WO2022262671A1

WO2022262671A1 - Macro heterocyclic compound and medical use thereof

Info

Publication number: WO2022262671A1
Application number: PCT/CN2022/098369
Authority: WO
Inventors: 刘国标; 王国政; 沙汉明; 尚飞; 闫旭
Original assignee: 中国医药研究开发中心有限公司
Priority date: 2021-06-15
Filing date: 2022-06-13
Publication date: 2022-12-22
Also published as: TW202317572A; CN115884776B; CN115884776A

Abstract

Disclosed are a macro heterocyclic compound and the medical use thereof. In particular, disclosed are a macrocyclic compound as shown in general formula (I), and a preparation method therefor, a pharmaceutical composition containing same, and the use thereof as a TRK kinase inhibitor. The compound can be used for treating diseases associated with TRK activity, such as cancer.

Description

Heterocyclic macrocycles and their medicinal uses

technical field

The present invention relates to a new class of macrocyclic compound, its preparation method, its pharmaceutical composition and its use as TRK kinase inhibitor. The compounds of the present invention can be used in the treatment of diseases associated with TRK activity, such as cancer.

Background technique

Tropomyosin-receptor kinase (TRK) is a kind of nerve growth factor receptor. The TRK family includes three highly homologous kinases, TRKA, TRKB, and TRKC, which are encoded by corresponding three genes NTRK1, NTRK2, and NTRK3 (Chao, Nat Rev Neurosci, 2003, 4: 299-309). After TRK kinase binds to the nerve growth factor ligand, it is activated through dimerization and autophosphorylation, and then activates the downstream PLγ, Ras/MAPK, and PI3K signaling pathways to regulate cell proliferation, differentiation, metabolism, and apoptosis; among them, Nerve growth factor (NGF) binds TRKA, derived neurotrophic factor (BDNF) binds TRKB, and neurotrophin 3 (NT3) binds TRKC (Cocco et al., Nature reviews. Clinical oncology, 2018, 15:731-747).

Activation of TRK receptors by NTRK fusions is a known driver of a variety of cancers. After the 3'-terminal tyrosine kinase (RTK) domain of NTRK gene is fused with the 5'-terminal gene of the partner gene, the formed TRK fusion protein is in a continuously active state, and the downstream signaling pathway is continuously activated, thereby promoting the development of TRK fusion tumors. Diffusion and growth. At present, NTRK fusion can be found in many types of tumors, such as colon cancer, lung cancer, thyroid cancer, pancreatic cancer, breast cancer, etc.; especially in some rare cancers, such as infantile fibrosarcoma, similar breast secretory carcinoma, breast secretory carcinoma , the incidence of NTRK gene fusion can reach more than 90% (Cocco, Scaltriti, Nature reviews. Clinical oncology, 2018, 15: 731-747). There are many types of NTRK fusion genes, such as TPM3-NTRK1, which was first discovered in colorectal cancer KM12 cells, and LMNA-NTRK1, CD74-NTRK1, MPRIP-NTRK1, ETV6-NTRK3, etc. (Amatu et al., Esmo Open, 2016, 1:1-9; Butti et al., Genomics, 1995, 28:15-24; Vaishnavi et al., Nature Medicine, 2013, 19:1469-1472).

For NTRK fusion tumors, a variety of TRK small molecule inhibitors have been developed in recent years. Among them, LOXO's Larotrectinib and ROCHE's Entrectinib are currently approved TRK-targeted drugs, which were approved by the US FDA in November 2018 and August 2019, respectively, for the treatment of TRK fusion-positive adult and childhood cancer patients . Larotrectinib is a selective TRK inhibitor. The results of three Phase I/II clinical trials showed that the overall effective rate of Larotrectinib in treating NTRK fusion patients was 75%, of which 13% showed complete response, and 55% of patients were treated for one year. Still progression-free survival (Hong et al., The Lancet Oncology, 2020, 21). Entrectinib is an inhibitor of TRK/ROS1/ALK. Based on three phase I/II clinical trials, the objective effective rate of entrectinib for patients with NTRK fusion was 57% (31/54), of which 4 cases (7%) were in complete remission, and the median effective time was 10 months (Cancer Discovery , 2017).

However, similar to other targeted therapies, acquired drug resistance mediated by NTRK mutations, such as NTRK1-G595R and G667C mutations, has emerged clinically, which limits the efficacy of TRK inhibitors. More effective small-molecule drugs that can overcome the resistance of the first-generation TRK inhibitors have also been developed and entered the clinical trial stage, which can show in vitro activity against multiple TRK mutants in a lower nM range. Selitrectinib (LOXO-195) overcomes drug resistance by targeting kinase domain mutations (solvent front, xDFG, and gatekeeper mutations) (Drilon et al., Cancer Discovery, 2017, 7:963-972). Repotrectinib (TPX-0005) targets solvent front base substitutions, such as TRKA G595R and TRKC G623R (Alexander et al., Cancer Discovery, 2018, 8:1227-1236). Domestic second-generation TRK inhibitors BPI-28592, AB-106, HG030, etc. have also entered the clinical trial stage.

In addition, TRK inhibitor-mediated adverse events occasionally occurred. A retrospective analysis involved 96 patients with advanced or unresectable solid tumors. During the treatment of TRK inhibitors, adverse reactions included weight gain, paresthesia, dizziness (ataxia or vertigo), etc., mostly Grade 1 to 2, with <5% of patients experiencing grade 3 toxicity (Drilon et al., Cancer Discovery, 2017, 7:400-409; Hong et al., Annals of Oncology, 2019, 30:325-331; Liu et al. , Ann Oncol, 2020, 31:1207-1215). Adverse reactions can be alleviated by dose adjustment or drug withdrawal. In addition, some patients who discontinue the drug will experience pain episodes. The pain caused by drug withdrawal is different from cancer pain and may be related to the effect of NGF on sensory nerve endings (Lim et al., Annals of Oncology, 2020).

Therefore, it is necessary to develop new and highly efficient TRK inhibitors, overcome TRK mutation resistance, and minimize the on-target toxicity of compounds.

Contents of the invention

After painstaking research, the present inventors have developed a new class of macrocyclic compounds, which can effectively inhibit TRK, and thus be effectively used in the treatment of diseases related to TRK kinase, such as cancer.

Therefore, the object of the present invention is to provide a compound represented by general formula (I) or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof, or Its pharmaceutically acceptable salts:

in,

Z ¹ , Z ² , Z ³ and Z ⁴ can be independently selected from carbon or nitrogen;

X is selected from a bond, -(CH ₂ ) _m -, -(CH=CH)-, -O-(CH ₂ ) _t -, -S-(CH ₂ ) _t -, -S(O)-(CH ₂ ) _t -, -S(O) ₂ -(CH ₂ ) _t - or -NR ⁶ -(CH ₂ ) _t -;

Y is -Q-(CH ₂ ) _v -, wherein Q is selected from

Where "*" represents the end where the Y group is connected to the aromatic ring core;

Ring A is selected from heteroaryl, aryl, cycloalkyl, heterocyclyl, said heteroaryl, aryl, cycloalkyl, heterocyclyl is optionally further selected from deuterium, alkyl, deuterated alkyl , haloalkyl, alkoxy, deuterated alkoxy, haloalkoxy, halogen, amino, hydroxyl, mercapto, nitro, cyano, oxo, alkenyl, alkynyl, cycloalkyl, heterocyclyl, Aryl, Heteroaryl, -(CH ₂ ) _q R ^a , -(CH ₂ ) _q OR ^a , -(CH ₂ ) _q C(O)R ^a , -(CH ₂ ) _q C(O)OR ^a , -(CH ₂ ) _q OC(O)R ^a , -(CH ₂ ) _q C(O)NR ^a R ^b , -(CH ₂ ) _q S(O) _p R ^a , -(CH ₂ ) _q NR ^a R ^b , -(CH ₂ ) _q S(O) _p NR ^a R ^b , -NR ^a C(O)NR ^b NR ^c , -(CH ₂ ) _q NR ^b C(O)R ^a , -(CH ₂ ) _q NR ^b C(O)OR ^a or -(CH ₂ ) _q NR ^b S(O) _p R ^a is replaced by one or more groups;

^R and R are each independently selected from ^hydrogen , halogen, nitro, hydroxyl, mercapto, cyano, amino, alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and Heteroaryl, said alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl are optionally further selected from halogen, amino, nitro, cyano, oxygen One or more groups of substituent, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl group replaced;

Alternatively, ^R1 and ^R2 together form

Alternatively, R and R ^together with the atoms they are connected to form ^a cycloalkyl or heterocyclyl, which is optionally further selected from the group consisting of halogen, amino, nitro, cyano, oxo One or more groups of radical, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl replaced by

R ³ and R ⁴ are each independently selected from hydrogen, halogen, alkyl;

R ⁵ is NR ⁸ R ⁹ ;

R ^is selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl, the alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl are optionally further selected from the group consisting of halogen, amino, nitro, cyano, oxo, hydroxy, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy, haloalkoxy Substituted by one or more groups of radical, cycloalkyl, heterocyclyl, aryl, heteroaryl;

Each R is ^{independently} selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl, the alkyl, alkenyl, alkynyl, cycloalkyl, Heterocyclyl, aryl and heteroaryl are optionally further selected from the group consisting of halogen, amino, nitro, cyano, oxo, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkane One or more groups of oxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl are substituted;

R ⁸ and R ⁹ are each independently selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl, the alkyl, alkenyl, alkynyl, cycloalkyl , heterocyclyl, aryl and heteroaryl are optionally further selected from halogen, amino, nitro, cyano, oxo, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, One or more groups of alkoxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl; or

R ⁸ and R ⁹ form a heterocyclic group together with the nitrogen atom connected to it, and the heterocyclic group is optionally further selected from the group consisting of deuterium, alkyl, deuterated alkyl, haloalkyl, alkoxy, deuterated alkoxy, One or more groups of haloalkoxy, halogen, amino, hydroxyl, mercapto, nitro, cyano, oxo, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl replace;

R ^a , R ^b , and R ^c are each independently selected from hydrogen, halogen, nitro, hydroxyl, mercapto, cyano, amino, alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, heterocyclyl, Aryl and heteroaryl, said alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl are optionally further selected from halogen, amino, nitro, cyano One or Replaced by multiple groups;

Or, any two adjacent or non-adjacent R ^a , R ^b , R ^c together with the atoms they connect form cycloalkyl, heterocyclyl, aryl and heteroaryl, wherein said cycloalkyl, hetero Cyclic, aryl and heteroaryl are optionally further selected from the group consisting of halogen, amino, nitro, cyano, oxo, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy Substituted by one or more groups of radical, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl;

n is an integer selected from 0 to 6;

m is an integer selected from 1 to 6;

t is an integer selected from 0 to 6;

v is an integer selected from 0 to 6;

p is 0, 1 or 2;

q is an integer of 0 to 6.

In a preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof, or a pharmaceutically acceptable salt thereof, which is a compound represented by general formula (II) or its mesomer, racemate, enantiomer, diastereoisomer, or in the form of a mixture, or a pharmaceutically acceptable salt thereof,

Wherein, X, Y, ring A, R ¹ to R ⁵ , and n are as defined in the general formula (I).

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, wherein,

X is selected from a bond, -(CH ₂ ) _m -, -(CH=CH)-, -O-(CH ₂ ) _t - or -S-(CH ₂ ) _t -;

m is an integer from 1 to 6;

t is an integer from 0 to 6;

Preferably, X is selected from a bond, _-CH2- , -( _CH2 ) _2- , -O-, -O-CH2-, -O-( _CH2 ) _2- or -( _CH =CH)-.

Y is -Q-(CH ₂ ) _v -, wherein Q is selected from

v is 0, 1 or 2;

R ⁷ is as defined in claim 1 .

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, wherein:

Ring A is selected from aryl or heteroaryl, preferably C ₆ -C ₁₀ aryl or 5-10 membered heteroaryl, more preferably phenyl or 5-6 membered heteroaryl such as pyridyl, pyrimidinyl, pyridazinyl , triazinyl, said aryl and heteroaryl are optionally further selected from deuterium, alkyl, deuterated alkyl, haloalkyl, alkoxy, deuterated alkoxy, haloalkoxy, halogen, amino, One or more groups of hydroxyl, mercapto, nitro, cyano, oxo, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl are substituted.

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, which is a compound represented by general formula (III) or its mesomer, racemate, enantiomer, diastereoisomer, or its mixture form, or its pharmaceutically acceptable salt,

Wherein, A ₁ , A ₂ , A ₃ , A ₄ are each independently selected from carbon or nitrogen;

Each R is ^{independently} selected from the group consisting of hydrogen, alkyl, deuterated alkyl, haloalkyl, alkoxy, deuterated alkoxy, haloalkoxy, halogen, amino, hydroxyl, mercapto, nitro, cyano, Oxo, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl; preferably hydrogen, halogen, oxo;

s is an integer from 0 to 3;

X, Y, R ¹ to R ⁵ , and n are as defined above.

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, which is a compound represented by general formula (IV) or its mesoform, racemate, enantiomer, diastereoisomer, or its mixture form, or its pharmaceutically acceptable salt,

s is an integer from 0 to 3;

X, R ¹ to R ⁵ , R ⁷ , and n are as defined above.

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, wherein R ¹ and R ² are each independently selected from hydrogen and C ₁ -C ₆ alkyl, and the C ₁ -C ₆ alkyl is optionally substituted by halogen; or ^R1 and ^R2 together form

preferred

And n is an integer of 1 to 3.

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, wherein, R ¹ and R ² form a C ₃ -C ₆ cycloalkyl group together with the atoms they are connected to, and the C ₃ -C ₆ cycloalkyl group is optionally further replaced by selected from halogen, amino, nitro, cyano, oxo, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy, haloalkoxy, cycloalkyl, heterocyclyl , aryl, heteroaryl one or more groups substituted.

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, wherein R ³ and R ⁴ are each independently selected from hydrogen or halogen, preferably hydrogen.

