NOVEL PURINE DERIVATIVE, INTERMEDIATE AND APPLICATION THEREOF IN PREPARING ANTICANCER MEDICINE

Abstract

The present invention disclosures a novel purine derivatives represented by formula (I) or a pharmaceutically acceptable salt thereof, intermediate and application thereof inpreparation of a medicament for treating or preventing a cancer. This compound is a novel PI3K inhibitor with an excellent inhibitory activity; and may be useful for treating a variety of malignant tumors.

Claims

1. A purine derivative represented by Formula (I), or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a crystal thereof, ##STR00035## in the formula, A is selected from the group consisting of —OH, —NH.sub.2, —SH, ##STR00036## B is —C.sub.nH.sub.2n—, n is 1, 2, 3 or 4; Z is selected from the group consisting of hydrogen, hydroxyl, C.sub.1-3 alkyl, fluorine, chlorine and bromine, or is C.sub.1-3 alkyl substituted by one or more selected from fluorine, chlorine and bromine.

2. A purine derivative represented by Formula (I), or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a crystal thereof, according to claim 1, wherein, Z is selected from the group consisting of hydrogen, hydroxyl, fluorine, chlorine, bromine, methyl, ethyl, isopropyl, trifluoromethyl, and pentafluoroethyl.

3. A purine derivative represented by Formula (I), or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a crystal thereof, according to claim 1, wherein, the structure of the purine derivative is represented by the following Formula (I-a): ##STR00037## wherein, A and B are defined the same as in claim 1, and Z.sub.1 is selected from the group consisting of hydrogen, hydroxyl, fluorine, chlorine, bromine, methyl, ethyl, isopropyl, trifluoromethyl, and pentafluoroethyl.

4. A purine derivative represented by Formula (I), or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a crystal thereof, according to claim 1, wherein, B is selected from the group consisting of —CH.sub.2—, —CH.sub.2CH.sub.2—, —CH.sub.2CH.sub.2CH.sub.2—, —CH(CH.sub.3)—, —CH(CH.sub.3)CH.sub.2—, —C(CH.sub.3).sub.2— and —CH.sub.2C(CH.sub.3).sub.2—.

5. A purine derivative represented by Formula (I), or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a crystal thereof, according to claim 1, wherein, the purine derivative is selected from compounds represented by the following formulas: ##STR00038##

6. A method for preparing a medicine for treating and/or preventing phosphatidylinositol-3-kinase (PI3K)-mediated diseases comprising providing a purine derivative represented by Formula (I), or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a crystal thereof according to claim 1 in preparing a medicine for treating and/or preventing phosphatidylinositol-3-kinase (PI3K)-mediated diseases.

7. The use according to claim 6, wherein, the phosphatidylinositol-3-kinase-mediated diseases include cancers, the cancers include renal carcinoma, liver cancer, colon cancer, gastrointestinal stromal tumor, non-small cell lung cancer, breast cancer, pancreatic cancer, glioma, lymphoma, fibrosarcoma, ovarian cancer, leukemia and prostate cancer.

8. A pharmaceutical composition, wherein, it contains a purine derivative represented by Formula (I), or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a crystal thereof according to claim 1, and a pharmaceutical acceptable carrier.

9. A pharmaceutical composition according to claim 8, wherein, the pharmaceutical composition is a pharmaceutical composition for treating cancers.

10. An intermediate for preparing a purine derivative represented by Formula (I), or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a crystal thereof according to claim 1, wherein, the intermediate has a structure represented by Formula (II): ##STR00039## in Formula (II), A.sub.1 is tert-butyldimethylsiloxy or A.sub.1 is the same as A in Formula (I); B and Z are respectively the same as B and Z in Formula (I), and Y is an amino protection group.

11. An intermediate according to claim 10, wherein, the amino protection group is tetrahydro-2H-pyran-2-yl.

12. An intermediate according to claim 10, wherein, the intermediate is selected from compounds represented by the following formulas: ##STR00040## THP is tetrahydro-2H-pyran-2-yl.

13. An intermediate according to claim 11, wherein, the intermediate is prepared by reacting ##STR00041## with a compound represented by Formula (III) ##STR00042## and in Formula (III), A.sub.1, B and Z are defined the same as in Formula (II).

14. An intermediate according to claim 13, wherein, in the process of preparing the intermediate represented by Formula (II), the reaction is carried out under an alkaline condition at a temperature of 30-120° C., and optionally under an inert atmosphere.

15. An intermediate according to claim 14, wherein, in the process of preparing the intermediate represented by Formula (II), the reaction is carried out at a temperature of 40-110° C., preferably at a temperature of 50-105° C., more preferably at a temperature of 60-100° C., and even more preferably at a temperature of 70-95° C.

