77(m,2H),7.69–7.56(m,1H),7.52–7.40(m,4H),7.34–7.27(m,3H),6.27,6.21(s,1H),4.05–3.94(m,1H),3.87–3.74(m,1H),3.35–3.24(m,1H),3.18–2.99(m,3H),2.37,2.31(s,3H),1.30(t,J＝7.3Hz,3H)。 Add 6-(ethylsulfonyl)-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1, 1'-Biphenyl]-4-yl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (100 mg, 0.165 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, DIEA (0.082 mL, 0.496 mmol) and acetyl chloride (0.024 mL, 0.331 mmol) were sequentially added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted for 30 minutes at room temperature. LC-MS monitored the reaction to be complete. The reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product. Column separation and purification (PE:EA=1:1-0:1) to obtain the crude product, and then reverse silica gel column separation and purification (acetonitrile:water=7:3) to obtain the target compound (25.0mg, three-step yield: 34.5%) , White solid). LC-MS(ESI)m/z:647.0[M+H] + ; 1 H NMR(400MHz,CDCl 3 )δ7.83–7.77(m,2H),7.69–7.56(m,1H),7.52–7.40 (m,4H),7.34--7.27(m,3H), 6.27, 6.21(s,1H), 4.05--3.94(m,1H), 3.87-3.74(m,1H), 3.35-3.24(m,1H) , 3.18-2.99 (m, 3H), 2.37, 2.31 (s, 3H), 1.30 (t, J = 7.3 Hz, 3H).
实施例8：2-乙酰基-N-(4’-(1,1,1,3,3,3-六氟-2-羟基丙基-2-基)-[1,1’-联苯]-4-基)-5-(甲基磺酰基)异吲哚啉-1-甲酰胺Example 8: 2-Acetyl-N-(4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropyl-2-yl)-[1,1'-biphenyl ]-4-yl)-5-(methylsulfonyl)isoindoline-1-carboxamide
Figure PCTCN2021093788-appb-000053
Figure PCTCN2021093788-appb-000053
将2-(4’-氨基-[1,1’-联苯]-4-基)-1,1,1,3,3,3-六氟丙-2-醇(50mg，0.149mmol)、2-乙酰基-5-(甲磺酰基)异吲哚啉-1-甲酸(46.5mg，0.164mmol)和TCFH(92mg，0.328mmol)加入到乙腈(5mL)中。向反应混合物中依次加入N-甲基咪唑(73.4mg，0.894mmol)。反应混合物在室温下搅拌反应3小时。加入EA(15mL)和水(10mL)。分出水相用EA(10mL)萃取。合并有机相用饱和食盐水洗涤，无水硫酸钠干燥，过滤。滤液减压浓缩得到粗产品。经柱层析分离纯化(C18，甲醇/水＝0～100％)得到目标化合物(30mg，收率33.5％，黄色固体)。LC-MS(ESI)m/z 601.2[M+H] +。 1H NMR(400MHz,DMSO-d 6)δ10.87,10.63(s,1H),8.79–8.76(m,1H),8.05–8.00(m,1H),7.95–7.91(m,1H),7.83–7.80(m,2H),7.79–7.70(m,7H),5.95–5.93,5.76–5.73(m,1H),5.09–5.03,4.93–4.88,4.85–4.78(m,2H),3.26–3.22(m,3H),2.17,2.02(s,3H). Combine 2-(4'-amino-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3-hexafluoropropan-2-ol (50mg, 0.149mmol), 2-Acetyl-5-(methylsulfonyl)isoindoline-1-carboxylic acid (46.5 mg, 0.164 mmol) and TCFH (92 mg, 0.328 mmol) were added to acetonitrile (5 mL). To the reaction mixture was sequentially added N-methylimidazole (73.4 mg, 0.894 mmol). The reaction mixture was stirred and reacted at room temperature for 3 hours. Add EA (15 mL) and water (10 mL). The aqueous phase was separated and extracted with EA (10 mL). The combined organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to obtain a crude product. Separation and purification by column chromatography (C18, methanol/water=0-100%) gave the target compound (30 mg, yield 33.5%, yellow solid). LC-MS(ESI) m/z 601.2 [M+H] + . 1 H NMR (400MHz, DMSO-d 6 ) δ 10.87, 10.63 (s, 1H), 8.79-8.76 (m, 1H), 8.05-8.00 (m, 1H), 7.95-7.91 (m, 1H), 7.83 --7.80 (m, 2H), 7.79 - 7.70 (m, 7H), 5.95 - 5.93, 5.76 - 5.73 (m, 1H), 5.09 - 5.03, 4.93 - 4.88, 4.85 - 4.78 (m, 2H), 3.26 - 3.22 (m, 3H), 2.17, 2.02 (s, 3H).
实施例9：2-乙酰基-N-(2-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺Example 9: 2-Acetyl-N-(2-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1' -Biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000054
Figure PCTCN2021093788-appb-000054
步骤1：1,1,1,3,3,3-六氟-2-(4-(4,4,5,5-四甲基-1,3,2-二氧杂硼杂环戊-2-基)苯基)丙-2-醇的合成Step 1: 1,1,1,3,3,3-hexafluoro-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane- Synthesis of 2-yl)phenyl)propan-2-ol
Figure PCTCN2021093788-appb-000055
Figure PCTCN2021093788-appb-000055
依次将2-(4-溴苯基)-1,1,1,3,3,3-六氟丙烷-2-醇(1000mg，3.10mmol)、联硼酸频那醇酯(865mg，3.41mmol)、乙酸钾(911mg，9.29mmol)和Pd(dppf)Cl 2(227mg，0.310mmol)加入到1,4-二氧六环(10mL)中。在氮气保护下，反应混合物在90℃下搅拌反应过夜。将反应混合物冷却至室温，过滤，滤液减压浓缩，得到目标化合物(1.00g，粗品，黑色油状)。LC-MS(ESI)m/z:369.1[M-H] -。 Combine 2-(4-bromophenyl)-1,1,1,3,3,3-hexafluoropropane-2-ol (1000mg, 3.10mmol) and pinacol diborate (865mg, 3.41mmol) in sequence , Potassium acetate (911 mg, 9.29 mmol) and Pd(dppf)Cl 2 (227 mg, 0.310 mmol) were added to 1,4-dioxane (10 mL). Under the protection of nitrogen, the reaction mixture was stirred overnight at 90°C. The reaction mixture was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain the target compound (1.00 g, crude product, black oil). LC-MS(ESI) m/z: 369.1 [MH] - .
步骤2：2-(4'-氨基-2'-氟-[1,1'-联苯]-4-基)-1,1,1,3,3,3,3-六氟丙烷-2-醇的合成Step 2: 2-(4'-amino-2'-fluoro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3,3-hexafluoropropane-2 -Synthesis of alcohol
Figure PCTCN2021093788-appb-000056
Figure PCTCN2021093788-appb-000056
将1,1,1,3,3,3-六氟-2-(4-(4,4,5,5-四甲基-1,3,2-二氧杂硼杂环戊-2-基)苯基)丙-2-醇(500mg，1.35mmol)、4-溴-3-氟苯胺(205mg，1.08mmol)、碳酸钾(373mg，2.70mmol)和Pd(dppf)Cl 2(98.9mg，0.135mmol)加入到1,4-二氧六环(5mL)和水(0.5mL)的混合溶剂中。在氮气保护下，反应混合物在100℃下搅拌反应2小时，LC-MS监测反应完全。将反应混合物冷却至室温，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE:EA＝10:1-2:1)得到粗品，再经反相柱分离纯化(乙腈：甲醇＝1:1)，得到目标化合物(30.0mg，三步收率4.40％，白色固体)。LC-MS(ESI)m/z:352.0[M-H] -。 1,1,1,3,3,3-hexafluoro-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2- (Yl)phenyl)propan-2-ol (500mg, 1.35mmol), 4-bromo-3-fluoroaniline (205mg, 1.08mmol), potassium carbonate (373mg, 2.70mmol) and Pd(dppf)Cl 2 (98.9mg , 0.135mmol) was added to the mixed solvent of 1,4-dioxane (5mL) and water (0.5mL). Under the protection of nitrogen, the reaction mixture was stirred and reacted at 100°C for 2 hours. LC-MS monitored that the reaction was complete. The reaction mixture was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product, which was separated and purified by silica gel column (PE:EA=10:1-2:1), and then separated and purified by a reverse phase column (acetonitrile: methanol=1). 1) to obtain the target compound (30.0 mg, three-step yield 4.40%, white solid). LC-MS(ESI) m/z: 352.0 [MH] - .
