ANTI-CANCER COMPOUNDS ACTING AS NON-PGP SUBSTRATE

Abstract

Provided are anti-cancer compounds which act as a non-PGP substrate, same being compounds of formula I-1, or a pharmaceutically acceptable salt, a prodrug or a solvate thereof, and the medical use of these compounds in the treatment of cancers, tumors, conditions caused by cancers or tumors, or cell proliferative diseases. Also provided is a method for treating cancers, tumors, conditions caused by cancers or tumors, or cell proliferative diseases using the anti-cancer compounds which act as non-PGP substrates as described above.

Claims

1. An anti-cancer compound for acting as a non-PGP substrate, wherein the compound is a compound having a formula I-1, or a pharmaceutically acceptable salt or a solvate thereof: ##STR00059## wherein R.sub.1 and R.sub.2 are respectively independently hydrogen, deuterium, an aryl group or a Z-substituted aryl group, a heteroaryl group, a heterocycle or a Z-substituted heteroaryl group, a C.sub.1-C.sub.6 alkyl group or a Z-substituted alkyl group, a C.sub.2-C.sub.6 alkenyl group or a Z-substituted alkenyl group, a C.sub.2-C.sub.6 alkynyl group or a Z-substituted alkynyl group, a C.sub.3-C.sub.8 cycloalkyl group or a Z-substituted cycloalkyl group; R.sub.3 is hydrogen, halogen, a cyano group or an isocyano group, a thiocyanato group or an isothiocyanato group, hydroxyl group, a thiol group, an amino group, oxime, hydrazone, OTs, OMs, a C.sub.1-C.sub.6 alkyl group or a Z-substituted alkyl group, a C.sub.2-C.sub.6 alkenyl group or a Z-substituted alkenyl group, a C.sub.2-C.sub.6 alkynyl group or a Z-substituted alkynyl group, a C.sub.3-C.sub.8 cycloalkyl group or a Z-substituted cycloalkyl group, a C.sub.6-C.sub.10 aryl group or a Z-substituted aryl group, a 4-15 membered heterocycle or a Z-substituted heterocycle, a 5-15 membered heteroaryl group or a Z-substituted heteroaryl group, a C.sub.1-C.sub.6 alkoxyl group or a Z-substituted C.sub.1-C.sub.6 alkoxyl group, or R.sub.3 is —CONR.sup.6R.sup.7, —SO.sub.2NR.sup.6R.sup.7, —SO.sub.2R.sup.6, —OCO—R.sup.6, —OCOO—R.sup.6, —COOR.sup.6, —NR.sup.6COR.sup.7, —OCOR.sup.6, —NR.sup.6SO.sub.2R.sup.7, and —NR.sup.6CONR.sup.7; R.sub.4 and R.sub.5 are respectively independently hydrogen, halogen, a cyano group or an isocyano group, a thiocyanato group or an isothiocyanato group, a hydroxyl group, a thiol group, an amino group, oxime, hydrazone, OTs, OMs, a C.sub.1-C.sub.6 alkyl group or a Z-substituted alkyl group, a C.sub.2-C.sub.6 alkenyl group or a Z-substituted alkenyl group, a C.sub.2-C.sub.6 alkynyl group or a Z-substituted alkynyl group, a C.sub.3-C.sub.8 cycloalkyl group or a Z-substituted cycloalkyl group, a C.sub.6-C.sub.10 aryl group or a Z-substituted aryl group, a 4-15 membered heterocycle or a Z-substituted heterocycle, a 5-15 membered heteroaryl group or a Z-substituted heteroaryl group, a C.sub.1-C.sub.6 alkoxyl group or a Z-substituted C.sub.1-C.sub.6 alkoxyl group, —CONR.sup.6R.sup.7, —SO.sub.2NR.sup.6R.sup.7, —SO.sub.2R.sup.6, —OCOO—R.sup.6, —COOR.sup.6, —NR.sup.6COR.sup.7, —OCOR.sup.6, —NR.sup.6SO.sub.2R.sup.7, —NR.sup.6CONR.sup.7, or R.sub.4, R.sub.5 and the atom of the bonding benzene ring bonded thereto form a 7-15 membered fused ring or a Z-substituted fused ring; R.sup.6 and R.sup.7 are each independently hydrogen, a cyano group or an isocyano group, a C.sub.1-C.sub.6 alkyl group or a Z-substituted alkyl group, a C.sub.2-C.sub.6 alkenyl group or a Z-substituted alkenyl group, a C.sub.2-C.sub.6 alkynyl group or a Z-substituted alkynyl group, a C.sub.3-C.sub.8 cycloalkyl group or a Z-substituted cycloalkyl group, a C.sub.6-C.sub.10 aryl group or a Z-substituted aryl group, a 4-15 membered heterocycle or a Z-substituted heterocycle, a 5-15 membered heteroaryl group or a Z-substituted heteroaryl group, a C.sub.1-C.sub.6 alkoxyl group or a Z-substituted C.sub.1-C.sub.6 alkoxyl group, or R.sup.6 and R.sup.7 and atoms bonded thereto form a 3-7 membered heterocyclyl group or a Z-substituted 3-7 membered heterocyclyl group; Cy is a 5-10 membered aromatic ring, heterocyclic ring or heteroaromatic ring, and hydrogens of the ring are each independently substituted by deuterium, halogen, a cyano group or an isocyano group, a thiocyanato group or an isothiocyanato group, a hydroxyl group, a thiol group, an amino group, oxime, hydrazone, OTs, OMs, a C.sub.1-C.sub.6 aliphatic group, or the hydrogens of the ring are each independently substituted by C.sub.1-C.sub.6 aliphatic group substituted by halogen, a cyano group, an isocyano group, a hydroxyl group, a thiol group, an amino group, oxime, hydrazone; R.sub.10 is a 3-18 membered cyclohydrocarbyl group, an aryl group or a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group or a Z-substituted C.sub.3-C.sub.18 cycloalkyl group, an aryl or a fused ring, heterocycle, a fused heterocyclyl group, a heteroaryl group or a C.sub.1-C.sub.18 hydrocarbyl group or a Z-substituted hydrocarbyl group; or R.sub.10 is -Q-Cz, Q is —O—, —S—, —CO—, —SO.sub.2—, —SO—, —OCO—, —OCOO—, —NR.sup.6CO—, —NR.sup.6SO.sub.2—, —OCONR.sup.6; and Cz is a 3-18 membered cyclohydrocarbyl group, an aryl group or a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group or a Z-substituted 3-18 membered cycloalkyl group, an aryl group or a fused ring, a heterocycle, a fused heterocyclyl group, a heteroaryl group or a C.sub.1-C.sub.18 hydrocarbyl group or a Z-substituted hydrocarbyl group; Y is —O— or —S— or —SO.sub.2—, —SO—; L and D are selected from the following three situations: (1) L is selected from —O—, —S—, —OCOO—, —NR.sup.6CO—, —OCO—, —NR.sup.6SO.sub.2—, —OCONR.sup.6—, quaternary ammonium, —OSO.sub.2, ##STR00060## R.sup.40 and R.sup.41 are independently hydrogen, a C.sub.1-C.sub.6 alkyl group, a C.sub.2-C.sub.6 alkenyl group, a C.sub.2-C.sub.6 alkynyl group, a C.sub.3-C.sub.8 cycloalkyl group, a C.sub.6-C.sub.10 aryl group, a 4-15 membered heterocycle or a 5-15 membered heteroaryl group; R.sup.42 is C.sub.2-C.sub.3 alkylenyl, heterylene or one to three C.sub.1-C.sub.6 alkyl-substituted C.sub.2-C.sub.3 alkylenyl, C.sub.1-C.sub.6 alkyl-substituted heterocycloalkylene; V(−) is any anion; D is a moiety for making D-OH an anti-cancer drug, wherein —OH is an aliphatic group, a phenolic hydroxyl group, or a —OH moiety attached to the phosphate ester; (2) L is selected from ##STR00061## R.sup.40 is defined as above; R.sup.43 is hydrogen or form to heterocycle with D, phenylene is Z-substituted or unsubstituted; and D is a moiety for making D-NR.sup.43H an anti-cancer drug; or (3) L is selected from a bond, —O—C(R.sup.40R.sup.41).sub.2, —O—C(R.sup.40R.sup.41)—R.sup.40R.sup.41 (+)—C(R.sup.40R.sup.41)—, or ##STR00062## wherein R.sup.40, R.sup.41 and V(−) are defined as above; and D is an anti-cancer drug with a tertiary or secondary nitrogen atom, wherein the tertiary or secondary nitrogen atom is bonded to L; and an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, an aryl group, a heterocycle, a heteroaryl group, and ether in the definitions of the L and D are Z-substituted or unsubstituted; the Z-substituted group is halogen, a cyano group or an isocyano group, a thiocyanato group or an isothiocyanato group, a hydroxyl group, a thiol group, an amino group, oxime, hydrazone, OTs, OMs, a C.sub.1-C.sub.3 alkyl group or a substituted alkyl group, a C.sub.2-C.sub.3 alkenyl group or a substituted alkenyl group, a C.sub.2-C.sub.3 alkynyl group or a substituted alkynyl group, a C.sub.3-C.sub.8 cycloalkyl group or a substituted cycloalkyl group, an aromatic ring, a heterocycle, a heteroaryl group and a fused ring or a substituted aryl group, heterocycle, heteroaryl group and a fused ring, wherein the substitution manners are mono-substituted or double-substituted; and the substituent is halogen, a cyano group or an isocyano group, a thiocyanato group or an isothiocyanato group, a hydroxyl group, a thiol group, an amino group, oxime, hydrazone, OTs, OMs; and the compound does not comprise ##STR00063## ##STR00064##

2. The compound of claim 1, wherein R.sub.10 is a 3-18 membered cyclic hydrocarbyl group, an aryl group or a fused ring, a heterocycle, fa used heterocycle, a heteroaryl group, or a Z-substituted C.sub.3-C.sub.18 cycloalkyl group, a Z-substituted aryl group or a fused ring, a Z-substituted heterocycle, a Z-substituted fused heterocyclic group, a Z-substituted heteroaryl group, or —CF.sub.3 or C1-substituted a hydrocarbyl group; or R.sub.10 is -Q-Cz, wherein Q is selected from the group consisting of —O—, —S—, —CO—, —SO.sub.2—, —SO—, —OCO—, —OCOO—, —NR.sup.6CO—, —NR.sup.6SO.sub.2—, —OCONR.sup.6; Cz is a 3-18 membered cyclohydrocarbyl group, or a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group or a Z-substituted 3-18-membered cycloalkyl group, a Z-substituted aryl group or a fused ring, a Z-substituted heterocycle, a Z-substituted fused heterocycle group, a Z-substituted heteroaryl group, or —CF.sub.3 or C1-substituted a hydrocarbyl group.

3. The compound of claim 1, wherein -D is —P(Z.sup.1)(Z.sup.5—X.sup.5—Y.sup.5).sub.n, wherein Z.sup.1 is O or S, Z.sup.5 is N, S, or O; X.sup.5 is any substituted ethylidene; Y.sup.5 is halogen or —OSO.sub.2—R.sup.20, R.sup.20 is any substituted hydrocarbyl group, aryl group, cycloalkyl group, heterocyclyl group and heteroaryl group, and n is 1 or 2; or Z.sup.1 is O or S; Z.sup.5—X.sup.5—Y.sup.5 is —NCH.sub.2CH.sub.2; or -L- is —O—; -D is —P(Z.sup.1)(Z.sup.5—X.sup.5—Y.sup.5).sub.n; Z.sup.1 is O or S; Z.sup.5 is N, S, or O; X.sup.5 is any substituted ethylidene; Y.sup.5 is halogen or —OSO.sub.2—R.sup.20, wherein R.sup.20 is any substituted hydrocarbyl group, aryl, cycloalkyl group, heterocyclyl group and heteroaryl group, and n is 1 or 2; or -L- is —O—; Z.sup.1 is O or S; and Z.sup.5—X.sup.5—Y.sup.5 is —NCH.sub.2CH.sub.2; or -L-D is —OP(Z.sup.1)(NR.sup.30CH.sub.2CH.sub.2Cl).sub.2, —OP(Z.sup.1)(NR.sup.30CH.sub.2CH.sub.2Br).sub.2, —OP(Z.sup.1)(NR.sup.30.sub.2)(N(CH.sub.2CH.sub.2X.sup.1).sub.2), —OP(Z.sup.1)(N(CH.sub.2).sub.2).sub.2, or —OP(Z.sup.1)(N(CH.sub.2CH.sub.2Cl).sub.2).sub.2, wherein every R.sup.30 is each independent hydrogen, a C.sub.1-C.sub.6 hydrocarbyl group, or two R.sup.30 group and the nitrogen atom bonded thereto form 5-7 membered heterocycle, Z.sup.1 is O or S, and X.sup.1 is Cl, Br or —SOS.sub.2Me; or -L-D is —OP(Z.sup.1)(NHCH.sub.2CH.sub.2Cl).sub.2, —OP(Z.sup.1)(NHCH.sub.2CH.sub.2Br).sub.2, —OP(Z.sup.1)(NH.sub.2)(N(CH.sub.2CH.sub.2X.sup.1).sub.2), —OP(Z.sup.1)(N(CH.sub.2).sub.2).sub.2, or —OP(Z.sup.1)(N(CH.sub.2CH.sub.2Cl).sub.2).sub.2, and X.sup.1 is Cl, Br or —SOS.sub.2Me.

4. The compound of claim 1, wherein L is selected from the group consisting of —O—, —S—, —OCOO—, —NR.sup.6CO—, —OCO—, —NR.sup.6SO.sub.2—, —OCONR.sup.6—, quaternary ammonium, and —OSO.sub.2—; -D is —P(Z′)(Z.sup.5—X.sup.5—Y.sup.5).sub.n, Z.sup.1 is O or S, Z.sup.5 is N, S or O, X.sup.5 is any substituted ethylidene, Y.sup.5 is halogen or —OSO.sub.2—R.sup.20, R.sup.20 is any substituted hydrocarbyl group, aryl group, cycloalkyl group, heterocyclyl group, or heteroaryl group, and n is 1 or 2.

5. The compound of claim 4, wherein Z.sup.1 is O or S; Z.sup.5—X.sup.5—Y.sup.5 is —NCH.sub.2CH.sub.2.

6. The compound of claim 1, wherein -L- is —O—; -D is —P(Z.sup.1)(Z.sup.5—X.sup.5—Y.sup.5).sub.n, and n is 1 or 2; Z.sup.1 is O or S; Z.sup.5 is N, S or O; X.sup.5 is any substituted ethylidene; Y.sup.5 is halogen or —OSO.sub.2—R.sup.20, R.sup.20 is any substituted hydrocarbyl group, aryl group, cycloalkyl group, heterocyclyl group, or heteroaryl group.

7. The compound of claim 6, wherein -L- is —O—; Z.sup.1 is O or S; Z.sup.5—X.sup.5—Y.sup.5 is —NCH.sub.2CH.sub.2.

8. The compound of claim 1, wherein -L-D is OP(Z.sup.1)(NR.sup.30CH.sub.2CH.sub.2Cl).sub.2, —OP(Z.sup.1)(NR.sup.30CH.sub.2CH.sub.2Br).sub.2, —OP(Z.sup.1)(NR.sup.30.sub.2)(N(CH.sub.2CH.sub.2X.sup.1).sub.2), —OP(Z.sup.1)(N(CH.sub.2).sub.2).sub.2, or —OP(Z.sup.1)(N(CH.sub.2CH.sub.2Cl).sub.2).sub.2, wherein every R.sup.30 is each independent hydrogen, a C.sub.1-C.sub.6 hydrocarbyl group, or two R.sup.30 group and the nitrogen atom bonded thereto form a 5-7 membered heterocycle, Z.sup.1 is O or S; X.sup.1 is Cl, Br or —SOS.sub.2Me.

9. The compound of claim 8, wherein -L-D is —OP(Z.sup.1)(NHCH.sub.2CH.sub.2Cl).sub.2, —OP(Z.sup.1)(NHCH.sub.2CH.sub.2Br).sub.2, —OP(Z.sup.1)(NH.sub.2)(N(CH.sub.2CH.sub.2X.sup.1).sub.2), —OP(Z.sup.1)(N(CH.sub.2).sub.2).sub.2, or —OP(Z.sup.1)(N(CH.sub.2CH.sub.2Cl).sub.2).sub.2; and X.sup.1 is Cl, Br or —SOS.sub.2Me.

