KIF18A INHIBITOR

Abstract

Disclosed in the present invention is a class of KIF18A inhibitors. Specifically, the present invention relates to a compound of general formula (1), a method for preparing same, and use of the compound of general formula (1) or an isomer thereof, a crystalline form thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof, or a solvate thereof as a KIF18A inhibitor in preparing an anti-tumor medicament.

Description

The present application claims priority to Chinese Patent Application No. 202210266719.4 filed on Mar. 17, 2022, which is incorporated herein by reference in its entirety.

TECHNICAL FIELD

The present invention relates to the field of pharmaceutical chemistry, and particularly to a class of compounds with an inhibitory effect on KIF18A protein, a method for preparing same, and use of the class of compounds in preparing anti-tumor medicaments.

BACKGROUND

Genomic instability is a common feature of most tumor cells. Most tumor cells exhibit abnormal gain or deletion of chromosomes. The chromosome instability of tumor cells leads to the interaction of abnormal chromosomes with mitotic spindle microtubules, which in turn causes chromosome segregation errors. Cells with chromosome instability develop increased spindle microtubule polymerization and reduced spindle microtubule-centromere contact turnover, as compared to cells with normal chromosomes. Therefore, anti-mitotic therapies directed against the microtubule backbone may be particularly effective for cells with chromosome instability.

Kinesins are a class of molecular motors that play important roles in cell division and intracellular vesicle and organelle transport. Mitotic kinesins play important roles in several aspects such as spindle assembly, chromosome segregation, centrosome segregation, and dynamics. Human kinesins are classified into 14 subfamilies based on differences in amino acid sequences of motor domains, and the ATPase activity located in the motor domains drives the proteins to move unidirectionally along the microtubules. The non-motor domains of these proteins are responsible for interacting with substrates, and a variety of different membranous organelles, signal transduction scaffold systems, and chromosomes serve as substrates with which the non-motor domains can interact. The kinesins gain energy through ATP hydrolysis, moving the substrates along polarized microtubules. Therefore, kinesins are commonly referred to as “plus-end” or “minus-end” directed motors.

KIF18A protein belongs to the kinesin-8 subfamily: KIF18A protein is overexpressed in various types of cancers, such as lung, ovarian, cervical, breast, pancreatic, prostate, colon, and bladder cancers. Studies suggest that KIF18A affects the dynamics of the plus-ends of the centromere microtubules so as to control correct chromosome positioning and spindle tension. In tumor cells with chromosome instability, abnormal microtubule dynamics make such cells particularly dependent on KIF18A protein to reduce spindle microtubule-centromere contact turnover and to limit microtubule growth (Nat Commun. 2021, 12, 1213). When KIF18A protein is deleted from tumor cells with chromosome instability, centrosomes of the cells are fragmented and mitotic progression is slowed or stopped. However, these phenomena do not occur in cells with normal chromosomes. Therefore, the activity of KIF18A protein does not have a significant effect on the proliferation of normal cells but is very critical for the growth of chromosomally unstable tumors. Accordingly, the development of KIF18A inhibitors is a new promising approach against tumors with chromosome instability.

SUMMARY

The present invention provides a compound of general formula (1) or an isomer thereof, a crystalline form thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof, or a solvate thereof:

• • wherein in general formula (1):
  • X¹ is —CR⁵═ or N:
  • X² is —CR⁶═ or N:
  • X³ is —CR⁷═ or N:
  • ring A is 7-10 membered cycloalkylene, 7-10 membered heterocycloalkylene, 7-10 membered heteroarylene, or 10-membered arylene, wherein the 7-10 membered cycloalkylene, 7-10 membered heterocycloalkylene, 7-10 membered heteroarylene, or 10-membered arylene may be optionally substituted with 0, 1, 2, or 3 groups selected from H, halogen, —C_1-4 hydrocarbyl, —C_1-4 halohydrocarbyl, or —O—C_1-4 hydrocarbyl; L is —(C═O)—NR³—**** or —NR³—(C═O)—****: **** represents attachment to a

end;

• • R¹ is —CN or —Z—R¹⁰, wherein Z is a chemical bond, —C_0-4 hydrocarbylene-, —NR¹¹—, —NR¹¹SO₂—, —SO₂NR¹¹—, —NR¹¹—S(═O)(═NH)—**, —S(═O)(═NH)—, —S—, —S(═O)—, —SO₂—, —C_0-4 hydrocarbylene-O—**, —(C═O)—, —(C═O)NR¹¹—, —C(═N—OH)—, or —NR¹¹(C═O)—**; or the group —Z—R¹⁰ is —N═S(═O)—(R¹⁰)₂, wherein the two R¹⁰ may be combined with the sulfur atom to which they are each attached to form a saturated or partially saturated 3-, 4-, 5-, or 6-membered monocyclic ring containing 0, 1, 2, or 3 N atoms and 0, 1 or 2 atoms selected from O and S: ** represents attachment to an R¹⁰ end:
  • R² is halogen or a group —Y—R¹², wherein Y is a chemical bond, —C_0-4 hydrocarbylene-, —N(C_0-1 hydrocarbyl)-C_0-4 hydrocarbylene-***, —C(═O)NR^a (C_1-4 hydrocarbyl)-***, —O—C_0-4 hydrocarbylene-***, —S—, —S(═O)—, —SO₂—, —SO₂NR¹²—***, or —S(═O)(═NH)—***: *** represents attachment to an R¹² end;
  • R³ is H or C_1-6 hydrocarbyl;
  • R⁵ is H, halogen, C_1-8 alkyl, or C_1-4 haloalkyl;
  • R⁶ is H, halogen, C_1-8 alkyl, C_1-4 haloalkyl, —OH, —O—R^6a, or —O—R^6b;
  • R⁷ is H, halogen, C_1-8 hydrocarbyl, or C_1-4 halohydrocarbyl;
  • R⁸ is selected from the group consisting of:

• • R^13a, R^13b, R^13c, R^13d, R^13e, R^13f, R^13g, R^13h, R¹³ⁱ, R^13j, R^13k, and R^13l are each independently H, halogen, R^13m, or R¹³ⁿ: or each of the pairs of R^13a/R^13b, R^13c/R^13d, R^13e/R^13f, R^13g/R^13h, R¹³ⁱ/R^13j, and R^13k/R^13l may independently form, with the carbon atom to which they are each attached, a saturated or partially saturated 3-, 4-, 5-, or 6-membered monocyclic ring spiro-linked to R⁸ ring, wherein the 3-, 4-, 5-, or 6-membered monocyclic ring contains 0, 1, 2, or 3 N atoms and 0, 1, or 2 atoms selected from O and S, and further, the 3-, 4-, 5-, or 6-membered monocyclic ring is substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, C_1-6 hydrocarbyl, C_1-4 halohydrocarbyl, —OR^a, —OC_1-4 halohydrocarbyl, CN, —NR^aR^a, and oxo;
  • R¹⁰ is H, R^10a, R^10b, or R^10c;
  • R¹¹ is H, R^11a, or R^11b;
  • R¹² is R^12a or R^12b;
  • R^6a, R^10a, R^11a, R^12a, or R^13m, in each case, is independently selected from a saturated, partially saturated, or unsaturated 3-, 4-, 5-, 6-, or 7-membered monocyclic ring or 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, or 12-membered bicyclic ring containing 0, 1, 2, or 3 N atoms and 0, 1 or 2 atoms selected from O and S, wherein the monocyclic ring and bicyclic ring may be each independently and optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, C_1-6 hydrocarbyl, C_1-4 halohydrocarbyl, —OR^a, —OC_1-4 halohydrocarbyl, CN, —C(═O)R^b, —C(═O)OR^a, —C(═O)NR^aR^a, —C(═NR^a)NR^aR^a, —OC(═O)R^b, —OC(═O)NR^aR^a, —OC_2-6 hydrocarbyl NR^aR^a, —OC_2-6 hydrocarbyl OR^a, —SR^a, —S(═O)R^b, —S(═O)₂R^b, —S(═O)—NR^aR^a, —NR^aR^a, —N(R^a)C(═O)R^b, —N(R^a)C(═O)OR^b, —N(R^a)C(═O)NR^aR^a, —N(R^a)C(═NR^a)NR^aR^a, —N(R^a)S(═O)₂R^b, —N(R^a)S(═O)₂NR^aR^a, —NR^aC_2-6 hydrocarbyl NR^aR^a, —NR^aC_2-6 hydrocarbyl OR^a, —C_1-6 hydrocarbyl NR^aR^a, —C_1-6 hydrocarbyl OR^a, —C_1-6 hydrocarbyl N(R^a)C(═O)R^b, —C_1-6 hydrocarbyl OC(═O)R^b, —C_1-6 hydrocarbyl C(═O)NR^aR^a, —C_1-6 hydrocarbyl C(═O)OR^a, R⁴, and oxo;
  • R^6b, R^10b, R^11b, R^12b, or R¹³ⁿ, in each case, is independently selected from C_1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, 3, 4, or 5 groups selected from F, Cl, Br, —R^a, —OR^a, —OC_1-4 halohydrocarbyl, and CN:

R^10c, in each case, is independently selected from C_1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, 3, 4, or 5 groups selected from F, Cl, Br, —R^a, —R^c, —OR^a, —OC_1-4 halohydrocarbyl, and CN;

• • R⁴, in each case, is independently selected from the group consisting of: a saturated, partially saturated, or unsaturated 3-, 4-, 5-, 6-, or 7-membered monocyclic ring or 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, or 12-membered bicyclic ring containing 0, 1, 2, or 3 N atoms and 0 or 1 atom selected from O and S, wherein the monocyclic ring and bicyclic ring may be each independently and optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, C_1-6 hydrocarbyl, C_1-4 halohydrocarbyl, —OR^a, —OC_1-4 halohydrocarbyl, CN, —C(═O)R^b, —C(═O)OR^a, —C(═O)NR^aR^a, —C(═NR^a)NR^aR^a, —OC(═O)R^b, —OC(═O)NR^aR^a, —OC_2-6 hydrocarbyl NR^aR^a, —OC_2-6 hydrocarbyl OR^a, —SR^a, —S(═O)R^b, —S(═O)₂R^b, —S(═O)₂NR^aR^a, —NR^aR^a, —N(R^a)C(═O)R^b, —N(R^a)C(═O)OR^b, —N(R^a)C(═O)NR^aR^a, —N(R^a)C(═NR^a)NR^aR^a, —N(R^a)S(═O)₂R^b, —N(R^a)S(═O)₂NR^aR^a, —NR^aC_2-6 hydrocarbyl NR^aR^a, —NR^aC_2-6 hydrocarbyl OR^a, —C_1-6 hydrocarbyl NR^aR^a, —C_1-6 hydrocarbyl OR^a, —C_1-6 hydrocarbyl N(R^a)C(═O)R^b, —C_1-6 hydrocarbyl OC(═O)R^b, —C_1-6 hydrocarbyl C(═O)NR^aR^a, —C_1-6 hydrocarbyl C(═O)OR^a, and oxo:
  • R^a, in each case, is independently H or R^b:
  • R^b, in each case, is independently C_1-6 hydrocarbyl, phenyl, or benzyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, or 3 groups selected from halogen, —OH, —OC_1-4 hydrocarbyl, —NH₂, —NHC_1-4 hydrocarbyl, —OC(═O)C_1-4 hydrocarbyl, or —N(C_1-4 hydrocarbyl) C_1-4 hydrocarbyl; and the phenyl and benzyl may be each independently and optionally substituted with 0, 1, 2, or 3 groups selected from halogen, C_1-4 hydrocarbyl, C_1-3 halohydrocarbyl, —OH, —OC_1-4 hydrocarbyl, —NH₂, —NHC_1-4 hydrocarbyl, —OC(═O)C_1-4 hydrocarbyl, or —N(C_1-4 hydrocarbyl) C_1-4 hydrocarbyl; and
  • R^c, in each case, is independently —OC(═O)C_1-5 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 1, 2, or 3 groups selected from —OH or —NH₂.

In another preferred embodiment, the general formula (1) has the following structure:

In another preferred embodiment, in the general formula (1), ring A is 9-10 membered cycloalkylene, 9-10 membered heterocycloalkylene, 9-10 membered heteroarylene, or 10-membered arylene, wherein the 9-10 membered cycloalkylene, 9-10 membered heterocycloalkylene, 9-10 membered heteroarylene, or 10-membered arylene may be optionally substituted with 0, 1, 2, or 3 groups selected from H, F, Cl, Br, —C_1-4 hydrocarbyl, —C_1-4 halohydrocarbyl, or —O—C_1-4 hydrocarbyl.

In another preferred embodiment, in the general formula (1), ring A is:

wherein * represents attachment to an L end; and the groups described above may be optionally substituted with 0, 1, 2, or 3 groups selected from H, F, Cl, Br, —CH₃, —CH₂CH₃, —CF₃, —CH₂CF₃, —OCH₃, or —OCH₂CH₃.

In another preferred embodiment, in the general formula (1), ring A is:

• • wherein * represents attachment to an L end; and the groups described above may be optionally substituted with 0, 1, 2, or 3 groups selected from H, F, Cl, Br, —CH₃, —CH₂CH₃, —CF₃, —CH₂CF₃, —OCH₃, or —OCH₂CH₃.

In another preferred embodiment, in the general formula (1), R³ is H, methyl, or ethyl, preferably H.

In another preferred embodiment, in the general formula (1), R^13c, R^13d, R^13e, R^13f, R^13g, R^13h, R¹³ⁱ, R^13j, R^13k, and R^13l are each independently H, halogen, C_1-6 hydrocarbyl, or C_1-4 halohydrocarbyl; and R^13a and R^13b in a pair of R^13a/R^13b may be combined with the carbon atom to which they are each attached to form a saturated 3-, 4-, or 5-membered monocyclic ring spiro-linked to R⁸ ring, wherein the monocyclic ring contains 0, 1, 2, or 3 N atoms and 0, 1, or 2 atoms selected from O and S; preferably, R^13c, R^13d, R^13e, R^13f, R^13g, R^13h, R¹³ⁱ, R^13j, R^13k, and R^13l are each independently H, methyl, or ethyl; and R^13a and R^13b in the pair of R^13a/R^13b may be combined with the carbon atom to which they are each attached to form a cyclopropyl, cyclobutyl, or cyclopentyl ring spiro-linked to R⁸ ring.

In another preferred embodiment, in the general formula (1), the structural unit

is:

preferably

In another preferred embodiment, in the general formula (1), Z is a chemical bond, —NH—, —NHSO₂—, —SO₂NH—, —S(═O)(═NH)—, —S—, —S(═O)—, —SO₂—, —(C═O)—, —(C═O)NH—, or —NH(C═O)—.

In another preferred embodiment, in the general formula (1), R¹⁰ is selected from: (a) H: or (b) C_1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, —OH, or —OCH₃; (c) a group such that when the group —Z—R¹⁰ is —N═S(═O)—(R¹⁰)₂, the two R¹⁰ may be combined with the sulfur atom to which they are each attached to form a saturated, partially saturated, or unsaturated 3-, 4-, 5-, 6-, or 7-membered monocyclic ring containing 0, 1, 2, or 3 N atoms and 0 or 1 atom selected from O and S, wherein the monocyclic ring is substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, C_1-6 hydrocarbyl, C_1-4 halohydrocarbyl, —C_1-6 hydrocarbylene OH, —OH, —OCH₃, —NH₂, or oxo; or (d) C_1-6 hydrocarbyl, wherein the C_1-6 hydrocarbyl may be optionally substituted with 1, 2, or 3 groups selected from —OC(═O)C_1-5 hydrocarbyl, wherein the C_1-5 hydrocarbyl may be optionally substituted with 1 or 2 groups selected from —OH or —NH₂; and the C_1-6 hydrocarbyl may be optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, —OH, or —OCH₃.

In another preferred embodiment, in the general formula (1), R¹ is —CN or a group —Z—R¹⁰, wherein Z is a chemical bond, —NH—, —NHSO₂—, —SO₂NH—, —S(═O)(═NH)—, —S—, —S(═O)—, —SO₂—, —(C═O)—, —(C═O)NH—, or —NH(C═O)—; and R¹⁰ is selected from:

• • (a) H;
  • (b) cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, oxiranyl, oxetanyl, tetrahydrofuranyl, azetidinyl, imidazolyl, morpholinyl, pyrrolidinyl, piperazinyl,

wherein each of the rings may be independently and optionally substituted with 0, 1, 2, or 3 groups selected from OH, F, methyl, —CH₂OH, —C(═O)OCH₃, —C(═O)OC(CH₃)₃, NH₂, CN, and oxo; preferably oxetanyl or cyclopropyl;

• • (c) C_1-6 hydrocarbyl substituted with 0, 1, 2, or 3 OH, F, —C(═O)OCH₃, —NH₂, —NH(CH₃), or —N(CH₃)₂: preferably C_1-6 hydrocarbyl substituted with 0, 1, 2, or 3 OH groups; and more preferably C_1-6 hydrocarbyl substituted with 1 OH group; or
  • (d) C_1-6 hydrocarbyl, wherein the C_1-6 hydrocarbyl may be optionally substituted with 1, 2 or 3 groups selected from

and the C_1-6 hydrocarbyl may be optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, —OH, or —OCH₃.