16. An intermediate according to claim 15, wherein, in the process of preparing the intermediate represented by Formula (II), the reaction is carried out at a temperature of 80-90° C.

17. An intermediate according to claim 14, wherein, the alkaline condition is formed by adding an alkaline substance, and the alkaline substance is selected from the group consisting of potassium acetate, potassium carbonate, potassium phenoxide, potassium phosphate, potassium tert-butoxide, sodium carbonate, sodium bicarbonate, sodium tert-butoxide, sodium methoxide, sodium ethoxide, triethylamine, tri-n-butylamine, diisopropylethylamine, and combinations thereof.

18. An intermediate according to claim 13, wherein, in the process of preparing the intermediate represented by Formula (II), the reaction is carried out in the presence of 2-dicyclohexylphosphino-2,4,6-triisopropylbiphenyl and/or tris(dibenzylideneacetone)dipalladium.

19. An intermediate according to claim 18, wherein, in the process of preparing the intermediate represented by Formula (II), the reaction is carried out in the co-presence of 2-dicyclohexylphosphino-2,4,6-triisopropylbiphenyl and tris(dibenzylideneacetone)dipalladium.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0040] FIG. 1 shows the relationship curves of the inhibition rates of Compound I-1 to Compound I-3 and the positive control compound GDC-0941 on PI3Kα.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

Definition of Terms

[0041] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs.

[0042] The term “isomer” refers to an isomer produced by the different arrangement of atoms in a molecule in space, and includes cis-trans isomers, enantiomers and conformational isomers. All stereoisomers are within the scope of the present disclosure. The compounds of the present disclosure may be a single stereoisomer or a mixture of other isomers such as a racemate, or a mixture of all other stereoisomers.

[0043] The term “salt” refers to a pharmaceutically acceptable salt formed by a compound of the present disclosure with an acid, the acid may be an organic or inorganic acid, specifically selected from the group consisting of phosphoric acid, sulfuric acid, hydrochloric acid, hydrobromic acid, citric acid, maleic acid, malonic acid, mandelic acid, succinic acid, fumaric acid, acetic acid, lactic acid, nitric acid, sulfonic acid, p-toluenesulfonic acid, malic acid, methanesulfonic acid or analogues thereof.

[0044] The term “solvate” refers to a form of a compound of the present disclosure that forms a solid or liquid complex by coordination with a solvent molecule. Hydrates are a special form of solvates in which coordination occurs with water. Within the scope of the present disclosure, the solvate is preferably a hydrate.

[0045] The term “crystal” refers to the various solid forms formed by the compounds described herein, including crystalline forms and amorphous forms.

[0046] The following embodiments may enable those skilled in the art to fully understand the present disclosure, but do not limit the present disclosure in any way. The structures of all compounds were confirmed by .sup.1H NMR or MS.

[0047] The compounds used in the embodiments are abbreviated as follows: [0048] DBU: 1,8-diazabicyclo[5.4.0]undec-7-ene; [0049] DMF: N,N-dimethylformamide; [0050] THF: tetrahydrofuran; [0051] Pd(dppf)Cl.sub.2: [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium; [0052] DTT: dithiothreitol; [0053] ATP: adenosine triphosphate; [0054] TK: tyrosine kinase; [0055] HEPES: 2-[4-(2-hydroxyethyl)-1-piperazinyl]ethanesulfonic acid.

Embodiment 1: Preparation of Compound 14

[0056] Compound I-1 was synthesized through the following route:

##STR00010##

1.1. Synthesis of Compound 2

[0057] Compound 2:

2-(4-isocyanatophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;

##STR00011##

[0058] Compound 1, namely 4-aminophenylboronic acid pinacol ester (10 g, 45.6 mmol), and triethylamine (13.8 g, 136.8 mmol) were added into 300 mL of dichloromethane, cooled to zero ° C., triphosgene (8.1 g, 27.4 mmol) was slowly added at zero ° C. in batches and then stirred at zero ° C. for 50 minutes to give a solution of Compound 2, which was used directly in the next step.

