1H-PYRAZOLO[4,3-H]QUINAZOLINE COMPOUND SERVING AS PROTEIN KINASE INHIBITOR

Abstract

A 1H-pyrazolo[4,3-H]quinazoline compound represented by formula (I) can be used for treating cell proliferation dysfunction, and is an broad-spectrum and strongly-active inhibitor for a cell cyclin-dependent kinase (CDK).

Description

FIELD OF THE INVENTION

The present disclosure provides a class of 1H-pyrazolo[4,3-H]quinazoline compounds as inhibitors of cyclin-dependent kinase (CDK), which have a broad-spectrum and strong inhibitory activity against CDK. The compounds of the present disclosure are effective in treating diseases such as cancer, inflammation, etc.

BACKGROUND OF THE INVENTION

Cancer is the second leading cause of death globally. According to the ‘Global Cancer Report 2014’ published by World Health Organization, the number of cancer patients and deaths worldwide is increasing alarmingly. Nearly half of the new cancer cases are in Asia, and most of them are in China. The report also predicts that the number of cancer cases worldwide will increase rapidly, from 14 million in 2012 to 19 million in 2025, and to 24 million by 2035, of which China will account for 21.9%. According to institutional data, in the past 30 years, cancer mortality rate in China has increased by 80%, and about 2.6 million cancer cases and 1.8 million deaths occur annually.

Cell cycle is an important part of cellular activities. Studies have shown that tumorigenesis and progression of many malignancies are closely related to the disorder of cell cycle regulation mechanism, so that tumors are considered as a kind of disease relating to cell cycle. Since the 1970s, three scientists from the United States and UK have successively discovered the important roles of cyclin-dependent kinase and cyclin in cell regulation, thus winning the 2001 Nobel Prize in Physiology/Medicine. With the great progress in the study of cell cycle regulation mechanism, especially the discovery of the core role of CDK in cell cycle regulation, cyclin-dependent kinase has become a hotspot of anticancer drug research in recent years. At present, CDK1, 2, 4, 6 and 7 are considered to be the major regulators of cell cycle.

In addition to the selective inhibitors of CDK4 and 6, pan-CDK inhibitors such as Dinaciclib (SCH-727965, MK-7965), which have inhibitory activities against CDK1, CDK2, CDK5, CDK9 and CDK12, have entered the stage of clinical trials, showing promising anticancer activities in targeted therapy for solid tumors.

More CDK inhibitors are needed to meet the clinical needs of various diseases. CDK inhibitors with higher effectiveness and selective activity show better therapeutic benefits for specific diseases (such as cancer, cardiovascular disorders, infectious diseases, autoimmune diseases, etc.) and therefore become the goal has been pursuing in the field.

SUMMARY OF THE INVENTION

The present disclosure provides a class of 1H-pyrazolo[4,3-H]quinazoline compounds as inhibitors of cyclin-dependent kinase, which have a broad-spectrum and strong inhibitory activity. The compounds of the present disclosure are effective in treating cell proliferative diseases, such as restenosis, cancer and inflammation. Compared with the existing drugs, the compounds of the present disclosure can further improve the pharmacokinetic properties, including the significant improvement in the metabolic stability and clearance rate over the existing compounds. Furthermore, the compounds of the present disclosure can be readily synthesized and can be administered to the patients by a variety of methods.

In one aspect, the present disclosure provides a compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug, or an isotope variant thereof, and mixtures thereof:

wherein:

A₁ is selected from CR₃ or N;

A₂ is selected from CR₃ or N;

A₃ is selected from CR₃ or N;

R₁ is selected from H, halogen, —CN, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl; wherein the said C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by oxo or thioxo;

R₂ is selected from H, halogen, —CN, —OR_a, —SR_a, —NR_a, —C(O)R_a, —C(O)R_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl; wherein the said C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by oxo or thioxo;

R₃ is selected from H, halogen, —CN, —NO₂, -L-OR_a, -L-SR_a, -L-NR_bR_c, -L-C(O)R_a, -L-C(O)OR_a, -L-C(O)NR_bR_c, -L-S(O)_mR_a, -L-S(O)_mOR_a, -L-S(O)_mNR_bR_c, —O—C_1-6 alkylene-R₆, C_1-6 alkyl, C_1-6 haloalkyl, -L′-C_3-7 cycloalkyl, -L′-3- to 11-membered heterocyclyl, -L′-C_6-10 aryl, or -L′-5- to 10-membered heteroaryl, each of which is optionally substituted by 1, 2, 3, 4, or 5 R₆ groups;

R₄ is selected from H, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R₅ is selected from H, halogen, —CN, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(O)O, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl; wherein the said C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by oxo or thioxo;

R₆ is selected from H, —NH₂, —NHC_1-6 alkyl, —N(C_1-6 alkyl)₂, C_1-6 alkyl, C_1-6 haloalkyl, —C_1-6 alkylene-OR_a, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl;

or two R₆ groups on the same carbon atom are taken together to form oxo or thioxo;

wherein:

R₄ is optionally substituted by 1, 2, or 3 R′ groups, wherein R′ is independently selected from H, halogen, —CN, —NO₂, —OR_a, —SR_a, —NR_bR_c, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

each of R₁-R₂ and R₅-R₆ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H, —OH, halogen, —NO₂, carbonyl, -L-CN, -L-OR_a, -L-SR_a, -L-NR_bR_c, -L-C(O)R_a, -L-C(S)R_a, -L-C(O)OR_a, -L-C(S)OR_a, -L-C(O)—NR_bR_c, -L-C(S)—NR_bR_c, -L-O—C(O)R_a, -L-O—C(S)R_a, -L-N(R_b)—C(O)—R_a, -L-N(R_b)—C(S)—R_a, -L-S(O)_mR_a, -L-S(O)_mOR_a, -L-S(O)_mNR_bR_c, -L-N(R_b)—S(O)_mR_a, -L-N(R_b)—S(O)_m—NR_bR_c, -L-N(R_b)—C(O)OR_a, -L-N(R_b)—C(S)OR_a, -L-O—C_1-6 alkylene-OR_a, -L-C(O)—C_1-6 alkylene-NR_bR_c, -L-N(R_b)—C(O)—NR_bR_c, -L-N(R_b)—C(S)—NR_bR_c, -L-O—C(O)—NR_bR_c, -L-O—C(S)—NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_2-6 alkenyl, C_2-6 alkynyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl; wherein the said C_1-6 alkyl, C_1-6 haloalkyl, C_2-6 alkenyl, C_2-6 alkynyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl is each further optionally substituted by one or more groups consisting of the following:

-L-CN, —NO₂, carbonyl, -L-OR_a, -L-SR_a, -L-NR_bR_c, -L-C(O)R_a, -L-C(S)R_a, -L-C(O)OR_a, -L-C(S)OR_a, -L-C(O)—NR_bR_c, -L-C(S)—NR_bR_c, -L-O—C(O)R_a, -L-O—C(S)R_a, -L-N(R_b)—C(O)—R_a, -L-N(R_b)—C(S)—R_a, -L-S(O)_mR_a, -L-S(O)_mOR_a, -L-S(O)_mNR_bR_c, -L-N(R_b)—S(O)_m—R_a, -L-N(R_b)—S(O)_m—R_bR_c, -L-N(R_b)—C(O)OR_a, -L-N(R_b)—C(S)OR_a, -L-O—C_1-6 alkylene-OR_a, -L-C(O)—C_1-6 alkylene-NR_bR_c, -L-N(R_b)—C(O)—NR_bR_c, -L-N(R_b)—C(S)—NR_bR_c, -L-O—C(O)—NR_bR_c, and -L-O—C(S)—NR_bR_c;

R_a is independently selected from H, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl;

R_b and R_c are independently selected from H, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl; or, R_b, R_c and N atom are taken together to form 3- to 7-membered heterocyclyl;

R_a, R_b and R_c are each further optionally substituted by one or more groups consisting of the following:

C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, and -L-5- to 10-membered heteroaryl;

L is selected from a chemical bond, —C_1-6 alkylene-, —C_2-6 alkenylene-, or —C_2-6 alkynylene-;

L′ is selected from a chemical bond, —O—, —NH—, —C(O)—, —C(O)NH—, —NHC(O)—, —C_1-6 alkylene-, —C_2-6 alkenylene-, or —C_2-6 alkynylene-; and

m represents 0, 1, or 2.

In another aspect, the present disclosure provides a pharmaceutical composition comprising a compound of the present disclosure, and optionally pharmaceutically acceptable excipients.

In another aspect, the present disclosure provides a pharmaceutical composition comprising a compound of the present disclosure and pharmaceutically acceptable excipients, which also includes other therapeutic agents.

In another aspect, the present disclosure provides a kit comprising a compound of the present disclosure, other therapeutic agents and pharmaceutically acceptable carriers, adjuvants or vehicles.

In another aspect, the present disclosure provides use of a compound of the present disclosure in the preparation of a medicament for the treatment and/or prevention of CDK-mediated diseases.

In another aspect, the present disclosure provides a method of treating and/or preventing CDK-mediated diseases in a subject, including administering a compound of the present disclosure or a composition of the present disclosure to the subject.

In another aspect, the present disclosure provides a compound or a composition of the present disclosure, for use in treating and/or preventing CDK-mediated diseases.

In a specific embodiment, the diseases described herein include cell proliferative diseases, which include but are not limited to cancers, cardiovascular disorders, infectious diseases, chronic inflammatory diseases, autoimmune disorders and other cell proliferative disorders. More specifically, the cancers described herein include, but are not limited to, solid tumors and hematological malignancies, such as breast cancer, neuroblastoma, malignant rhabdomyoma, well-differentiated and dedifferentiated liposarcoma, glioma, lung cancer, colorectal cancer, gastric cancer, gastrointestinal stromal tumors (GIST), hepatocellular carcinoma, prostatic tumors, sarcoma, ovarian cancer, cervical cancer, pancreatic cancer, melanoma, thyroid cancer, carcinoma of bile duct, endometrial cancer, renal cancer, mesothelioma, lymphoma, leukemia, non-Hodgkin's lymphoma, mantle cell lymphoma, anaplastic large cell lymphoma, acute myeloid leukemia (AML), and multiple myeloma. The cardiovascular disorders described herein include restenosis, atherosclerosis, vascular smooth muscle proliferation and intimal hyperplasia secondary to balloon angioplasty, and other vascular disorders caused by abnormal cell proliferation. The infectious diseases described herein include infections of fungi, protozoan parasites (such as Plasmodium falciparum) and DNA and RNA virus, such as herpes simplex virus (HSV) infections. The chronic inflammatory diseases described herein are such as rheumatoid arthritis. Other cell proliferative disorders described herein include psoriasis (characterized by excessive proliferation of keratinocytes), glomerulonephritis and lupus.

Other objects and advantages of the present disclosure will be apparent to those skilled in the art from the subsequent specific embodiments, examples and claims.

Definitions

Chemical Definitions

Definitions of specific functional groups and chemical terms are described in more detail hereafter.

When a range of values is listed, each value and sub-range within the range are intended to be included. For example, “C_1-6 alkyl” is intended to include C₁, C₂, C₃, C₄, C₅, C₆, C_1-6, C_1-5, C_1-4, C_1-3, C_1-2, C_2-6, C_2-5, C_2-6, C_2-3, C_3-6, C_3-5, C_3-4, C_4-6, C_4-5 and C_5-6 alkyl.

“C_1-6 alkyl” refers to a radical of a straight or branched, saturated hydrocarbon group having 1 to 6 carbon atoms. In some embodiments, C_1-4 alkyl is preferred. Examples of C_1-6 alkyl include methyl (C₁), ethyl (C₂), n-propyl (C₃), iso-propyl (C₃), n-butyl (C₄), tert-butyl (C₄), sec-butyl (C₄), iso-butyl (C₄), n-pentyl (C₅), 3-pentyl (C₅), pentyl (C₅), neopentyl (C₅), 3-methyl-2-butyl (C₅), tert-pentyl (C₅) and n-hexyl (C₆). The term “C_1-6 alkyl” also includes heteroalkyl, wherein one or more (e.g., 1, 2, 3 or 4) carbon atoms are substituted with heteroatoms (e.g., oxygen, sulfur, nitrogen, boron, silicon, phosphorus). Alkyl groups can be optionally substituted with one or more substituents, for example, with 1 to 5 substituents, 1 to 3 substituents or 1 substituent. Conventional abbreviations of alkyl include Me (—CH₃), Et (—CH₂CH₃), iPr (—CH(CH₃)₂), nPr (—CH₂CH₂CH₃), n-Bu (—CH₂CH₂CH₂CH₃) or i-Bu (—CH₂CH(CH₃)₂).

“C_2-6 alkenyl” refers to a radical of a straight or branched hydrocarbon group having 2 to 6 carbon atoms and at least one carbon-carbon double bond. In some embodiments, C_2-4 alkenyl is preferred. Examples of C_2-6 alkenyl include vinyl (C₂), 1-propenyl (C₃), 2-propenyl (C₃), 1-butenyl (C₄), 2-butenyl (C₄), butadienyl (C₄), pentenyl (C₅), pentadienyl (C₅), hexenyl (C₆), etc. The term “C_2-6 alkenyl” also includes heteroalkenyl, wherein one or more (e.g., 1, 2, 3 or 4) carbon atoms are replaced by heteroatoms (e.g., oxygen, sulfur, nitrogen, boron, silicon, phosphorus). The alkenyl groups can be optionally substituted with one or more substituents, for example, with 1 to 5 substituents, 1 to 3 substituents or 1 substituent.

“C_2-6 alkynyl” refers to a radical of a straight or branched hydrocarbon group having 2 to 6 carbon atoms, at least one carbon-carbon triple bond and optionally one or more carbon-carbon double bonds. In some embodiments, C_2-4 alkynyl is preferred. Examples of C_2-6 alkynyl include, but are not limited to, ethynyl (C₂), 1-propynyl (C₃), 2-propynyl (C₃), 1-butynyl (C₄), 2-butynyl (C₄), pentynyl (C₅), hexynyl (C₆), etc. The term “C_2-6 alkynyl” also includes heteroalkynyl, wherein one or more (e.g., 1, 2, 3 or 4) carbon atoms are replaced by heteroatoms (e.g., oxygen, sulfur, nitrogen, boron, silicon, phosphorus). The alkynyl groups can be substituted with one or more substituents, for example, with 1 to 5 substituents, 1 to 3 substituents or 1 substituent.

“—C_1-6 alkylene-, —C_2-6 alkenylene- or —C_2-6 alkynylene-” refers to a divalent group of the “C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl” as defined above.

“C_1-6 alkylene” refers to a divalent group formed by removing another hydrogen of the C_1-6 alkyl, and can be a substituted or unsubstituted alkylene. In some embodiments, C_1-4 alkylene is particularly preferred. The unsubstituted alkylene groups include, but are not limited to, methylene (—CH₂—), ethylene (—CH₂CH₂—), propylene (—CH₂CH₂CH₂—), butylene (—CH₂CH₂CH₂CH₂—), pentylene (—CH₂CH₂CH₂CH₂CH₂—), hexylene (—CH₂CH₂CH₂CH₂CH₂CH₂—), etc. Examples of substituted alkylene groups, such as those substituted with one or more alkyl (methyl) groups, include, but are not limited to, substituted methylene (—CH(CH₃)—, —C(CH₃)₂—), substituted ethylene (—CH(CH₃)CH₂—, —CH₂CH(CH₃)—, —C(CH₃)₂CH₂—, —CH₂C(CH₃)₂—), substituted propylene (—CH(CH₃)CH₂CH₂—, —CH₂CH(CH₃)CH₂—, —CH₂CH₂CH(CH₃)—, —C(CH₃)₂CH₂CH₂—, —CH₂C(CH₃)₂CH₂—, —CH₂CH₂C(CH₃)₂—), etc.

“C_2-6 alkenylene” refers to a C_2-6 alkenyl group wherein another hydrogen is removed to provide a divalent radical of alkenylene, and which may be substituted or unsubstituted alkenylene. In some embodiments, C_2-4 alkenylene is particularly preferred. Exemplary unsubstituted alkenylene groups include, but are not limited to, ethenylene (—CH═CH—) and propenylene (e.g., —CH═CHCH₂—, —CH₂—CH═CH—). Exemplary substituted alkenylene groups, e.g., substituted with one or more alkyl (methyl) groups, include but are not limited to, substituted ethylene (—C(CH₃)═CH—, —CH═C(CH₃)—), substituted propylene (e.g., —C(CH₃)═CHCH₂—, —CH═C(CH₃)CH₂—, —CH═CHCH(CH₃)—, —CH═CHC(CH₃)₂—, —CH(CH₃)—CH═CH—, —C(CH₃)₂—CH═CH—, —CH₂—C(CH₃)═CH—, —CH₂—CH═C(CH₃)—), and the like.

“C_2-6 alkynylene” refers to a C_2-6 alkynyl group wherein another hydrogen is removed to provide a divalent radical of alkynylene, and which may be substituted or unsubstituted alkynylene. In some embodiments, C_2-4 alkynylene is particularly preferred. Exemplary alkynylene groups include, but are not limited to, ethynylene (—C≡C—), substituted or unsubstituted propynylene (—C≡CCH₂—), and the like.

“Halo” or “halogen” refers to fluorine (F), chlorine (Cl), bromine (Br) and iodine (I).

“C_1-6 haloalkyl” represents the “C_1-6 alkyl” described above, which is substituted with one or more halogen groups. Examples include the mono-, di-, poly-halogenated, including perhalogenated, alkyl. A monohalogen substituent may have one iodine, bromine, chlorine or fluorine atom in the group; a dihalogen substituent and a polyhalogen substituent may have two or more identical halogen atoms or a combination of different halogens. Examples of preferred haloalkyl groups include monofluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, pentafluoroethyl, heptafluoropropyl, difluorochloromethyl, dichlorofluoromethyl, difluoroethyl, difluoropropyl, dichloroethyl and dichloropropyl. The haloalkyl groups can be substituted at any available point of attachment, for example, with 1 to 5 substituents, 1 to 3 substituents or 1 substituent.

“C_3-7 cycloalkyl” refers to a radical of non-aromatic cyclic hydrocarbon group having 3 to 7 ring carbon atoms and zero heteroatoms. In some embodiments, C_3-6 cycloalkyl is particularly preferred, and C₅₄ cycloalkyl is more preferred. The cycloalkyl also includes a ring system in which the cycloalkyl described herein is fused with one or more aryl or heteroaryl groups, wherein the point of attachment is on the cycloalkyl ring, and in such case, the number of carbon atoms continues to represent the number of carbon atoms in the cycloalkyl system. Exemplary cycloalkyl groups include, but are not limited to, cyclopropyl (C₃), cyclopropenyl (C₃), cyclobutyl (C₄), cyclobutenyl (C₄), cyclopentyl (C₅), cyclopentenyl (C₅), cyclohexyl (C₆), cyclohexenyl (C₆), cyclohexadienyl (C₆), cycloheptyl (C₇), cycloheptenyl (C₇), cycloheptadienyl (C₇), cycloheptatrienyl (C₇), etc. The cycloalkyl can be substituted with one or more substituents, for example, with 1 to 5 substituents, 1 to 3 substituents or 1 substituent.

“3- to 11-membered heterocyclyl” refers to a radical of 3- to 11-membered non-aromatic ring system having ring carbon atoms and 1 to 5 ring heteroatoms, wherein each of the heteroatoms is independently selected from nitrogen, oxygen, sulfur, boron, phosphorus and silicon. In the heterocyclyl containing one or more nitrogen atoms, the point of attachment can be a carbon or nitrogen atom as long as the valence permits. In some embodiments, 3- to 9-membered heterocyclyl is preferred, which is a radical of 3- to 9-membered non-aromatic ring system having ring carbon atoms and 1 to 5 ring heteroatoms. In some embodiments, 3- to 7-membered heterocyclyl is preferred, which is a radical of 3- to 7-membered non-aromatic ring system having ring carbon atoms and 1 to 4 ring heteroatoms. 3- to 6-membered heterocyclyl is preferred, which is a radical of 3- to 6-membered non-aromatic ring system having ring carbon atoms and 1 to 3 ring heteroatoms. 4- to 6-membered heterocyclyl is preferred, which is a radical of 4- to 6-membered non-aromatic ring system having ring carbon atoms and 1 to 3 ring heteroatoms. 5- to 6-membered heterocyclyl is more preferred, which is a radical of 5- to 6-membered non-aromatic ring system having ring carbon atoms and 1 to 3 ring heteroatoms. The heterocyclyl also includes a ring system wherein the heterocyclyl described above is fused with one or more cycloalkyl groups, wherein the point of attachment is on the cycloalkyl ring, or the heterocyclyl described above is fused with one or more aryl or heteroaryl groups, wherein the point of attachment is on the heterocyclyl ring; and in such cases, the number of ring members continues to represent the number of ring members in the heterocyclyl ring system. Exemplary 3-membered heterocyclyl groups containing one heteroatom include, but are not limited to, aziridinyl, oxiranyl and thiorenyl. Exemplary 4-membered heterocyclyl groups containing one heteroatom include, but are not limited to, azetidinyl, oxetanyl and thietanyl. Exemplary 5-membered heterocyclyl groups containing one heteroatom include, but are not limited to, tetrahydrofuranyl, dihydrofuranyl, tetrahydrothiophenyl, dihydrothienyl, pyrrolidinyl, dihydropyrrolyl and pyrrolyl-2,5-dione. Exemplary 5-membered heterocyclyl groups containing two heteroatoms include, but are not limited to, dioxolanyl, oxasulfuranyl, disulfuranyl, and oxazolidin-2-one. Exemplary 5-membered heterocyclyl groups containing three heteroatoms include, but are not limited to, triazolinyl, oxadiazolinyl, and thiadiazolinyl. Exemplary 6-membered heterocyclyl groups containing one heteroatom include, but are not limited to, piperidyl, tetrahydropyranyl, dihydropyridyl and thianyl. Exemplary 6-membered heterocyclyl groups containing two heteroatoms include, but are not limited to, piperazinyl, morpholinyl, dithianyl and dioxanyl. Exemplary 6-membered heterocyclyl groups containing three heteroatoms include, but are not limited to, triazinanyl. Exemplary 7-membered heterocycly groups containing one heteroatom include, but are not limited to, azepanyl, oxepanyl and thiepanyl. Exemplary 5-membered heterocyclyl groups fused with a C₆ aryl (also referred as 5,6-bicyclic heterocyclyl herein) include, but are not limited to, indolinyl, isoindolinyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, benzoxazolinonyl, etc. Exemplary 6-membered heterocyclyl groups fused with a C₆ aryl (also referred as 6,6-bicyclic heterocyclyl herein) include, but are not limited to, tetrahydroquinolinyl, tetrahydroisoquinolinyl, etc. The heterocyclyl can be substituted with one or more substituents, for example, with 1 to 5 substituents, 1 to 3 substituents or 1 substituent.