In another preferred embodiment, in the general formula (1), the group —Z—R¹⁰ is —N═S(═O)—(R¹⁰)₂, wherein the two R¹⁰ may be combined with the sulfur atom to which they are each attached to form a saturated or partially saturated 3-, 4-, 5-, or 6-membered monocyclic ring containing 0, 1, 2, or 3 N atoms and 0, 1, or 2 atoms selected from O and S; preferably, the group —Z—R¹⁰ is selected from

In another preferred embodiment, in the general formula (1), R¹ is a group —Z—R¹⁰, wherein Z is —NHSO₂— or —SO₂NH—; and R¹⁰ is oxetanyl or cyclopropyl; or R¹⁰ is C_1-6 hydrocarbyl substituted with 0, 1, 2, or 3 OH groups; or R¹⁰ is C_1-6 hydrocarbyl, wherein the C_1-6 hydrocarbyl may be optionally substituted with 1, 2 or 3 groups selected from

In another preferred embodiment, in the general formula (1), R¹⁰ is selected from C_1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, or 3 groups selected from

preferably

Z is —NHSO₂— or —SO₂NH—; and Z is preferably —NHSO₂—.

In another preferred embodiment, in the general formula (1), R¹⁰ is selected from C_1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 1, 2, or 3 groups selected from

Z is —NHSO₂— or —SO₂NH—.

In another preferred embodiment, in the general formula (1), R² is halogen or a group —Y—R¹², wherein Y is a chemical bond, —NH—, —NH—(CH₂)_0-4—, or —O—(CH₂)_0-4—; and R¹² is a saturated, partially saturated, or unsaturated 3-, 4-, 5-, 6-, or 7-membered monocyclic ring or 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, or 12-membered bicyclic ring containing 0, 1, 2, or 3 N atoms and 0 or 1 atom selected from O and S, wherein the monocyclic ring and bicyclic ring may be each independently and optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, C_1-6 hydrocarbyl, C_1-4 halohydrocarbyl, —OH, —OC_1-4 halohydrocarbyl, CN, R¹⁴, and oxo; or R¹² is C_1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, 3, 4, or 5 groups selected from F, Cl, Br, —OH, —OC_1.4 halohydrocarbyl, or CN.

In another preferred embodiment, in the general formula (1), R² is a saturated 5- or 6-membered monocyclic ring, wherein each of the rings contains 0, 1, or 2 N atoms and 0 or 1 O atom, and each of the rings is substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, C_1-6 hydrocarbyl, C_1.4 halohydrocarbyl, —OH, —OC_1-4 halohydrocarbyl, CN, R¹⁴, and oxo.

In another preferred embodiment, in the general formula (1), R² is: (a) halogen; (b) a group —Y—R¹², wherein Y is a chemical bond; and R¹² is morpholinyl, piperidinyl, azetidinyl, pyrrolidinyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, piperazinyl, tetrahydrofuranyl,

wherein each of the rings is substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, methyl, CF₃, —OH, —OCHF₂, CN, and oxo; or (c) a group —Y—R¹², wherein Y is —NH—, —O—, —O—(CH₂)—, —O—(CH₂)—(CH₂)—, or —O—(CH₂)—(CH₂)—(CH₂)—, and R¹² is

or R¹² is C_1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, 3, 4, or 5 groups selected from F, Cl, Br, methyl, CF₃, —OH, or CN.

In another preferred embodiment, in the general formula (1), R² is morpholinyl or piperidinyl, wherein the morpholinyl and piperidinyl may be optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, methyl, CF₃, —OH, —OCHF₂, and CN.

In another preferred embodiment, in the general formula (1), R² is piperidinyl substituted with 1, 2, or 3 fluorine groups.

In another preferred embodiment, in the general formula (1), R² is:

In another preferred embodiment, in the general formula (1), R² is morpholinyl substituted with 1, 2, or 3 methyl groups.

In another preferred embodiment, in the general formula (1), R² is

In another preferred embodiment, in the general formula (1), R¹⁰ is selected from cyclopropyl, cyclobutyl, cyclopentyl, oxetanyl, azetidinyl, tetrahydrofuranyl, and 1,3,4-oxathiazinanyl.

In another preferred embodiment, in the general formula (1), R⁵ is H or F, preferably H.

In another preferred embodiment, in the general formula (1), R⁶ is H or F, preferably H.

In another preferred embodiment, in the general formula (1), R⁷ is H.

In various different embodiments of the present invention, the compound of general formula (1) has one of the following structures:

In various different embodiments of the present invention, the compound of general formula (1) also has one of the following structures:

The present invention is further intended to provide a pharmaceutical composition comprising a pharmaceutically acceptable carrier, diluent, and/or excipient, as well as the compound of general formula (1) or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof of the present invention as an active ingredient.

The present invention is still further intended to provide use of the compound of general formula (1) or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof of the present invention or the pharmaceutical composition described above in preparing a medicament for treating, regulating, or preventing a disease related to KIF18A protein.

The present invention is even further intended to provide a method for treating, regulating, or preventing a related disease mediated by KIF18A protein, comprising administering to a subject a therapeutically effective amount of the compound of general formula (1) or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof of the present invention or the pharmaceutical composition described above.

Through synthesis and careful studies of various classes of new compounds with KIF18A protein inhibitory effects, the inventors have discovered that the compound of general formula (1) has surprisingly strong KIF18A protein inhibition activity.

It should be understood that both the aforementioned general description and the following detailed description of the present invention are exemplary and explanatory, and are intended to provide further explanation of the present invention claimed.

Synthesis of Compounds 35

Methods for preparing the compound of general formula (1) of the present invention are specifically described below, but these specific methods do not limit the present invention in any way.

The compound of general formula (1) described above may be synthesized using standard synthetic techniques or well-known techniques in combination with the methods described herein. In addition, the solvents, temperatures, and other reaction conditions mentioned herein may vary. Starting materials for the synthesis of the compounds may be obtained synthetically or commercially. The compounds described herein and other related compounds with different substituents may be synthesized using well-known techniques and starting materials, including the methods found in March, ADVANCED ORGANIC CHEMISTRY, 4^th Ed., (Wiley 1992): Carey and Sundberg, ADVANCED ORGANIC CHEMISTRY, 4^th Ed., Vols. A and B (Plenum 2000, 2001); and Green and Wuts, PROTECTIVE GROUPS IN ORGANIC SYNTHESIS, 3^rd Ed., (Wiley 1999). General methods for preparing the compounds may be altered by using appropriate reagents and conditions for introducing different groups into the molecular formulas provided herein.

In one aspect, the compounds described herein are prepared according to methods well known in the art. However, the conditions of the methods, such as reactants, solvents, bases, the amount of the compound used, reaction temperature, and time required for the reaction are not limited to the following explanation. The compounds of the present invention may also be conveniently prepared by optionally combining various synthetic methods described herein or known in the art, and such combinations may be easily determined by those skilled in the art to which the present invention pertains. In one aspect, the present invention further provides a method for preparing the compound of general formula (1), wherein the compound of general formula (1) may be prepared by the following general reaction scheme 1, 2, 3, or 4

• • Embodiments of the compound of general formula (1) may be prepared according to general reaction scheme 1, wherein R¹, R², ring A, R⁸, X¹, X², and X³ are as defined above: W¹ represents fluorine, chlorine, bromine, or iodine; H represents hydrogen; N represents nitrogen; R¹ reagent is, for example, (1) 1-methylcyclopropane-1-sulfonamide, (2) 3-methyloxetan-3-amine, (3) tert-butyl 3-mercaptoazetidine-1-carboxylate, (4) ethyl 2-sulfamoylpropionate, (5) 2-hydroxypropane-1-sulfonamide, (6) 2-hydroxyethane-1-sulfonamide, (7) ethyl iodoacetate, (8) 2-mercaptopropan-1-ol, (9) 2-mercapto-2-methylpropan-1-ol, (10) 2-aminoethan-1-ol, or (11) cyclopropanethiol. As shown in general reaction scheme 1, compound 1-1 and compound 1-2 undergo an amidation reaction to generate compound 1-3, and compound 1-3 reacts with R¹ reagent 1-4 to generate compound 1-5.

Embodiments of the compound of general formula (1) may be prepared according to general reaction scheme 2, wherein R¹, R², ring A, R⁸, X¹, X², and X³ are as defined above; W¹ represents fluorine, chlorine, bromine, or iodine; H represents hydrogen; N represents nitrogen; R¹ reagent is, for example, (1) 1-methylcyclopropane-1-sulfonamide, (2) 3-methyloxetan-3-amine, (3) tert-butyl 3-mercaptoazetidine-1-carboxylate, (4) ethyl 2-sulfamoylpropionate, (5) 2-hydroxypropane-1-sulfonamide, (6) 2-hydroxyethane-1-sulfonamide, (7) ethyl iodoacetate, (8) 2-mercaptopropan-1-ol, (9) 2-mercapto-2-methylpropan-1-ol, (10) 2-aminoethan-1-ol, or (11) cyclopropanethiol. As shown in general reaction scheme 2, compound 2-1 and compound 2-2 undergo an amidation reaction to generate compound 2-3, and compound 2-3 reacts with R¹ reagent 2-4 to generate compound 2-5.

Embodiments of the compound of general formula (1) may be prepared according to general reaction scheme 3, wherein R¹, R², ring A, R⁸, X¹, X², and X³ are as defined above; W¹ represents fluorine, chlorine, bromine, or iodine; H represents hydrogen; N represents nitrogen; P¹ is an ester group-protecting group; R¹ reagent is, for example, (1) 1-methylcyclopropane-1-sulfonamide, (2) 3-methyloxetan-3-amine, (3) tert-butyl 3-mercaptoazetidine-1-carboxylate, (4) ethyl 2-sulfamoylpropionate, (5) 2-hydroxypropane-1-sulfonamide, (6) 2-hydroxyethane-1-sulfonamide, (7) ethyl iodoacetate, (8) 2-mercaptopropan-1-ol, (9) 2-mercapto-2-methylpropan-1-ol, (10) 2-aminoethan-1-ol, or (11) cyclopropanethiol. As shown in general reaction scheme 3, compound 3-1 reacts with R¹ reagent 3-2 to generate compound 3-3, compound 3-3 loses the ester group-protecting group P¹ to give compound 3-4, and compound 3-4 and compound 3-5 undergo an amidation reaction to generate compound 3-6.

Embodiments of the compound of general formula (1) may be prepared according to general reaction scheme 4, wherein R¹, R², ring A, R⁸, X¹, X², and X³ are as defined above: W¹ represents fluorine, chlorine, bromine, or iodine: H represents hydrogen; N represents nitrogen: P² is an amino-protecting group: R¹ reagent is, for example, (1) 1-methylcyclopropane-1-sulfonamide, (2) 3-methyloxetan-3-amine, (3) tert-butyl 3-mercaptoazetidine-1-carboxylate, (4) ethyl 2-sulfamoylpropionate, (5) 2-hydroxypropane-1-sulfonamide, (6) 2-hydroxyethane-1-sulfonamide, (7) ethyl iodoacetate, (8) 2-mercaptopropan-1-ol, (9) 2-mercapto-2-methylpropan-1-ol, (10) 2-aminoethan-1-ol, or (11) cyclopropanethiol. As shown in general reaction scheme 4, compound 4-1 reacts with R¹ reagent 4-2 to generate compound 4-3, compound 4-3 loses the amino-protecting group P² to give compound 4-4, and compound 4-4 and compound 4-5 undergo an amidation reaction to generate compound 4-6.

Further Forms of Compounds

“Pharmaceutically acceptable” herein refers to a substance, such as a carrier or diluent, which will not lead to loss of biological activity or properties in a compound and is relatively non-toxic. For example, when an individual is given a substance, such substance will not cause undesired biological effects or interact with any component contained therein in a deleterious manner.

The term “pharmaceutically acceptable salt” refers to a form of a compound that does not cause significant irritation to the organism receiving the administration or eliminate the biological activity and properties of the compound. In certain specific aspects, the pharmaceutically acceptable salt is obtained by subjecting the compound of the general formula to a reaction with acids or bases, wherein the acids or bases include, but are not limited to, those found in Stahl and Wermuth, Handbook of Pharmaceutical Salts: Properties, Selection. and Use. 1^st Ed. (Wiley. 2002).

It should be understood that references to pharmaceutically acceptable salts include solvent addition forms or crystalline forms, especially solvates or polymorphs. A solvate contains either stoichiometric or non-stoichiometric amount of solvent and is selectively formed during crystallization in a pharmaceutically acceptable solvent such as water and ethanol. Hydrates are formed when the solvent is water, or alcoholates are formed when the solvent is ethanol. The solvates of the compound of general formula (1) are conveniently prepared or formed according to methods described herein. For example, hydrates of the compound of general formula (1) are conveniently prepared by recrystallization in a mixed solvent of water/organic solvent, wherein the organic solvent used includes, but is not limited to, tetrahydrofuran, acetone, ethanol, or methanol. Furthermore, the compounds described herein may be present in either a non-solvated form or a solvated form. In general, the solvated forms are considered equivalent to the non-solvated forms for purposes of the compounds and methods provided herein.

In other specific examples, the compound of general formula (1) is prepared in different forms including, but not limited to, amorphous, pulverized, and nanoparticle forms. In addition, the compound of general formula (1) includes crystalline forms, but may also be polymorphs. Polymorphs include different lattice arrangements of the same elements of a compound. Polymorphs generally have different X-ray diffraction spectra, infrared spectra, melting points, density, hardness, crystalline forms, optical and electrical properties, stability, and solubility. Different factors such as recrystallization solvent, crystallization rate, and storage temperature may lead to a single dominant crystalline form.

In another aspect, the compound of general formula (1) may have a chiral center and/or axial chirality, and thus may be present in the form of a racemate, a racemic mixture, a single enantiomer, a diastereomeric compound, a single diastereomer, and a cis-trans isomer. Each chiral center or axial chirality will independently produce two optical isomers, and all possible optical isomers, diastereomeric mixtures, and pure or partially pure compounds are included within the scope of the present invention. The present invention is meant to include all such isomeric forms of these compounds.

The compound of the present invention may contain unnatural proportions of atomic isotopes at one or more of the atoms that constitute the compound. For example, the compound may be labeled with radioactive isotopes, such as tritium (³H), iodine-125 (¹²⁵I), and C-14 (¹⁴C). For another example, deuterium can be used to substitute a hydrogen atom to form a deuterated compound. The bond formed by deuterium and carbon is stronger than that formed by common hydrogen and carbon, and compared with an undeuterated medicament, the deuterated medicament generally has the advantages of reduced adverse effects, increased medicament stability, enhanced efficacy, prolonged in vivo half-life and the like. All isotopic variations of the compound of the present invention, whether radioactive or not, are intended to be encompassed within the scope of the present invention.

Terminology

Unless otherwise stated, the terms used in the present application, including those in the specification and claims, are defined as follows. It must be noted that in the specification and the appended claims, the singular forms “a” and “an” include plural meanings unless clearly indicated otherwise. Unless otherwise stated, conventional methods for mass spectrometry, nuclear magnetic resonance spectroscopy, HPLC, protein chemistry, biochemistry, recombinant DNA techniques, and pharmacology are used. As used herein, “or” or “and” refers to “and/or” unless otherwise stated.

Unless otherwise specified, “Cap hydrocarbyl” means a hydrocarbyl group containing a minimum of a and a maximum of β carbon atoms in a branched or linear relationship, wherein a and B represent integers. The hydrocarbyl described in this section may also contain one or two double or triple bonds. A designation of Co hydrocarbyl represents a direct bond. Examples of the C_1-6 hydrocarbyl include, but are not limited to, the following:

Unless otherwise specified, “C_α-β halohydrocarbyl” means a hydrocarbyl group, as described above, in which any number (at least one) of the hydrogen atoms attached to the hydrocarbyl chain are replaced by F, Cl, Br, or I.

Unless otherwise specified, “oxo” and “thio” represent ═O (e.g., carbonyl) and ═S (e.g., thiocarbonyl), respectively.

Unless otherwise specified, “halo” or “halogen” means a halogen atom selected from F, Cl, Br, and I.

Unless otherwise specified, “alkoxy” refers to an alkyl group that bonds to the rest of the molecule through an ether oxygen atom. Representative alkoxy groups are those having 1-6 carbon atoms, such as methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy; and tert-butoxy. As used herein, “alkoxy” includes unsubstituted and substituted alkoxy, particularly alkoxy substituted with one or more halogens. Preferred alkoxy is selected from OCH₃, OCF₃, CHF₂O, CF₃CH₂O, ^i-PrO, ^n-PrO, ^i-BuO, ^n-BuO, and ^t-BuO. Unless otherwise specified, “cycloalkyl” refers to a monocyclic non-aromatic hydrocarbon ring system. The ring carbon atoms of the cycloalkyl may optionally be oxidized to form an oxo or sulfido group. The cycloalkyl further includes cycloalkylene. In some embodiments, the cycloalkyl contains 0, 1, or 2 double bonds. In some embodiments, the cycloalkyl contains 1 or 2 double bonds (partially unsaturated cycloalkyl). Examples of the cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptatrienyl,

and the like.