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, wherein R ⁵ is NR ⁸ R ⁹ ; wherein R ⁸ and R ⁹ are each independently selected from hydrogen and C ₁ -C ₆ alkyl, preferably hydrogen.

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, wherein R ⁷ is hydrogen or C ₁ -C ₆ alkyl, and the C ₁ -C ₆ alkyl is optionally further selected from halogen, amino, nitro, One or more groups of cyano, oxo, hydroxyl, mercapto, carboxyl, ester, hydroxyalkyl, alkoxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl Substitution, preferably ^R7 is hydrogen.

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, which is a compound represented by general formula (V) or its mesoform, racemate, enantiomer, diastereoisomer, or its mixture form, or its pharmaceutically acceptable salt,

in,

R ¹ and R ² are each independently selected from hydrogen and C ₁ -C ₆ alkyl, said C ₁ -C ₆ alkyl is optionally substituted by halogen, and n is an integer from 1 to 3, preferably n is 1; or

R ¹ and R ² together with the atoms to which they are attached form a C ₃ -C ₆ cycloalkyl group;

^R3 and ^R4 are each independently selected from hydrogen or halogen, preferably hydrogen;

R ⁵ is NR ⁸ R ⁹ ; wherein R ⁸ and R ⁹ are each independently selected from hydrogen and C ₁ -C ₆ alkyl, preferably hydrogen;

R ⁷ is hydrogen or C ₁ -C ₆ alkyl, preferably hydrogen;

R ¹⁰ is selected from hydrogen, halogen, C _1- C ₆ alkyl, C _1- C ₆ deuterated alkyl, C _1- C ₆ haloalkyl, C _1- C ₆ alkoxy, C _1- C ₆ deuterated Alkoxy, C ₁ -C ₆ haloalkoxy, preferably hydrogen or halogen.

In another preferred embodiment of the present invention, the compound represented by the general formula (I) according to the present invention or its mesoform, racemate, enantiomer, diastereoisomer , or a mixture thereof, or a pharmaceutically acceptable salt thereof, which is a compound represented by general formula (VI) or its mesoform, racemate, enantiomer, diastereoisomer, or its mixture form, or its pharmaceutically acceptable salt,

in,

R ¹ and R ² are each independently selected from hydrogen and C ₁ -C ₆ alkyl, said C ₁ -C ₆ alkyl is optionally substituted by halogen, and n is an integer from 1 to 3; or

R ⁷ is hydrogen or C ₁ -C ₆ alkyl, preferably hydrogen;

Typical compounds of the invention include, but are not limited to:

or a mesoform, a racemate, an enantiomer, a diastereoisomer, or a mixture thereof, or a pharmaceutically acceptable salt thereof.

The present invention further provides a method for preparing the compound represented by general formula (IV) or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof, or its pharmaceutically The method with salt, it comprises the following steps:

In the presence of a condensing agent, the compound (IV-1) undergoes an intramolecular condensation reaction to obtain a compound of the general formula (IV). The condensing agent is preferably 1-ethyl-(3-dimethylaminopropyl) carbonyl diethylene Amine hydrochloride and 1-hydroxybenzotriazole;

Wherein, A ₁ , A ₂ , A ₃ , A ₄ , R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁷ , R ¹⁰ , s and n are as defined in general formula (IV).

The present invention further provides a pharmaceutical composition, which comprises the compound represented by general formula (I) to general formula (VI) or its mesoform, racemate, enantiomer according to the present invention , diastereoisomers, or a mixture thereof, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.

The present invention also relates to compounds represented by general formula (I) to general formula (VI) according to the present invention or their mesoforms, racemates, enantiomers, diastereoisomers, Use thereof in the form of a mixture thereof, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising the same in the preparation of a tropomyosin receptor kinase (TRK) inhibitor.

The present invention also relates to compounds represented by general formula (I) to general formula (VI) according to the present invention or their mesoforms, racemates, enantiomers, diastereoisomers, or a mixture thereof, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising it in the preparation of a medicament for preventing or/and treating a disease associated with tropomyosin receptor kinase (TRK) activity, the disease preferably Neuroblastoma, melanoma, ovarian cancer, colorectal cancer, gastric cancer, lung cancer, breast cancer, glioblastoma, medulloblastoma, head and neck cancer, salivary gland cancer, and papillary thyroid cancer.

The present invention also relates to a compound represented by general formula (I) to general formula (VI) or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof , or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising the same, for use as a tropomyosin receptor kinase (TRK) inhibitor.

The present invention also relates to a compound represented by general formula (I) to general formula (VI) or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof , or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising it, which is used for the prevention or/and treatment of diseases associated with tropomyosin receptor kinase (TRK) activity, preferably neurocytoma, melanoma, Ovarian cancer, colorectal cancer, gastric cancer, lung cancer, breast cancer, glioblastoma, medulloblastoma, head and neck cancer, salivary gland cancer, and papillary thyroid cancer.

The present invention further relates to a method for inhibiting tropomyosin receptor kinase (TRK), which comprises administering an effective amount of the compounds represented by general formula (I) to general formula (VI) according to the present invention to patients in need. or a mesoform, a racemate, an enantiomer, a diastereoisomer, or a mixture thereof, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising the same.

The present invention further relates to a method for preventing or/and treating diseases associated with tropomyosin receptor kinase (TRK) activity, which comprises administering a preventive or therapeutically effective amount of the general medicine according to the present invention to a patient in need thereof. Compounds represented by formula (I) to general formula (VI) or their mesoforms, racemates, enantiomers, diastereoisomers, or mixtures thereof, or pharmaceutically acceptable salts thereof Or a pharmaceutical composition comprising it, wherein the disease is preferably neurocytoma, melanoma, ovarian cancer, colorectal cancer, gastric cancer, lung cancer, breast cancer, glioblastoma, medulloblastoma, head and neck cancer , salivary gland carcinoma, and papillary thyroid carcinoma.

Detailed Description of the Invention

The compounds of the present invention can form pharmaceutically acceptable acid addition salts with acids according to conventional methods in the field to which the present invention belongs. Examples of inorganic acid salts include hydrochloride, hydrobromide, hydroiodide, nitrate, sulfate, hydrogensulfate, phosphate, hydrogenphosphate, and the like. Examples of organic acid salts include acetate, trifluoroacetate, gluconate, lactate, salicylate, citrate, tartrate, ascorbate, succinate, maleate, fumarate salt, formate, benzoate, methanesulfonate, ethanesulfonate, p-toluenesulfonate, etc.

The compounds of the present invention can form pharmaceutically acceptable base addition salts with bases according to conventional methods in the field to which the present invention belongs. Examples of alkali metal salts include sodium salts, potassium salts, and the like. Examples of alkaline earth metal salts include magnesium salts, calcium salts, and the like. Examples of organic amine salts include triethylamine salts, pyridinium salts, procaine salts, picoline salts, dicyclohexylamine salts, diethanolamine salts, triethanolamine salts, tris(hydroxymethyl)aminomethane salts, and the like. Examples of amino acid addition salts include arginine salts, lysine salts, ornithine salts, serine salts, glycinate salts, aspartic acid salts, glutamic acid salts, and the like.

The pharmaceutical composition containing the active ingredient may be in a form suitable for oral administration, such as tablets, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups or elixir. Oral compositions can be prepared according to any method known in the art for the preparation of pharmaceutical compositions, and such compositions can contain one or more ingredients selected from the group consisting of sweeteners, flavoring agents, coloring agents and preservatives, To provide pleasing and palatable medicinal preparations. Tablets contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients suitable for the manufacture of tablets. These excipients can be inert excipients such as calcium carbonate, sodium carbonate, lactose, calcium or sodium phosphate; granulating and disintegrating agents such as microcrystalline cellulose, croscarmellose sodium, corn starch or alginic acid; binders such as starch, gelatin, polyvinylpyrrolidone or acacia; and lubricants such as magnesium stearate, stearic acid or talc. These tablets may be uncoated or may be coated by known techniques to mask the taste of the drug or to delay disintegration and absorption in the gastrointestinal tract, thus providing sustained release over an extended period of time. For example, water-soluble taste-masking materials such as hydroxypropylmethylcellulose or hydroxypropylcellulose, or time-extending materials such as ethylcellulose, cellulose acetate butyrate may be used.

Hard gelatin capsules in which the active ingredient is admixed with an inert solid diluent such as calcium carbonate, calcium phosphate, or kaolin, or in which the active ingredient is admixed with a water-soluble carrier such as polyethylene glycol or an oil vehicle such as peanut oil, liquid paraffin, or olive oil may also be used. Soft gelatin capsules provide an oral formulation.

Aqueous suspensions contain the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions. Such excipients are suspending agents, such as sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, polyvinylpyrrolidone, and acacia; dispersing or wetting agents, which may be natural The resulting phospholipids such as lecithin, or condensation products of alkylene oxides with fatty acids, such as polyoxyethylene stearate, or condensation products of ethylene oxide with long-chain fatty alcohols, such as heptadecanylethyleneoxycetate Heptadecaethyleneoxy cetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitols, such as polyethylene oxide sorbitan monooleate, or ethylene oxide with fatty acids and hexitols Condensation products of anhydride-derived partial esters, such as polyethylene oxide sorbitan monooleate. Aqueous suspensions may also contain one or more preservatives, such as ethyl or n-propylparaben, one or more coloring agents, one or more flavoring agents and one or more sweeteners. Flavoring agents such as sucrose, saccharin, or aspartame.

Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil, such as arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as liquid paraffin. Oily suspensions may contain a thickening agent, such as beeswax, hard paraffin or cetyl alcohol. Sweetening and flavoring agents as mentioned above may be added to provide a palatable preparation. These compositions can be preserved by the addition of antioxidants such as butylated hydroxyanisole or alpha-tocopherol.

The pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil such as olive oil or arachis oil, or a mineral oil such as liquid paraffin or mixtures thereof. Suitable emulsifiers may be naturally occurring phospholipids, such as soybean lecithin, and esters or partial esters derived from fatty acids and hexitol anhydrides, such as sorbitan monooleate, and the condensation of said partial esters with ethylene oxide Products such as polyethylene oxide sorbitan monooleate. The emulsions may also contain sweetening, flavoring, preservative and antioxidant agents. Syrups and elixirs may be formulated with sweetening agents, for example glycerol, propylene glycol, sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative, coloring agents and antioxidants.

The pharmaceutical compositions of the present invention may be in the form of sterile injectable aqueous solutions. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution. The sterile injectable preparation may be a sterile injectable oil-in-water microemulsion in which the active ingredient is dissolved in the oily phase. For example, the active ingredient is dissolved in a mixture of soybean oil and lecithin. The oil solution is then treated in a mixture of water and glycerol to form a microemulsion. The injectable solution or microemulsion can be injected into the patient's bloodstream by local bolus injection. Alternatively, solutions and microemulsions are preferably administered in a manner that maintains a constant circulating concentration of the compounds of the invention. To maintain this constant concentration, a continuous intravenous delivery device can be used.

The pharmaceutical composition of the present invention may be in the form of sterile injectable aqueous or oily suspension for intramuscular and subcutaneous administration. This suspension may be formulated according to the known art using those suitable dispersing or wetting agents and suspending agents which have been mentioned above. The sterile injectable preparation can also be a sterile injectable solution or suspension prepared in a non-toxic parenterally acceptable diluent or solvent, for example a solution in 1,3-butanediol. In addition, sterile fixed oils are conveniently employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are prepared as injectables.

The compounds of this invention may be administered in the form of suppositories for rectal administration. These pharmaceutical compositions can be prepared by mixing the drug with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid in the rectum and will therefore melt in the rectum to release the drug. Such materials include cocoa butter, glycerinated gelatin, hydrogenated vegetable oils, polyethylene glycols of various molecular weights and mixtures of fatty acid esters of polyethylene glycols.

It is well known to those skilled in the art that the dosage of the drug depends on many factors, including but not limited to the following factors: the activity of the specific compound used, the patient's age, the patient's body weight, the patient's health status, the patient's behavior, the patient's Diet, administration time, administration method, excretion rate, drug combination, etc. In addition, the optimal treatment method such as the treatment mode, the daily dosage of the compound of the general formula or the type of pharmaceutically acceptable salt can be verified according to the traditional treatment plan.

The present invention can contain the compound represented by the general formula (I), and its pharmaceutically acceptable salt, hydrate or solvate as the active ingredient, mixed with a pharmaceutically acceptable carrier or excipient to prepare a composition, and Prepared into clinically acceptable dosage forms. The derivatives of the present invention can be used in combination with other active ingredients as long as they do not produce other adverse effects such as allergic reactions and the like. The compound of the present invention can be used as the only active ingredient, and can also be used in combination with other drugs for treating diseases related to tyrosine kinase activity. Combination therapy is achieved by the simultaneous, separate or sequential administration of the individual therapeutic components.

Unless stated to the contrary, the terms used in the specification and claims have the following meanings.