1.2. Synthesis of Compound 3

[0059] Compound 3:

1-(4-(hydroxymethyl)phenyl)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea;

##STR00012##

[0060] P-aminobenzyl alcohol (8.4 g, 68 mmol) was added to the above-mentioned solution of Compound 2 at zero degree Celsius, then the system was stirred at zero degree Celsius for 15 minutes, warmed to room temperature, and stirred at room temperature for another 3 hours. LC-MS detection showed the reaction completion, the reaction solution was concentrated and spin-dried, and extracted with dichloromethane, and the organic phase was washed with sodium bicarbonate solution and saturated sodium chloride solution, dried over anhydrous sodium sulfate, and filtered, and the filtrate was spin-dried, and purified by column chromatography (dichloromethane/methanol=40:1) to give yellow solid, namely Compound 3 (11 g, yield=60%). Measured: ESI-MS m/z=369 [M+1].sup.+. .sup.1H NMR (DMSO-d6, 400 MHz): δ 9.02 (s, 1H), 8.89 (s, 1H), 7.60-7.58 (d/J=8 Hz, 2H), 7.49-7.47 (d,J=8.4 Hz, 2H), 7.42-7.40 (d,J=8 Hz, 2H), 7.24-7.21 (d,J=8.4 Hz, 2H), 5.06 (m, 1H), 4.44-4.42 (d,J=5.6 Hz, 2H), 1.28 (s, 12H).

1.3. Synthesis of Compound 5

[0061] Compound 5: 4-(2-chloro-7H-purin-6-yl)morpholine

##STR00013##

[0062] 2,6-dichloropurine (18.9 g, 0.1 mol, Compound 4) was dissolved in methanol (400 mL) and cooled to zero degree Celsius, morpholine (13 mL, 0.15 mol) was slowly added dropwise in the range of 0 to 5 degrees Celsius, then stirred at zero degree Celsius for 15 minutes, warmed to room temperature, and stirred at room temperature for another 3 hours. LC-MS detection showed the reaction completion, a large amount of yellow solid was precipitated and filtered, and the filter cake was washed with 20 mL of methanol, 50 mL of water and 50 mL of ethyl ether to give off-white solid, namely Compound 5 (21.1 g, yield=88%). Measured: ESI-MS m/z=240 [M+1].sup.+. .sup.1H NMR (DMSO-d6, 400 MHz): δ 11.23 (s, 1H), 8.16 (s, 1H), 4.19 (m, 4H), 3.74-3.71 (m, 4H).

1.4. Synthesis of Compound 6

[0063] Compound 6:

4-(2-chloro-7-(tetrahydro-2H-pyran-2-yl)-7H-purin-6-yl)morpholine

##STR00014##

[0064] Compound 5 (16.0 g, 0.067 mol) was suspended in ethyl acetate (480 mL), and 3,4-dihydro-2H-pyran (8.4 g, 0.1 mol, DHP) and monohydrate 4-methylbenzenesulfonic acid (1.0 g, 5.2 mmol, TsOH) were added at room temperature. The reaction mixture was stirred at 75 degrees Celsius overnight to give a black solution. The reaction mixture was cooled to room temperature, washed with saturated sodium bicarbonate aqueous solution, then the organic phase was dried over anhydrous sodium sulfate, and filtered. The filtrate was vacuum concentrated to dry methyl tertiary-butyl ether(20 mL) and petroleum ether(50 mL) were added to the residual, and the system was stirred for 0.5 h and filtered, and the filter cake was vacuum dried to give Compound 6 (20.0 g, yield=92.6%). Measured: ESI-MS m/z=324 [M+1].sup.+. .sup.1H NMR (CDCl.sub.3, 400 MHz): δ 7.91 (s, 1H), 5.72-5.69 (m, 1H), 4.29-3.73 (m, 10H), 2.10-2.02 (m, 2H), 1.91-1.65 (m, 4H).

1.5. Synthesis of Compound 7

[0065] Compound 7:

1-(4-(hydroxymethyl)phenyl)-3-(4-(6-morpholino-7-tetrahydro-2H-pyran-2-yl)-7H-purin-2-yl)phenyl)urea

##STR00015##

[0066] Compound 6 (2.0 g, 6.2 mmol) was dissolved in 1,4-dioxane (25 mL) and water (3 mL), and then Compound 3 (2.3 g, 6.2 mmol), sodium bicarbonate (1.7 g, 20.4 mmol), XPhos (400 mg, 2-dicyclohexylphosphino-2,4,6-triisopropylbiphenyl) and Pd.sub.2(dba).sub.3 (180 mg, tris(dibenzylideneacetone)dipalladium) were added, then the system was replaced with nitrogen for 3 times. The system was stirred at 85 degrees Celsius for 2 days under nitrogen atmosphere. The reaction solution was vacuum concentrated, then water (20 mL) was added, and the reaction solution was extracted with ethyl aceteate (50 mL*2), the organic phases were dried over anhydrous sodium sulfate and filtered, and the filtrate was vacuum concentrated to dry. Methyl tertiary-butyl ether (30 mL) was added, and the system was stirred at morn temperature for 0.5 h and filtered, and the filter cake was vacuum dried to give offwhite solid Compound 7 (1.3 g, yield>39.6%). Measured: ESI-MS m/z=530[M+1].sup.+.