The 3- to 11-membered heterocyclyl also includes spiroheterocyclyl, that is, a group in which two rings (e.g., a heterocycle and a carbocycle) share a carbon atom, wherein at least one of the rings is a heterocyclyl as defined above. More specifically, the spiroheterocyclyl is a spiro ring formed by two 4-membered rings, two 5-membered rings, two 6-membered rings, one 4-membered ring and one 5-membered ring, one 4-membered ring and one 6-membered ring, or one 5-membered ring and one 6-membered ring, wherein at least one of the rings is a 4- to 6-membered heterocyclyl as defined above. The 4- to 6-membered heterocyclyl containing 1, 2 or 3 O, N or S heteroatoms is preferred. The 4- to 6-membered heterocyclyl containing 1 N heteroatom is more preferred. Specific spiroheterocyclyl groups include, but are not limited to:

Specific examples of preferred heterocyclyl groups include, pyrrolinyl, imidazolidinyl, pyrazolidinyl, tetrahydropyranyl, dihydropyranyl, dihydrofuranyl, thiazolidinyl, dihydrothiazolyl, 2,3-dihydro-benzo[1,4]dioxol, indolinyl, isoindolinyl, dihydrobenzothiophene, dihydrobenzofuranyl, isodihydrobenzopyranyl, dihydrobenzopyranyl, 1,2-dihydroisoquinoline, 1,2,3,4-tetrahydroisoquinoline, 1,2,3,4-tetrahydroquinoline, 2,3,4,4a,9,9a-hexahydro-1H-3-azafluorene, 5,6,7-trihydro-1,2,4-triazolo[3,4-a]isoquinolyl, 3,4-dihydro-2H-benzo[1,4]oxazinyl, benzo[1,4]dioxol, 2,3-dihydro-lH-lk′-benzo[d]isothiazol-6-yl, 2,3-di-benzo[1,4]dioxinyl, dihydrobenzofuran, 2-oxoaziridin-1-yl, 2-oxoazetidin-1-yl, 2-oxopyrrolidin-1-yl, 2-oxopiperidin-1-yl, 2-oxoazepan-1-yl, 2-oxoazocan-1-yl, 2-oxoazonan-1-yl, 2-oxoazecan-1-yl, aziridine, azetidine, pyrrolidinyl, piperidine, azepane, azocane, azonane, azecane, piperidyl, piperazinyl, morpholinyl, diazaspiro[3.3]heptane, diazaspiro[3.4]octane, diazaspiro[3.5]nonane, diazaspiro[4.4]nonane, diazaspiro[4.5]decane, and diazaspiro[5.5]undecane.

“C_6-10 aryl” refers to a radical of monocyclic or polycyclic (e.g., bicyclic) 4n+2 aromatic ring system having 6-10 ring carbon atoms and zero heteroatoms (e.g., having 6 or 10 shared π electrons in a cyclic array). In some embodiments, the aryl group has six ring carbon atoms (“C₆ aryl”; for example, phenyl). In some embodiments, the aryl group has ten ring carbon atoms (“C₁₀ aryl”; for example, naphthyl, e.g., 1-naphthyl and 2-naphthyl). The aryl group also includes a ring system in which the aryl ring described above is fused with one or more cycloalkyl or heterocyclyl groups, and the point of attachment is on the aryl ring, in which case the number of carbon atoms continues to represent the number of carbon atoms in the aryl ring system. The aryl can be substituted with one or more substituents, for example, with 1 to 5 substituents, 1 to 3 substituents or 1 substituent.

“5- to 10-membered heteroaryl” refers to a radical of 5- to 10-membered monocyclic or bicyclic 4n+2 aromatic ring system (e.g., having 6 or 10 shared π electrons in a cyclic array) having ring carbon atoms and 1-4 ring heteroatoms, wherein each heteroatom is independently selected from nitrogen, oxygen and sulfur. In the heteroaryl group containing one or more nitrogen atoms, the point of attachment can be a carbon or nitrogen atom as long as the valence permits. Heteroaryl bicyclic systems may include one or more heteroatoms in one or two rings. Heteroaryl also includes ring systems wherein the heteroaryl ring described above is fused with one or more cycloalkyl or heterocyclyl groups, and the point of attachment is on the heteroaryl ring. In such case, the number the carbon atoms continues to represent the number of carbon atoms in the heteroaryl ring system. In some embodiments, 5- to 6-membered heteroaryl groups are particularly preferred, which are radicals of 5- to 6-membered monocyclic or bicyclic 4n+2 aromatic ring systems having ring carbon atoms and 1-4 ring heteroatoms. Exemplary 5-membered heteroaryl groups containing one heteroatom include, but are not limited to, pyrrolyl, furyl and thienyl. Exemplary 5-membered heteroaryl groups containing two heteroatoms include, but are not limited to, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, and isothiazolyl. Exemplary 5-membered heteroaryl groups containing three heteroatoms include, but are not limited to, triazolyl, oxadiazolyl (such as, 1,2,4-oxadiazoly), and thiadiazolyl. Exemplary 5-membered heteroaryl groups containing four heteroatoms include, but are not limited to, tetrazolyl. Exemplary 6-membered heteroaryl groups containing one heteroatom include, but are not limited to, pyridyl. Exemplary 6-membered heteroaryl groups containing two heteroatoms include, but are not limited to, pyridazinyl, pyrimidinyl, and pyrazinyl. Exemplary 6-membered heteroaryl groups containing three or four heteroatoms include, but are not limited to, triazinyl and tetrazinyl, respectively. Exemplary 7-membered heteroaryl groups containing one heteroatom include, but are not limited to, azepinyl, oxepinyl, and thiepinyl. Exemplary 5,6-bicyclic heteroaryl groups include, but are not limited to, indolyl, isoindolyl, indazolyl, benzotriazolyl, benzothiophenyl, isobenzothiophenyl, benzofuranyl, benzoisofuranyl, benzimidazolyl, benzoxazolyl, benzoisoxazolyl, benzoxadiazolyl, benzothiazolyl, benzoisothiazolyl, benzothiadiazolyl, indolizinyl and purinyl. Exemplary 6,6-bicyclic heteroaryl groups include, but are not limited to, naphthyridinyl, pteridinyl, quinolyl, isoquinolyl, cinnolinyl, quinoxalinyl, phthalazinyl and quinazolinyl. The heteroaryl can be substituted with one or more substituents, for example, with 1 to 5 substituents, 1 to 3 substituents or 1 substituent.

Specific examples of preferred heteroaryl groups include: pyrrolyl, imidazolyl, pyrazolyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazolyl (4H-1,2,4-triazolyl, 1H-1,2,3-triazolyl, 2H-1,2,3-triazolyl, pyranyl, 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, oxazolyl, isoxazolyl, oxazolyl (1,2,4-oxazolyl, 1,3,4-oxazolyl, 1,2,5-oxazolyl, thiazolyl, thiadiazolyl (1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl).

“carbonyl”, whether used alone or in conjunction with other terms (e.g., aminocarbonyl), is represented by —C(O)—.

“Oxo” represents ═O.

“Thioxo” represents ═S.

Alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl as defined herein are optionally substituted groups.

Exemplary substituents on carbon atoms include, but are not limited to, halogen, —CN, —NO₂, —N₃, —SO₂H, —SO₃H, —OH, —OR^aa, —ON(R^bb)₂, —N(R^bb)₂, —N(R^bb)₃⁺X⁻, —N(OR^cc)R^bb, —SH, —SR^aa, —SSR^cc—, —C(═O)R^aa, —CO₂H, —CHO, —C(OR^cc)₂, —CO₂R^aa, —OC(═O)R^aa, —OCO₂R^aa, —C(═O)N(R^bb)₂, —OC(═O)N(R^bb)₂, —NR^bbC(═O)R^aa, —NR^bbCO₂R^aa, —NR^bbC(═O)N(R^aa)₂, —C(═NR^bb)R^aa, —C(═NR^bb)OR^aa, —OC(═NR^bb)R^aa, —OC(═NR^bb)OR^aa, —C(═NR^bb)N(R^bb)₂, —OC(═NR^bb)N(R^bb)₂, —NR^bbC(═NR^bb)N(R^bb)₂, —C(═O)NR^bbSO₂R^aa, —NR^bbSO₂R^aa, —SO₂N(R^bb)₂, —SO₂R^aa, —SO₂OR^aa, —OSO₂R^aa, —S(═O)R^aa, —OS(═O)R^aa, —Si(R^aa)₃, —OSi(R^aa)₃, —C(═S)N(R^bb)₂, —C(═O)SR^aa, —C(═S)SR^aa, —SC(═S)SR^aa, —SC(═O)SR^aa, —OC(═O)SR^aa, —SC(═O)OR^aa, —SC(═O)R^aa, —P(═O)₂R^aa, —OP(═O)₂R^aa, —P(═O)(R^aa)₂, —OP(═O)(R^aa)₂, —OP(═O)(OR^aa)₂, —P(═O)₂N(R^bb)₂, —OP(═O)₂N(R^aa)₂, —P(═O)(NR^bb)₂, —OP(═O)(NR^bb)₂, —NR^bbP(═O)(OR^cc)₂, —NR^bbP(═O)(NR^bb)₂, —P(R^aa)₂, —P(R^aa)₃, —OP(R^aa)₂, —OP(R^aa)₃, —B(R^aa)₂, —B(OR^aa)₂, —BR^aa(OR^aa), alkyl, haloalkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl, wherein each of the alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl is independently substituted with 0, 1, 2, 3, 4 or 5 R^dd groups;

or two geminal hydrogen on a carbon atom are replaced with ═O, ═S, ═NN(R^bb)₂, ═NNR^bbC(═O)R^aa, ═NNR^bbC(═O)OR^aa, ═NNR^bbS(═O)₂R^aa, ═NR^bb or ═NOR^cc groups;

each of the R^aa is independently selected from alkyl, haloalkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl, or two of the R^aa groups are combined to form a heterocyclyl or heteroaryl ring, wherein each of the alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl is independently substituted with 0, 1, 2, 3, 4 or 5 R^d groups;

each of the R^bb is independently selected from hydrogen, —OH, —OR^aa, —N(R^cc)₂, —CN, —C(═O)R^aa, —C(═O)N(R^cc)₂, —CO₂R^aa, —SO₂R^aa, —C(═NR^cc)OR^aa, —C(═NR^cc)N(R^cc)₂, —SO₂N(R^cc)₂, —SO₂R^cc, —SO₂OR^cc, —SOR^aa, —C(═S)N(R^cc)₂, —C(═O)SR^cc, —C(═S)SR^cc, —P(═O)₂R^aa, —P(═O)(R^aa)₂, —P(═O)₂N(R^cc)₂, —P(═O)(NR^cc)₂, alkyl, haloalkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl, or two R^bb groups are combined to form a heterocyclyl or a heteroaryl ring, wherein each of the alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl is independently substituted with 0, 1, 2, 3, 4 or 5 R^dd groups;

each of the R^cc is independently selected from hydrogen, alkyl, haloalkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl, or two R^cc groups are combined to form a heterocyclyl or a heteroaryl ring, wherein each of the alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl is independently substituted with 0, 1, 2, 3, 4 or 5 R^dd groups;

each of the R^dd is independently selected from halogen, —CN, —NO₂, —N₃, —SO₂H, —SO₃H, —OH, —OR^ee—, —ON(R^ff)₂, —N(R^ff)₂, —N(R^ff)₃⁺X⁻, —N(OR^ee)R^ff, —SH, —SR^ee, —SSR^ee, —C(═O)R^ee, —CO₂H, —CO₂R^ee, —OC(═O)R^ee, —OCO₂R^ee, —C(═O)N(R^ff)₂, —OC(═O)N(R^ff)₂, —NR^ffC(═O)R^ee, —NR^ffCO₂R^ee, —NR^ffC(═O)N(R^ff)₂, —C(═NR^ff)OR^ee, —OC(═NR^ff)R^ee, —OC(═NR^ff)OR^ee, —C(═NR^ff)N(R^ff)₂, —OC(═NR^ff)N(R^ff)₂, —NR^ffC(═NR^ff)N(R^ff)₂, —NR^ffSO₂R^ee, —SO₂N(R^ff)₂, —SO₂R^ee, —SO₂OR^ee, —OSO₂R^ee, —S(═O)R^ee, —Si(R^ee)₃, —OSi(R^ee)₃, —C(═S)N(R^ff)₂, —C(═O)SR^ee, —C(═S)SR^ee, —SC(═S)SR^ee, —P(═O)₂R^ee, —P(═O)(R^ee)₂, —OP(═O)(R^ee)₂, —OP(═O)(OR^ee)₂, alkyl, haloalkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, wherein each of the alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl is independently substituted with 0, 1, 2, 3, 4 or 5 R^gg groups, or two geminal R^dd substituents can be combined to form ═O or ═S;

each of the R^ee is independently selected from alkyl, haloalkyl, alkenyl, alkynyl, carbocyclyl, aryl, heterocyclyl, and heteroaryl, wherein each of the alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl is independently substituted with 0, 1, 2, 3, 4 or 5 R^gg groups;

each of the R^ff is independently selected from hydrogen, alkyl, haloalkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl, or two R^ff groups are combined to form a heterocyclyl or a heteroaryl ring, wherein each of the alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl is independently substituted with 0, 1, 2, 3, 4 or 5 R^gg groups;

each of the R^gg is independently selected from halogen, —CN, —NO₂, —N₃, —SO₂H, —SO₃H, —OH, —OC_1-6 alkyl, —ON(C_1-6 alkyl)₂, —N(C_1-6 alkyl)₂, —N(C_1-6 alkyl)₃⁺X⁻, —NH(C_1-6 alkyl)₂⁺X⁻, —NH₂(C_1-6 alkyl)⁺X⁻, —NH₃⁺X⁻, —N(OC_1-6 alkyl(C_1-6 alkyl), —N(OH)(C_1-6 alkyl), —NH(OH), —SH, —SC_1-6 alkyl, —SS(C_1-6 alkyl), —C(═O)(C_1-6 alkyl), —CO₂H, —CO₂(C_1-6 alkyl), —OC(═O)(C_1-6 alkyl), —OCO₂(C_1-6 alkyl), —C(═O)NH₂, —C(═O)N(C_1-6 alkyl)₂, —OC(═O)NH(C_1-6 alkyl), —NHC(═O)(C_1-6 alkyl), —N(C_1-6 alkyl)C(═O)(C_1-6 alkyl), —NHCO₂(C_1-6 alkyl), —NHC(═O)N(C_1-6 alkyl)₂, —NHC(═O)NH(C_1-6 alkyl), —NHC(═O)NH₂, —C(═NH)O(C_1-6 alkyl), —OC(═NH)(C_1-6 alkyl), —OC(═NH)OC_1-6 alkyl, —C(═NH)N(C_1-6 alkyl)₂, —C(═NH)NH(C_1-6 alkyl), —C(═NH)NH₂, —OC(═NH)N(C_1-6 alkyl)₂, —OC(NH)NH(C_1-6 alkyl), —OC(NH)NH₂, —NHC(NH)N(C_1-6 alkyl)₂, —NHC(═NH)NH₂, —NHSO₂(C_1-6 alkyl), —SO₂N(C_1-6 alkyl)₂, —SO₂NH(C_1-6 alkyl), —SO₂NH₂, —SO₂C_1-6 alkyl, —SO₂OC_1-6 alkyl, —OSO₂C_1-6 alkyl, —SOC_1-6 alkyl, —Si(C_1-6 alkyl)₃, —OSi(C_1-6 alkyl)₃, —C(═S)N(C_1-6 alkyl)₂, C(═S)NH(C_1-6 alkyl), C(═S)NH₂, —C(═O)S(C_1-6 alkyl), —C(═S)SC_1-6 alkyl, —SC(═S)SC_1-6 alkyl, —P(═O)₂(C_1-6 alkyl), —P(═O)(C_1-6 alkyl)₂, —OP(═O)(C_1-6alkyl)₂, —OP(═O)(OC_1-6 alkyl)₂, C_1-6alkyl, C_1-6 haloalkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₇ carbocyclyl, C₆-C₁₀ aryl, C₃-C₇ heterocyclyl, C₅-C₁₀ heteroaryl; or two geminal R^gg substituents may combine to form ═O or ═S; wherein X⁻ is a counter-ion.

Exemplary substituents on nitrogen atoms include, but are not limited to, hydrogen, —OH, —OR^aa, —N(R^cc)₂, —CN, —C(═O)R^aa, —C(═O)N(R^cc)₂, —CO₂R^aa, —SO₂R^aa, —C(═NR^bb)R^aa, —C(═NR^cc)OR^aa, —C(═NR^cc)N(R^cc)₂, —SO₂N(R^cc)₂, —SO₂R^cc, —SO₂OR_a, —SOR^aa, —C(═S)N(R^cc)₂, —C(═O)SR^cc, —C(═S)SR^cc, —P(═O)₂R^aa, —P(═O)(R^aa)₂, —P(═O)₂N(R^cc)₂, —P(═O)(NR^cc)₂, alkyl, haloalkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl, or two R^cc groups attached to a nitrogen atom combine to form a heterocyclyl or a heteroaryl ring, wherein each of the alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl is independently substituted with 0, 1, 2, 3, 4 or 5 R^dd groups, and wherein R^aa, R^bb, R^cc and R^dd are as described herein.

Other Definitions

The term “cancer” includes, but is not limited to, the following cancers: breast, ovary, cervix, prostate, testis, esophagus, stomach, skin, lung, bone, colon, pancreas, thyroid, biliary tract, buccal cavity and pharynx (mouth), lips, tongue, oral cavity, pharynx, small intestine, colorectal, large intestine, rectum, cancer of brain and central nervous system, glioblastoma, neuroblastoma, keratoacanthoma, epidermoid carcinoma, large cell carcinoma, adenocarcinoma, adenoma, follicular carcinoma, undifferentiated carcinoma, papillary carcinoma, seminoma, melanoma, sarcoma, bladder cancer, liver cancer, kidney cancer, bone marrow disorder, lymphatic disorder, Hodgkin's disease, hairy cell carcinoma and leukemia.

The term “treating” as used herein relates to reversing, alleviating or inhibiting the progression or prevention of the disorders or conditions to which the term applies, or of one or more symptoms of such disorders or conditions. The noun “treatment” as used herein relates to the action of treating, which is a verb, and the latter is as just defined.

The term “pharmaceutically acceptable salt” as used herein refers to those carboxylate and amino acid addition salts of the compounds of the present disclosure, which are suitable for the contact with patients' tissues within a reliable medical judgment, and do not produce inappropriate toxicity, irritation, allergy, etc. They are commensurate with a reasonable benefit/risk ratio, and are effective for their intended use. The term includes, if possible, the zwitterionic form of the compounds of the disclosure.

The term “salt” refers to a relatively non-toxic addition salt of inorganic and organic acids to the compounds of the present disclosure. These salts can be prepared in situ during the final separation and purification of the compounds, or by isolating salts produced by separately reacting the purified compound in the free base form with a suitable organic or inorganic acid. As long as the compounds of the present disclosure are basic compounds, they are capable of forming a plurality of different salts with various inorganic and organic acids. Although such salts must be pharmaceutically acceptable for animal administration, it is often necessary in practice that the pharmaceutically unacceptable salts of the basic compounds are first isolated from the reaction mixture, and then they are simply treated with an alkaline agent to convert to the free base compound, followed by the conversion of the free base to pharmaceutically acceptable acid addition salts. The acid addition salts of the basic compounds are prepared by contacting the free base form with a sufficient amount of the acid required in a conventional manner to form the salts. The free base can be regenerated by contacting the salt form with the base in a conventional manner and then isolating the free base. The free base forms are somewhat different from their respective salt forms in some physical properties, such as solubility in polar solvents. But for the purposes of the present disclosure, the salts are still equivalent to their respective free bases.

The pharmaceutically acceptable base addition salts are formed with metals or amines, such as alkali metal and alkaline earth metal hydroxides or organic amines. Examples of the metals used as cations include sodium, potassium, magnesium, calcium, etc. Examples of suitable amines are N,N′-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, ethylenediamine, N-methylglucamine and procaine.

The base addition salt of the acidic compound can be prepared by contacting the free acid form with a sufficient amount of the required base to form a salt in a conventional manner. The free acid can be regenerated by contacting the salt form with an acid in a conventional manner and then isolating the free acid. The free acid forms are somewhat different from their respective salt forms in their physical properties, such as solubility in polar solvents. But for the purposes of the present disclosure, the salts are still equivalent to their respective free acids.

The salts can be prepared from the inorganic acids, which include sulfates, pyrosulfates, bisulfates, sulfites, bisulfites, nitrates, phosphates, monohydrogen phosphates, dihydrogen phosphates, metaphosphates, pyrophosphates, chlorides, bromides and iodides. Examples of the acids include hydrochloric acid, nitric acid, sulfuric acid, hydrobromic acid, hydroiodic acid, phosphoric acid, etc. The representative salts include hydrobromide, hydrochloride, sulfate, bisulfate, nitrate, acetate, oxalate, valerate, oleate, palmitate, stearate, laurate, borate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, naphthalate, methanesulfonate, glucoheptanate, lactobionate, lauryl sulfonate, isethionate, etc. The salts can also be prepared from the organic acids, which include aliphatic monocarboxylic and dicarboxylic acids, phenyl-substituted alkanoic acids, hydroxyalkanoic acids, alkanedioic acid, aromatic acids, aliphatic and aromatic sulfonic acids, etc. The representative salts include acetate, propionate, octanoate, isobutyrate, oxalate, malonate, succinate, suberate, sebacate, fumarate, maleate, mandelate, benzoate, chlorobenzoate, methyl benzoate, dinitrobenzoate, naphthoate, besylate, tosylate, phenylacetate, citrate, lactate, maleate, tartrate, methanesulfonate, etc. The pharmaceutically acceptable salts can include cations based on alkali metals and alkaline earth metals, such as sodium, lithium, potassium, calcium, magnesium, etc., as well as non-toxic ammonium, quaternary ammonium, and amine cations including, but not limited to, ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, ethylamine, etc. Salts of amino acids are also included, such as arginine salts, gluconates, galacturonates, etc. (for example, see Berge S. M. et al., “Pharmaceutical Salts,” J. Pharm. Sci., 1977; 66: 1-19 for reference).

Examples of pharmaceutically acceptable non-toxic amides of the compounds of the disclosure include C₁-C₆ alkyl esters, wherein the alkyl group is straight or branched. Acceptable esters also include C₅-C₇ cycloalkyl esters as well as arylalkyl esters, such as, but not limited to, benzyl esters. C₁-C₄ alkyl esters are preferred. Esters of the compounds of the disclosure can be prepared according to the conventional methods, for example, March's Advanced Organic Chemistry, 5 Edition, M. B. Smith & J. March, John Wiley & Sons, 2001.

Examples of pharmaceutically acceptable non-toxic amides of the compounds of the disclosure include amides derived from ammonia, primary C₁-C₆ alkylamines and secondary C₁-C₆ dialkylamines, wherein the alkyl group is straight or branched. In the case of the secondary amine, the amine may also be in the form of a 5- or 6-membered heterocycle containing one nitrogen atom. Amides derived from ammonia, C₁-C₃ alkyl primary amine and C₁-C₂ dialkyl secondary amine are preferred. Amides of the compounds of the present disclosure can be prepared according to the conventional methods, for example, March's Advanced Organic Chemistry, 5 Edition, M. B. Smith & J. March, John Wiley & Sons, 2001.

The term “prodrug” refers to a compound that is rapidly converted in vivo to give the parent compound of the above formula, for example, by means of hydrolysis in the blood. For a detailed discussion, see T. Higuchi and V. Stella, “Pro-drugs as Novel Delivery Systems,” Vol. 14 of the A. C. S. Symposium Series and Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987, both of which were introduced herein as references.

“Subjects” to which administration is contemplated include, but are not limited to, humans (e.g., males or females of any age group, e.g., paediatric subjects (e.g., infants, children, adolescents) or adult subjects (e.g., young adults, middle-aged adults or older adults) and/or non-human animals, such as mammals, e.g., primates (e.g., cynomolgus monkeys, rhesus monkeys), cattle, pigs, horses, sheep, goats, rodents, cats and/or dogs. In some embodiments, the subject is a human. In some embodiments, the subject is a non-human animal. The terms “humam”, “patient” and “subject” can be used interchangeably herein.

“Disease,” “disorder,” and “condition” can be used interchangeably herein.

Unless indicated, otherwise the term “treatment” as used herein includes the effect on a subject who is suffering from a particular disease, disorder, or condition, which reduces the severity of the disease, disorder, or condition, or delays or slows the progression of the disease, disorder or condition (“therapeutic treatment”). The term also includes the effect that occurs before the subject begins to suffer from a specific disease, disorder or condition (“prophylactic treatment”).

Generally, the “effective amount” of a compound refers to an amount sufficient to elicit a target biological response. As understood by those skilled in the art, the effective amount of the compound of the disclosure can vary depending on the following factors, such as the desired biological endpoint, the pharmacokinetics of the compound, the diseases being treated, the mode of administration, and the age, health status and symptoms of the subjects. The effective amount includes therapeutically effective amount and prophylactically effective amount.