10. The compound of claim 1, wherein R.sub.10 is a 5-18 membered cycloalkyl group, an aryl group or a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group, or a Z-substituted 5-18 membered cycloalkyl group, an aryl group or a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group, or a —CF.sub.3 or C1 substituted hydrocarbyl group; or R.sub.10 is —O-Cz, Cz is a 5-18 membered cycloalkyl group, an aryl group, a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group, or a Z-substituted 5-18 membered cycloalkyl, an aryl group, a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group, or a —CF.sub.3 or C1 substituted hydrocarbyl group.

11. The compound of claim 1, wherein R.sub.10 is 7-18 membered a cycloalkyl group, an aryl group, a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group, or a Z-substituted 7-18 membered cycloalkyl group, an aryl group, a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group, or a —CF.sub.3 or C1 substituted hydrocarbyl group; or R.sub.10 is —O-Cz, Cz is a 7-18 membered cycloalkyl group, an aryl group, a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group, or a Z-substituted 7-18 membered cycloalkyl group, an aryl group, a fused ring, a heterocycle, a fused heterocycle, a heteroaryl group, or a —CF.sub.3 or C1 substituted hydrocarbyl group.

12. The compound of claim 1, wherein the compound comprises the structure of formula I-2: ##STR00065## wherein Cx is selected from biphenyl, Z-substituted biphenyl, phenylpyridyl, Z-substituted phenylpyridyl, and substituted biphenyl and phenylpyridyl having a substituent of —CONR.sup.6R.sup.7, —SO.sub.2NR.sup.6R.sup.7, —SO.sub.2R.sup.6, —OCOO—R.sup.6, —COOR.sup.6, —NR.sup.6COR.sup.7, —OCOR.sup.6, —NR.sup.6SO.sub.2R.sup.7, —NR.sup.6SO.sub.2NR.sup.6R.sup.7, —COR.sup.6, or —NR.sup.6CONR.sup.7.

13. The compound of claim 12, wherein —Y— is connected to a para-position of a carbon atom connecting two benzenes of —Cx, and a substituent on biphenyl is F or methyl.

14. The compound of claim 12, wherein Cx is selected from —F, —CF.sub.3, or —CH.sub.3 substituted biphenyl and phenylpyridine.

15. The compound of claim 1, wherein R.sub.3, R.sub.4, and R.sub.5 are each independent hydrogen.

16. The compound of claim 1, wherein R.sub.1, R.sub.2 are each independent hydrogen, deuterium, —CH.sub.3,—CD.sub.3, or —CF.sub.3.

17. The compound of claim 1, wherein Y is —O—.

18. The compound of claim 1, wherein Cy is a 5-10 membered heteroaryl group or a benzene ring, or hydrogens thereon are each independent substituted by deuterium, halogen, a cyano group or an isocyano group, a thiocyanato group or an isothiocyanato group, hydroxyl, a thiol group, an amino group, oxime, hydrazone, OTs, OMs, or a C.sub.1-C.sub.6 aliphatic group; or substituted by a C.sub.1-C.sub.6 aliphatic group substituted by halogen, a cyano group or an isocyano group, a hydroxyl group, a thiol group, an amino group, oxime, or hydrazone.

19. The compound of claim 1, wherein a substituent on Cy is hydrogen, deuterium, halogen, —CH.sub.3, or —CF.sub.3.

20. The compound of claim 1, wherein Cy is selected from a 5-8 membered aromatic heterocycle, and a heteroatom is N, S or O, the number of the heteroatom is 1, 2, or 3.

21. The compound of claim 1, wherein the compound is selected from the structures below: ##STR00066## ##STR00067## ##STR00068##

22. The compound of claim 1, wherein D-OH is selected from the anti-cancer drug containing —OH below: gemcitabine, estramusting, pudnimnstine, chlorozotocin, ranimustine, mannomustine, mitobronitol, dibromodulcitol, aclacinomycins, anthramycin, bleomycin, carubicin, doxorubicin, carzinophilin, chromomycin, dactinomycin, daunorubicin, mycophenolic acid, nogalamycin, olivomycin, peplomycin, plicamycin, puromycin, streptonigrin, streptozocin, tubercidin, ubenimex, zinostatin, zorubicin, denopterin, fludarabine, ancitabine, azacitidine, 6-azauridine, cytarabine, dideoxyuridine, doxifluridine, enocitabine, floxuridine, L-asparaginase, pulmozyme, aceglatone, elliptinium acetate, etoglucid, interferon-alpha, interferon-beta, interferon-gamma, interleukin-2, lentinan, mitoxantrone, mopidamol, pentostatin, pirarubicin, podophyllinic acid, sizofiran, paclitaxel, teniposide, tenuazonic acid vinblastine, and vincristine; D-NR.sup.43H is selected from the anti-cancer drug below: erlotinib, meturedepa, uredepa, imatinib, trimethylolomelamine, gefitinib, uracil mustard, carmustine, chlorozotocin, fotemustine, nimustine, ranimustine, dacarbazine, mannomustine, actinomycin, anthramycin, bleomycin, cactinomycin, carubicin, doxorubicin, carzinophilin, dactinomycin, peplomycin, puromycin, streptozocin, ubenimex, zinostatin, denopterin, pteropterin, trimetrexate, 6-mercaptopurine, thiamiprine, thioguanine, 6-azauridine, carmofur, dideoxyuridine, doxifluridine, enocitabine, floxuridine, 5-fluorouracil, tegafur, L-asparaginase, pulmozyme, amsacrine, bisantrene, demecolcine, diaziquone, elliptinium acetate, flutamide, hydroxyurea, interferon-alpha, interferon-beta, interferon-gamma, interleukin-2, mitoxantrone, nitracrine, pentostatin, phenamet, 2-ethylhydrazide, procarbazine, razoxane, erlotonib, urethane, vinblastine, and vincristine; and the anti-cancer drug containing a secondary or tertiary nitrogen is selected from: altretamine, triethylenemelamine, chlorambuci, chlornaphazine, estramustine, gefitinib, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, novembichin, phenesterine, prednimustine, trofosfamide, uracil mustard, carmustine, chlorozotocin, fotemustine, nimustine, ranimustine, dacarbazine, pipobroman, actinomycin, anthramycin, carzinophilin, dactinomycin, nogalamycin, porfiromycin, puromycin, streptozocin, tubercidin, fludarabine, ancitabine, azacitidine, cytarabine, dideoxyuridine, enocitabine, floxuridine, L-asparaginase, pulmozyme, aldophosphamide glycoside, bestrabucil, diaziquone, interferon-alpha, interferon-beta, interferon-gamma, interleukin-2, mitoguazone, mopidamo, nitracrine, pentostatin, phenamet, razoxane, spirogermanium, tamoxifen, triaziquone, 2,2′,2″-trichlorotriethylamine, vinblastine, and vincristine.

23. A method of treating a cancer, a tumor expressing AKR1C3 enzyme, or a disease or cell proliferative disease caused by the cancer or the tumor expressing AKR1C3 enzyme, the method comprising: administering an effective amount of a drug comprising the compound of claim 1.

24. The method of claim 23, wherein the cancer or the tumor is a cancer or a tumor of central nervous system, and the disease comprises pain.

25. The method of claim 23, wherein the cancer or the tumor is a primary brain cancer or a primary tumor, or a metastatic cancer or a metastatic tumor transferred to the brain.

26. (canceled)

27. (canceled)

28. The method of claim 23, wherein the compound is selected from: ##STR00069## ##STR00070## ##STR00071## ##STR00072## ##STR00073## ##STR00074##

29. (canceled)

Description

DETAILED DESCRIPTION

[0114] The present disclosure will be described below with reference to specific examples. Those skilled in the art can understand that these examples are only for illustrating the present invention and do not limit the scope of the present disclosure in any way.

[0115] The experimental methods described in the following embodiments are normal methods if there is no special illustration. The raw materials of drugs and reagents are purchased products for commercial if there is no special illustration.

[0116] The definitions below are provided to help readers. All terms, symbols and other scientific or medical terms used herein are indicated to the meanings commonly understood by person having ordinary skill in the chemical and medical fields. In some situations, terms with commonly understood meanings are defined herein for clear explanation and/or for immediate reference. Additionally, definitions herein should not be explained to have material difference with the terms commonly understood in the art.

[0117] All indicated numerical values (e.g., pH, temperature, time, concentration, and weight, including the ranges thereof) are usually the approximation with the increment (+) or decrement (−) of 0.1, 1.0, or 10.0. All indicated numerical values are understood to have the term “about” in front. The agents herein are exemplary and the equivalents thereof are known in the art.

[0118] The term “C.sub.x-C.sub.y” or “C.sub.x-y” in front of the group refers to the range of the number of the carbon atoms in the group. For example, C.sub.1-C.sub.6 alkyl group refers to the alkyl group with at least 1 and at most 6 carbon atoms.

[0119] The term “alkoxyl group” refers to an —O— alkyl group.

[0120] The term “amino group” refers to NR.sup.pR.sup.q, wherein R.sup.p and R.sup.q are independently hydrogen or a C.sub.1-C.sub.6 alkyl group, or R.sup.p and R.sup.q and the nitrogen atom bonded thereto form a 4-15 membered heterocycle.

[0121] The term “aryl group” refers to the aromatic group with carbon atoms, a single ring (e.g., phenyl), or a multiple fused ring (e.g., naphthyl or anthryl) and without heteroatom. For the multicyclic ring system with fused, bridged, or spiro aromatic ring and non-aromatic ring but without heteroatom on the ring, the term “aryl” or “Ar” is acceptable when the attachment point is located in the carbon atom on the aromatic ring (e.g., 5,6,7,8-tetrahydronaphth-2-yl group is an aryl group due to the attachment point is located in the 2-position of aromatic phenyl group).

[0122] According to the detailed description of the present disclosure, C.sub.6-C.sub.10 aryl group may be a phenyl group, a naphthyl group, and any substituted phenyl groups and or naphthyl groups.

[0123] The term “heteroaryl group” refers to an aromatic group having 1-14 carbon atoms and 1-6 heteroatoms selected from oxygen, nitrogen, and sulfur and includes a single ring (e.g., imidazol-2-yl, and imidazol-5-yl) and a multicyclic ring system (e.g., imidazopyridyl, benzotriazolyl, benzimidazol-2-yl, and benzimidazol-6-yl). For the multicyclic ring system with aromatic ring and non-aromatic ring including fused ring, bridged ring and spiro ring, the term “heteroaryl” (e.g., 1,2,3,4-tetrahydroquinolin-6-yl and 5,6,7,8-tetrahydroquinolin-3-yl) is applied when at least one heteroatom is existed, and the attachment point is located at an atom on the aromatic ring. In some embodiments, the nitrogen and/or sulfur atom of the heteroaryl group is optionally oxidized to be a moiety of the N-oxide (N—O), sulfinyl or sulfonyl. The term “heteroaryl” or “5-15 membered heteroaryl” includes (but no limited thereto) acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiophenyl, benzoxazolyl, benzothiazolyl, benzotriazole, benzotetrazole, benzisoxazolyl, benzisothiazolyl, benzothienyl, benzimidazolinyl, carbazolyl, NH-carbazolyl, carbolinyl, chromanyl, chromenyl, cinnolinyl, dithiazinyl, furanyl, furazanyl, imidazolidyl, imidazolinyl, imidazopyridyl, imidazolyl, indazolyl, indolenyl, indolinyl, indolizinyl, indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl, isoquinolyl, isothiazolyl, isoxazolyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, oxazolidinyl, oxazolyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, hexahydropyrazinyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl, pyrazolyl, azosinyl, pyridoxazolyl, pyrido-oxazolyl, pyrido-imidazolyl, pyrido-thiazolyl, pyridinyl, pyridyl, pyrrolyl, quinazolinyl, quinolyl, quinolinyl, quinuclidinyl, tetrahydroisoquinolyl, tetrahydroquinolyl, tetrazolyl, thiadiazinyl, thiadiazolyl, thianthranyl, thiazolyl, thienyl, thienothiazolyl, thieno-oxazolyl, thieno-imidazolyl, triazinyl, xanthenyl.

[0124] The term “alkyl group” refers to an aliphatic group with carbon atoms. In some embodiments, alkyl group refers to univalent aliphatic group with 1-6 carbon atoms. The term “C.sub.x-y alkyl” refers to an alkyl group with x-y carbon atoms. The term “alkyl” includes linear hydrocarbyl group and branched hydrocarbyl group. For example, methyl (CH.sub.3—), ethyl (CH.sub.3CH.sub.2—), n-propyl (CH.sub.3CH.sub.2CH.sub.2—), isopropyl ((CH.sub.3).sub.2CH—), n-butyl (CH.sub.3CH.sub.2CH.sub.2CH.sub.2—), isobutyl ((CH.sub.3).sub.2CHCH.sub.2—), sec-butyl ((CH.sub.3)(CH.sub.3CH.sub.2)CH—), tert-butyl ((CH.sub.3).sub.3C—), n-pentyl, and neopentyl.

[0125] The term “cycloalkyl group” refers to saturated or unsaturated cyclic group with at least 3 carbon atoms and without heteroatom, and the cyclic group includes a single ring, a fused ring, a bridged ring and a spiro ring. For the multicyclic ring system with aromatic ring and non-aromatic ring and without heteroatom, the term “cycloalkyl” is applied when the attachment point is located at the carbon on the non-aromatic ring (e.g., 5,6,7,8-tetrahydronaphth-5-yl). The term “cycloalkyl” or “C.sub.3-C.sub.8 cycloalkyl” includes cycloalkenyl e.g., adamantlyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclooctyl and cyclohexenyl.

[0126] The term “heterocyclic”, “heterocycle”, “heterocycloalkyl group” or “heterocyclyl group” refers to a saturated or unsaturated cyclic group with carbon atoms and 1-6 heteroatoms selected from nitrogen, oxygen, and sulfur, and the cyclic group includes a single ring, a fused ring, a bridged ring and a spiro ring. For a multicyclic ring system with a aromatic ring and a non-aromatic ring and without heteroatom, the term “heterocyclic”, “heterocycle”, “heterocycloalkyl group” or “heterocyclyl group” is applied when the attachment point is located at the atom on the non-aromatic ring (e.g., 1,2,3,4-tetrahydro-quinolin-3-yl, 5,6,7,8-tetrahydro-quinolin-6-yl, and decahydroquinolin-6-yl). In some embodiments, heterocyclyl group is 3-15 membered, 4-14 membered, 5-13 membered, 7-12 membered or 5-7 membered heterocycle. In some other embodiments, heterocycle contains 4 heteroatoms. In some other embodiments, heterocycle contains 3 heteroatoms. In some other embodiments, heterocycle contains 2 heteroatoms at most. In some embodiments, the nitrogen and/or sulfur atom of heterocycloalkyl group is oxidized to be a moiety of the N-oxide, sulfinyl or sulfonyl. The term “heterocyclyl group” includes (but no be limited thereto) tetrahydrofuranyl, piperidyl, N-methyl-piperid-3-yl, hexahydropyrazinyl, N-methyl-pyrrolidin-3-yl, pyrrolidin-3-yl, 2-pyrrolidon-1-yl, morpholinyl and pyrrolidinyl. The numerical multiplier of the indicated number of carbon atoms (e.g., C.sub.3-C.sub.10) refers to the total number of the carbon atoms excepts for the number of the heteroatoms of the moiety of heterocyclyl group. The divalent heterocyclyl group contains the appropriate content of hydrogen.

[0127] The term “ether” refers to C.sub.1-C.sub.6 alkyl group with 1-3 substituted C.sub.1-C.sub.6 alkoxyl group. Alkoxyl group refers to —O-alkyl.

[0128] The term “halogen” or “halogeno” refers to one or more of fluorine, chlorine, bromine and iodine.