步骤3：1-((2-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲基磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁酯的合成Step 3: 1-((2-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
Figure PCTCN2021093788-appb-000057
Figure PCTCN2021093788-appb-000057
将2-(4'-氨基-2'-氟-[1,1'-联苯]-4-基)-1,1,1,3,3,3,3-六氟丙烷-2-醇(30.0mg，0.085mmol)和2-(叔丁氧基羰基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酸(30.2mg，0.085mmol)溶于无水DCM(3mL)中。在室温下，依次将HATU(48.4mg，0.127mmol)和DIEA(0.042mL，0.255mmol)加入到反应液中。加完后，反应混合物在室温下搅拌反应2小时，LC-MS监测反应完全。将反应液倒入水(20mL)中，用DCM(15mLx2)萃取，合并有机相，依次用饱和碳酸氢钠(20mL)和饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩，得到目标化合物(80.0mg，粗品，棕色液体)。LC-MS(ESI)m/z:689.1[M-H] -。 2-(4'-amino-2'-fluoro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3,3-hexafluoropropan-2-ol (30.0mg, 0.085mmol) and 2-(tert-butoxycarbonyl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid (30.2mg, 0.085mmol) ) Was dissolved in anhydrous DCM (3mL). At room temperature, HATU (48.4 mg, 0.127 mmol) and DIEA (0.042 mL, 0.255 mmol) were sequentially added to the reaction solution. After the addition, the reaction mixture was stirred at room temperature for 2 hours, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with DCM (15mL×2), the organic phases were combined, washed with saturated sodium bicarbonate (20mL) and saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, The filtrate was concentrated under reduced pressure to obtain the target compound (80.0 mg, crude product, brown liquid). LC-MS(ESI) m/z: 689.1 [MH] - .
步骤4：N-(2-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐的合成Step 4: N-(2-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4 -Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
Figure PCTCN2021093788-appb-000058
Figure PCTCN2021093788-appb-000058
将1-((2-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲基磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁酯(80.0mg)溶于DCM(1mL)中。在冰浴下，将4mol/L盐酸二氧六环溶液(1mL)滴加到反应液中。加完后，撤掉冰浴，反应混合物在室温下继续搅拌反应2小时，LC-MS监测反应完全。将反应液减压浓缩，得到目标化合物(70.0mg，粗品，棕色油状)。LC-MS(ESI)m/z:591.0[M+H] +。 Add 1-((2-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- (Yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (80.0 mg) was dissolved in DCM (1 mL). Under an ice bath, 4 mol/L hydrochloric acid dioxane solution (1 mL) was added dropwise to the reaction solution. After the addition, the ice bath was removed, and the reaction mixture was stirred and reacted at room temperature for 2 hours. LC-MS monitored that the reaction was complete. The reaction solution was concentrated under reduced pressure to obtain the target compound (70.0 mg, crude product, brown oil). LC-MS(ESI) m/z: 591.0 [M+H] + .
步骤5：2-乙酰基-N-(2-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺的合成Step 5: 2-Acetyl-N-(2-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'- Synthesis of biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000059
Figure PCTCN2021093788-appb-000059
将N-(2-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐(70.0mg，0.119mmol)溶于无水DCM(3mL)中。在室温下，依次将三乙胺(0.049mL，0.356mmol)和乙酰氯(0.021mL，0.296mmol)滴加到反应液中。加完后，反应液在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液直接浓缩并溶于甲醇(3mL)中，在室温下，将1mol/L氢氧化钠水溶液(2mL)滴加到反应液中。加完后，在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液倒入水(20mL)中，用EA(15mLx2)萃取，合并有机相，用饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝1:1-0:1)得到粗品，再经反相柱分离纯化(乙腈：水＝7:3)得到目标化合物(10.0mg，三步收率18.6％，白色固体)。LC-MS(ESI)m/z:633.0[M+H] +。 1H NMR(400MHz,CDCl 3)δ9.51(s,1H),7.90–7.85(m,2H),7.80–7.74(m,2H),7.62–7.56(m,3H),7.54–7.50(m,1H),7.37–7.33(m,1H),7.24–7.20(m,2H),6.23(s,1H),3.89–3.82(m,2H),3.27–3.18(m,1H),3.14–3.05(m,5H),2.35(s,3H). N-(2-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl )-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (70.0 mg, 0.119 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.049 mL, 0.356 mmol) and acetyl chloride (0.021 mL, 0.296 mmol) were sequentially added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product. Column separation and purification (PE:EA=1:1-0:1) to obtain the crude product, and then reverse phase column separation and purification (acetonitrile:water=7:3) to obtain the target compound (10.0mg, three-step yield 18.6%, white solid). LC-MS(ESI) m/z: 633.0 [M+H] + . 1 H NMR(400MHz, CDCl 3 ) δ9.51(s,1H), 7.90-7.85(m,2H), 7.80-7.74(m,2H), 7.62-7.56(m,3H), 7.54-7.50(m ,1H),7.37–7.33(m,1H),7.24–7.20(m,2H), 6.23(s,1H), 3.89–3.82(m,2H), 3.27–3.18(m,1H), 3.14–3.05 (m,5H),2.35(s,3H).
实施例10：2-乙酰基-N-(2-氯-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺Example 10: 2-Acetyl-N-(2-chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1' -Biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000060
Figure PCTCN2021093788-appb-000060
步骤1：2-(4'-氨基-2'-氯-[1,1'-联苯]-4-基)-1,1,1,3,3,3,3-六氟丙烷-2-醇的合成Step 1: 2-(4'-Amino-2'-chloro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3,3-hexafluoropropane-2 -Synthesis of alcohol
Figure PCTCN2021093788-appb-000061
Figure PCTCN2021093788-appb-000061
将1,1,1,3,3,3-六氟-2-(4-(4,4,5,5-四甲基-1,3,2-二氧杂硼杂环戊-2-基)苯基)丙-2-醇(500mg，1.35mmol)、4-溴-3-氯苯胺(223mg，1.08mmol)、碳酸钾(373mg，2.70mmol)和Pd(dppf)Cl 2(98.9mg，0.135mmol)加入到1,4-二氧六环(5mL)和水(0.5mL)的混合溶剂中。在氮气保护下，反应混合物在100℃下搅拌反应2小时，LC-MS监测反应完全。将反应混合物冷却至室温，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE:EA＝10:1-2:1)得到粗品，再经反相柱分离纯化(乙腈：甲醇＝1:1)，得到目标化合物(310mg，三步收率43.5％，白色固体)。LC-MS(ESI)m/z:368.0[M-H] -。 1,1,1,3,3,3-hexafluoro-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2- Yl)phenyl)propan-2-ol (500mg, 1.35mmol), 4-bromo-3-chloroaniline (223mg, 1.08mmol), potassium carbonate (373mg, 2.70mmol) and Pd(dppf)Cl 2 (98.9mg , 0.135mmol) was added to the mixed solvent of 1,4-dioxane (5mL) and water (0.5mL). Under the protection of nitrogen, the reaction mixture was stirred and reacted at 100°C for 2 hours. LC-MS monitored that the reaction was complete. The reaction mixture was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product, which was separated and purified by silica gel column (PE:EA=10:1-2:1), and then separated and purified by a reverse phase column (acetonitrile: methanol=1). 1) to obtain the target compound (310 mg, yield 43.5% in three steps, white solid). LC-MS(ESI) m/z: 368.0 [MH] - .