The term "alkyl" refers to a saturated aliphatic hydrocarbon group, which is a straight or branched chain group containing 1 to 20 carbon atoms, preferably an alkyl group containing 1 to 12 carbon atoms, more preferably 1 to 6 carbon atoms atom of the alkyl group. Non-limiting examples include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, sec-butyl, n-pentyl, 1,1-dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1-ethylpropyl, 2-methylbutyl, 3-methylbutyl, n-hexyl, 1-ethyl-2- Methylpropyl, 1,1,2-trimethylpropyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 2,2-dimethylbutyl, 1,3 -Dimethylbutyl, 2-ethylbutyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 2,3-dimethylbutyl, n-heptyl, 2 -Methylhexyl, 3-methylhexyl, 4-methylhexyl, 5-methylhexyl, 2,3-dimethylpentyl, 2,4-dimethylpentyl, 2,2-dimethyl Pentyl, 3,3-dimethylpentyl, 2-ethylpentyl, 3-ethylpentyl, n-octyl, 2,3-dimethylhexyl, 2,4-dimethylhexyl, 2 ,5-dimethylhexyl, 2,2-dimethylhexyl, 3,3-dimethylhexyl, 4,4-dimethylhexyl, 2-ethylhexyl, 3-ethylhexyl, 4-ethylhexyl ylhexyl, 2-methyl-2-ethylpentyl, 2-methyl-3-ethylpentyl, n-nonyl, 2-methyl-2-ethylhexyl, 2-methyl-3-ethyl 2,2-diethylhexyl, 2,2-diethylpentyl, n-decyl, 3,3-diethylhexyl, 2,2-diethylhexyl, and various branched chain isomers. More preferred are lower alkyl groups containing 1 to 6 carbon atoms, non-limiting examples include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, sec-butyl Base, n-pentyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, 2-methylbutyl, 3-methylbutyl, n-hexyl, 1-ethyl-2-methylpropyl, 1,1,2-trimethylpropyl, 1,1-dimethylbutyl, 1,2-dimethyl Dimethylbutyl, 2,2-dimethylbutyl, 1,3-dimethylbutyl, 2-ethylbutyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl group, 2,3-dimethylbutyl group, etc. Alkyl groups may be substituted or unsubstituted, and when substituted, substituents may be substituted at any available point of attachment, said substituents being preferably one or more of the following groups independently selected from alkyl radical, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkane Oxy group, heterocycloalkoxy group, cycloalkylthio group, heterocycloalkylthio group, oxo group, carboxyl group or carboxylate group.

The term "alkenyl" means an alkyl group as defined above consisting of at least two carbon atoms and at least one carbon-carbon double bond, for example vinyl, 1-propenyl, 2-propenyl, 1-, 2- or 3- -butenyl etc. Alkenyl groups may be substituted or unsubstituted, and when substituted, the substituents are preferably one or more of the following groups independently selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkylthio, Alkylamino, halogen, mercapto, hydroxy, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, heterocycle Alkylthio.

The term "alkynyl" refers to an alkyl group as defined above consisting of at least two carbon atoms and at least one carbon-carbon triple bond, eg ethynyl, propynyl, butynyl and the like. Alkynyl groups may be substituted or unsubstituted, and when substituted, the substituents are preferably one or more of the following groups independently selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkylthio, Alkylamino, halogen, mercapto, hydroxy, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, heterocycle Alkylthio.

The term "cycloalkyl" refers to a saturated or partially unsaturated monocyclic or polycyclic cyclic hydrocarbon substituent, the cycloalkyl ring containing 3 to 20 carbon atoms, preferably containing 3 to 12 carbon atoms, more preferably containing 3 to 6 carbon atoms. Non-limiting examples of monocyclic cycloalkyls include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cyclohexadienyl, cycloheptyl, cycloheptatriene Base, cyclooctyl, etc.; polycyclic cycloalkyl includes spiro ring, fused ring and bridged ring cycloalkyl.

The term "spirocycloalkyl" refers to a polycyclic group of 5 to 20 membered monocyclic rings sharing one carbon atom (called a spiro atom), which may contain one or more double bonds, but none of the rings has complete conjugation The π-electron system. Preferably it is 6 to 14 yuan, more preferably 7 to 10 yuan. According to the number of spiro atoms shared between the rings, the spirocycloalkyl group can be divided into single spirocycloalkyl, double spirocycloalkyl or polyspirocycloalkyl, preferably single spirocycloalkyl and double spirocycloalkyl. More preferably, it is a 4-membered/4-membered, 4-membered/5-membered, 4-membered/6-membered, 5-membered/5-membered or 5-membered/6-membered monospirocycloalkyl group. Non-limiting examples of spirocycloalkyl groups include:

The term "fused cycloalkyl" refers to a 5 to 20 membered all-carbon polycyclic group in which each ring of the system shares an adjacent pair of carbon atoms with other rings in the system, wherein one or more rings may contain one or Multiple double bonds, but none of the rings have a fully conjugated π-electron system. Preferably it is 6 to 14 yuan, more preferably 7 to 10 yuan. According to the number of rings, it can be divided into bicyclic, tricyclic, tetracyclic or polycyclic condensed cycloalkyl groups, preferably bicyclic or tricyclic, more preferably 5-membered/5-membered or 5-membered/6-membered bicycloalkyl groups. Non-limiting examples of fused cycloalkyl groups include:

The term "bridged cycloalkyl" refers to a 5 to 20 membered, all-carbon polycyclic group having any two rings sharing two carbon atoms not directly attached, which may contain one or more double bonds, but none of the rings has a complete Conjugated π-electron systems. Preferably it is 6 to 14 yuan, more preferably 7 to 10 yuan. According to the number of constituent rings, it can be divided into bicyclic, tricyclic, tetracyclic or polycyclic bridged cycloalkyl groups, preferably bicyclic, tricyclic or tetracyclic, more preferably bicyclic or tricyclic. Non-limiting examples of bridged cycloalkyl groups include:

The cycloalkyl ring may be fused to an aryl, heteroaryl or heterocycloalkyl ring where the ring bonded to the parent structure is a cycloalkyl, non-limiting examples include indanyl, tetrahydronaphthalene base, benzocycloheptyl, etc. Cycloalkyl groups may be optionally substituted or unsubstituted, and when substituted, the substituents are preferably one or more of the following groups independently selected from alkyl, alkenyl, alkynyl, alkoxy, alkane Thio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio , heterocycloalkylthio, oxo, carboxyl or carboxylate.

The term "heterocyclyl" refers to a saturated or partially unsaturated monocyclic or polycyclic cyclic hydrocarbon substituent comprising 3 to 20 ring atoms, one or more of which is selected from nitrogen, oxygen or S(O) _m (where m is an integer from 0 to 2), but excluding ring portions of -OO-, -OS- or -SS-, the remaining ring atoms being carbon. Preferably contain 3 to 12 ring atoms, of which 1 to 4 are heteroatoms; most preferably contain 3 to 8 ring atoms, of which 1 to 3 are heteroatoms; most preferably contain 5 to 7 ring atoms, of which 1 to 2 or 1 to 3 are heteroatoms. Non-limiting examples of monocyclic heterocyclyl groups include pyrrolidinyl, imidazolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, dihydroimidazolyl, dihydrofuranyl, dihydropyrazolyl, dihydropyrrolyl, piperidine group, piperazinyl, morpholinyl, thiomorpholinyl, homopiperazinyl, pyranyl, etc., preferably 1, 2, 5-oxadiazolyl, pyranyl or morpholinyl. Polycyclic heterocyclyls include spiro, fused and bridged heterocyclyls.

The term "spiroheterocyclyl" refers to a polycyclic heterocyclic group that shares one atom (called a spiro atom) between 5 to 20-membered monocyclic rings, wherein one or more ring atoms are selected from nitrogen, oxygen or S(O ) _m (wherein m is an integer from 0 to 2), the remaining ring atoms are carbon. It may contain one or more double bonds, but none of the rings has a fully conjugated pi-electron system. Preferably it is 6 to 14 yuan, more preferably 7 to 10 yuan. According to the number of spiro atoms shared between the rings, the spiroheterocyclyl can be divided into single spiroheterocyclyl, double spiroheterocyclyl or polyspiroheterocyclyl, preferably single spiroheterocyclyl and double spiroheterocyclyl. More preferably, it is a 4-membered/4-membered, 4-membered/5-membered, 4-membered/6-membered, 5-membered/5-membered or 5-membered/6-membered monospiro heterocyclic group. Non-limiting examples of spiroheterocyclyls include:

The term "fused heterocyclyl" refers to a 5 to 20 membered polycyclic heterocyclic group in which each ring in the system shares an adjacent pair of atoms with other rings in the system, and one or more rings may contain one or more double bond, but none of the rings has a fully conjugated π-electron system, where one or more ring atoms are heteroatoms selected from nitrogen, oxygen, or S(O) _m (where m is an integer from 0 to 2), and the remaining ring The atom is carbon. Preferably it is 6 to 14 yuan, more preferably 7 to 10 yuan. According to the number of constituent rings, it can be divided into bicyclic, tricyclic, tetracyclic or polycyclic fused heterocyclic groups, preferably bicyclic or tricyclic, more preferably 5-membered/5-membered or 5-membered/6-membered bicyclic fused heterocyclic groups. Non-limiting examples of fused heterocyclic groups include:

The term "bridged heterocyclyl" refers to a 5 to 14 membered polycyclic heterocyclic group in which any two rings share two atoms not directly attached, which may contain one or more double bonds, but none of the rings has a complete shared bond. A pi-electron system of a yoke wherein one or more ring atoms are heteroatoms selected from nitrogen, oxygen or S(O) _m (where m is an integer from 0 to 2) and the remaining ring atoms are carbon. Preferably it is 6 to 14 yuan, more preferably 7 to 10 yuan. According to the number of constituent rings, it can be divided into bicyclic, tricyclic, tetracyclic or polycyclic bridged heterocyclic groups, preferably bicyclic, tricyclic or tetracyclic, more preferably bicyclic or tricyclic. Non-limiting examples of bridged heterocyclyl groups include:

The heterocyclyl ring may be fused to an aryl, heteroaryl, or cycloalkyl ring where the ring bonded to the parent structure is a heterocyclyl, non-limiting examples of which include:

Wait.

Heterocyclic groups may be optionally substituted or unsubstituted, and when substituted, the substituents are preferably one or more of the following groups independently selected from alkyl, alkenyl, alkynyl, alkoxy, alk Thio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio , heterocycloalkylthio, oxo, carboxyl or carboxylate.

The term "aryl" refers to a 6 to 14 membered all-carbon monocyclic or fused polycyclic (that is, rings sharing adjacent pairs of carbon atoms) group, preferably 6 to 10 membered, having a conjugated pi-electron system, such as benzene base and naphthyl. Phenyl is more preferred. The aryl ring may be fused to a heteroaryl, heterocyclyl or cycloalkyl ring, where the ring bonded to the parent structure is an aryl ring, non-limiting examples of which include:

Aryl groups may be substituted or unsubstituted, and when substituted, the substituents are preferably one or more of the following groups independently selected from alkyl, alkenyl, alkynyl, alkoxy, alkylthio, Alkylamino, halogen, mercapto, hydroxy, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, heterocycle Alkylthio, carboxyl or carboxylate.

The term "heteroaryl" refers to a heteroaromatic system comprising 1 to 4 heteroatoms, 5 to 14 ring atoms, wherein the heteroatoms are selected from oxygen, sulfur and nitrogen. Heteroaryl is preferably 5 to 10 membered, containing 1 to 3 heteroatoms; more preferably 5 or 6 membered, containing 1 to 2 heteroatoms; preferred examples are imidazolyl, furyl, thienyl, thiazolyl, pyryl Azolyl, oxazolyl, pyrrolyl, tetrazolyl, pyridyl, pyrimidinyl, thiadiazole, pyrazinyl, etc., preferably imidazolyl, thiazolyl, pyrazolyl or pyrimidinyl, thiazolyl; more preferably pyrazolyl or thiazolyl. The heteroaryl ring may be fused to an aryl, heterocyclyl or cycloalkyl ring, wherein the ring bonded to the parent structure is a heteroaryl ring, non-limiting examples of which include:

Heteroaryl groups may be optionally substituted or unsubstituted, and when substituted, the substituents are preferably one or more of the following groups independently selected from alkyl, alkenyl, alkynyl, alkoxy, alkane Thio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio , heterocycloalkylthio, carboxyl or carboxylate.

The term "alkoxy" refers to -O-(alkyl) and -O-(unsubstituted cycloalkyl), wherein alkyl and cycloalkyl are as defined above. Non-limiting examples of alkoxy include: methoxy, ethoxy, propoxy, butoxy, cyclopropoxy, cyclobutoxy, cyclopentyloxy, cyclohexyloxy. Alkoxy may be optionally substituted or unsubstituted, and when substituted, the substituent is preferably one or more of the following groups independently selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkoxy Thio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio , heterocycloalkylthio, carboxyl or carboxylate.

The term "haloalkyl" refers to an alkyl group substituted with one or more halo, wherein alkyl is as defined above.

The term "haloalkoxy" refers to an alkoxy group substituted with one or more halogens, wherein alkoxy group is as defined above.

The term "deuteroalkyl" refers to an alkyl group substituted with one or more deuteriums, wherein alkyl is as defined above.

The term "hydroxyalkyl" refers to an alkyl group substituted with one or more hydroxy groups, wherein alkyl is as defined above.

The term "hydroxyl" refers to a -OH group.

The term "halogen" refers to fluorine, chlorine, bromine or iodine.

The term "amino" refers to _-NH2 .

The term "cyano" refers to -CN.

The term "nitro" refers to _-NO2 .

The term "oxo" refers to =O.

The term "thio" refers to =S.

The term "carboxy" refers to -C(O)OH.

The term "mercapto" refers to -SH.

The term "ester group" refers to -C(O)O(alkyl) or -C(O)O(cycloalkyl), wherein alkyl and cycloalkyl are as defined above.

The term "acyl" refers to compounds containing the group -C(O)R, where R is alkyl, cycloalkyl, heterocyclyl, aryl, heteroaryl as defined above.

The term "sulfonyl" refers to compounds containing the group -S(O ₎ 2R, where R is alkyl, cycloalkyl, heterocyclyl, aryl, heteroaryl as defined above.

Compounds of the invention may be in deuterated form. Each available hydrogen atom attached to a carbon atom can be independently replaced by a deuterium atom. Those skilled in the art can refer to the relevant literature to synthesize the deuterated form of the compound. Commercially available deuterated starting materials can be used in the preparation of deuterated forms of the compounds, or they can be synthesized using conventional techniques using deuterated reagents.

"Optional" or "optionally" means that the subsequently described event or circumstance can but need not occur, and that the description includes instances where the event or circumstance occurs or does not occur. For example, a "heterocyclic group optionally substituted with an alkyl group" means that an alkyl group may but need not be present, and the description includes cases where the heterocycle group is substituted with an alkyl group and cases where the heterocycle group is not substituted with an alkyl group .