Unless indicated, otherwise the “therapeutically effective amount” of the compound as used herein is an amount sufficient to provide therapeutic benefits in the course of treating a disease, disorder or condition, or to delay or minimize one or more symptoms associated with the disease, disorder or condition. The therapeutically effective amount of a compound refers to the amount of the therapeutic agent that, when used alone or in combination with other therapies, provides a therapeutic benefit in the treatment of a disease, disorder or condition. The term “therapeutically effective amount” can include an amount that improves the overall treatment, reduces or avoids the symptoms or causes of the disease or condition, or enhances the therapeutic effect of other therapeutic agents.

Unless indicated, otherwise the “prophylactically effective amount” of the compound as used herein is an amount sufficient to prevent a disease, disorder or condition, or an amount sufficient to prevent one or more symptoms associated with a disease, disorder or condition, or an amount sufficient to prevent the recurrence of a disease, disorder or condition. The prophylactically effective amount of a compound refers to the amount of a therapeutic agent that, when used alone or in combination with other agents, provides a prophylactic benefit in the prevention of a disease, disorder or condition. The term “prophylactically effective amount” can include an amount that improves the overall prevention, or an amount that enhances the prophylactic effect of other preventive agents.

“Combination” and related terms refer to the simultaneous or sequential administration of the compounds of the present disclosure and other therapeutic agents. For example, the compounds of the present disclosure can be administered simultaneously or sequentially in separate unit dosage with other therapeutic agents, or simultaneously in a single unit dosage with other therapeutic agents.

DETAILED DESCRIPTION OF THE INVENTION

As used herein, “compounds of the present disclosure” refer to the compounds of formula (I) or formula (II) below, or pharmaceutically acceptable salts, enantiomers, diastereomers, racemates, solvates, hydrates, polymorphs, prodrugs or isotope variants thereof, and mixtures thereof.

Compounds are generally described herein using standard nomenclature. It should be understood, unless otherwise specified, that compounds with asymmetric center(s) include all optical isomers and mixtures thereof. Furthermore, unless otherwise specified, all isomer compounds and carbon-carbon double bonds included in the present disclosure may be in the form of Z and E. Compounds which exist in different tautomeric forms, one of which is not limited to any particular tautomer, but is intended to cover all tautomeric forms. The general formulas are used for certain compounds, including descriptions and variables. Unless otherwise specified, each variable in such formula is defined independently of any other variable and multiple variables that independently define any one of the variables at each occurrence.

In one embodiment, the present disclosure refers to a compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug, or an isotope variant thereof, and mixtures thereof:

wherein:

A₁ is selected from CR₃ or N;

A₂ is selected from CR₃ or N;

A₃ is selected from CR₃ or N;

R₁ is selected from H, halogen, —CN, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl; wherein the said C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by oxo or thioxo;

R₂ is selected from H, halogen, —CN, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(O)OR_a, —C(O)NR_a, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl; wherein the said C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by oxo or thioxo;

R₃ is selected from H, halogen, —CN, —NO₂, -L-OR_a, -L-SR_a, -L-NR_bR_c, -L-C(O)R_a, -L-C(O)OR_a, -L-C(O)NR_bR_c, -L-S(O)_mR_a, -L-S(O)_mOR_a, -L-S(O)_mNR_bR_c, —O—C_1-6 alkylene-R₆, C_1-6 alkyl, C_1-6 haloalkyl, -L′-C_3-7 cycloalkyl, -L′-3- to 11-membered heterocyclyl, -L′-C_6-10 aryl, or -L′-5- to 10-membered heteroaryl, each of which is optionally substituted by 1, 2, 3, 4, or 5 R₆ groups;

R₄ is selected from H, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R₅ is selected from H, halogen, —CN, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl; wherein the said C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by oxo or thioxo;

R₆ is selected from H, —NH₂, —NHC_1-6 alkyl, —N(C_1-6 alkyl)₂, C_1-6 alkyl, C_1-6 haloalkyl, —C_1-6 alkylene-OR_a, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl;

or two R₆ groups on the same carbon atom are taken together to form oxo or thioxo;

wherein:

R₄ is optionally substituted by 1, 2, or 3 R′ groups, wherein R′ is independently selected from H, halogen, —CN, —NO₂, —OR_a, —SR_a, —NR_bR_c, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

each of R₁-R₂ and R₅-R₆ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H, —OH, halogen, —NO₂, carbonyl, -L-CN, -L-OR_a, -L-SR_a, -L-NR_bR_c, -L-C(O)R_a, -L-C(S)R_a, -L-C(O)OR_a, -L-C(S)OR_a, -L-C(O)—NR_bR_c, -L-C(S)—NR_bR_c, -L-O—C(O)R_a, -L-O—C(S)R_a, -L-N(R_b)—C(O)—R_a, -L-N(R_b)—C(S)—R_a, -L-S(O)_mR_a, -L-S(O)_mOR_a, -L-S(O)_mNR_bR_c, -L-N(R_b)—S(O)_m—R_a, -L-N(R_b)—S(O)_m—NR_bR_c, -L-N(R_b)—C(O)OR_a, -L-N(R_b)—C(S)OR_a, -L-O—C_1-6 alkylene-OR_a, -L-C(O)—C_1-6 alkylene-NR_bR_c, -L-N(R_b)—C(O)—NR_bR_c, -L-N(R_b)—C(S)—NR_bR_c, -L-O—C(O)—NR_bR_c, -L-O—C(S)—NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_2-6 alkenyl, C_2-6 alkynyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl; wherein the said C_1-6 alkyl, C_1-6 haloalkyl, C_2-6 alkenyl, C_2-6 alkynyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl is each further optionally substituted by one or more groups consisting of the following:

-L-CN, —NO₂, carbonyl, -L-OR_a, -L-SR_a, -L-NR_bR_c, -L-C(O)R_a, -L-C(S)R_a, -L-C(O)OR_a, -L-C(S)OR_a, -L-C(O)—NR_bR_c, -L-C(S)—NR_bR_c, -L-O—C(O)R_a, -L-O—C(S)R_a, -L-N(R_b)—C(O)—R_a, -L-N(R_b)—C(S)—R_a, -L-S(O)_mR_a, -L-S(O)_mOR_a, -L-S(O)_mNR_bR_c, -L-N(R_b)—S(O)_m—R_a, -L-N(R_b)—S(O)_m—R_bR_c, -L-N(R_b)—C(O)OR_a, -L-N(R_b)—C(S)OR_a, -L-O—C_1-6 alkylene-OR_a, -L-C(O)—C_1-6 alkylene-NR_bR_c, -L-N(R_b)—C(O)—NR_bR_c, -L-N(R_b)—C(S)—NR_bR_c, -L-O—C(O)—NR_bR_c, and -L-O—C(S)—NR_bR_c;

R_a is independently selected from H, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl;

R_b and R_c are independently selected from H, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, or -L-5- to 10-membered heteroaryl; or, R_b, R_c and N atom are taken together to form 3- to 7-membered heterocyclyl;

R_a, R_b and R_c are each further optionally substituted by one or more groups consisting of the following:

C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, -L-C_3-7 cycloalkyl, -L-3- to 7-membered heterocyclyl, -L-C_6-10 aryl, and -L-5- to 10-membered heteroaryl;

L is selected from a chemical bond, —C_1-6 alkylene-, —C_2-6 alkenylene- or —C_2-6 alkynylene-;

L′ is selected from a chemical bond, —O—, —NH—, —C(O)—, —C(O)NH—, —NHC(O)—, —C_1-6 alkylene-, —C_2-6 alkenylene- or —C_2-6 alkynylene-; and

m represents 0, 1, or 2.

A₁, A₂ and A₃

In a specific embodiment, A₁ is CR₃; in another specific embodiment, A₁ is CH; in another specific embodiment, A₁ is C(OMe); in another specific embodiment, A₁ is N.

In a specific embodiment, A₂ is CR₃; in another specific embodiment, A₂ is CH; in another specific embodiment, A₂ is CR_3a, and R_3b has the same definition as R₃; in another specific embodiment, A₂ is N.

In a specific embodiment, A₃ is CR₃; in another specific embodiment, A₃ is CH; in another specific embodiment, A₂ is CR_3a, and R_3a has the same definition as R₃; in another specific embodiment, A₃ is CMe; in another specific embodiment, A₃ is N.

R₁

In a specific embodiment, R₁ is H; in another specific embodiment, R₁ is halogen; in another specific embodiment, R₁ is —CN; in another specific embodiment, R₁ is —OR_a; in another specific embodiment, R₁ is —SR_a; in another specific embodiment, R₁ is —NR_bR_c; in another specific embodiment, R₁ is —C(O)R_a; in another specific embodiment, R₁ is —C(O)O; in another specific embodiment, R₁ is —C(O)NR_bR_c; in another specific embodiment, R₁ is C_1-6 alkyl; in another specific embodiment, R₁ is Me; in another specific embodiment, R₁ is C_1-6 haloalkyl; in another specific embodiment, R₁ is C_3-7 cycloalkyl; in another specific embodiment, R₁ is 3- to 7-membered heterocyclyl; in another specific embodiment, R₁ is C_6-10 aryl; in another specific embodiment, R₁ is 5- to 10-membered heteroaryl.

In the specific embodiment of R₁ as mentioned above, the said C_3-7 cycloalkyl, or 3- to 7-membered heterocyclyl is optionally substituted by oxo; in the specific embodiment of R₁ as mentioned above, the said C_3-7 cycloalkyl, or 3- to 7-membered heterocyclyl is optionally substituted by thioxo.

R₂

In a specific embodiment, R₂ is H; in another specific embodiment, R₂ is halogen; in another specific embodiment, R₂ is —CN; in another specific embodiment, R₂ is —OR_a; in another specific embodiment, R₂ is —SR_a; in another specific embodiment, R₂ is —NR_bR_c; in another specific embodiment, R₂ is —C(O)R_a; in another specific embodiment, R₂ is —C(O)OR_a; in another specific embodiment, R₂ is —C(O)NR_bR_c; in another specific embodiment, R₂ is C_1-6 alkyl; in another specific embodiment, R₂ is C_1-6 haloalkyl; in another specific embodiment, R₂ is C_3-7 cycloalkyl; in another specific embodiment, R₂ is 3- to 7-membered heterocyclyl; in another specific embodiment, R₂ is C_6-10 aryl; in another specific embodiment, R₂ is 5- to 10-membered heteroaryl.

In the specific embodiment of R₂ as mentioned above, the C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by oxo; in the specific embodiment of R₂ as mentioned above, the C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by thioxo.

In more specific embodiment of R₂, R₂ is selected from H, —CN, 5 to 6-membered heteroaryl, and 3- to 7-membered heterocyclyl which is optionally substituted by oxo or thioxo; in another more specific embodiment, the R₂ is selected from H, —CN, 5 to 6-membered heteroaryl, and 3- to 7-membered heterocyclyl which is optionally substituted by oxo or thioxo, wherein the 5 to 6-membered heteroaryl and 3- to 7-membered heterocyclyl are selected from the group consisting of:

* is the point of attachment to the parent core.

In more specific embodiment of R₂, R₂ is selected from H, —CN and 5 to 6-membered heteroaryl, wherein the 5 to 6-membered heteroaryl is selected from the group consisting of:

* is the point of attachment to the parent core.

R₃

In a specific embodiment, R₃ is H; in another specific embodiment, R₃ is halogen; in another specific embodiment, R₃ is —CN; in another specific embodiment, R₃ is —NO₂; in another specific embodiment, R₃ is -L-OR_a; in another specific embodiment, R₃ is -L-SR_a; in another specific embodiment, R₃ is -L-NR_bR_c; in another specific embodiment, R₃ is -L-C(O)R_a; in another specific embodiment, R₃ is -L-C(O)OR_a; in another specific embodiment, R₃ is -L-C(O)NR_bR_a; in another specific embodiment, R₃ is -L-S(O)_mR_a; in another specific embodiment, R₃ is -L-S(O)_mOR_a; in another specific embodiment, R₃ is -L-S(O)_mNR_bR_c; in another specific embodiment, R₃ is —O—C_1-6 alkylene-R₆; in another specific embodiment, R₃ is C_1-6 alkyl; in another specific embodiment, R₃ is C_1-6 haloalkyl; in another specific embodiment, R₃ is -L′-C_3-7 cycloalkyl; in another specific embodiment, R₃ is -L′-3- to 11-membered heterocyclyl; in another specific embodiment, R₃ is -L′-3- to 9-membered heterocyclyl; in another specific embodiment, R₃ is -L′-C_6-10 aryl; in another specific embodiment, R₃ is -L′-5- to 10-membered heteroaryl.

In the specific embodiment of R₃ as mentioned above, each of the groups is optionally substituted by 1, 2, 3, 4, or 5 R₆ groups. In a specific embodiment, each of the groups is optionally substituted by 1 R₆ group; in another specific embodiment, the groups are substituted by 2 R₆ groups; in another specific embodiment, the groups are substituted by 3 R₆ groups; in another specific embodiment, the groups are substituted by 4 R₆ groups; in another specific embodiment, the groups are substituted by 5 R₆ groups.

In a more specific embodiment, R₃ is selected from -L′-3- to 11-membered heterocyclyl, wherein the said 3- to 11-membered heterocyclyl is selected from the group consisting of:

In a more specific embodiment, R₃ is selected from H, -L-OR_a, —O—C_1-6 alkylene-R₆, C_1-6 alkyl or -L′-3- to 11-membered heterocyclyl, wherein the said 3- to 11-membered heterocyclyl is selected from the group consisting of:

In a specific embodiment, R₄ is H; in another specific embodiment, R₄ is —C(O)R_a; in another specific embodiment, R₄ is —C(O)OR_a; in another specific embodiment, R₄ is —C(O)NR_bR_c; in another specific embodiment, R₄ is C_1-6 alkyl; in another specific embodiment, R₄ is C_1-6 haloalkyl; in another specific embodiment, R₄ is C_3-7 cycloalkyl; in another specific embodiment, R₄ is 3- to 7-membered heterocyclyl; in another specific embodiment, R₄ is C_6-10 aryl; in another specific embodiment, R₄ is 5- to 10-membered heteroaryl.

In the specific embodiment of R₄ as mentioned above, the groups are optionally substituted by 1, 2, or 3 R′ groups. In a specific embodiment, the groups are optionally substituted by 1 R′ group; in another specific embodiment, the groups are optionally substituted by 2 R′ groups; in another specific embodiment, the groups are optionally substituted by 3 R′ groups.

In the specific embodiment as mentioned above, R′ is H; in another specific embodiment, R′ is halogen; in another specific embodiment, R′ is —CN; in another specific embodiment, R′ is —NO₂; in another specific embodiment, R′ is —OR_a; in another specific embodiment, R′ is —SR_a; in another specific embodiment, R′ is —NR_bR_c; in another specific embodiment, R′ is —C(O)OR_a; in another specific embodiment, R′ is —C(O)NR—R_a; in another specific embodiment, R′ is C_1-6 alkyl; in another specific embodiment, R′ is C_1-6 haloalkyl; in another specific embodiment, R′ is C_3-7 cycloalkyl; in another specific embodiment, R′ is 3- to 7-membered heterocyclyl; in another specific embodiment, R′ is C_6-10 aryl; in another specific embodiment, R′ is 5- to 10-membered heteroaryl.

R₅

In a specific embodiment, R₄ is H; In a specific embodiment, R₅ is halogen; In a specific embodiment, R₅ is —CN; In a specific embodiment, R₅ is —OR_a; In a specific embodiment, R₅ is —SR_a; In a specific embodiment, R₅ is —NR_bR_c; In a specific embodiment, R₅ is —C(O)R_a; In a specific embodiment, R₅ is —C(O)OR_a; In a specific embodiment, R₅ is —C(O)NR_bR_c; in another specific embodiment, R₅ is C_1-6 alkyl; in another specific embodiment, R₅ is C_1-6 haloalkyl; in another specific embodiment, R₅ is C_3-7 cycloalkyl; in another specific embodiment, R₅ is 3- to 7-membered heterocyclyl; in another specific embodiment, R₅ is C_6-10 aryl; in another specific embodiment, R₅ is 5- to 10-membered heteroaryl.

In the specific embodiment of R₅ as mentioned above, the C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by oxo; in the specific embodiment of R₅ as mentioned above, the C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by thioxo.

R₆

In a specific embodiment, R₆ is H; in another specific embodiment, R₆ is —NH₂; in another specific embodiment, R₆ is —NHC_1-6 alkyl; in another specific embodiment, R₆ is —N(C_1-6 alkyl)₂; in another specific embodiment, R₆ is C_1-6 alkyl; in another specific embodiment, R₆ is C_1-6 haloalkyl; in another specific embodiment, R₆ is —C_1-6 alkylene-OR_a; in another specific embodiment, R₆ is -L-C_3-7 cycloalkyl; in another specific embodiment, R₆ is -L-3- to 7-membered heterocyclyl; in another specific embodiment, R₆ is -L-C_6-10 aryl; in another specific embodiment, R₆ is -L-5- to 10-membered heteroaryl; in another specific embodiment, two R₆ on the same carbon atom are taken together to form oxo. In another specific embodiment, two R₆ on the same carbon atom are taken together to form thioxo.

L

In a specific embodiment, L is a chemical bond; in another specific embodiment, L is —C_1-6 alkylene-; in another specific embodiment, L is —C_2-6 alkenylene-; in another specific embodiment, L is —C_2-6 alkynylene-.

L′

In a specific embodiment, L′ is a chemical bond; in another specific embodiment, L′ is —O—; in another specific embodiment, L′ is —NH—; in another specific embodiment, L′ is —C(O)—; in another specific embodiment, L′ is —C(O)NH—; in another specific embodiment, L′ is —NHC(O)—; in another specific embodiment, L′ is —C_1-6 alkylene-; in another specific embodiment, L′ is —C_2-6 alkenylene-; in another specific embodiment, L′ is —C_2-6 alkynylene-.

m

In a specific embodiment, m is 0; in another specific embodiment, m is 1; in another specific embodiment, m is 2.

Any technical solution in any one of the above embodiments, or any combination thereof, may be combined with any technical solution in any one of the above embodiments, or any combination thereof. For example, any technical solution of A₁, or any combination thereof, may be combined with any technical solution of A₂, A₃, R₁-R₆, R′, R″, R_a, R_b, R_c, L, L′ and m, etc or any combination thereof. The present disclosure is intended to include all combination of such technical solutions, which are not exhaustively listed here to save space.

In a more specific embodiment, the present disclosure provides the technical solution 1, which refers to a compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug, or an isotope variant thereof, and mixtures thereof:

wherein,

A₁ is N; A₂ is CR₃; A₃ is CR₃;

R₁ is H;

R₂ is selected from H, halogen, —CN, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl; wherein the said C_3-7 cycloalkyl or 3- to 7-membered heterocyclyl is optionally substituted by oxo or thioxo;

R₃ is selected from H, halogen, —CN, C_1-6 alkyl, C_1-6 haloalkyl, -L′-C_3-7 cycloalkyl, -L′-3- to 11-membered heterocyclyl, -L′-C_6-10 aryl, or -L′-5- to 10-membered heteroaryl, each of which is optionally substituted by 1, 2, 3, 4, or 5 R₆ groups;

R₄ is selected from C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R₅ is selected from H, halogen, —CN, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl or C_1-6 haloalkyl;

R₆ is selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

or two R₆ groups on the same carbon atom are taken together to form oxo or thioxo;

wherein:

R₂ and R₅-R₆ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H, halogen, —NO₂, —CN, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(S)R_a, —C(O)OR_a, —C(S)OR_a, —C(O)—NR_bR_c, —C(S)—NR_bR_c, —O—C(O)R_a, —O—C(S)R_a, —N(R_b)—C(O)—R_a, —N(R_b)—C(S)—R_a, —O—C_1-6 alkylene-OR_a, —C(O)—C_1-6 alkylene-NR_bR_c, —N(R_b)—C(O)—NR_bR_c, —N(R_b)—C(S)—NR_bR_c, —O—C(O)—NR_bR_c, —O—C(S)—NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_2-6 alkenyl or C_2-6 alkynyl;

R is independently selected from H, C_1-6 alkyl, C_1-6 haloalkyl, —C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R_b and R_c are independently selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl; or, R_b, R_c and N atom are taken together to form 3- to 7-membered heterocyclyl; and

L′ is selected from a chemical bond, —C(O)—, —C_1-6 alkylene-, —C_2-6 alkenylene- or —C_2-6 alkynylene-.

In another more specific embodiment, the present disclosure provides the technical solution 2, which refers to the compound of the technical solution 1, wherein

R₂ is selected from H, halogen, —CN, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

preferably, R₂ is selected from H, halogen, —CN, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

preferably, R₂ is selected from H, halogen, —CN, C_1-6 alkyl, —C(O)F or C_6-10 aryl;

preferably, R₂ is selected from H, —C(O)R_a, —C(O)OR_a or —C(O)NR_bR_c;

preferably, R₂ is selected from H or —C(O)R_a;

preferably, R₂ is —C(O)R_a.

In another more specific embodiment, the present disclosure provides the technical solution 3, which refers to the compound of the technical solution 1 or 2, wherein

R₃ is selected from H, halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, or 3- to 11-membered heterocyclyl, each of which is optionally substituted by 1, 2, 3, 4, or 5 R₆ groups;

preferably, R₃ is selected from H, halogen, C_1-6 alkyl or 3- to 11-membered heterocyclyl, each of which is optionally substituted by 1, 2, 3, 4, or 5 R₆ groups;

preferably, R₃ is selected from H, C_3-7 cycloalkyl, or 3- to 11-membered heterocyclyl, each of which is optionally substituted by 1, 2, 3, 4, or 5 R₆ groups;

preferably, R₃ is selected from H or 3- to 11-membered heterocyclyl, each of which is optionally substituted by 1, 2, 3, 4, or 5 R₆ groups.

In another more specific embodiment, the present disclosure provides the technical solution 4, which refers to the compound of any one of the technical solutions 1-3, wherein

R₄ is selected from C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, or 3- to 7-membered heterocyclyl;

preferably, R₄ is selected from C_1-6 alkyl or C_3-7 cycloalkyl;

preferably, R₄ is selected from isopropyl or cyclopentyl;

preferably, R₄ is isopropyl.

In another more specific embodiment, the present disclosure provides the technical solution 5, which refers to the compound of any one of the technical solutions 1-4, wherein

R₆ is selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, or 3- to 7-membered heterocyclyl; or two R₆ groups on the same carbon atom are taken together to form oxo or thioxo;

preferably, R₆ is selected from H, C_1-6 alkyl or C_1-6 haloalkyl; or two R₆ groups on the same carbon atom are taken together to form oxo or thioxo;

preferably, R₆ is selected from H, C_1-6 alkyl or C_1-6 haloalkyl.

In another more specific embodiment, the present disclosure provides the technical solution 6, which refers to the compound of any one of the technical solutions 1-5, wherein

R₂ and R₆ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H, halogen, —NO₂, —CN, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(S)R_a, —C(O)OR_a, —C(S)OR_a, —C(O)—NR_bR_c, —C(S)—NR_bR_c, —O—C(O)R_a, —O—C(S)R_a, —N(R_b)—C(O)—R_a, —N(R_b)—C(S)—R_a, C_1-6 alkyl, C_1-6 haloalkyl, C_2-6 alkenyl or C_2-6 alkynyl;

preferably, R₂ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H, halogen, —NO₂, —CN, —OR_a, —SR_a or —NR_bR_c;

preferably, R₂ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H or —O.

In another more specific embodiment, the present disclosure provides the technical solution 7, which refers to the compound of any one of the technical solutions 1-6, wherein

R_a is independently selected from H, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R_a is independently selected from H or C_1-6 alkyl.

In another more specific embodiment, the present disclosure provides the technical solution 8, which refers to the compound of any one of the technical solutions 1-7, wherein

R_b and R_c are independently selected from H, C_1-6 alkyl or C_1-6 haloalkyl; or, R_b, R_c and N atom are taken together to form 3- to 7-membered heterocyclyl;

preferably, R_b and R_c are independently selected from H, C_1-6 alkyl or C_1-6 haloalkyl.