Unless otherwise specified, “aryl” refers to an aromatic hydrocarbon group, which is monocyclic or polycyclic: for example, a monocyclic aryl ring is fused to one or more carbocyclic aromatic groups. Examples of aryl include, but are not limited to, phenyl, naphthyl, and phenanthryl.

Unless otherwise specified, “arylene” refers to a divalent aryl as defined above. Examples of arylene include, but are not limited to, phenylene, naphthylene, and phenanthrylene.

Unless otherwise specified, “heteroaryl” refers to an aromatic group containing one or more heteroatoms (O, S, or N), and the heteroaryl is monocyclic or polycyclic. For example, a monocyclic heteroaryl ring is fused to one or more carbocyclic aromatic groups or other monocyclic heterocycloalkyl groups. Examples of heteroaryl include, but are not limited to, pyridinyl, pyridazinyl, imidazolyl, pyrimidinyl, pyrazolyl, triazolyl, pyrazinyl, quinolinyl, isoquinolinyl, furanyl, thienyl, isoxazolyl, thiazolyl, oxazolyl, isothiazolyl, pyrrolyl, indolyl, benzimidazolyl, benzofuranyl, benzothiazolyl, benzothienyl, benzoxazolyl, benzopyridinyl, pyrrolopyrimidinyl, 1H-pyrrolo[3,2-b]pyridinyl, 1H-pyrrolo[2,3-c]pyridinyl, 1H-pyrrolo[3,2-c]pyridinyl, 1H-pyrrolo[2,3-b]pyridinyl,

Unless otherwise specified, “heteroarylene” refers to a divalent heteroaryl as defined above.

Unless otherwise specified, “heterocycloalkyl” refers to a non-aromatic ring or ring system, which may optionally contain one or more alkenylene as part of the ring structure, having at least one heteroatom ring member independently selected from boron, phosphorus, nitrogen, sulfur, oxygen, and phosphorus. Partially unsaturated heterocycloalkyl may be referred to as “heterocycloalkenyl” if heterocycloalkyl contains at least one double bond, or “heterocycloalkynyl” if the heterocycloalkyl contains at least one triple bond. Heterocycloalkyl may include monocyclic, bicyclic, spiro ring, or polycyclic systems (e.g., having two fused or bridged rings). In some embodiments, heterocycloalkyl is a monocyclic group having 1, 2, or 3 heteroatoms independently selected from nitrogen, sulfur, and oxygen. The ring carbon atoms and heteroatoms of heterocycloalkyl may optionally be oxidized to form oxo or thio groups or other oxidized bonds (e.g., C(O), S(O), C(S) or S(O)₂, N-oxides, etc.), or the nitrogen atoms may be quaternized. Heterocycloalkyl may be attached via a ring carbon atom or a ring heteroatom. In some embodiments, heterocycloalkyl contains 0 to 3 double bonds. In some embodiments, heterocycloalkyl contains 0 to 2 double bonds. The definition of heterocycloalkyl further includes moieties (also referred to as partially unsaturated heterocyclic rings) having one or more aromatic rings fused to (i.e., sharing a bond with) the heterocycloalkyl ring, for example, benzo-derivatives of piperidine, morpholine, azepin, thienyl, or the like. Heterocycloalkyl containing a fused aromatic ring may be attached via any ring atom, including ring atoms of the fused aromatic ring. Examples of heterocycloalkyl include, but are not limited to, azetidinyl, azepinyl, dihydrobenzofuranyl, dihydrofuranyl, dihydropyranyl, N-morpholinyl, 3-oxa-9-azaspiro[5.5]undecyl, 1-oxa-8-azaspiro[4.5] decyl, piperidinyl, piperazinyl, oxopiperazinyl, pyranyl, pyrrolidinyl, quininyl, tetrahydrofuranyl, tetrahydropyranyl, 1,2,3,4-tetrahydroquinolinyl, tropanyl, 4,5,6,7-tetrahydrothiazolo[5,4-c]pyridinyl, 4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine, N-methylpiperidinyl, tetrahydroimidazolyl, pyrazolidinyl, butyrolactam, valerolactam, imidazolidinonyl, hydantoinyl, dioxolanyl, phthalimidyl, pyrimidine-2,4(1H,3H)-dione, 1,4-dioxanyl, morpholinyl, thiomorpholinyl, thiomorpholinyl-S-oxide, thiomorpholinyl-S,S-oxide, piperazinyl, pyranyl, pyridonyl, 3-pyrrolinyl, thiopyranyl, pyronyl, tetrahydrothienyl, 2-azaspiro[3.3]heptanyl, indolinyl,

Unless otherwise specified, “heterocycloalkylidene” means a divalent heterocycloalkyl group as defined above. Unless otherwise specified, “bicyclic ring” means a group that features two connecting rings. The bicyclic ring may be a carbocyclic ring (all ring atoms are carbon atoms) or a heterocyclic ring (ring atoms include, for example, 1, 2, or 3 heteroatoms, such as N, O, or S, in addition to carbon atoms). These two rings may be aliphatic (e.g., decalin and norbornane), or may be aromatic (e.g., naphthalene), or a combination of aliphatic and aromatic (e.g., tetralin). Bicyclic rings include: (a) spirocyclic compounds, wherein the two rings share only one single atom (the spiro atom, which is typically a quaternary carbon); examples of the spirocyclic compounds include, but are not limited to:

• • (b) fused bicyclic compounds, wherein the two rings share two adjacent atoms, that is, the rings share a covalent bond, i.e., the bridgehead atoms are directly connected (e.g., α-thujene and decalin); examples of the fused bicyclic rings include, but are not limited to:

• • (c) bridged bicyclic compounds, wherein the two rings share three or more atoms and the two bridgehead atoms are separated by a bridge containing at least one atom; for example, norbornane, also known as bicyclo[2.2.1]heptane, can be thought of as a pair of cyclopentane rings, each sharing three of their five carbon atoms; examples of the bridged bicyclic rings include, but are not limited to:

Unless otherwise specified, “carbocyclic ring” or “carbocyclic”, by itself or in combination with other terms, represents a cyclic form of “C_α-β hydrocarbyl”. Examples of the carbocyclic ring include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptatrienyl, norcamphanyl, norpinanyl, norcarnyl, bicyclo[1.1.1]pentyl, bicyclo[2.1.1]hexyl, and the like.

Unless otherwise specified, “heterocyclic ring” or “heterocyclic” means a ring containing at least one carbon atom and at least one other atom selected from N, O, and S. Examples of the heterocyclic ring that may be found in the claims include, but are not limited to, the following:

“Optional” or “optionally” means that the subsequently described event or circumstance may, but does not necessarily, occur, and the description includes instances where the event or circumstance occurs and instances where it does not.

“Saturated, partially saturated, or unsaturated” includes substituents saturated with hydrogen, substituents completely unsaturated with hydrogen, and substituents partially saturated with hydrogen.

When one of the variables is selected from a chemical bond, it means that the two groups linked by this variable are linked directly. For example, when L in X-L-Y represents a chemical bond, it means that the structure is actually X-Y.

When the number of a group is 0, such as —N(C₀ hydrocarbyl)-C_0-4 hydrocarbyl-, it means that the linker group is —NH—C_0-4 hydrocarbyl-.

When the number of a linker group is 0, such as —(CH₂)₀—, it means that the linker group is a chemical bond.

Unless otherwise stated, the absolute configuration of a stereogenic center is represented by a wedged solid bond () and a wedged dashed bond (), and the relative configuration of a stereogenic center is represented by a straight solid bond () and a straight dashed bond (). A wavy line () represents a wedged solid bond () or a wedged dashed bond (), or a wavy line () represents a straight solid bond () or a straight dashed bond ().

Unless otherwise stated, a single bond or a double bond is represented by .

Specific Pharmaceutical and Medical Terminology

The term “acceptable”, as used herein, means that a formulation component or an active ingredient does not unduly adversely affect a general therapeutic target's health.

The terms “treatment.” “treatment course,” and “therapy”, as used herein, include alleviating, inhibiting, or ameliorating a symptom or condition of a disease: inhibiting the development of complications: ameliorating or preventing underlying metabolic syndrome: inhibiting the development of a disease or symptom, e.g., controlling the progression of a disease or condition: alleviating a disease or symptom; leading to disease or symptom regression; and alleviating a complication caused by a disease or symptom, or preventing or treating a sign caused by a disease or symptom. As used herein, a compound or pharmaceutical composition, when administered, can ameliorate a disease, symptom, or condition, which particularly refers to ameliorating the severity; delaying the onset, slowing the progression, or reducing the duration of the disease. Fixed or temporary administration, or continuous or intermittent administration, may be attributed to or associated with the administration.

The “active ingredient” refers to the compound of general formula (1), and pharmaceutically acceptable inorganic or organic salts of the compound of general formula (1). The compounds of the present invention may contain one or more asymmetric centers (chiral center or axial chirality) and thus occur in the form of a racemate, racemic mixture, single enantiomer, diastereomeric compound, and single diastereomer. Asymmetric centers that may be present depend on the nature of the various substituents on the molecule. Each of these asymmetric centers will independently produce two optical isomers, and all possible optical isomers, diastereomeric mixtures, and pure or partially pure compounds are included within the scope of the present invention. The present invention is meant to include all such isomeric forms of these compounds.

The terms such as “compound”, “composition”, “agent”, or “medicine or medicament” are used interchangeably herein and all refer to a compound or composition that, when administered to an individual (human or animal), is capable of inducing a desired pharmacological and/or physiological response by local and/or systemic action.

The term “administered, administering, or administration” refers herein to the direct administration of the compound or composition, or the administration of a prodrug, derivative, analog, or the like of the active compound.

Although the numerical ranges and parameters defining the broad scope of the present invention are approximations, the related numerical values set forth in the specific examples have been presented herein as precisely as possible. Any numerical value, however, inherently contains a standard deviation necessarily resulting from certain methods of testing. Herein, “about” generally means that the actual numerical value is within a particular numerical value or range±10%, 5%, 1%, or 0.5%. Alternatively, the term “about” indicates that the actual numerical value falls within the acceptable standard error of a mean, as considered by those skilled in the art. All ranges, quantities, numerical values, and percentages used herein (e.g., to describe an amount of a material, a length of time, a temperature, an operating condition, a quantitative ratio, and the like) are to be understood as being modified by the word “about”, except in the experimental examples or where otherwise explicitly indicated. Accordingly, unless otherwise contrarily stated, the numerical parameters set forth in the specification and the appended claims are all approximations that may vary as desired. At the very least, these numerical parameters should be understood as the significant digits indicated or the numerical value obtained using conventional rounding rules.

Unless otherwise defined in the specification, the scientific and technical terms used herein have the same meaning as commonly understood by those skilled in the art. Furthermore, nouns in their singular forms used in the specification encompass their plural forms, unless contradicted by context: nouns in their plural forms used also encompass their singular forms.

Therapeutic Use

The present invention provides use of the compound of general formula (1) or the pharmaceutical composition of the present invention in inhibiting KIF18A protein, therefore, in treating one or more disorders related to the activity of KIF18A protein. Therefore, in certain embodiments, the present invention provides a method for treating a disorder mediated by KIF18A protein, the method comprising a step of administering to a patient in need thereof the compound or the pharmaceutically acceptable composition thereof of the present invention. In some embodiments, a method for treating cancer is provided, the method comprising administering to an individual in need thereof an effective amount of any of the aforementioned pharmaceutical compositions comprising the compound of structural general formula (1). In some embodiments, the cancer is mediated by KIF18A protein. In other embodiments, the cancer is a hematologic cancer and a solid tumor, preferably a tumor with chromosome instability, including, but not limited to, hematologic malignancies (leukemias, lymphomas, and myelomas including multiple myeloma, myelodysplastic syndrome and myeloproliferative family syndrome), solid tumors (carcinomas such as prostate, breast, lung, colon, pancreas, kidney, ovary and soft tissue cancers, osteosarcoma, and interstitial tumors), and the like. Leukemia, breast cancer, lung cancer, pancreatic cancer, colon cancer, bladder cancer, brain cancer, urothelial cancer, prostate cancer, liver cancer, ovarian cancer, head and neck cancer, gastric cancer, mesothelioma, or all cancer metastases are preferred: in other embodiments, the cancer is colon cancer, ovarian cancer, breast cancer, uterine cancer, cervical cancer, fallopian tube cancer, peritoneal cancer, lung cancer, liver cancer, head and neck cancer, pancreatic cancer, prostate cancer, oral cancer, esophageal cancer, and cancer metastases of these cancers: in other embodiments, the breast cancer is preferably triple negative breast cancer: in other embodiments, the ovarian cancer is preferably high-grade ovarian cancer, more preferably platinum-resistant high-grade ovarian cancer, and more preferably platinum-resistant high-grade serous ovarian cancer: in other embodiments, the peritoneal cancer is preferably primary peritoneal cancer: in other embodiments, the uterine cancer is preferably serous endometrial cancer.

Route of Administration

The compound and the pharmaceutically acceptable salt thereof disclosed herein can be prepared into various formulations comprising a safe and effective amount of the compound or the pharmaceutically acceptable salt thereof disclosed herein, and a pharmaceutically acceptable excipient or carrier, wherein the “safe and effective amount” means that the amount of the compound is sufficient to significantly improve the condition without causing serious adverse effects. The safe and effective amount of the compound is determined according to the age, condition, course of treatment, and other specific conditions of a treated subject.

The “pharmaceutically acceptable excipient or carrier” refers to one or more compatible solid or liquid fillers or gel substances that are suitable for human use and must be of sufficient purity and sufficiently low toxicity. “Compatible” means that the components of the composition are capable of intermixing with the compound of the present invention and with each other, without significantly diminishing the pharmaceutical efficacy of the compound. Examples of pharmaceutically acceptable excipients or carriers include cellulose and its derivatives (e.g., sodium carboxymethylcellulose, sodium ethylcellulose, or cellulose acetate), gelatin, talc, solid lubricants (e.g., stearic acid or magnesium stearate), calcium sulfate, vegetable oil (e.g., soybean oil, sesame oil, peanut oil, or olive oil), polyols (e.g., propylene glycol, glycerol, mannitol, or sorbitol), emulsifiers (e.g., Tween R), wetting agents (e.g., sodium lauryl sulfate), colorants, flavoring agents, stabilizers, antioxidants, preservatives, pyrogen-free water, etc.

When the compound of the present invention is administered, it may be administered orally, rectally, parenterally (intravenously; intramuscularly, or subcutaneously), or topically.

Solid dosage forms for oral administration include capsules, tablets, pills, pulvises, and granules. In these solid dosage forms, the active compound is mixed with at least one conventional inert excipient (or carrier), such as sodium citrate or dicalcium phosphate, or with the following ingredients: (a) fillers or extenders, such as starch, lactose, sucrose, glucose, mannitol, and silicic acid: (b) binders, such as hydroxymethyl cellulose, alginate, gelatin, polyvinylpyrrolidone, sucrose, and acacia: (c) humectants, such as glycerol: (d) disintegrants, such as agar, calcium carbonate, potato or tapioca starch, alginic acid, certain complex silicates, and sodium carbonate: (e) solution retarders, such as paraffin: (f) absorption accelerators, such as quaternary ammonium compounds: (g) wetting agents, such as cetyl alcohol and glycerol monostearate: (h) adsorbents, such as kaolin; and (i) lubricants, such as talc, calcium stearate, magnesium stearate, solid polyethylene glycol, and sodium lauryl sulfate, or mixtures thereof. In the case of capsules, tablets, and pills, the dosage forms may further comprise buffers.

Solid dosage forms such as tablets, dragees, capsules, pills, and granules can be prepared using coatings and shells such as enteric coatings and other materials well known in the art. They may comprise opacifying agents, and the active compound or compound in such a composition may be released in a certain part of the digestive tract in a delayed manner. Examples of embedding components that can be used are polymeric substances and wax-based substances. If necessary, the active compound can also be in microcapsule form with one or more of the above-mentioned excipients.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs. In addition to the active compound, the liquid dosage form may comprise inert diluents commonly used in the art, such as water or other solvents, solubilizers and emulsifiers, for example, ethanol, isopropanol, ethyl carbonate, ethyl acetate, propylene glycol, 1,3-butanediol, dimethylformamide, and oils, especially cottonseed oil, peanut oil, corn germ oil, olive oil, castor oil, and sesame oil, or mixtures of these substances.

Besides such inert diluents, the composition may further comprise adjuvants, such as wetting agents, emulsifiers, suspending agents, sweeteners, flavoring agents, and perfuming agents.

Suspensions, in addition to the active compound, may comprise suspending agents, such as ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum methylate and agar, or mixtures of these substances.