[0129] The term “alkenyl group” refers to a linear hydrocarbyl group or a branched hydrocarbyl group with carbon atoms. For example, the alkenyl group refers to a linear hydrocarbyl group or a branched hydrocarbyl group with 2-6 or 2-4 carbon atoms and with at least one unsaturated position of vinyl (>C═<). For example, the term “C.sub.x-y alkenyl” refers to an alkenyl group with x-y carbon atoms. The term “C.sub.x-y alkenyl” is vinyl, allyl, 1,3-butadienyl etc.

[0130] The term “alkynyl group” refers to a linear univalent hydrocarbyl group or a branched univalent hydrocarbyl group, containing at least a triple bond, with more than two carbon atoms, and in some embodiments with 2-6 or 2-4 carbons. The term “alkynyl group” also refers to these alkyl group with a triple bond and a double bond. For example, the term “C.sub.2-6 alkynyl” includes ethynyl and propynyl etc.

[0131] The term “aminophosphate ester alkylating agent” refers to an alkylating agent having at least one Z.sup.5—X.sup.5—Y.sup.5 bonded to —O—P(Z1). In Z.sup.5—X.sup.5—Y.sup.5, Z.sup.5 is a heteroatom, such as nitrogen, sulfur, or oxygen; X.sup.5 is an optionally-substituted ethylene group; Y.sup.5 is a halogeno or another leaving group; or Z.sup.5—X.sup.5—Y.sup.5 forms a moiety of NCH.sub.2CH.sub.2, and Z.sup.1 is as defined above. The alkylating agent may react with a DNA, another nucleic acid, or a protein. In some situations, the alkylating agent may cross-link DNA.

[0132] The group may be substituted by one or more substituents (e.g., 1, 2, 3, 4, or 5 substituents). Preferably, the substituent is selected from the group consisting of an oxo group, a halogeno, —CN, NO.sub.2.sup.+, —N.sub.2.sup.+, —CO.sub.2R.sup.100, —OR.sup.100, —SR.sup.100, —SOR.sup.100, —SO.sub.2R.sup.100, —NR.sup.100SO.sub.2R.sup.100, —NR.sup.101R.sup.102, —CONR.sup.101R.sup.102, —SO.sub.2NR.sup.101R.sup.102, C1-C6 alkyl, a C1-C6 alkoxyl group, —CR.sup.100═C(R.sup.00).sub.2, —CCR.sup.100, a C.sub.3-C.sub.10 cycloalkyl group, a C.sub.3-C.sub.10 heterocyclyl group, and the divalent substituent e.g., —O—(CH.sub.2)—O— or —O—(CH.sub.2).sub.2—O—, wherein the divalent substituent is unsubstituted or substituted by 1-4 methyl, wherein R.sup.100, R.sup.101 and R.sup.102 is respectively independently hydrogen, a C.sub.1-C.sub.8 alkyl group, a C.sub.3-C.sub.12 cycloalkyl group, a C.sub.3-C.sub.10 heterocyclyl group, a C.sub.6-C.sub.12 aryl group, and a C.sub.2-C.sub.12 heteroaryl group, or R.sup.100 and R.sup.102 and the nitrogen atom bonded thereto form 5-7 membered heterocycle; wherein the alkyl group, cycloalkyl group, aryl group and heteroaryl group are respectively optionally substituted by 1-3 halogeno, 1-3 C.sub.1-C.sub.6 alkyl group, 1-3 C.sub.1-C.sub.6 haloalkyl group or 1-3 C.sub.1-C.sub.6 alkoxyl group. Preferably, the substituent is selected from the group consisting of chlorine, fluorine, —OCH.sub.3, methyl. ethyl, isopropyl, cyclopropyl, —CO.sub.2H (and a salt thereof), C.sub.1-C.sub.6 alkyl ester, CONMe.sub.2, CONHMe, CONH.sub.2, —SO.sub.2Me, —SO.sub.2NH.sub.2, —SO.sub.2NMe.sub.2, —SO.sub.2NHMe, —NHSO.sub.2Me, —NHSO.sub.2CF.sub.3, —NHSO.sub.2CH.sub.2Cl, —NH.sub.2, —OCF.sub.3, —CF.sub.3 and —OCHF.sub.2.

[0133] The term “alkylene” refers to a divalent saturated aliphatic group having carbon atoms. In some embodiments, the alkylene refers to a divalent aliphatic group with 1-6 carbon atoms and loses one more hydrogen atom. The term “C.sub.u-v alkylene” refers to an alkylene with from u to v carbon atoms. The term “alkylene” includes a linear hydrocarbyl group or a branched hydrocarbyl group. For example, the alkylene includes methylene, ethylene, propylene, 2-methyl propene, and amylene etc.

[0134] The term “heteroalkylene” refers to the carbon atom on alkylene chain is substituted by a heteroatom (e.g., O, S, N, or P) or substituted by a substituent containing a heteroatom.

[0135] The term “drug” used herein with respect to D includes (but not limited thereto) gemcitabine, erlotinib, meturedepa, uredepa, altretamine, imatinib, triethylenemelamine, 2,4,6-trimethylmelamine, chlorambucil, chlornaphazine, estramustine, gefitinib, afatinib, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, novembichin, phenesterine, prednimustine, trofosfamide, uracil mustard, carmustine, chlorozotocin, fotemustine, nimustine, ranimustine, dacarbazine, mannomustine, mitobronitol, mitolactol, pipobroman, aclacinomycins, actinomycin, anthramycin, azaserine, bleomycin, cactinomycin, carubicin, doxorubicin, carzinophilin, chromomycin, dactinomycin, daunorubicin, daunomycin, 6-diazo-5-oxo-L-norleucine, mycophenolic acid, nogalamycin, olivomycin, peplomycin, plicamycin, porfiromycin, puromycin, streptonigrin, streptozocin, tubercidin, ubenimex, zinostatin, zorubicin, denopterin, pteropterin, trimetrexate, fludarabine, mercaptopurine, thiamiprine, tioguanine, ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, dideoxyuridine, doxifluridine, enocitabine, floxuridine, fluorouracil, tegafur, L-asparaginase, pulmozyme, aceglatone, aldo-isophosphamide glycoside, aminolevulinic acid, amsacrine, bestrabucil, bisantrene, defofamide, demecolcine, diaziquone, elfornithine, elliptinium acetate, etoglucid, flutamide, hydroxyurea, interferon-α, interferon-β, interferon-γ, interleukin-2, lentinan, mitoguazone, mitoxantrone, mopidamol, nitracrine, pentostatin, phenamet, pirarubicin, podophyllinic acid, 2-ethylhydrazide, procarbazine, razoxane, sizofiran, spirogermanium, paclitaxel, tamoxifen, erlotonib, teniposide, tenuazonic acid, trisethyleneiminoquinone, 2,2′,2″-triclorotriethylamine, urethane, vinblastine, and vincristine.

[0136] The term “administering” or “applying” a drug refers to directly administering or applying a drug (which may be administered or applied to a patient by a medical professional or maybe self-administered or applied) and/or indirectly administering or applying a drug, which may be a drug-prescribing behavior. For example, a physician instructing a patient to self-administer or administer a drug and/or providing a prescription for the drug to the patient is administering or applying the drug to the patient.

[0137] The term “cancer” refers to the potentially unlimited growth leukemia, lymphoma, cancers and other malignant tumors (including solid tumors) which are partially expanded via the invasion and fully expanded via the metastasis. Examples for the cancer includes (but not be limited thereto) the cancer of the adrenal gland, bone, brain, breast, bronchus, colon, rectum, gallbladder, head, neck, kidney, throat, liver, lung, nervous tissue, pancreas, prostate, parathyroid, thyroid, skin, and stomach. Some other embodiments of the cancer include acute and chronic lymphocytic and granulocytic tumors, adenocarcinoma, adenoma, basal cell carcinoma, cervical intraepithelial neoplasia, cancer in situ, Ewing's sarcoma, epidermoid carcinoma, giant cell tumor, multiform neuroglioblastoma, hair cell tumor, intestinal ganglioma and proliferative corneal nerve tumor, islet cell carcinoma, Kaposi's sarcoma, leiomyoma, leukemia, lymphoma, malignant carcinoid tumor, malignant melanoma, malignant hypercalcemia, equine tumor, myeloid epithelial cancer, metastatic skin cancer and mucosal neuroma, myeloma, mycosis fungoides, neuroblastoma, osteosarcoma, osteogenic and other sarcoma, ovarian tumor, pheochromocytoma, polycythemia vera, primary brain tumor, small cell lung cancer, ulcerative and papillary squamous cell carcinoma, hyperplasia, seminoma, soft tissue sarcoma, retinoblastoma, rhabdomyosarcoma, renal cell tumor, local skin lesions, reticular cell sarcoma and Wilm's tumor.

[0138] The terms “patient” and “individual” may be exchanged and refer to a mammal in need of the cancer therapy. Generally, the patient refers to a human. Generally, the patient refers to a human diagnosed with cancer. In some embodiments, the terms “patient” and “individual” refer to a non-human mammal that may be used to select, characterize, and evaluate the drug and therapy. For example, the non-human mammal is the non-human primates, dog, cat, rabbit, pig, mouse, or rat.

[0139] The term “prodrug” refers to a compound transformed via metabolism or other ways to a biologically active or more active compound (or a drug) after administering or applying. Relative to the drug, the prodrug is chemically modified in such a way that it is less active or inactive relative to the drug, but the chemical modification results in the production of the corresponding drug through metabolism or other biological processes after administration of the prodrug. Relative to the active drug, prodrugs may have altered metabolic stability, transport characteristics, fewer side effects or lower toxicity, or improved flavor. Please refer to the reference documents, such as Nogrady (1985) Medicinal Chemistry A Biochemical Approach, Oxford University Press, New York, pp. 388-392, which is entirely incorporated herein by reference. On the other hand, the prodrug may be synthesized by a reactant other than the corresponding drug.

[0140] The term “solid tumor” refers to (but is not limited thereto) a solid tumor of a metastatic tumor in the bone, brain, liver, lung, lymph glands, prostate, skin, and sarcoma soft tissue.

[0141] The term “cancer or tumor of the central nervous system” refers to the benign tumor or the malignant tumor (cancer) in the skull or other central nervous systems, including meningioma, hypophysoma, craniopharyngioma, neurinoma, glioma, ependymoma, primitive neurectodermal tumor, lymphoma of the central nervous system, germ cell tumor, and metastatic tumor.

[0142] The term “therapeutically effective dose” of the drug refers to the amount of the drug having the expected therapeutic effect (e.g., the relief, improvement, ease, or elimination of one or more cancers in the patient) when administered or applied to a patient having a cancer. The therapeutic effect does not necessarily have to occur by administering or applying a single dose and may only occur by administering or applying a series of doses. Therefore, the therapeutically effective dose may be administered or applied once or repeatedly.

[0143] The term “therapy” of a condition of an illness or a patient refers to obtain beneficial or expected results (including the clinical outcome) by adopting steps. For the purpose of the present disclosure, the beneficial or expected results include (but is not limited thereto) the relief or improvement of one or more cancer symptoms, the weakening of the disease degree, the delay or ease of the disease course, the improvement, relief or stability of the disease state, or other beneficial results. In some cases, the therapy of the cancer may be used to partially react to the cancer or to stabilize the disease.

[0144] The term “tumor cell” refers to the tumor of any suitable species, such as mammals, e.g., the mouse, rat, dog, cat, horse, or human.

[0145] The above description of the specific embodiments of the present disclosure does not limit the present disclosure, and those skilled in the art can make various changes or deformations according to the present disclosure.

[0146] The present disclosure is based on the three following applications: [0147] (1) The patent application no. PCT/US2016/021581 and the patent publication no. WO2016/145092 correspond to the China patent application no. 2016800150788 and the China patent publication no. CN107530556A. [0148] (2) The patent application no. PCT/US2016/025665 and the patent publication no. WO2016/061342 correspond to the China patent application no. 2016800200132 and the China patent publication no. CN108136214A. [0149] (3) The patent application no. PCT/US2016/062114 and the patent publication no. WO2017/087428 correspond to the China patent application no. 2016800446081 and the China patent publication no. CN108290911A.

[0150] Hence, the above three applications are hereby incorporated by reference into the text of the present application.

[0151] The experiments and embodiments of the present disclosure are shown as follows.

[0152] The experiments of the inhibitory activity of the proliferation of the cancer cells in vitro, and the experimental data of the interaction of P-GP glycoprotein of the compounds designed and synthesized by the applicant are disclosed below. Hereby declared, the right of the following experimental data is belonged to the applicant.

[0153] P-glycoprotein (P-GP, also known as multidrug resistance protein), which is a high-molecular-weight protein discovered on the plasma membrane of the multidrug-resistant tumor cell, has a transport-pump-like structure. P-GP pumps out a variety of chemotherapy drugs out of cells and reduces intracellular drug concentration. Therefore, the P-GP is closely related to the resistance in clinical chemotherapy.

[0154] The role of the chemotherapy drug for treating the tumor or cancer of the central nervous system (such as the brain) is limited. The limitation is mainly due to the blood-brain barrier (BBB), the low permeability of the chemotherapy drug to the tumor system, or the tumor tissue caused by BBB, i.e., the chemotherapy drug may not eliminate the cancer cells by passing through the blood-brain barrier and entering the brain.

[0155] The process that the small molecules (e.g., the chemotherapy drug) pass through the blood-brain barrier is more complicated. The blood-brain barrier, located between the systemic blood circulation and the cerebrospinal fluid, is formed by specialized brain microvascular endothelial cells, along with surrounding cells and perivascular astrocytes through tight junctions between adjacent cells when most molecules are forced to pass through, rather than forming a physical barrier around vascular endothelial cells.

[0156] The small hydrophilic molecules are allowed to pass through the membrane transportation system of the BBB, whereas the bulky hydrophilic molecules, such as many chemotherapy drugs and macromolecular drugs, are excluded from the central nervous system unless they may be actively transported by specific proteins. More particularly, the “efflux pumps” of BBB for protecting the brain tissue (e.g., P-gp) may actively exclude some chemotherapy drugs and bulky molecular drugs.

[0157] Therefore, even that the small hydrophilic molecular chemotherapy drugs, including small molecule targeted antitumor drug molecule, may pass through the blood-brain barrier and enter the brain to play a role. However, the small hydrophilic molecular chemotherapy drugs may not work because they are excluded from the central nervous system under the action of the P-GP. In other words, the transmembrane structure of P-GP has the function of the energy dependent “drug pump,” which may pump out the hydrophobic lipophilic drugs (e.g., VCR, Dox, and VP-16) and decrease the intracellular drug concentration, so that the cytotoxicity is decreased or complete loss of cytotoxicity.

[0158] For the reasons described above, the experimental data of the interaction between P-GP and the compound is used to evaluate the effective degree of the compound on the inhibitory activity of the proliferation of the tumor cells in the central nervous system.

[0159] The applicant declares that some of the specific compounds disclosed in the following experiments can be synthesized based on the specific synthetic methods and synthetic routes of the compounds disclosed in the present invention, with reference to similar methods and operations disclosed in patent publications (the patent application no. PCT/US2016/021581 and the patent publication no. WO2016/145092 correspond to the China patent application no. 2016800150788 and the China patent publication no. CN107530556A; the patent application no. PCT/US2016/025665 and the patent publication no. WO2016/061342 correspond to the China patent application no. 2016800200132 and the China patent publication no. CN108136214A; the patent application no. PCT/US2016/062114 and the patent publication no. WO2017/087428 correspond to the China patent application no. 2016800446081 and the China patent publication no. CN108290911A) or other publications. And the applicant has confirmed the structures by NMR and mass spectrometry.