In another specific embodiment, the present disclosure provides the technical solution 9, which refers to the compound of formula (II), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug, or an isotope variant thereof, and mixtures thereof:

wherein,

R₂ is selected from H, halogen, —CN, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R₃ is selected from the groups consisting of the following:

R_3a is selected from H, halogen, —CN, —NO₂, C_1-6 alkyl or C_1-6 haloalkyl;

R_3b is selected from H, halogen, —CN, —NO₂, C_1-6 alkyl or C_1-6 haloalkyl;

R_3c, R_3d, R_3e and R_3f are independently selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R₄ is selected from C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 11-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R₂ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H, halogen, —CN, —NO₂, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(S)R_a, —C(O)OR_a, —C(S)OR_a, —C(O)—NR_bR_c, —C(S)—NR_bR_c, —O—C(O)R_a, —O—C(S)R_a, —N(R_b)—C(O)—R_a, —N(R_b)—C(S)—R_a, —O—C_1-6 alkylene-OR_a, —C(O)—C_1-6 alkylene-NR_bR_c, —N(R_b)—C(O)—NR_bR_c, —N(R_b)—C(S)—NR_bR_c, —C(O)—NR_bR_c, —O—C(S)—NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_2-6 alkenyl or C_2-6 alkynyl;

R is independently selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R_b and R_c are independently selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl.

In another more specific embodiment, the present disclosure provides the technical solution 10, which refers to the compound of the technical solution 9, wherein

R₂ is selected from H, —CN, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

preferably, R₂ is selected from H, halogen, —CN, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

preferably, R₂ is selected from H, —CN, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

preferably, R₂ is selected from H, halogen, CN, C_1-6 alkyl, —C(O)R_a or C_6-10 aryl;

preferably, R₂ is selected from H, CN, C_1-6 alkyl, —C(O)R_a or C_6-10 aryl;

preferably, R₂ is selected from H, —C(O)R_a, —C(O)OR_a or —C(O)NR_bR_c;

preferably, R₂ is selected from H or —C(O)R_a;

preferably, R₂ is selected from H, Br, CN, Me, CH₃C(O)— or Ph(OMe)₂;

preferably, R₂ is selected from H, CN, Me, CH₃C(O)— or Ph(OMe)₂;

preferably, R₂ is selected from H or CH₃C(O)—;

preferably, R₂ is CH₃C(O)—.

In another more specific embodiment, the present disclosure provides the technical solution 11, which refers to the compound of any one of the technical solutions 9-10, wherein

R₃ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

preferably, R³ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

In another more specific embodiment, the present disclosure provides the technical solution 12, which refers to the compound of any one of the technical solutions 9-11, wherein

R_3a is selected from H, halogen or C_1-6 alkyl;

preferably, R_3a is selected from H, F or Me;

preferably, R_3a is H.

In another more specific embodiment, the present disclosure provides the technical solution 13, which refers to the compound of any one of the technical solutions 9-12, wherein

R_3b is selected from H, halogen or C_1-6 alkyl;

preferably, R_3b is selected from H, For Me;

preferably, R_3b is H.

In another more specific embodiment, the present disclosure provides the technical solution 14, which refers to the compound of any one of the technical solutions 9-13, wherein

R_3c, R_3d, R_3e and R_3f are independently selected from H, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R_3c, R_3d, R_3e and R_3f are independently selected from H or C_1-6 alkyl;

preferably, R_3c is selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

preferably, R_3c is selected from H, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R_3c is selected from H or C_1-6 alkyl.

In another more specific embodiment, the present disclosure provides the technical solution 15, which refers to the compound of any one of the technical solutions 9-14, wherein

R₄ is selected from C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, or 3- to 11-membered heterocyclyl;

preferably, R₄ is selected from C_1-6 alkyl or C_3-7 cycloalkyl;

preferably, R₄ is selected from ethyl, isopropyl, cyclopropyl or cyclopentyl;

preferably, R₄ is selected from isopropyl or cyclopentyl;

preferably, R₄ is isopropyl.

In another more specific embodiment, the present disclosure provides the technical solution 16, which refers to the compound of any one of the technical solutions 9-15, wherein

R₂ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H, halogen, —CN, —NO₂ or —OR_a;

R₂ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from —OR_a.

In another more specific embodiment, the present disclosure provides the technical solution 17, which refers to the compound of any one of the technical solutions 9-16, wherein

R_a is independently selected from H, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R_a is independently selected from H or C_1-6 alkyl.

In another more specific embodiment, the present disclosure provides the technical solution 18, which refers to the compound of any one of the technical solutions 9-17, wherein

R_b and R_c are independently selected from H, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R_b and R_c are independently selected from H or C_1-6 alkyl.

In another specific embodiment, the present disclosure provides the technical solution 19, which is the compound of formula (II), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug, or an isotope variant thereof, and mixtures thereof:

wherein,

R₂ is selected from —CN, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R₃ is selected from the groups consisting of the following:

R_3a is H;

R_3b is selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R_3c is selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R₄ is selected from C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 11-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R₂ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H, halogen, —CN, —NO₂, —OR_a, —SR_a, —NR_bR_c, —C(O)R_a, —C(S)R_a, —C(O)OR_a, —C(S)OR_a, —C(O)—NR_bR_c, —C(S)—NR_bR_c, —O—C(O)R_a, —O—C(S)R_a, —N(R_b)—C(O)—R_a, —N(R_b)—C(S)—R_a, —O—C_1-6 alkylene-OR_a, —C(O)—C_1-6 alkylene-NR_bR_c, —N(R_b)—C(O)—NR_bR_c, —N(R_b)—C(S)—NR_bR_c, —O—C(O)—NR_bR_c, —O—C(S)—NR_bR_c, C_1-6 alkyl, C_1-6 haloalkyl, C_2-6 alkenyl or C_2-6 alkynyl;

R_a is independently selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

R_b and R_c are independently selected from H, C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl.

In another more specific embodiment, the present disclosure provides the technical solution 20, which refers to the compound of the technical solution 19, wherein

R₂ is selected from —CN, —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

preferably, R₂ is selected from —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R₂ is selected from —C(O)R_a, —C(O)OR_a, —C(O)NR_bR_c or C_1-6 alkyl;

preferably, R₂ is selected from CN, C_1-6 alkyl, —C(O)R_a or C_6-10 aryl;

preferably, R₂ is selected from C_1-6 alkyl or —C(O)R_a;

preferably, R₂ is selected from CN, Me, CH₃C(O)— or Ph(OMe)₂;

preferably, R₂ is selected from Me or CH₃C(O)—;

preferably, R₂ is H.

In another more specific embodiment, the present disclosure provides the technical solution 21, which refers to the compound of any one of the technical solutions 19-20, wherein

R₃ is selected from the groups consisting of the following:

preferably, R₃ is

preferably, R₃ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

preferably, R₃ is selected from the groups consisting of the following:

In another more specific embodiment, the present disclosure provides the technical solution 22, which refers to the compound of any one of the technical solutions 19-21, wherein

R_3b is selected from C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C_6-10 aryl, or 5- to 10-membered heteroaryl;

preferably, R_3b is selected from H, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R_3b is selected from C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R_3b is selected from H or C_1-6 alkyl;

preferably, R_3b is C_1-6 alkyl;

preferably, R_3b is selected from H or Me;

preferably, R_3b is selected from Me;

preferably, R_3b is H.

In another more specific embodiment, the present disclosure provides the technical solution 23, which refers to the compound of any one of the technical solutions 19-22, wherein

R_3c is selected from H, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R₃, is selected from C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R₃, is selected from H or C_1-6 alkyl;

preferably, R₃, is C_1-6 alkyl.

In another more specific embodiment, the present disclosure provides the technical solution 24, which refers to the compound of any one of the technical solutions 19-23, wherein

R₄ is selected from C_1-6 alkyl, C_1-6 haloalkyl, C_3-7 cycloalkyl, or 3- to 11-membered heterocyclyl;

preferably, R₄ is selected from C_1-6 alkyl or C_3-7 cycloalkyl;

preferably, R₄ is selected from ethyl, isopropyl, cyclopropyl or cyclopentyl;

preferably, R₄ is selected from isopropyl or cyclopentyl;

preferably, R₄ is isopropyl.

In another more specific embodiment, the present disclosure provides the technical solution 25, which refers to the compound of any one of the technical solutions 19-24, wherein

R₂ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from H, halogen, —CN, —NO₂ or —OR_a;

preferably, R₂ is optionally substituted by 1, 2, or 3 R″ groups, wherein R″ is independently selected from —OR_a.

In another more specific embodiment, the present disclosure provides the technical solution 26, which refers to the compound of any one of the technical solutions 19-25, wherein

R_a is independently selected from H, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R_a is independently selected from H or C_1-6 alkyl.

In another more specific embodiment, the present disclosure provides the technical solution 27, which refers to the compound of any one of the technical solutions 19-26, wherein

R_b and R_c are independently selected from H, C_1-6 alkyl or C_1-6 haloalkyl;

preferably, R_b and R_c are independently selected from H or C_1-6 alkyl.

The compounds of the present disclosure may include one or more asymmetric centers, and thus may exist in a variety of stereoisomeric forms, for example, enantiomers and/or diastereomers. For example, the compounds of the present disclosure may be in the form of an individual enantiomer, diastereomer or geometric isomer (e.g., cis- and trans-isomers), or may be in the form of a mixture of stereoisomers, including racemic mixture and a mixture enriched in one or more stereoisomers. The isomers can be separated from the mixture by the methods known to those skilled in the art, including chiral high pressure liquid chromatography (HPLC) and the formation and crystallization of chiral salts; or preferred isomers can be prepared by asymmetric synthesis.

It will be understood by those skilled in the art that the organic compounds can form complexes with solvents in which they are reacted or from which they are precipitated or crystallized. These complexes are known as “solvates.” Where the solvent is water, the complex is known as “hydrate.” The present disclosure encompasses all solvates of the compounds of the present disclosure.

The term “solvate” refers to forms of a compound or a salt thereof, which are associated with a solvent, usually by a solvolysis reaction. This physical association may include hydrogen bonding. Conventional solvents include water, methanol, ethanol, acetic acid, DMSO, THF, diethyl ether, etc. The compounds described herein can be prepared, for example, in crystalline form, and can be solvated. Suitable solvates include pharmaceutically acceptable solvates and further include both stoichiometric solvates and non-stoichiometric solvates. In some cases, the solvates will be capable of isolation, for example, when one or more solvent molecules are incorporated into the crystal lattice of a crystalline solid. “Solvate” includes both solution-phase and isolatable solvates. Representative solvates include hydrates, ethanolates and methanolates.

The term “hydrate” refers to a compound that is associated with water. Generally, the number of water molecules contained in a hydrate of a compound is in a definite ratio to the number of the compound molecules in the hydrate. Therefore, hydrates of a compound can be represented, for example, by a general formula R.xH₂O, wherein R is the compound, and x is a number greater than 0. Given compounds can form more than one type of hydrates, including, for example, monohydrates (x is 1), lower hydrates (x is a number greater than 0 and smaller than 1, for example, hemihydrates (R.0.5H₂O)) and polyhydrates (x is a number greater than 1, for example, dihydrates (R.2H₂O) and hexahydrates (R.6H₂O)).

Compounds of the present disclosure may be in an amorphous or a crystalline form (polymorph). Furthermore, the compounds of the present disclosure may exist in one or more crystalline forms. Therefore, the present disclosure includes all amorphous or crystalline forms of the compounds of the present disclosure within its scope. The term “polymorph” refers to a crystalline form of a compound (or a salt, hydrate or solvate thereof) in a particular crystal packing arrangement. All polymorphs have the same elemental composition. Different crystalline forms generally have different X-ray diffraction patterns, infrared spectra, melting points, density, hardness, crystal shapes, optical and electrical properties, stability, and solubility. Recrystallization solvents, rate of crystallization, storage temperatures, and other factors may cause one crystalline form to dominate. Various polymorphs of a compound can be prepared by crystallization under different conditions.

The present disclosure also comprises compounds that are labeled with isotopes, which are equivalent to those described in formula (I), but one or more atoms are replaced by atoms having an atom mass or mass number that are different from that of atoms that are common in nature. Examples of isotopes which may be introduced into the compounds of the disclosure include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine and chlorine, such as ²H, ³H, ¹³C, ¹¹C, ¹⁴C, ¹⁵N, ¹⁸O, ¹⁷O, ³¹P, ³²P, ³⁵S, ¹⁸F and ³⁶Cl, respectively. Compounds of the present disclosure that comprise the above isotopes and/or other isotopes of other atoms, prodrugs thereof and pharmaceutically acceptable salts of said compounds or prodrugs all are within the scope of the present disclosure. Certain isotope-labeled compounds of the present disclosure, such as those incorporating radioactive isotopes (e.g., ³H and ¹⁴C), can be used for the measurement of the distribution of drug and/or substrate in tissue. Tritium, which is ³H and carbon-14, which is ¹⁴C isotope, are particularly preferred, because they are easy to prepare and detect. Furthermore, replaced by heavier isotopes, such as deuterium, which is ²H, may provide therapeutic benefits due to the higher metabolic stability, such as prolonging the half-life in vivo or decreasing the dosage requirements, and thus may be preferred in some cases. Isotope-labeled compounds of formula (I) of the present disclosure and prodrugs thereof can be prepared generally by using readily available isotope-labeled reagents to replace non-isotope-labeled reagents in the following schemes and/or the procedures disclosed in the examples and preparation examples.

In addition, prodrugs are also included within the context of the present disclosure. The term “prodrug” as used herein refers to a compound that is converted into an active form that has medical effects in vivo by, for example, hydrolysis in blood. Pharmaceutically acceptable prodrugs are described in T. Higuchi and V. Stella, Prodrugs as Novel Delivery Systems, A.C.S. Symposium Series, Vol. 14, Edward B. Roche, ed., Bioreversible Carriers in Drug Design, American Pharmaceutical Association and Pergamon Press, 1987, and D. Fleisher, S. Ramon and H. Barbra “Improved oral drug delivery: solubility limitations overcome by the use of prodrugs”, Advanced Drug Delivery Reviews (1996) 19(2) 115-130, each of which are incorporated herein by reference.

The prodrugs are any covalently bonded compounds of the present disclosure, which release the parent compound in vivo when the prodrug is administered to a patient. Prodrugs are typically prepared by modifying functional groups in such a way that the modifications can be cleaved either by routine manipulation or decompose in vivo to yield the parent compound. Prodrugs include, for example, compounds of the present disclosure wherein the hydroxyl, amino or sulfhydryl groups are bonded to any group that, when administered to a patient, cleaves to form the hydroxyl, amino or sulfhydryl groups. Thus, representative examples of prodrugs include (but are not limited to) the acetate/acetamide, formate/formamide and benzoate/benzamide derivatives of the hydroxyl, amino or sulflhydryl functional groups of the compounds of formula (I). Furthermore, in the case of carboxylic acid (—COOH), esters such as methyl esters and ethyl esters, etc. can be employed. The ester itself may be active in their own and/or hydrolyzable under in vivo conditions in the human body. Suitable pharmaceutically acceptable in vivo hydrolysable ester groups include those groups that can readily break down in the human body to release the parent acids or salts thereof.

The present disclosure also provides a pharmaceutical formulation comprising a therapeutically effective amount of a compound of formula (I), or therapeutically acceptable salts thereof, and pharmaceutically acceptable carriers, diluents or excipients thereof. All of these forms belong to the present disclosure.

The preferred compounds disclosed herein include but are not limited to the following compounds, or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug, or an isotope variant thereof, and mixtures thereof:

Pharmaceutical Compositions, Formulations and Kits

In another aspect, the present disclosure provides a pharmaceutical composition comprising a compound of the present disclosure (also referred to as the “active ingredient”) and pharmaceutically acceptable excipients. In some embodiments, the pharmaceutical composition comprises an effective amount of the compound of the present disclosure. In some embodiments, the pharmaceutical composition comprises a therapeutically effective amount of the compound of the present disclosure. In some embodiments, the pharmaceutical composition comprises a prophylactically effective amount of the compound of the present disclosure.

Pharmaceutically acceptable excipients for use in the present disclosure refer to the non-toxic carriers, adjuvants or vehicles, which do not destroy the pharmacological activity of the compounds formulated together. Pharmaceutically acceptable carriers, adjuvants, or vehicles that can be used in the compositions of the present disclosure include (but are not limited to) ion exchangers, alumina, aluminum stearate, lecithin, serum proteins (such as human serum proteins), buffer substances (such as phosphate), glycine, sorbic acid, potassium sorbate, mixture of partial glycerides of saturated plant fatty acids, water, salts or electrolytes (such as protamine sulfate), disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, silica gel, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substance, polyethylene glycol, sodium carboxymethyl cellulose, polyacrylate, wax, polyethylene-polyoxypropylene block polymers, polyethylene glycol and lanolin.

The present disclosure also includes kits (e.g., pharmaceutical packs). The kits provided may include a compound of the present disclosure, other therapeutic agent(s), and a first and a second containers (e.g., vials, ampoules, bottles, syringes, and/or dispersible packages or other suitable containers) containing the compound of the present disclosure and other therapeutic agent(s). In some embodiments, the provided kits can also optionally include a third container containing a pharmaceutically acceptable excipient for diluting or suspending the compound of the present disclosure and/or other therapeutic agent(s). In some embodiments, the compound of the present disclosure provided in the first container and other therapeutic agent(s) provided in the second container are combined to form a unit dosage form.

Administration

The pharmaceutical composition provided by the present disclosure can be administered by a variety of routes including, but not limited to, oral administration, parenteral administration, inhalation administration, topical administration, rectal administration, nasal administration, buccal administration, vaginal administration, administration by implant or other means of administration. For example, parenteral administration as used herein includes subcutaneous administration, intradermal administration, intravenous administration, intramuscular administration, intra-articular administration, intra-arterial administration, intrasynovial administration, intrasternal administration, intracerebroventricular administration, intralesional administration, and intracranial injection or infusion techniques.

Generally, the compounds provided herein are administered in an effective amount. The amount of the compound actually administered will typically be determined by a physician, in the light of the relevant circumstances, including the condition to be treated, the route of administration selected, the actual compound administered, the age, weight and response of the individual patient, the severity of the patient's symptoms, etc.

When used to prevent the conditions described in the present disclosure, the compounds provided herein will be administered to a subject at risk of developing the conditions, typically based on the physician's recommendation and administered under the supervision of the physician, at the dosage level described above. Subjects at risk of developing the particular conditions generally include those who have a family history of the conditions, or those who have been identified by genetic testing or screening to be particularly susceptible to developing the conditions.

The pharmaceutical compositions provided herein can also be administered chronically (“chronic administration”). Chronic administration refers to the administration of a compound or pharmaceutical composition thereof for a long period of time, for example, 3 months, 6 months, 1 year, 2 years, 3 years, 5 years, etc., or can be continuously administered indefinitely, for example, for the rest of the subject's life. In some embodiments, the chronic administration is intended to provide a constant level of the said compound in the blood over a long period of time, for example, within the therapeutic window.

Pharmaceutical compositions of the present disclosure can be further delivered using various dosing methods. For example, in some embodiments, pharmaceutical compositions can be administered by bolus injection, for example, to increase the concentration of the compound in the blood to an effective level. The bolus dose depends on the desired systemic level of the active ingredient throughout the body, for example, intramuscular or subcutaneous bolus dose allows a slow release of the active ingredient, while the bolus that is delivered directly to the vein (e.g., via IV intravenous drip) allows a much faster delivery which quickly raises the concentration of the active ingredient in the blood to an effective level. In other embodiments, pharmaceutical compositions can be administered in a form of continuous infusion, for example, via IV intravenous drip, thereby providing a steady state concentration of the active ingredient in the subject's body. Moreover, in other embodiments, a bolus dose of the pharmaceutical compositions can be administered first, followed by continuous infusion.

The compositions for oral administration can be in the form of bulk liquid solution or suspension or bulk powder. More commonly, however, in order to facilitate the precise dosing, the compositions are provided in unit dosage form. The term “unit dosage form” refers to physical discrete units suitable as unitary dosages for human patients and other mammals, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effects with suitable pharmaceutical excipients. Typical unit dosage forms include prefilled, pre-measured ampoules or syringes of the liquid compositions, or pills, tablets, capsules, etc. in the case of solid compositions. In such compositions, the said compound generally will be the minor component (about 0.1 to about 50% by weight, or preferably about 1 to about 40% by weight), with the remainder being various carriers or excipients and processing aids useful for forming the desired dosing form.

For oral dosage, a representative scheme is one to five, especially two to four, and typically three oral doses per day. Using these dosing patterns, each dose provides from about 0.01 to about 20 mg/kg of the compound of the present disclosure, with preferred doses each providing from about 0.1 to about 10 mg/kg, and especially from about 1 to about 5 mg/kg.

Transdermal doses are generally selected to provide similar or lower blood levels than are achieved using injection doses, usually in an amount of from about 0.01 to about 20% by weight, preferably from about 0.1 to about 20% by weight, preferably from about 0.1 to about 10% by weight, and more preferably from about 0.5 to about 15% by weight.

The injection dose level ranges from about 0.1 mg/kg/hr to at least 10 mg/kg/hr, all for from about 1 to about 120 hours, especially from 24 to 96 hours. In order to achieve a sufficient level of steady state, a preloading bolus of from about 0.1 mg/kg to about 10 mg/kg or more can also be administered. For human patients of 40 to 80 kg, the maximum total dose should not exceed approximately 2 g/day.

Liquid forms suitable for oral administration may include suitable aqueous or nonaqueous carriers, buffers, suspending agents and dispersants, coloring agents, flavoring agents, etc. Solid forms may include, for example, any of the following components, or compounds having the similar properties: binders, for example, microcrystalline cellulose, tragacanth gum or gelatin; excipients, for example, starch or lactose; disintegrants, for example, alginic acid, Primogel or corn starch; lubricants, for example, magnesium stearate; glidants, for example, colloidal silica; sweeteners, for example, sucrose or saccharin; or flavoring agents, for example, peppermint, methyl salicylate or orange flavouring.

Injectable compositions are typically based on the injectable sterile saline or phosphate-buffered saline, or other injectable excipients known in the art. As previously mentioned, in such compositions, the active ingredients will typically be the minor component, often from about 0.05 to 10% by weight, with the remainder being injectable excipients, etc.

The transdermal compositions are typically formulated as topical ointments or creams containing the active ingredients. When formulated as an ointment, the active ingredients are typically combined with paraffin or water miscible ointment base. Alternatively, the active ingredients can be formulated as a cream with, for example, oil-in-water cream base. Such transdermal formulations are well-known in the art and generally include other ingredients for enhancing stable skin penetration of the active ingredients or the formulations. All such known transdermal formulations and components are included within the scope of the present disclosure.

The compounds of the present disclosure may also be administered by transdermal devices. Thus, transdermal administration can be accomplished using a patch either of reservoir or porous membrane type, or of a plurality of solid substrates.

The above components of the compositions for oral administration, injection or topical administration are only representative. Other materials and processing techniques, etc., are described in the Section 8 of Remington's Pharmaceutical Sciences, 17th edition, 1985, Mack Publishing Company, Easton, Pa., which is incorporated herein by reference.

Compounds of the present disclosure may also be administered in a sustained release form or from a sustained release delivery system. Description of the representative sustained release materials can be found in Remington's Pharmaceutical Sciences.

The present disclosure also relates to pharmaceutically acceptable formulations of the compounds of the present disclosure. In one embodiment, the formulation comprises water. In another embodiment, the formulation comprises cyclodextrin derivative. The most common cyclodextrins are alpha-, beta- and gamma-cyclodextrins consisting of 6, 7 and 8 alpha-1,4-linked glucose units, respectively, optionally including one or more substituents on the linked sugar moiety, including, but are not limited to, methylated, hydroxyalkylated, acylated, and sulfoalkyl ether substitution. In some embodiments, the cyclodextrin is sulfoalkyl ether beta-cyclodextrin, e.g., sulfobutyl ether beta-cyclodextrin, also known as Captisol. See, for example, U.S. Pat. No. 5,376,645. In some embodiments, the formulation comprises hexapropyl-β-cyclodextrin (e.g., 10-50% in water).