1.6. Synthesis of Compound I-1

[0067] Compound I-1:

1-(4-(hydroxymethyl)phenyl)-3-(4-(6-morpholino-7H-purin-2-yl)phenyl)urea

##STR00016##

[0068] Compound 7 (1.4 g, 10.6 mmol) was suspended in 1,4-dioxane (5 mL), a solution of hydrogen chloride in dioxane (4N, 15 mL) was added, the system was stirred at room temperature overnight. The reaction was complete as determined by LCMS. The system was filtered, and the filter cake was washed with dioxane, and vacuum dried to give yellow solid Compound I-1 (1.0 g, yield>21%). Measured: .sup.1H NMR (DMSO-d6, 400 MHz): δ 8.36 (s, 1H), 8.24-8.22 (m, 2H), 7.64-7.62 (d,J=8.8 Hz, 2H), 7.50-7.37 (m, 3H), 7.27-7.25 (d,J=8.4 Hz, 1H), 4.72 (s, 1H), 4.45 (s, 1H), 4.28 (m, 4H) 3.82 (m, 4H). LCMS [mobile phase: from 95% water (0.1% TFA) and 5% CH.sub.3CN to 5% water (0.1% TFA) and 95% CH.sub.3CN in 6.5 min, finally under these conditions for 0.5 min.] purity is >90%, Rt=3.699 min; MS Calcd.: 445; MS Found: 446 [M+H].sup.+.

Embodiment 2: Preparation of Compound I-2

[0069] Compound I-2 was synthesized through the following route:

##STR00017##

2.1. Synthesis of Compound 9

[0070] Compound 9: (4-nitro-2-(trifluoromethyl)phenyl)methanol;

##STR00018##

[0071] Compound 8 (25.0 g, 106.4 mmol) was dissolved in tetrahydrofuran (100 mL), sodium borohydride (11.5 g, 319.1 mmol) was slowly added in an ice bath, and boron trifluoride diethyl etherate (20 mL) was slowly added dropwise, and stirred at room temperature overnight. After TLC detection showed the reaction completion, 100 mL of brine was added, and the system was extracted with ethyl acetate (300 mL×3), and the organic phases were dried over sodium sulfate and concentrated to give Compound 9 (14.5 g, yield=61%). Measured: ESI-MS m/z=222 [M+1].sup.+.

2.2. Synthesis of Compound 10

[0072] Compound 10:

tert-butyldimethyl((4-nitro-2-(trifluoromethyl)benzyl)oxy)silane;

##STR00019##

[0073] Compound 9 (14.0 g, 63.6.4 mmol), tert-butyldimethylsilyl chloride (19.2 g, 127.27 mmol), triethylamine (16.1 g, 159.1 mmol) and p-dimethylaminopyridine (0.78 g, 6.36 mmol) were added to dichloromethane (120 mL) in ice bath, and then the reaction solution was stirred at room temperature for 2 h. After TLC detection showed the reaction completion, 100 mL of brine: was added, and the system was extracted with dichloromethane (200 mL×3), and the organic phases were concentrated by drying with sodium sulfate and purified by column chromatography (petroleum ether/ethyl acetate=100:1-50:1) to give Compound 10 (15.0 g, yield=70%), which was directly used in the next step.

2.3. Synthesis of Compound 11

[0074] Compound 11:

4-(((tert-butyl dimethylsilyl)oxy)methyl)-3-(trifluoromethyl)aniline;

##STR00020##

[0075] Compound 10 (15.0 g, 44.78 mmol) was dissolved in ethanol/water (200 mL/80 mL), ammonium chloride (15.0 g, 268.68 mmol) was added, and the system was warmed to a temperature of 80° C., then iron powder (11.0 g, 201.49 mmol) la was added, the reaction was carried out at this temperature for 1 h. After LCMS detection showed the reaction completion, brine (100 mL) was added, and the system was extracted with ethyl acetate (200 mL×3), and the organic phases were dried over sodium sulfate and concentrated to give Compound 11 (11.0 g, yield=80%). Measured: ESI-MS m/z=306 [M+1].sup.+. .sup.1H NMR (CDCl.sub.3, 400 MHz): δ 7.49 (d, J=8.0 Hz, 1H), 6.90 (s, 1H), 6.83 (d,J=8.0 Hz, 1H), 4.78 (s, 2H), 0.94 (s, 9H), 0.09 (s, 6H).

2.4. Synthesis of Compound 12

[0076] Compound 12:

1-(4-(((tert-butyldimethylsilyl)oxy)methyl)-3-(trifluoromethyl)phenyl)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea;

##STR00021##

[0077] Compound 11 (6.0 g, 19.68 mol) was dissolved in tetrahydrofuran (90 mL), and then Compound 8 (12.0 g, 49.19 mmol) was added. The system reacted at room temperature overnight. After LCMS detection showed the reaction completion, the reaction solution was vacuum concentrated, and purified by column chromatography (petroleum ether/ethyl acetate=10:1-5:1) to give Compound 12 (5.5 g, yield=50%). Measured: ESI-MS m/z=551.6[M+1].sup.+.