Compositions for parenteral injection may comprise physiologically acceptable sterile aqueous or anhydrous solutions, dispersions, suspensions or emulsions, and sterile powders for redissolving into sterile injectable solutions or dispersions. Suitable aqueous and non-aqueous carriers, diluents, solvents, or excipients include water, ethanol, polyols, and suitable mixtures thereof.

Dosage forms for topical administration of the compound of the present invention include ointments, pulvises, patches, sprays, and inhalants. The active ingredient is mixed under sterile conditions with a physiologically acceptable carrier and any preservatives, buffers, or propellants that may be required if necessary.

The compound of the present invention may be administered alone or in combination with other pharmaceutically acceptable compounds. When the pharmaceutical composition is used, a safe and effective amount of the compound of the present invention is administered to a mammal (such as a human) to be treated, wherein the administration dose is a pharmaceutically effective administration dose. For a human of 60 kg, the daily dose of administration is usually 1-2000 mg, preferably 50-1000 mg. In determining a specific dose, such factors as the route of administration, the health condition of the patient, and the like will also be considered, which are well known to skilled physicians.

The above features mentioned in the present invention or those mentioned in the examples may be combined arbitrarily: All the features disclosed in this specification may be used with any composition form and the various features disclosed in this specification may be replaced with any alternative features that provide the same, equivalent, or similar purpose. Thus, unless otherwise expressly stated, the features disclosed herein are merely general examples of equivalent or similar features.

DETAILED DESCRIPTION

Various specific aspects, features, and advantages of the compounds, methods, and pharmaceutical compositions described above will be set forth in detail in the following description, which will make the content of the present invention very clear. It should be understood that the detailed description and examples below describe specific embodiments for reference only. After reading the description of the present invention, those skilled in the art can make various changes or modifications to the present invention, and such equivalents also fall within the scope of the present invention defined herein.

In all examples, ¹H-NMR spectra were recorded with a Varian Mercury 400 nuclear magnetic resonance spectrometer, and chemical shifts are expressed in δ (ppm); silica gel for separation was 200-300 mesh silica gel if not specified, and the ratio of the eluents was volume ratio. The following abbreviations are used in the present invention: (Boc)₂O for di-tert-butyl dicarbonate; BINAP for 2,2′-bis(diphenylphosphino)-1,1′-binaphthalene: BOPCl for bis(2-oxo-3-oxazolidinyl) phosphinic chloride; t-BuONa for sodium tert-butoxide; CDCl₃ for deuterated chloroform; Cs₂CO₃ for cesium carbonate; CuI for cuprous iodide; EtOAc for ethyl acetate; Hexane for n-hexane; HPLC for high-performance liquid chromatography; MeCN for acetonitrile; DCE for 1,2-dichloroethane; DCM for dichloromethane; DIPEA for diisopropylethylamine; 1,4-Dioxane for 1,4-dioxane; DMF for N,N-dimethylformamide; DMAP for 4-(dimethylamino)pyridine; DMSO for dimethyl sulfoxide; h for hour; HATU for N-[(dimethylamino)-1H-1,2,3-triazolo-[4,5-b]pyridin-1-methylene]-N-methylmethanaminium hexafluorophosphate-N-oxide; IPA for isopropanol; min for minute; K₂CO₃ for potassium carbonate; KOAc for potassium acetate; K₃PO₄ for potassium phosphate; LiBH₄ for lithium borohydride; min for minute; MeOH for methanol; MS for mass spectrometry; NMR for nuclear magnetic resonance; Pd/C for palladium on carbon; Pd(PPh₃)₄ for tetrakis(triphenylphosphine)palladium; Pd₂(dba)₃ for tris(dibenzylideneacetone)dipalladium(0); Pd(OAc)₂ for palladium acetate; PE for petroleum ether; RuPhos Pd G₃ for (2-dicyclohexylphosphino-2′,6′-diisopropoxy-11′-biphenyl)[2-(2′-amino-11′-biphenyl)]palladium(II) methanesulfonate; Sarcosine for sarcosine; TFA for trifluoroacetic acid; T₃P for 1-propanephosphonic anhydride; XantPhos for 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; TLC for thin-layer chromatography; and XPhos for 2-dicyclohexylphosphonium-2′,4′, 6′-triisopropylbiphenyl.

Example 1. Synthesis of Compound 1

Step 1: Synthesis of Compound Int_1-2

• • int_1-1 (15 g, 56.3 mmol) was dissolved in methanol (150 mL), and concentrated sulfuric acid (2.5 mL) was added. The mixture was heated to 80° C. and reacted for 4 h, and LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product, and the crude product was dissolved in ethyl acetate. The organic phase was washed with a saturated sodium bicarbonate solution and then with saturated brine, dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a white solid (14 g, yield: 89%). The solid was used directly in the next step.

ESI-MS m/z: 281 [M+H]⁺

Step 2: Synthesis of Compound Int_1-4

int_1-2 (14 g, 49.9 mmol) was dissolved in DMSO (100 mL), and cesium carbonate (23.4 g, 71.7 mmol) and int_1-3 (6.98 g, 62.8 mmol) were added. The mixture was heated to 90° C. and reacted for 24 h, and LC-MS monitoring showed the reaction was complete. The reaction solution was diluted with water (500 mL), and the aqueous phase was extracted with ethyl acetate (100 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, EtOAc:Hexane=1:1) to give the target product (16.3 g, yield: 88%).

ESI-MS m/z: 372 [M+H]⁺.

Step 3: Synthesis of Compound Int_1-5

int_1-4 (16.3 g, 43.9 mmol) was dissolved in a mixed solvent of methanol (100 mL) and water (10 mL), and lithium hydroxide (2.1 g, 87.8 mmol) was added at room temperature. The mixture was stirred at room temperature for 6 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product (17 g). The crude product was directly used in the next step.

ESI-MS m/z: 358 [M+H]⁺.

Step 4: Synthesis of Compound Int_1-7

int_1-5 (1.1 g, 3.08 mmol) was dissolved in DCM (10 mL), and oxalyl chloride (888.4 mg, 7 mmol) was added. The reaction solution was stirred at room temperature for 2 h and then concentrated under reduced pressure to remove the solvent, thus giving a solid. The solid was dissolved in DCM (10 mL), and int_1-6 (783.2 mg, 3.08 mmol) and pyridine (730 mg, 9.24 mmol) were added. The reaction solution was stirred at 40° C. for 10 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, PE:EtOAc=100:1) to give a solid (1.3 g, yield: 71.4%).

ESI-MS m/z: 594 [M+H]⁺.

Step 5: Synthesis of Compound 1

int_1-8 (291 mg, 2.374 mmol), sarcosine (209.1 mg, 2.348 mmol), cuprous iodide (227 mg, 1.174 mmol), and potassium phosphate (1.5 g, 7.041 mmol) were dissolved in DMF (20 mL). The solution was purged with argon three times, and int_1-7 (1.3 g, 2.19 mmol) was added. Under argon atmosphere, the reaction solution was heated to 90° C. and reacted for 3 h. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography (SiO₂, EtOAc:Hexane=1:1) to give a solid (1 g, yield: 77.5%).

¹H NMR (400 MHZ, DMSO-d6) δ 11.53 (s, 1H), 7.80 (d, J=8.5 Hz, 1H), 7.41 (d, J=2.0 Hz, 1H), 7.13 (d, J=2.2 Hz, 1H), 7.06-6.95 (m, 2H), 4.51 (t, J=8.7 Hz, 2H), 3.73 (t, J=6.6 Hz, 2H), 3.23-3.08 (m, 6H), 2.94 (t, J=5.1 Hz, 4H), 2.15-1.96 (m, 4H), 1.53 (s, 4H), 0.33 (s, 4H).

ESI-MS m/z: 591 [M+H]⁺.

Example 2. Synthesis of Compound 65

Step 1: Synthesis of Compound Int_65-2

int_65-1 (17.6 g, 101 mmol) was dissolved in THF (200 mL), and n-BuLi (2.5 M, 60.8 mL) was slowly added dropwise to the reaction solution at −78° C. under nitrogen atmosphere. After the reaction solution was reacted at −78° C. for 0.5 h, ethylene oxide (22.3 g, 506 mmol, 25.3 mL) was added dropwise to the reaction solution at −78° C., and the reaction solution was reacted at −78° C. for 1 h, then slowly heated to room temperature, and reacted for another 1.5 h. LC-MS monitoring showed the reaction was complete. A saturated ammonium chloride solution (200 mL) was added to the reaction solution to quench the reaction. The aqueous phase was extracted with ethyl acetate (200 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product (16 g, yield: 72.5%). The crude product was directly used in the next step.

¹H NMR (400 MHZ, DMSO-d6) δ=8.09 (d, J=4.9 Hz, 1H), 7.37 (d, J=4.9 Hz, 1H), 5.16-5.06 (m, 2H), 4.79 (t, J-5.3 Hz, 1H), 3.73-3.64 (m, 2H), 3.57-3.53 (m, 3H), 2.86 (t, J=6.7 Hz, 2H).

Step 2: Synthesis of Compound Int_65-3

int_65-2 (16.0 g, 73.5 mmol) was dissolved in methanol (200 mL), and a hydrochloric acid solution (12 M, 30.6 mL) was added at 0° C. The mixture was heated to 25° C. and reacted for 3 h, and LC-MS monitoring showed the reaction was complete. At 0° C., 1 N NaOH was added to the reaction solution to adjust the pH to 7. The aqueous phase was extracted with ethyl acetate (300 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product (10 g, yield: 78.3%). The crude product was directly used in the next step.

¹H NMR (400 MHZ, DMSO-d6) δ=8.09 (d, J=4.9 Hz, 1H), 7.37 (d, J=4.9 Hz, 1H), 5.16-5.06 (m, 2H), 4.79 (t, J=5.3 Hz, 1H), 3.73-3.64 (m, 2H), 3.57-3.53 (m, 3H), 2.86 (t, J=6.7 Hz, 2H).

Step 3: Synthesis of Compound Int_65-4

int_1-4 (9.50 g, 54.7 mmol) was dissolved in a mixed solvent of THF (200 mL) and water (50 mL), and I₂ (13.8 g, 54.7 mmol, 11.0 mL) and K₂CO₃ (15.1 g, 109 mmol) were added at room temperature. The reaction solution was stirred at room temperature for 2 h. LC-MS monitoring showed the reaction was complete. 100 mL of water was added to the reaction solution. The aqueous phase was extracted with ethyl acetate (100 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, PE:EtOAc=1:1) to give a solid (13 g, yield: 79.3%).

¹H NMR (400 MHZ, DMSO-d6) δ=10.10 (s, 1H), 7.58 (s, 1H), 3.63 (t, J=6.3 Hz, 2H), 2.75 (t, J=6.3 Hz, 2H).

Step 4: Synthesis of Compound Int_65-5

int_65-4 (7.10 g, 23.7 mmol) and PPh₃ (9.33 g, 35.5 mmol) were dissolved in THF (100 mL), and DIAD (7.19 g, 35.5 mmol, 6.91 mL) was slowly added dropwise to the reaction solution at 0° C. under nitrogen atmosphere. The reaction solution was heated to 70° C. and stirred for 1 h. LC-MS monitoring showed the reaction was complete. 100 mL of water was added to the reaction solution. The aqueous phase was extracted with ethyl acetate (100 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, PE:EtOAc=3:1) to give a solid (11 g, yield: 65.9%).

¹H NMR (400 MHZ, CHLOROFORM-d) δ=7.42 (s, 1H), 4.64 (t, J=8.9 Hz, 2H), 3.31-3.19 (m, 2H).

Step 5: Synthesis of Compound Int_65-7

int_65-5 (1.19 g, 4.26 mmol) and int_65-6 (5.16 g, 42.6 mmol) were mixed, and the reaction solution was heated to 140° C. and stirred for 16 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was diluted with water (30 mL), and the aqueous phase was extracted with ethyl acetate (30 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, EtOAc:Hexane=5:1) to give the target product (0.35 g, yield: 22.4%).

¹H NMR (400 MHZ, CHLOROFORM-d) δ=7.08 (s, 1H), 4.58 (t, J=8.9 Hz, 2H), 3.77-3.68 (m, 4H), 3.15 (t, J=8.9 Hz, 2H), 2.03-1.89 (m, 4H).

Step 6: Synthesis of Compound Int_65-8

int_65-7 (0.35 g, 955 μmol), NH₂Boc (223 mg, 1.91 mmol), RuPhos Pd G3 (79.9 mg, 95.5 μmol), and K₃PO₄ (405 mg, 1.91 mmol) were dissolved in 1,4-dioxane (5 mL), and the reaction solution was heated to 80° C. and stirred for 16 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was diluted with water (30 mL), and the aqueous phase was extracted with ethyl acetate (30 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product (0.2 g, yield: 58.8%). The crude product was directly used in the next step.

¹H NMR (400 MHZ, CHLOROFORM-d) δ=7.08 (s, 1H), 4.58 (t, J=8.9 Hz, 2H), 3.77-3.68 (m, 4H), 3.15 (t, J=8.9 Hz, 2H), 2.03-1.89 (m, 4H).

Step 7: Synthesis of Compound Int_65-9

int_65-8 (0.20 g, 562 μmol) was dissolved in dichloromethane (5 mL), and a hydrochloric acid/dioxane solution (4 M, 5 mL) was added at 0° C. The mixture was heated to 25° C. and reacted for 2 h, and LC-MS monitoring showed the reaction was complete. Ammonia water was added to the reaction solution to adjust the pH to 9 at 0° C. The aqueous phase was extracted with ethyl acetate (30 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, PE:EtOAc=1:1) to give a solid (108 mg, yield: 75.1%).

¹H NMR (400 MHz, CHLOROFORM-d) δ=5.89 (s, 1H), 4.40 (t, J=8.7 Hz, 2H), 3.64-3.54 (m, 4H), 2.99 (t, J=8.6 Hz, 2H), 2.03-1.86 (m, 4H).

Step 8: Synthesis of Compound Int_65-10

int_1-5 (70 mg, 0.196 mmol) was dissolved in DCM (3 mL), and oxalyl chloride (253.8 mg, 2 mmol) was added. The reaction solution was stirred at room temperature for 2 h and then concentrated under reduced pressure to remove the solvent, thus giving an acyl chloride solid. int_65-9 (50 mg, 0.196 mmol) was dissolved in THF (5 mL), and sodium hydride (30 mg, 0.75 mmol, 60% purity) was added at 0° C. under nitrogen atmosphere. The reaction solution was heated to room temperature and reacted for 1 h, and then the reaction solution was cooled to 0° C. The acyl chloride prepared above was slowly added to the reaction solution, and the reaction solution was heated to 45° C. and stirred for 12 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (92 mg, yield: 79%).

ESI-MS m/z: 595 [M+H]⁺.

Step 9: Synthesis of Compound 65

int_1-8 (39 mg, 0.309 mmol), dimethylcyclohexane-1,2-diamine (11 mg, 0.077 mmol), cuprous iodide (15 mg, 0.077 mmol), and potassium phosphate (98 mg, 0.464 mmol) were dissolved in DMF (5 mL). The solution was purged with argon three times, and int_65-10 (92 mg, 0.155 mmol) was added. Under argon atmosphere, the reaction solution was heated to 100° C. and reacted for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography to give a solid (50 mg, yield: 55%).

¹H NMR (400 MHz, DMSO-d6) δ 12.74 (s, 1H), 8.02 (d, J=8.6 Hz, 1H), 7.74 (s, 1H), 7.21 (d, J=2.1 Hz, 1H), 7.07 (dd, J=8.6, 2.1 Hz, 1H), 4.54 (t, J=8.8 Hz, 2H), 3.73 (t, J=6.5 Hz, 2H), 3.66 (t, J=5.8 Hz, 4H), 3.17 (t, J=8.8 Hz, 2H), 2.94 (t, J=5.3 Hz, 4H), 2.16-1.93 (m, 4H), 1.69 (s, 4H), 0.36 (s, 4H).

ESI-MS m/z: 592 [M+H]⁺.

Example 3. Synthesis of Compound 129

Step 1: Synthesis of Compound Int_129-2

int_129-1 (28.7 g, 131 mmol) was dissolved in acetonitrile (50 mL), and potassium acetate (29.1 g, 296 mmol), ICl (21.4 g, 131 mmol, 6.71 mL), and CH₃ COOH (60 mL) were added. The mixture was heated to 50° C. and reacted for 42 h, and TLC monitoring showed the reaction was complete. 500 mL of water was added to the reaction solution. The aqueous phase was extracted with ethyl acetate (500 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a white solid (42 g, yield: 92.8%). The solid was directly used in the next step.

Step 2: Synthesis of Compound Int_129-4

int_129-2 (37.0 g, 107 mmol) was dissolved in acetonitrile (500 mL), and int_129-3 (11.1 g, 112 mmol), CuI (409 mg, 2.15 mmolq), TEA (21.8 g, 215 mmol), and Pd(PPh₃)₂Cl₂ (755 mg, 1.08 mmol) were added. The reaction solution was reacted at 20° C. for 3 h under nitrogen atmosphere, and then heated to 80° C. and reacted for 8 h. LC-MS monitoring showed the reaction was complete. The reaction solution was diluted with water (500 mL), and the aqueous phase was extracted with ethyl acetate (500 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, EtOAc:Hexane=1:10 to 3:1) to give the target product (12 g, yield: 35.5%).