步骤2：1-((2-氯-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲基磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁酯的合成Step 2: 1-((2-Chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
Figure PCTCN2021093788-appb-000062
Figure PCTCN2021093788-appb-000062
将2-(4'-氨基-2'-氯-[1,1'-联苯]-4-基)-1,1,1,3,3,3,3-六氟丙烷-2-醇(83.2mg，0.225mmol)和2-(叔丁氧基羰基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酸(80.0mg，0.225mmol)溶于无水DCM(3mL)中。在室温下，依次将HATU(111mg，0.293mmol)和DIEA(0.112mL，0.675mmol)加入到反应液中。加完后，反应混合物在室温下搅拌反应2小时，LC-MS监测反应完全。将反应液倒入水(20mL)中，用DCM(15mLx2)萃取，合并有机相，依次用饱和碳酸氢钠(20mL)中和饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩，得到目标化合物(150mg，粗品，棕色油状)。LC-MS(ESI)m/z:705.1[M-H] -。 2-(4'-amino-2'-chloro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3,3-hexafluoropropan-2-ol (83.2mg, 0.225mmol) and 2-(tert-butoxycarbonyl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid (80.0mg, 0.225mmol) ) Was dissolved in anhydrous DCM (3mL). At room temperature, HATU (111 mg, 0.293 mmol) and DIEA (0.112 mL, 0.675 mmol) were sequentially added to the reaction solution. After the addition, the reaction mixture was stirred at room temperature for 2 hours, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with DCM (15mLx2), the organic phases were combined, washed with saturated sodium bicarbonate (20mL) and saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, and filtered The filtrate was concentrated under reduced pressure to obtain the target compound (150 mg, crude product, brown oil). LC-MS(ESI) m/z: 705.1 [MH] - .
步骤3：N-(2-氯-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐的合成Step 3: N-(2-Chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4 -Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
Figure PCTCN2021093788-appb-000063
Figure PCTCN2021093788-appb-000063
将1-((2-氯-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲基磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁酯(150mg)溶于DCM(1.5mL)中。在冰浴下，将4mol/L盐酸二氧六环溶液(1.5mL)滴加到反应液中。加完后，撤掉冰浴，反应混合物在室温下继续搅拌反应2小时，LC-MS监测反应完全。将反应液减压浓缩，得到目标化合物(140mg，粗品，棕色油状)。LC-MS(ESI)m/z:605.1[M-H] -。 Add 1-((2-chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- (Yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (150 mg) was dissolved in DCM (1.5 mL). Under an ice bath, 4 mol/L hydrochloric acid dioxane solution (1.5 mL) was added dropwise to the reaction solution. After the addition, the ice bath was removed, and the reaction mixture was stirred and reacted at room temperature for 2 hours. LC-MS monitored that the reaction was complete. The reaction solution was concentrated under reduced pressure to obtain the target compound (140 mg, crude product, brown oil). LC-MS(ESI) m/z: 605.1 [MH] - .
步骤4：2-乙酰基-N-(2-氯-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺的合成Step 4: 2-Acetyl-N-(2-chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'- Synthesis of biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000064
Figure PCTCN2021093788-appb-000064
将N-(2-氯-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐(140mg，0.231mmol)溶于无水DCM(3mL)中。在室温下，依次将三乙胺(0.096mL，0.692mmol)和乙酰氯(0.041mL，0.577mmol)滴加到反应液中。加完后，反应液在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液直接浓缩并溶于甲醇(3mL)中，在室温下，将1mol/L氢氧化钠水溶液(2mL)滴加到反应液中。加完后，在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液倒入水(20mL)中，用EA(15mLx2)萃取，合并有机相，用饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝1:1-0:1)得到粗品，再经反相柱分离纯化(乙腈：水＝7:3)得到目标化合物(49.3mg，三步收率12.9％，白色固体)。LC-MS(ESI)m/z:649.0[M+H] +。 1H NMR(400MHz,CDCl 3)δ9.38(d,J＝11.7Hz,1H),7.88–7.83(m,2H),7.80–7.68(m,3H),7.53–7.45(m,3H),7.43–7.38(m,1H),7.25–7.23(m,1H),6.20(s,1H),3.91–3.79(m,3H),3.26–3.15(m,1H),3.11–3.03(m,4H),2.32(s,3H). N-(2-chloro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4-yl )-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (140 mg, 0.231 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.096 mL, 0.692 mmol) and acetyl chloride (0.041 mL, 0.577 mmol) were sequentially added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product. Column separation and purification (PE:EA=1:1-0:1) to obtain the crude product, and then reverse phase column separation and purification (acetonitrile:water=7:3) to obtain the target compound (49.3mg, three-step yield 12.9%, white solid). LC-MS(ESI) m/z: 649.0 [M+H] + . 1 H NMR(400MHz, CDCl 3 )δ9.38(d,J=11.7Hz,1H), 7.88–7.83(m,2H), 7.80–7.68(m,3H), 7.53–7.45(m,3H), 7.43–7.38(m,1H), 7.25–7.23(m,1H), 6.20(s,1H), 3.91–3.79(m,3H), 3.26–3.15(m,1H), 3.11–3.03(m,4H) ), 2.32(s, 3H).
实施例11：N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-2-丙酰基-1,2,3,4-四氢异喹啉-1-甲酰胺Example 11: N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl] -4-yl)-6-(methylsulfonyl)-2-propionyl-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000065
Figure PCTCN2021093788-appb-000065
步骤1：1-((2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁基酯的合成Step 1: 1-((2'-Fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl] Synthesis of -4-yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester
Figure PCTCN2021093788-appb-000066
Figure PCTCN2021093788-appb-000066
将2-(叔丁氧基羰基)-6-(乙基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酸(553mg，1.56mmol)和2-(4'-氨基-2-氟-[1,1'-联苯]-4-基)-1,1,1,3,3,3,3-六氟丙烷-2-醇(550mg，1.56mmol)溶于无水DCM(6mL)中。在室温下，依次将HATU(770mg，2.02mmol)和DIEA(0.772mL，4.67mmol)加入到反应液中。加完后，反应混合物在室温下搅拌反应2小时，TLC监测反应完全。将反应液倒入水(20mL)中，用DCM(15mLx2)萃取，合并有机相，依次用饱和碳酸氢钠(20mL)和饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩，得到目标化合物(1.00g，粗品，淡棕色固体)。Combine 2-(tert-butoxycarbonyl)-6-(ethylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid (553mg, 1.56mmol) and 2-(4'- Amino-2-fluoro-[1,1'-biphenyl]-4-yl)-1,1,1,3,3,3,3-hexafluoropropane-2-ol (550mg, 1.56mmol) dissolved in Anhydrous DCM (6 mL). At room temperature, HATU (770 mg, 2.02 mmol) and DIEA (0.772 mL, 4.67 mmol) were sequentially added to the reaction solution. After the addition, the reaction mixture was stirred at room temperature for 2 hours, and TLC monitored the reaction to be complete. The reaction solution was poured into water (20mL), extracted with DCM (15mLx2), the organic phases were combined, washed with saturated sodium bicarbonate (20mL) and saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, The filtrate was concentrated under reduced pressure to obtain the target compound (1.00 g, crude product, light brown solid).