"Substituted" means that one or more hydrogen atoms in a group, preferably up to 5, more preferably 1 to 3 hydrogen atoms are independently substituted by the corresponding number of substituents. It goes without saying that substituents are only in their possible chemical positions and that a person skilled in the art can determine (by experiment or theory) possible or impossible substitutions without undue effort. For example, an amino or hydroxyl group with free hydrogen may be unstable when bonded to a carbon atom with an unsaturated (eg, ethylenic) bond.

"Pharmaceutical composition" means a mixture containing one or more compounds described herein, or a physiologically/pharmaceutically acceptable salt or prodrug thereof, and other chemical components, and other components such as a physiologically/pharmaceutically acceptable carrier and excipients. The purpose of the pharmaceutical composition is to promote the administration to the organism, facilitate the absorption of the active ingredient and thus exert biological activity.

"Pharmaceutically acceptable salt" refers to the salt of the compound of the present invention, which is safe and effective when used in mammals, and has proper biological activity.

Synthetic method of the invented compound

In order to accomplish the object of the present invention, the present invention adopts the following synthetic scheme to prepare the compound of the present invention.

Compounds of general formula (V) are synthesized according to scheme 1:

Step 1: Under basic conditions, compound Va is subjected to a substitution reaction with compound Vj to obtain compound Vb, and the basic conditions are preferably N,N-diisopropylethylamine;

Step 2: In the presence of a catalyst, compound Vb is demethylated to obtain compound Vc, and the catalyst is preferably boron tribromide;

Step 3: Under basic conditions, compound Vc is reacted with N-phenylbis(trifluoromethanesulfonyl)imide to obtain compound Vd, and the basic conditions are preferably N,N-diisopropylethylamine;

Step 4: In the presence of a catalyst, compound Vd is coupled with compound Vi to obtain compound Ve, and the catalyst is preferably tetrakistriphenylphosphine palladium;

Step 5: In the presence of a catalyst, reducing compound Ve to obtain compound Vf, the catalyst is preferably palladium hydroxide carbon;

Step 6: deprotecting compound Vf to obtain compound Vg under acidic conditions, preferably hydrochloric acid;

Step 7: Under basic conditions, compound Vg is hydrolyzed to obtain compound Vh, and the basic conditions are preferably sodium hydroxide;

Step 8: In the presence of a catalyst, the compound Vh undergoes an intramolecular condensation reaction to obtain a compound of the general formula (V), and the catalyst is preferably EDCI and HOBT;

in,

R ^d is selected from chlorine, bromine, iodine, OMs or OTs, preferably OTs;

R ^e is selected from methyl or ethyl, preferably ethyl;

R ¹ to R ⁵ , R ⁷ , R ¹⁰ , and n are as defined in the general formula (V).

The compound of general formula (VI) is synthesized according to scheme 2:

Step 1: Under basic conditions, compound Vc is reacted with VIa to obtain compound VIb, and the basic conditions are preferably N,N-diisopropylethylamine;

Step 2: deprotecting compound VIb to obtain compound VIc under acidic conditions, preferably hydrochloric acid;

Step 3: Under basic conditions, compound VIc is hydrolyzed to obtain compound VId, and the basic conditions are preferably sodium hydroxide;

Step 4: In the presence of a catalyst, the compound VId undergoes an intramolecular condensation reaction to obtain a compound of the general formula (VI), and the catalyst is preferably EDCI and HOBT;

in,

R ^e is selected from methyl or ethyl, preferably ethyl;

R ¹ to R ⁵ , R ⁷ , R ¹⁰ , and n are as defined in the general formula (VI).

detailed description

The compounds of the invention and their preparation are further understood by the examples, which illustrate some of the methods of making or using the compounds. However, it is to be understood that these examples do not limit the scope of the present invention. Variations of the invention now known or further developed are considered to fall within the scope of the invention described and claimed herein.

The compounds of the present invention are prepared utilizing convenient starting materials and general preparative procedures. The present invention gives typical or preferred reaction conditions, such as reaction temperature, time, solvent, pressure, molar ratio of reactants. But unless otherwise specified, other reaction conditions can also be adopted. Optimum conditions may vary with specific reactants or solvents used, but in general, reaction optimization steps and conditions can be identified.

In addition, some protecting groups may be used in the present invention to protect certain functional groups from unnecessary reactions. Suitable protecting groups for various functional groups and their protection or deprotection conditions are widely known to those skilled in the art. For example, "Protecting Groups in Organic Preparations" by T.W. Greene and G.M. Wuts (3rd edition, Wiley, New York, 1999 and citations in the book) describes in detail the protection or deprotection of a large number of protecting groups.

The separation and purification of compounds and intermediates takes appropriate methods and steps according to specific needs, such as filtration, extraction, distillation, crystallization, column chromatography, preparative thin-layer plate chromatography, preparative high-performance liquid chromatography or a combination of the above methods. For its specific usage method, please refer to the examples described in the present invention. Of course, other similar separation and purification means can also be used. They can be characterized using conventional methods, including physical constants and spectral data.

Compound structures were determined by nuclear magnetic resonance (NMR) or/and mass spectroscopy (MS). NMR shifts are given in units of 10 ^-6 (ppm). The determination of NMR is a Brukerdps 300 type nuclear magnetic analyzer, and the determination solvent is deuterated dimethyl sulfoxide (DMSO-d ₆ ), deuterated chloroform (CDCl ₃ ), deuterated methanol (CD ₃ OD), and the internal standard is tetramethyl sulfoxide. trimethylsilane (TMS).

LC (Agilent 1260 Infinity)/MS (G6125B) mass spectrometer (manufacturer: Agilent) was used for the determination of MS.

The lc6000 high performance liquid chromatograph (manufacturer: Innovation Tongheng) was used for the preparative liquid chromatography.

Thin-layer chromatography (TLC) uses Qingdao Ocean Chemical GF254 silica gel plate, the specification of the silica gel plate used for reaction monitoring TLC is 0.20mm ~ 0.25mm, and the specification of silica gel plate used for separation and purification TLC It is 0.5mm.

Silica gel column chromatography uses Qingdao ocean silica gel 100-200 mesh, 200-300 mesh and 300-400 mesh silica gel as the carrier.

The known starting materials of the present invention can be adopted or synthesized according to methods known in the art, or can be purchased from Wanghua Mall, Beijing Coupling, Sigma, Bailingwei, Yi Shiming, Shanghai Shuya, Shanghai Yinuokai, Anaiji Chemical, Shanghai Biide, Nanjing Yaoshi and other companies.

Unless otherwise specified in the examples, the reactions can all be carried out under a nitrogen atmosphere.

The argon atmosphere or nitrogen atmosphere means that the reaction bottle is connected to an argon or nitrogen balloon with a volume of about 1 L.

Reaction solvents, organic solvents or inert solvents are each expressed as the solvent used does not participate in the reaction under the described reaction conditions, including, such as benzene, toluene, acetonitrile, tetrahydrofuran (THF), dimethylformamide (DMF), chloroform , dichloromethane, ether, methanol, nitrogen-methylpyrrolidinone (NMP), pyridine, etc. Unless otherwise specified in the examples, the solution refers to an aqueous solution.

The chemical reactions described in the present invention are generally carried out under normal pressure. The reaction time and conditions are, for example, between -78°C and 200°C under one atmospheric pressure, and the reaction is completed within about 1 to 24 hours. If the reaction is overnight, the reaction time is generally 16 hours. Unless otherwise specified in the examples, the reaction temperature is room temperature, which is 20°C to 30°C.

The monitoring of the reaction process in the embodiment adopts thin layer chromatography (TLC), and the system of developing agent used in the reaction has: A: dichloromethane and methanol system, B: sherwood oil and ethyl acetate system, C: acetone, The volume ratio of the solvent is adjusted according to the polarity of the compound.

The eluent system of the column chromatography that purifies compound adopts and the developer system of thin-layer chromatography include: A: dichloromethane and methanol system, B: sherwood oil and ethyl acetate system, the volume ratio of solvent is according to the compound It can be adjusted according to the polarity, and it can also be adjusted by adding a small amount of basic or acidic reagents such as triethylamine and trifluoroacetic acid.

Unless otherwise defined, all professional and scientific terms used herein have the same meanings as commonly understood by those skilled in the art. In addition, any methods and materials similar or equivalent to those described can be applied to the method of the present invention.

Example

Examples 1-A and 1-B: (1 ³ E, 1 ⁴ E, 2 ¹ R, 2 ² R, 2 ⁵ S, 6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl-2 ³ ,7-Diaza-1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0 ]Hexane heterocyclooctane-8-one and (1 ³ E,1 ⁴ E,2 ¹ R,2 ² S,2 ⁵ S,6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl -2 ³ ,7-Diaza-1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1 .0] Preparation of Hexanocyclooctan-8-one

Step 1: Preparation of tert-butyl 2-(5-fluoro-2-methoxypyridin-3-yl)-2,5-dihydro-1H-pyrrole-1-carboxylate (1m)

At room temperature, 3-bromo-5-fluoro-2-methoxypyridine (10.0g, 48.5mmol), 2,3-dihydro-1H-pyrrole-1-carboxylic acid tert-butyl ester (12.3g, 72.8mmol ), triphenylphosphine (2.54 g, 9.72 mmol), potassium carbonate (20.2 g, 110 mmol) and palladium acetate (1.09 g, 4.85 mmol) were dissolved in 100 mL of dioxane. Under nitrogen atmosphere, it was stirred at 100°C for 18 hours. Cooled down to room temperature, added 500mL water, extracted with ethyl acetate (200mL x 3), washed with saturated brine (200mL x 1), dried over anhydrous sodium sulfate, filtered, the filtrate was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography Separation and purification (mobile phase: EA/PE=50:1) gave 8.20 g of the title compound as a white solid, yield: 58.1%.

LCMS: m/z 295.14 [M+H] ⁺ .

Step 2: Preparation of tert-butyl 2-(5-fluoro-2-methoxypyridin-3-yl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (1n)

At room temperature, tert-butyl 2-(5-fluoro-2-methoxypyridin-3-yl)-2,5-dihydro-1H-pyrrole-1-carboxylate (5.00 g, 16.9 mmol) was dissolved in Add palladium acetate (380 mg, 1.69 mmol) to 50 mL of anhydrous diethyl ether. At 0°C, slowly add diazomethane diethyl ether solution (84.5mL, 1M) dropwise (at 0°C, add 1-methyl-1 - methylene urea, stirred for ten minutes, left to stand, and the upper yellow ether solution was separated to obtain the ether solution of diazomethane). Stir at room temperature for 1 hour, filter, wash the filter cake with ether, concentrate the filtrate under reduced pressure to obtain a residue, and purify the residue by preparative liquid chromatography (column model: Gemini-C18 150x 21.2mm, 5um, mobile phase: acetonitrile/water , Gradient: 20%-80%) to obtain 2.50 g of the title compound as an oil, yield: 47.9%.

LCMS: m/z 309.15 [M+H] ⁺ .

Step 3: Preparation of 2-(5-fluoro-2-methoxypyridin-3-yl)-3-azabicyclo[3.1.0]hexane (1a)

At room temperature, tert-butyl 2-(5-fluoro-2-methoxypyridin-3-yl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (1.43g, 4.63mmol) Dissolve in 20ml DCM, add 4mol/L dioxane hydrochloride solution (5mL). Stir overnight at room temperature. Concentration under reduced pressure gave 1.05 g of the title compound as a white solid, yield: 92.9%.

LC-MS: m/z 209.10 [M+H] ⁺ .

Step 4: Preparation of (Z)-3-amino-4,4,4-trichloro-2-cyanobut-2-enoic acid ethyl ester (1r)

Dissolve ethyl cyanoacetate (20.0g, 177mmol), trichloroacetonitrile (38.2g, 266mmol) and triethylamine (8.94g, 88.5mmol) in 200mL absolute ethanol at 0°C, and stir at room temperature for 16 hours . It was concentrated under reduced pressure, and the residue was separated and purified by silica gel column chromatography (mobile phase: EA/PE=1:3) to obtain 44.0 g of the title compound as a yellow solid, yield: 96.7%.

LC-MS: m/z 256.96 [M+H] ⁺ .

Step 5: Preparation of ethyl 3,5-diamino-1H-pyrazole-4-carboxylate (1s)

At room temperature, (Z)-3-amino-4,4,4-trichloro-2-cyanobut-2-enoic acid ethyl ester (44.0g, 171mmol) and an aqueous solution of hydrazine hydrate (50%, 38.3g , 385mmol) was dissolved in 120mL N,N-dimethylformamide and stirred at 100°C for 2 hours. Concentrate under reduced pressure, dissolve the residue in 50 mL of dichloromethane, and let stand overnight. After filtration, the filter cake (50 mL×2) was washed with dichloromethane to obtain 16.5 g of the title compound as a brown solid, yield: 56.7%.

LC-MS: m/z 171.08 [M+H] ⁺ .

Step 6: Preparation of ethyl 2-amino-5-oxo-4,5-dihydropyrazolo[1,5-a]pyrimidine-3-carboxylate (1t)

At room temperature, sodium ethoxide (4.16g, 61.2mmol) was dissolved in 40mL of absolute ethanol, and ethyl 3,5-diamino-1H-pyrazole-4-carboxylate (2.60g, 15.3mmol) and 1,3 -Dimethylpyrimidine-2,4(1H,3H)-dione (2.14g, 15.3mmol), stirred at 90°C for 4 hours. Cool to room temperature, adjust the pH to 7-8 with 1N hydrochloric acid, filter, and wash the filter cake (20 mL×2) with absolute ethanol to obtain 1.28 g of the title compound as a yellow solid, yield: 37.6%.

LC-MS: m/z 223.08 [M+H] ⁺ .

Step 7: Preparation of ethyl 2-amino-5-(tosyloxy)pyrazolo[1,5-a]pyrimidine-3-carboxylate (1j)

Dissolve ethyl 2-amino-5-oxo-4,5-dihydropyrazolo[1,5-a]pyrimidine-3-carboxylate (1.08g, 4.86mmol) in 30ml DCM, add DIEA ( 1.96g, 19.4mmol), p-toluenesulfonyl chloride (1.02g, 5.34mmol), and stirred overnight at room temperature. Quenched with water, extracted with DCM (30mL x 3), washed with saturated brine (30mL x 2), dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to give the title compound 1.65g as a light yellow solid, yield: 90.1% .

