PYRIMIDINE COMPOUND AS AXL INHIBITOR

Abstract

A pyrimidine compound as an AXL inhibitor is provided. The structure of the pyrimidine compound is as shown in general formula I, and the definition of each substituent is as described in the description. The present invention further provides a preparation method for the pyrimidine compound. The pyrimidine compound of the present invention has significant AXL inhibitory activity, and can be used as an AXL inhibitor.

##STR00001##

Claims

1. A compound of Formula I or a pharmaceutically acceptable salt of the compound, ##STR00463## wherein X is CH or N; R.sup.1 is a 5-12 membered saturated heterocyclic ring or a 5-8 membered saturated carbocyclic ring optionally substituted by one or more C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, halogen, cyano, deuterium, or hydroxyl, and R.sup.1 is not ##STR00464## R.sup.2 is halogen; ring A is selected from the group consisting of phenyl, 5-6 membered heteroaryl, and 9-12 membered benzoheterocyclyl, wherein the phenyl and the 5-6 membered heteroaryl are optionally substituted by one or more R.sup.3, and the 9-12 membered benzoheterocyclyl is optionally substituted by ##STR00465##  or one or more R.sup.3; R.sup.3 is selected from the group consisting of deuterium, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkox 1, C.sub.3-10 cycloalkyloxyl, ##STR00466## and ##STR00467##  wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by hydroxyl, halogen, cyano, C.sub.1-3 alkoxyl, or 4-7 membered heterocycloalkyl; R.sup.4 and R.sup.5 are independently selected from the group consisting of C.sub.1-6 alkyl, hydroxyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.1-6 alkoxyl, and C.sub.3-10 cycloalkyl, wherein the C.sub.1-6 alkyl is optionally substituted by deuterium, hydroxyl, halogen, cyano, or C.sub.1-3 alkoxyl; or R.sup.4 and R.sup.5 is configured to form a 3-6 membered phosphorus-containing saturated monocyclic ring together with adjacent P atom; R.sup.6 is selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.1-6 alkoxyl, C.sub.3-10 cycloalkyl, 4-7 membered heterocycloalkyl, and 5-7 membered heteroaryl; R.sup.7 and R.sup.8 are independently selected from the group consisting of hydrogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, C.sub.3-10 cycloalkyl, 4-7 membered heterocycloalkyl, and 5-7 membered heteroaryl, wherein the C.sub.1-6 alkyl is optionally substituted by hydroxyl, halogen, cyano, or C.sub.1-3 alkoxyl; or R.sup.7 and R.sup.8 form a 3-6 membered nitrogen-containing saturated monocyclic ring together with their adjacent N atom; R.sup.9 and R.sup.10 are independently selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, and C.sub.3-10 cycloalkyl; R.sup.11 is selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, 4-7 membered heterocycloalkyl, and 5-7 membered heteroaryl; and R.sup.12 is selected from the group consisting of C.sub.3-10 cycloalkyl, 4-7 membered heterocycloalkyl, and 5-7 membered heteroaryl, the C.sub.3-10 cycloalkyl, the 4-7 membered heterocycloalkyl, or the 5-7 membered heteroaryl is optionally substituted by one or more hydroxyl, halogen, cyano, C.sub.1-6 alkyl, or 3-7 membered heterocycloalkyl.

2. The compound of the Formula I or the pharmaceutically acceptable salt of the compound according to claim 1, wherein R.sup.1 is a 5-8 membered saturated heterocyclic ring or a 5-8 membered saturated carbocyclic ring optionally substituted by one or more C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, halogen, cyano, deuterium, or hydroxyl, and R.sup.1 is not ##STR00468##  and ##STR00469## or, R.sup.1 is a 5-12 membered saturated heterocyclic ring or a 5-7 membered saturated carbocyclic ring-optionally substituted by one or more C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, halogen, cyano, deuterium, or hydroxyl, and R.sup.1 is not ##STR00470##

3. The compound of the Formula I or the pharmaceutically acceptable salt of the compound according to claim 1, wherein the ring A is phenyl, furyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, benzo five-membered heterocyclyl, or benzo six-membered heterocyclyl groups, wherein the phenyl, the furyl, the thienyl, the pyrrolyl, the pyrazolyl, the imidazolyl, the thiazolyl, the oxazolyl, the 1,2,3-triazolyl, the 1,2,4-triazolyl, the pyridyl, the pyrimidinyl, the pyridazinyl, the pyrazinyl, the benzo five-membered heterocyclyl, or the benzo six-membered heterocyclyl groups are optionally substituted by one or more R.sup.3.

4. The compound of the Formula I or the pharmaceutically acceptable salt of the compound according to claim 1, wherein R.sup.3 is selected from the group consisting of deuterium, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, C.sub.3-10 cycloalkyloxyl, ##STR00471##  wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by hydroxyl, halogen, cyano, C.sub.1-3 alkoxyl, or 4-7 membered heterocycloalkyl; or, R.sup.3 is selected from the group consisting of deuterium, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, ##STR00472##  wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by hydroxyl, halogen, cyano, C.sub.1-3 alkoxyl, or 4-7 membered heterocycloalkyl.