步骤2：N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐的合成Step 2: N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride
Figure PCTCN2021093788-appb-000067
Figure PCTCN2021093788-appb-000067
将1-((2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)氨基甲酰基)-6-(甲磺酰基)-3,4-二氢异喹啉-2(1H)-甲酸叔丁基酯(1.00g)溶于DCM(5mL)中。在冰浴下，将4mol/L盐酸二氧六环溶液(5mL)滴加到反应液中。加完后，撤掉冰浴，反应混合物在室温下继续搅拌反应2小时，LC-MS监测反应完全。将反应液减压浓缩，得到目标化合物(700mg，粗品，黄色固体)。LC-MS(ESI)m/z:591.1[M+H] +。 Add 1-((2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4 -Yl)carbamoyl)-6-(methylsulfonyl)-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (1.00 g) was dissolved in DCM (5 mL). Under an ice bath, 4 mol/L hydrochloric acid dioxane solution (5 mL) was added dropwise to the reaction solution. After the addition, the ice bath was removed, and the reaction mixture was stirred and reacted at room temperature for 2 hours. LC-MS monitored that the reaction was complete. The reaction solution was concentrated under reduced pressure to obtain the target compound (700 mg, crude product, yellow solid). LC-MS(ESI) m/z: 591.1 [M+H] + .
步骤3：N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-2-丙酰基-1,2,3,4-四氢异喹啉-1-甲酰胺的合成Step 3: N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]- Synthesis of 4-yl)-6-(methylsulfonyl)-2-propionyl-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000068
Figure PCTCN2021093788-appb-000068
将N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐(100mg，0.169mmol)溶于无水DCM(3mL)中。在室温下，依次将三乙胺(0.071mL，0.508mmol)和丙酰氯(0.037mL，0.423mmol)滴加到反应液中。加完后，反应液在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液直接浓缩并溶于甲醇(3mL)中，在室温下，将1mol/L氢氧化钠水溶液(2mL)滴加到反应液中。加完后，在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液倒入水(20mL)中，用EA(15mLx2)萃取，合并有机相，用饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝1:1-0:1)得到粗品，再经反相柱分离纯化(乙腈：水＝7:3)得到目标化合物(31.1mg，三步收率21.6％，白色固体)。LC-MS(ESI)m/z:647.1[M+H] +。 1H NMR(400MHz,CDCl 3)δ8.26–7.94(m,1H),7.90–7.73(m,2H),7.43–7.30(m,4H),7.12–6.76(m,3H),6.48(s,1H),4.44–4.22(m,1H),3.75–3.62(m,1H),3.60–3.39(m,1H),3.14–2.90(m,5H),2.73–2.58(m,1H),1.45(t,3H). N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (100 mg, 0.169 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.071 mL, 0.508 mmol) and propionyl chloride (0.037 mL, 0.423 mmol) were sequentially added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product. Column separation and purification (PE:EA=1:1-0:1) to obtain the crude product, and then reverse phase column separation and purification (acetonitrile:water=7:3) to obtain the target compound (31.1mg, three-step yield 21.6%, white solid). LC-MS(ESI) m/z: 647.1 [M+H] + . 1 H NMR(400MHz, CDCl 3 )δ8.26-7.94(m,1H), 7.90-7.73(m,2H), 7.43-7.30(m,4H), 7.12-6.76(m,3H), 6.48(s ,1H),4.44-4.22(m,1H),3.75-3.62(m,1H), 3.60-3.39(m,1H),3.14-2.90(m,5H),2.73-2.58(m,1H),1.45 (t,3H).
实施例12：2-(环丙烷羰基)-N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺Example 12: 2-(Cyclopropanecarbonyl)-N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[ 1,1'-Biphenyl)-4-yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
Figure PCTCN2021093788-appb-000069
Figure PCTCN2021093788-appb-000069
将N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐(100mg，0.169mmol)溶于无水DCM(3mL)中。在室温下，依次将三乙胺(0.071mL，0.508mmol)和环丙基甲酰氯(0.0385mL，0.423mmol)滴加到反应液中。加完后，反应液在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液直接浓缩并溶于甲醇(3mL)中，在室温下，将1mol/L氢氧化钠水溶液(2mL)滴加到反应液中。加完后，在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液倒入水(20mL)中，用EA(15mLx2)萃取，合并有机相，用饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝1:1-0:1)得到粗品，再经反相柱分离纯化(乙腈：水＝7:3)得到目标化合物(41.7mg，三步收率28.4％，白色固体)。LC-MS(ESI)m/z:700.0[M+ACN+H] +。 1H NMR(400MHz,DMSO-d 6)δ10.83,10.70(s,1H),7.88–7.78(m,3H),7.74– 7.62(m,3H),7.60–7.46(m,4H),6.16,5.90(s,1H),4.39–4.19(m,1H),4.05–3.83(m,2H),3.27–3.22(m,1H),3.18(s,3H),3.10–3.01(m,1H),2.15–2.07(m,1H),0.88–0.68(m,4H). N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (100 mg, 0.169 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.071 mL, 0.508 mmol) and cyclopropylformyl chloride (0.0385 mL, 0.423 mmol) were sequentially added dropwise to the reaction solution. After the addition, the reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was directly concentrated and dissolved in methanol (3 mL), and a 1 mol/L sodium hydroxide aqueous solution (2 mL) was added dropwise to the reaction solution at room temperature. After the addition, the reaction was continued to be stirred at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with EA (15mLx2), the organic phases were combined, washed with saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain a crude product. Column separation and purification (PE:EA=1:1-0:1) to obtain the crude product, and then reverse phase column separation and purification (acetonitrile:water=7:3) to obtain the target compound (41.7mg, three-step yield 28.4%, white solid). LC-MS(ESI) m/z: 700.0 [M+ACN+H] + . 1 H NMR (400MHz, DMSO-d 6 ) δ 10.83, 10.70 (s, 1H), 7.88-7.78 (m, 3H), 7.74-7.62 (m, 3H), 7.60-7.46 (m, 4H), 6.16 ,5.90(s,1H), 4.39–4.19(m,1H), 4.05–3.83(m,2H), 3.27–3.22(m,1H), 3.18(s,3H), 3.10–3.01(m,1H) , 2.15-2.07(m,1H), 0.88-0.68(m,4H).