2.5. Synthesis of Compound 13

[0078] Compound 13:

1-(4-(((tert-butyldimethylsilyl)oxy)methyl)-3-(trifluoromethyl)phenyl)-3-(4-(6-mor pholino-7-(tetrahydro-2H-pyran-2-yl)-7H-purin-2-yl)phenyl)urea

##STR00022##

[0079] Compound 12 (5.5 g, 10.0 mmol) was dissolved in 1,4-dioxane (80 mL)/water (5 mL), then Compound 6 (3.6 g, 11.00 mmol), sodium bicarbonate (2.6 g, 30.0 mmol), XPhos (476 mg, 1.0 mmol) and Pd.sub.2(dba).sub.3 (184 mg, 0.20 mmol) were added. The reaction was carried out at 85° C.: overnight. After LCMS detection showed the reaction completion, 35 mL of brine was added, and the system was extracted with ethyl acetate (100 mL×3), the organic phase was dried over sodium sulfate, concentrated, and purified by column chromatography (petroleum ether/ethyl acetate=5:1-1:1) to give a crude product, which was purified by reverse column to give Compound 13 (2.0 g, yield=28%). Measured: ESI-MS m/z=712.9[M+1].sup.+. .sup.1H NMR (CDCl.sub.3, 400 MHz): δ 8.40-8.38 (m, 2H), 7.95 (s, 1H), 7.69-7.67 (m, 1H), 7.60-7.57 (m, 2H), 7.41 (d,J=8.4 Hz, 2H), 7.08 (s, 1H), 7.00 (s, 1H), 5.86-5.82 (m, 1H), 4.83 (s, 2H), 4.35 (brs, 4H), 4.19-4.16 (m, 1H), 3.87-3.78 (m, 5H), 2.16-1.99 (m, 3H), 1.84-1.73 (m, 3H), 0.93 (s, 9H), 0.09 (s, 6H).

2.6. Synthesis of Compound I-2

[0080] Compound I-2:

1-(4-(hydroxymethyl)-3-(trifluoromethyl)phenyl)-3-(4-(6-morpholino-7H-purin-2-yl)phenyl)urea

##STR00023##

[0081] Compound 13 (2.0 g, 2.81 mmol) was dissolved in 1,4-dioxane (8 mL), and then water (30 mL) and 1 M of a solution of hydrochloride acid in dioxan (80 mL) were added. The system was stirred at room temperature overnight, and after LCMS detection showed the reaction completion, the system was filtered. The obtained insolubles were respectively slurried with water, acetonitrile, and methyl tert-butyl ether, and dried to give Compound I-2 (1.3 g, yield 92%). Measured: .sup.1H NMR (DMSO-d6, 400 MHz): δ 9.50-9.44 (m, 2H), 8.29-8.27 (m, 3H), 7.97 (s, 1H), 7.68-7.59 (m, 4H), 4.61 (s, 2H), 4.29 (brs, 4H), 3.80-3.78 (m, 4H). .sup.1H NMR (DMSO-d6+D.sub.2O, 400 MHz): δ 9.36-9.32 (m, 0.3H), 8.29-8.26 (m, 3H), 7.97 (s, 1H), 7.68-7.60 (m, 4H), 4.61 (s, 2H), 4.29 (brs, 4H), 3.80-3.78 (m, 4H), LCMS [mobile phase: from 95% water (0.02% NH.sub.4Ac) and 5% CH.sub.3CN to 5% water (0.02% NH.sub.4Ac) and 95% CH.sub.3CN in 6.5 min, finally under these conditions for 0.5 min.] purity is >97%, Rt=3.485 min; MS Calcd.: 513; MS Found: 514 [M+H].sup.+.

Embodiment 3: Preparation of Compound I-3

[0082] Compound I-3 was synthesized through the following route:

##STR00024## ##STR00025##

3.1. Synthesis of Compound 15

[0083] Compound 15: 4-(2-(benzyloxy)ethyl)morpholine;

##STR00026##

[0084] Compound 14 (32.8 g, 0.25 mol) was dissolved in DMF (200 mL), NaH (10 g, 0.25 mol) was added in batches in an ice-water bath, and the system was stirred at room temperature for 1.5 hours, and then benzyl bromide (39.3 g, 0.23 mol) was added dropwise. The reaction solution was stirred at room temperature for 16 hours, vacuum concentrated, then ethyl acetate (100 mL) was added and the reaction solution was washed with water and saturated brine. The organic phase was vacuum concentrated, and purified by silica gel column (DCM:MeOH=10:1) to give colorless oil, namely Compound 15 (40 g, yield 78%). Measured: ESI-MS m/z=222 [M+1].sup.+.