¹H NMR: (400 MHZ, CHLOROFORM-d) δ 8.19 (d, J=17.4 Hz, 2H), 6.91 (s, 1H), 0.19 (s, 9H).

Step 3: Synthesis of Compound Int_129-6

int_129-4 (11 g, 35.0 mmol) was dissolved in methylbenzene (300 mL), and int_129-5 (4.40 g, 36.3 mmol), BINAP (4.36 g, 7.00 mmol), t-BuONa (6.73 g, 70.0 mmol), and Pd(OAc)₂ (785 mg, 3.50 mmol) were added at room temperature. The reaction solution was heated to 110° C. and stirred for 16 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. Methylbenzene was removed under reduced pressure, and the reaction solution was diluted with water (200 mL). The aqueous phase was extracted with ethyl acetate (200 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, EtOAc:Hexane=1:10 to 3:1) to give the target product (6.4 g, yield: 64.8%).

¹H NMR (400 MHZ, CHLOROFORM-d) δ 8.08 (d, J=2.0 Hz, 1H), 7.71-7.46 (m, 2H), 6.84 (d, J=2.1 Hz, 1H), 3.54-3.47 (m, 2H), 3.45-3.44 (m, 1H), 3.56-3.36 (m, 1H), 2.20-2.09 (m, 4H).

ESI-MS m/z: 283 [M+H]⁺.

Step 4: Synthesis of Compound Int_129-7

int_129-6 (4.50 g, 15.9 mmol) was dissolved in ethanol (50 mL), and Fe (8.90 g, 159 mmol) and an ammonium chloride solution (8.53 g, 159 mmol, 3.5 M) were added at room temperature. The reaction solution was heated to 70° C. and stirred for 0.5 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was filtered to give a filtrate, and the filtrate was concentrated under reduced pressure to give a crude product (3 g, yield: 74.6%). The crude product was directly used in the next step.

ESI-MS m/z: 253 [M+H]⁺.

Step 5: Synthesis of Compound Int_129-8

int_1-5 (3.50 g, 9.80 mmol) was dissolved in DCM (50 mL), and HATU (6.71 g, 17.6 mmol) and DIPEA (4.56 g, 35.3 mmol) were added. The reaction solution was stirred at room temperature for 0.5 h, and int_129-7 (4.20 g, 11.76 mmol) was then added. The reaction solution was heated to 50° C. and stirred for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, PE:EtOAC=10:1 to 3:1) to give a solid (5 g, yield: 71.9%).

¹H NMR (400 MHz, CHLOROFORM-d) δ 12.32 (s, 1H), 8.03-7.86 (m, 1H), 7.72-7.47 (m, 4H), 7.18 (d, J=10.6 Hz, 2H), 6.70 (d, J=1.4 Hz, 1H), 5.23 (s, 2H), 3.47 (br t, J=5.3 Hz, 4H), 3.02 (br t, J=5.0 Hz, 4H), 2.31-2.02 (m, 4H), 1.75-1.45 (m, 5H).

ESI-MS m/z: 592 [M+H]⁺.

Step 6: Synthesis of Compound 129

int_1-8 (1.03 g, 8.24 mmol), dimethylcyclohexane-1,2-diamine (781 mg, 5.50 mmol), cuprous iodide (1.05 g, 5.50 mmol), and Cs₂CO₃ (3.58 g, 11.0 mmol) were dissolved in DMF (70 mL). The solution was purged with argon three times, and int_129-8 (3.25 g, 5.50 mmol) was added. The reaction solution was heated to 110° C. and reacted for 16 h under argon atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography (SiO₂, DCM:MeOH=10:1 to 1:1) to give a solid (1.5 g, yield: 46.4%).

¹H NMR (400 MHZ, DMSO-d6) δ 11.70 (s, 2H), 7.94 (d, J=2.1 Hz, 1H), 7.86-7.76 (m, 2H), 7.14 (d, J=2.1 Hz, 1H), 7.07 (d, J=1.9 Hz, 1H), 7.01 (dd, J=8.5, 2.0 Hz, 1H), 6.93 (d, J=2.1 Hz, 1H), 3.74 (t, J=6.6 Hz, 2H), 3.44 (t, J=5.7 Hz, 4H), 3.29 (d, J=6.6 Hz, 2H), 2.96 (t, J=5.2 Hz, 4H), 2.24-2.07 (m, 4H), 1.55 (s, 4H), 0.33 (s, 4H).

ESI-MS m/z: 589 [M+H]⁺.

Example 4. Synthesis of Compound 385

Step 1: Synthesis of Compound Int_385-2

int_385-1 (5.00 g, 20.7 mmol) was dissolved in DMF (50 mL), and t-BuOK (2.44 g, 21.8 mmol) was added at 0° C. under nitrogen atmosphere. After 0.5 h of reaction, CH₃I (5.41 g, 37.3 mmol, 98% purity) was added at 0° C. The reaction solution was heated to 25° C. and reacted for 1 h, and TLC monitoring showed the reaction was complete. 50 mL of water was added to the reaction solution, and a precipitate precipitated out. The mixture was filtered to give a filter cake, and the filter cake was washed with water (100 mL×2) and dried to give a yellow solid (5 g, crude product). The solid was used directly in the next step.

¹H NMR: (400 MHZ, CHLOROFORM-d) δ 4.14 (s, 3H) 6.59 (d, J=3.25 Hz, 1H) 7.08 (d, J=3.25 Hz, 1H) 8.19 (d, J=2.13 Hz, 1H) 8.40 (d, J=2.13 Hz, 1H).

Step 2: Synthesis of Compound Int_385-4

int_385-2 (4.80 g, 18.8 mmol) was dissolved in methylbenzene (50 mL), and RuPhos Pd G3 (1.57 g, 1.88 mmol), Cs₂CO₃ (12.3 g, 37.6 mmol), and int_385-3 (4.56 g, 37.6 mmol) were added. The reaction solution was heated to 100° C. and reacted for 16 h under nitrogen atmosphere, and TLC monitoring showed the reaction was complete. The reaction solution was diluted with water (100 mL), and the aqueous phase was extracted with ethyl acetate (100 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, EtOAc:Hexane=1:30 to 1:3) to give the target product (3.4 g, yield: 61.2%).

Step 3: Synthesis of Compound Int_385-5

int_385-4 (3.40 g, 11.5 mmol) was dissolved in ethanol (35 mL), and Fe (6.43 g, 115 mmol, 10.0 eq) and an ammonium chloride solution (6.16 g, 115 mmol, 3.4 M) were added at room temperature. The reaction solution was stirred at 70° C. for 0.5 h. TLC monitoring showed the reaction was complete. The reaction solution was diluted with water (20 mL), and the aqueous phase was extracted with ethyl acetate (20 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product (3.7 g). The crude product was directly used in the next step.

¹H NMR: (400 MHZ, CHLOROFORM-d) δ 6.82 (d, J=2.9 Hz, 1H), 6.75 (s, 1H), 6.46 (s, 1H), 6.22 (d, J=2.9 Hz, 1H), 3.98 (s, 3H), 3.18 (br d, J=10.9 Hz, 2H), 2.96-2.89 (m, 2H), 2.19-2.01 (m, 6H).

Step 4: Synthesis of Compound Int_385-6

int_1-5 (3.50 g, 9.80 mmol) was dissolved in DCM (50 mL), and HATU (5.59 g, 14.7 mmol) and DIPEA (3.80 g, 29.4 mmol) were added. The reaction solution was stirred at room temperature for 0.5 h, and int_385-5 (2.60 g, 9.80 mmol) was then added. The reaction solution was heated to 50° C. and stirred for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, PE:EtOAc=1:0 to 3:1) to give a solid (1.25 g, yield: 21.1%).

ESI-MS m/z: 605 [M+H]⁺.

Step 5: Synthesis of Compound 385

int_385-6 (1.25 g, 2.07 mmol), dimethylcyclohexane-1,2-diamine (29.4 mg, 206 μmol), cuprous iodide (393 mg, 2.07 mmol), and Cs₂CO₃ (1.35 g, 4.14 mmol) were dissolved in DMF (25 mL). The solution was purged with argon three times, and int_1-8 (388 mg, 3.10 mmol) was added. The reaction solution was heated to 90° C. and reacted for 3 h under argon atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography (SiO₂, EtOAc:Hexane=1:20 to 1:1) to give a solid (0.53 g, yield: 42.8%).

¹H NMR: (400 MHz, DMSO-d6) δ 11.76 (s, 1H), 10.06 (s, 1H), 7.94-7.85 (m, 2H), 7.22-7.20 (m, 1H), 7.19 (d, J=1.8 Hz, 2H), 7.06 (dd, J=2.1, 8.6 Hz, 1H), 6.39 (d, J=3.0 Hz, 1H), 4.94 (t, J=5.6 Hz, 1H), 4.08 (s, 3H), 3.77 (q, J=6.3 Hz, 2H), 3.42 (br s, 4H), 3.03-2.85 (m, 6H), 2.35-2.13 (m, 4H), 1.61 (br s, 4H), 0.37 (s, 4H).

ESI-MS m/z: 602 [M+H]⁺.

Example 5. Synthesis of Compound 513

Step 1: Synthesis of Compound Int_513-2

int_513-1 (25.0 g, 84.2 mmol), K₂CO₃ (34.9 g, 252 mmol), and Mel (119 g, 842 mmol, 52.4 mL) were dissolved in acetone (250 mL), and the reaction solution was heated to 60° C. and reacted for 18 h under nitrogen atmosphere. TLC monitoring showed the reaction was complete. Water (200 mL) was added to the reaction solution to quench the reaction. The aqueous phase was extracted with dichloromethane (200 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (ISCO®; 120 g SepaFlash® Silica Flash Column, Eluent of 0-7% Ethyl acetate/Petroleum ether gradient @ 80 mL/min) to give a solid (23 g, yield: 87.8%).

¹H NMR (400 MHZ, DMSO-d6) δ=8.49 (m, 2H) 3.91 (s, 3H).

Step 2: Synthesis of Compound Int_513-3

int_513-2 (12.0 g, 38.5 mmol), NH₂ Boc (4.52 g, 38.5 mmol), Cs₂CO₃ (25.1 g, 77.1 mmol), and XantPhos Pd G3 (1.83 g, 1.93 mmol) were dissolved in methylbenzene (120 mL). The reaction solution was heated to 100° C. and reacted for 3 h under nitrogen atmosphere, and LC-MS monitoring showed the reaction was complete. Water (500 mL) was added to the reaction solution. The aqueous phase was extracted with dichloromethane (500 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (ISCOR; 200 g SepaFlash® Silica Flash Column, Eluent of 0-10% Ethyl acetate/Petroleum ether gradient @ 80 mL/min) to give a solid (9 g, yield: 67.1%).

¹H NMR (400 MHZ, DMSO-d6) δ=9.16 (s, 1H) 8.77 (d, J=2.81 Hz, 1H) 8.12 (d, J=2.81 Hz, 1H) 3.84 (s, 3H) 1.51 (s, 9H).

Step 3: Synthesis of Compound Int_513-5

int_513-3 (4 g, 11.52 mmol), int_513-4 (2.79 g, 23.0 mmol), Pd₂(dba)₃ (1.06 g, 1.15 mmol, 0.10 eq), Xantphos (1.33 g, 2.30 mmol, 0.20 eq), and Cs₂CO₃ (7.51 g, 23.0 mmol, 2.00 eq) were dissolved in methylbenzene (100 mL), and the reaction solution was heated to 100° C. and stirred for 3 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. 50 mL of water was added to the reaction solution. The aqueous phase was extracted with dichloromethane (50 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (ISCO®; 40 g SepaFlash R Silica Flash Column, Eluent of 0-20% Ethyl acetate/Petroleum ether gradient @ 50 mL/min) to give a solid (1.78 g, yield: 39.8%).

¹H NMR (400 MHZ, DMSO-d6) δ=8.71 (s, 1H) 8.46 (d, J=2.50 Hz, 1H) 7.51 (d, J=2.75 Hz, 1H) 3.87 (m, 3H) 3.19 (br t, J=5.19 Hz, 4H) 2.16 (m, 4H) 1.49 (s, 9H).

Step 4: Synthesis of Compound Int_513-6

int_513-5 (1.78 g, 4.60 mmol) was dissolved in ethyl acetate (10 mL), and a HCl/ethyl acetate solution (2.50 M, 2.00 mL) was slowly added dropwise to the reaction solution under nitrogen atmosphere. The reaction solution was heated to 40° C. and stirred for 3 h. LC-MS monitoring showed the reaction was complete. The reaction solution was distilled under reduced pressure to give a crude product (1.65 g, yield: 99.8%). The crude product was directly used in the next step.

ESI-MS m/z: 288 [M+H]⁺

Step 5: Synthesis of Compound Int_513-7

int_513-6 (798 mg, 2.78 mmol) was dissolved in DCM (10 mL), and BBr₃ (2.79 g, 11.1 mmol, 1.07 mL) was added to the reaction solution at 0° C. under nitrogen atmosphere. The reaction solution was slowly heated to room temperature and reacted for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was diluted with water (50 mL), and the aqueous phase was extracted with dichloromethane (50 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (ISCOR; 40 g SepaFlash® Silica Flash Column, Eluent of 0-30% Ethyl acetate/Petroleum ether gradient @ 50 mL/min) to give the target product (0.52 g, yield: 68.4%).

¹H NMR (400 MHZ, DMSO-d6) δ=7.35 (d, J=2.69 Hz, 1H) 7.25 (d, J=2.69 Hz, 1H) 4.09 (br s, 1H) 3.17 (s, 2H) 2.94 (br t, J=5.20 Hz, 4H) 2.18 (m, 4H).

Step 6: Synthesis of Compound Int_513-8

int_513-7 (0.52 g, 1.90 mmol) was dissolved in trimethyl orthoformate (50.3 g, 474 mmol, 52.0 mL), and the reaction solution was heated to 105° C. and stirred for 18 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was distilled under reduced pressure to give a crude product (0.5 g). The crude product was directly used in the next step.

ESI-MS m/z: 284 [M+H]⁺.

Step 7: Synthesis of Compound Int_513-9

int_513-8 (0.50 g, 1.77 mmol) and Pd/C (0.05 g, 1.77 mmol, 10% purity) were dissolved in methanol (5 mL). The reaction solution was reacted at 25° C. for 18 h under hydrogen atmosphere, and LC-MS monitoring showed the reaction was complete. The reaction solution was filtered, and the filtrate was distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography (ISCO®; 80 g SepaFlash® Silica Flash Column, Eluent of 30% Ethyl acetate/Petroleum ether gradient @ 80 mL/min) to give a solid (0.3 g, yield: 68.2%).

¹H NMR (400 MHZ, DMSO-d6) δ=7.35 (d, J=2.69 Hz, 1H) 7.25 (d, J=2.69 Hz, 1H) 4.09 (br s, 1H) 3.17 (s, 2H) 2.94 (br t, J=5.20 Hz, 4H) 2.18 (m, 4H).

Step 8: Synthesis of Compound Int_513-10

int_1-5 (124 mg, 0.3 mmol) was dissolved in DCM (10 mL), and oxalyl chloride (253.8 mg, 2 mmol) was added. The reaction solution was stirred at room temperature for 2 h and then concentrated under reduced pressure to remove the solvent, thus giving an acyl chloride solid. int_513-9 (76 mg, 0.3 mmol) was dissolved in THF (5 mL), and sodium hydride (72 mg, 1.8 mmol, 60% purity) was added at 0° C. under nitrogen atmosphere. The reaction solution was heated to room temperature and reacted for 1 h, and then the reaction solution was cooled to 0° C. The acyl chloride prepared above was slowly added to the reaction solution, and the reaction solution was heated to 40° C. and stirred for 12 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (100 mg, yield: 56.2%).

ESI-MS m/z: 593 [M+H]⁺.

Step 9: Synthesis of Compound 513

int_1-8 (63 mg, 0.51 mmol), dimethylcyclohexane-1,2-diamine (12 mg, 0.085 mmol), cuprous iodide (16 mg, 0.085 mmol), and potassium phosphate (108 mg, 0.51 mmol) were dissolved in DMF (5 mL). The solution was purged with argon three times, and int_513-10 (100 mg, 0.17 mmol) was added. Under argon atmosphere, the reaction solution was heated to 100° C. and reacted for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography to give a solid (33 mg, yield: 33%).

¹H NMR (400 MHZ, DMSO-d6) δ 11.71 (s, 1H), 10.09 (s, 1H), 8.67 (s, 1H), 7.87 (d, J=1.7 Hz, 1H), 7.82 (d, J=8.5 Hz, 1H), 7.21 (d, J=1.8 Hz, 1H), 7.15 (d, J=2.1 Hz, 1H), 7.01 (dd, J=8.5, 2.1 Hz, 1H), 3.74 (t, J=6.6 Hz, 2H), 3.50 (t, J=5.8 Hz, 4H), 2.96 (t, J=5.3 Hz, 4H), 2.15 (tt, J=13.4, 5.6 Hz, 4H), 1.53 (s, 4H), 0.32 (s, 4H).