Treatment

The present disclosure provides the methods for treating the following disorders or conditions in mammals (including humans): cell proliferative disorders, e.g. cancer, vascular smooth muscle hyperplasia associated with atherosclerosis, postoperative vascular stenosis, restenosis, and endometriosis; infections, including viral infections, e.g. DNA viruses such as herpes, and RNA viruses such as HIV, and fungal infections; autoimmune diseases, e.g. psoriasis and inflammation, such as rheumatoid arthritis, lupus, type I diabetes, diabetic nephropathy, multiple sclerosis and glomerulonephritis; organ transplant rejection, including host versus graft disease. The methods comprise administering to the mammal a therapeutically effective amount of a compound of the present disclosure or a composition thereof.

The present disclosure further provides compounds of the present disclosure useful for the treatment of abnormal cell proliferation, such as cancer. The present disclosure further provides a method of treating abnormal cell proliferation, such as cancers selected from the following: breast, ovary, cervix, prostate, testis, esophagus, stomach, skin, lung, bone, colon, pancreas, thyroid, biliary tract, buccal cavity and pharynx (mouth), lips, tongue, oral cavity, pharynx, small intestine, colorectal, large intestine, rectum, cancer of brain and central nervous system, glioblastoma, neuroblastoma, keratoacanthoma, epidermoid carcinoma, large cell carcinoma, adenocarcinoma, adenoma, follicular carcinoma, undifferentiated carcinoma, papillary carcinoma, seminoma, melanoma, sarcoma, bladder cancer, liver cancer, kidney cancer, bone marrow disorder, lymphatic disorder, Hodgkin's disease, hairy cell carcinoma and leukemia, comprising administering to the subjects in need of such treatment a therapeutically effective amount of a compound of the present disclosure or a composition thereof.

Further, the present disclosure relates to a method of treating a subject having a disease caused by proliferation of vascular smooth muscle cells. Compounds of the present disclosure effectively inhibit the proliferation and migration of vascular smooth muscle cells. The method comprises administering to the subject in need of the treatment a compound of the present disclosure or a composition thereof in an amount sufficient to inhibit the proliferation and/or migration of the vascular smooth muscle.

The present disclosure further provides a method of treating a subject suffering from gout, comprising administering to the subject in need of treatment a compound of the present disclosure or a composition thereof in an amount sufficient to treat the condition.

The present disclosure further provides a method of treating a subject having a renal disease, such as a polycystic kidney disease, comprising administering to the subject in need of treatment an amount of a compound of the present disclosure or a composition thereof in an amount sufficient to treat the condition.

Due to their inhibitory activity against CDK and other kinases, the compounds of the present disclosure are also useful research tools for studying the mechanism of action of these kinases in vitro and in vivo.

Compounds of the present disclosure are useful in the treatment of cancers (e.g., leukemia and cancers of lung, breast, prostate and skin, such as melanoma) and other proliferative diseases including, but are not limited to, psoriasis, HSV, HIV, restenosis, and atherosclerosis. In order to treat cancers using a compound of the present disclosure, a therapeutically effective amount of a pharmaceutically acceptable composition comprising at least one compound of the present disclosure is administered to the patient in need of such treatment, for example, who has cancer or another proliferative disorder.

The effective amount of a compound of the present disclosure is generally administered in a single or multiple doses at an average daily dose of from 0.01 mg to 50 mg of the compound per kilogram of patient's body weight, preferably from 0.1 mg to 25 mg of the compound per kilogram of patient's body weight. Generally, the compounds of the present disclosure may be administered to the patient in need of such treatment in a daily dosage ranges from about 1 mg to about 3500 mg per patient, preferably from 10 mg to 1000 mg. For example, the daily dosage per patient can be 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 500, 600, 700, 800, 900 or 1000 mg. It can be administered one or more times daily, weekly (or at intervals of several days) or on an intermittent schedule. For example, the compounds can be administered one or more times per day on a weekly basis (e.g., every Monday), continually or for several weeks, such as 4-10 weeks. Alternatively, the administration may be continued for several days (e.g., 2-10 days), followed by a few days (e.g., 1-30 days) without administration of the compound, and the cycle may be repeated indefinitely or repeated for a given number of times, such as 4-10 cycles. For example, the compounds of the present disclosure may be administered daily for 5 days, then intermittently for 9 days, and then administered daily for 5 days, then intermittently for 9 days, and so on, repeating the cycle indefinitely or repeating 4-10 times.

Combination Therapy

Compounds or compositions of the present disclosure may be administered simultaneously with, prior to, or subsequent to one or more additional pharmaceutical agents, which may be useful as combination therapy. The pharmaceutical agents include therapeutically active agents. Pharmaceutical agents also include prophylactically active agents. Pharmaceutical agents include small organic molecules such as pharmaceutical compounds (e.g., compounds approved for human or veterinary use by the U.S. Food and Drug Administration as provided in the Code of Federal Regulations (CFR)), peptides, proteins, carbohydrates, monosaccharides, oligosaccharides, polysaccharides, nuclear proteins, mucoproteins, lipoproteins, synthetic polypeptides or proteins, small molecules linked to proteins, glycoproteins, steroids, nucleic acids, DNAs, RNAs, nucleotides, nucleosides, oligonucleotides, antisense oligonucleotides, lipids, hormones, vitamins and cells. In some embodiments, the additional pharmaceutical agent is a pharmaceutical agent for treating and/or preventing the diseases described herein. Each additional pharmaceutical agent can be administered at a dose and/or on a time schedule determined by the pharmaceutical agent. The additional pharmaceutical agents may also be administered together with each other and/or with the compounds or compositions described herein, in a single dose, or administered separately in different doses. Specific combinations employed in this regimen will take into account the compatibility of the compounds of the present disclosure with the additional pharmaceutical agent(s) and/or the desired therapeutic and/or prophylactic effects to be achieved. Generally, it is expected that the additional pharmaceutical agent(s) utilized in combination be utilized at levels that do not exceed the levels at which they are utilized individually. In some embodiments, the levels used in combination will be lower than those utilized individually.

The additional pharmaceutical agents include, but are not limited to, anti-proliferative agents, anticancer agents, anti-angiogenic agents, anti-inflammatory agents, immunosuppressants, antibacterial agents, antiviral agents, cardiovascular agents, lipid-lowering agents, anti-diabetic agents, anti-allergic agents, contraceptive agents and analgesics. In one embodiment, the additional pharmaceutical agent is an anti-proliferative agent. In one embodiment, the additional medicament is an anticancer agent. In one embodiment, the additional medicament is an anti-leukemia agent. In one embodiment, the additional pharmaceutical agent is ABITREXATE (methotrexate), ADE, Adriamycin RDF (doxorubicin hydrochloride), Ambochlorin (chlorambucil), ARRANON (nelarabine), ARZERRA (ofatumumab), BOSULIF (bosutinib), BUSULFEX (busulfan), CAMPATH (alemtuzumab), CERUBIDINE (daunorubicin hydrochloride), CLAFEN (cyclophosphamide), CLOFAREX (clofarabine), CLOLAR (clofarabine), CVP, CYTOSAR-U (cytarabine), CYTOXAN (cyclophosphamide), ERWINAZE (asparaginase erwinia chrysogenum), FLUDARA (fludarabine phosphate), FOLEX (methotrexate), FOLEX PFS (methotrexate), GAZYVA (obinutuzumab), GLEEVEC (imatinib mesylate), Hyper-CVAD, ICLUSIG (ponatinib hydrochloride), IMBRUVICA (ibrutinib), LEUKERAN (chlorambucil), LINFOLIZIN (chlorambucil), MARQIBO (vincristine sulfate liposome), METHOTREXATE LPF (methotrexate), MEXATE (methotrexate), MEXATE-AQ (methotrexate), Mitoxantrone Hydrochloride, MUSTARGEN (mechlorethamine hydrochloride), MYLERAN (busulfan), NEOSAR (cyclophosphamide), ONCASPAR (pegaspargase), PURINETHOL (mercaptopurine), PURIXAN (mercaptopurine), Rubidomycin (daunorubicin hydrochloride), SPRYCEL (dasatinib), SYNRIBO (omacetaxine mepesuccinate), TARABINE PFS (cytarabine), TASIGNA (nilotinib), TREANDA (bendamustine hydrochloride), TRISENOX (arsenic trioxide), VINCASAR PFS (vincristine sulfate), ZYDELIG (idelalisib) or combinations thereof. In one embodiment, the additional pharmaceutical agent is an anti-lymphoma drug. In one embodiment, the additional medicament is ABITREXATE (methotrexate), ABVD, ABVE, ABVE-PC, ADCETRIS (brentuximab vedotin), ADRIAMYCIN PFS (doxorubicin hydrochloride), ADRIAMYCIN RDF (doxorubicin hydrochloride), AMBOCHLORIN (chlorambucil), AMBOCLORIN (chlorambucil), ARRANON (nelarabine), BEACOPP, BECENUM (carmustine), BELEODAQ (belinostat), BEXXAR (tositumomab and iodine-I 131 tositumomab), BICNU (carmustine), BLENOXANE (bleomycin), CARMUBRIS (carmustine), CHOP, CLAFEN (cyclophosphamide), COPP, COPP-ABV, CVP, CYTOXAN (cyclophosphamide), DEPOCYT (cytarabine liposome), DTIC-DOME (dacarbazine), EPOCH, FOLEX (methotrexate), FOLEX PFS (methotrexate), FOLOTYN (pralatrexate), HYPER-CVAD, ICE, IMBRUVICA (ibrutinib), INTRON A (recombinant intergeron alfa-2b), ISTODAX (romidepsin), LEUKERAN (chlorambucil), LINFOLIZIN (chlorambucil), Lomustine, MATULANE (procarbazine hydrochloride), METHOTREXATE LPF (methotrexate), MEXATE (methotrexate), MEXATE-AQ (methotrexate), MOPP, MOZOBIL (plerixafor), MUSTARGEN (mechlorethamine hydrochloride), NEOSAR (cyclophosphamide), OEPA, ONTAK (denileukin diftitox), OPPA, R-CHOP, REVLIMID (lenalidomine), RITUXAN (rituximab), STANFORD V, TREANDA (bendamustine hydrochloride), VAMP, VELBAN (vinblastine sulfate), VELCADE (bortezomib), VELSAR (vinblastine sulfate), VINCASAR PFS (vinblastine sulfate), ZEVALIN (ibritumomab tiuxetan), ZOLINZA (vorinostat), ZYDELIG (idelalisib) or combinations thereof. In one embodiment, the additional pharmaceutical agent is REVLIMID (lenalidomide), DACOGEN (decitabine), VIDAZA (azacitidine), CYTOSAR-U (cytarabine), IDAMYCIN (idarubicin), CERUBIDINE (daunorubicin), LEUKERAN (chlorambucil), NEOSAR (cyclophosphamide), FLUDARA (fludarabine), LEUSTATIN (cladribine) or combinations thereof. In one embodiment, the additional pharmaceutical agent is ABITREXATE (methotrexate), ABRAXANE (paclitaxel albumin stabilized nanoparticles), AC, AC-T, ADE, ADRIAMYCIN PFS (doxorubicin hydrochloride), ADRUCIL (fluorouracil), AFINITOR (everolimus), AFINITOR DISPERZ (everolimus), ALDARA (imiquimod), ALIMTA (pemetrexed disodium), AREDIA (pamidronate disodium), ARIMIDEX (anastrozole), AROMASIN (exemestane), AVASTIN (bevacizumab), BECENUM (carmustine), BEP, BICNU (carmustine), BLENOXANE (bleomycin), CAF, CAMPTOSAR (irinotecan hydrochloride), CAPOX, CAPRELSA (vandetanib), CARBOPLATIN-TAXOL, CARMUBRIS (carmustine), CASODEX (bicalutamide), CEENU (lomustine), CERUBIDINE (daunorubicin hydrochloride), CERVARIX (recombinant HPV bivalent vaccine), CLAFEN (cyclophosphamide), CMF, COMETRIQ (carbatinib-s-malate), COSMEGEN (dactinomycin), CYFOS (ifosfamide), CYRAMZA (ramucirumab), CYTOSAR-U (cytarabine), CYTOXAN (cyclophosphamide), DACOGEN (decitabine), DEGARELIX, DOXIL (doxorubicin hydrochloride liposome), Doxorubicin Hydrochloride, DOX-SL (doxorubicin hydrochloride liposome), DTIC-DOME (dacarbazine), EFUDEX (fluorouracil), ELLENCE (epirubicin hydrochloride), ELOXATIN (oxaliplatin), ERBITUX (cetuximab), ERIVEDGE (vismodegib), ERIVEDGE (etoposide phosphate), EVACET (doxorubicin hydrochloride liposome), FARESTON (toremifene), FASLODEX (fulvestrant), FEC, FEMARA (letrozole), FLUOROPLEX (fluorouracil), FOLEX (methotrexate), FOLEX PFS (methotrexate), FOLFIRI, FOLFIRI-BEVACIZUMAB, FOLFIRI-CETUXIMAB, FOLFIRINOX, FOLFOX, FU-LV, GARDASIL (recombinant human papillomavirus (HPV) quadrivalent vaccine), GEMCITABINE-CISPLATIN, GEMCITABINE-OXALIPLATIN, GEMZAR (gemcitabine hydrochloride), GILOTRIF (alfatinib dimaleate), GLEEVEC (imatinib mesylate), GLIADEL (carmustine implant), GLIADEL WAFER (carmustine implant), HERCEPTIN (trastuzumab), HYCAMTIN (topotecan hydrochloride), IFEX (ifosfamide), IFOSFAMIDUM (ifosfamide), INLYTA (axitinib), INTRON A (recombinant interferon alfa-2b), IRESSA (gefitinib), IXEMPRA (ixapione), JAKAFI (ruxolitinib phosphate), JEVTANA (cabazitaxel), KADCYLA (ado-trastuzumab emtansine), KEYTRUDA (pembrolizumab), KYPROLIS (carfilzomib), LIPODOX (doxorubicin hydrochloride liposome), LUPRON (leuprorelin acetate), LUPRON DEPOT (leuprorelin acetate), LUPRON DEPOT-3 MONTH (leuprorelin acetate), LUPRON DEPOT-4 MONTH (leuprorelin acetate), LUPRON DEPOT-PED (leuprorelin acetate), MEGACE (megestrol acetate), MEKINIST (trametinib), METHAZOLASTONE (temozolomide), METHOTREXATE LPF (methotrexate), MEXATE (methotrexate), MEXATE-AQ (methotrexate), Mitoxantrone Hydrochloride, MITOZYTREX (mitomycin-c), MOZOBIL (plerixafor), MUSTARGEN (mechlorethamine hydrochloride), MUTAMYCIN (mitomycin-c), MYLOSAR (azacitidine), NAVELBINE (vinorelbine tartrate), NEOSAR (cyclophosphamide), NEXAVAR (sorafenib tosylate), NOLVADEX (tamoxifen citrate), NOVALDEX (tamoxifen citrate), OFF, PAD, PARAPLAT (carboplatin), PARAPLATIN (carboplati), PEG-INTRON (peginterferon alfa-2b), Pemetrexed Disodium, PERJETA (pertuzumab), PLATINOL (cisplatin), PLATINOL-AQ (cisplatin), POMALYST (pomalidomide), Prednisone, PROLEUKIN (aldesleukin), PROLIA (denosumab), PROVENGE (sipuleucel-t), REVLIMID (lenalidomide), RUBIDOMYCIN (daunorubicin hydrochloride), SPRYCEL (dasatinib), STIVARGA (regorafenib), SUTENT (sunitinib malate), SYLATRON (peginterferon alfa-2b), SYLVANT (cetuximab), SYNOVIR (thalidomide), TAC, TAFINLAR (dabrafenib), TARABINE PFS (cytarabine), TARCEVA (erlotinib hydrochloride), TASIGNA (nilotinib), TAXOL (paclitaxel), TAXOTERE (docetaxel), TEMODAR (temozolomide), THALOMID (thalidomide), TOPOSAR (etoposide), TORISEL (temsirolimus), TPF, TRISENOX (arsenic trioxide), TYKERB (lapatinib ditosylate), VECTIBIX (panitumumab), VEIP, VELBAN (vinblastine sulfate), VELCADE (bortezomib), VELSAR (vinblastine sulfate), VEPESID (etoposide), VIADUR (leuprorelin acetate), VIDAZA (azacitidine), VINCASAR PFS (vincristine sulfate), VOTRIENT (pazopanib hydrochloride), WELLCOVORIN (leucovorin calcium), XALKORI (crizotinib), XELODA (capecitabine), XELOX, XGEVA (denosumab), XOFIGO (radium 223 dichloride), XTANDI (enzalutamide), YERVOY (ipilimumab), ZALTRAP (ziv-aflibercept), ZELBORAF (vemurafenib), ZOLADEX (goserelin acetate), ZOMETA (zoledronic acid), ZYKADIA (ceritinib), ZYTIGA (abiraterone acetate) or combinations thereof.

In one embodiment, the additional pharmaceutical agent is an antiviral agent. In one embodiment, the additional pharmaceutical agent is selected from epigenetic or transcriptional modulators (e.g., DNA methyltransferase inhibitors, histone deacetylase inhibitors (HDAC inhibitors), lysine methyltransferase inhibitors), anti-mitotic drugs (e.g., taxanes and vinca alkaloids), hormone receptor modulators (e.g., estrogen receptor modulators and androgen receptor modulators), cell signaling pathway inhibitors (e.g., tyrosine kinase inhibitors), modulators of protein stability (e.g., proteasome inhibitors), Hsp90 inhibitors, glucocorticoids, all-trans retinoic acids, and other agents that promote differentiation. In one embodiment, compounds or pharmaceutical compositions of the present disclosure may be administered in combination with anti-cancer therapy including, but not limited to, surgery, radiation therapy, transplantation (e.g., stem cell transplantation, bone marrow transplantation), immunotherapy and chemotherapy.

EXAMPLES

The following examples are provided to provide those skilled in the art with a complete disclosure and description of how to implement, prepare and evaluate the methods and compounds claimed herein, and are intended to be illustrative only and not limiting the scope of the invention.

The preparation protocol of the compound disclosed herein is shown, for example, in Scheme 1.

The compound of formula I could be prepared according to the general scheme as shown above. Firstly, the compound (1) is reacted with ethanol in the presence of the catalyst 4-methylbenzenesulfonic acid, to afford the enol ether intermediate (2), which is reacted with N,N-dimethylformamide dimethyl acetal to get the enamine intermediate (3). (3) is reacted with alkylhydrazine hydrochloride to form an pyrazole ring to afford intermediate (4). After that, the resulting product is once again reacted with N,N-dimethylformamide dimethyl acetal to afford enamine intermediate (5). Then, (5) is reacted with S-methylisothiourea hydrochloride to form a pyrimidine ring, to give a tricyclic intermediate (6). (6) is reacted with manganese oxide to form the aromatic intermediate (7). (7) may be reacted with N-bromosuccimide in the presence of catalyst AIBN to prepare (8). (8) is subjected to a corresponding cross-coupling reaction under the catalyst of Palladium, respectively, to obtain (9), (10), (11) and (12). The methylthio group in intermediate (7-12) is oxidized with Davis oxidant to afford methylsulfinyl intermediate (13). The compound (13) is coupled with amine (14), to afford the compound of formula (I).

Example 1

Preparation of 1-isopropyl-N-(5-(piperazin-1-yl)pyridin-2-yl)-1H-pyrazolo[4,3-h]quinazolin-8-amine hydrochloride (I-1)

1-Isopropyl-1,4,5,6-tetrahydro-7H-indazol-7-one (4a)

A crude intermediate 3 (25 g, 128.2 mmol) was dissolved in methanol (500 mL), to which glacial acetic acid (50 mL) and isopropylhydrazine hydrochloride (42.5 g, 384.6 mmol) were added at room temperature, and the mixture was stirred at this temperature for 10 hours. After completion of the reaction, the mixture was concentrated under reduced pressure to remove most of the solvent, and the resulting residue was isolated by flash silica gel column chromatography (petroleum ether: ethyl acetate=10:1) to afford a white solid as the title compound 4a (18.5 g, 103.8 mmol, S1%). ¹H NMR (400 MHz, chloroform-d, ppm) δ 7.37 (s, 1H), 5.44 (p, J=6.6 Hz, 1H), 2.75 (t, J=6.1 Hz, 2H), 2.55 (dd, J=7.1, 5.6 Hz, 2H), 2.09 (p, J=6.3 Hz, 2H), 1.46 (d, J=6.6 Hz, 6H).

(Z)-6-((dimethylamino)methylene)-1-isopropyl-1,4,5,6-tetrahydro-7H-indazol-7-one (5a)

A solution of 4a (18 g, 101.1 mmol) and N,N-dimethylformamide dimethyl acetal (67.1 mL, 505.3 mmol) in N,N-dimethylformamide (200 mL) was stirred at 120° C. for 13 hours. After the reaction mixture was cooled to room temperature, it was concentrated under reduced pressure to afford a brown oil as the title compound 5a (20.5 g, 87.9 mmol, 87%) as a crude, which can be used in the next reaction without further purification. LC-MS (ESI), for C₁₃H₂₀N₃O [M+H]⁺: m/z=234.2.

1-Isopropyl-8-(methylthio)-4,5-dihydro-1H-pyrazolo[4,3-H]quinazoline (6a)

5a (20 g, 85.8 mmol) and S-methylisothiourea sulfate (73.6 g, 257.4 mmol) were suspended in N,N-dimethylformamide (600 mL), and the mixture was heated to 110° C., and stirred for 16 hours. After the reaction mixture was cooled to room temperature, it was concentrated under reduced pressure to remove most of the solvent. The resulting residue was diluted by adding ethyl acetate (300 mL) and water (500 mL), and the water layer was separated, and extracted with ethyl acetate (3×150 mL). The organic phases were combined, washed with brine (2×100 mL), dried over anhydrous sodium fulfate, filtered, concentrated, and the resulting residue was purified by flash silica gel column chromatography (petroleum ether/ethyl acetate=1:1 to 0:1) to afford a brown solid as the title compound 6a (9.6 g, 36.9 mmol, 43%). ¹H NMR (400 MHz, chloroform-d, ppm) δ 8.32 (s, 1H), 7.41 (s, 1H), 5.84 (p, J=6.6 Hz, 1H), 2.86 (dd, J=8.1, 5.9 Hz, 2H), 2.78 (ddd, J=8.5, 6.3, 1.7 Hz, 2H), 2.19 (s, 3H), 1.56 (d, J=6.6 Hz, 6H). LC-MS (ESI), for C₁₃H₁₇N₄S [M+H]⁺: m/z=261.2.

1-Isopropyl-8-(methylthio)-1H-pyrazolo[4,3-H]quinazoline (7a)

6a (9.5 g, 36.5 mmol) was dissolved in acetonitrile (150 mL), to which 2-iodoxybenzoic acid (20.4 g, 73.0 mmol) was added, and the mixture was heated to 75° C., and stirred for 16 hours. After the reaction mixture was cooled to room temperature, it was filtered, and concentrated. The resulting residue was purified by flash column chromatography to afford a light yellow solid as the title compound 7a (7.64 g, 29.6 mmol, 81%). ¹H NMR (600 MHz, chloroform-d, ppm) δ 9.24 (s, 1H), 8.11 (s, 1H), 7.66 (d, J=8.5 Hz, 1H), 7.43 (d, J=8.6 Hz, 1H), 6.34 (p, J=6.7 Hz, 1H), 2.35 (s, 3H), 1.70 (d, J=6.6 Hz, 6H). LC-MS (ESI), for C₁₃H₁₅N₄S [M+H]⁺: m/z=259.1.

1-Isopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13a)

7a (7.3 g, 28.3 mmol) was dissolved in chloroform (150 mL), to which 2-phenylsulfonyl-3-phenyloxaziridine (8.9 g, 34.0 mmol) was added, and the mixture was stirred at room temperature for 18 hours. The mixture was concentrated, and the crude was purified by flash column chromatography (petroleum ether/acetone=2:1 to 0:1) to afford an off-white solid as the title compound 13a (7.1 g, 25.8 mmol, 91%). LC-MS (ESI), for C₁₃H₁₅N₄OS [M+H]⁺: m/z=275.1.