实施例13：N 1-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-N 2-甲基-6-(甲基磺酰基)-3,4-二氢异喹啉-1,2(1H)-二甲酰胺 Example 13: N 1 -(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl ]-4-yl)-N 2 -methyl-6-(methylsulfonyl)-3,4-dihydroisoquinoline-1,2(1H)-dimethylamide
Figure PCTCN2021093788-appb-000070
Figure PCTCN2021093788-appb-000070
将N-(2'-氟-4'-(1,1,1,3,3,3-六氟-2-羟基丙烷-2-基)-[1,1'-联苯]-4-基)-6-(甲基磺酰基)-1,2,3,4-四氢异喹啉-1-甲酰胺盐酸盐(100mg，0.169mmol)溶于无水DCM(3mL)中。在室温下，依次将三乙胺(0.071mL，0.508mmol)和甲胺基甲酰氯(39.6mg，0.423mmol)加到反应液中。加完后，反应液在室温下继续搅拌反应30分钟，LC-MS监测反应完全。将反应液倒入水(20mL)中，用DCM(15mLx2)萃取，合并有机相，依次用饱和碳酸氢钠(20mL)和饱和氯化铵(20mL)洗涤，用无水硫酸钠干燥，过滤，滤液减压浓缩得到粗品，经硅胶柱分离纯化(PE：EA＝1:1-0:1)得到粗品，再经反相柱分离纯化(乙腈：水＝7:3)，得到目标化合物(41.7mg，三步收率28.5％，白色固体)。LC-MS(ESI)m/z:648.0[M+H] +。 1H NMR(400MHz,DMSO-d 6)δ10.60(s,1H),7.84–7.75(m,3H),7.73–7.63(m,3H),7.58–7.47(m,4H),6.71–6.65(m,1H),5.83(s,1H),3.91–3.81(m,1H),3.56–3.48(m,1H),3.22–3.13(m,4H),3.02–2.92(m,1H),2.62(d,J＝4.1Hz,3H). N-(2'-fluoro-4'-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-[1,1'-biphenyl]-4- Yl)-6-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide hydrochloride (100 mg, 0.169 mmol) was dissolved in anhydrous DCM (3 mL). At room temperature, triethylamine (0.071 mL, 0.508 mmol) and methylcarbamoyl chloride (39.6 mg, 0.423 mmol) were sequentially added to the reaction solution. After the addition, the reaction solution was stirred and reacted at room temperature for 30 minutes, and the reaction was completed as monitored by LC-MS. The reaction solution was poured into water (20mL), extracted with DCM (15mL×2), the organic phases were combined, washed with saturated sodium bicarbonate (20mL) and saturated ammonium chloride (20mL), dried with anhydrous sodium sulfate, filtered, The filtrate was concentrated under reduced pressure to obtain the crude product, which was separated and purified by silica gel column (PE:EA=1:1-0:1), and then separated and purified by reverse phase column (acetonitrile:water=7:3) to obtain the target compound (41.7). mg, three-step yield 28.5%, white solid). LC-MS(ESI) m/z: 648.0 [M+H] + . 1 H NMR (400MHz, DMSO-d 6 ) δ 10.60 (s, 1H), 7.84-7.75 (m, 3H), 7.73-7.63 (m, 3H), 7.58-7.47 (m, 4H), 6.71-6.65 (m,1H),5.83(s,1H),3.91--3.81(m,1H),3.56--3.48(m,1H),3.22--3.13(m,4H),3.02-2.92(m,1H),2.62 (d,J=4.1Hz,3H).
活性实施例1：体外测定化合物对RORγt荧光素酶报告基因的抑制作用Activity Example 1: In vitro determination of compound's inhibitory effect on RORγt luciferase reporter gene
本实验基本上按照文献(Current Chemical Genomics,2010,4,43-49)所述的方法进行。This experiment is basically carried out according to the method described in the literature (Current Chemical Genomics, 2010, 4, 43-49).
将RORγ-LBD编码序列插入到pBIND质粒(Promega,E1581)。该表达载体和报告载体(携带稳定整合的GAL4启动子驱动的荧光素酶报告基因的pGL4.35)在HEK293T宿主细胞中共表达。当抑制剂与相应的嵌合受体结合时，嵌合受体与报告基因载体上的GAL4结合位点结合并抑制报告基因表达。根据化学发光信号的强弱来判定化合物对RORγ上的抑制活性。The RORγ-LBD coding sequence was inserted into the pBIND plasmid (Promega, E1581). The expression vector and the reporter vector (pGL4.35 carrying the luciferase reporter gene driven by the stably integrated GAL4 promoter) are co-expressed in HEK293T host cells. When the inhibitor binds to the corresponding chimeric receptor, the chimeric receptor binds to the GAL4 binding site on the reporter gene carrier and inhibits reporter gene expression. According to the strength of the chemiluminescence signal, the inhibitory activity of the compound on RORγ was judged.
试剂与耗材Reagents and consumables
Figure PCTCN2021093788-appb-000071
Figure PCTCN2021093788-appb-000071
实验方法：experimental method:
1.准备实验化合物1. Prepare the test compound
1.1所有待测化合物用DMSO进行3倍梯度稀释，10个稀释梯度，起始浓度为10mM。1.1 All test compounds were diluted with DMSO in a 3-fold gradient, 10 dilution gradients, and the starting concentration was 10 mM.
1.2阳性对照AZD-0284用DMSO进行3倍梯度稀释，10个稀释梯度，起始浓度为10mM。1.2 The positive control AZD-0284 was diluted with DMSO in a 3-fold gradient, 10 dilution gradients, and the initial concentration was 10mM.
1.3准备1000×阳性对照(10mM AZD-0284)和1000×阴性对照(100％DMSO)。1.3 Prepare 1000× positive control (10mM AZD-0284) and 1000× negative control (100% DMSO).
1.4将化合物板子封闭并震荡5min。1.4 Seal the compound plate and shake for 5 min.
2.实验过程2. Experimental process
2.1细胞悬浊液制备和种板2.1 Cell suspension preparation and seeding
a)所有细胞都按照ATCC标准操作培养，HEK293T在指数生长期进行实验。a) All cells were cultured in accordance with ATCC standards, and HEK293T was tested in the exponential growth phase.
b)弃去培养基。b) Discard the medium.
c)用PBS清洗细胞2次。c) Wash the cells twice with PBS.
d)加入胰酶消化液消化细胞，用完全培养基终止消化。d) Add trypsin digestion solution to digest the cells, and terminate the digestion with complete medium.
e)收集细胞并计数，只有在细胞活率大于90％时才可以进行实验。e) Collect the cells and count them. Only when the cell viability rate is greater than 90% can the experiment be carried out.
f)种6*10 6HEK293T细胞到100mm细胞培养皿中。 f) Seed 6*10 6 HEK293T cells into a 100mm cell culture dish.
g)将种好细胞的培养皿置于37℃，5％CO2培养箱过夜培养。g) Place the culture dish with the seeded cells in a 37°C, 5% CO2 incubator for overnight culture.
2.2细胞转染2.2 Cell transfection
a)将Trans-IT转染试剂放置室温平衡；a) Place the Trans-IT transfection reagent at room temperature to equilibrate;
b)加20μl转染试剂600μl Opti-MEM TM培养基，注意不要碰到管壁，用移液枪吹吸混匀，室温静置5分钟； b) Add 20μl of transfection reagent and 600μl of Opti-MEM TM medium, take care not to touch the tube wall, blow and mix with a pipette, and let it stand at room temperature for 5 minutes;
c)加入10μg质粒到转染试剂中(见步骤2.2.b)，室温静置20分钟；质粒：分别加入5μg pBIND-RORγ和5μg pGL4.35质粒c) Add 10μg plasmid to the transfection reagent (see step 2.2.b), let stand at room temperature for 20 minutes; Plasmid: add 5μg pBIND-RORγ and 5μg pGL4.35 plasmid respectively
d)将混好DNA的转染试剂加到100mm细胞培养皿中(见步骤2.1)；d) Add the transfection reagent mixed with DNA to a 100mm cell culture dish (see step 2.1);
e)将培养皿置于37℃，5％CO2培养箱培养5h。e) Place the petri dish in a 37°C, 5% CO2 incubator for 5 hours.