3.2. Synthesis of Compound 16

[0085] Compound 16: 4-(2-((4-nitrobenzyl)oxy)ethyl)morpholine;

##STR00027##

[0086] Compound 15 (40.0 g, 0.18 mol) was dissolved in acetic anhydride (200 mL), cooled to 5° C. in an ice-water bath, fuming nitric acid (60 ml) was added dropwise, and stirred at 5° C. for 4 hours. The reaction solution was slowly poured into aqueous sodium carbonate solution to make pH>8, and extracted with ethyl acetate. The organic phase was washed with water and saturated brine, vacuum concentrated, and purified by silica gel column (DCM:MeOH=10:1) to give colorless oil, namely Compound 16 (30.1 g, yield 62%). Measured: ESI-MS m/z=267 [M+1].sup.+.

3.3. Synthesis of Compound 17

[0087] Compound 17: 4-((2-morpholinoethoxy)methyl)aniline;

##STR00028##

[0088] Compound 16 (5.0 g, 0.018 mol) was dissolved in ethyl acetate (200 mL), 10% palladium on carbon (1.0 g) were added, and the system was replaced with hydrogen for 3 times, and stirred at room temperature for 16 hours under hydrogen atmosphere. The reaction solution was filtered, and the filtrate was vacuum concentrated to dryness to give a red crude, namely Compound 17 (4.5 g), which was directly used in the next step. Measured: ESI-MS m/z=237 [M+1].sup.+.

3.4. Synthesis of Compound 18

[0089] Compound 18:

1-(4-((2-morpholinoethoxy)methyl)phenyl)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea;

##STR00029##

[0090] To a dichloromethane solution of Compound 2 (100 mL, from 6.6 g of Compound 1, 30 mmol) was added dropwise a dichloromethane solution(30 mL) of Compound 17 (5.9 g, 25 mmol) in an ice bath. The reaction solution was stirred overnight at room temperature, washed with aqueous sodium bicarbonate solution, washed with water, and the organic phase was vacuum concentrated, and purified by silica gel column (DCM:MeOH=10:1) to give yellow solid, namely Compound 18 (8.7 g, yield 72.3%). Measured: ESI-MS m/z=482[M+1].sup.+.

3.5. Synthesis of Compound 19

[0091] Compound 19:

1-(4-(6-morpholino-7-(tetrahydro-2H-pyran-2-yl)-7H-purin-2-yl)phenyl)-3-(4-((2-morpholinoethoxy)methyl)phenyl)urea

##STR00030##

[0092] Compound 18 (3.8 g, 8.28 mmol) was dissolved in 1,4-dioxane (80 mL)/water (8 mL), then Compound 6 (3.0 g, 9.29 mmol), sodium bicarbonate (2.1 g, 24.84 mmol), XPhos (395 mg) and Pd.sub.2(dba).sub.3 (152 mg) were added. The reaction was carried out at 85° C. overnight. After LCMS detection showed the reaction completion, 20 mL, of brine was added, and the system was extracted with ethyl acetate, the organic phase was dried over sodium sulfate, concentrated, and purified by silica gel column (dichloromethane/methanol=30:1-10:1), and then purified by a reverse column to give Compound 19 (1.5 g, yield=29%). Measured: ESI-MS m/z=643.8 [M+1].sup.+. .sup.1H NMR (DMSO-d6, 400 MHz): δ 8.89 (s, 1H), 8.72 (s, 1H), 8.35-8.33 (m, 3H), 7.57 (d,J=8.8 Hz, 2H), 7.45 (d,J=8.0, 2H), 7.24 (d, J=8.0 Hz, 2H), 5.80-5.75 (m, 1H), 4.39 (s, 2H), 4.30 (brs, 3H), 4.06-4.03 (m, 1H), 3.78-3.71 (m, 5H), 3.56-3.49 (m, 6H), 3.36-3.35 (m, 1H), 2.51-2.47 (m, 2H), 2.39 (brs, 4H), 2.31-2.22 (m, 1H), 1.99-1.97 (m, 2H), 1.79-1.76 (m, 1H), 1.64-1.60 (m, 2H).