Tert-butyl 4-(6-((1-isopropyl-1H-pyrazolo[4,3-H]quinazolin-8-yl)amino)pyridin-3-yl)piperazine-1-carboxylate (I-1a)

13a (82.2 mg, 0.3 mmol) and tert-butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate 14a (83.5 mg, 0.3 mmol) were suspended in xylene (0.6 mL), the atmosphere was replaced with argon for 3 times, and the mixture was heated to 130° C. for 21 hours. After the reaction mixture was cooled to room temperature, a small amount of ethyl acetate was added, and the stirring was continued for about 2 hours, during which period a yellow solid was precipitated out from the reaction mixture. The mixture was suction filtered, and the resulting residue was washed with petroleum ether/ethyl acetate (2:1, 2×2 mL), dried in vacuum to afford a light yellow powder as the title compound I-1a (30.7 mg, 21.1%). ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.18 (s, 1H), 8.44 (s, 1H), 8.33 (d, J=9.0 Hz, 1H), 8.16-8.04 (m, 2H), 7.56 (d, J=8.5 Hz, 1H), 7.41-7.31 (m, 2H), 6.42 (hept, J=6.6 Hz, 1H), 3.74-3.55 (m, 4H), 3.25-3.04 (m, 4H), 1.69 (d, J=6.6 Hz, 7H), 1.50 (s, 9H).

1-Isopropyl-N-(5-(piperazin-1-yl)pyridin-2-yl)-1H-pyrazolo[4,3-H]quinazolin-8-amine hydrochloride (I-1)

I-1a (20 mg, 0.041 mmol) was dissolved in dichloromethane/methanol (1:1, 2 mL), to which HCl (4M, 1,4-dioxane solution, 0.82 mL) was added, and the mixture was stirred at room temperature for 3 hours. After that, it was concentrated under reduced pressure, and the resulting crude was stirred in ethyl acetate for 1 hour, filtered, to afford a yellow powder as the title compound I-1 (17.2 mg, 99%). ¹H NMR (400 MHz, water-d₂, ppm) δ 9.19 (s, 1H), 7.94 (s, 1H), 7.78 (d, J=9.4 Hz, 1H), 7.59 (d, J=8.6 Hz, 1H), 7.48 (d, J=8.6 Hz, 1H), 7.35 (s, 1H), 7.01 (d, J=9.4 Hz, 1H), 5.90 (dq, J=13.1, 6.2 Hz, 1H), 3.62-3.47 (m, 4H), 3.47-3.31 (m, 4H), 1.60 (d, J=6.6 Hz, 6H).

TABLE 1
Examples I-2 to I-34
Side chains	Products	Side chains	Products

By referring to the synthetic method of I-1 in Example 1, compounds I-2 (12.9 mg, 29.4 μmol, 21%), I-3 (11.7 mg, 26.6 μmol, 19%), I-10 (11.1 mg, 25.2 μmol, 18%), I-11 (13.6 mg, 30.8 μmol, 22%), I-12 (10.4 mg, 23.8 μmol, 17%), I-13 (14.6 mg, 32.2 μmol, 23%), I-14 (12.7 mg, 28.8 μmol, 20%), I-22 (9.8 mg, 22.4 μmol, 16%), I-25 (8.4 mg, 18.2 μmol, 13%), I-26 (5.8 mg, 12.6 μmol, 9%), and I-27 (4.7 mg, 9.8 μmol, 7%) were prepared from 13a (39.0 mg, 0.14 mmol) and 14 series (2 equiv.).

By referring to the synthetic method of I-1a in Example 1, compounds I-4 (14.6 mg, 36.4 μmol, 26%), I-5 (18.1 mg, 43.4 μmol, 31%), I-6 (15.7 mg, 37.8 μmol, 27%), I-7 (19.2 mg, 46.2 μmol, 33%), I-8 (18.1 mg, 42.0 μmol, 30%), I-9 (15.7 mg, 36.4 μmol, 26%), I-15 (15.8 mg, 40.6 μmol, 29%), I-16 (16.4 mg, 40.6 μmol, 29%), I-17 (18.7 mg, 44.8 μmol, 32%), I-18 (12.4 mg, 30.8 μmol, 22%), I-19 (14.1 mg, 35.0 μmol, 25%), I-20 (14.6 mg, 35.0 μmol, 25%), I-21 (11.7 mg, 28.0 μmol, 20%), I-23 (18.4 mg, 47.6 μmol, 34%), I-24 (5.4 mg, 12.6 μmol, 9%), I-28 (6.7 mg, 15.4 μmol, 11%), I-29 (5.1 mg, 11.2 μmol, 8%), I-30 (3.2 mg, 7.0 μmol, 5%), I-31 (6.5 mg, 12.6 μmol, 9%), I-32 (11.8 mg, 30.8 μmol, 22%), I-33 (7.9 mg, 21.0 μmol, 15%), and I-34 (9.4 mg, 23.8 μmol, 17%) were prepared from 13a (39.0 mg, 0.14 mmol) and 14 series (2 equiv.).

I-2 ¹H NMR (400 MHz, water-d₂, ppm) δ 9.26 (s, 1H), 7.98 (d, J=9.0 Hz, 1H), 7.87 (s, 1H), 7.65-7.54 (m, 2H), 7.12 (d, J=9.1 Hz, 1H), 5.95 (dd, J=13.5, 7.1 Hz, 1H), 3.61 (t, J=4.9 Hz, 4H), 3.33 (d, J=5.0 Hz, 4H), 2.58 (s, 3H), 1.66 (d, J=6.6 Hz, 6H).

I-3 ¹H NMR (400 MHz, water-d₂, ppm) δ 9.23 (s, 1H), 7.94 (s, 1H), 7.69-7.45 (m, 3H), 6.79 (s, 1H), 5.93 (p, J=6.6 Hz, 1H), 3.53 (t, J=5.0 Hz, 4H), 3.22 (d, J=5.0 Hz, 4H), 2.38 (s, 3H), 1.60 (d, J=6.7 Hz, 6H).

I-4 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.30 (d, J=9.0 Hz, 1H), 8.13-8.06 (m, 3H), 7.56 (d, J=8.6 Hz, 1H), 7.39-7.31 (m, 2H), 6.43 (p, J=6.7 Hz, 1H), 3.23 (t, J=5.0 Hz, 4H), 2.63 (t, J=4.9 Hz, 4H), 2.39 (s, 3H), 1.69 (d, J=6.6 Hz, 6H).

I-5 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.22 (s, 1H), 8.17 (s, 1H), 8.10 (s, 1H), 8.07 (s, 1H), 7.58 (d, J=8.6 Hz, 1H), 7.35 (d, J=8.6 Hz, 1H), 6.45 (q, J=6.6 Hz, 1H), 3.72 (q, J=7.1 Hz, 1H), 3.04 (t, J=4.8 Hz, 4H), 2.63 (s, 3H), 2.43 (s, 3H), 2.40 (s, 3H), 1.70 (d, J=6.6 Hz, 6H).

I-6 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.18 (d, J=8.7 Hz, 1H), 8.08 (s, 1H), 7.99 (s, 1H), 7.56 (d, J=8.6 Hz, 1H), 7.43 (d, J=8.7 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 6.42 (p, J=6.7 Hz, 1H), 3.02-2.88 (m, 4H), 2.62 (s, 4H), 2.51 (s, 3H), 2.39 (s, 3H), 1.68 (d, J=6.6 Hz, 6H).

I-7 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.30 (d, J=9.0 Hz, 1H), 8.16 (s, 1H), 7.56 (d, J=8.6 Hz, 1H), 7.39-7.32 (m, 2H), 6.43 (p, J=6.7 Hz, 1H), 3.24 (t, J=5.0 Hz, 4H), 2.67 (t, J=5.0 Hz, 4H), 2.51 (q, J=7.2 Hz, 2H), 1.70 (s, 3H), 1.68 (s, 3H), 1.15 (t, J=7.2 Hz, 3H).

I-8 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.21 (s, 1H), 8.12-8.05 (m, 3H), 7.58 (d, J=8.5 Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 6.45 (p, J=6.7 Hz, 1H), 3.05 (t, J=4.7 Hz, 4H), 2.65 (s, 3H), 2.53 (q, J=7.2 Hz, 2H), 2.43 (s, 3H), 1.71 (s, 3H), 1.69 (s, 3H), 1.16 (t, J=7.2 Hz, 3H).

I-9 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.18 (d, J=8.6 Hz, 1H), 8.08 (s, 1H), 8.00 (s, 1H), 7.56 (d, J=8.6 Hz, 1H), 7.44 (d, J=8.6 Hz, 1H), 7.33 (d, J=8.6 Hz, 1H), 6.42 (dt, J=13.2, 6.8 Hz, 1H), 2.98 (t, J=4.6 Hz, 4H), 2.66 (s, 4H), 2.53 (d, J=7.5 Hz, 5H), 1.68 (d, J=6.7 Hz, 6H), 1.16 (t, J=7.2 Hz, 3H).

I-10a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.22 (s, 1H), 8.29 (s, 1H), 8.14 (s, 1H), 8.09 (d, J=3.5 Hz, 2H), 7.61 (d, J=8.6 Hz, 1H), 7.38 (d, J=8.6 Hz, 1H), 6.30 (dt, J=13.3, 6.5 Hz, 1H), 3.73-3.59 (m, 4H), 3.24 (d, J=4.4 Hz, 4H), 1.65 (d, J=6.6 Hz, 6H), 1.50 (s, 9H).

I-10 LC-MS (ESI), for C₂₁H₂₄FN₈ [M+H]⁺: m/z=407.2, 408.1.

I-11a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.22 (s, 1H), 8.21 (d, J=8.4 Hz, 1H), 8.11 (d, J=4.8 Hz, 2H), 7.60 (d, J=8.6 Hz, 1H), 7.45-7.32 (m, 2H), 6.39 (p, J=6.7 Hz, 1H), 3.71-3.52 (m, 4H), 3.14-2.95 (m, 4H), 1.70 (d, J=6.7 Hz, 6H), 1.50 (s, 9H).

I-11 LC-MS (ESI), for C₂₁H₂₄FN₈ [M+H]⁺: m/z=407.2, 408.2.

I-12a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.34-8.29 (m, 1H), 8.09 (s, 1H), 8.06 (s, 1H), 8.05-8.03 (m, 1H), 7.57 (d, J=8.6 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 6.42 (p, J=6.7 Hz, 1H), 4.40 (s, 1H), 4.01 (d, J=13.2 Hz, 1H), 3.72 (d, J=6.7 Hz, 1H), 3.46 (d, J=11.5 Hz, 1H), 3.35-3.25 (m, 2H), 2.97 (dd, J=11.7, 3.9 Hz, 1H), 2.79 (td, J=11.7, 3.5 Hz, 1H), 1.70 (d, J=6.6 Hz, 6H), 1.50 (s, 10H), 1.36 (d, J=6.8 Hz, 3H).

I-12 LC-MS (ESI), for C₂₂H₂₇N₈ [M+H]⁺: m/z=403.3.

I-13a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.31 (d, J=9.0 Hz, 1H), 8.18-8.01 (m, 3H), 7.57 (d, J=8.6 Hz, 1H), 7.39-7.29 (m, 2H), 6.43 (dt, J=13.3, 6.7 Hz, 1H), 4.35-4.22 (m, 2H), 3.31 (d, J=11.6 Hz, 2H), 2.94 (dd, J=11.7, 4.1 Hz, 2H), 1.70 (d, J=6.7 Hz, 5H), 1.51 (s, 8H), 1.41 (d, J=6.8 Hz, 6H).

I-13 LC-MS (ESI), for C₂₃H₂₉N₈ [M+H]⁺: m/z=417.2.

I-14a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.13 (s, 1H), 8.25 (d, J=9.0 Hz, 1H), 8.08 (s, 1H), 7.96-7.88 (m, 2H), 7.55 (d, J=8.6 Hz, 1H), 7.33 (d, J=8.6 Hz, 1H), 7.15 (dd, J=9.1, 3.0 Hz, 1H), 6.43 (p, J=6.6 Hz, 1H), 3.84-3.79 (m, 2H), 3.72 (dd, J=6.8, 3.4 Hz, 3H), 3.39 (t, J=5.6 Hz, 2H), 3.27 (s, 2H), 1.70 (s, 3H), 1.68 (s, 3H), 1.51 (s, 9H), 1.47 (s, 6H).

I-14 LC-MS (ESI), for C₂₃H₂₉N₈ [M+H]⁺: m/z=417.2.

I-15 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.32 (d, J=9.0 Hz, 1H), 8.09 (s, 1H), 8.05 (d, J=2.9 Hz, 1H), 8.01 (s, 1H), 7.57 (d, J=8.6 Hz, 1H), 7.38-7.31 (m, 2H), 6.42 (p, J=6.7 Hz, 1H), 3.96-3.87 (m, 4H), 3.23-3.14 (m, 4H), 1.69 (d, J=6.7 Hz, 6H).

I-16 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.17 (s, 1H), 8.32 (d, J=9.1 Hz, 2H), 8.08 (s, 2H), 7.56 (d, J=8.5 Hz, 1H), 7.34 (dd, J=8.7, 4.3 Hz, 2H), 6.43 (dt, J=13.3, 6.6 Hz, 1H), 4.09-4.01 (m, 1H), 3.90-3.76 (m, 2H), 3.40 (dd, J=19.4, 11.6 Hz, 2H), 2.89 (td, J=11.5, 3.2 Hz, 1H), 2.55 (t, J=10.8 Hz, 1H), 1.70 (d, J=6.6 Hz, 6H), 1.29 (d, J=6.3 Hz, 3H).

I-17 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.31 (d, J=9.1 Hz, 1H), 8.25 (s, 1H), 8.14-7.96 (m, 2H), 7.56 (d, J=8.5 Hz, 1H), 7.43-7.29 (m, 2H), 6.43 (dt, J=13.2, 6.7 Hz, 1H), 3.86 (dd, J=8.9, 5.1 Hz, 2H), 3.40 (d, J=10.7 Hz, 2H), 2.48 (t, J=11.0 Hz, 2H), 1.70 (d, J=6.6 Hz, 6H), 1.30 (d, J=6.3 Hz, 6H).

I-18 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.21 (d, J=8.7 Hz, 1H), 8.09 (s, 1H), 8.03 (s, 1H), 7.57 (d, J=8.6 Hz, 1H), 7.42 (d, J=8.7 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 6.43 (p, J=6.7 Hz, 1H), 3.94-3.83 (m, 4H), 3.72 (q, J=7.2 Hz, 1H), 2.97-2.89 (m, 4H), 2.53 (s, 3H), 1.69 (d, J=6.6 Hz, 6H).

I-19 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.21 (d, J=8.7 Hz, 1H), 8.09 (s, 1H), 8.02 (s, 1H), 7.57 (d, J=8.6 Hz, 1H), 7.42 (d, J=8.7 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 6.43 (p, J=6.6 Hz, 1H), 3.96-3.84 (m, 4H), 2.95-2.88 (m, 4H), 2.53 (s, 3H), 1.69 (d, J=6.6 Hz, 6H).

I-20 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.17 (s, 1H), 8.22 (d, J=13.8 Hz, 2H), 8.10 (s, 1H), 8.05 (s, 1H), 7.58 (d, J=8.6 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 6.44 (dt, J=13.2, 6.6 Hz, 1H), 3.99 (d, J=11.9 Hz, 1H), 3.90-3.78 (m, 2H), 2.96 (q, J=11.0, 10.3 Hz, 3H), 2.70-2.62 (m, 1H), 2.44 (s, 3H), 1.70 (d, J=6.6 Hz, 6H), 1.24 (d, J=6.3 Hz, 3H).

I-21 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.20 (d, J=8.7 Hz, 1H), 8.08 (s, 1H), 8.03 (s, 1H), 7.57 (d, J=8.6 Hz, 1H), 7.40 (d, J=8.7 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 6.43 (dt, J=13.1, 6.6 Hz, 1H), 3.99 (d, J=10.8 Hz, 1H), 3.91-3.78 (m, 2H), 2.98-2.82 (m, 3H), 2.63-2.45 (m, 4H), 1.70 (d, J=6.6 Hz, 6H), 1.24 (d, J=6.3 Hz, 3H).

I-22a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.12 (s, 1H), 8.20 (d, J=9.1 Hz, 1H), 8.07 (s, 1H), 8.03 (s, 1H), 7.91 (s, 1H), 7.53 (d, J=8.6 Hz, 1H), 7.32 (d, J=8.6 Hz, 1H), 7.11 (dd, J=9.1, 2.8 Hz, 1H), 6.43 (p, J=6.7 Hz, 1H), 3.60 (dd, J=11.8, 5.6 Hz, 6H), 3.38 (t, J=5.2 Hz, 1H), 3.28 (t, J=6.0 Hz, 1H), 2.02 (h, J=6.4 Hz, 2H), 1.68 (d, J=6.7 Hz, 6H), 1.42 (d, J=20.8 Hz, 9H).

I-22 LC-MS (ESI), for C₂₂H₂₇N₈ [M+H]⁺: m/z=403.3.

I-23 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.14 (s, 1H), 8.27 (d, J=9.1 Hz, 1H), 8.10-8.03 (m, 3H), 7.55 (d, J=8.6 Hz, 1H), 7.38-7.35 (m, 1H), 7.35-7.32 (m, 1H), 6.43 (p, J=6.7 Hz, 1H), 3.26-3.09 (m, 4H), 1.76 (q, J=5.8 Hz, 4H), 1.69 (d, J=6.6 Hz, 6H), 1.65-1.55 (m, 6H).

I-24 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.14 (s, 1H), 8.29 (d, J=9.0 Hz, 1H), 8.10-8.03 (m, 3H), 7.56 (d, J=8.6 Hz, 1H), 7.37 (dd, J=9.1, 3.0 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 6.43 (p, J=6.7 Hz, 1H), 3.79-3.62 (m, 3H), 2.78 (td, J=12.1, 2.4 Hz, 2H), 2.37 (s, 7H), 2.01 (d, J=12.5 Hz, 2H), 1.75 (t, J=6.0 Hz, 2H), 1.69 (d, J=6.7 Hz, 6H).

I-25a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.20 (d, J=8.7 Hz, 1H), 8.08 (s, 1H), 8.05 (s, 1H), 7.57 (d, J=8.6 Hz, 1H), 7.39 (d, J=8.7 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 6.42 (p, J=6.6 Hz, 1H), 3.61 (t, J=4.9 Hz, 4H), 2.87 (t, J=4.9 Hz, 4H), 2.53 (s, 3H), 1.69 (d, J=6.6 Hz, 6H), 1.50 (s, 9H).

I-25 LC-MS (ESI), for C₂₄H₂₉N₈ [M+H]⁺: m/z=429.3.

I-26a ¹H NMR (600 MHz, chloroform-d, ppm) δ 9.12 (s, 1H), 8.23 (d, J=8.8 Hz, 1H), 8.08 (s, 1H), 7.94 (s, 1H), 7.65 (d, J=2.8 Hz, 1H), 7.54 (d, J=8.5 Hz, 1H), 7.33 (d, J=8.5 Hz, 1H), 6.88 (dd, J=8.8, 2.9 Hz, 1H), 6.42 (p, J=6.7 Hz, 1H), 3.70 (s, 4H), 3.43 (t, J=5.5 Hz, 4H), 1.82 (t, J=5.5 Hz, 4H), 1.68 (d, J=6.6 Hz, 6H), 1.47 (s, 9H).

I-26 LC-MS (ESI), for C₂₄H₂₉N₈ [M+H]⁺: m/z=429.3.

I-27a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.11 (s, 1H), 8.19 (d, J=8.9 Hz, 1H), 8.07 (s, 1H), 7.88 (s, 1H), 7.73 (s, 1H), 7.53 (d, J=8.6 Hz, 1H), 7.32 (d, J=8.6 Hz, 1H), 6.95 (dd, J=9.0, 2.9 Hz, 1H), 6.44 (dt, J=13.5, 6.7 Hz, 1H), 3.62-3.32 (m, 6H), 3.20 (s, 2H), 1.95 (t, J=6.9 Hz, 2H), 1.68 (d, J=6.6 Hz, 4H), 1.63 (d, J=6.8 Hz, 6H), 1.48 (s, 9H).

I-27 LC-MS (ESI), for C₂₅H₃₁N₈ [M+H]⁺: m/z=443.3.

I-28 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.17 (s, 1H), 8.40 (d, J=9.0 Hz, 1H), 8.10 (t, J=4.2 Hz, 3H), 7.59 (d, J=8.5 Hz, 1H), 7.42-7.33 (m, 2H), 6.40 (dt, J=12.9, 6.3 Hz, 1H), 3.84-3.74 (m, 4H), 3.26-3.15 (m, 4H), 1.70 (d, J=6.7 Hz, 6H).

I-29 ¹H NMR (400 MHz, DMSO-d₆, ppm) δ 10.03 (s, 1H), 9.36 (s, 1H), 8.22 (s, 1H), 8.15 (s, 1H), 8.06 (s, 1H), 7.66 (d, J=8.5 Hz, 1H), 7.51 (d, J=8.5 Hz, 1H), 6.42-6.35 (m, 2H), 3.45-3.37 (m, 4H), 2.40 (s, 3H), 1.58 (d, J=6.6 Hz, 6H).

I-30 LC-MS (ESI), for C₂₂H₂₆N₇O₂S [M+H]⁺: m/z=452.2.

I-31 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.25 (s, 1H), 8.65 (s, 1H), 8.55 (d, J=8.6 Hz, 1H), 8.47 (d, J=2.2 Hz, 1H), 8.11 (s, 1H), 7.85 (dd, J=8.7, 2.2 Hz, 1H), 7.64 (d, J=8.5 Hz, 1H), 7.39 (d, J=8.6 Hz, 1H), 6.39 (p, J=6.6 Hz, 1H), 4.79-4.55 (m, 1H), 4.12-3.90 (m, 1H), 3.28-2.77 (m, 3H), 2.76-2.37 (m, 8H), 2.30 (s, 3H), 2.01-1.88 (m, 2H), 1.71 (d, J=6.7 Hz, 6H), 1.60-1.49 (m, 2H).

I-32 LC-MS (ESI), for C₂₂H₂₁N₆O [M+H]⁺: m/z=385.2.

I-33 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.07 (s, 1H), 7.96 (s, 1H), 7.39 (d, J=8.6 Hz, 1H), 7.24 (d, J=8.6 Hz, 1H), 7.06 (dt, J=9.5, 4.6 Hz, 1H), 6.90-6.78 (m, 1H), 5.73 (s, 1H), 5.58 (d, J=8.4 Hz, 1H), 4.10 (d, J=10.0 Hz, 2H), 3.94-3.85 (m, 2H), 2.57-2.48 (m, 1H), 2.10 (m, 1H), 1.52 (s, 6H).

I-34 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.05 (s, 1H), 7.95 (s, 1H), 7.38 (d, J=8.6 Hz, 1H), 7.22 (d, J=9.3 Hz, 1H), 7.04 (d, J=7.8 Hz, 1H), 6.94 (d, J=10.0 Hz, 1H), 6.92-6.86 (m, 1H), 5.65 (s, 1H), 5.33 (s, 1H), 4.08 (s, 2H), 3.91 (q, J=9.2, 8.7 Hz, 2H), 3.21 (s, 2H), 2.50 (q, J=9.0 Hz, 2H), 2.07 (m, 2H), 1.51 (s, 6H).

Preparation of Intermediate 1-cyclopentyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13b)

By referring to the synthetic method of 13a in Example 1, the compound 13b (0.76 g, 2.53 mmol, 19%) was prepared from 3 (2.6 g, 13.3 mmol) via five reaction steps. LC-MS (ESI), for C₁₅H₁₇N₄OS [M+H]⁺: m/z=301.1.

TABLE 2
Examples I-35 to I-44
Side chains	Products	Side chains	Products

By referring to the synthetic method of I-1 in Example 1, compounds I-35 (15.5 mg, 34.5 μmol, 23%), I-36 (13.3 mg, 28.5 μmol, 19%/), and I-37 (10.4 mg, 22.5 μmol, 15%) were prepared from 13b (45.0 mg, 0.15 mmol) and 14 series (2 equiv.).