2.3化合物的处理2.3 Treatment of compounds
a)将稀释好的化合物用Echo550转移25nl到细胞培养板中(6007680-50,PE)；a) Transfer 25nl of the diluted compound to the cell culture plate (6007680-50, PE) with Echo550;
b)将细胞(见步骤2.2)接种到384细胞培养板中(6007680-50,PE)，每孔15,000细胞数，25μl含5％炭吸附FBS培养基；b) Inoculate the cells (see step 2.2) into a 384 cell culture plate (6007680-50, PE), 15,000 cells per well, 25μl FBS medium containing 5% carbon adsorption;
c)细胞在37℃，5％CO2培养箱中过夜培养c) The cells are cultured overnight in a 37°C, 5% CO2 incubator
2.4化合物的检测：2.4 Detection of compounds:
a)将Steady-Glo TM检测试剂放置室温； a) Put the Steady-Glo TM detection reagent at room temperature;
b)将384细胞板(见步骤2.3)放置室温；b) Place the 384 cell plate (see step 2.3) at room temperature;
c)每孔加入25μL Steady-Glo TM检测试剂于细胞培养板(见步骤2.4b)； c) Add 25μL Steady-Glo TM detection reagent to each well on the cell culture plate (see step 2.4b);
d)将板子放到振荡器上避光震荡5min；d) Put the board on the oscillator to avoid light and shake for 5 minutes;
e)用Envision 2104检测化学发光值。e) Use Envision 2104 to detect the chemiluminescence value.
％Inhibition的计算：Calculation of %Inhibition:
Figure PCTCN2021093788-appb-000072
Figure PCTCN2021093788-appb-000072
RLU cmpd:测试化合物的荧光值 RLU cmpd : the fluorescence value of the test compound
Figure PCTCN2021093788-appb-000073
阳性对照平均值
Figure PCTCN2021093788-appb-000073
Positive control mean
Figure PCTCN2021093788-appb-000074
阴性对照平均值
Figure PCTCN2021093788-appb-000074
Negative control mean
用Graphad8.0通过拟合％Inhibition和化合物浓度的log值来计算化合物的IC 50。测定结果显示，本发明的化合物对RORγt荧光素酶报告基因有较好的抑制活性(如表1所示)。 Compound with Graphad8.0 calculated IC 50 and% Inhibition by fitting the log of compound concentration. The measurement results show that the compound of the present invention has a good inhibitory activity on the RORγt luciferase reporter gene (as shown in Table 1).
表1.实施例化合物对RORγt荧光素酶报告基因抑制活性测定Table 1. Determination of the inhibitory activity of the example compounds on the RORγt luciferase reporter gene
实施例Example IC 50(nM) IC 50 (nM) Emax％Emax%
11 15.4615.46 101.5101.5
33 106106 97.0797.07
44 34.5634.56 100.2100.2
55 15.8415.84 99.599.5
77 76.376.3 97.3297.32
88 24.9824.98 98.2998.29
99 185.9185.9 99.2699.26
1010 22.5422.54 101.1101.1
1111 76.3376.33 101.6101.6
1212 144.6144.6 103.5103.5
1313 697.8697.8 96.8796.87
AZD-0284AZD-0284 34.8134.81 99.7999.79
注：Emax％为相对于AZD-0284 10μM时的相对最大抑制率。Note: Emax% is the relative maximum inhibition rate relative to AZD-0284 at 10μM.
活性实施例2：化合物对人PBMC Th17细胞分化抑制实验Activity Example 2: The compound inhibits the differentiation of human PBMC Th17 cells
试验材料：experiment material:
Figure PCTCN2021093788-appb-000075
Figure PCTCN2021093788-appb-000075
实验方法：首先将PBMC细胞复苏铺板，然后用刺激因子(anti-hCD28：5μg/mL；rhTGF-β1：5ng/mL；rhIL-6：20ng/mL；rhIL-23：10ng/Ml)刺激PBMC细胞分化至Th17，同时加入不同浓度化合物，最大浓度从3μM开始，48小时后收集上清进行IL-17ELISA检测，与溶剂组比较，测定化合物抑制Th17细胞分泌IL-17的抑制率，用Graphad8.0拟合IC 50值。 Experimental method: first resuscitate PBMC cells and plate them, and then stimulate PBMC cells with stimulating factors (anti-hCD28: 5μg/mL; rhTGF-β1: 5ng/mL; rhIL-6: 20ng/mL; rhIL-23: 10ng/Ml) Differentiate to Th17, and add different concentrations of compounds at the same time. The maximum concentration starts from 3μM. After 48 hours, the supernatant is collected for IL-17 ELISA. Compared with the solvent group, the inhibitory rate of the compound to inhibit the secretion of IL-17 from Th17 cells is determined by Graphad8.0 Fit the IC 50 value.
测定结果显示，本发明的化合物对人PBMC具有较好的抑制Th17细胞分化分泌IL-17的能力(如表2所示)。The assay results show that the compound of the present invention has a better ability to inhibit the differentiation and secretion of IL-17 from Th17 cells to human PBMC (as shown in Table 2).
表2.化合物抑制Th17细胞分化分泌IL-17实验结果Table 2. Experimental results of compounds inhibiting the differentiation of Th17 cells and secreting IL-17
实施例Example IC 50(nM) IC 50 (nM) Emax％Emax%
11 28.7528.75 83.1883.18
44 87.3287.32 83.483.4
55 55.6955.69 100.89100.89
88 38.3838.38 83.1583.15
AZD-0284AZD-0284 28.4128.41 78.5478.54
注:Emax％为最大抑制率。Note: Emax% is the maximum inhibition rate.
活性实施例3：人和小鼠肝微粒体代谢稳定性实验Activity Example 3: Metabolic stability test of human and mouse liver microsomes
根据本领域常规的体外代谢稳定性研究的标准方法，例如(Kerns,Edward H.and Di Li(2008).Drug-like Properties:Concepts,Structure Design and Methods:from ADME to Toxicity Optimization.San Diego:Academic Press；Di,Li等人，Optimization of a Higher Throughput Microsomal Stability Screening Assay for Profiling Drug Discovery Candidates,J.Biomol.Screen.2003,8(4),453.)中所述的方法，类似地如下进行本发明化合物的肝微粒体代谢稳定性试验。According to the standard methods of in vitro metabolic stability research routine in this field, for example (Kerns, Edward H. and Di Li (2008). Drug-like Properties: Concepts, Structure Design and Methods: from ADME to Toxicity Optimization. San Diego: Academic Press; Di, Li et al., Optimization of a Higher Throughput Microsomal Stability Screening Assay for Profiling Drug Discovery Candidates, J. Biomol. Screen. 2003, 8(4), 453.), similarly proceed as follows Metabolic stability test of liver microsomes of the invention compound.
孵育体系包含0.5mg蛋白/mL微粒体、辅助因子、PBS，37℃预孵育3min，加入底物(即待测化合物)启动反应。在反应开始0、1、5、10、15、20、30、60min取样，加入适当终止物终止反应。The incubation system contains 0.5 mg protein/mL microsomes, cofactors, and PBS, pre-incubated at 37°C for 3 minutes, and the substrate (ie, test compound) is added to initiate the reaction. Samples were taken at 0, 1, 5, 10, 15, 20, 30, 60 min at the beginning of the reaction, and appropriate terminator was added to terminate the reaction.
Figure PCTCN2021093788-appb-000076
Figure PCTCN2021093788-appb-000076
样品处理(n＝3)：各加合适样品，涡旋后高速离心，取上清液，采用HPLC-MS/MS对底物进行检测。把0min时间点峰面积作为100％。其他时间点的峰面积转换为百分剩余量，各时间点的百分剩余量的自然对数对孵育时间作图，直线回归求算出斜率(-k)，然后按固有清除率(Clint)＝(k*孵育液体积)/肝微粒体质量，计算出Clint(uL/min/mg)及化合物半衰期(T1/2，min)。结果见表3。Sample processing (n=3): add appropriate samples to each, vortex and centrifuge at high speed, take the supernatant, and use HPLC-MS/MS to detect the substrate. The peak area at the time of 0 min is regarded as 100%. The peak area at other time points is converted into percentage residual amount, the natural logarithm of the percentage residual amount at each time point is plotted against the incubation time, and the slope (-k) is calculated by linear regression, and then the inherent clearance rate (Clint) = (k*Incubation volume)/weight of liver microsomes, Clint (uL/min/mg) and compound half-life (T1/2, min) are calculated. The results are shown in Table 3.