ESI-MS m/z: 590 [M+H]⁺.

Example 6. Synthesis of Compound 522

Step 1: Synthesis of Compound Int_522-2

int_522-1 (620 mg, 1.87 mmol) and int_522-2 (226 mg, 1.87 mmol) were dissolved in 1,4-dioxane (15 mL), and cesium carbonate (913 mg, 2.8 mmol), Pd₂(dba)₃ (171 mg, 0.187 mmol), and XantPhOS (108 mg, 0.187 mmol) were added to the reaction solution. The reaction solution was heated to 100° C. and stirred for 18 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was diluted with water (30 mL), and the aqueous phase was extracted with ethyl acetate (30 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product, and the crude product was purified by column chromatography (SiO₂, EtOAc:Hexane=1:25) to give the target product (486 mg, yield: 70%).

ESI-MS m/z: 372 [M+H]⁺.

Step 2: Synthesis of Compound Int_522-4

int_522-3 (486 mg, 1.309 mmol), NH₂Boc (460 mg, 3.8 mmol), Pd₂(dba)₃ (24 mg, 0.026 mmol), X-PhOS (18 mg, 0.039 mmol), and cesium carbonate (633 mg, 1.95 mmol) were dissolved in 1,4-dioxane (5 mL), and the reaction solution was heated to 100° C. and stirred for 16 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was diluted with water (30 mL), and the aqueous phase was extracted with ethyl acetate (30 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product, and the crude product was purified by column chromatography (SiO₂, EtOAc:Hexane=1:10) to give the target product (406 mg, yield: 68.3%).

ESI-MS m/z: 453 [M+H]⁺.

Step 3: Synthesis of Compound Int_522-5

int_522-4 (400 mg, 0.878 mmol) was dissolved in dichloromethane (10 mL), and trifluoroacetic acid (4 mL) was added at 0° C. The mixture was heated to 25° C. and reacted for 2 h, and LC-MS monitoring showed the reaction was complete. A saturated sodium bicarbonate solution was added to the reaction solution at 0° C. to adjust the pH to 7. The aqueous phase was extracted with dichloromethane (30 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (220 mg, yield: 100%).

ESI-MS m/z: 253 [M+H]⁺.

Step 4: Synthesis of Compound Int_522-6

int_1-5 (140 mg, 0.396 mmol) was dissolved in DCM (10 mL), and oxalyl chloride (253.8 mg, 2 mmol) was added. The reaction solution was stirred at room temperature for 2 h and then concentrated under reduced pressure to remove the solvent, thus giving an acyl chloride solid. int_522-5 (100 mg, 0.396 mmol) was dissolved in DCM (10 mL), and DIPEA (255 mg, 1.98 mmol) was added under nitrogen atmosphere. Then the reaction solution was cooled to 0° C., and the acyl chloride prepared above was slowly added to the reaction solution. The reaction solution was heated to room temperature and stirred for 1 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (106 mg, yield: 45.2%).

ESI-MS m/z: 592 [M+H]⁺.

Step 5: Synthesis of Compound 522

int_1-8 (45 mg, 0.358 mmol), dimethylcyclohexane-1,2-diamine (13 mg, 0.0895 mmol), cuprous iodide (17 mg, 0.0895 mmol), and potassium phosphate (114 mg, 0.537 mmol) were dissolved in DMF (10 mL). The solution was purged with argon three times, and int_522-6 (106 mg, 0.179 mmol) was added. Under argon atmosphere, the reaction solution was heated to 100° C. and reacted for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography to give a solid (10 mg, yield: 9.5%).

¹H NMR (400 MHZ, DMSO-d6) δ 12.69 (s, 1H), 11.33 (s, 1H), 8.12-7.99 (m, 2H), 7.44 (t, J=2.8 Hz, 1H), 7.21 (d, J=2.1 Hz, 1H), 7.07 (dd, J=8.5, 2.1 Hz, 1H), 6.44 (d, J=2.9 Hz, 1H), 3.73 (t, J=6.5 Hz, 2H), 3.52 (t, J=5.7 Hz, 4H), 2.96 (s, 4H), 2.30-2.11 (m, 4H), 1.67 (s, 4H), 0.37 (s, 4H).

ESI-MS m/z: 589 [M+H]⁺.

Example 7. Synthesis of Compound 530

Step 1: Synthesis of Compound Int_530-2

int_530-1 (7.40 g, 42.5 mmol) was dissolved in concentrated sulfuric acid (50 mL), and NBS (8.32 g, 46.74 mmol) was added to the reaction solution. The reaction solution was heated to 50° C. and stirred for 5 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was slowly added to ice water (200 mL). The aqueous phase was extracted with ethyl acetate (200 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography to give the target product (9 g, yield: 83.7%).

¹H NMR (400 MHZ, CHLOROFORM-d) δ=9.26 (dd, J=1.6, 4.1 Hz, 1H), 8.89 (d, J=2.5 Hz, 1H), 8.82 (d, J=2.5 Hz, 1H), 8.46-8.40 (m, 1H), 7.69 (dd, J=4.3, 8.3 Hz, 1H).

Step 2: Synthesis of Compound Int_530-4

int_522-2 (9.00 g, 35.6 mmol), int_522-3 (6.46 g, 53.6 mmol), Cs₂CO₃ (23.1 g, 71.1 mmol), and RuPhos Pd G3 (2.97 g, 3.56 mmol) were dissolved in methylbenzene (100 mL), and the reaction solution was heated to 80° C. and stirred for 16 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was diluted with water (200 mL), and the aqueous phase was extracted with ethyl acetate (200 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography to give the target product (4 g, yield: 38.4%).

ESI-MS m/z: 294 [M+H]⁺.

Step 3: Synthesis of Compound Int_530-5

int_530-4 (2.00 g, 6.82 mmol) was dissolved in methanol (30 mL), and Pd/C (1.00 g, 10% purity) was added. The reaction solution was reacted at 25° C. for 16 h under hydrogen atmosphere, and LC-MS monitoring showed the reaction was complete. The reaction solution was filtered, and the filtrate was distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (2.2 g, yield: 61.3%).

¹H NMR (400 MHZ, CHLOROFORM-d) δ=8.57 (br d, J=2.5 Hz, 1H), 7.79 (br d, J=8.1 Hz, 1H), 7.23-7.13 (m, 2H), 6.60-6.46 (m, 2H), 4.05-3.63 (m, 2H), 3.39 (br t, J=4.8 Hz, 4H), 2.35-2.14 (m, 4H).

Step 4: Synthesis of Compound Int_530-6

int_1-5 (124 mg, 0.3 mmol) was dissolved in DCM (10 mL), and oxalyl chloride (253.8 mg, 2 mmol) was added. The reaction solution was stirred at room temperature for 2 h and then concentrated under reduced pressure to remove the solvent, thus giving an acyl chloride solid. int_530-5 (80 mg, 0.3 mmol) was dissolved in DCM (10 mL), and NaH (72 mg, 1.8 mmol, 60% purity) was added under nitrogen atmosphere. Then the reaction was cooled to 0° C., and the acyl chloride prepared above was slowly added to the reaction solution. The reaction solution was heated to 40° C. and stirred for 12 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (58 mg, yield: 32.2%).

ESI-MS m/z: 603 [M+H]⁺

Step 5: Synthesis of Compound 530

int_1-8 (19 mg, 0.15 mmol), dimethylcyclohexane-1,2-diamine (7 mg, 0.05 mmol), cuprous iodide (10 mg, 0.05 mmol), and potassium phosphate (63 mg, 0.3 mmol) were dissolved in DMF (5 mL). The solution was purged with argon three times, and int_530-6 (58 mg, 0.1 mmol) was added. Under argon atmosphere, the reaction solution was heated to 100° C. and reacted for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography to give a solid (14 mg, yield: 98.1%).

¹H NMR (400 MHZ, CHLOROFORM-d) δ 12.84 (s, 1H), 8.85-8.75 (m, 1H), 8.27 (s, 1H), 8.21 (s, 1H), 8.13 (d, J=8.2 Hz, 1H), 7.45-7.29 (m, 2H), 7.04 (d, J=32.6 Hz, 2H), 4.15 (s, 2H), 3.55 (d, J=6.4 Hz, 4H), 3.34 (s, 2H), 3.12 (s, 4H), 2.32 (d, J=14.4 Hz, 4H), 1.71 (s, 4H), 0.45 (s, 4H).

ESI-MS m/z: 600 [M+H]⁺.

Example 10. Synthesis of Compound 537

Step 1: Synthesis of Compound Int_537-2

int_1-5 (100 mg, 0.28 mmol) was dissolved in DCM (10 mL), and oxalyl chloride (253.8 mg, 2 mmol) was added. The reaction solution was stirred at room temperature for 2 h and then concentrated under reduced pressure to remove the solvent, thus giving an acyl chloride solid. int_537-1 (71.7 mg, 0.28 mmol) was dissolved in DCM (10 mL), and NaH (112 mg, 2.8 mmol, 60% purity) was added under nitrogen atmosphere. Then the reaction solution was cooled to 0° C., and the acyl chloride prepared above was slowly added to the reaction solution. The reaction solution was heated to 45° C. and stirred for 3 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (127 mg, yield: 76.1%).

ESI-MS m/z: 596 [M+H]⁺.

Step 2: Synthesis of Compound 537

int_1-8 (25 mg, 0.2 mmol), dimethylcyclohexane-1,2-diamine (18 mg, 0.125 mmol), cuprous iodide (26 mg, 0.125 mmol), and potassium phosphate (164 mg, 0.747 mmol) were dissolved in DMF (5 mL). The solution was purged with argon three times, and int_537-2 (120 mg, 0.2 mmol) was added. Under argon atmosphere, the reaction solution was heated to 100° C. and reacted for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography to give a solid (76 mg, yield: 64.1%).

ESI-MS m/z: 593 [M+H]⁺.

Example 9. Synthesis of Compound 539

Step 1: Synthesis of Compound Int_539-2

int_539-1 (500 mg, 2.34 mmol) was dissolved in concentrated sulfuric acid (6 mL), and KNO₃ (356 mg, 3.51 mmol) was added to the reaction solution. The reaction solution was heated to room temperature and stirred for 2 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was slowly added to ice water (50 mL). The aqueous phase was extracted with dichloromethane (50 mL×3), and the organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography to give the target product (395 mg, yield: 65.2%).

ESI-MS m/z: 258 [M+H]⁺.

Step 2: Synthesis of Compound Int_539-4

int_539-2 (300 mg, 1.16 mmol), int_539-3 (155 mg, 1.27 mmol), Cs₂CO₃ (756 mg, 2.32 mmol), and RuPhos Pd G3 (97 mg, 0.116 mmol) were dissolved in 1,4-dioxane (20 mL), and the reaction solution was heated to 100° C. and stirred for 12 h under nitrogen atmosphere. LC-MS monitoring showed the reaction was complete. The reaction solution was diluted with water (20 mL), and the aqueous phase was extracted with ethyl acetate (20 mL×3). The organic phase was dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography to give the target product (200 mg, yield: 44.4%).

ESI-MS m/z: 299 [M+H]⁺.

Step 3: Synthesis of Compound Int_539-5

int_530-4 (200 mg, 0.67 mmol) was dissolved in methanol (15 mL), and Pd/C (200 mg, 10% purity) was added. The reaction solution was reacted at 25° C. for 16 h under hydrogen atmosphere, and LC-MS monitoring showed the reaction was complete. The reaction solution was filtered, and the filtrate was distilled under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (140 mg, yield: 78.2%).

ESI-MS m/z: 269 [M+H]⁺.

Step 4: Synthesis of Compound Int_539-6

int_1-5 (200 mg, 0.559 mmol) was dissolved in DCM (10 mL), and oxalyl chloride (253.8 mg, 2 mmol) was added. The reaction solution was stirred at room temperature for 2 h and then concentrated under reduced pressure to remove the solvent, thus giving an acyl chloride solid. int_539-5 (120 mg, 0.447 mmol) was dissolved in DCM (10 mL), and DIPEA (173 mg, 1.34 mmol) was added under nitrogen atmosphere. Then the reaction solution was cooled to 0° C., and the acyl chloride prepared above was slowly added to the reaction solution. The reaction solution was heated to 40° C. and stirred at room temperature for 1 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (235 mg, yield: 74.3%).

ESI-MS m/z: 608 [M+H]⁺.

Step 5: Synthesis of Compound 539

int_1-8 (97 mg, 0.773 mmol), dimethylcyclohexane-1,2-diamine (27 mg, 0.193 mmol), cuprous iodide (37 mg, 0.193 mmol), and potassium phosphate (246 mg, 1.158 mmol) were dissolved in DMF (15 mL). The solution was purged with argon three times, and int_539-6 (235 mg. 0.386 mmol) was added. Under argon atmosphere, the reaction solution was heated to 100° C. and reacted for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography to give a solid (160 mg, yield: 68.6%).

¹H NMR (400 MHZ, DMSO-d6) δ 11.51 (s, 1H), 7.80 (d, J=8.5 Hz, 1H), 7.28 (d, J=2.3 Hz, 1H), 7.13 (d, J=2.1 Hz, 1H), 7.03 (d, J=2.4 Hz, 1H), 7.00 (dd, J=8.5, 2.1 Hz, 1H), 4.17-4.10 (m, 2H), 3.73 (t, J=6.6 Hz, 2H), 3.31 (s, 2H), 3.05 (t, J=5.5 Hz, 4H), 2.93 (t, J=5.3 Hz, 4H), 2.72 (t, J=6.5 Hz, 2H), 2.06 (q, J=6.0 Hz, 4H), 1.90 (p, J=6.1 Hz, 2H), 1.53 (t, J=5.3 Hz, 4H), 0.33 (s, 4H).

ESI-MS m/z: 605 [M+H]⁺.

Example 10. Synthesis of Compound 583

Step 1: Synthesis of Compound Int_583-2

int_1-5 (100 mg, 0.28 mmol) was dissolved in DCM (10 mL), and oxalyl chloride (253.8 mg, 2 mmol) was added. The reaction solution was stirred at room temperature for 2 h and then concentrated under reduced pressure to remove the solvent, thus giving an acyl chloride solid. int_530-5 (74 mg, 0.28 mmol) was dissolved in DCM (10 mL), and NaH (112 mg, 2.8 mmol, 60% purity) was added under nitrogen atmosphere. Then the reaction solution was cooled to 0° C., and the acyl chloride prepared above was slowly added to the reaction solution. The reaction solution was heated to 45° C. and stirred for 3 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (150 mg, yield: 88.8%).

ESI-MS m/z: 604 [M+H]⁺.

Step 2: Synthesis of Compound 583

int_1-8 (34 mg, 0.249 mmol), dimethylcyclohexane-1,2-diamine (18 mg, 0.125 mmol), cuprous iodide (26 mg, 0.125 mmol), and potassium phosphate (164 mg, 0.747 mmol) were dissolved in DMF (5 mL). The solution was purged with argon three times, and int_583-2 (150 mg, 0.249 mmol) was added. Under argon atmosphere, the reaction solution was heated to 100° C. and reacted for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography to give a solid (57 mg, yield: 38%).

¹H NMR (400 MHZ, DMSO-d6) δ 12.93 (s, 1H), 8.70 (dd, J=4.2, 1.8 Hz, 1H), 8.22 (dd, J=8.5, 1.8 Hz, 1H), 8.09 (s, 1H), 8.05 (d, J=8.6 Hz, 1H), 7.59 (dd, J=8.4, 4.1 Hz, 1H), 7.21 (d, J=2.1 Hz, 1H), 7.07 (dd, J=8.7, 2.1 Hz, 1H), 4.17 (t, J=5.3 Hz, 4H), 3.73 (t, J=6.5 Hz, 2H), 2.99 (d, J=6.7 Hz, 4H), 2.15 (dq, J=14.0, 7.2, 5.8 Hz, 4H), 1.73 (s, 4H), 0.39 (s, 4H).

ESI-MS m/z: 601 [M+H]⁺.

Example 11. Synthesis of Compound 584

Step 1: Synthesis of Compound Int_584-3

int_584-1 (100 mg, 0.341 mmol) was dissolved in DCM (5 mL), and oxalyl chloride (253.8 mg, 2 mmol) was added. The reaction solution was stirred at room temperature for 2 h and then concentrated under reduced pressure to remove the solvent, thus giving an acyl chloride solid. int_584-2 (90 mg, 0.321 mmol) was dissolved in THF (5 mL), and NaH (112 mg, 2.8 mmol, 60% purity) was added under nitrogen atmosphere. Then the reaction solution was cooled to 0° C., and the acyl chloride prepared above was slowly added to the reaction solution. The reaction solution was heated to 45° C. and stirred for 12 h. LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography to give a solid (150 mg, yield: 83.8%).