LC-MS: m/z 377.08 [M+H]+.

Step 8: 2-Amino-5-(2-(5-fluoro-2-methoxypyridin-3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1 ,5-a] Preparation of ethyl pyrimidine-3-carboxylate (1b)

Dissolve 2-(5-fluoro-2-methoxypyridin-3-yl)-3-azabicyclo[3.1.0]hexane (1.08g, 4.41mmol) in 30ml n-butanol, add DIEA ( 1.98g, 15.3mmol), 2-amino-5-(tosyloxy)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid ethyl ester (1.65g, 4.39mmol), stirring at 105°C overnight. Concentrate under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-2:3) to obtain 1.41 g of the title compound as a light yellow solid, yield: 77.8%.

LC-MS: m/z 413.17 [M+H] ⁺ .

Step 9: 2-Amino-5-(2-(5-fluoro-2-hydroxypyridin-3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5 -a] Preparation of ethyl pyrimidine-3-carboxylate (1c)

2-amino-5-(2-(5-fluoro-2-methoxypyridin-3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5 -a] ethyl pyrimidine-3-carboxylate (1.62g, 3.93mmol) was dissolved in 30mL MeCN and 6mL DCM, NaI (3.54g, 23.6mmol) and AlCl ₃ (3.14g, 23.6mmol) were added at 0°C, Stir at 25°C for 3 hours. The reaction solution was poured into ice water, extracted with DCM (50mL x 3), washed with saturated sodium sulfite solution (50mL x 1), washed with saturated brine (50mL x 1), dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to obtain 1.41 g of the title compound as yellow oil, yield: 89.7%.

LC-MS: m/z 399.15 [M+H] ⁺ .

Step 10: 2-Amino-5-(2-(5-fluoro-2-(((trifluoromethanesulfonyl)oxy)pyridin-3-yl)-3-azabicyclo[3.1.0]hexyl- Preparation of 3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid ethyl ester (1d)

2-amino-5-(2-(5-fluoro-2-hydroxypyridin-3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a ] Pyrimidine-3-carboxylic acid ethyl ester (1.19g, 2.99mmol) was dissolved in 20mL DMF, TEA (604mg, 5.98mmol) and 1,1,1-trifluoro-N-phenyl-N-(trifluoro Methanesulfonyl)methanesulfonamide (PhN(Tf) ₂ ), stirred overnight at room temperature. Quenched with water, extracted with EA (20mL x 3), washed with saturated brine (20mL x 2), dried over anhydrous sodium sulfate, filtered, the filtrate was concentrated under reduced pressure, and the residue was separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-2:3), to obtain 1.05 g of the title compound as a yellow solid, yield: 66.4%.

LC-MS: m/z 531.10 [M+H] ⁺ .

Step 11: (R,E)-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)but-3-en-2-yl ) Preparation of tert-butyl carbamate (1i)

(R)-But-3-yn-2-ylcarbamate tert-butyl ester (1.00g, 5.92mmol), pinacol borate (1.80g, 7.09mmol), triflate ketone (107mg, 0.296mmol), triphenylphosphine (155mg, 0.592mmol), sodium tert-butoxide (56.8mg, 0.592mmol) were dissolved in dioxane (25mL), methanol (56.8mg, 17.8mmol) was added, under nitrogen atmosphere , and stirred at room temperature for 2 hours. Add 50mL water to quench, EA extract (30mL x 3), wash with saturated brine (50mL x 1), dry over anhydrous sodium sulfate, filter, the filtrate is concentrated under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile Phase: PE/EA=100:1-19:1), to obtain 1.68 g of the title compound as a colorless oil, yield: 95.4%.

LC-MS: m/z 298.21 [M+H] ⁺ .

Step 12: 2-Amino-5-(2-(2-((R,E)-3-((tert-butoxycarbonyl)amino)but-1-en-1-yl)-5-fluoropyridine- Preparation of ethyl 3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (1e)

Compound 1d (500 mg, 0.943 mmol), compound 1i (350 mg, 1.18 mmol) were dissolved in ethylene glycol dimethyl ether (12 ml), and saturated sodium bicarbonate solution (4 mL) and tetrakistriphenylphosphine palladium (109 mg, 0.0943 mmol), stirred at 90°C for 2 hours. Quenched with water, extracted with EA (10mL x 3), washed with saturated brine (20mL x 1), dried over anhydrous sodium sulfate, filtered, the filtrate was concentrated under reduced pressure, and the residue was separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-3:7), to obtain 300 mg of the title compound as a yellow solid, yield: 57.7%.

LC-MS: m/z 552.27 [M+H] ⁺ .

Step 13: 2-Amino-5-(2-(2-((R)-3-((tert-butoxycarbonyl)amino)butyl)-5-fluoropyridin-3-yl)-3-aza Preparation of ethyl bicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (1f)

Compound 1e (300 mg, 0.542 mmol) was dissolved in 5 mL of methanol, palladium hydroxide on carbon (10%) (600 mg) was added, and stirred overnight at room temperature under hydrogen atmosphere. Filter, wash the filter cake (10mL x 3) with methanol, and concentrate the filtrate under reduced pressure to obtain 270 mg of the title compound as a light yellow solid, yield: 89.1%.

LC-MS: m/z 554.28 [M+H] ⁺ .

Step 14: 2-Amino-5-(2-(2-((R)-3-aminobutyl)-5-fluoropyridin-3-yl)-3-azabicyclo[3.1.0]hexa-3 -yl) pyrazolo[1,5-a]pyrimidine-3-carboxylate ethyl ester (1g)

Compound 1f (270 mg, 0.487 mmol) was dissolved in 5 mL of DCM, 2.5 mL of dioxane hydrochloride solution (4 mol/L) was added, and stirred at room temperature for 1 hour. Concentrate under reduced pressure, add 15mL saturated sodium bicarbonate solution, extract with DCM (10mL x 3), wash with saturated brine (20mL x 1), dry over anhydrous sodium sulfate, filter, and concentrate the filtrate under reduced pressure to obtain 240 mg of the title compound as a light yellow solid (Crude).

LC-MS: m/z 454.23 [M+H] ⁺ .

Step 15: 2-Amino-5-(2-(2-((R)-3-aminobutyl)-5-fluoropyridin-3-yl)-3-azabicyclo[3.1.0]hexa-3 -yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (1h)

Compound 1g (240mg, 0.529mmol) was dissolved in a mixed solvent of 6mL ethanol and 3mL water at room temperature, sodium hydroxide (211mg, 5.29mmol) was added, stirred overnight at 50°C, and continued to stir at 70°C for 3 hours. Add saturated citric acid solution at 0°C to adjust the pH to 6-7, and concentrate under reduced pressure to obtain 1.03 g of the title compound (crude product) as a pale yellow solid.

LC-MS: m/z 426.20 [M+H] ⁺ .

Step 16: (1 ³ E, 1 ⁴ E, 2 ¹ R, 2 ² R, 2 ⁵ S, 6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl-2 ³ ,7-diazepine -1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexaneheterocyclooctane -8-one and (1 ³ E,1 ⁴ E,2 ¹ R,2 ² S,2 ⁵ S,6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl-2 ³ ,7-di Aza-1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexaneheterocycle Preparation of Octan-8-one

Compound 1h (1.03g, 0.487mmol) was dissolved in 10ml of dichloromethane and 5ml of DMF mixed solvent, EDCI (280mg, 1.46mmol) and HOBT (197mg, 1.46mmol) were added, and stirred for 10 minutes. Triethylamine (147mg, 1.46mmol) was added and stirred overnight at room temperature. Add 20mL water to quench, EA extract (20mL x 3), wash with saturated brine (20mL x 1), dry over anhydrous sodium sulfate, filter, the filtrate is concentrated under reduced pressure, and the residue is separated by high performance preparative liquid chromatography (chromatographic column Model: Daisogei 30mm*250mm, C18-3, 10um 100A, mobile phase: acetonitrile/water (0.05% formic acid), 2-22min, gradient: 30%-50%), the title compound (1-A) was obtained as white solid 9 mg and (1-B) 7 mg, yield: 4.54%, 3.53%.

Compound 1-A: retention time 16.9min

LC-MS: m/z 408.19 [M+H] ⁺ ;

¹ H NMR (400MHz,DMSO-d ₆ )δ8.38(m,2H),8.19(d,1H),7.36-7.26(m,1H),6.19(d,1H),5.84(br,2H), 5.56(br,1H),4.28-4.17(m,1H),4.15-4.04(m,1H),3.78(d,1H),3.54-3.40(m,1H),2.86-2.64(m,2H), 2.16-1.98 (m, 2H), 1.57-1.48 (m, 1H), 1.33-1.10 (m, 3H), 0.99-0.89 (m, 1H), 0.55-0.46 (m, 1H).

Compound 1-B: retention time 20.5min

LC-MS: m/z 408.19 [M+H] ⁺ ;

¹ H NMR (400MHz,DMSO-d ₆ )δ:8.49-8.40(m,1H),8.35(d,1H),7.57(d,1H),7.43(d,1H),6.22(d,1H), 5.85(s,2H),5.41(br,1H),4.27-4.13(m,1H),4.10-3.94(m,1H),3.81(d,1H),3.72-3.57(m,1H),3.08- 2.82(m,2H),2.31-2.15(m,1H),2.06-1.94(m,1H),1.52-1.41(m,1H),1.10(d,3H),0.895-0.85(m,1H), 0.46-0.37(m,1H).

Example 2: (3'E,4'E)-2'-amino-5'-fluorospiro[cyclopropane-1,6'-2 ³ ,7-diaza-1(5,3)-pyridine Azolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexaneheterocyclooctane]-8'-one (2) preparation of

Step 1: (E)-(1-(2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)cyclopropane base) preparation of tert-butyl carbamate (2a)

(1-Ethynylcyclopropyl) tert-butyl carbamate (450mg, 2.49mmol), biborpinacol ester (758mg, 2.98mmol), copper trifluoromethanesulfonate (45.0mg, 0.124mmol), Tris Phenylphosphine (65.1mg, 0.249mmol) was dissolved in dioxane (15ml), sodium tert-butoxide (23.9mg, 0.249mmol) and methanol (239mg, 7.47mmol) were added, and stirred at room temperature for 3 Hour. Quenched with water, extracted with EA (10mL x 3), washed with saturated brine (20mL x 1), dried over anhydrous sodium sulfate, filtered, the filtrate was concentrated under reduced pressure, and the residue was separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-5:1), to obtain 410 mg of the title compound as a white solid, yield: 53.4%.

LC-MS: m/z 310.27 [M+H] ⁺ .

Other steps are the same as the preparation method of Example 1, except that (E)-(1-(2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborane -2-yl)vinyl)cyclopropyl)tert-butyl carbamate (2a) instead of (R,E)-(4-(4,4,5,5-tetramethyl-1,3,2-di Oxaboran-2-yl)but-3-en-2-yl)carbamate tert-butyl ester (1i) to give the title compound 2.

LC-MS: m/z 420.19 [M+H] ⁺ .

¹ H NMR (400 MHz, CD ₃ OD) δ: 8.41(s,1H), 8.28(d,1H), 8.11(d,1H), 7.29(d,1H), 6.24(d,1H), 5.64( s,1H),4.20-4.15(m,1H),3.78-3.70(m,2H),3.08-3.02(m,1H),2.61-2.56(m,1H),2.16-1.71(m,2H), 1.59-1.51 (m, 2H), 1.17-1.08 (m, 2H), 0.99-0.82 (m, 2H), 0.66-0.58 (m, 1H), 0.51-0.45 (m, 1H).

Examples 3-A and 3-B: (1 ³ E, 1 ⁴ E, 2 ¹ R, 2 ² R, 2 ⁵ S, 6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl-4 -oxa-2 ³ ,7-diaza-1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)- Bicyclo[3.1.0]hexanocyclooctan-8-one and (1 ³ E,1 ⁴ E,2 ¹ R,2 ⁴ R,2 ⁵ S,6R)-1 ² -amino-3 ⁵ -fluoro -6-Methyl-4-oxa-2 ³ ,7-diaza-1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina- Preparation of 2(3,2)-bicyclo[3.1.0]heterocyclooctan-8-one

Step 1: Preparation of (R)-2-((tert-butoxycarbonyl)amino)propyl 4-methylbenzenesulfonate (3a)

Dissolve tert-butyl (R)-(1-hydroxypropan-2-yl)carbamate (1.00 g, 5.71 mmol) in 25 mL of DCM, add p-toluenesulfonyl chloride (1.14 g, 6.00 mmol) and TEA (1.44 g , 14.3mmol), stirred overnight at room temperature. Concentrate under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-5:1) to obtain 1.22 g of the title compound as a light yellow solid, yield: 64.9%.

LC-MS: m/z 330.13 [M+H] ⁺ .

Step 2: 2-Amino-5-(2-(2-((R)-2-((tert-butoxycarbonyl)amino)propoxy)-5-fluoropyridin-3-yl)-3-nitrogen Preparation of ethyl heterobicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (3b)

2-amino-5-(2-(5-fluoro-2-hydroxypyridin-3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a ] Pyrimidine-3-carboxylic acid ethyl ester (1c) (500mg, 1.26mmol) was dissolved in 25mL DMF, cesium carbonate (1.23g, 3.77mmol) and (R)-2-((tert-butoxycarbonyl)amino ) Propyl 4-methylbenzenesulfonate (829mg, 2.51mmol), stirred overnight at 80°C. Add 30mL of water to dilute, extract with EA (20mL x 3), wash with saturated brine (20mL x 2), dry over anhydrous sodium sulfate, filter, the filtrate is concentrated under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile phase : PE/EA=100:1-3:2), to obtain 400 mg of the title compound as a white solid, yield: 57.3%.

LC-MS: m/z 556.26 [M+H] ⁺ .