表3.人和小鼠肝微粒体代谢稳定性实验结果Table 3. Results of the metabolic stability test of human and mouse liver microsomes
Figure PCTCN2021093788-appb-000077
Figure PCTCN2021093788-appb-000077
上述实验结果表明本发明的化合物具有很好的代谢稳定性。The above experimental results show that the compound of the present invention has good metabolic stability.
活性实施例4：化合物在小鼠中PK测定Activity Example 4: Compound PK determination in mice
每个化合物的PK测定方法如下：6只C57BL/6小鼠(来源上海灵畅生物科技有限公司)分为两组，每组3只。其中一组通过静脉(IV)给药，剂量为1mg/kg，溶媒为5％DMSO/95％(20％Captisol)；一组通过口服(PO)灌胃给药，剂量为5mg/kg，溶媒为0.5％CMC-Na/0.5％Tween 80。 每一组在给药后0、0.083、0.25、0.5、1、2、4、6、8、24h分别通过小腿隐静脉采血。将约40μL血液收集到含EDTA-K2的抗凝管中。在收集完成后迅速将采血管倒置至少5次，以确保混合均匀，然后放置在冰上。采集到的各时间点血液在4℃，8000rpm离心5分钟以获得血浆。另取1.5mL离心管标记好化合物名称，动物编号，时间点，将血浆转移至该管中。血浆保存在-80℃直至分析。The PK determination method of each compound is as follows: 6 C57BL/6 mice (from Shanghai Lingchang Biotechnology Co., Ltd.) were divided into two groups, 3 mice in each group. One group was administered intravenously (IV) with a dose of 1 mg/kg and the vehicle was 5% DMSO/95% (20% Captisol); one group was administered by oral (PO) intragastric administration with a dose of 5 mg/kg and the vehicle It is 0.5% CMC-Na/0.5% Tween 80. Blood was collected from the saphenous vein of the calf in each group at 0, 0.083, 0.25, 0.5, 1, 2, 4, 6, 8, and 24 hours after administration. Collect about 40 μL of blood into an anticoagulation tube containing EDTA-K2. After the collection is complete, quickly invert the blood collection tube at least 5 times to ensure uniform mixing, and then place it on ice. The blood collected at each time point was centrifuged at 4°C and 8000 rpm for 5 minutes to obtain plasma. Another 1.5 mL centrifuge tube is labeled with the compound name, animal number, and time point, and the plasma is transferred to the tube. The plasma was stored at -80°C until analysis.
采用UPLC-MS/MS方法测定血浆中化合物浓度，用Phoenix WinNolin 6.4药代动力学软件对所得数据进行药代动力学参数计算。The UPLC-MS/MS method was used to determine the concentration of the compound in the plasma, and the Phoenix WinNolin 6.4 pharmacokinetic software was used to calculate the pharmacokinetic parameters of the obtained data.
具体实验结果如下，结果表明化合物药代吸收较好，具有药代动力学优势。本发明化合物的AUC 0-last(ng/mL*hr)和生物利用度都显著提高，显示其具有更好的成药性 The specific experimental results are as follows, and the results show that the compound has better pharmacokinetic absorption and has pharmacokinetic advantages. The AUC 0-last (ng/mL*hr) and bioavailability of the compound of the present invention are significantly improved, showing that it has better druggability
表4.实施例化合物体内PK结果Table 4. In vivo PK results of example compounds
Figure PCTCN2021093788-appb-000078
Figure PCTCN2021093788-appb-000078
以上实验中使用对照化合物的结构如下：The structure of the control compound used in the above experiment is as follows:
Figure PCTCN2021093788-appb-000079
Figure PCTCN2021093788-appb-000079
本领域技术人员将了解，上文描述本质上为示例性及说明性的，且欲说明本发明及其优选实施方案。通过常规实验，技术人员将了解可作出明显修正及变化而不悖离本发明的精神。在随附申请专利范围内的所有此类修正欲包括于其中。因此，本发明意欲并非由上述描述而是由以下权利要求范围及其等效物定义。Those skilled in the art will understand that the above description is exemplary and illustrative in nature, and is intended to illustrate the present invention and its preferred embodiments. Through routine experiments, the skilled person will understand that obvious modifications and changes can be made without departing from the spirit of the present invention. All such amendments within the scope of the attached patent application are intended to be included. Therefore, the present invention is intended to be defined not by the above description but by the following claims and their equivalents.
本说明书中所引用的所有公开出版物以引用方式并入本文中。All publications cited in this specification are incorporated herein by reference.

Claims (15)

  1. 式(I)的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，The compound of formula (I), its stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates,
    Figure PCTCN2021093788-appb-100001
    Figure PCTCN2021093788-appb-100001
    其中：in:
    R 1和R 2各自独立地选自氢、卤素、氰基、硝基、C 1-C 6烷基、-O-C 1-C 6烷基、-S-C 1-C 6烷基、-NH-C 1-C 6烷基、-N-(C 1-C 6烷基) 2、-C 1-C 6烷基-O-C 1-C 6烷基、-C 1-C 6烷基-S-C 1-C 6烷基、-C 1-C 6烷基-NH-C 1-C 6烷基或-C 1-C 6烷基-N(C 1-C 6烷基) 2，其中所述C 1-C 6烷基任选被卤素或氰基取代； R 1 and R 2 are each independently selected from hydrogen, halogen, cyano, nitro, C 1 -C 6 alkyl, -OC 1 -C 6 alkyl, -SC 1 -C 6 alkyl, -NH-C 1 -C 6 alkyl, -N-(C 1 -C 6 alkyl) 2 , -C 1 -C 6 alkyl -OC 1 -C 6 alkyl, -C 1 -C 6 alkyl -SC 1- C 6 alkyl, -C 1 -C 6 alkyl-NH-C 1 -C 6 alkyl or -C 1 -C 6 alkyl-N(C 1 -C 6 alkyl) 2 , wherein the C 1 -C 6 alkyl is optionally substituted by halogen or cyano;
    R 3选自H、-C 1-C 6烷基、-C 3-C 7环烷基、-4-7元杂环烷基、-NR aR a或-OR a，其中C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基任选被独立地选自以下的取代基取代：卤素、氰基、硝基、任选被卤素取代的C 3-C 7环烷基、R a、-OR a、-SR a或-NR aR a，其中R a选自H或任选被卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个R a可以与它们所连接的N原子一起形成4-7元含氮杂环烷基； R 3 is selected from H, -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl, -NR a R a or -OR a, wherein C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally substituted with substituents independently selected from the group consisting of halogen, cyano, nitro, C 3 optionally substituted by halogen -C 7 -cycloalkyl, R a, -OR a, -SR a , or -NR a R a, wherein R a is selected from H or optionally halogen-substituted C 1 -C 6 alkyl, or connected to the same two R a may be formed on the N-atom together with the N atom to which they are attached, 4-7 membered nitrogen-containing heterocyclic group;
    R 4选自-C 1-C 6烷基、-C 3-C 7环烷基、-4-7元杂环烷基或任选被C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基取代的氨基，其中所述C 1-C 6烷基、C 3-C 7环烷基或4-7元杂环烷基任选被各自独立地选自以下的取代基取代：卤素、氰基、硝基、R a、-OR a、-SR a、-NR aR a或任选被卤素取代的C 3-C 7环烷基，其中R a选自H或任选被卤素取代的C 1-C 6烷基，或者连接在同一个N原子上的两个基团可以与它们所连接的N原子一起形成4-7元含氮杂环烷基； R 4 is selected from -C 1 -C 6 alkyl, -C 3 -C 7 cycloalkyl, -4-7 membered heterocycloalkyl or optionally C 1 -C 6 alkyl, C 3 -C 7 ring Alkyl or 4-7 membered heterocycloalkyl substituted amino, wherein the C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or 4-7 membered heterocycloalkyl are optionally selected independently of each other from the following substituents: halogen, cyano, nitro, R a, -OR a, -SR a, -NR a R a optionally substituted with halogen or C 3 -C 7 cycloalkyl group, wherein R a Two groups selected from H or C 1 -C 6 alkyl optionally substituted by halogen, or two groups attached to the same N atom can form 4-7 membered nitrogen-containing heterocycloalkanes together with the N atom to which they are attached base;
    R 5和R 6各自独立地选自H、卤素、氰基或任选被卤素或氰基取代的C 1-C 6烷基； R 5 and R 6 are each independently selected from H, halogen, cyano or C 1 -C 6 alkyl optionally substituted by halogen or cyano;
    m和p各自独立地选自0、1或2，且m and p are each independently selected from 0, 1, or 2, and
    n选自0或1。n is selected from 0 or 1.