ESI-MS m/z: 556 [M+H]⁺.

Step 2: Synthesis of Compound 584

int_1-8 (84 mg, 0.674 mmol), dimethylcyclohexane-1,2-diamine (32 mg, 0.225 mmol), cuprous iodide (43 mg, 0.225 mmol), and potassium phosphate (286 mg, 1.348 mmol) were dissolved in DMF (10 mL). The solution was purged with argon three times, and int_584-3 (150 mg, 0.270 mmol) was added. Under argon atmosphere, the reaction solution was heated to 100° C. and reacted for 16 h. LC-MS monitoring showed the reaction was complete. The reaction solution was cooled to room temperature, concentrated to dryness by rotary evaporation, and purified by column chromatography to give a solid (50 mg, yield: 30.9%).

¹H NMR (400 MHZ, DMSO-d6) δ 9.67 (s, 1H), 8.97 (dt, J=4.1, 2.1 Hz, 1H), 8.47 (dd, J=8.3, 1.9 Hz, 1H), 8.18 (d, J=2.0 Hz, 1H), 7.98 (d, J=8.6 Hz, 1H), 7.72-7.58 (m, 2H), 7.11 (d, J=2.4 Hz, 1H), 6.98 (dd, J=8.6, 2.3 Hz, 1H), 3.73 (t, J=6.8 Hz, 2H), 3.55 (t, J=5.5 Hz, 4H), 3.22 (t, J=6.7 Hz, 2H), 2.86 (t, J=5.2 Hz, 4H), 2.24 (q, J=12.2 Hz, 4H), 1.51 (s, 4H), 0.32 (d, J=2.3 Hz, 4H).

Example 12. Synthesis of Compound 595

Step 1: Synthesis of Compound Int_595-2

1 (0.50 g, 846 μmol) was dissolved in tetrahydrofuran (10 mL), and int_595-1 (919 mg, 4.23 mmol), BOPCl (538 mg, 2.12 mmol), 3-nitro-4H-1,2,4-triazole (241 mg, 2.12 mmol), and DIPEA (547 mg, 4.23 mmol) were added. The mixture was reacted at room temperature for 4 h, and LC-MS monitoring showed the reaction was complete. The reaction solution was filtered to give a filtrate, and the filtrate was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, PE/EtOAc=10/0 to 1/1) to give the target product (0.6 g, yield: 89.7%).

ESI-MS m/z: 790 [M+H]⁺.

Step 2: Synthesis of Compound 595

int_595-2 (0.60 g, 759 μmol) was dissolved in a HCl/dioxane solution (4 M, 6 mL). The solution was reacted at room temperature for 2 h, and LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product, and a saturated NaHCO₃ solution (6 mL) was added to the crude product to adjust the pH to 7-8. The aqueous phase was extracted with dichloromethane (6 mL×3), and the organic phases were combined, dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give the target product (490 mg, yield: 90.3%).

¹H NMR (400 MHZ, CHLOROFORM-d) δ 12.13 (s, 1H), 8.17 (d, J=8.5 Hz, 1H), 7.31 (s, 1H), 7.26 (d, J=1.9 Hz, 1H), 7.06 (s, 1H), 6.98 (dd, J=1.9, 8.5 Hz, 1H), 4.60-4.46 (m, 4H), 3.43-3.35 (m, 2H), 3.27-3.20 (m, 5H), 3.17 (t, J=8.8 Hz, 2H), 3.00 (br t, J=5.1 Hz, 4H), 2.15-1.92 (m, 5H), 1.58 (br s, 4H), 0.90 (dd, J=6.9, 11.5 Hz, 6H), 0.35 (s, 4H).

ESI-MS m/z: 690 [M+H]⁺.

Example 13. Synthesis of Compound 611

Step 1: Synthesis of Compound Int_611-1

385 (0.58 g, 985 μmol) was dissolved in tetrahydrofuran (10 mL), and int_595-1 (1.07 g, 4.93 mmol), BOPCl (627 mg, 2.46 mmol), 3-nitro-4H-1,2,4-triazole (281 mg, 2.46 mmol), and DIPEA (637 mg, 4.93 mmol) were added. The mixture was reacted at room temperature for 4 h, and LC-MS monitoring showed the reaction was complete. The reaction solution was filtered to give a filtrate, and the filtrate was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, PE/EtOAc=5/1 to 3/1) to give the target product (0.17 g, yield: 38.5%).

ESI-MS m/z: 788 [M+H]⁺.

Step 2: Synthesis of Compound 611

int_611-1 (0.93 g, 1.18 mmol) was dissolved in a HCl/dioxane solution (4 M, 2.95 mL). The solution was reacted at room temperature for 0.5 h, and LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product, and a saturated NaHCO₃ solution (10 mL) was added to the crude product to adjust the pH to 7-8. The aqueous phase was extracted with dichloromethane (10 mL×3), and the organic phases were combined, dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give the target product (130 mg, yield: 28.5%).

¹H NMR (400 MHZ, DMSO-d6) δ 12.29 (s, 1H), 8.20-8.18 (d, J=8.4 Hz, 1H), 7.62 (s, 1H), 7.54 (s, 1H), 7.28 (d, J=2.0 Hz, 1H), 7.19-7.14 (m, 1H), 7.08 (d, J=2.1 Hz, 1H), 6.69 (d, J=2.0 Hz, 1H), 4.51 (t, J=5.8 Hz, 2H), 3.45 (m, 4H), 3.39 (m, 2H), 3.25-3.16 (m, 1H), 3.12 (br s, 4H), 2.39-2.22 (m, 4H), 2.01-1.83 (m, 1H), 1.81-1.64 (m, 4H), 0.97-0.87 (m, 6H), 0.48 (s, 4H).

ESI-MS m/z: 688 [M+H]⁺.

Example 14. Synthesis of Compound 643

Step 1: Synthesis of Compound Int_643-1

385 (0.50 g, 831 μmol) was dissolved in tetrahydrofuran (10 mL), and int_595-1 (902 mg, 4.15 mmol), BOPCl (528 mg, 2.08 mmol), 3-nitro-4H-1,2,4-triazole (237 mg, 2.08 mmol), and DIPEA (537 mg, 4.15 mmol) were added. The mixture was reacted at room temperature for 4 h, and LC-MS monitoring showed the reaction was complete. The reaction solution was filtered to give a filtrate, and the filtrate was concentrated under reduced pressure to give a crude product. The crude product was purified by column chromatography (SiO₂, PE/EtOAc=10/0 to 1/1) to give the target product (0.5 g, yield: 75.1%).

ESI-MS m/z: 801 [M+H]⁺.

Step 2: Synthesis of Compound 643

int_643-1 (0.50 g, 624.3 μmol) was dissolved in a HCl/dioxane solution (4 M, 5 mL). The solution was reacted at room temperature for 2 h, and LC-MS monitoring showed the reaction was complete. The reaction solution was concentrated under reduced pressure to give a crude product, and a saturated NaHCO₃ solution (5 mL) was added to the crude product to adjust the pH to 7-8. The aqueous phase was extracted with dichloromethane (5 mL×3), and the organic phases were combined, dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure to give the target product (130 mg, yield: 28.5%).

¹H NMR (400 MHZ, CHLOROFORM-d) δ 12.27 (s, 1H), 8.29 (d, J=8.5 Hz, 1H), 7.86 (d, J=1.6 Hz, 1H), 7.44 (d, J=1.6 Hz, 1H), 7.37 (d, J=1.6 Hz, 1H), 7.11 (br d, J=7.0 Hz, 1H), 7.01-6.97 (m, 1H), 6.51-6.47 (m, 1H), 4.73-4.50 (m, 2H), 4.18-4.09 (m, 3H), 3.57-3.47 (m, 2H), 3.35 (br d, J=10.4 Hz, 2H), 3.11 (br t, J=5.2 Hz, 7H), 2.13 (br s, 5H), 1.65 (br s, 4H), 1.06-0.96 (m, 6H), 0.46-0.37 (m, 4H).

ESI-MS m/z: 701 [M+H]⁺.

The target compounds 2-64, 66-128, 130-384, 386-512, 514-521, 523-529, 531-536, 538, 540-582, 585-594, 596-610, 612-642, and 644-814 in Table 1 were obtained by using the above synthesis methods with different starting materials.

TABLE 1
Compound	Compound structure	MS (M + H)+
2		571
3		571
4		563
5		584
6		567
7		542
8		573
9		573
10		553
11		559
12		557
13		605
14		605
15		585
16		585
17		591
18		571
19		571
20		563
21		584
22		567
23		542
24		573
25		573
26		553
27		559
28		557
29		605
30		605
31		585
32		585
33		591
34		571
35		571
36		563
37		584
38		567
39		542
40		573
41		573
42		553
43		559
44		557
45		605
46		605
47		585
48		585
49		591
50		571
51		571
52		563
53		584
54		567
55		542
56		573
57		574
58		553
59		559
60		557
61		605
62		605
63		585
64		585
65		592
66		572
67		572
68		564
69		585
70		568
71		543
72		574
73		574
74		554
75		560
76		558
77		606
78		606
79		586
80		586
81		592
82		572
83		572
84		564
85		585
86		568
87		543
88		574
89		574
90		554
91		560
92		558
93		606
94		606
95		586
96		586
97		592
98		572
99		572
100		564
101		585
102		568
103		543
104		574
105		574
106		554
107		560
108		558
109		606
110		606
111		586
112		586
113		592
114		572
115		572
116		564
117		585
118		568
119		543
120		574
121		574
122		554
123		560
124		558
125		606
126		606
127		586
128		586
129		589
130		569
131		569
132		561
133		582
134		565
135		540
136		571
137		571
138		551
139		557
140		555
141		603
142		603
143		583
144		583
145		589
146		569
147		569
148		561
149		582
150		565
151		540
152		571
153		571
154		551
155		557
156		555
157		603
158		603
159		583
160		583
161		589
162		569
163		569
164		561
165		582
166		565
167		540
168		571
169		571
170		551
171		557
172		555
173		603
174		603
175		583
176		583
177		589
178		569
179		569
180		561
181		582
182		565
183		540
184		571
185		571
186		551
187		557
188		555
189		603
190		603
191		583
192		583
193		590
194		570
195		570
196		562
197		583
198		566
199		541
200		572
201		572
202		552
203		558
204		556
205		604
206		604
207		584
208		584
209		590
210		570
211		570
212		562
213		583
214		566
215		541
216		572
217		572
218		552
219		558
220		556
221		604
222		604
223		584
224		584
225		590
226		570
227		570
228		562
229		583
230		566
231		541
232		572
233		572
234		552
235		558
236		556
237		604
238		604
239		584
240		584
241		590
242		570
243		570
244		562
245		583
246		566
247		541
248		572
249		572
250		552
251		558
252		556
253		604
254		604
255		584
256		584
257		604
258		584
259		584
260		576
261		597
262		580
263		555
264		586
265		586
266		566
267		572
268		570
269		618
270		618
271		598
272		598
273		604
274		584
275		584
276		576
277		597
278		580
279		555
280		586
281		586
282		566
283		572
284		570
285		618
286		618
287		598
288		598
289		604
290		584
291		584
292		576
293		597
294		580
295		555
296		586
297		586
298		566
299		572
300		570
301		618
302		618
303		598
304		598
305		604
306		584
307		584
308		576
309		597
310		580
311		555
312		586
313		586
314		566
315		572
316		570
317		618
318		618
319		598
320		598
321		605
322		585
323		585
324		577
325		598
326		581
327		556
328		587
329		587
330		567
331		573
332		571
333		619
334		619
335		599
336		599
337		605
338		585
339		585
340		577
341		598
342		581
343		556
344		587
345		587
346		567
347		573
348		571
349		619
350		619
351		599
352		599
353		605
354		585
355		585
356		577
357		598
358		581
359		556
360		587
361		587
362		567
363		573
364		571
365		619
366		619
367		599
368		599
369		605
370		585
371		585
372		577
373		598
374		581
375		556
376		587
377		587
378		567
379		573
380		571
381		619
382		619
383		599
384		599
385		602
386		582
387		582
388		574
389		595
390		578
391		553
392		584
393		584
394		564
395		570
396		568
397		616
398		616
399		596
400		596
401		602
402		582
403		582
404		574
405		595
406		578
407		553
408		584
409		584
410		564
411		570
412		568
413		616
414		616
415		596
416		596
417		602
418		582
419		582
420		574
421		595
422		578
423		553
424		584
425		584
426		564
427		570
428		568
429		616
430		616
431		596
432		596
433		602
434		582
435		582
436		574
437		595
438		578
439		553
440		584
441		584
442		564
443		570
444		568
445		616
446		616
447		596
448		596
449		603
450		583
451		583
452		575
453		596
454		579
455		554
456		585
457		585
458		565
459		571
460		569
461		617
462		617
463		597
464		597
465		603
466		583
467		583
468		575
469		596
470		579
471		554
472		585
473		585
474		565
475		571
476		569
477		617
478		617
479		597
480		597
481		603
482		583
483		583
484		575
485		596
486		579
487		554
488		585
489		585
490		565
491		571
492		569
493		617
494		617
495		597
496		597
497		603
498		583
499		583
500		575
501		596
502		579
503		554
504		585
505		585
506		565
507		571
508		569
509		617
510		617
511		597
512		597
513		590
514		591
515		606
516		607
517		590
518		591
519		606
520		607
521		588
522		589
523		590
524		591
525		589
526		590
527		603
528		603
529		599
530		600
531		603
532		589
533		589
534		590
535		589
536		590
537		593
538		594
539		605
540		606
541		604
542		605
543		607
544		608
545		605
546		605
547		605
548		606
549		606
550		606
551		633
552		633
553		633
554		633
555		634
556		634
557		634
558		634
559		631
560		631
561		631
562		631
563		632
564		632
565		632
566		632
567		646
568		646
569		646
570		646
571		647
572		647
573		647
574		647
575		644
576		644
577		644
578		644
579		645
580		645
581		645
582		645
583		601
584		601
585		607
586		608
587		706
588		706
589		707
590		707
591		690
592		690
593		690
594		690
595		690
596		690
597		690
598		690
599		691
600		691
601		691
602		691
603		691
604		691
605		691
606		691
607		688
608		688
609		688
610		688
611		688
612		688
613		688
614		688
615		688
616		689
617		689
618		689
619		689
620		689
621		689
622		689
623		703
624		703
625		703
626		703
627		703
628		703
629		703
630		703
631		704
632		704
633		704
634		704
635		704
636		704
637		704
638		704
639		701
640		701
641		701
642		701
643		701
644		701
645		701
646		701
647		702
648		702
649		702
650		702
651		702
652		702
653		702
654		702
655		689
656		689
657		689
658		689
659		689
660		689
661		689
662		689
663		690
664		690
665		690
666		690
667		690
668		690
669		690
670		690
671		687
672		687
673		687
674		687
675		687
676		687
677		687
678		687
679		688
680		688
681		688
682		688
683		688
684		688
685		688
686		688
687		689
688		689
689		689
690		689
691		689
692		689
693		689
694		689
695		690
696		690
697		690
698		690
699		690
700		690
701		690
702		690
703		699
704		699
705		699
706		699
707		699
708		699
709		699
710		699
711		700
712		700
713		700
714		700
715		700
716		700
717		700
718		700
719		704
720		704
721		704
722		704
723		704
724		704
725		704
726		704
727		705
728		705
729		705
730		705
731		705
732		705
733		705
734		705
735		648
736		662
737		676
738		690
739		649
740		663
741		667
742		691
743		662
744		676
745		690
746		704
747		663
748		677
749		691
750		705
751		704
752		704
753		704
754		704
755		704
756		704
757		704
758		704
759		705
760		705
761		705
762		705
763		705
764		705
765		705
766		705
767		718
768		718
769		718
770		718
771		718
772		718
773		718
774		718
775		719
776		719
777		719
778		719
779		719
780		719
781		719
782		719
783		676
784		676
785		676
786		676
787		676
788		676
789		676
790		676
791		677
792		677
793		677
794		677
795		677
796		677
797		677
798		677
799		690
800		690
801		690
802		690
803		690
804		690
805		690
806		690
807		691
808		691
809		691
810		691
811		691
812		691
813		691
814		691

Biological Example 1. Assay for In Vitro Inhibition of Enzymatic Activity of KIF18A by Compounds of the Present Invention

KIF18A enzyme assay: The enzymatic activity of KIF18A after treatment with the compounds was measured by an assay of microtubule-stimulated ATPase activity. ADP generated from the ATPase reaction was measured in this assay. The compounds were serially diluted 2-fold in DMSO over a range of 22 concentration points. Recombinant human KIF18A (1-467His-tagged) protein was expressed using a baculovirus system. Concentrations of KIF18A protein, microtubules, and ATP in the reaction were optimized for a standardized homogenous enzyme assay using an ADP-Glo kinase/ATPase assay kit. A reaction buffer [(15 mM Tris, pH 7.5), 10 mM MgCl₂, 0.01% PluronicF-68, 1 μM paclitaxel, and 30 μg/mL pig microtubules] was prepared. The compounds and KIF18A protein (30 nM) were added to the prepared reaction buffer, and the reaction mixture was incubated at room temperature for 15 min, followed by addition of ATP (Km, 75 μM). The resulting reaction mixture was incubated at room temperature for another 15 min. 5 μL of ADP-Glo reagent and 2.5 μL of the reaction mixture were mixed and the resulting mixture was incubated at room temperature for 40 min. 10 μL of ADP-Glo detection reagent was added and the mixture was incubated at room temperature for 40 min. Luminescence was measured using a microplate reader and compared with that of the DMSO group, and then the inhibition percentages and IC₅₀ values of the compounds were calculated. The results are shown in Table 2 below.