1. The Evaluation of the Potential of the Sample as the P-Gp Substrate, which Took MDCKII-MDR1 Cells as the Model and Verapamil as the Inhibitor

[0160] The preparation of the bacteria for the penetration test: [0161] (1) MDCKII-MDR1 cells were cultured in the cell culture bottle. The conditions of the incubator were 37° C., 5% of CO.sub.2, and 95% of the relative humidity. When the cell growth confluence was up to 70-90%, the cells were inoculated to the transwell. [0162] (2) Before the cell inoculation, 50 μL of the culture medium was respectively added to every well of the upper compartment of the transwell, and 25 mL of the culture medium was added to the lower compartment. The transwell was incubated in the incubator under 37° C. and 5% CO.sub.2. After 1 hour, the transwell may be used to inoculate the cells. [0163] (3) After the cells were incubated, the cell suspension was transferred to a round bottom centrifuge tube, and the cell suspension was centrifuged at 120 g for 5 min. [0164] (4) Cells were resuspended in the culture medium, and the final concentration was 1.56×10.sup.6 cells/mL. The cell suspension was transferred to the upper compartment of the 96-well transwell, wherein each upper compartment contains 50 μL of the cell suspension. The final inoculum density was 5.45×10.sup.5 cells/cm.sup.2. [0165] (5) The culture medium was replaced after inoculating for 48 h. After culturing for 4-8 days, the medium was changed every other day. [0166] (6) The process of replacing the culture medium was as the follow. The upper compartment and the lower compartment were separated. The medium in the lower compartment was discarded, and then the medium in the upper compartment was discarded. Finally, 75 μL of fresh medium was added to each upper compartment and 25 mL of fresh medium was added to the lower compartment.

[0167] Evaluation of the Cell Monolayer Integrity [0168] (1) The MDCKII-MER1 cells should be totally confluent and complete the differentiation after culturing for 4-8 days. The MDCKII-MER1 cells can be used for the penetration test at this time. [0169] (2) Millipore was used to measure the resistance of the cell monolayer, and the resistance of every well was recorded. [0170] (3) After the measuring, the transwell was put back to the incubator. [0171] (4) The calculation of the resistance: measured resistance (ohms)×area of the membrane=TEER value (ohm-cm.sup.2). If TERR value was <42 ohm-cm.sup.2, the well would not be used to the penetration test.

[0172] Penetration Test of the Drug [0173] (1) The transwell of the MDCKII-MER1 cells was taken out from the incubator. The cell monolayer was rinsed two times by the buffer solution and incubated at 37° C. for 30 min. [0174] (2) The transport rate of the compound from the top to the bottom was tested. 75 L of the buffer solution contained the sample was added to each upper compartment, and 235 μL of the buffer solution was added to each lower compartment. [0175] (3) The transport rate that the compound was transported from the bottom to the top was tested. 75 μL of the buffer solution was added to each upper compartment, and 235 μL of the buffer solution contained the sample was added to each lower compartment. [0176] (4) 50 μL of the sample was transferred to the acetonitrile containing the internal standard (100 nM Alprazolam, 200 nM Labetalol, 200 nM caffeine and 2 μM Ketoprofen), and the mixture was as the dosing sample at 0 min. [0177] (5) For testing the transportation that the sample was under the condition that the P-GP inhibitor Verapamil was added. Verapamil was both added to the buffer salt of the dosing end and the receiving end of the transwell contained MDCKII-MDR1 cells, and the final concentration was 100 μM. [0178] (6) The transportation of the up and down were merged up, the sample was incubated at 37° C. for 2 h. [0179] (7) After the incubation was finished, 50 μL of the samples from each well of the upper compartment and the lower compartment were respectively added to the sample tubes. 200 μL of the acetonitrile containing the internal standard (100 nM Alprazolam, 200 nM Labetalol, 200 nM caffeine and 2 μM Ketoprofen) was added to each sample tube. After the sample tubes were vortexed for 10 min, the sample tubes were centrifuged at 3220 g for 30 min. 100 μL of the supernatant was taken to be diluted with the same volume of the water, and the LC-MS/MS analysis was executed. Each sample was adopted to the three parallel incubation. [0180] (8) After the cell monolayer was incubated for 2 h, the integrity of the cell monolayer was evaluated by the migration assay using the fluorescence yellow, the fluorescence yellow storage solution was diluted by the buffer solution, and the final concentration was 100 μM/L. 100 μL of the fluorescence yellow solution was added to each well of the upper compartment, and 300 μL of the buffer was added to each well of the lower compartment. After the transwell was incubated at 37° C. for 30 min, 80 L of the solution from each well of the upper compartment and the lower compartment was respectively transferred to a new 96-well plate. ELISA (Enzyme-linked Immunosorbent Assay) reader was used to perform the fluorimetry with the excitation wavelength of 480 nm and the emission wavelength of 530 nm.

[0181] Data Analysis

[0182] The peak area was calculated by the result of the ion chromatography. The permeability coefficient (Papp, unit: cm/s×10.sup.−6) of the compound was calculated by the formula:

[00001]$P_{\mathrm{app}}=\frac{V_A}{\mathrm{Area}\times \mathrm{time}}\times \frac{{\left[\mathrm{drug}\right]}_{\mathrm{acceptor}}}{{\left[\mathrm{drug}\right]}_{\mathrm{intial},\mathrm{donor}}}$

[0183] In the formula, “V.sub.A” refers to the volume of the solution on the acceptor (Ap.fwdarw.B1 was 0.235 mL, B1.fwdarw.Ap was 0.075 mL), “Area” refers to the area of the permeable membrane of the 96-well transwell (0.143 cm.sup.2), “time” refers to the incubation time (s), “[drug].sub.acceptor” refers to the drug concentration of the acceptor after the incubation, and “[drug].sub.initial,donor” refers to the initial concentration of the drug administration before the incubation.

[0184] The efflux ratio was calculated by the formula:

[00002]$\mathrm{Efflux}\mathrm{Ratio}=\frac{P_{\mathrm{app}\left(B-A\right)}}{P_{\mathrm{app}\left(A-B\right)}}$

[0185] In the formula, “P.sub.app (B-A)” refers to the permeability coefficient from the lower compartment to the upper compartment, and the term “P.sub.app (A-B)” refers to the permeability coefficient from the upper compartment to the lower compartment.

[0186] The recovery rate was calculated by the formula:

[00003]$\mathrm{Recovery}\%=\frac{{\left[\mathrm{drug}\right]}_{\mathrm{acceptor}}\times {V_A\left[\mathrm{drug}\right]}_{\mathrm{donor}}\times V_D}{{\left[\mathrm{drug}\right]}_{\mathrm{initial},\mathrm{donor}}\times V_D}\times 100$

[0187] In the formula, “V.sub.A” refers to the volume of the solution on the acceptor (mL), “V.sub.D” refers to the volume of the solution on the donor (mL), “[drug].sub.acceptor” refers to the drug concentration of the acceptor after the incubation, “[drug].sub.donor” refers to the drug concentration of the donor after the incubation, and the term “[drug].sub.initial,donor” refers to the initial concentration of the drug administration before the incubation.

[0188] The LY Leakage of the cell monolayer was calculated by the formula:

[00004]$\mathrm{LY}\mathrm{Leakage}=\left(\frac{I_{\mathrm{acceptor}}\times 0.3}{I_{\mathrm{acceptor}}\times 0.3+I_{\mathrm{donor}}\times 0.1}\right)\times 100$

[0189] In the formula, “I.sub.acceptor” refers to the fluorescence intensity of the acceptor (0.3 mL), “I.sub.donor” refers to the fluorescence intensity of the donor (0.1 mL), expressed by % LY. LY<1.5% refers to the cell monolayer was intact.

[0190] The efflux ratios of different compounds that were in the presence of or in the absence of P-glycoprotein inhibitor, Verapamil, were obtained after respectively testing a part of the compounds.

[0191] The efflux ratios of Metoptolol, Prazosin and Imatinib were also tested as the control groups.

[0192] There were two efflux ratios of one compound (in the absence of Verapamil and in the presence of Verapamil). The closer these two values were, the less effective the P-GP on the drug, i.e., the drug was not the substrate of the P-GP and could enter the blood-brain barrier.

2. The Evaluation of the Inhibitory Effect of the Prepared Compounds to the Proliferation of the Cancer Cells

[0193] The cytotoxicity analysis of the human tumor cell lines in vitro was used.

[0194] The report of the proliferation of the non-small cell lung cancer (NSCLC) human tumor line H460 in vitro was shown in the below table of the compounds.

[0195] IC50 (half maximal inhibitory concentration) values were in nanomoles and were obtained by the following. Cells were exposed in the compounds with different concentration for 2 hours. The compounds were washed off, and fresh medium was added into plates. A growth rate and a cell-survival rate were obtained by cell staining and compared with a control group treated with the medium only.

[0196] Particularly, exponentially growing cells were inoculated in a 96-well plate for 24 h and under the conditions of 37° C., 5% CO.sub.2, 95% air and 100% relative humidity, and then the tested compound was added. The compound was dissolved in 100% DMSO at 200 times of the desired final test concentration. When the drug was added, the compound was further diluted at 4 times of the desired final test concentration by the complete medium. 50 μL aliquots of the compound with specific concentration were added to the microwells contained 150 μL of medium, and then the final drug concentration was obtained. After the drug was added, the plate was further incubated for 2 h under the conditions of 37° C., 5% CO.sub.2, 95% air and 100% relative humidity, then the drug was washed, and the fresh medium was added, and then the plate was further incubated for 70 h under the conditions of 37° C., 5% CO.sub.2, 95% air and 100% relative humidity. After the incubation was finished, the Alamar Blue was used to analyze and quantify the alive cells. The 50% inhibitory concentration (IC.sub.50) caused by the drug was calculated by the computer software and the result was shown in the table below.

[0197] Similarly, to further prove that the compound was activated by the AKR1C3 (the member C3 of the aldo-keto reductase family 1), the proliferation test of some compounds on the cancer cells H460 was carried out in the presence of the specific AKR1C3 inhibitor (3 μmol concentration). Before 2 h of the compound was prepared, the compound with the inhibitor was added to the cell culture. The inhibitor was

##STR00019##

by reference to Flanagan et al., compound 36 in Bioorganic and Medicinal Chemistry (2014) pp. 962-977.

TABLE-US-00001 Efflux ratio (MDCK-MDR1) Inhibitory effect of the Without With proliferation of the cancer cells Number compound Verapamil Verapamil IC.sub.50 (nM) IC.sub.50 of +TH3021 (nM)  1 [00020] 1   0.57 0.87 40  2 [00021]  1.53 0.46 1.89 105.4  3 [00022] 1.2 0.59 1.84 47.78  4 [00023]  0.87 0.59 0.67 16.34  5 [00024]  1.69 0.61 0.59 5.037  6 [00025] untested untested 0.46 38.23  7 [00026]  1.54 0.54 0.71 19.72  8 [00027] untested untested <1.5 26.83  9 [00028] untested untested <1.5 56.15 10 [00029]  1.43 0.61 1.15 29.63 11 [00030] untested untested 0.2108 92.23 12 [00031] untested untested <1.5 11.4 13 [00032] untested untested 29.99 1887 14 [00033]  1.26 0.75 11.39 >1000 15 [00034]  1.36 1.12 6.782 1913 16 [00035]  1.96 0.71 7.258 >500 17 [00036] untested untested 35.45 >10000 18 [00037] untested untested 312.9 >10000 19 [00038] untested untested 46.81 >10000 Control Metoptolol  0.96 untested untested untested group Prazosin  2.87 0.57 untested untested Imatinib 18.06 0.90 untested untested

3. The Compound Preparation and the Spectrum

[0198] “THF” refers to tetrahydrofuran; “DCM” refers to dichloromethane; “EA” or “EtOAc” refers to ethyl acetate; “TEA” refers to triethylamine; “HPLC” refers to high performance liquid chromatography; “MTBE” refers to methyl tert-butyl ether; “DMAP” refers to 4-dimethylaminopyridine; “DBAD” refers to di-tert-butyl azodicarboxylate; “TFA” refers to trifluoroacetate; “LCMS” refers to liquid chromatography-mass spectrometry; “EtOH” refers to ethanol; “t-BuOH” refers to tert-butanol; “DMF” refers to 2,5-dimethylfuran; “PE” refers to petroleum ether; “eq” refers to the chemical equivalence; “TBAF” refers to tetra-n-butylammonium fluoride; and “DIPEA” refers to N,N-diisopropylamine.

[0199] All chemical agents, drugs which were not indicated the source were analytical reagent (AR) or chemical pure (CP) and were purchased from commercial reagent companies.

[0200] Other English abbreviations were by reference to the explanation in organic chemistry.

[0201] Synthesis of Compound 1

##STR00039## [0202] Compound 1-A1 (80.0 mg, 0.266 mmol, synthesized by the synthesis method of compound 3-A4) and 1-A2 (78.3 mg, 0.380 mmol, purchased) were dissolved in acetone (4 mL), then Cs.sub.2CO.sub.3 (199.3 mg, 0.612 mmol) was added and the solution was stirred at room temperature. HPLC was used to detect the extent of reaction. After 2 h, the reaction was finished. The solid was removed by the suction filtration, the original solution was concentrated and separated by column chromatography. The solution after preparation was extracted by DCM (10 mL×3), concentrated, freeze-dried, and then the pure product of compound 1 was obtained (17 mg, percent yield 13.1%, light yellow solid). [0203] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.02 (d, J=8.4 Hz, 1H), 7.48 (dd, J=7.2, 5.5 Hz, 2H), 7.39 (t, J=8.6 Hz, 1H), 7.30 (d, J=8.5 Hz, 1H), 7.19 (s, 1H), 7.14 (t, J=8.7 Hz, 2H), 6.89 (dd, J=8.5, 2.0 Hz, 1H), 6.83 (dd, J=11.1, 2.3 Hz, 1H), 5.19 (d, J=8.0 Hz, 2H), 2.21-2.12 (m, 8H). [0204] MS: Calculated 487.1, found 488.1 ([M+H].sup.+).

[0205] Synthesis of Compound 2

##STR00040## [0206] Compound 1-A1 (150.0 mg, 0.50 mmol, synthesized by the synthesis method of compound 3-A4) and compound 2-A2 (134 mg, 0.71 mmol, purchased) were dissolved in acetone (10 mL), then Cs.sub.2CO.sub.3 (199.3 mg, 0.612 mmol) was added and the solution was stirred at room temperature. HPLC was used to detect the extent of reaction. After 2 h, the reaction was finished. The solution was separated by the suction filtration with the diatomaceous earth. The filter cake was washed by EtOAc (10 mL×3) and combined the organic phase. The original solution was concentrated and separated by column chromatography. The solution after preparation was extracted by DCM (10 mL×3), concentrated at 35° C., freeze-dried, and then the pure product of compound 2 was obtained (26 mg, percent yield 11.1%, light yellow oily substance). [0207] .sup.1H-NMR (400 MHz, MeOD): δ8.01 (d, J=8.4 Hz 1H), 7.68-7.62 (m, 4H), 7.31 (d, J=8.4 Hz 1H), 7.20-7.15 (m, 5H), 5.18 (d, J=8.4 Hz 2H), 2.17-2.10 (m, 8H). [0208] MS: Calculated 469.1, found 470.2 ([M+H].sup.+).

[0209] Synthesis of Compound 3

##STR00041##

[0210] The Synthesis of Compound 3-A2 [0211] Under nitrogen protection, compound 3-A1 (5 g, 24.62 mmol, purchased) was dissolved in anhydrous THF (50 mL) and the solution was lowered to 0° C. The gas was exchanged 3 times, borane-tetrahydrofuran complex (61.5 mL, 61.5 mmol, 1 mol/L in THF) was slowly dripped to the reaction solution. The solution was kept at 0° C. for 30 min, and then warmed up to 65° C. After 3 h, the reaction was finished. The reaction solution was naturally cooled to room temperature and slowly added to cold water (300 g). The reaction solution was extracted by DCM (50 mL×3). The organic phase was washed by 1 M HCl (50 mL×3), washed by water, and washed by brine, concentrated, and dried to obtain the product (4.6 g, percent yield 98.9%, off-white solid). [0212] .sup.1H-NMR (400 MHz, DMSO-d6): δ 8.04 (dd, J=9.2, 6.1 Hz, 1H), 7.58 (dd, J=11.7, 5.8 Hz, 1H), 5.72 (s, 1H), 4.63 (s, 2H). [0213] MS: Calculated MS: 189.1, found: 188.0 ([M−H].sup.−).