  2. 根据权利要求1的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，其中R 1和R 2各自独立地为H或卤素。 The compound according to claim 1, its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate, wherein R 1 and R 2 are each independently H or halogen.
  3. 根据权利要求1的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，其中R 1和R 2各自独立地为C 1-C 6烷基或-O-C 1-C 6烷基，其中的C 1- C 6烷基任选被卤素取代。 The compound according to claim 1, its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate, wherein R 1 and R 2 are each independently C 1 -C 6 alkyl group or -OC 1 -C 6 alkyl group, wherein the C 1 -C 6 alkyl group is optionally substituted by halogen.
  4. 根据权利要求1-3任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，其中R 3为-C 1-C 6烷基，优选C 1-C 3烷基。 The compound according to any one of claims 1 to 3, its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate, wherein R 3 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl.
  5. 据权利要求1-3任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，其中R 3为-C 3-C 7环烷基，优选环丙基、环丁基或环戊基。 The compound according to any one of claims 1 to 3, its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate, wherein R 3 is -C 3 -C 7 Cycloalkyl, preferably cyclopropyl, cyclobutyl or cyclopentyl.
  6. 据权利要求1-3任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，其中R 3为-NR aR a，其中R a独立地选自H或任选被一个或多个卤素取代的C 1-C 3烷基。 The compound according to any one of claims 1 to 3, its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate, wherein R 3 is -NR a R a wherein R a is independently selected from H or optionally substituted with one or more halogen C 1 -C 3 alkyl.
  7. 据权利要求1-6任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，其中R 4为-C 1-C 6烷基，优选C 1-C 3烷基。 The compound, its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate according to any one of claims 1 to 6, wherein R 4 is -C 1 -C 6 alkyl, preferably C 1 -C 3 alkyl.
  8. 据权利要求1-7任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，其中R 5和R 6各自独立地选自卤素或被卤素取代的C 1-C 6烷基，优选R 5和R 6均为-CF 3。 The compound according to any one of claims 1-7, its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate, wherein R 5 and R 6 are each independently It is selected from halogen or C 1 -C 6 alkyl substituted by halogen, preferably R 5 and R 6 are both -CF 3 .
  9. 化合物，选自Compound selected from
    Figure PCTCN2021093788-appb-100002
    Figure PCTCN2021093788-appb-100002
    Figure PCTCN2021093788-appb-100003
    Figure PCTCN2021093788-appb-100003
    其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物。Its stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates.
  10. 根据权利要求1至9任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物，用作药物、尤其是用作RORγt抑制剂，或用于治疗、尤其是用于治疗或预防与RORγt有关的疾病。The compound according to any one of claims 1 to 9, its stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates, for use as a medicine, especially as RORγt Inhibitors, or for the treatment, especially for the treatment or prevention of diseases related to RORγt.
  11. 药物组合物，包含根据权利要求1至9任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物和可药用赋形剂。A pharmaceutical composition comprising a compound according to any one of claims 1 to 9, its stereoisomers, tautomers, stable isotopic variants, pharmaceutically acceptable salts or solvates, and pharmaceutically acceptable excipients Shape agent.
  12. 用于在哺乳动物、特别是人中预防或治疗与RORγt有关的疾病的方法，该方法包括施用有效量的根据权利要求1至9任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物或根据权利要求11的药物组合物。A method for preventing or treating diseases related to RORγt in mammals, especially humans, the method comprising administering an effective amount of a compound according to any one of claims 1 to 9, its stereoisomers, and tautomers A compound, a stable isotope variant, a pharmaceutically acceptable salt or solvate, or a pharmaceutical composition according to claim 11.
  13. 根据权利要求1至9任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物或根据权利要求11的药物组合物用于预防或治疗与RORγt有关的疾病的用途。The compound according to any one of claims 1 to 9, its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate or the pharmaceutical composition according to claim 11 For the prevention or treatment of diseases related to RORγt.
  14. 根据权利要求1至9任一项的化合物、其立体异构体、互变异构体、稳定的同位素变体、药学上可接受的盐或溶剂合物或根据权利要求11的药物组合物在制备用于预防或治疗与RORγt有关的疾病的药物中的用途。The compound according to any one of claims 1 to 9, its stereoisomer, tautomer, stable isotope variant, pharmaceutically acceptable salt or solvate or the pharmaceutical composition according to claim 11 Use in the preparation of medicines for preventing or treating diseases related to RORγt.
  15. 根据权利要求10的化合物、根据权利要求12的方法或根据权利要求13或14的用途，其中的与RORγt有关的疾病选自银屑病、类风湿性关节炎、银屑病性关节炎、强直性脊柱炎、多发性硬化、系统性红斑狼疮、移植物抗宿主疾病、炎症性肠病、克隆氏病、溃疡性结肠炎、慢性阻塞性肺病、哮喘、血管球性肾炎、狼疮性肾炎、心肌炎、甲状腺炎、干眼症、葡萄膜炎、白塞病、过敏性皮肤炎、粉刺、硬皮病、支气管炎、皮肌过敏性鼻炎、坏死性小肠结肠炎、肝纤维化、非酒精性脂肪性肝炎(NASH)、新冠病毒肺炎、胰岛素依赖性I型糖尿病、三阴乳腺癌和前列腺癌。The compound according to claim 10, the method according to claim 12, or the use according to claim 13 or 14, wherein the disease associated with RORγt is selected from the group consisting of psoriasis, rheumatoid arthritis, psoriatic arthritis, and rigidity. Spondylitis, multiple sclerosis, systemic lupus erythematosus, graft-versus-host disease, inflammatory bowel disease, Crohn's disease, ulcerative colitis, chronic obstructive pulmonary disease, asthma, globular nephritis, lupus nephritis, myocarditis , Thyroiditis, dry eye, uveitis, Behcet's disease, allergic dermatitis, acne, scleroderma, bronchitis, dermatomuscular allergic rhinitis, necrotizing enterocolitis, liver fibrosis, non-alcoholic fat Hepatitis (NASH), New Coronavirus Pneumonia, Insulin-dependent Type I Diabetes, Triple Negative Breast Cancer and Prostate Cancer.
PCT/CN2021/093788 2020-05-15 2021-05-14 BIARYL COMPOUND CAPABLE OF SERVING AS RORγ MODULATOR WO2021228216A1 (en)

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