TABLE 2
The inhibitory activity of the compounds of the
present invention against KIF18A (IC50, nM)
Com-		Com-		Com-		Com-
pound	IC50	pound	IC50	pound	IC50	pound	IC50
1	+++	2	+++	3	+++	4	+++
5	+++	6	+++	7	+++	8	+++
9	+++	10	+++	11	+++	12	+++
13	+++	14	+++	15	+++	16	+++
17	+++	18	+++	19	+++	20	+++
21	+++	22	+++	23	+++	24	+++
25	+++	26	+++	27	+++	28	+++
29	+++	30	+++	31	+++	32	+++
33	+++	34	+++	35	+++	36	+++
37	+++	38	+++	39	+++	40	+++
41	+++	42	+++	43	+++	44	+++
45	+++	46	+++	47	+++	48	+++
49	+++	50	+++	51	+++	52	+++
53	+++	54	+++	55	+++	56	+++
57	+++	58	+++	59	+++	60	+++
61	+++	62	+++	63	+++	64	+++
65	+++	66	+++	67	+++	68	+++
69	+++	70	+++	71	+++	72	+++
73	+++	74	+++	75	+++	76	+++
77	+++	78	+++	79	+++	80	+++
81	+++	82	+++	83	+++	84	+++
85	+++	86	+++	87	+++	88	+++
89	+++	90	+++	91	+++	92	+++
93	+++	94	+++	95	+++	96	+++
97	+++	98	+++	99	+++	100	+++
101	+++	102	+++	103	+++	104	+++
105	+++	106	+++	107	+++	108	+++
109	+++	110	+++	111	+++	112	+++
113	+++	114	+++	115	+++	116	+++
117	+++	118	+++	119	+++	120	+++
121	+++	122	+++	123	+++	124	+++
125	+++	126	+++	127	+++	128	+++
129	+++	130	+++	131	+++	132	+++
133	+++	134	+++	135	+++	136	+++
137	+++	138	+++	139	+++	140	+++
141	+++	142	+++	143	+++	144	+++
145	+++	146	+++	147	+++	148	+++
149	+++	150	+++	151	+++	152	+++
153	+++	154	+++	155	+++	156	+++
157	+++	158	+++	159	+++	160	+++
161	+++	162	+++	163	+++	164	+++
165	+++	166	+++	167	+++	168	+++
169	+++	170	+++	171	+++	172	+++
173	+++	174	+++	175	+++	176	+++
177	+++	178	+++	179	+++	180	+++
181	+++	182	+++	183	+++	184	+++
185	+++	186	+++	187	+++	188	+++
189	+++	190	+++	191	+++	192	+++
193	+++	194	+++	195	+++	196	+++
197	+++	198	+++	199	+++	200	+++
201	+++	202	+++	203	+++	204	+++
205	+++	206	+++	207	+++	208	+++
209	+++	210	+++	211	+++	212	+++
213	+++	214	+++	215	+++	216	+++
217	+++	218	+++	219	+++	220	+++
221	+++	222	+++	223	+++	224	+++
225	+++	226	+++	227	+++	228	+++
229	+++	230	+++	231	+++	232	+++
233	+++	234	+++	235	+++	236	+++
237	+++	238	+++	239	+++	240	+++
241	+++	242	+++	243	+++	244	+++
245	+++	246	+++	247	+++	248	+++
249	+++	250	+++	251	+++	252	+++
253	+++	254	+++	255	+++	256	+++
257	+++	258	+++	259	+++	260	+++
261	+++	262	+++	263	+++	264	+++
265	+++	266	+++	267	+++	268	+++
269	+++	270	+++	271	+++	272	+++
273	+++	274	+++	275	+++	276	+++
277	+++	278	+++	279	+++	280	+++
281	+++	282	+++	283	+++	284	+++
285	+++	286	+++	287	+++	288	+++
289	+++	290	+++	291	+++	292	+++
293	+++	294	+++	295	+++	296	+++
297	+++	298	+++	299	+++	300	+++
301	+++	302	+++	303	+++	304	+++
305	+++	306	+++	307	+++	308	+++
309	+++	310	+++	311	+++	312	+++
313	+++	314	+++	315	+++	316	+++
317	+++	318	+++	319	+++	320	+++
321	+++	322	+++	323	+++	324	+++
325	+++	326	+++	327	+++	328	+++
329	+++	330	+++	331	+++	332	+++
333	+++	334	+++	335	+++	336	+++
337	+++	338	+++	339	+++	340	+++
341	+++	342	+++	343	+++	344	+++
345	+++	346	+++	347	+++	348	+++
349	+++	350	+++	351	+++	352	+++
353	+++	354	+++	355	+++	356	+++
357	+++	358	+++	359	+++	360	+++
361	+++	362	+++	363	+++	364	+++
365	+++	366	+++	367	+++	368	+++
369	+++	370	+++	371	+++	372	+++
373	+++	374	+++	375	+++	376	+++
377	+++	378	+++	379	+++	380	+++
381	+++	382	+++	383	+++	384	+++
385	+++	386	+++	387	+++	388	+++
389	+++	390	+++	391	+++	392	+++
393	+++	394	+++	395	+++	396	+++
397	+++	398	+++	399	+++	400	+++
401	+++	402	+++	403	+++	404	+++
405	+++	406	+++	407	+++	408	+++
409	+++	410	+++	411	+++	412	+++
413	+++	414	+++	415	+++	416	+++
417	+++	418	+++	419	+++	420	+++
421	+++	422	+++	423	+++	424	+++
425	+++	426	+++	427	+++	428	+++
429	+++	430	+++	431	+++	432	+++
433	+++	434	+++	435	+++	436	+++
437	+++	438	+++	439	+++	440	+++
441	+++	442	+++	443	+++	444	+++
445	+++	446	+++	447	+++	448	+++
449	+++	450	+++	451	+++	452	+++
453	+++	454	+++	455	+++	456	+++
457	+++	458	+++	459	+++	460	+++
461	+++	462	+++	463	+++	464	+++
465	+++	466	+++	467	+++	468	+++
469	+++	470	+++	471	+++	472	+++
473	+++	474	+++	475	+++	476	+++
477	+++	478	+++	479	+++	480	+++
481	+++	482	+++	483	+++	484	+++
485	+++	486	+++	487	+++	488	+++
489	+++	490	+++	491	+++	492	+++
493	+++	494	+++	495	+++	496	+++
497	+++	498	+++	499	+++	500	+++
501	+++	502	+++	503	+++	504	+++
505	+++	506	+++	507	+++	508	+++
509	+++	510	+++	511	+++	512	+++
513	+++	514	+++	515	+++	516	+++
517	+++	518	+++	519	+++	520	+++
521	+++	522	+++	523	+++	524	+++
525	+++	526	+++	527	+++	528	+++
529	++	530	+++	531	++	532	+++
533	+++	534	+++	535	+++	536	+++
537	+++	538	+++	539	+++	540	+++
541	+++	542	+++	543	+++	544	+++
545	+++	546	+++	547	+++	548	+++
549	+++	550	+++
+++ means that IC50 is less than or equal to 100 nM.
++ means that IC50 is 100 nM to 500 nM.
+ means that IC50 is greater than 500 nM.

As can be seen from the data in Table 2, the compounds of the present invention have good inhibitory activity against the enzymatic activity of KIF18A.

Biological Example 2. In Vitro Anti-Proliferative Activity of Compounds of the Present Invention Against HT-29 Cells

HT-29 cells were seeded on a 384-well plate at 3000 cells/well. After overnight adherence culture, DMSO or the compounds serially diluted in a 1:5 ratio from 5 μM were added. The viability was assessed 72 h after dosing by measuring the intracellular ATP content. The inhibition percentages of viable cells by the compounds were calculated by comparing with the DMSO group, and the IC so values were also calculated. The results are shown in Table 3 below.

TABLE 3
The anti-proliferative activity of the compounds of
the present invention against HT-29 cells (IC50, nM)
Com-		Com-		Com-		Com-
pound	IC50	pound	IC50	pound	IC50	pound	IC50
1	9	4	63	5	88	7	73
33	52	49	61	65	8	66	85
68	51	69	71	71	56	81	51
97	57	113	81	129	40	513	71
522	69	530	36	537	95	539	43
583	38	584	70	AMG650	89

The reference compound AMG650 is compound 4 in WO2020132648A1.

As can be seen from the data in Table 3, some of the compounds of the present invention have stronger anti-proliferative activities against HT-29 cells than AMG650.

Biological Example 3. In Vitro Anti-Proliferative Activity of Compounds of the Present Invention Against HCT116 Cells

HCT116 cells were seeded on a 384-well plate at 3000 cells/well. After overnight adherence culture, DMSO or the compounds serially diluted in a 1:5 ratio from 5 μM were added. The viability was assessed 72 h after dosing by measuring the intracellular ATP content. The inhibition percentages of viable cells by the compounds were calculated by comparing with the DMSO group, and the IC₅₀ values were also calculated. The results are shown in Table 4 below.

TABLE 4
The anti-proliferative activity of the compounds of
the present invention against HCT116 cells (IC50, nM)
Compound	IC50	Compound	IC50	Compound	IC50	Compound	IC50
1	>10000	2	>10000	3	>10000	4	>10000
5	>10000	6	>10000	7	>10000	33	>10000
49	>10000	65	>10000	66	>10000	67	>10000
68	>10000	69	>10000	70	>10000	71	>10000
81	>10000	97	>10000	113	>10000	129	>10000
385	>10000	513	>10000	522	8187	530	>10000
537	>10000	539	>10000	583	>10000	584	>10000
AMG650	>10000

As can be seen from the data in Table 4, none of the compounds of the present invention has anti-proliferative activity against HCT116 cells.

Although specific embodiments of the present invention have been described above, it will be appreciated by those skilled in the art that these embodiments are merely illustrative and that many changes or modifications can be made to these embodiments without departing from the principles and spirit of the present invention. The protection scope of the present invention is therefore defined by the appended claims.

Claims

1. A compound of general formula (1) or an isomer thereof, a crystalline form thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof, or a solvate thereof:

2. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein the general formula (1) has the following structure:

3. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), ring A is 9-10 membered cycloalkylene, 9-10 membered heterocycloalkylene, 9-10 membered heteroarylene, or 10-membered arylene, wherein the 9-10 membered cycloalkylene, 9-10 membered heterocycloalkylene, 9-10 membered heteroarylene, or 10-membered arylene may be optionally substituted with 0, 1, 2, or 3 groups selected from H, F, Cl, Br, —C1-4 hydrocarbyl, —C1-4 halohydrocarbyl, or —O—C1-4 hydrocarbyl.

4. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), ring A is:

5. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), ring A is:

6. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), R3 is H, methyl, or ethyl, preferably H.

7. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), R13c, R13d, R13e, R13f, R13g, R13h, R13i, R13j, R13k, and R13l are each independently H, halogen, C1-6 hydrocarbyl, or C1-4 halohydrocarbyl; and R13a and R13b in a pair of R13a/R13b may be combined with the carbon atom to which they are each attached to form a saturated 3-, 4-, or 5-membered monocyclic ring spiro-linked to R8 ring, wherein the monocyclic ring contains 0, 1, 2, or 3 N atoms and 0, 1, or 2 atoms selected from O and S; preferably, R13c, R13d, R13e, R13f, R13g, R13h, R13i, R13j, R13k, and R13l are each independently H, methyl, or ethyl; and R13a and R13b in the pair of R13a/R13b may be combined with the carbon atom to which they are each attached to form a cyclopropyl, cyclobutyl, or cyclopentyl ring spiro-linked to R8 ring.

8. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), the structural unit

9. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), Z is a chemical bond, —NH—, —NHSO2—, —SO2NH—, —S(═O)(═NH)—, —S—, —S(═O)—, —SO2—, —(C═O)—, —(C═O)NH—, or —NH(C═O)—.

10. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein, in the general formula (1), R10 is selected from: (a) H; or (b) C1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, —OH, or —OCH3; or (c) a group such that when the group —Z—R10 is —N═S(═O)—(R10)2, the two R10 may be combined with the sulfur atom to which they are each attached to form a saturated, partially saturated, or unsaturated 3-, 4-, 5-, 6-, or 7-membered monocyclic ring containing 0, 1, 2, or 3 N atoms and 0 or 1 atom selected from O and S, wherein the monocyclic ring is substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, —C1-6 hydrocarbyl, —C1-4 halohydrocarbyl, —C1-6 hydrocarbylene OH, —OH, —OCH3, —NH2, or oxo; or (d) C1-6 hydrocarbyl, wherein the C1-6 hydrocarbyl may be optionally substituted with 1, 2, or 3 groups selected from —OC(═O)C1-5 hydrocarbyl, wherein the C1-5 hydrocarbyl may be optionally substituted with 1 or 2 groups selected from —OH or —NH2; and the C1-6 hydrocarbyl may be optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, —OH, or —OCH3.

11. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), R1 is —CN or a group —Z—R10, wherein Z is a chemical bond, —NH—, —NHSO2—, —SO2NH—, —S(═O)(═NH)—, —S—, —S(═O)—, —SO2—, —(C═O)—, —(C═O)NH—, or —NH(C═O)—; and R10 is selected from: (a) H;(b) cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, oxiranyl, oxetanyl, tetrahydrofuranyl, azetidinyl, imidazolyl, morpholinyl, pyrrolidinyl, piperazinyl,

12. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), the group —Z—R10 is —N═S(═O)—(R10)2, wherein the two R10 may be combined with the sulfur atom to which they are each attached to form a saturated or partially saturated 3-, 4-, 5-, or 6-membered monocyclic ring containing 0, 1, 2, or 3 N atoms and 0, 1 or 2 atoms selected from O and S; preferably, the group —Z—R10 is selected from

13. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), R1 is a group —Z—R10, wherein Z is —NHSO2— or —SO2NH—; and R10 is oxetanyl or cyclopropyl; or R10 is C1-6 hydrocarbyl substituted with 0, 1, 2, or 3 OH groups; or R10 is C1-6 hydrocarbyl, wherein the C1-6 hydrocarbyl may be optionally substituted with 1, 2, or 3 groups selected from

14. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), R10 is selected from C1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, or 3 groups selected from

15. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), R10 is selected from C1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 1, 2 or 3 groups selected from

16. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), R2 is halogen or a group —Y—R12, wherein Y is a chemical bond, —NH—, —NH—(CH2)0-4—, or —O—(CH2)0-4—; and R12 is a saturated, partially saturated, or unsaturated 3-, 4-, 5-, 6-, or 7-membered monocyclic ring or 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, or 12-membered bicyclic ring containing 0, 1, 2, or 3 N atoms and 0 or 1 atom selected from O and S, wherein the monocyclic ring and bicyclic ring may be each independently and optionally substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, C1-6 hydrocarbyl, C1-4 halohydrocarbyl, —OH, —OC1-4 halohydrocarbyl, CN, R14, and oxo; or R12 is C1-6 hydrocarbyl, wherein the hydrocarbyl may be optionally substituted with 0, 1, 2, 3, 4, or 5 groups selected from F, Cl, Br, —OH, —OC1-4 halohydrocarbyl, or CN.

17. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), R2 is a saturated 5- or 6-membered monocyclic ring, wherein each of the rings contains 0, 1 or 2 N atoms and 0 or 1 O atom, and each of the rings is substituted with 0, 1, 2, or 3 groups selected from F, Cl, Br, C1-6 hydrocarbyl, C1-4 halohydrocarbyl, —OH, —OC1-4 halohydrocarbyl, CN, R14, and oxo; or in the general formula (1), R2 is: (a) halogen; (b) a group —Y—R12, wherein Y is a chemical bond; and R12 is morpholinyl, piperidinyl, azetidinyl, pyrrolidinyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, piperazinyl, tetrahydrofuranyl,

18-23. (canceled)

24. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein in the general formula (1), R10 is selected from cyclopropyl, cyclobutyl, cyclopentyl, oxetanyl, azetidinyl, tetrahydrofuranyl, or 1,3,4-oxathiazinanyl; R5 is H or F; R6 is H or F; and R7 is H.

25-27. (canceled)

28. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein the compound has one of the following structures:

29. The compound or the isomer thereof, the crystalline form thereof, the pharmaceutically acceptable salt thereof, the hydrate thereof, or the solvate thereof according to claim 1, wherein the compound has one of the following structures:

30-32. (canceled)