3.6. Synthesis of Compound I-3

[0093] Compound I-3:

1-(4-(6-morpholino-7H-purin-2-yl)phenyl)-3-(4-((2-morpholinoethoxy)methyl)phenyl)urea

##STR00031##

[0094] Compound 19 (2.5 g, 3.89 mmol) was dissolved in a 0.3 Ni solution (60 mL) of hydrochloric acid in 1,4-dioxane, and then water (5 mL) was added. The system was stirred at room temperature for 2 h, and after LCMS detection showed the reaction completion, the system was filtered. The obtained insolubles were respectively slurried with acetonitrile, ethyl acetate and methyl Cert-butyl ether, and dried to give Compound I-3 (2.0 g, yield 91%). Measured: .sup.1H NMR (DMSO-d6, 400 MHz): δ 10.99 (s, 1H), 9.92 (s, 1H), 9.69 (s, 1H), 8.40 (s, 1H), 8.28 (d,J=8.4 Hz, 2H), 7.63 (d, J=9.2 Hz, 2H), 7.49 (d,J=8.4 Hz, 2H), 7.29 (d,J=8.41 Hz, 2H), 4.47 (s, 2H), 4.29 (brs, 4H), 3.96-3.93 (m, 2H), 3.85-3.79 (m, 8H), 3.42-3.34 (m, 4H), 3.16-3.09 (m, 2H). .sup.1H NMR (DMSO-d6+D.sub.2O, 400 MHz): δ 8.38-8.37 (m, 1H), 8.25 (d,J=8.4 Hz, 2H), 7.63 (d,J=8.4 Hz, 2H), 7.49 (d,J=7.2 Hz, 2H), 7.31 (d,J=8.4 Hz, 2H), 4.49 (s, 2H), 4.29 (brs, 4H), 3.81-3.75 (m, 10H), 3.43-3.35 (m, 4H), 3.17-3.11 (m, 2H). LCMS [mobile phase: from 95% water (0.02% NH.sub.4Ac) and 5% acetonitrile to 5% water (0.02% NIH.sub.4Ac) and 95% acetonitrile in 6.5 min, finally under these conditions for 1 min.] purity is >97%, Rt=3.258 min; MS Calcd.: 558; MS Found: 559 ([M+1].sup.+).

Embodiment 4: Biological Activity Experiment of the Compounds of the Embodiments

[0095] PI3-Kinase (human) HTRF™ Assay kit (PI3-Kinase (human) HTRF™ Assay kit detection method is an international general method) was used to detect the half inhibitory concentration of PI3K alpha enzyme (IC50 determination)) of the 3 compounds, namely Compound I-1, Compound I-2, Compound I-3 (in the following experiments, they were respectively given code RMP-D06, RMP-D07, RMP-D08) in the embodiments, and the compound GDC-0941 was used as a positive control. Positive control substance: GDC0941 (Pictilisib) with the following structural formula:

##STR00032##

7.1 Materials and Instruments

[0096] 2104 EnVision® Multilabel Reader (Cat: 2104-0010, PerkinElmer);

[0097] 384 well opaque balck plate (Cat. 6007270, PerkinElmer);

[0098] PI3-Kinase (human) HTRF™ Assay kit (Cat. 33-016, Millipore);

[0099] 4× Reaction Buffer (Cat. 33-002, Millipore); PIP2 1 mM (Cat. 33-004, Millipore); Stop A (Cat, 33-306, Millipore); Stop B (Cat. 33-008, Millipore); DM A (Cat. 33-010, Millipore); DM B (Cat. 33-012, Millipore); DM C (Cat. 33-014, Millipore); PI3k alpha (Cat. 14-602, Millipore); ATP 10 mM (cat PV3227, Invitrogen); DTT 1M (cat D5545, Sigma);

[0100] Compounds to be tested: Compound I-1, Compound I-2, Compound I-3 (in the following experiments, they were respectively given codes RMP-D06, RMP-D07, RMP-D08), and GDC-0941.

7.2 Reagent Preparation

[0101] 1× Reaction Buffer

[0102] 4× Reaction Buffer was diluted to 1× with ddH.sub.2O, and 1M DTT was added to make the final concentration of 5 mM. Prepare fresh before each use. For example, to prepare 10 mL 1× Reaction Buffer, adding 2.5 mL 4× Reaction Buffer, 50 μL 1 M DTT, and 7.45 mL ddH.sub.2O, Throughout the experiment, freshly prepared 1× Reaction Buffer was used to prepare ATP working solution, substrate and enzyme mixed working solution, etc..

[0103] 4× Compound Working Solution

[0104] The compound to be tested was dissolved in DMSO to 1 mM as a storage solution, and then diluted with DMSO in a 4-fold ratio for a total of 10 concentration points. 1 μL of each was added to 24 μL 1× Reaction Buffer. 5 μL of each diluted solution was added into a 384-well plate and contained 1% DMSO.

[0105] 2×PIP2 Working Solution

[0106] 1× reaction buffer was used to prepare 2×PIP2 working solution to make the final concentration of 20 μM and PIP2 reaction final concentration of 10 μM, for example, to prepare 1 ml 1× reaction buffer/PIP2 working solution, add 20 μL of PIP2 to 980 μL 1× reaction buffer. This working solution should be prepared with 0.1-0.2 ml more to meet the control usage and dead volume.