[0214] Synthesis of Compound 3-A3 [0215] Under nitrogen protection, POCl.sub.3 (610 mg, 3.97 mmol) was added to anhydrous DCM (5 mL), and compound 3-A2 (500 mg, 2.64 mmol) was added. The reaction solution was lowered to −20° C. TEA (454 mg, 4.49 mmol) in DCM (3 mL) was slowly added to the reaction solution. The reaction solution was kept at −20° C. for 30 min. After 3 h, the reaction of 3-A2 was finished. The reaction solution was cooled to −40° C., and 2-bromoethylamine hydrobromide (1.6 g, 7.92 mmol) was slowly added, TEA (801 mg, 7.92 mmol) in DCM was dropwise added to the solution. The reaction solution was kept at −40° C. for 30 min, and the reaction was finished. 5 mL of H.sub.2O was slowly added, and the reaction solution was naturally warmed up to room temperature. The reaction solution was extracted by DCM (8 mL×3), the organic phase was washed by H.sub.2O (5 mL×2), concentrated, dried, and separated by column chromatography (100-200 mesh silica gel, EA: n-heptane=1:1-EA) to obtain the product (260 mg, yield 20.5%, off-white solid). [0216] .sup.1H NMR (400 MHz, CDCl.sub.3): δ 7.81 (dd, J=8.6, 5.9 Hz, 1H), 7.48 (dd, J=10.5, 5.7 Hz, 1H), 5.14 (d, J=7.6 Hz, 2H), 3.52-3.34 (m, 8H). [0217] MS: Calculated 480.9, found 481.9 ([M+H]+).

[0218] Synthesis of Compound 3-A4 [0219] Under nitrogen protection, compound 3-A3 (5 g, 24.62 mmol, purchased) was dissolved in THF (4 mL) and acetone (6 mL), the reaction solution was warmed up to 59° C. After 4 h, the reaction was finished. The reaction solution was cooled to room temperature, removed by the suction filtration with the diatomaceous earth. The solid was washed by acetone (5 mL), and the original solution was concentrated to obtain the crude product (190 mg, light-yellow solid). The next step was executed directly. [0220] .sup.1H-NMR (400 MHz, MeOD): δ 7.99 (dd, J=9.1, 6.0 Hz, 1H), 7.61 (dd, J=10.9, 5.8 Hz, 1H), 5.30 (d, J=7.9 Hz, 2H), 2.32-1.95 (m, 8H). [0221] MS: Calculated 319.1, found 320.0 ([M+H]+).

[0222] Synthesis of Compound 3 [0223] Under nitrogen protection, compound 3-A4 (80 mg, 0.25 mmol) and 4-hydroxy-4′-fluorobiphenyl (71 mg, 0.38 mmol) were dissolved in acetone (5 mL), CsCO.sub.3 was added (205 mg, 0.63 mmol). The reaction solution was stirred for 3 h. After 3 h, the reaction was finished. The solution was separated by the suction filtration with the diatomaceous earth. The solid was washed by acetone (3 mL), the original solution was concentrated. After the column chromatography, the pure product was obtained (17 mg, percent yield 14.0%, white solid). [0224] .sup.1H-NMR (400 MHz, MeOD): δ 7.91 (d, J=9.1 Hz, 1H), 7.67-7.61 (m, 4H), 7.30 (d, J=6.0 Hz, 1H), 7.20-7.14 (m, 4H), 5.25 (d, J=8.0 Hz, 2H), 2.15-2.10 (m, 8H). [0225] MS: Calculated 487.1, found 488.0 ([M+H].sup.+).

[0226] Synthesis of Compound 4

##STR00042##

[0227] Synthesis of Compound 4-A3 [0228] Under nitrogen protection, compound 4-A1 (1.0 g, 5.24 mmol, purchased) and compound 4-A2 (909 mg, 5.76 mmol, purchased) were added in the mixed solution of 1,4-dioxane (18 mL) and H.sub.2O (2 mL), K.sub.2CO.sub.3 (2.2 g, 15.71 mmol) was added to the reaction solution. N.sub.2 was exchanged 3 times, Pd(OAc).sub.2 (59 mg, 0.26 mmol) and PPh.sub.3 (69 mg, 0.26 mmol) were added to the reaction solution. N.sub.2 was exchanged 3 times again, the reaction solution was warmed up to 100° C. After 1.5 h, the reaction was finished.

[0229] Post treatment: the reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth and washed by DCM. The original solution was extracted by DCM (5 mL×3), concentrated, dried and separated by reversed-phase chromatography (water:MeCN=50%:50%), then the product was obtained (238 mg, percent yield 20.3%, yellow solid). [0230] .sup.1H-NMR (400 MHz, MeOD): δ7.39-7.33 (m, 1H), 7.16 (t, J=8.4 Hz, 1H), 7.03-6.97 (m, 2H), 6.68 (dd, J=8.4 Hz, 2.4 Hz, 1H), 6.60 (dd, J=12.0, 2.4 Hz, 1H). [0231] MS: Calculated 224.1, found 223.0 ([M−H].sup.−).

[0232] Synthesis of Compound 4 [0233] Under nitrogen protection, compound 4-A3 (80 mg, 0.27 mmol) and compound 1-A1 (101 mg, 0.45 mmol, synthesized by the synthesis method of compound 3-A4) were dissolved in acetone (5 mL), Cs.sub.2CO.sub.3 (216 mg, 0.66 mmol) was added to the reaction solution, and then the reaction solution was stirred. After 1.5 h, the reaction was finished. [0234] Post treatment: the reaction solution was separated by the suction filtration with the diatomaceous earth and washed by DCM. The original solution was concentrated, dried, separated by column chromatography and freeze-dried to obtain the product (35.5 mg, percent yield 26.4%, light yellow oily substance). [0235] .sup.1H-NMR (400 MHz, MeOD): δ8.06 (d, J=8.4 Hz, 1H), 7.48-7.40 (m, 3H), 7.32 (s, 1H), 7.10-7.05 (m, 2H), 6.99-6.95 (m, 2H), 5.23 (d, J=8.4 Hz, 2H), 2.22-2.13 (m, 8H). [0236] MS: Calculated 505.1, found 506.1 ([M+H].sup.+).

[0237] Synthesis of Compound 5

##STR00043##

[0238] Synthesis of Compound 5-A3 [0239] Under nitrogen protection, compound 5-A1 (1.0 g, 5.24 mmol, purchased) and compound 5-A2 (886 mg, 5.76 mmol, purchased) were added in the mixed solution of 1,4-dioxane (18 mL) and H.sub.2O (2 mL), and then K.sub.2CO.sub.3 (2.2 g, 15.71 mmol) was added to the reaction solution. N.sub.2 was exchanged 3 times, Pd(OAc).sub.2 (59 mg, 0.26 mmol) and PPh.sub.3 (69 mg, 0.26 mmol) were added to the solution. N.sub.2 was exchanged 3 times again, the temperature was warmed up to 100° C. After 1.5 h, the reaction was finished. [0240] Post treatment: The reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth and washed by DCM. The original solution was extracted by DCM (5 mL×3), concentrated, dried and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=5:1) to obtain the product (895 mg, percent yield 77.6%, off-white solid). [0241] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.16-7.12 (m, 1H), 7.06 (t, J=8.4 Hz, 1H), 6.99-6.89 (m, 2H), 6.72-6.65 (m, 2H), 6.32 (s, 1H), 2.19 (s, 3H). [0242] MS: Calculated 220.1, found 219.1 ([M−H].sup.−).

[0243] Synthesis of Compound 5 [0244] Under nitrogen protection, compound 5-A3 (80 mg, 0.27 mmol) and compound 1-A1 (95 mg, 0.45 mmol, synthesized by the synthesis method of compound 3-A4) were dissolved in acetone (5 mL), Cs.sub.2CO.sub.3 (216 mg, 0.66 mmol) was added to the reaction solution, then the solution was stirred for 2 h at room temperature, and the reaction was finished.

[0245] Post treatment: The reaction solution was separated by the suction filtration with the diatomaceous earth and washed by DCM. The original solution was concentrated, separated by column chromatography and freeze-dried to obtain the product (13 mg, percent yield 7.1%, yellow oily substance). [0246] .sup.1H-NMR (400 MHz, MeOD): δ 8.06 (d, J=8.4 Hz, 1H), 7.40 (d, J=8.4 Hz, 1H), 7.33-7.27 (m, 2H), 7.24-7.16 (m, 1H), 7.06-7.04 (m, 1H), 7.01-6.93 (m, 3H), 5.24 (d, J=8.4 Hz, 2H), 2.22-2.16 (m, 11H). [0247] MS: Calculated 501.1, found 502.1 ([M+H]+).

[0248] Synthesis of Compound 6

##STR00044## [0249] Under nitrogen protection, compound 6-A1 (80 mg, 0.266 mmol, synthesized by the synthesis method of compound 3-A4) and compound 6-A2 (73.2 mg, 0.452 mmol, purchased) were dissolved in acetone (5 mL), Cs.sub.2CO.sub.3 (216.3 mg, 0.664 mmol) was added to the reaction solution, and then the reaction solution was stirred at room temperature. After 1.5 h, the reaction was finished. [0250] Post treatment: The reaction solution was separated by the suction filtration with the diatomaceous earth and the solid was washed by DCM. The original solution was concentrated, separated by column chromatography to obtain the pure product (17.4 mg, percent yield 14.7%, light-yellow oily substance). [0251] .sup.1H-NMR (400 MHz, MeOD): δ8.45 (d, J=2.8 Hz, 1H), 8.08 (d, J=8.4 Hz, 1H), 7.69 (d, J=8.8 Hz, 1H), 7.41-7.39 (m, 2H), 7.23 (s, 1H), 5.21 (d, J=8.0 Hz, 2H), 2.22-2.13 (m, 8H). [0252] MS: Calculated 444.1, found 445.1 ([M+H]+).

[0253] Synthesis of Compound 7

##STR00045## [0254] Compound 7-A1 (94 mg, 0.50 mmol) and compound 7-A2 (100 mg, 0.33 mmol, synthesized by the synthesis method of compound 3-A4) were dissolved in acetone (5 mL), Cs.sub.2CO.sub.3 (372 mg, 0.83 mmol) was added to acetone, and then the reaction solution was stirred at room temperature. HPLC was used to detect the extent of reaction. After 1.0 h, the reaction was finished. [0255] The reaction solution was separated by the suction filtration with the diatomaceous earth and the solid was washed by DCM (10 mL×3). The original solution was concentrated, separated by column chromatography, extracted by DCM (10 mL×3) and freeze-dried to obtain compound 7 (42 mg, percent yield 26.9%, light-yellow oily substance). [0256] .sup.1H-NMR (400 MHz, MeOD): δ8.43 (d, J=2.7 Hz, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.02 (dd, J=8.8, 5.4 Hz, 2H), 7.91 (d, J=8.7 Hz, 1H), 7.57 (dd, J=8.7, 2.9 Hz, 1H), 7.42 (d, J=7.8 Hz, 1H), 7.29 (s, 1H), 7.21 (t, J=8.8 Hz, 2H), 5.22 (d, J=8.4 Hz, 2H), 2.26-2.08 (m, 8H). [0257] MS: Calculated 470.1, found 471.1 ([M+H].sup.+).

[0258] Synthesis of Compound 8

##STR00046## [0259] Compound 8-A1 (3.0 g, 17.2 mmol, purchased) was added in the mixed solution of 1,4-dioxane and H.sub.2O (9:1, 60 mL), K.sub.2CO.sub.3 (4.7 mg, 34.4 mmol) was added to the solution. N.sub.2 was exchanged 3 times, PPh.sub.3 (225 mg, 0.86 mmol) and Pd(OAc).sub.2 (193 mg, 0.86 mmol) were added in proper order, and then N.sub.2 was exchanged 3 times again. The reaction was reacted at 100° C. HPLC was used to detect the extent of reaction, and the reaction was finished after 10 h. [0260] The reaction solution was separated by the suction filtration with the diatomaceous earth and the solid was washed by DCM (15 mL×3). The solid was washed. The original solution was concentrated, dry packed, separated by column chromatography (Heptane:EtOAc=5:1), and mixed with MTBE (3 mL) to obtain compound 8-A2 (1.5 g, percent yield 42.0%, white solid). [0261] .sup.1H-NMR (300 MHz, MeOD): δ8.19 (s, 1H), 7.78-7.75 (m, 1H), 7.58 (d, J=8.4 Hz, 1H), 7.29 (d, J=8.4 Hz, 1H), 7.08-7.05 (m, 2H). [0262] MS: Calculated 207.0, found 208.2 ([M+H].sup.+).

[0263] Compound 8-A2 (103 mg, 0.50 mmol) and compound 8-A3 (100 mg, 0.33 mmol, synthesized by the synthesis method of compound 3-A4) were dissolved in acetone (5 mL), Cs.sub.2CO.sub.3 (270 mg, 0.83 mmol) was added to the reaction solution, then the reaction solution was stirred at room temperature, the reaction solution was light yellow. HPLC was used to detect the extent of reaction and the reaction was finished after 2.0 h [0264] The reaction solution was separated by the suction filtration with the diatomaceous earth and the solid was washed by acetone (10 mL×3). The original solution was concentrated, separated by column chromatography, extracted by DCM (10 mL×3) and freeze-dried to obtain compound 8 (26 mg, percent yield 16.0%, yellow liquid). [0265] .sup.1H-NMR (400 MHz, MeOD): δ8.47 (d, J=2.8 Hz, 1H), 8.10 (d, J=8.4 Hz, 1H), 7.95-7.92 (m, 1H), 7.85-7.82 (m, 1H), 7.59-7.57 (m, 1H), 7.46-7.44 (m, 1H), 7.33 (s, 1H), 7.11-7.08 (m, 2H), 5.23 (d, J=8.4 Hz, 2H), 2.19-2.15 (m, 8H). [0266] MS: Calculated 488.1, found 489.1 ([M+H].sup.+).

[0267] Synthesis of Compound 9

##STR00047## [0268] Under nitrogen protection, compound 9-A1 (80 mg, 0.266 mmol, synthesized by the synthesis method of compound 3-A4) and compound 9-A2 (58 mg, 0.452 mmol, purchased) were dissolved in acetone (5 mL), Cs.sub.2CO.sub.3 (216.3 mg, 0.664 mmol) was added to the reaction solution, and then the reaction solution was stirred at room temperature. After 1.5 h, the reaction was finished. [0269] The reaction solution was separated by the suction filtration with the diatomaceous earth and the solid was washed by DCM. The original solution was concentrated, separated by HPLC to obtain the pure product (19.8 mg, percent yield 18.1%, yellow liquid). [0270] .sup.1H-NMR (400 MHz, MeOD): δ8.18 (d, J=2.8 Hz, 1H), 8.09 (d, J=8.4 Hz, 1H), 7.55-7.44 (m, 3H), 7.30 (s, 1H), 5.22 (d, J=8.0 Hz, 2H), 2.22-2.15 (m, 8H). [0271] MS (retention time 3.103 min): Calculated 410.1, found 411.0 ([M+H]+).

[0272] Synthesis of Compound 10

##STR00048## [0273] Under nitrogen protection, 2-bromo-5-fluoropyridine (compound 10-A1, 2.0 g, 11.36 mmol) and 4-hydroxyphenylboronic acid (compound 10-A2, 1.9 g, 13.64 mmol) were added to the mixed solution of DME (40 mL) and H.sub.2O (9 mL). N.sub.2 was exchanged 3 times, Pd(PPh.sub.3).sub.4 (396 mg, 0.35 mmol) and Na.sub.2CO.sub.3 (2.4 g, 22.73 mmol) were added, then N.sub.2 was exchanged 3 times again. The reaction solution was warmed up to 80° C. HPLC was used to detect the extent of reaction. After 2.5 h, the reaction was finished. [0274] The reaction solution was cooled to room temperature and extracted by EtOAc (60 mL×3). The organic phase was washed by water, washed by brine, and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=15:1-12:1) to obtain the compound 10-A3 (1.4 g, percent yield 54.1%, light yellow solid). [0275] .sup.1H-NMR (300 MHz, MeOD): δ8.43 (d, J=2.7 Hz, 1H), 7.81-7.77 (m, 3H), 7.64-7.58 (m, 1H), 6.87 (d, J=8.7 Hz, 1H). [0276] MS: Calculated 189.1, found 190.1 ([M+H]+).

[0277] Under nitrogen protection, compound 10-A4 (80 mg, 0.27 mmol, synthesized by the synthesis method of compound 3-A4) and compound 10-A3 (88 mg, 0.45 mmol) were dissolved in acetone (5 mL), Cs.sub.2CO.sub.3 (216 mg, 0.66 mmol) was added to the solution, and then the solution was stirred at room temperature. After 2 h, the reaction was finished.