By referring to the synthetic method of I-1a in Example 1, compounds I-38 (12.8 mg, 30.0 μmol, 20%/), I-39 (17.2 mg, 39.0 μmol, 26%), I-40 (21.2 mg, 46.5 μmol, 31%), I-41 (13.0 mg, 28.5 μmol, 19%/), I-42 (11.8 mg, 28.5 μmol, 19%/), I-43 (13.5 mg, 31.5 μmol, 21%), and I-44 (10.3 mg, 24.0 μmol, 16%) were prepared from 13b (45.0 mg, 0.15 mmol) and 14 series (2 equiv.).

I-35 ¹H NMR (400 MHz, methanol -d₄, ppm) δ 9.54 (s, 1H), 8.20 (s, 1H), 8.10 (s, 1H), 7.85 (d, J=8.7 Hz, 1H), 7.65 (d, J=8.7 Hz, 1H), 7.51 (s, 1H), 6.70-6.60 (m, 1H), 3.46 (dd, J=6.5, 3.4 Hz, 4H), 3.32 (d, J=5.5 Hz, 4H), 2.61 (s, 3H), 2.34 (dtd, J=13.1, 8.7, 7.8, 3.8 Hz, 2H), 2.27-2.12 (m, 2H), 2.12-1.96 (m, J=5.0 Hz, 2H), 1.86 (dtd, J=12.0, 7.5, 3.4 Hz, 2H).

I-36 ¹H NMR (400 MHz, methanol -d₄, ppm) δ 9.54 (s, 1H), 8.20 (s, 1H), 8.10 (s, 1H), 7.85 (d, J=8.7 Hz, 1H), 7.65 (d, J=8.7 Hz, 1H), 7.51 (s, 1H), 6.70-6.60 (m, 1H), 3.46 (dd, J=6.5, 3.4 Hz, 4H), 3.32 (d, J=5.5 Hz, 4H), 2.61 (s, 3H), 2.34 (dtd, J=13.1, 8.7, 7.8, 3.8 Hz, 2H), 2.27-2.12 (m, 2H), 2.12-1.96 (m, J=5.0 Hz, 2H), 1.86 (dtd, J=12.0, 7.5, 3.4 Hz, 2H).

I-37a ¹H NMR (600 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.19 (d, J=8.6 Hz, 1H), 8.08 (s, 1H), 8.00 (s, 1H), 7.56 (d, J=8.5 Hz, 1H), 7.38 (d, J=8.7 Hz, 1H), 7.34 (d, J=8.5 Hz, 1H), 6.58 (p, J=7.6 Hz, 1H), 3.64-3.59 (m, 4H), 2.91-2.84 (m, 4H), 2.53 (s, 3H), 2.32-2.23 (m, 4H), 2.06 (ddd, J=9.4, 6.5, 3.6 Hz, 2H), 1.80 (q, J=6.0 Hz, 2H), 1.50 (s, 11H).

I-37 LC-MS (ESI), for C₂₄H₂₉N₈[M+H]⁺: m/z=429.3.

I-38 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.14 (s, 1H), 8.28 (d, J=9.1 Hz, 1H), 8.07 (s, 2H), 8.02 (s, 1H), 7.55 (dd, J=8.6, 2.9 Hz, 1H), 7.33 (dt, J=5.9, 2.6 Hz, 2H), 6.58 (dd, J=9.1, 6.4 Hz, 1H), 3.22 (t, J=3.4 Hz, 4H), 2.64 (d, J=5.4 Hz, 4H), 2.39 (d, J=2.8 Hz, 3H), 2.26 (d, J=8.4 Hz, 4H), 2.04 (s, 2H), 1.79 (s, 2H).

I-39 ¹H NMR (600 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.28 (d, J=9.0 Hz, 1H), 8.14 (s, 1H), 8.09 (d, J=3.0 Hz, 1H), 8.07 (s, 1H), 7.55 (d, J=8.5 Hz, 1H), 7.37-7.31 (m, 2H), 6.59 (p, J=7.6 Hz, 1H), 3.24 (t, J=5.0 Hz, 4H), 2.68 (t, J=5.0 Hz, 4H), 2.52 (q, J=7.2 Hz, 2H), 2.31-2.22 (m, 4H), 2.05 (dt, J=10.0, 4.4 Hz, 2H), 1.79 (q, J=6.1 Hz, 2H), 1.16 (t, J=7.2 Hz, 3H).

I-40 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.17 (d, J=8.7 Hz, 1H), 8.06 (d, J=8.8 Hz, 2H), 7.55 (d, J=8.5 Hz, 1H), 7.44 (d, J=8.7 Hz, 1H), 7.33 (d, J=8.6 Hz, 1H), 6.59 (p, J=7.7 Hz, 1H), 2.98 (t, J=4.7 Hz, 4H), 2.83-2.57 (m, 4H), 2.53 (d, J=7.7 Hz, 5H), 2.26 (tt, J=12.9, 6.2 Hz, 4H), 2.10-1.98 (m, 2H), 1.85-1.72 (m, 2H), 1.16 (t, J=7.2 Hz, 3H).

I-41 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.20 (s, 2H), 8.07 (d, J=4.4 Hz, 2H), 7.57 (d, J=8.5 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 6.64-6.55 (m, 1H), 3.06 (t, J=4.7 Hz, 4H), 2.87-2.59 (m, 4H), 2.55 (q, J=7.2 Hz, 2H), 2.41 (s, 3H), 2.34-2.19 (m, 4H), 2.09-1.97 (m, 2H), 1.78-1.73 (m, 2H), 1.17 (t, J=7.2 Hz, 3H).

I-42 ¹H NMR (600 MHz, chloroform-d, ppm) δ 9.15 (s, 1H), 8.31 (d, J=9.0 Hz, 1H), 8.08 (s, 1H), 8.06 (d, J=3.0 Hz, 1H), 8.04 (s, 1H), 7.56 (d, J=8.5 Hz, 1H), 7.35-7.31 (m, 2H), 6.59 (p, J=7.6 Hz, 1H), 3.94-3.89 (m, 4H), 3.19-3.15 (m, 4H), 2.27 (p, J=6.7 Hz, 4H), 2.06 (q, J=6.4 Hz, 2H), 1.80 (t, J=6.1 Hz, 2H).

I-43 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.19 (d, J=8.7 Hz, 1H), 8.06 (d, J=7.1 Hz, 2H), 7.56 (d, J=8.6 Hz, 1H), 7.41 (d, J=8.7 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 6.59 (p, J=7.6 Hz, 1H), 3.96-3.80 (m, 4H), 2.99-2.84 (m, 4H), 2.53 (s, 3H), 2.26 (ddt, J=9.7, 7.5, 3.7 Hz, 4H), 2.12-2.00 (m, 2H), 1.80 (dqt, J=11.9, 8.0, 4.0 Hz, 2H).

I-44 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.18 (s, 1H), 8.34 (s, 1H), 8.22 (s, 1H), 8.08 (d, J=3.0 Hz, 2H), 7.57 (d, J=8.5 Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 6.59 (p, J=7.0 Hz, 1H), 4.02-3.73 (m, 4H), 3.11-2.86 (m, 4H), 2.42 (s, 3H), 2.36-2.19 (m, J=7.4, 6.8 Hz, 4H), 2.11-1.94 (m, 2H), 1.84-1.69 (m, 2H).

Preparation of Intermediate 1-ethyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13c)

By referring to the synthetic method of 13a in Example 1, the compound 13c (0.53 g, 2.05 mmol, 21%) was prepared from 3 (1.9 g, 9.74 mmol) via five reaction steps. ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.21 (s, 1H), 8.06 (s, 1H), 7.63 (d, J=8.6 Hz, 1H), 7.40 (d, J=8.6 Hz, 1H), 5.16 (q, J=7.2 Hz, 2H), 2.52 (s, 3H), 1.60 (t, J=7.2 Hz, 3H); LC-MS (ESI), for C₁₂H₁₃N₄OS [M+H]⁺: m/z=261.1.

TABLE 3
Examples I-45 to I-52
Side chains	Products	Side chains	Products

By referring to the synthetic method of I-a in Example 1, compounds -45 (6.8 mg, 16.5 μmol, 11%), I-46 (12.2 mg, 28.5 μmol, 19%), and I-47 (8.4 mg, 19.5 μmol, 13%) were prepared from 13c (39.0 mg, 0.15 mmol) and 14 series (2 equiv.).

By referring to the synthetic method of I-1a in Example 1, compounds I-48 (12.1 mg, 30.0 μmol, 20%), I-49 (14.4 mg, 34.5 μmol, 23%), I-50 (12.4 mg, 33.0 μmol, 22%), I-51 (15.7 mg, 39.0 μmol, 26%), and I-52 (11.1 mg, 28.5 μmol, 19%) were prepared from 13c (39.0 mg, 0.15 mmol) and 14 series (2 equiv.).

I-45a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.36 (d, J=9.0 Hz, 1H), 8.26 (s, 1H), 8.08 (d, J=2.9 Hz, 1H), 8.05 (s, 1H), 7.56 (d, J=8.6 Hz, 1H), 7.41-7.32 (m, 2H), 5.19 (q, J=7.2 Hz, 2H), 3.73-3.52 (m, 4H), 3.23-3.04 (m, 4H), 1.65-1.59 (m, 6H), 1.50 (s, 9H).

I-45 LC-MS (ESI), for C₂₀H₂₃N₈[M+H]⁺: m/z=375.2.

I-46a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.23 (s, 1H), 8.30 (s, 1H), 8.15 (s, 1H), 8.12 (s, 1H), 8.06 (s, 1H), 7.60 (d, J=8.6 Hz, 1H), 7.38 (d, J=8.6 Hz, 1H), 5.16 (q, J=7.2 Hz, 2H), 3.75-3.57 (m, 4H), 3.32-3.14 (m, 4H), 1.56 (t, J=7.2 Hz, 3H), 1.51 (s, 9H).

I-46 LC-MS (ESI), for C₂₀H₂₂FN₈ [M+H]⁺: m/z=393.2, 394.1.

I-47 LC-MS (ESI), for C₂₀H₂₂FN₈ [M+H]⁺: m/z=393.1, 394.2.

I-48 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.37-8.24 (m, 2H), 8.09 (d, J=2.9 Hz, 1H), 8.04 (s, 1H), 7.55 (d, J=8.6 Hz, 1H), 7.41-7.30 (m, 2H), 5.19 (q, J=7.2 Hz, 2H), 3.32-3.15 (m, 4H), 2.75-2.58 (m, 4H), 2.51 (q, J=7.2 Hz, 2H), 1.61 (t, J=7.2 Hz, 3H), 1.15 (t, J=7.2 Hz, 3H).

I-49 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.17 (s, 1H), 8.40 (s, 1H), 8.25 (s, 1H), 8.11 (s, 1H), 8.06 (s, 1H), 7.57 (d, J=8.6 Hz, 1H), 7.35 (d, J=8.6 Hz, 1H), 5.23 (q, J=7.2 Hz, 2H), 3.05 (t, J=4.7 Hz, 4H), 2.65 (s, 3H), 2.52 (q, J=7.2 Hz, 2H), 2.41 (s, 3H), 1.61 (t, J=7.2 Hz, 3H), 1.15 (t, J=7.2 Hz, 3H).

I-50 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.17 (s, 1H), 8.36 (d, J=9.1 Hz, 2H), 8.09 (d, J=2.8 Hz, 1H), 8.05 (s, 1H), 7.56 (d, J=8.5 Hz, 1H), 7.42-7.31 (m, 2H), 5.19 (q, J=7.2 Hz, 2H), 4.00-3.83 (m, 4H), 3.25-3.09 (m, 4H), 1.62 (t, J=7.2 Hz, 3H).

I-51 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.25 (s, 2H), 8.07 (d, J=9.4 Hz, 2H), 7.57 (d, J=8.6 Hz, 1H), 7.36 (d, J=8.6 Hz, 1H), 5.24 (q, J=7.2 Hz, 2H), 3.03 (t, J=4.7 Hz, 4H), 2.61 (s, 4H), 2.40 (d, J=10.9 Hz, 6H), 1.61 (t, J=7.2 Hz, 3H).

I-52 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.28 (s, 1H), 8.12 (s, 1H), 8.06 (d, J=4.7 Hz, 2H), 7.58 (d, J=8.6 Hz, 1H), 7.36 (d, J=8.6 Hz, 1H), 5.24 (q, J=7.2 Hz, 2H), 3.94-3.82 (m, 4H), 3.05-2.94 (m, 4H), 2.43 (s, 3H), 1.63 (d, J=7.2 Hz, 3H).

Preparation of Intermediate 1-cyclopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13d)

By referring to the synthetic method of 13a in Example 1, the compound 13d (312.8 mg, 1.15 mmol, 14%) was prepared from 3 (1.6 g, 8.2 mmol) via five reaction steps. ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.31 (d, J=1.8 Hz, 1H), 8.16 (s, 1H), 8.02 (d, J=8.7 Hz, 1H), 7.74 (d, J=8.7 Hz, 1H), 4.11 (td, J=7.1, 3.6 Hz, 1H), 2.44 (s, 3H), 1.41 (dd, J=8.0, 6.0 Hz, 2H), 1.22-1.14 (m, 2H). LC-MS (ESI), for C₁₃H₁₃N₄OS [M+H]⁺: m/z=273.1.

TABLE 4
Examples I-53 to I-60
Side chains	Products	Side chains	Products

By referring to the synthetic method of I-1 in Example 1, compounds I-53 (8.2 mg, 19.5 μmol, 15%), and I-54 (7.4 mg, 16.9 μmol, 13%) were prepared from 13d (35.0 mg, 0.13 mmol) and 14 series (2 equiv.).

By referring to the synthetic method of I-1a in Example 1, compounds I-55 (10.2 mg, 24.7 μmol, 19%), I-56 (9.7 mg, 23.4 μmol, 18%), I-57 (12.8 mg, 29.9 μmol, 23%), I-58 (10.6 mg, 27.3 μmol, 21%), I-59 (10.4 mg, 26.0 μmol, 20%), and I-60 (12.0 mg, 29.9 μmol, 23%) were prepared from 13d (35.0 mg, 0.13 mmol) and 14 series (2 equiv.).

I-53 ²H NMR (400 MHz, water-d₂, ppm) δ 9.07 (s, 1H), 7.82 (d, J=4.6 Hz, 1H), 7.71 (s, 1H), 7.57-7.47 (m, 1H), 7.39 (d, J=9.4 Hz, 1H), 7.31 (s, 1H), 6.99 (s, 1H), 4.51-4.45 (p, J=6.7 Hz, 1H), 3.49 (s, 4H), 3.41 (s, 4H), 1.27 (d, J=7.2 Hz, 2H), 1.18 (s, 2H).

I-54 ²H NMR (400 MHz, chloroform-d, ppm) δ 9.23 (s, 1H), 8.28 (s, 1H), 8.14 (s, 1H), 7.99 (s, 1H), 7.59 (d, J=8.6 Hz, 1H), 7.39 (d, J=8.6 Hz, 1H), 5.00 (tt, J=7.6, 4.0 Hz, 1H), 3.69-3.62 (m, 4H), 3.21 (s, 4H), 1.51 (s, 10H), 1.46-1.41 (m, 3H), 1.20 (tt, J=7.7, 4.2 Hz, 2H).

I-55 ²H NMR (400 MHz, chloroform-d, ppm) δ 9.23 (s, 1H), 8.28 (s, 1H), 8.14 (s, 1H), 7.99 (s, 1H), 7.59 (d, J=8.6 Hz, 1H), 7.39 (d, J=8.6 Hz, 1H), 5.00 (tt, J=7.6, 4.0 Hz, 1H), 3.69-3.62 (m, 4H), 3.21 (s, 4H), 1.51 (s, 10H), 1.46-1.41 (m, 3H), 1.20 (tt, J=7.7, 4.2 Hz, 2H).

I-56 ²H NMR (400 MHz, chloroform-d, ppm) δ 9.09 (s, 1H), 8.39 (s, 1H), 7.92 (q, J=7.9, 5.2 Hz, 2H), 7.50 (d, J=8.6 Hz, 1H), 7.31 (d, J=8.6 Hz, 1H), 4.89 (d, J=8.9 Hz, 1H), 3.65-3.51 (m, 2H), 3.31 (d, J=8.0 Hz, 4H), 3.19 (s, 4H), 1.44-1.34 (m, 2H), 1.19-1.13 (m, 5H).

I-57 ²H NMR (400 MHz, chloroform-d, ppm) δ 9.18 (s, 1H), 8.36 (s, 1H), 8.19 (s, 1H), 8.08 (s, 1H), 7.98 (s, 1H), 7.56 (d, J=8.6 Hz, 1H), 7.37 (d, J=8.6 Hz, 1H), 5.10 (tt, J=7.6, 3.9 Hz, 1H), 3.08 (s, 4H), 2.71 (s, 2H), 2.58 (d, J=7.4 Hz, 2H), 2.30 (d, J=0.7 Hz, 2H), 1.52-1.43 (m, 2H), 1.28-1.17 (m, 5H).

I-58 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.50 (d, J=9.1 Hz, 1H), 8.02 (d, J=2.9 Hz, 1H), 7.98 (s, 1H), 7.55 (d, J=8.6 Hz, 1H), 7.36 (d, J=8.6 Hz, 1H), 7.29 (dd, J=9.2, 2.9 Hz, 1H), 5.02 (tt, J=7.5, 3.9 Hz, 1H), 3.95-3.85 (m, 4H), 3.20-3.13 (m, 4H), 1.48 (td, J=5.3, 4.5, 3.1 Hz, 2H), 1.23-1.19 (m, 2H).

I-59 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.19 (s, 1H), 8.39 (s, 1H), 8.34 (s, 1H), 8.05 (s, 1H), 7.98 (s, 1H), 7.57 (d, J=8.6 Hz, 1H), 7.37 (d, J=8.6 Hz, 1H), 5.09 (tt, J=7.6, 3.9 Hz, 1H), 3.98-3.79 (m, 4H), 3.09-2.89 (m, 4H), 2.33 (s, 3H), 1.52-1.41 (m, 2H), 1.23-1.18 (m, 2H).

I-60 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.49 (d, J=9.1 Hz, 1H), 8.19 (s, 1H), 8.02 (d, J=3.0 Hz, 1H), 7.97 (s, 1H), 7.55 (d, J=8.6 Hz, 1H), 7.36 (d, J=8.6 Hz, 1H), 7.28 (dd, J=9.1, 2.8 Hz, 1H), 5.02 (tt, J=7.6, 3.9 Hz, 1H), 4.05 (ddd, J=11.5, 3.5, 1.4 Hz, 1H), 3.85 (dd, J=11.5, 2.6 Hz, 1H), 3.80 (ddd, J=10.5, 5.9, 2.5 Hz, 1H), 3.40 (dt, J=11.5, 2.1 Hz, 1H), 3.37-3.31 (m, 1H), 2.87 (td, J=11.6, 3.4 Hz, 1H), 2.53 (dd, J=11.5, 10.1 Hz, 1H), 1.28 (d, J=6.3 Hz, 3H), 1.22 (tt, J=7.6, 4.0 Hz, 3H).

Preparation of Intermediate 4-bromo-1-isopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13e)

4-Bromo-1-isopropyl-8-(methylthio)-1H-pyrazolo[4,3-H]quinazoline (8)

7a (2.5 g, 9.69 mmol), N-bromosuccimide (1.7 g, 9.69 mmol) and azobisisobutyronitrile (478.0 mg, 2.91 mmol) were suspended in toluene (100 mL), and the atmosphere was replaced with argon for 3 times. The reaction was heated to 100° C., and stirred for 10 hours. After being concentrated under reduced pressure to remove most of the solvent, the resulting residue was purified by flash silica gel column chromatography (petroleum ether/ethyl acetate=3:1) to afford a light yellow powder as the title compound 8 (682 mg, 2.03 mmol, 21%). ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.22 (s, 1H), 8.19 (s, 1H), 7.67 (s, 1H), 6.26 (p, J=6.6 Hz, 1H), 2.23 (s, 3H), 1.68 (d, J=6.6 Hz, 6H).

4-Bromo-1-isopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13e)

By referring to the synthetic method of 13a, the title compound 13e (532 mg, 1.51 mmol, 78%) was prepared from 8 (650 g, 1.93 mmol) and 2-phenylsulfonyl-3-phenyloxaziridine (605 mg, 2.32 mmol, 1.2 equiv.). LC-MS (ESI), for C₁₃H₁₄BrN₄OS [M+H]⁺: m/z=353.1, 355.1.

TABLE 5
Examples I-61 to I-65
Side chains	Products	Side chains	Products

By referring to the synthetic method of I-1 in Example 1, compounds I-61 (7.8 mg, 15.6 μmol, 13%), and I-62 (6.9 mg, 13.2 μmol, 11%) were prepared from 13e (42.2 mg, 0.12 mmol) and 14 series (2 equiv.).

By referring to the synthetic method of I-1a in Example 1, compounds I-63 (9.8 mg, 20.4 μmol, 17%), I-64 (9.5 mg, 19.2 μmol, 16%), and I-65 (11.8 mg, 25.2 μmol, 21%) were prepared from 13e (42.2 mg, 0.12 mmol) and 14 series (2 equiv.).

I-61 LC-MS (ESI), for C₂₁H₂₄BrN₈ [M+H]⁺: m/z=467.1, 469.1.

I-62 LC-MS (ESI), for C₂₁H₂₃BrFN₈ [M+H]⁺: m/z=485.1, 487.1.

I-63 LC-MS (ESI), for C₂₂H₂₆BrN₈ [M+H]⁺: m/z=481.1, 483.1.

I-64 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.06 (s, 1H), 8.23 (d, J=9.0 Hz, 1H), 8.09 (s, 1H), 8.07 (d, J=2.9 Hz, 1H), 8.03 (s, 1H), 7.51 (s, 1H), 7.35 (dd, J=9.0, 3.0 Hz, 1H), 6.38 (s, 1H), 3.27-3.22 (m, 4H), 2.67 (t, J=5.0 Hz, 3H), 2.51 (d, J=7.3 Hz, 2H), 1.68 (d, J=6.6 Hz, 6H), 1.25 (s, 2H), 1.15 (s, 3H).

I-65 LC-MS (ESI), for C₂₁H₂₃BrN₇O [M+H]⁺: m/z=468.1, 470.1.

Preparation of Intermediate 1-isopropyl-4-methyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13f)

1-Isopropyl-4-methyl-8-(methylthio)-1H-pyrazolo[4,3-H]quinazoline (9) PGP-1

8 (500 mg, 1.49 mmol) was suspended in N,N-dimethylformamide (6 mL), to which trimethylboroxine (3.5M in THF, 2 mL), potassium carbonate (4.3 g, 31.2 mmol), [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) chloride (220.0 mg, 0.30 mmol) and deionized water (3.6 mL) were added sequentially, and the atmosphere was replaced with argon for three times. The reaction mixture was heated to 100° C., and stirred for 10 hours. After cooling to room temperature, the reaction mixture was diluted by adding ethyl acetate (100 mL) and water (150 mL), the organic layer was separated, and the water layer was extracted with ethyl acetate (2×100 mL). The organic layers were combined, washed again with water (50 mL) and brine (50 mL), dried over anhydrous sodium fulfate, suction filtered, and concentrated, the resulting residue was isolated by flash silica gel column chromatography (petroleum ether/ethyl acetate=4:1) to afford a brown powder as the title compound 9 (360 mg, 1.32 mmol, 89%). ¹H NMR (600 MHz, chloroform-d, ppm) δ 9.25 (s, 1H), 8.20 (s, 1H), 6.44 (p, J=6.6 Hz, 1H), 2.74 (s, 3H), 2.43 (s, 3H), 1.79 (d, J=6.7 Hz, 6H).

1-Isopropyl-4-methyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13f)

By referring to the synthetic method of 13a, the title compound 13f (light yellow solid, 340 mg, 1.18 mmol, 90%) was prepared from 9 (355 mg, 1.31 mmol) and 2-phenylsulfonyl-3-phenyloxaziridine (410 mg, 1.57 mmol, 1.2 equiv.). LC-MS (ESI), for C₁₄H₁₇N₄OS [M+H]⁺: m/z=289.1.