Step 3: 2-Amino-5-(2-(2-((R)-2-aminopropoxy)-5-fluoropyridin-3-yl)-3-azabicyclo[3.1.0]hexyl- Preparation of 3-yl)pyrazolethyl[1,5-a]pyrimidine-3-carboxylic acid ethyl ester (3c)

Compound 3b (400mg, 0.719mmol) was dissolved in DCM (10ml), added with 4mol/L dioxane hydrochloride solution (3mL), and stirred at room temperature for 2 hours. Concentrate under reduced pressure, add 20mL saturated sodium bicarbonate solution, extract with DCM (10mL x 3), wash with saturated brine (20mL x 1), dry over anhydrous sodium sulfate, filter, and concentrate the filtrate under reduced pressure to obtain a light yellow semi-solid title Compound 370 mg (crude product).

LC-MS: m/z 456.21 [M+H] ⁺ .

Step 4: 2-Amino-5-(2-(2-((R)-2-aminopropoxy)-5-fluoropyridin-3-yl)-3-azabicyclo[3.1.0]hexyl- Preparation of 3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (3d)

Compound 3c (320mg, 0.702mmol) was dissolved in a mixed solvent of 10mL ethanol and 1mL water, sodium hydroxide (281mg, 7.02mmol) was added, and stirred at 65°C overnight. At 0°C, adjust the pH to 8 with 1mol/L hydrochloric acid. Concentrate under reduced pressure at 25°C to obtain 860 mg of the title compound (crude product) as a pale yellow solid.

LC-MS: m/z 428.18 [M+H] ⁺ .

Step 5: (1 ³ E, 1 ⁴ E, 2 ¹ R, 2 ² R, 2 ⁵ S, 6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl-4-oxa-2 ³ , 7-diaza-1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexyl Alkacyclooctan-8-one and (1 ³ E,1 ⁴ E,2 ¹ R,2 ⁴ R,2 ⁵ S,6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl-4 -oxa-2 ³ ,7-diaza-1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)- Preparation of bicyclo[3.1.0]hexanocyclooctan-8-one

Compound 3d (860mg, 0.702mmol) was dissolved in 10ml of dichloromethane and 4ml of DMF mixed solvent, EDCI (405mg, 2.11mmol) and HOBT (285mg, 2.11mmol) were added, and stirred for 10 minutes. Triethylamine (213 mg, 2.11 mmol) was added and stirred at room temperature overnight. Add 20mL water to quench, EA extract (20mL x 3), wash with saturated brine (20mL x 1), dry over anhydrous sodium sulfate, filter, the filtrate is concentrated under reduced pressure, and the residue is separated by high performance preparative liquid chromatography (chromatographic column Model: Daisogei 30mm*250mm, C18-5, 10um 100A, mobile phase: acetonitrile/water (0.05% formic acid), gradient: 1-10min, 35%, 10-20min, 38%), the title compound was obtained as light yellow solid (3-A) 18 mg and (3-B) 27 mg, yield: 6.25%, 9.38%.

Compound 3-A: retention time 14.5min

LC-MS: m/z 410.17 [M+H] ⁺ ;

¹ H NMR (400MHz,DMSO-d ₆ )δ9.25(d,1H),8.35(d,1H),8.06(d,1H),7.63(dd,1H),6.18(d,1H),5.83( br,2H),5.61(br,1H),4.75(dd,1H),4.31-4.20(m,1H),4.17-4.05(m,2H),3.77(br,1H),2.13-2.01(m, 1H), 1.68-1.57(m, 1H), 1.37(d, 3H), 0.95-0.82(m, 1H), 0.41-0.34(m, 1H).

Compound 3-B: retention time 16.2min

LC-MS: m/z 410.17 [M+H] ⁺ ;

¹ H NMR (400MHz,DMSO-d ₆ )δ8.79(br,1H),8.35(d,1H),8.08(d,1H),7.67(dd,1H),6.21(d,1H),5.87( br,2H),5.69(br,1H),4.90-4.78(m,1H),4.3-4.22(m,1H),4.15-3.98(m,2H),3.84-3.77(m,1H),2.06- 1.94 (m, 1H), 1.61-1.52 (m, 1H), 1.42 (d, 3H), 0.90-0.82 (m, 1H), 0.32-0.25 (m, 1H).

Example 4: (1 ³ E,1 ⁴ E,5R)-1 ² -amino-3 ⁵ -fluoro-5-methyl-3 ¹ ,3 ² -dihydro-2 ³ ,6-diaza-1 (5,3)-pyrazolo[1,5-a]pyrimidina-3(3,1)-pyridina-2(3,2)-bicyclo[3.1.0]hexepepane-3 Preparation of ² ,7-diketone (4)

Step 1: 2-Amino-5-(2-(1-((R)-2-((tert-butoxycarbonyl)amino)propyl)-5-fluoro-2-oxo-1,2-dihydro Preparation of ethyl pyridin-3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (4a).

2-amino-5-(2-(5-fluoro-2-hydroxypyridin-3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a ] Ethyl pyrimidine-3-carboxylate (1c) (1.00 g, 5.71 mmol) was dissolved in 25 mL of DCM, p-toluenesulfonyl chloride (1.14 g, 6.00 mmol) and triethylamine (1.44 g, 14.3 mmol) were added, room temperature Stir overnight. Concentrate under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-5:1) to obtain 1.22 g of the title compound as a light yellow solid, yield: 64.9%.

LC-MS: m/z 330.13 [M+H] ⁺ .

Other steps are the same as the preparation method of Example 3, except that 2-amino-5-(2-(1-((R)-2-((tert-butoxycarbonyl)amino)propyl)-5-fluoro- 2-oxo-1,2-dihydropyridin-3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid Ethyl ester (4a) instead of 2-amino-5-(2-(2-((R)-2-((tert-butoxycarbonyl)amino)propoxy)-5-fluoropyridin-3-yl)- 3-Azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid ethyl ester (3b) to obtain the title compound 4.

LC-MS: m/z 410.17 [M+H] ⁺ .

¹ H NMR (400MHz,DMSO-d ₆ )δ8.26(d,1H),7.88-7.82(m,1H),7.47(dd,1H),6.75(d,1H),6.17(d,1H), 5.98(br,2H),5.29(s,1H),4.64-4.54(m,1H),4.19-4.07(m,1H),4.00-3.93(m,1H),3.92-3.83(m,1H), 3.78 (d, 1H), 2.07-1.96 (m, 1H), 1.70-1.61 (m, 1H), 1.37 (d, 3H), 1.00-1.91 (m, 1H), 0.45-0.37 (m, 1H).

Example 5: (1 ³ E,1 ⁴ E,5S)-1 ² -amino-3 ⁵ -fluoro-5-methyl-4-oxa-2 ³ ,7-diaza-1(5,3 )-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexaneheterocyclooctane-8-one (5 ) preparation

Step 1: Preparation of (S)-1-((tert-butoxycarbonyl)amino)propan-2-yl 4-methylbenzenesulfonate (5a)

Dissolve tert-butyl (S)-(2-hydroxypropyl)carbamate (1.00 g, 5.71 mmol) in 25 mL of DCM, add p-toluenesulfonyl chloride (1.14 g, 6.00 mmol) and TEA (1.44 g, 14.3 mmol) ), stirred overnight at room temperature. Concentrate under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-5:1) to obtain 640 mg of the title compound as a light yellow solid, yield: 34.0%.

LC-MS: m/z 330.13 [M+H] ⁺ .

Other steps are the same as in Example 3, except that (S)-1-((tert-butoxycarbonyl)amino)propan-2-yl 4-methylbenzenesulfonate (5a) is used instead of (R)-2 -((tert-butoxycarbonyl)amino)propyl 4-methylbenzenesulfonate (3a), the title compound 5 was obtained.

LC-MS: m/z 410.17 [M+H] ⁺ .

¹ H NMR (300MHz,DMSO-d ₆ )δ9.23(d,1H),8.35(d,1H),8.05(d,1H),7.63-7.56(m,1H),6.18(d,1H), 5.82(br,2H),5.58-5.54(m,1H),5.16-5.04(m,1H),4.15-4.08(m,1H),4.01-3.90(m,1H),3.76(d,1H), 3.15-3.04(m,1H),2.10-1.98(m,1H),1.65-1.58(m,1H),1.47(d,3H),0.94-0.85(m,1H),0.41-0.33(m,1H ).

Example 6: (1 ³ E,1 ⁴ E,7R)-1 ² -amino-3 ⁵ -fluoro-7-methyl-4-oxa-2 ³ ,8-diaza-1(5,3 )-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexaneheterocyclononan-9-one (6 ) preparation

Step 1: Preparation of (R)-2-(4-hydroxybut-2-yl)isoindoline-1,3-dione (6a)

(R)-3-Aminobutan-1-ol (1.00 g, 11.2 mmol) was dissolved in xylene (15 ml), and phthalic anhydride (1.75 g, 11.8 mmol) was added. Stir overnight at 140°C in a sealed tube. Concentrate under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-3:1) to obtain 2.43 g of the title compound as a light yellow solid, yield: 98.8%.

LC-MS: m/z 220.09 [M+H] ⁺ .

Step 2: Preparation of (R)-3-(1,3-dioxoisoindolin-2-yl)butyl 4-methylbenzenesulfonate (6b)

Dissolve (R)-2-(4-hydroxybut-2-yl)isoindoline-1,3-dione (1.43g, 6.53mmol) in dichloromethane, add p-toluenesulfonyl chloride (1.37g , 7.17mmol) and triethylamine (1.65g, 16.3mmol), stirred overnight at room temperature. Concentrate under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-5:1) to obtain 1.47 g of the title compound as light yellow oil, yield: 60.5%.

LC-MS: m/z 374.10 [M+H] ⁺ .

Step 3: 2-Amino-5-(2-(2-((R)-3-(1,3-dioxoisoindolin-2-yl)butoxy)-5-fluoropyridine-3 Preparation of -yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid ethyl ester (6c)

2-amino-5-(2-(5-fluoro-2-hydroxypyridin-3-yl)-3-azabicyclo[3.1.0]hex-3-yl)pyrazolo[1,5-a ]pyrimidine-3-carboxylic acid ethyl ester (1c) (500mg, 1.26mmol) and (R)-3-(1,3-dioxoisoindoline-2-yl)butyl 4-methylbenzenesulfonate Ester (6b) was dissolved in 15 mL of DMF, cesium carbonate (1.23 g, 3.77 mmol) was added, and stirred overnight at 80°C. Add 30mL of water to dilute, extract with EA (20mL x 3), wash with saturated brine (30mL x 1), dry over anhydrous sodium sulfate, filter, the filtrate is concentrated under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile phase PE/EA=1:1), to obtain 260 mg of the title compound as a light yellow solid, yield: 34.6%.

LC-MS: m/z 600.23 [M+H] ⁺ .

Step 4: 2-Amino-5-(2-(2-((R)-3-aminobutoxy)-5-fluoropyridin-3-yl)-3-azabicyclo[3.1.0]hexyl- Preparation of 3-yl)pyrazolethyl[1,5-a]pyrimidine-3-carboxylic acid ethyl ester (6d)

Compound 6c (230 mg, 0.384 mmol) was dissolved in 8 mL of ethanol, hydrazine hydrate (123 mg, 1.92 mmol) was added, and stirred at 70°C for 2 hours. Add 15 mL of water for dilution, extract with EA (10 mL x 3), wash with saturated brine (20 mL x 1), dry over anhydrous sodium sulfate, filter, and concentrate the filtrate under reduced pressure to obtain 160 mg of the title compound as a white solid, yield: 88.9%.

LC-MS: m/z 466.23 [M+H] ⁺ .

Step 5: 2-Amino-5-(2-(2-((R)-3-aminobutoxy)-5-fluoropyridin-3-yl)-3-azabicyclo[3.1.0]hexyl- Preparation of 3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (6e)

Compound 6d (140mg, 0.298mmol) was dissolved in a mixed solvent of 5mL ethanol and 0.5mL water at room temperature, sodium hydroxide (119mg, 2.98mmol) was added, and stirred overnight at 65°C. Add 1 mol/L hydrochloric acid solution at 0°C to adjust the pH to 8-9, and concentrate under reduced pressure at room temperature to obtain 330 mg of the title compound (crude product) as a white-yellow solid.

LC-MS: m/z 442.19 [M+H] ⁺ .

Step 6: (1 ³ E,1 ⁴ E,7R)-1 ² -amino-3 ⁵ -fluoro-7-methyl-4-oxa-2 ³ ,8-diaza-1(5,3) -Pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexaneheterocyclononan-9-one (6) preparation of

Compound 6e (330mg, 0.298mmol) was dissolved in 5ml of dichloromethane and 2ml of DMF mixed solvent, EDCI (172mg, 0.894mmol) and HOBT (121mg, 0.894mmol) were added, and stirred for 10 minutes. Triethylamine (90.3 mg, 0.894 mmol) was added and stirred overnight at room temperature. Add 20mL water to quench, EA extract (15mL x 3), wash with saturated brine (20mL x 1), dry over anhydrous sodium sulfate, filter, concentrate under reduced pressure, and the residue is separated by high performance preparative liquid chromatography (column type : Daisogei 30mm*250mm, C18, 10um 100A, mobile phase: acetonitrile/water (0.05% formic acid), gradient: 30%-70%), obtain the title compound 28mg of pale yellow solid, yield: 22.2%.

LC-MS: m/z 424.18 [M+H] ⁺ .

¹ H NMR (300MHz, DMSO-d ₆ ) δ: 8.33 (br, 1H), 8.08 (d, 1H), 7.97 (s, 1H), 7.60 (d, 1H), 6.18 (d, 1H), 6.08 ( br,2H),5.68-5.64(m,1H),4.79-4.67(m,1H),4.27-4.20(m,2H),4.06-4.01(m,1H),3.83-3.76(m,1H), 2.38-2.28(m,1H),2.05-1.99(m,2H),1.63-1.55(m,1H),1.26(d,3H),0.93-0.87(m,1H),0.46-0.38(m,1H ).