[0278] Post treatment: The reaction solution was separated by the suction filtration with the diatomaceous earth and washed by DCM. The original solution was concentrated, separated by column chromatography and freeze-dried to obtain compound 10 (2 mg, percent yield 1.5%, yellow oily substance). [0279] .sup.1H-NMR (400 MHz, MeOD): δ 8.52 (d, J=2.8 Hz, 1H), 8.04 (dd, J=8.6, 3.1 Hz, 3H), 7.92 (dd, J=8.8, 4.3 Hz, 1H), 7.68 (dd, J=8.4, 2.9 Hz, 1H), 7.35 (d, J=8.3 Hz, 1H), 7.22 (s, 1H), 7.17 (d, J=8.8 Hz, 2H), 5.20 (d, J=8.3 Hz, 2H), 2.28-2.03 (m, 8H). [0280] MS: Calculated 470.1, found 471.1 ([M+H].sup.+).

[0281] Synthesis of Compound 11

##STR00049##

[0282] Compound 11-A1 (4.0 g, 20.9 mmol) and B.sub.2pin.sub.2 (8.0 g, 31.4 mmol) were added in the mixed solution of 1,4-dioxane and H.sub.2O (9:1, 40 mL), and then KOAc (4.7 mg, 34.4 mmol) and Pd(PPh.sub.3).sub.4 (1.21 g, 1.1 mmol) were added to the reaction solution. N.sub.2 was exchanged 3 times, and the reaction was reacted at 95° C. HPLC was used to detect the extent of reaction.

[0283] After the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth and the solid was washed by EtOAc (10 mL×3), the original solution was concentrated, extracted by EtOAc (30 mL×3), washed by water (40 mL), washed by brine (40 mL×2), dried by MgSO.sub.4 and concentrated, and separated by column chromatography (Heptane:EtOAc=10:1) to obtain compound 11-A2 (1.8 g, percent yield 36.7%, white solid). [0284] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.61 (t, J=7.6 Hz, 1H), 6.61 (dd, J=8.0, 2.0 Hz, 1H), 6.52 (dd, J=10.8, 2.0 Hz, 1H), 5.39 (s, 1H), 1.34 (s, 12H). [0285] MS: Calculated 238.1, found 239.2 ([M+H]+).

[0286] Compound 11-A2 (1.15 g, 4.83 mmol) was dissolved in the mixed solution of 1,4-dioxane and H.sub.2O (9:1) and the solution was under nitrogen protection, K.sub.3PO.sub.4 (1.5 g, 7.1 mmol) and 2-bromo-5-fluoropyridine (500 mg, 2.8 mmol) were added to the reaction solution. N.sub.2 was exchanged 3 times, and the reaction was reacted at 90° C. HPLC was used to detect the extent of reaction.

[0287] After the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth and the solid was washed by EtOAc (20 mL×3), the original solution was concentrated, washed by water (10 mL), dried by Na.sub.2SO.sub.4 and concentrated, and separated by column chromatography (200-300 mesh silica gel, Heptane:EA=3:1) to obtain compound 11-A3 (500 mg, percent yield 76.2%, white solid). [0288] .sup.1H-NMR (400 MHz, MeOD): δ10.24 (s, 1H), 8.64 (d, J=2.4 Hz 1H), 7.78-7.73 (m, 3H), 6.75-6.73 (m, 1H), 6.69-6.65 (m, 1H). [0289] MS: Calculated 207.1, found 208.2 ([M+H]+).

[0290] Compound 11-A4 (80 mg, 0.27 mmol, synthesized by the synthesis method of compound 3-A4) was dissolved in acetone (5 mL), Cs.sub.2CO.sub.3 (199 mg, 0.612 mmol) was added to the reaction solution, and then the solution was stirred at room temperature. HPLC was used to detect the extent of reaction, and the reaction was finished after 1.5 h. [0291] The reaction solution was separated by the suction filtration with the diatomaceous earth and the solid was washed by EtOAc (10 mL×3), the original solution was concentrated, separated by column chromatography, extracted by DCM (10 mL×3) and freeze-dried to obtain compound 11 (17 mg, percent yield 13.1%, light yellow oily substance). [0292] .sup.1H-NMR (400 MHz, MeOD): δ8.57 (d, J=2.8 Hz, 1H), 8.08 (d, J=8.4 Hz, 1H), 7.94 (t, J=9.6 Hz, 1H), 7.86-7.83 (m, 1H), 7.72-7.67 (m, 1H), 7.44 (d, J=8.4 Hz 1H), 7.34 (s, 1H), 7.00-6.95 (m, 2H), 5.23 (d, J=8.4 Hz, 2H), 2.22-2.14 (m, 8H). [0293] MS: Calculated 488.1, found 489.2 ([M+H].sup.+).

[0294] Synthesis of Compound 12

##STR00050## [0295] Compound 12-A1 (4.0 g, 19.9 mmol) and 4-fluorophenylboronic acid (3.3 g, 23.9 mmol) were added to the mixed solution of 1,4-dioxane and H.sub.2O (9:1, 40 mL), K.sub.2CO.sub.3 (8.2 g, 59.7 mmol) was added to the reaction solution, and N.sub.2 was exchanged 3 times. PPh.sub.3 (262 mg, 1.0 mmol) and Pd(OAc).sub.2 (224 mg, 0.995 mmol) were added to the reaction solution, and N.sub.2 was exchanged 3 times again. The reaction was reacted at 100° C. HPLC was used to detect the extent of reaction. [0296] After the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth and the solid was washed by EtOAc, the original solution was concentrated, extracted by EtOAc (20 mL×3), dried, concentrated, and separated by column chromatography to obtain compound 12-A2 (700 mg, percent yield 16.2%, white solid). [0297] .sup.1H-NMR (400 MHz, DMSO): δ7.34-7.31 (m, 2H), 7.21 (t, J=8 Hz, 2H), 7.10 (d, J=8 Hz, 1H), 6.85 (s, 1H), 6.81 (d, J=8 Hz, 1H), 3.75 (s, 3H), 2.18 (s, 3H).

[0298] Compound 12-A2 (510 mg, 2.36 mmol) was dissolved in DCM (18 mL), and the reaction solution was cooled to 0° C. After the BBr.sub.3 (1.2 g, 4.72 mmol) was added to the reaction solution, the temperature was natural warmed up to room temperature, and the reaction solution was stirred at room temperature for 1 h. HPLC was used to detect the extent of reaction until the reaction was finished. [0299] Post treatment: the reaction solution was quenched by water (15 mL), extracted by DCM (10 mL×5) and dried to obtain the crude product, and the crude product was separated by column chromatography to obtain compound 12-A3 (300 mg, percent yield 62.9%, light yellow liquid). [0300] .sup.1H-NMR (400 MHz, DMSO): δ9.40 (s, 1H), 7.32-7.28 (m, 2H), 7.20 (t, J=8 Hz, 2H), 6.99 (d, J=8 Hz, 1H), 6.68 (s, 1H), 6.66-6.63 (m, 1H), 2.14 (s, 3H). [0301] MS: Calculated 202.1, found 200.6 ([M−H].sup.−).

[0302] Compound 12-A4 (80 mg, 0.27 mmol, synthesized by the synthesis method of compound 3-A4) and compound 12-A3 (76.8 mg, 0.38 mmol) were dissolved in acetone (4 mL), Cs.sub.2CO.sub.3 (199 mg, 0.61 mmol) was added to the reaction solution, and then the solution was stirred at room temperature. HPLC was used to detect the extent of reaction. After 1.5 h, the reaction was finished. [0303] The solid of the reaction solution was separated by the suction filtration, the original solution was concentrated, separated by column chromatography, extracted by DCM (10 mL×3), concentrated at 35° C. water bath, and freeze-dried to obtain compound 12 (21 mg, percent yield 16.4%, yellow oily substance). [0304] .sup.1H-NMR (400 MHz, CD.sub.3OD): δ 8.00 (d, J=8.4 Hz, 1H), 7.35-7.29 (m, 3H), 7.25 (d, J=8.4 Hz, 1H), 7.19-7.14 (m, 3H), 7.03 (d, J=2.0 Hz, 1H), 6.97-6.94 (m, 1H), 5.19 (d, J=8.4 Hz, 2H). 2.25 (s, 3H). 2.18-2.12 (m, 8H). [0305] MS: Calculated 483.1, found 484.1 ([M+H].sup.+).

[0306] Synthesis of Compound 13

##STR00051## [0307] Under nitrogen protection, m-bromophenol (13-A0, 1.5 g, 8.57 mmol) and 4-fluorophenylboronic acid (13-A1, 1.0 g, 7.15 mmol) were added to the mixed solution of 1,4-dioxane (30 mL) and H.sub.2O (5 mL). N.sub.2 was exchanged 3 times, Pd(OAc).sub.2 (224 mg, 0.995 mmol), PPh.sub.3 (94 mg, 0.36 mmol) and K.sub.2CO.sub.3 (3.0 g, 21.44 mmol) were added to the reaction solution and N.sub.2 was exchanged 3 times again, the reaction solution was warmed up to 100° C. The reaction was under supervision for 1 h and the reaction was finished. [0308] Post treatment: the reaction solution was cooled to room temperature, extracted by EtOAc (50 mL×3) after the suction filtration. The organic phase was washed by water, washed by brine, separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=12:1-9:1) to obtain compound 13-A2 (1.1 g, percent yield 76.2%, white solid). [0309] .sup.1H-NMR (300 MHz, MeOD): δ7.59-7.54 (m, 2H), 7.23-7.10 (m, 3H), 7.04-6.99 (m, 2H), 6.76 (dd, J=8.1, 1.5 Hz, 1H). [0310] MS: Calculated 188.1, found 189.1 ([M+H].sup.+).

[0311] Compound 13-A2 (580 mg, 3.08 mmol) and 3-fluoro-4-nitrobenzoaldehyde (434 mg, 2.57 mmol) were dissolved in MeCN (10 mL), K.sub.2CO.sub.3 (887 mg, 6.42 mmol) was added to the reaction solution under nitrogen, and the reaction solution was warmed up to 80° C., the reaction was under supervision for 2 h and the reaction was finished. [0312] The reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth, washed by DCM. The original solution was concentrated and separated by column chromatography (MeCN:H.sub.2O=50%:50%) to obtain compound 13-A3 (320 mg, percent yield 33.7%, yellow oily substance). [0313] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 9.98 (s, 1H), 8.05 (d, J=8.4 Hz, 1H), 7.71 (d, J=1.6 Hz, 1H), 7.69-7.43 (m, 5H), 7.28-7.27 (m, 1H), 7.15-7.11 (m, 2H), 7.08-7.05 (m, 1H).

[0314] Under nitrogen protection, compound 13-A3 (350 mg, 1.04 mmol) and TMSCF.sub.3 (296 mg, 2.08 mmol) were dissolved in THF (4 mL). After the reaction solution was cooled to 0° C., TBAF (0.01 mL, 0.01 mmol, 1M in THF) was added to the reaction solution and the temperature was kept at 0° C. for 30 min. After the reagent 14-A3 was totally vanished, 3N HCl (2 mL) was added to the reaction solution, and the solution became clear. The reaction solution was keeping stirring for 1 h to totally transfer to the product. [0315] The reaction solution was extracted by DCM (5 mL×3). The organic phase was washed by water (5 mL×3), dried, concentrated, and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=12:1-10:1) to obtain the product (350 mg, percent yield 82.8%, yellow solid). [0316] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.00 (d, J=8.4 Hz, 1H), 7.53-7.34 (m, 5H), 7.24-7.23 (m, 2H), 7.15-7.11 (m, 2H), 7.03-7.00 (m, 1H), 5.03-5.02 (m, 1H). [0317] MS: Calculated 407.1, found 408.0 ([M+H]+).

[0318] Under nitrogen protection, POCl.sub.3 (188 mg, 1.23 mmol) was dissolved in DCM (5 mL), and the reaction solution was cooled to −40° C. Compound 13-A4 (250 mg, 0.61 mmol) was dissolved in DCM (2 mL) and added to the reaction solution with TEA (155 mg, 1.53 mmol), the reaction solution was kept at −40° C. After 3 h, compound 15-A3 was totally transferred to intermediate, 2-bromoethylamine hydrobromide (1.0 g, 4.91 mmol) and TEA (497 mg, 4.91 mmol) were added to the reaction solution. The reaction was supervised and finished after 30 min. [0319] NH.sub.4Cl (5 mL) was added to the reaction solution at 0° C., the reaction solution was extracted by DCM (20 mL×3). The organic phase was washed by water, washed by brine, dried, concentrated, and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=2:1-1:1) to obtain compound 13-A5 (200 mg, percent yield 46.6%, yellow solid). [0320] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.01 (d, J=8.4 Hz, 1H), 7.54-7.33 (m, 5H), 7.25 (d, J=2.0 Hz, 1H), 7.18 (s, 1H), 7.15-7.10 (m, 2H), 7.03 (d, J=1.2 Hz, 1H), 5.70-5.60 (m, 1H), 3.38-3.08 (m, 8H). [0321] MS: Calculated 699.0, found 699.9 ([M+H]+).

[0322] Under nitrogen protection, compound 13-A5 (150 mg, 0.22 mmol) was dissolved in THF (15 mL), Ag.sub.2O (497 mg, 2.1 mmol) and DIPEA (277 mg, 2.1 mmol) were added to the reaction solution, the reaction solution was warmed up to 65° C. and stirred for 1.5 h. [0323] After the reaction was finished, the reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth, the solid was washed by DCM, the original solution was concentrated and separated by column chromatography to obtain compound 13 (56 mg, percent yield 48.6%, white solid). [0324] .sup.1H-NMR (400 MHz, MeOD): δ 8.08 (d, J=8.4 Hz, 1H), 7.67-7.59 (m, 2H), 7.56-7.46 (m, 3H), 7.31 (d, J=2.2 Hz, 2H), 7.22-7.13 (m, 2H), 7.10-7.05 (m, 1H), 6.05-5.95 (m, 1H), 2.29-1.89 (m, 8H). [0325] MS: Calculated 537.1, found 538.1 ([M+H].sup.+).

[0326] Synthesis of Compound 14

##STR00052## [0327] Compound 14-A1 (500 mg, 2.96 mmol) and compound 14-A0 (554 mg, 2.69 mmol) were dissolved in MeCN (10 mL), K.sub.2CO.sub.3 (743 mg, 5.38 mmol) was added to the solution under nitrogen, the reaction solution was warmed up to 80° C., and the reaction was supervised and finished after 1.5 h. [0328] The reaction solution was cooled down to room temperature, washed by DCM. The original solution was concentrated and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=15:1-10:1) to obtain the product (535 mg, percent yield 56.0%, brown oily substance). [0329] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 9.99 (s, 1H), 8.05 (d, J=8.4 Hz, 1H), 7.71 (d, J=8.4 Hz, 1H), 7.56-7.55 (m, 3H), 7.41 (dd, J1=8.4 4.8 Hz, 1H), 7.16 (d, J=8.4 Hz, 2H), 7.00-6.91 (m, 2H).

[0330] Under nitrogen protection, compound 14-A2 (400 mg, 1.13 mmol) and TMSCF.sub.3 (320 mg, 2.25 mmol) were dissolved in THF (4 mL), the reaction solution was cooled down to 0° C., TBAF (0.02 ml, 0.02 mmol, 1M in THF) was added, and the temperature was kept at 0° C. for 30 min. After compound 14-A2 was totally vanished, 3N HCl (2 mL) was added to the reaction solution, and the reaction solution was became clear. The reaction solution was keeping stirred for 1 h, extracted by DCM (5 mL×3). The organic phase was washed by water (5 mL×3), dried and concentrated to obtain the crude product (405 mg, percent yield 56.4%, yellow solid). The crude product was used to the next reaction directly. [0331] MS: Calculated 425.3, found 426.0 ([M+1].sup.+).