[0107] 2× PIP2/Kinase Working Solution

[0108] The kinase was diluted with 2× PIP2 working solution, and the concentration of the kinase working solution was 10 ng/well.

[0109] Kinase-Free Control (it can be Regarded as 100% Inhibition)

[0110] That is, 2× PIP2 working solution.

[0111] 4× ATP Working Solution

[0112] 10 mM ATP was diluted to 40 μM with 1× reaction buffer. In a 20 μL kinase reaction system, the concentration of ATP was 10 μM. For example, to prepare 2 ml ATP working solution, take 8 μL 10 mM ATP and add it to 1992 μL 1× reaction buffer.

[0113] Stop Solution

[0114] Stop A and Stop B were mixed in a ratio of 3:1 and can be used after at least 2 hours at room temperature. The stop solution can be stable for 12 hours at room temperature.

[0115] Test Solution

[0116] DMC, DMA and DMB were mixed in a ratio of 18:1:1, and can be used after at least 2 hours at room temperature. The test solution can be stable for 12 hours at room temperature.

7.3 Experimental Procedure

[0117]

TABLE-US-00001 Screening Control group group 100% 0% inhibition Kinase + inhibition With kinase and Reagent compound Kinase-free no compound Kinase 4× Compound  5 μL — — response 4% DMSO —  5 μL  5 μL 2× PIP2 — 10 μL — 2× PIP2/kinase 10 μL — 10 μL 4× ATP  5 μL  5 μL  5 μL [00033] Test Stop Solution  5 μL  5 μL  5 μL Test Solution  5 μL  5 μL  5 μL [00034] Excitation at 320 nM, and emission signal detection at 665 nm, 620 nm

[0118] Data Analysis

[0119] Calculation of the Emission Ratio (ER) of Each Well

[0120] Emission Ratio (ER)=665 nM Emission signal/620 nm Emission signal

[0121] The average emission intensity ratio (Emission Ratio) of the 100% inhibition control is recorded as: ER.sub.100%

[0122] The average Emission Ratio of the 0% inhibition control is recorded as: ER.sub.0%

[0123] Calculation of the Inhibition Rate

[0124] The inhibition rate is calculated with the following formula:

Inhibition rate=(ER.sub.sample˜ER.sub.0%)/(ER.sub.100%˜ER.sub.0%)×100%[(ERpositive−ERsample)/(ERpositive−ERnegative)*100%]

7.4 Experimental Results

[0125] PI3-Kinase (human) HTRF™ Assay kit was used to detect the inhibition rate of the 3 compounds on PI3K-alpha enzyme at different concentrations, with the concentration of DMSO controlled to 1%, double holes for each concentration, and selecting GDC-0941 as a positive reference substance. The measurement results are shown in FIG. 1. According to the test results, the half inhibitory concentration (IC.sub.50) of each compound on PI3K-alpha enzyme is summarized in Table 1 below.

TABLE-US-00002 TABLE 1 the half inhibitory concentrations (IC.sub.50) of the tested compounds on PI3K-alpha Compound IC.sub.50 (nM) RMP-D06 22.6 RMP-D07 214.8 RMP-D08 46.15 GDC0941 31.28

[0126] The above experiments proved the inhibitory effect of the novel purine derivative of the present disclosure on phosphatidylinositol-3-kinase (PI3K), indicating that the novel purine derivative (including its pharmaceutically acceptable salts, etc.) of the present disclosure is a kind of new PI3K inhibitor. Therefore, it can be used to treat phosphatidylinositol-3-kinase-mediated diseases, and its treatable malignancies include but are not limited to renal carcinoma, liver cancer, colon cancer, gastrointestinal stromal tumor, non-small cell lung cancer, breast cancer, pancreatic cancer, glioma, lymphoma, fibrosarcoma, ovarian cancer, leukemia and prostate cancer, etc..

[0127] The other compounds of the present disclosure have basically the same structure as Compound I-1 to Compound I-3, and it can be expected that they have excellent activities comparable to Compound I-1 to Compound I-3. This class of compounds is the world's first new type of compound, which has shown obvious strong activity, and will be used in further new drug research to invent domestically-made innovative drugs, to use in cheap anti-cancer drugs with strong effects and small side effects urgently needed in the market.

[0128] The explanation on the above embodiments is only to help understanding of the method and its core concept of the present disclosure. It should be noted that, for those ordinary skilled in the art, various improvements and modifications can be made without depart from the technical principle of the present disclosure, and these improvements and modifications should be covered by the protective scope of the present disclosure.