Examples 7-A and 7-B: (1 ³ E, 1 ⁴ E, 2 ¹ R, 2 ² R, 2 ⁵ S, 4E, 6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl -2 ³ ,7-Diaza-1(5,3)-pyrimazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1 .0] hexane heterocyclooct-4-en-8-one and (1 ³ E, 1 ⁴ E, 2 ¹ R, 2 ² S, 2 ⁵ S, 4E, 6R)-1 ² -amino-3 ⁵ -Fluoro-6-methyl-2 ³ ,7-diaza-1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3 ,2) Preparation of -bicyclo[3.1.0]hexanocyclooct-4-en-8-one

Step 1: 2-Amino-5-(2-(2-(R,E)-3-aminobut-1-en-1-yl)-5-fluoropyridin-3-yl)-3-azabicyclo Preparation of [3.1.0]hex-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid ethyl ester (7a)

Compound 1e (270 mg, 0.490 mmol) was dissolved in 5 mL of DCM, 2.5 mL of dioxane hydrochloride solution (4 mol/L) was added, and stirred at room temperature for 1 hour. Concentrate under reduced pressure, add 15mL saturated sodium bicarbonate solution, extract with DCM (10mL x 3), wash with saturated brine (20mL x 1), dry over anhydrous sodium sulfate, filter, and concentrate the filtrate under reduced pressure to obtain 240 mg of the title compound as a light yellow solid (Crude).

LC-MS: m/z 452.21 [M+H] ⁺ .

Step 2: 2-Amino-5-(2-(2-(R,E)-3-aminobut-1-en-1-yl)-5-fluoropyridin-3-yl)-3-azabicyclo Preparation of [3.1.0]hex-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (7b)

Compound 7a (240mg, 0.490mmol) was dissolved in a mixed solvent of 6mL ethanol and 3mL water at room temperature, sodium hydroxide (196mg, 4.90mmol) was added, stirred overnight at 50°C, and continued to stir at 70°C for 3 hours. Add saturated citric acid solution at 0°C to adjust the pH to 6-7, and concentrate under reduced pressure to obtain 1.03 g of the title compound (crude product) as a pale yellow solid.

LC-MS: m/z 424.18 [M+H] ⁺ .

Step 3: (1 ³ E, 1 ⁴ E, 2 ¹ R, 2 ² R, 2 ⁵ S, 4E, 6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl-2 ³ ,7-di Aza-1(5,3)-pyrimazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexaneheterocycle Oct-4-en-8-one and (1 ³ E,1 ⁴ E,2 ¹ R,2 ² S,2 ⁵ S,4E,6R)-1 ² -amino-3 ⁵ -fluoro-6-methyl -2 ³ ,7-Diaza-1(5,3)-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1 .0] Preparation of hexaneheterocyclooct-4-en-8-one

Compound 7b (1.03g, 0.487mmol) was dissolved in 10ml of dichloromethane and 5ml of DMF mixed solvent, EDCI (280mg, 1.46mmol) and HOBT (197mg, 1.46mmol) were added, and stirred for 10 minutes. Triethylamine (147mg, 1.46mmol) was added and stirred overnight at room temperature. Add 20mL water to quench, EA extract (20mL x 3), wash with saturated brine (20mL x 1), dry over anhydrous sodium sulfate, filter, the filtrate is concentrated under reduced pressure, and the residue is separated by high performance preparative liquid chromatography (chromatographic column Model: Daisogei 30mm*250mm, C18-3, 10um 100A, mobile phase: acetonitrile/water (0.05% formic acid), 2-25min, gradient: 30%-60%), the title compound (7-A) was obtained as white solid 6 mg and (7-B) 9 mg, yield: 3.03%, 4.54%.

Compound 7-A: retention time 17.5min

LC-MS: m/z 406.17 [M+H] ⁺ ;

¹ H NMR (400MHz,DMSO-d ₆ )δ8.38(m,2H),8.19(d,1H),7.36-7.26(m,1H),6.71-6.82(m,2H),6.19(d,1H ),5.84(br,2H),5.56(br,1H),4.28-4.17(m,1H),4.15-4.04(m,1H),3.78(d,1H),3.54-3.40(m,1H), 1.57-1.48(m,1H),1.33-1.10(m,3H),0.99-0.89(m,1H),0.55-0.46(m,1H).

Compound 7-B: retention time 21.2min

LC-MS: m/z 406.17 [M+H] ⁺ ;

¹ H NMR (400MHz,DMSO-d ₆ )δ:8.49-8.40(m,1H),8.35(d,1H),7.57(d,1H),7.43(d,1H),6.71-6.82(m,2H ),6.22(d,1H),5.85(s,2H),5.41(br,1H),4.27-4.13(m,1H),4.10-3.94(m,1H),3.81(d,1H),3.72- 3.57 (m, 1H), 1.52-1.41 (m, 1H), 1.10 (d, 3H), 0.895-0.85 (m, 1H), 0.46-0.37 (m, 1H).

Example 8: (1 ³ E,1 ⁴ E,5R)-1 ² -amino-35-fluoro-5-methyl-4-methylene-2 ³ ,6-diaza-1(5,3 )-pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexacycloheptane-7-one (8 ) preparation

Step 1: tert-butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-3-en-2-yl)carbamate Preparation of (8d)

(R)-But-3-yn-2-ylcarbamate tert-butyl ester (1.00g, 5.92mmol), pinacol borate (1.80g, 7.09mmol), ketone chloride (58.6mg, 0.592 mmol), sodium tert-butoxide (85.2 mg, 0.888 mmol) were dissolved in toluene (25 mL), and tri-tert-butylphosphine (2 mL, 10% in n-heptane), methanol ( 379mg, 11.8mmol), stirred at -50°C for 1 hour under nitrogen atmosphere. Concentrate under reduced pressure, and the residue is separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-3:1) to obtain 1.40 g of the title compound as a colorless oil, yield: 80%.

LC-MS: m/z 298.21 [M+H] ⁺ .

Step 2: 2-Amino-5-(2-(2-(R)-3-(tert-butoxycarbonyl)amino)but-1-en-2-yl)-5-fluoropyridin-3-yl) Preparation of ethyl 3-azabicyclo[3.1.0]hexan-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (8a)

Compound 1d (500 mg, 0.943 mmol), compound 8d (350 mg, 1.18 mmol) were dissolved in ethylene glycol dimethyl ether (12 ml), and saturated sodium bicarbonate solution (4 mL) and tetrakistriphenylphosphine palladium (109 mg, 0.0943 mmol), stirred at 90°C for 2 hours. Quenched with water, extracted with EA (10mL x 3), washed with saturated brine (20mL x 1), dried over anhydrous sodium sulfate, filtered, the filtrate was concentrated under reduced pressure, and the residue was separated and purified by silica gel column chromatography (mobile phase: PE/EA=100:1-3:7), to obtain 300 mg of the title compound as a yellow solid, yield: 57.7%.

LC-MS: m/z 552.27 [M+H] ⁺ .

Step 3: 2-Amino-5-(2-(R)-3-aminobut-1-en-2-yl)-5-fluoropyridin-3-yl)-3-azabicyclo[3.1.0] Preparation of ethyl hexane-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (8b)

Compound 8a (270 mg, 0.487 mmol) was dissolved in 5 mL of DCM, 2.5 mL of dioxane hydrochloride solution (4 mol/L) was added, and stirred at room temperature for 1 hour. Concentrate under reduced pressure, add 15mL saturated sodium bicarbonate solution, extract with DCM (10mL x 3), wash with saturated brine (20mL x 1), dry over anhydrous sodium sulfate, filter, and concentrate the filtrate under reduced pressure to obtain 240 mg of the title compound as a light yellow solid (Crude).

LC-MS: m/z 452.21 [M+H] ⁺ .

Step 4: 2-Amino-5-(2-(R)-3-aminobut-1-en-2-yl)-5-fluoropyridin-3-yl)-3-azabicyclo[3.1.0] Preparation of Hexan-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (8c)

Compound 8b (240mg, 0.529mmol) was dissolved in a mixed solvent of 6mL ethanol and 3mL water at room temperature, sodium hydroxide (211mg, 5.29mmol) was added, stirred overnight at 50°C, and continued to stir at 70°C for 3 hours. Add saturated citric acid solution at 0°C to adjust the pH to 6-7, and concentrate under reduced pressure to obtain 1.03 g of the title compound (crude product) as a pale yellow solid.

LC-MS: m/z 424.18 [M+H] ⁺ .

Step 5: (1 ³ E,1 ⁴ E,5R)-1 ² -amino-35-fluoro-5-methyl-4-methylene-2 ³ ,6-diaza-1(5,3) -pyrazolo[1,5-a]pyrimidina-3(3,2)-pyridina-2(3,2)-bicyclo[3.1.0]hexacycloheptan-7-one (8) preparation of

Compound 8c (1.03g, 0.487mmol) was dissolved in 10ml of dichloromethane and 5ml of DMF mixed solvent, EDCI (280mg, 1.46mmol) and HOBT (197mg, 1.46mmol) were added, and stirred for 10 minutes. Triethylamine (147mg, 1.46mmol) was added and stirred overnight at room temperature. Add 20mL water to quench, EA extract (20mL x 3), wash with saturated brine (20mL x 1), dry over anhydrous sodium sulfate, filter, the filtrate is concentrated under reduced pressure, and the residue is separated by high performance preparative liquid chromatography (chromatographic column Model: Daisogei 30mm*250mm, C18, 10um 100A, mobile phase: acetonitrile/water (0.05% formic acid), gradient: 30%-70%), the title compound was obtained as a white solid 1.6mg, yield: 0.81%.

LC-MS: m/z 406.17 [M+H] ⁺ .

¹ H NMR (400MHz,DMSO-d ₆ )δ8.38(m,2H),8.19(d,1H),7.36-7.26(m,1H),6.19(d,1H),6.14(d,1H), 5.84(br,2H),5.56(br,1H),5.35(d,1H),4.28-4.17(m,1H),4.15-4.04(m,1H),3.78(d,1H),3.54-3.40( m, 1H), 1.57-1.48(m, 1H), 1.33-1.10(m, 3H), 0.99-0.89(m, 1H), 0.55-0.46(m, 1H).

biological test

Test Example 1: Inhibitory activity of compounds of the present invention on TRK kinase

use

The KinEASE ^TM (Cisbio, 62TKOPEC) kit detects the inhibitory activity of the compounds of the present invention on TRKA, TRKA-G595R, and TRKA-G667C kinases. The buffer (buffer) that comes with the HRTF detection kit includes 5mM MgCl ₂ and 1mM DTT. The inhibitory level of the compound on the kinase is evaluated by detecting the phosphorylation level of the substrate in the kinase reaction. TRKA and TRKA(G667C) proteins were purchased from Bioduro, and TRKA(G595R) proteins were purchased from Signalchem, Cat. No. H2714-7.

experimental method:

First, the compound to be tested was dissolved in DMSO (Sigma, Cat. No. D8418), the initial concentration of the experiment was 10 uM, 3-fold dilution, and 10 gradients. Add reaction buffer, TRK kinase, and diluted test compound to a 384-well reaction plate (LABCYTE, product number LP-0200), mix well, and incubate at room temperature for 30 minutes. Add TK antibody (Cisbio, 62TKOPEC), ATP (Sigma, R0441), 1× reaction buffer to the reaction plate, centrifuge at 1000 rpm for 1 minute, and incubate at room temperature for 60 minutes. Finally, add the detection reagent to the reaction plate and incubate for 60 minutes. Luminescence values at wavelengths of 665 nm and 612 nm were read using an Envision plate reader (PerkinElmer). The ratio of 665/612 was positively correlated with substrate phosphorylation, thereby detecting the activity of TRKA kinase.

For the experimental data, the log value of the compound concentration is used on the X-axis; the percentage inhibition level is used on the Y-axis. GraphPad prism 6.0 software is used for nonlinear fitting to obtain the relationship between dose and effect, and the IC ₅₀ value of the compound is calculated using the following formula:

Y＝Bottom+(Top-Bottom)/(1+10^((LogIC ₅₀ -X)*HillSlope))

X is the log value of the compound concentration; Y is the inhibition level of the kinase. Top and Bottom are the Y values of the highest and lowest plateau periods of the curve; Hillslope is the Hill constant.

Table 1 The compounds of the present invention inhibit the IC values of TRKA, TRKA- _G595R , and TRKA-G667C kinases

Conclusion: As shown in the above table, the compound of the present invention can effectively inhibit the activity of TRKA, TRKA-G595R and TRKA-G667C kinases.

Test Example 2: Test of the inhibitory level of the compound of the present invention on tumor cell proliferation

Detect the inhibition level of the test compound on BaF3 TPM3-NTRK1-WT, BaF3 TPM3-NTRK1-G595R, BaF3 TPM3-NTRK1-G667C stably transfected cell lines, and screen candidate compounds according to the detection index IC ₅₀ .

experimental method:

Parental BaF3 and stable transfected cell lines (purchased from National Experimental Cell Resource Sharing Service Platform) were cultured in RPMI1640 (Invitrogen, A10491-01), adding 10% FBS (Gbico, 10099141), double antibodies (1% penicillin and streptomycin Invitrogen, 15140122) and puromycin (Puromycin, 0.8 μg/mL, Invitrogen, QLL-41-02). After the cells grow to the logarithmic phase, the cells are collected by centrifugation, and the cell viability is detected by the trypan blue method to ensure that the cell viability is greater than 90%. The cells were adjusted to a density of 1×10 ⁵ cells/mL, and the cells were seeded in a white transparent bottom 384-well plate (Corning, 3570), 500 cells/well. Add the compound to be tested, dissolve the compound in DMSO, and dilute; the initial concentration starts from 10 mM, and it is diluted 3 times, and 10 concentration gradients are set, with 3 replicate wells for each gradient. 37 ℃, 5% CO2 co-cultivation 72h. Using the CELL Titer-GLO luminescence method, the total ATP content was detected to determine the level of cell proliferation. The cells in the 384-well plate were taken out and equilibrated at room temperature for 30 minutes, and 20 μL CellTiter Glo (Promega, product number G7572) was added to each well, vortexed to mix, and incubated at room temperature for 10 minutes.