[0332] Under nitrogen protection, POCl.sub.3 (209 mg, 1.36 mmol, J&K Scientific) was dissolved in DCM (5 mL), and the reaction solution was cooled to −40° C. Compound 14-A3 (290 mg, 0.68 mmol) was dissolved in DCM (2 mL) and added to the reaction solution with TEA (173 mg, 1.70 mmol), the reaction solution was kept at −40° C. After 2 h, compound 15-A3 was totally transferred to intermediate, 2-bromoethylamine hydrobromide (1.0 g, 4.91 mmol) and TEA (497 mg, 4.91 mmol) were added to the reaction solution. The reaction was supervised and finished after 30 min. [0333] Saturated NH.sub.4Cl (5 mL) solution was added to the reaction solution at 0° C., the reaction solution was extracted by DCM (20 mL×3). The organic phase was washed by water, washed by brine, dried, concentrated, and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=5:1-3:1) to obtain compound 14-A4 (250 mg, percent yield 51.1%, yellow solid). [0334] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.00 (d, J=8.4 Hz, 1H), 7.54 (d, J=7.6 Hz, 2H), 7.44-7.38 (m, 1H), 7.35 (d, J=8.4 Hz, 1H), 7.21 (s, 1H), 7.13 (d, J=8.8 Hz, 1H), 7.00-6.95 (m, 2H), 5.68-5.62 (m, 1H), 3.42-3.11 (m, 8H). [0335] MS: Calculated 717.2, found 717.9 ([M+H]+).

[0336] Under nitrogen protection, compound 14-A4 (230 mg, 0.32 mmol) was dissolved in THF (15 mL), Ag.sub.2O (372 mg, 1.60 mmol) and DIPEA (207 mg, 1.60 mmol) were added to the reaction solution, the reaction solution was warmed up to 65° C. and stirred for 1.5 h. [0337] After the reaction was finished, the reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth. The solid was washed by DCM, the original solution was concentrated and separated by column chromatography to obtain the pure product of compound 14 (102 mg, percent yield 57.5%, white solid). [0338] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.01 (d, J=8.4 Hz, 1H), 7.54 (d, J=1.6 Hz, 2H), 7.51-7.36 (m, 2H), 7.24 (s, 1H), 7.12-7.11 (m, 2H), 6.97-6.93 (m, 2H), 5.72-5.69 (m, 1H), 2.26-2.01 (m, 8H). [0339] MS: Calculated 555.1, found 556.1 ([M+H]+).

[0340] Synthesis of Compound 15

##STR00053## [0341] Under nitrogen protection, 4-bromo-3-fluorophenol (5.0 g, 26.2 mmol, purchased, 97%) and 4-fluorophenylboronic acid (4.0 g, 28.8 mmol) were dissolved in the mixed solution of dioxane and water (100 mL, dioxane:water=9:1), K.sub.2CO.sub.3 (10.8 g, 78.6 mmol) was added to the reaction solution, the gas was exchanged 3 times, Pd(OAc).sub.2 (295 mg, 1.31 mmol) and PPh.sub.3 (345 mg, 1.31 mmol, J&K Scientific, 97%) were added to the reaction solution, the gas was exchanged 3 times again, the reaction solution was warmed up to 100° C. and stirred overnight. [0342] After the reaction was finished, the reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth, washed by EA, the original solution was concentrated and pH was adjusted by 1N HCl to 3. The original solution was extracted by EA (50 mL×3), washed by water (10 mL×3), washed by brine, dried, concentrated and separated by column chromatography (100-200 mesh silica gel, n-heptane:EA=20:1) to obtain compound 15-A0 (3.5 g, percent yield 64.8%, white solid). [0343] .sup.1H-NMR (300 M, DMSO-d6): δ10.02 (s, 1H), 7.52-7.47 (m, 2H), 7.34-7.23 (m, 3H), 6.71-6.64 (m, 2H). [0344] MS: Calculated 206.1, found 204.8 ([M−H].sup.−).

[0345] Under nitrogen protection, compound 15-A1 (930 mg, 5.50 mmol, 97%) and compound 16-A0 (1.36 g, 6.60 mmol) were dissolved in acetonitrile (20 mL), K.sub.2CO.sub.3 (1.52 g, 11.0 mmol, J&K Scientific, 99%) was added, the reaction solution was warmed up to 85° C. and stirred for 2 h, and the reaction was finished. [0346] The reaction solution was cooled down to room temperature, separated by the suction filtration, the original solution was concentrated and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=15:1) to obtain compound 15-A2 (1.10 g, percent yield 56.4%, light yellow solid). [0347] .sup.1H-NMR (400 MHz, DMSO-d6): δ10.05 (s, 1H), 8.30 (d, J=8.3 Hz, 1H), 7.92 (dd, J=8.3, 1.5 Hz, 1H), 7.78 (d, J=1.5 Hz, 1H), 7.69-7.55 (m, 3H), 7.36-7.28 (m, 2H), 7.27-7.21 (m, 1H), 7.09 (dd, J=8.5, 2.3 Hz, 1H).

[0348] Under nitrogen protection, compound 15-A2 (700 mg, 1.970 mmol) was dissolved in anhydrous THF (10 mL), TTMS (476 mg, 3.35 mmol, 98%) was added to the reaction solution, the reaction solution was kept at 0° C. for 1.5 h and the reaction was finished. 3N HCl (2 mL) was added to the reaction solution, and the reaction solution was natural warmed up to room temperature and stirred for 1 h. [0349] 5 mL H.sub.2O was added to the reaction solution, the reaction solution was extracted by DCM (10 mL×3), washed by water (5 mL×3), dried, concentrated, and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=15:1-10:1) to obtain compound 15-A3 (810 mg, percent yield 96.7%, yellow oily substance). [0350] .sup.1H-NMR (400 MHz, DMSO-d6): δ8.19 (d, J=8.5 Hz, 1H), 7.63-7.52 (m, 4H), 7.44 (s, 1H), 7.32 (t, J=8.9 Hz, 2H), 7.21 (d, J=5.8 Hz, 1H), 7.14 (dd, J=11.7, 2.4 Hz, 1H), 6.97 (dd, J=8.5, 2.1 Hz, 1H), 5.44-5.37 (m, 1H).

[0351] Under nitrogen protection, POCl.sub.3 (580 mg, 3.76 mmol, 97%) was dissolved in anhydrous DCM (10 mL), and the reaction solution was cooled to −40° C. Compound 15-A3 (800 mg, 1.88 mmol) in DCM (4 mL) was added, and TEA (476 mg, 4.70 mmol) was added to the reaction solution, the reaction solution was kept at −40° C. to −35° C. for 2 h. LC-MS was used to detect the extent of reaction. When compound 15-A3 was vanished and transferred to intermediate, and the temperature was −40° C., 2-bromoethylamine hydrobromide (3.08 g, 15.04 mmol) was added, TEA (1.52 g, 15.04 mmol) in DCM (2 mL) was added to the reaction solution, the temperature was kept at −40° C. for 1 h, and the intermediate was totally transferred. [0352] The reaction solution was natural warmed up to room temperature, saturated NH.sub.4Cl aqueous solution (5 mL) was added to the reaction solution. The reaction solution was extracted by DCM (10 mL×3), washed by water (3 mL×3), dried, concentrated, and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=1:1-100% EA) to obtain compound 15-A4 (600 mg, percent yield 44.4%, white solid). [0353] .sup.1H-NMR (400 M, CDCl.sub.3): δ 8.04 (d, J=8.4 Hz, 1H), 7.55-7.47 (m, 2H), 7.46-7.38 (m, 2H), 7.27 (s, 1H), 7.19-7.10 (m, 2H), 6.95-6.83 (m, 2H), 5.69 (dd, J=11.4, 6.1 Hz, 1H), 3.50-3.18 (m, 8H). [0354] MS: Calculated 716.9, found 717.8 ([M+H].sup.+).

[0355] Under nitrogen protection, compound 15-A4 (600 mg, 0.837 mmol) was dissolved in THF (15 mL), Ag.sub.2O (1.16 mg, 5.02 mmol) and DIPEA (649 mg, 5.02 mmol) were added to the reaction solution, the reaction solution was warmed up to 65° C. and stirred for 3 h. [0356] After the reaction was finished, the reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth, the solid was washed by DCM, the original solution was concentrated, 1.5 mL of anhydrous diethyl ether was added to the reaction solution, and the reaction solution was separated by column chromatography to obtain the pure product of compound 15 (56 mg, percent yield 48.6%, white solid). [0357] .sup.1H-NMR (400 MHz, MeOD): δ8.12 (t, J=8.1 Hz, 1H), 7.55 (m, 4H), 7.45 (s, 1H), 7.19 (t, J=8.8 Hz, 2H), 6.98 (dd, J=7.8, 5.3 Hz, 2H), 6.15-5.98 (m, 1H), 2.39-1.93 (m, 8H). [0358] MS: Calculated 555.1, found 556.1 ([M+H].sup.+).

[0359] Synthesis of Compound 16

##STR00054## [0360] Under nitrogen protection, compound 16-A1 (1.7 g, 11 mmol), compound 16-A2 (2 g, 10 mmol), Pd(OAc).sub.2 (21.5 mg, 0.1 mmol) and PPh.sub.3 (39 mg, 0.15 mmol) and K.sub.2CO.sub.3 (2.8 g, 20 mmol) were dissolved in dioxane (20 mL) and water (2 mL), the reaction solution was warmed up to 80° C. and stirred overnight. [0361] After the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth, concentrated, stirred, and separated by column chromatography (100-200 mesh silica gel, n-heptane:EA=5:1) to obtain compound 16-A3 (900 mg, percent yield 40%, white solid). [0362] .sup.1H-NMR (300 MHz, DMSO): δ 10.17 (s, 1H), 7.55-7.08 (m, 3H), 6.79-6.50 (m, 3H). MS: Calculated 224.0, found 222.6[(M−H).sup.−].

[0363] Under nitrogen protection, compound 16-A3 (550 mg, 2.2 mmol) and 3-fluoro-4-nitrobenzoaldehyde (370 mg, 2.2 mmol) were dissolved in MeCN (5 mL), K.sub.2CO.sub.3 (830 mg, 6 mmol) was added under nitrogen, the reaction solution was warmed up to 80° C. and stirred for 4 h. [0364] After the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth, concentrated, stirred, separated by column chromatography (100-200 mesh silica gel, n-heptane:EA=10:1) to obtain the crude product of compound 16-A4 (700 mg, purity 76.2%, white solid), and the crude product was used to the next step directly. [0365] .sup.1H-NMR (300 MHz, DMSO): δ 10.03 (s, 1H), 8.31 (d, J=8.2 Hz, 1H), 7.94 (d, J=8.4 Hz, 1H), 7.83 (s, 1H), 7.59-7.50 (m, 2H), 7.40 (t, J=8.8 Hz, 1H), 7.32-7.16 (m, 2H), 7.10 (d, J=8.6 Hz, 1H).

[0366] Under nitrogen protection, compound 16-A4 (680 mg, 1.82 mmol) and TTMS (510 mg, 3.6 mmol) were dissolved in THF (8 mL), TBAF (0.1 mL, 0.1 mmol, 1M, Energy Chemical) in THF was added to the reaction solution at 0° C., and the temperature was kept at for 6 h. 1N HCl (2 mL) was added to the reaction solution and the reaction solution was stirred for 10 min. [0367] The reaction solution was concentrated to separated THF, the crude product was extracted by water (10 mL) and DCM (20 mL), the organic phase was separated by concentration and stir, the crude product was separated by column chromatography (100-200 mesh silica gel, n-heptane:EA=10:1) to obtain compound 16-A5 (400 mg, percent yield 49.6%, purity 90%). [0368] .sup.1H-NMR (300 MHz, DMSO): δ 8.19 (d, J=7.8 Hz, 1H), 7.76 (t, J=8.5 Hz, 1H), 7.57-7.51 (m, 2H), 7.38 (s, 1H), 7.28-7.19 (m, 3H), 6.89 (dd, J=8.8, 1.7 Hz, 1H), 5.40-5.36 (m, 1H).

[0369] Under nitrogen protection, POCl.sub.3 (168 mg, 1.1 mmol, J&K Scientific) was dissolved in ultra-dry DCM (5 mL), and the reaction solution was cooled to −30° C. Compound 16-A5 (220 mg, 0.5 mmol) was dissolved in DCM (5 mL) and TEA (170 mg, 1.65 mmol) was added, the temperature was kept at −30° C. After 6 h, the raw materials were totally vanished, 2-bromoethylamine hydrobromide (897 mg, 4.4 mmol) was added to the reaction solution at −30° C., and then TEA (440 mg, 4.4 mmol) was added.

[0370] After the reaction was finished, the temperature was cooled down to 0° C., saturated NH.sub.4Cl aqueous solution (10 mL) was added to the reaction solution. The reaction solution was extracted by DCM (15 mL×2), washed by water (5 mL×4), dried, and concentrated to obtain the crude product of compound 16-A6 (250 mg, yellow solid).

[0371] The crude product was used to the next step directly. [0372] MS: Calculated 732.9, found 733.9 ([M+H]+).

[0373] Under nitrogen protection, compound 16-A6 (250 mg, 0.34 mmol) was dissolved in THF (10 mL), Ag.sub.2O (210 mg, 1.7 mmol) and DIPEA (220 mg, 1.7 mmol) were added to the reaction solution, and the temperature was warmed up to 65° C. [0374] After 2h, the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth, the solid was washed by DCM (20 mL), the original solution was concentrated and separated by column chromatography to obtain the pure product of compound 16 (22 mg, percent yield 11%, white solid). [0375] .sup.1H-NMR (400 MHz, DMSO): δ 8.26 (d, J=8.5 Hz, 1H), 7.67 (d, J=8.5 Hz, 1H), 7.59-7.48 (m, 3H), 7.41 (dt, J=10.3, 2.5 Hz, 1H), 7.24-7.19 (m, 2H), 7.03 (dd, J=8.5, 2.3 Hz, 1H), 6.36-6.32 (m, 1H), 2.20-1.91 (m, 8H). [0376] MS: Calculated 573.1, found 574.1 ([M+H]+).

[0377] Synthesis of Compound 17

##STR00055## [0378] Under nitrogen protection, 2-bromo-5-hydroxypyridine (3.0 g, 17.2 mmol) and 4-fluorophenylboronic acid (compound 17-A0, 2.7 g, 19.0 mmol) were dissolved in the mixed solution of dioxane and water (60 mL, dioxane:water=9:1), the gas was exchanged 3 times, Pd(OAc).sub.2 (193 mg, 0.86 mmol) and PPh.sub.3 (225 mg, 0.86 mmol) were added to the reaction solution, the gas was exchanged 3 times again, the reaction solution was warmed up to 100° C. and stirred overnight. [0379] After the reaction was finished, the reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth and washed by EA. The original solution was concentrated, 15 mL of water was added to the reaction solution, the reaction solution was extracted by EA (50 mL×3), washed by water (10 mL×3), washed by brine, dried, concentrated, and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=15:1) to obtain compound 17-A1 (1.2 g, percent yield 36.9%, white solid). [0380] .sup.1H-NMR (400 M, DMSO-d6): δ 10.03 (s, 1H), 8.20 (d, J=2.7 Hz, 1H), 8.00 (dd, J=8.8, 5.6 Hz, 2H), 7.78 (d, J=8.6 Hz, 1H), 7.32-7.18 (m, 3H). [0381] MS: Calculated 189.1, found 190.2 ([M+H].sup.+).

[0382] Under nitrogen protection, compound 17-A1 (600 mg, 3.55 mmol) and compound 18-A0 (806 mg, 4.26 mmol) were dissolved in acetonitrile (15 mL), K.sub.2CO.sub.3 (980 mg, 7.1 mmol), the reaction solution was warmed up to 85° C. and stirred for 2 h. [0383] After the reaction was finished, the reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth, the original solution was concentrated and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=10:1) to obtain compound 17-A2 (760 mg, percent yield 63.3%, light yellow solid). [0384] .sup.1H-NMR (400 MHz, DMSO-d6): δ ppm 10.03 (s, 1H), 8.59 (d, J=2.8 Hz, 1H), 8.31 (d, J=8.3 Hz, 1H), 8.19-8.11 (m, 2H), 8.07 (d, J=8.7 Hz, 1H), 7.90 (dd, J=8.3, 1.6 Hz, 1H), 7.78-7.70 (m, 2H), 7.37-7.26 (m, 2H). [0385] MS: Calculated 338.1, found 339.0 ([M+H].sup.+).