TABLE 6
Examples I-66 to I-70
Side chains	Products	Side chains	Products

By referring to the synthetic method of I-1 in Example 1, compounds I-66 (12.6 mg, 28.8 μmol, 20%), and I-67 (13.4 mg, 29.4 μmol, 21%) were prepared from 13f (40.0 mg, 0.14 mmol) and 14 series (2 equiv.).

By referring to the synthetic method of I-1a in Example 1, compounds I-68 (9.3 mg, 22.4 μmol, 16%), I-69 (15.7 mg, 36.4 μmol, 26%), and I-70 (8.5 mg, 21.0 μmol, 15%) were prepared from 13f (40.0 mg, 0.14 mmol) and 14 series (2 equiv.).

I-66 ¹H NMR (400 MHz, water-d₂, ppm) δ 9.03 (s, 1H), 7.97 (s, 1H), 7.82 (s, 1H), 7.43 (s, 1H), 7.14 (brs, 2H), 5.89 (s, 1H), 3.48 (d, J=23.7 Hz, 8H), 1.58 (brs, 6H).

I-67a ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.14 (s, 1H), 8.27 (s, 1H), 8.14 (s, 1H), 8.09 (s, 1H), 7.12 (s, 1H), 6.30 (p, J=6.7 Hz, 1H), 3.67 (t, J=4.7 Hz, 4H), 3.25 (t, J=4.8 Hz, 4H), 2.63 (s, 3H), 1.65 (d, J=6.4 Hz, 6H), 1.50 (s, 9H).

I-67 LC-MS (ESI), for C₂₂H₂₆FN₈ [M+H]⁺: m/z=421.2, 422.2.

I-68 LC-MS (ESI), for C₂₃H₂₉N₈ [M+H]⁺: m/z=417.2.

I-69 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.07 (s, 1H), 8.30 (d, J=9.1 Hz, 1H), 8.08 (s, 1H), 8.06 (d, J=3.0 Hz, 1H), 7.99 (s, 1H), 7.36 (dd, J=9.0, 3.0 Hz, 1H), 7.09 (d, J=1.3 Hz, 1H), 6.42 (p, J=6.7 Hz, 1H), 3.27 (t, J=4.8 Hz, 4H), 2.73 (s, 4H), 2.62 (d, J=1.1 Hz, 3H), 2.58 (d, J=9.0 Hz, 2H), 1.69 (d, J=6.6 Hz, 6H), 1.24 (t, J=7.0 Hz, 3H).

I-70 ¹H NMR (400 MHz, Chloroform-d) δ 9.09 (s, 1H), 8.29 (d, J=17.4 Hz, 2H), 8.08 (s, 1H), 8.06 (d, J=2.9 Hz, 1H), 7.34 (dd, J=9.0, 3.0 Hz, 1H), 7.09 (s, 1H), 6.42 (p, J=6.7 Hz, 1H), 3.91 (t, J=4.7 Hz, 4H), 3.26-3.11 (m, 4H), 2.62 (s, 3H), 1.69 (d, J=6.6 Hz, 6H).

Preparation of Intermediate 1-isopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline-4-carbonitrile (13g)

1-Isopropyl-8-(methylthio)-1H-pyrazolo[4,3-H]quinazoline-4-carbonitrile (10)

8 (360 mg, 1.07 mmol) was dissolved in acetonitrile (10 mL), to which cuprous cyanide (192 mg, 2.14 mmol) and tetrakis(triphenylphosphine)palladium (243 mg, 0.21 mmol) were added, and the atmosphere was replaced with argon for three times. The reaction was heated to 100° C. and stirred for 10 hours. After the reaction mixture was cooled to room temperature, it was suction filtered with celite cake, the filtrate was concentrated, and the resulting residue was isolated by flash silica gel column chromatography (petroleum ether/ethyl acetate=2:1) to afford a yellow powder as the title compound 10 (233 mg, 0.824 mmol, 77%). ²H NMR (600 MHz, chloroform-d, ppm) δ 9.25 (s, 1H), 8.20 (s, 1H), 7.26 (s, 1H), 6.44 (dq, J=13.3, 6.6 Hz, 1H), 2.74 (s, 3H), 2.51 (s, 3H), 1.79 (d, J=6.7 Hz, 6H).

1-Isopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline-4-carbonitrile (13g)

By referring to the synthetic method of 13a, the title compound 13g (light yellow solid, 224 mg, 0.75 mmol, 93%) was prepared from 10 (230 mg, 0.81 mmol) and 2-phenylsulfonyl-3-phenyloxaziridine (254 mg, 0.97 mmol, 1.2 equiv.). LC-MS (ESI), for C₁₄H₁₄N₅OS [M+H]⁺: m/z=300.1.

TABLE 7
Examples I-71 to I-74
Side chains	Products	Side chains	Products

By referring to the synthetic method of I-1 in Example 1, compounds I-71 (4.2 mg, 9.4 μmol, 7%), and I-72 (3.7 mg, 8.0 μmol, 6%) were prepared from 13g (40 mg, 0.134 mmol) and 14 series (2 equiv.).

By referring to the synthetic method of I-1a in Example 1, compounds I-73 (6.5 mg, 14.7 μmol, 11%), and I-74 (5.0 mg, 12.1 μmol, 9%) were prepared from 13g (40 mg, 0.134 mmol) and 14 series (2 equiv.).

I-71 ¹H NMR (400 MHz, methanol -d₄, ppm) δ 9.60 (s, 1H), 8.33 (s, 1H), 8.24 (s, 1H), 8.22 (d, J=3.0 Hz, 1H), 7.88 (d, J=2.9 Hz, 1H), 7.65 (d, J=9.6 Hz, 1H), 6.46 (p, J=6.7 Hz, 1H), 3.89 (t, J=4.8 Hz, 4H), 3.28 (t, J=4.8 Hz, 4H), 1.67 (d, J=6.6 Hz, 6H).

I-72 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.35 (s, 1H), 8.40 (s, 1H), 7.40 (s, 1H), 7.22 (s, 1H), 6.79 (s, 1H), 6.27 (p, J=6.7 Hz, 1H), 3.67 (d, J=5.3 Hz, 4H), 3.20 (d, J=5.3 Hz, 4H), 1.64 (d, J=6.6 Hz, 6H), 1.52 (s, 9H).

I-73 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.16 (s, 1H), 8.20 (s, 1H), 8.18 (d, J=8.5 Hz, 1H), 8.03 (d, J=2.9 Hz, 1H), 7.81 (s, 1H), 7.36 (dd, J=9.1, 2.9 Hz, 1H), 7.30 (s, 1H), 6.33 (p, J=6.7 Hz, 1H), 3.62 (q, J=7.1 Hz, 2H), 3.37-3.32 (m, 4H), 2.74 (brs, 4H), 1.64 (d, J=6.7 Hz, 6H), 1.17 (t, J=7.1 Hz, 3H).

I-74 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.19 (s, 1H), 8.41 (s, 1H), 8.26 (d, J=9.1 Hz, 2H), 8.10 (d, J=2.9 Hz, 1H), 7.80 (s, 1H), 7.36 (dd, J=9.1, 3.0 Hz, 1H), 6.36 (p, J=6.7 Hz, 1H), 3.64 (t, J=5.1 Hz, 4H), 3.16 (t, J=5.1 Hz, 4H), 1.69 (d, J=6.6 Hz, 6H).

Preparation of 4-(1-butoxyvinyl)-1-isopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13h)

4-(1-Butoxyvinyl)-1-isopropyl-8-(methylthio)-1H-pyrazolo[4,3-H]quinazoline (11)

8 (240 mg, 0.45 mmol), vinyl n-butyl ether (0.54 mL, 3.75 mmol), palladium acetate (40 mg, 0.18 mmol), 1,3-bis(diphenylphosphino)propane (82.4 mg, 0.2 mmol) and triethylamine (75 μL, 0.54 mmol) were suspended in 1-butyl-3-methylimidazolium tetrafluoroborate (10 mL), and the atmosphere was sufficiently replaced with argon for 3 times. The reaction was heated to 100° C. and stirred for 10 hours. After the reaction mixture was cooled to room temperature, it was diluted with ethyl acetate (20 mL), suction filtered with celite cake, the filtrate was concentrated, and the resulting residue was isolated by flash silica gel column chromatography (petroleum ether/ethyl acetate=2:1) to afford a brown powder as the title compound 11 (121 mg, 0.34 mmol, 76%). ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.25 (s, 1H), 7.62 (s, 1H), 8.16 (s, 1H), 6.44 (dq, J=13.3, 6.7 Hz, 1H), 4.58 (d, J=2.3 Hz, 1H), 4.37 (d, J=2.4 Hz, 1H), 3.84 (t, J=6.8 Hz, 2H), 2.35 (s, 3H), 1.72 (d, J=6.6 Hz, 6H), 1.69-1.60 (m, 2H), 1.42-1.35 (m, 2H), 0.92 (t, J=7.4 Hz, 3H).

4-(1-Butoxyvinyl)-1-isopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13h)

By referring to the synthetic method of 13a, the title compound 13h (light yellow solid, 142.9 mg, 0.384 mmol, 95%) was prepared from 11 (120 mg, 0.337 mmol) and 2-phenylsulfonyl-3-phenyloxaziridine (106 mg, 0.404 mmol, 1.2 equiv.). LC-MS (ESI), for C₁₉H₂₅N₄O₂S [M+H]⁺: m/z=373.1.

TABLE 8
Examples I-75 to I-79
Side chains	Products	Side chains	Products

By referring to the synthetic method of I-1 in Example 1, compounds I-75 (3.7 mg, 8.0 μmol, 11%), and I-76 (2.5 mg, 5.1 μmol, 7%) were prepared from 13h (27 mg, 72.5 μmol) and 14 series (2 equiv.).

By referring to the synthetic method of I-1a in Example 1, compounds I-77 (4.2 mg, 9.4 μmol, 13%), I-78 (3.7 mg, 8.0 μmol, 11%), and I-79 (4.4 mg, 10.2 μmol, 14%) were prepared from 13h (27 mg, 72.5 μmol) and 14 series (2 equiv.).

I-75 ¹H NMR (400 MHz, methanol -d₄, ppm) δ 9.45 (s, 1H), 8.45 (s, 1H), 8.14 (s, 1H), 8.05 (d, J=3.0 Hz, 1H), 7.81 (d, J=2.9 Hz, 1H), 7.66 (d, J=9.6 Hz, 1H), 6.31 (p, J=6.7 Hz, 1H), 3.83 (t, J=4.8 Hz, 4H), 3.34 (t, J=4.8 Hz, 4H), 2.78 (s, 3H), 1.68 (d, J=6.6 Hz, 6H).

I-76 LC-MS (ESI), for C₂₃H₂₆FN₈O [M+H]⁺: m/z=449.2, 450.2.

I-77 LC-MS (ESI), for C₂₄H₂₉N₈O [M+H]⁺: m/z=445.3.

I-78 ¹H NMR (400 MHz, chloroform-d, ppm) δ 9.26 (s, 1H), 8.21 (s, 1H), 8.10 (d, J=8.5 Hz, 1H), 8.05 (d, J=2.9 Hz, 1H), 7.81 (s, 1H), 7.45 (dd, J=9.1, 2.9 Hz, 1H), 7.33 (s, 1H), 6.26 (p, J=6.7 Hz, 1H), 3.81 (q, J=7.1 Hz, 2H), 3.45 (m, 4H), 3.02 (brs, 4H), 2.71 (s, 3H), 1.65 (d, J=6.7 Hz, 6H), 1.16 (t, J=7.1 Hz, 3H).

I-79 LC-MS (ESI), for C₂₃H₂₆N₇O₂[M+H]⁺: m/z=432.2.

4-(3,5-Dimethoxyphenyl)-1-isopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13i)

8 (200 mg, 0.595 mmol), 3,5-dimethoxyphenyl boronic acid (217 mg, 1.19 mmol), [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride and potassium carbonate (132 mg, 0.18 mmol) were suspended in 1,2-dichloroethane (10 mL), and the atmosphere was sufficiently replaced with argon for 3 times. The reaction was heated to 100° C. and stirred for 10 hours. After the reaction mixture was cooled to room temperature, it was diluted with ethyl acetate (20 mL), suction filtered with celite cake, the filtrate was concentrated, and the resulting residue was isolated by flash silica gel column chromatography (petroleum ether/ethyl acetate=2:1) to afford a brown powder as the title compound 12 (200 mg, 0.51 mmol, 85%). ²H NMR (400 MHz, chloroform-d, ppm) δ 9.28 (s, 1H), 8.24 (s, 1H), 7.46 (s, 1H), 6.86 (d, J=2.4 Hz, 2H), 6.57 (t, J=2.4 Hz, 1H), 6.41 (p, J=7.2 Hz, 1H), 3.88 (s, 6H), 2.34 (s, 3H), 1.72 (d, J=6.6 Hz, 6H).

4-(3,5-Dimethoxyphenyl)-1-isopropyl-8-(methylsulfinyl)-1H-pyrazolo[4,3-H]quinazoline (13i)

By referring to the synthetic method of 13a, the title compound 13i (light yellow solid, 167.0 mg, 0.41 mmol, 85%) was prepared from 12 (180 mg, 0.46 mmol) and 2-phenylsulfonyl-3-phenyloxaziridine (144 mg, 0.55 mmol, 1.2 equiv.). LC-MS (ESI), for C₂₁H₂₃N₄O₃S [M+H]⁺: m/z=411.1.

TABLE 9
Examples I-80 to I-82
Side chains	Products	Side chains	Products

By referring to the synthetic method of I-1 in Example 1, the compound I-80 (6.4 mg, 11.4 μmol, 9%) was prepared from 13i (50 mg, 0.127 mmol) and 14 series (2 equiv.).

By referring to the synthetic method of I-1a in Example 1, compounds I-81 (4.9 mg, 8.9 μmol, 7%), and I-82 (4.7 mg, 8.9 μmol, 7%) were prepared from 13i (50 mg, 0.127 mmol) and 14 series (2 equiv.).

I-80 LC-MS (ESI), for C₂₉H₃₃N₈O₂[M+H]⁺: m/z=525.3.

I-81 LC-MS (ESI), for C₃₁H₃₇N₈O₂[M+H]⁺: m/z=553.3.

I-82 LC-MS (ESI), for C₃₉H₃₂N₇O₃[M+H]⁺: m/z=526.2.

Example 83

Potency determination of biochemical kinase inhibition test. Kinase activity test and IC50 determination. Firstly, 10 ng of recombinant CDK4/Cyclin D1 (Life Technologies PV4204) was diluted in kinase buffer (20 mM Tris pH 7.5, 10 mM MgCl₂, 0.01% NP-40, 2 mM DTT), and was incubated with inhibitors at the indicated concentration at room temperature for 30 minutes. The kinase reaction was initiated by adding 1 μg (1.5 μM) of recombinant retinoblastoma protein, 5 μM ATP and 10μ Ci γ-32P-ATP. The reaction was incubated at 30° C. for 20 minutes, and was terminated by adding 2×Laemmli sample buffer, heated at 95° C. for three minutes, and the resulting solution was dissolved with 12% acrylamide SDS-PAGE and autoradiographed. A densitometer (Bio-Rad) was used to quantify the corresponding phosphorylated substrate protein bands. The resulting density values were plotted as a function of the log drug concentration using Prism 4 Graphpad software. IC50 values were determined by plotting a non-linear regression curve with a variable slope.

The inhibitory activity of the compounds disclosed herein against CDK6/cyclin D1 was tested by a similar method.

Results of the enzyme inhibitory activity of the most representative compounds of the present disclosure are shown in the following table. The compounds were tested in a three-fold serial dilution from the starting concentration of 10 μM, over 10-fold of IC50. The control compound, staurosporine, was tested in a four-fold serial dilution from the starting concentration of 20 μM, over 10-fold of IC50. These reactions took place in the presence of 10 μM ATP.

	compound No.	CDK4/D1 (nM)	CDK6/D1 (nM)
	I-1	<1	<1
	I-2	1-5	1-5
	I-3	5-10	10-20
	I-4	1-5	1-5
	I-5	5-10	10-20
	I-6	1-5	<1
	I-7	1-5	1-5
	I-8	5-10	10-20
	I-9	1-5	<1
	I-10	5-10	10-20
	I-11	1-5	5-10
	I-12	5-10	5-10
	I-13	5-10	5-10
	I-14	10-20	10-20
	I-15	1-5	1-5
	I-16	5-10	5-10
	I-17	5-10	5-10
	I-18	1-5	<1
	I-19	20-50	10-20
	I-20	20-50	20-50
	I-21	5-10	10-20
	I-22	10-20	10-20
	I-23	50-100	50-100
	I-24	20-50	20-50
	I-25	1-5	1-5
	I-26	1-5	1-5
	I-27	20-50	20-50
	I-28	10-20	10-20
	I-29	20-50	20-50
	I-30	10-20	10-20
	I-31	50-100	50-100
	I-32	20-50	20-50
	I-33	50-100	50-100
	I-34	50-100	50-100
	I-35	1-5	1-5
	I-36	10-20	10-20
	I-37	1-5	<1
	I-38	1-5	5-10
	I-39	<1	1-5
	I-40	1-5	1-5
	I-41	10-20	10-20
	I-42	1-5	1-5
	I-43	1-5	1-5
	I-44	10-20	10-20
	I-45	10-20	5-10
	I-46	20-50	10-20
	I-47	10-20	5-10
	I-48	10-20	5-10
	I-49	20-50	10-20
	I-50	10-20	5-10
	I-51	20-50	10-20
	I-52	10-20	10-20
	I-53	10-20	5-10
	I-54	20-50	10-20
	I-55	20-50	10-20
	I-56	10-20	5-10
	I-57	10-20	10-20
	I-58	10-20	5-10
	I-59	10-20	10-20
	I-60	10-20	10-20
	I-61	10-20	10-20
	I-62	20-50	10-20
	I-63	10-20	10-20
	I-64	10-20	10-20
	I-65	10-20	10-20
	I-66	10-20	1-5
	I-67	20-50	10-20
	I-68	10-20	1-5
	I-69	10-20	1-5
	I-70	10-20	10-20
	I-71	10-20	1-5
	I-72	20-50	10-20
	I-73	10-20	1-5
	I-74	10-20	1-5
	I-75	1-5	<1
	I-76	10-20	5-10
	I-77	5-10	<1
	I-78	1-5	<1
	I-79	5-10	<1
	I-80	5-10	1-5
	I-81	5-10	1-5
	I-82	5-10	1-5

It is worth noting that most of the compounds of the present disclosure also have selectivity between CDK6/cyclin D1 and CDK4/cyclin D1 in terms of their enzyme inhibitory activity. For example, the selectivity of compounds I-6, I-9, I-18, I-37, I-75, I-77, I-78 and I-79 for CDK6/cyclin D1 is more than 10 times of that for CDK4/cyclin D1; the selectivity of compounds I-68 and I-69 for CDK6/cyclin D1 is more than 5 times of that for CDK4/cyclin D1; the selectivity of compounds I-45, 1-48, 1-50, 1-56, 1-58, 1-66, I-71, I-73, I-74, I-80, I-81 and I-82 for CDK6/cyclin D1 is about 3 times of that for CDK4/cyclin D1; and the selectivity of compounds I-46, I-47, I-49, I-51, I-53, I-54, I-55, I-62, I-67, I-72 and I-76 for CDK6/cyclin D1 is about 2 times of that for CDK4/cyclin Di.

While the present disclosure has been described in detail with reference to the specific preferred embodiments, it cannot be concluded that the specific embodiments of the present disclosure are limited to these descriptions. Those skilled in the art will appreciate that several simple deductions or substitutions may be made without departing from the spirit of the present disclosure, which should be regarded to be within the scope of the present disclosure.

Claims

1. A compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug, or an isotope variant thereof, and mixtures thereof:

2. A compound of formula (II), or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof:

3. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 2, wherein R2 is selected from H, halogen, CN, C1-6 alkyl, —C(O)Ra, or C6-10 aryl;R3 is selected from the groups consisting of the following:

4. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 2, wherein R2 is selected from H, halogen, —CN, —C(O)Ra, —C(O)ORa, —C(O)NRbRc, C1-6 alkyl, C1-6 haloalkyl, C3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C6-10 aryl, or 5- to 10-membered heteroaryl;R3 is selected from the groups consisting of the following:

5. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 2, wherein R2 is selected from H, halogen, CN, C1-6 alkyl, —C(O)Ra, or C6-10 aryl;R3 is selected from the groups consisting of the following:

6. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 2, wherein R2 is selected from H, —CN, —C(O)Ra, —C(O)ORa, —C(O)NRbRc, C1-6 alkyl, C1-6 haloalkyl, C3-7 cycloalkyl, 3- to 7-membered heterocyclyl, C6-10 aryl, or 5- to 10-membered heteroaryl;R3 is selected from the groups consisting of the following:

7. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 2, wherein R2 is selected from H, CN, C1-6 alkyl, —C(O)Ra, or C6-10 aryl;R3 is selected from the groups consisting of the following:

8. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 2, wherein R2 is selected from —C(O)Ra, —C(O)ORa, or —C(O)NRbRc;R3 is selected from the groups consisting of the following:

9. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 2, wherein R2 is —C(O)Ra;R3 is selected from the groups consisting of the following:

10. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 1, which is a compound of formula (II):

11. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 10, wherein R2 is selected from CN, C1-6 alkyl, —C(O)Ra, or C6-10 aryl;R3 is selected from the groups consisting of the following:

12. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 10, wherein R2 is selected from —C(O)Ra, —C(O)ORa, —C(O)NRbRc, C1-6 alkyl, or C1-6 haloalkyl;R3 is

13. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 10, wherein R2 is selected from —C(O)Ra, —C(O)ORa, —C(O)NRbRc, or C1-6 alkyl;R3 is

14. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 10, wherein R2 is selected from C1-6 alkyl or —C(O)Ra;R3 is

15. A compound of formula (II), or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof:

16. The compound, or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug, or the isotope variant thereof, and mixtures thereof according to claim 15, wherein R2 is H;R3 is selected from the groups consisting of the following:

17. A compound, or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug or a isotope variant thereof according to claim 1, wherein the said compound is selected from the group consisting of:

18. A pharmaceutical composition, comprising a compound according to claim 1, or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug or a isotope variant thereof, and pharmaceutically acceptable excipients; optionally, the pharmaceutical composition further comprises one or more other therapeutic agents.

19. A method of treating and/or preventing a CDK mediated disease in a subject, comprising administering to the subject a compound according to claim 1, or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug or a isotope variant thereof.

20. The method of claim 19, wherein the CDK-mediated diseases comprise cell proliferative disorders, including but are not limited to cancers, cardiovascular disorders, infectious diseases, chronic inflammatory diseases, autoimmune disorders and other cell proliferative disorders; more specifically, the cancers described herein include, but are not limited to, solid tumors and hematological malignancies, such as breast cancer, neuroblastoma, malignant rhabdomyoma, well-differentiated and dedifferentiated liposarcoma, glioma, lung cancer, colorectal cancer, gastric cancer, gastrointestinal stromal tumors (GIST), hepatocellular carcinoma, prostatic tumors, sarcoma, ovarian cancer, cervical cancer, pancreatic cancer, melanoma, thyroid cancer, carcinoma of bile duct, endometrial cancer, renal cancer, mesothelioma, lymphoma, leukemia, non-Hodgkin's lymphoma, mantle cell lymphoma, anaplastic large cell lymphoma, acute myeloid leukemia (AML), and multiple myeloma; more specifically, the cardiovascular disorders described herein are such as restenosis, atherosclerosis, vascular smooth muscle proliferation and intimal hyperplasia secondary to balloon angioplasty, and other vascular disorders caused by abnormal cell proliferation; more specifically, the infectious diseases described herein include infections of fungi, protozoan parasites (such as Plasmodium falciparum), and DNA and RNA virus, such as herpes simplex virus (HSV) infection; more specifically, the chronic inflammatory diseases described herein are such as rheumatoid arthritis; more specifically, other cell proliferative disorders described herein include psoriasis (characterized by excessive proliferation of keratinocytes), glomerulonephritis, lupus, etc.