The luminescence value was read with a multifunctional microplate reader (Biotek, model Cytation 3). GraphPad Prism 6.0 software was used to analyze the Log values of compound responses at different concentrations to determine IC ₅₀ .

See Table 2 below for the IC ₅₀ values of the compounds of the present invention on the inhibition of various cell proliferations.

Table 2 The compounds of the present invention inhibit the IC ₅₀ value of BaF3 TPM3-NTRK1-WT, BaF3 TPM3-NTRK1-G595R, BaF3 TPM3-NTRK1-G667C cells

Conclusion: As shown in the above table, the compound of the present invention has significant inhibitory effect on the proliferation of NTRK fusion and NTRK mutant cell lines.

Test example 3: Rat pharmacokinetic experiment of the compound of the present invention

The experimental animals were male SD rats aged 6-8 weeks, purchased from Beijing Weitong Lihua Experimental Animal Technology Co., Ltd., and raised in an SPF environment with a temperature of 20-26°C, a daily temperature difference of no more than 4°C, and a relative humidity of 40-70°C. %RH, 12h/12h alternate lighting every day. The experimental animals went through an adaptation period of 3-5 days, and the animals administered orally were fasted overnight (>12h) one day before the experiment, without water.

Each compound to be tested is divided into intravenous administration group (1mg/kg, n=3, vehicle: 10%DMSO+90% (20%HP-β-CD)) and intragastric administration group (10mg/kg, n =3, 0.5% Tween 80+0.5% CMC-Na). The compound solution preparation process is as follows: Intravenous injection of drugs, using DMSO and 20% HP-β-CD as solvents, first dissolving the drug in 10% DMSO, distilling to volume with 20% HP-β-CD, adjusting the concentration to 0.2 mg/mL That’s it; gavage drug, with Tween 80 and CMC-Na as solvent, first mix the drug with 0.5% Tween 80, then use 0.5% CMC-Na to make up the volume, mix well, and obtain the compound drug concentration of 1mg/ mL of suspension.

Animals were anesthetized by inhalation, and 0.2 mL of orbital blood was collected, placed in a sodium heparin anticoagulant tube, and the anticoagulant tube was gently shaken to prevent coagulation. The sample collection time points are: gavage group: before administration and 15min, 30min, 1h, 2h, 4h, 6h after administration; intravenous group: before administration and after administration 5min, 15min, 30min, 1h, 2h, 4h . Within 60 minutes of blood collection, centrifuge at 3000 rpm for 10 minutes with a Sorvall ST 8R high-speed low-temperature centrifuge. The upper layer of plasma was collected and stored in a freezer at -20°C for later use. The concentration of the compound in the sample was detected by the analytical method of LC-MS/MS. Use MAS Studio (V1.3.1stable) software to calculate and obtain the blood drug concentration-time curve of the compound in mice, as well as the main PK parameters: AUC0-t, Cmax, Tmax, T _1/2 and F%, F% = (AUCpo x dose iv)/(AUCiv x dose po) x 100%.

The pharmacokinetic parameters of the compounds of the present invention in rats are shown in Table 3 below.

Table 3 The pharmacokinetic parameters of the compounds of the present invention in rats

Conclusion: The compound of the present invention has good pharmacokinetic parameters and is suitable for the development of oral medicine.

Claims

A compound represented by general formula (I) or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof, or a pharmaceutically acceptable salt thereof:

in,

Z 1 , Z 2 , Z 3 and Z 4 can be independently selected from carbon or nitrogen;

X is selected from a bond, -(CH 2 ) m -, -(CH=CH)-, -O-(CH 2 ) t -, -S-(CH 2 ) t -, -S(O)-(CH 2 ) t -, -S(O) 2 -(CH 2 ) t - or -NR 6 -(CH 2 ) t -;

Y is -Q-(CH 2 ) v -, wherein Q is selected from

Where "*" represents the end where the Y group is connected to the aromatic ring core;

Ring A is selected from heteroaryl, aryl, cycloalkyl, heterocyclyl, said heteroaryl, aryl, cycloalkyl, heterocyclyl is optionally further selected from deuterium, alkyl, deuterated alkyl , haloalkyl, alkoxy, deuterated alkoxy, haloalkoxy, halogen, amino, hydroxyl, mercapto, nitro, cyano, oxo, alkenyl, alkynyl, cycloalkyl, heterocyclyl, Aryl, Heteroaryl, -(CH 2 ) q R a , -(CH 2 ) q OR a , -(CH 2 ) q C(O)R a , -(CH 2 ) q C(O)OR a , -(CH 2 ) q OC(O)R a , -(CH 2 ) q C(O)NR a R b , -(CH 2 ) q S(O) p R a , -(CH 2 ) q NR a R b , -(CH 2 ) q S(O) p NR a R b , -NR a C(O)NR b NR c , -(CH 2 ) q NR b C(O)R a , -(CH 2 ) q NR b C(O)OR a or -(CH 2 ) q NR b S(O) p R a is replaced by one or more groups;

R and R are each independently selected from hydrogen , halogen, nitro, hydroxyl, mercapto, cyano, amino, alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and Heteroaryl, said alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl are optionally further selected from halogen, amino, nitro, cyano, oxygen One or more groups of substituent, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl group replaced;

Alternatively, R1 and R2 together form

Alternatively, R and R together with the atoms they are connected to form a cycloalkyl or heterocyclyl, which is optionally further selected from the group consisting of halogen, amino, nitro, cyano, oxo One or more groups of radical, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl replaced by

R 3 and R 4 are each independently selected from hydrogen, halogen, alkyl;

R 5 is NR 8 R 9 ;

R is selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl, the alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl are optionally further selected from the group consisting of halogen, amino, nitro, cyano, oxo, hydroxy, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy, haloalkoxy Substituted by one or more groups of radical, cycloalkyl, heterocyclyl, aryl, heteroaryl;

Each R is independently selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl, the alkyl, alkenyl, alkynyl, cycloalkyl, Heterocyclyl, aryl and heteroaryl are optionally further selected from the group consisting of halogen, amino, nitro, cyano, oxo, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkane One or more groups of oxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl are substituted;

R 8 and R 9 are each independently selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl, the alkyl, alkenyl, alkynyl, cycloalkyl , heterocyclyl, aryl and heteroaryl are optionally further selected from halogen, amino, nitro, cyano, oxo, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, One or more groups of alkoxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl; or

R 8 and R 9 form a heterocyclic group together with the nitrogen atom connected to it, and the heterocyclic group is optionally further selected from the group consisting of deuterium, alkyl, deuterated alkyl, haloalkyl, alkoxy, deuterated alkoxy, One or more groups of haloalkoxy, halogen, amino, hydroxyl, mercapto, nitro, cyano, oxo, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl replace;

R a , R b , and R c are each independently selected from hydrogen, halogen, nitro, hydroxyl, mercapto, cyano, amino, alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, heterocyclyl, Aryl and heteroaryl, said alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl and heteroaryl are optionally further selected from halogen, amino, nitro, cyano One or Replaced by multiple groups;

Or, any two adjacent or non-adjacent R a , R b , R c together with the atoms they connect form cycloalkyl, heterocyclyl, aryl and heteroaryl, wherein said cycloalkyl, hetero Cyclic, aryl and heteroaryl are optionally further selected from the group consisting of halogen, amino, nitro, cyano, oxo, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy Substituted by one or more groups of radical, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl;

n is an integer selected from 0 to 6;

m is an integer selected from 1 to 6;

t is an integer selected from 0 to 6;

v is an integer selected from 0 to 6;

p is 0, 1 or 2;

q is an integer of 0 to 6.
The compound represented by the general formula (I) according to claim 1 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof, or its druggable A salt, which is a compound represented by general formula (II) or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof, or a pharmaceutically acceptable salt thereof ,

Wherein, X, Y, ring A, R 1 to R 5 , and n are as defined in claim 1.
The compound represented by the general formula (I) according to claim 1 or 2 or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof, or pharmaceutically acceptable salt, wherein,

X is selected from a bond, -(CH 2 ) m -, -(CH=CH)-, -O-(CH 2 ) t - or -S-(CH 2 ) t -;

m is an integer from 1 to 6;

t is an integer from 0 to 6;

Preferably, X is selected from a bond, -CH2- , -( CH2 ) 2- , -O-, -O-CH2-, -O-( CH2 ) 2- or -( CH =CH)-.
The compound represented by the general formula (I) according to any one of claims 1 to 3 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, wherein,

Y is -Q-(CH 2 ) v -, wherein Q is selected from
Where "*" represents the end where the Y group is connected to the aromatic ring core;

v is 0, 1 or 2;

R 7 is as defined in claim 1 .
The compound represented by the general formula (I) according to any one of claims 1 to 4 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, wherein:

Ring A is selected from aryl or heteroaryl, preferably C 6 -C 10 aryl or 5-10 membered heteroaryl, more preferably phenyl or 5-6 membered heteroaryl such as pyridyl, pyrimidinyl, pyridazinyl , triazinyl, said aryl and heteroaryl are optionally further selected from deuterium, alkyl, deuterated alkyl, haloalkyl, alkoxy, deuterated alkoxy, haloalkoxy, halogen, amino, One or more groups of hydroxyl, mercapto, nitro, cyano, oxo, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl are substituted.
The compound represented by the general formula (I) according to any one of claims 1 to 5 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, which is a compound represented by general formula (III) or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof, or a pharmaceutically acceptable salt thereof,

Wherein, A 1 , A 2 , A 3 , A 4 are each independently selected from carbon or nitrogen;

Each R is independently selected from the group consisting of hydrogen, alkyl, deuterated alkyl, haloalkyl, alkoxy, deuterated alkoxy, haloalkoxy, halogen, amino, hydroxyl, mercapto, nitro, cyano, Oxo, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl; preferably hydrogen, halogen, oxo;

s is an integer from 0 to 3;

X, Y, R 1 to R 5 , n are as defined in the preceding claims.
The compound represented by the general formula (I) according to any one of claims 1 to 6 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, which is a compound represented by general formula (IV) or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof, or a pharmaceutically acceptable salt thereof,

Wherein, A 1 , A 2 , A 3 , A 4 are each independently selected from carbon or nitrogen;

Each R is independently selected from the group consisting of hydrogen, alkyl, deuterated alkyl, haloalkyl, alkoxy, deuterated alkoxy, haloalkoxy, halogen, amino, hydroxyl, mercapto, nitro, cyano, Oxo, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl; preferably hydrogen, halogen, oxo;

s is an integer from 0 to 3;

X, R 1 to R 5 , R 7 , n are as defined in the preceding claims.
The compound represented by the general formula (I) according to any one of claims 1 to 7 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof,

Wherein, R 1 and R 2 are each independently selected from hydrogen and C 1 -C 6 alkyl, said C 1 -C 6 alkyl is optionally substituted by halogen; or R 1 and R 2 together form
preferred

n is an integer of 1 to 3.
The compound represented by the general formula (I) according to any one of claims 1 to 7 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, wherein, R 1 and R 2 form a C 3 -C 6 cycloalkyl group together with the atoms they are connected to, and the C 3 -C 6 cycloalkyl group is optionally further selected from halogen, Amino, nitro, cyano, oxo, hydroxyl, mercapto, carboxyl, ester, alkyl, hydroxyalkyl, haloalkyl, alkoxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, One or more groups of heteroaryl are substituted.
The compound represented by the general formula (I) according to any one of claims 1 to 9 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, wherein R3 and R4 are each independently selected from hydrogen or halogen, preferably hydrogen.
The compound represented by the general formula (I) according to any one of claims 1 to 10 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, wherein,

R 5 is NR 8 R 9 ; wherein R 8 and R 9 are each independently selected from hydrogen and C 1 -C 6 alkyl, preferably hydrogen.
The compound represented by the general formula (I) according to any one of claims 1 to 11 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, wherein R 7 is hydrogen or C 1 -C 6 alkyl, and the C 1 -C 6 alkyl is optionally further selected from halogen, amino, nitro, cyano, oxygen Substituent, hydroxyl, mercapto, carboxyl, ester, hydroxyalkyl, alkoxy, haloalkoxy, cycloalkyl, heterocyclyl, aryl, heteroaryl, preferably R 7 is hydrogen.
The compound represented by the general formula (I) according to any one of claims 1 to 12 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, wherein the compound is selected from:
A method for preparing a compound represented by general formula (IV) or its mesoform, racemate, enantiomer, diastereoisomer, or a mixture thereof, or a pharmaceutically acceptable salt thereof , which includes the following steps:

In the presence of a condensing agent, the compound (IV-1) undergoes an intramolecular condensation reaction to obtain a compound of the general formula (IV). The condensing agent is preferably 1-ethyl-(3-dimethylaminopropyl) carbonyl diethylene Amine hydrochloride and 1-hydroxybenzotriazole;

Wherein, A 1 , A 2 , A 3 , A 4 , R 1 , R 2 , R 3 , R 4 , R 5 , R 7 , R 10 , s and n are as defined in claim 7.
A pharmaceutical composition comprising the compound represented by the general formula (I) according to any one of claims 1 to 13 or its mesoform, racemate, enantiomer, diastereomer An enantiomer, or a mixture thereof, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
The compound represented by the general formula (I) according to any one of claims 1 to 13 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition according to claim 15 in the preparation of a tropomyosin receptor kinase (TRK) inhibitor.
The compound represented by the general formula (I) according to any one of claims 1 to 13 or its mesoform, racemate, enantiomer, diastereoisomer, or mixture thereof form, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition according to claim 15 in the preparation of a medicine for preventing or/and treating a disease associated with tropomyosin receptor kinase (TRK) activity, said disease Neurocytoma, melanoma, ovarian cancer, colorectal cancer, gastric cancer, lung cancer, breast cancer, glioblastoma, medulloblastoma, head and neck cancer, salivary gland cancer and papillary thyroid cancer are preferred.