[0386] Under nitrogen protection, compound 17-A2 (700 mg, 2.07 mmol) was dissolved in THF (10 mL), TTMS (500 mg, 3.52 mmol) was added to the reaction solution, the reaction solution was cooled down to 0° C., TBAF (0.03 mL, 1M in THF) was added, the temperature was kept at 0° C., and the reaction was finished. [0387] 3N HCl (2 mL) was added to the reaction solution, the reaction solution was natural warmed up to room temperature and stirred for 1 h. 5 mL water was added to the reaction solution, the reaction solution was extracted by DCM (10 mL×3), washed by water, dried, concentrated, and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=15:1-10:1) to obtain compound 17-A3 (550 mg, percent yield 65.1%, yellow oily substance). [0388] .sup.1H-NMR (400 MHz, DMSO-d6): δ8.52 (d, J=2.9 Hz, 1H), 8.19 (d, J=8.5 Hz, 1H), 8.16-8.10 (m, 2H), 8.06 (d, J=8.8 Hz, 1H), 7.64 (dd, J=8.8, 2.9 Hz, 1H), 7.55 (dd, J=8.7, 3.3 Hz, 1H), 7.38 (s, 1H), 7.36-7.28 (m, 2H), 7.18 (dd, J=5.8, 3.4 Hz, 1H), 5.43-5.34 (m, 1H). [0389] MS: Calculated 408.1, found 409.2 ([M+H]+).

[0390] Under nitrogen protection, POCl.sub.3 (414 mg, 2.70 mmol) was dissolved in DCM (10 mL), and the temperature was cooled to −40° C. Compound 17-A3 (550 mg, 1.35 mmol) was dissolved in DCM (4 mL) and added to the reaction solution with TEA (342 mg, 3.36 mmol), the temperature was kept at −40° C. to −35° C. for 2 h. LC-MS was used to detect the extent of reaction. When compound 17-A3 was vanished, transferred to intermediate, and the temperature was −40° C., 2-bromoethylamine hydrobromide (2.2 g, 10.8 mmol) was added to the reaction solution, TEA (101 g, 10.8 mmol) in DCM (2 mL) was added, the temperature was kept at −40° C. for 1 h, and the intermediate was totally transferred. [0391] The reaction solution was natural warmed up to 0° C., saturated NH.sub.4Cl aqueous solution (5 mL) was added. The reaction solution was extracted by DCM (10 mL×3), washed by water (3 mL×3), dried, concentrated and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=1:1-100% EA) to obtain compound 17-A4 (520 mg, percent yield 55.0%, white solid). [0392] .sup.1H-NMR (400 M, CDCl.sub.3): δ 8.49 (d, J=2.7 Hz, 1H), 8.06 (dd, J=8.4, 2.7 Hz, 1H), 8.01-7.94 (m, 2H), 7.77 (d, J=8.7 Hz, 1H), 7.54-7.48 (m, 1H), 7.43 (d, J=8.3 Hz, 1H), 7.26-7.24 (m, 1H), 7.18 (t, J=8.7 Hz, 2H), 5.69 (dq, J=12.3, 6.2 Hz, 1H), 3.49-3.16 (m, 8H). [0393] MS: Calculated 700.0, found 700.9 ([M+H]+).

[0394] Under nitrogen protection, compound 17-A4 (520 mg, 0.743 mmol) was dissolved in THF (15 mL), Ag.sub.2O (1.03 g, 4.46 mmol) and DIPEA (580 mg, 4.46 mmol) were added to the reaction solution, the reaction solution was warmed up to 65° C. and stirred for 3 h. [0395] After the reaction was finished, the reaction solution was cooled to room temperature, separated by the suction filtration with the diatomaceous earth, the solid was washed by DCM, the original solution was concentrated and separated by column chromatography to obtain the pure product of compound 18 (106.7 mg, percent yield 26.7%, white solid). [0396] .sup.1H-NMR (400 MHz, MeOD): δ8.43 (d, J=2.9 Hz, 1H), 8.16 (d, J=8.5 Hz, 1H), 8.07-7.97 (m, 2H), 7.92 (d, J=8.8 Hz, 1H), 7.65-7.54 (m, 2H), 7.46 (s 1H), 7.24-7.19 (m, 2H), 6.13-6.03 (m, 1H), 2.26-2.08 (m, 8H). [0397] MS: Calculated 538.1, found 539.1 ([M+H].sup.+).

[0398] Synthesis of Compound 18

##STR00056## [0399] Under nitrogen protection, compound 18-A1 (500 mg, 2.65 mmol) and compound 18-A2 (460 mg, 2.65 mmol), Pd(PPh.sub.3).sub.4 (300 mg, 5.2 mmol) were dissolve in toluene (10 mL) and water (1 mL). The reaction solution was warmed up to 80° C. and stirred overnight. [0400] After the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth, concentrated, stirred, and separated by column chromatography (100-200 mesh silica gel, n-heptane:EA=10:1) to obtain compound 18-A3 (600 mg, percent yield 94.7%, white solid). [0401] .sup.1H-NMR (300 MHz, DMSO): δ 10.24 (s, 1H), 8.26 (d, J=2.4 Hz, 1H), 8.19 (d, J=8.1 Hz, 2H), 7.91 (d, J=8.7 Hz, 1H), 7.78 (d, J=8.1 Hz, 2H), 7.29 (dd, J=8.6, 2.7 Hz, 1H). [0402] MS: Calculated 239.0, found 240.0 ([M+H]+).

[0403] Under nitrogen protection, compound 18-A3 (870 mg, 2.9 mmol) and 3-fluoro-4-nitrobenzoaldehyde (490 mg, 2.9 mmol) were dissolved in MeCN (8 mL), K.sub.2CO.sub.3 (830 mg, 6 mmol) was added to the reaction solution, the reaction solution was warmed up to 80° C. and stirred for 4 h. [0404] After the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth, concentrated, stirred, and separated by column chromatography (100-200 mesh silica gel, n-heptane:EA=10:1) to obtain compound 18-A4 (640 mg, white solid). [0405] .sup.1H-NMR (300 MHz, CDCl.sub.3): δ 10.03 (s, 1H), 8.57 (d, J=2.7 Hz, 1H), 8.15-8.12 (m, 3H), 7.87-7.75 (m, 4H), 7.60-7.51 (m, 2H). [0406] MS: Calculated 388.0, found 389.1 ([M+H]+).

[0407] Under nitrogen protection, compound 18-A4 (640 mg, 1.64 mmol) and TTMS (430 mg, 3 mmol) were dissolved in THF (5 mL), TBAF in THF (0.1 mL, 0.1 mmol, 1M) was added at 0° C., the reaction solution was kept at for 6 h, 1N HCl (2 mL) was added and stirred for 10 min. THF in the reaction solution was separated by concentrated. The crude product was extracted by water (10 mL) and DCM (20 mL), the organic phase was separated by concentrated and stirred, and the crude product was separated by column chromatography (100-200 mesh silica gel, n-heptane:EA=10:1) to obtain the product (640 mg, percent yield 85.2%, light yellow solid). [0408] .sup.1H-NMR (300 MHz, DMSO): δ 8.59 (d, J=2.7 Hz, 1H), 8.30 (d, J=7.5 Hz, 2H), 8.19 (t, J=9.2 Hz, 2H), 7.86 (d, J=8.5 Hz, 2H), 7.72-7.65 (m, 1H), 7.59-7.56 (m, 1H), 7.43 (s, 1H), 7.20 (d, J=5.8 Hz, 1H), 5.39-5.37 (m, 1H). [0409] MS: Calculated 458.0, found: 459.0 ([M+H]+).

[0410] Under nitrogen protection, POCl.sub.3 (200 mg, 1.3 mmol, 97%) was dissolved in ultra-dry DCM (10 mL), and the temperature was cooled to −30° C. Compound 18-A5 (300 mg, 0.65 mmol) in DCM (5 mL) was added, TEA (270 mg, 2.6 mmol) was added, the temperature was kept at −30° C. to −35° C., the raw materials were totally vanished after 6 h. 2-Bromoethylamine hydrobromide (1.1 g, 5.2 mmol) was added to the reaction solution at −30° C., and TEA (530 mg, 5.2 mmol) was added.

[0411] After the reaction was finished, the reaction solution was cooled down to 0° C., saturated NH.sub.4Cl aqueous solution (10 mL) was added. The reaction solution was extracted by DCM (15 mL×2), washed by water (5 mL×4), dried, and concentrated to obtain 200 mg of the crude product, the crude product was yellow solid and used to the next reaction directly. [0412] 1H NMR (400 MHz, CDCl.sub.3): δ 8.46 (d, J=2.6 Hz, 1H), 8.07-7.99 (m, 3H), 7.78-7.75 (m, 1H), 7.68 (d, J=8.2 Hz, 2H), 7.48-7.33 (m, 3H), 5.65-5.61 (m, 1H), 3.51-3.04 (m, 10H). [0413] MS: Calculated 747.9, found 748.9 ([M+H]+).

[0414] Under nitrogen protection, compound 18-A6 (150 mg, 0.23 mmol) was dissolved in THF (10 mL), Ag.sub.2O (170 mg, 1.38 mmol, Energy Chemical) and DIPEA (163 mg, 1.38 mmol) were added to the reaction solution, the temperature was warmed up to 65° C. to reaction.

[0415] After 2 h, the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth, the solid was washed by DCM (20 mL), and the original solution was concentrated and separated by column chromatography to obtain the pure product of compound 18 (41 mg, percent yield 36%, white solid). [0416] .sup.1H-NMR (400 MHz, DMSO): δ 8.61 (d, J=2.8 Hz, 1H), 8.31 (d, J=8.2 Hz, 2H), 8.27 (d, J=8.5 Hz, 1H), 8.21 (d, J=8.8 Hz, 1H), 7.87 (d, J=8.4 Hz, 2H), 7.72 (dd, J=8.8, 2.9 Hz, 1H), 7.65 (d, J=8.5 Hz, 1H), 7.56 (s, 1H), 6.32-6.28 (m, 1H), 2.17-1.90 (m, 8H). [0417] MS: Calculated 588.1, found 589.1 ([M+H].sup.+).

[0418] Synthesis of Compound 19

##STR00057##

[0419] Under nitrogen protection, 2-bromo-5-hydroxypyridine (1.5 g, 8.52 mmol, purchased) and 4-fluorophenylboronic acid (1.4 g, 10.23 mmol) were added to the mixed solution of DME (33 mL) and H.sub.2O (7 mL), the nitrogen was exchanged 3 times, Pd(PPh.sub.3).sub.4 (300 mg, 0.26 mmol) and Na.sub.2CO.sub.3 (1.8 g, 17.05 mmol) were added, the nitrogen was exchanged 3 times again, and the reaction solution was warmed up to 80° C. to reaction. The reaction was under supervision for 2.5 h.

[0420] After the reaction was finished, the reaction solution was cooled down to room temperature, extracted by EtOAc (50 mL×3), the organic phase was washed by water, washed by brine, and separated by column chromatography (200-300 mesh silica gel:n-heptane:EA=12:1-9:1) to obtain the product (1.4 g, percent yield 86.8%, white solid). [0421] .sup.1H-NMR (300 MHz, MeOD): δ8.43 (d, J=2.7 Hz, 1H), 7.81-7.77 (m, 3H), 7.64-7.58 (m, 1H), 6.87 (d, J=8.7 Hz, 2H). [0422] MS: Calculated 189.1, found 190.1 ([M+H]+).

[0423] Under nitrogen protection, compound 19-A3 (i.e. no. 46 compound, 100 mg, 0.27 mmol) was dissolved in acetone (5 mL), compound 19-A2 (10 mg, 0.54 mmol) and Cs.sub.2CO.sub.3 (309 mg, 0.95 mmol) was stirred at room temperature and stirred for 2 h. [0424] After the reaction was finished, the reaction solution was separated by the suction filtration with the diatomaceous earth, the solid was washed by acetone, the original solution was concentrated and separated by column chromatography to obtain the pure product of compound 20 (17 mg, percent yield 11.7%, brown solid). [0425] .sup.1H-NMR (400 MHz, MeOD): δ 8.52 (d, J=2.9 Hz, 1H), 8.10 (d, J=8.5 Hz, 1H), 8.06 (d, J=8.8 Hz, 2H), 7.92 (dd, J=8.8, 4.3 Hz, 1H), 7.68 (dt, J=8.6, 2.9 Hz, 1H), 7.54 (d, J=8.6 Hz, 1H), 7.37 (s, 1H), 7.19 (d, J=8.8 Hz, 2H), 6.06-5.99 (m, 1H), 2.27-1.97 (m, 8H). [0426] MS: Calculated 538.1, found 539.1 ([M+H]+).

[0427] Synthesis of Compound 46

##STR00058## [0428] Under nitrogen protection, compound 46-A2 (2.0 g, 11.8 mmol, purchased) and TMSCF.sub.3 (2.5 g, 17.7 mmol) were dissolved in THF (20 mL), the reaction solution was cooled down to 0° C., TBAF (2.6 ml, 0.26 mmol, 1M in THF) was added. After the temperature was kept at 0° C. for 30 min, compound 46-A2 was totally vanished, 3N HCl (2 mL) was added, the reaction solution was became clear and keeping stirring at 0° C. for 30 min, the mixture was totally transferred to the product. [0429] The product was extracted by DCM (10 ml×3), the organic phase was washed by water (10 ml×3), dried, concentrated, and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=12:1-10:1) to obtain compound 46-A3 (1.5 g, percent yield 53.2%, yellow oily substance). [0430] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.13-8.09 (m, 1H), 7.60 (d, J=11.6 Hz, 1H), 7.43 (d, J=8.4 Hz, 1H), 5.12-5.18 (m, 1H), 3.06 (d, J=4.4 Hz, 1H).

[0431] Under nitrogen protection, POCl.sub.3 (963 mg, 4.61 mmol) was dissolved in DCM (10 mL), and the temperature was cooled to −40° C. Compound 46-A3 (1.5 g, 6.27 mmol) was dissolved in DCM (20 mL) and added to the reaction solution with TEA (10.1 g, 0.1 mmol), the temperature was kept at −40° C. to −35° C. After 2 h. Compound 46-A3 was transferred to intermediate, 2-bromoethylamine hydrobromide (11.99 g, 50.16 mmol) and TEA (10.1 g, 0.1 mol) were added to the reaction solution, and the reaction solution was under supervision. After 30 min, the reaction was finished. [0432] Saturated NH.sub.4Cl aqueous solution (20 mL) was added to the reaction solution at 0° C., the reaction solution was extracted by DCM (50 mL×3), the organic phase was washed by water, washed by brine, dried, concentrated and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=5:1-1:1) to obtain compound 46-A4 (1.6 g, percent yield 65.3%, yellow oily substance). [0433] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.15-8.11 (m, 1H), 7.47 (d, J=11.6 Hz, 1H), 7.44 (d, J=8.8 Hz, 1H), 5.78-5.30 (m, 1H), 3.53-3.05 (m, 10H). [0434] MS: Calculated 529.9, found 531.9 ([M+H].sup.+).

[0435] Under nitrogen protection, compound 46-A4 (1.6 g, 3.0 mmol) was dissolved in THF (20 mL), Ag.sub.2O (4.2 g, 18.0 mmol) and DIPEA (2.3 g, 18.0 mmol) were added to the reaction solution, the reaction solution was warmed up to 65° C. and stirred for 1.5 h. [0436] After the reaction was finished, the reaction solution was cooled to room temperature and separated by the suction filtration with the diatomaceous earth, the solid was washed by DCM, the original solution was concentrated and separated by column chromatography (200-300 mesh silica gel, n-heptane:EA=5:1-1:1) to obtain the crude product, and the crude product was separated by column chromatography to obtain the pure product of compound 46 (30 mg, white solid). [0437] .sup.1H NMR (400 MHz, MeOD): δ8.24-8.20 (m, 1H), 7.70 (d, J=11.6 Hz, 1H), 7.63 (d, J=8.8 Hz, 1H), 6.14-6.10 (m, 1H), 2.28-2.14 (m, 8H). [0438] MS: Calculated 369.1, found 370.1 ([M+H].sup.+).