5. The compound of the Formula I or the pharmaceutically acceptable salt of the compound according to claim 1, wherein the compound has a structure shown in the following Formula I-1 or I-2, ##STR00473## wherein definitions of R.sup.1, R.sup.2, and ring A are as defined in the compound of the Formula I.

6. A compound of Formula II or a pharmaceutically acceptable salt of the compound, ##STR00474## wherein definitions of X, R.sup.1, R.sup.2, and R.sup.3 are consistent with those defined in the compound of the Formula I; n is an integer from 0 to 4; R.sup.a is deuterium, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, C.sub.3-10 cycloalkyloxyl, ##STR00475##  wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by one or more deuterium, methoxyl, hydroxyl, halogen, or cyano; wherein definitions of R.sup.4, R.sup.5, R.sup.7, R.sup.8, and R.sup.12 are consistent with those defined in the compound of the Formula I; preferably, the compound of the Formula II has a structure shown in the following Formula II-1, ##STR00476## wherein definitions of R.sup.1, R.sup.2, R.sup.3, R.sup.a, and n are consistent with those defined in the compound of the Formula II.

7. The compound of the Formula II according to claim 6, wherein the compound has a structure shown in the following Formula III, ##STR00477## wherein definitions of X, R.sup.1, R.sup.2, R.sup.3, and R.sup.a are consistent with those defined in the compound of the Formula II; preferably, the compound of the Formula II has a structure shown in the following Formula III-1, ##STR00478## wherein definitions of R.sup.1, R.sup.2, R.sup.3, and R.sup.a are consistent with those defined in the compound of the Formula II.

8. A compound of Formula IV or a pharmaceutically acceptable salt of the compound, ##STR00479## wherein definitions of X, R.sup.1 and R.sup.2 are consistent with those defined in the compound of Formula I; n is an integer from 0 to 4; ring B is selected from the group consisting of phenyl 5-6 membered heteroaryl, and 9-12 membered benzoheterocyclyl optionally substituted by ##STR00480## R.sup.b is deuterium, halogen C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, C.sub.3-10 cycloalkyloxyl, ##STR00481##  wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by one or more methoxyl, hydroxyl, deuterium, halogen, or cyano; wherein definitions of R.sup.4, R.sup.5, R.sup.7, R.sup.8, and R.sup.12 are consistent with those defined in the compound of the Formula I; preferably, the compound of the Formula IV has a structure shown in the following Formula IV-1: ##STR00482## wherein definitions of R.sup.1, R.sup.2, R.sup.b, n, and ring B are consistent with those defined in the compound of the Formula IV; preferably, the compound of the Formula IV has a structure shown in the following Formula V: ##STR00483## wherein definitions of X, R.sup.1, R.sup.2, R.sup.b and n are consistent with those defined in the compound of the Formula IV; preferably, the compound of the Formula IV has a structure shown in the following Formula VI, or a pharmaceutically acceptable salt of the compound: ##STR00484## wherein definitions of X, R.sup.1, R.sup.2, and R.sup.b are consistent with those defined in the compound of the Formula IV.

9. A compound selected from the group consisting of the following formulars or a pharmaceutically acceptable salt of the compound: ##STR00485## ##STR00486## ##STR00487## ##STR00488## ##STR00489## ##STR00490## ##STR00491## ##STR00492## ##STR00493## ##STR00494## ##STR00495## ##STR00496## ##STR00497## ##STR00498## ##STR00499## ##STR00500## ##STR00501## ##STR00502## ##STR00503## ##STR00504## ##STR00505## ##STR00506## ##STR00507## ##STR00508## ##STR00509## ##STR00510## ##STR00511## ##STR00512## ##STR00513## ##STR00514## ##STR00515## ##STR00516## ##STR00517## ##STR00518## ##STR00519##

10. A method for preparing a compound of Formula I, comprising the following step: synthesis scheme 1: ##STR00520## wherein definitions of R.sup.1, R.sup.2, X, and ring A are consistent with those defined in the Formula I; and a compound of the Formula H-1-3 is prepared from a compound of the Formula H-1-1 and a compound of the Formula H-1-2 in the presence of a first solvent and an alkaline, and the compound of the Formula I is prepared from a compound of the formula H-1-3 and a compound of the Formula H-1-4 in the presence of a second solvent and an acid.

11. A method for preparing a compound of Formula I-1, II-1, III-1 or IV-1, comprising the following step: synthesis scheme 2: ##STR00521## wherein definitions of R.sup.2 and ring A are consistent with those defined in the Formula I-1, and definition of R.sup.1 is consistent with that defined in the Formula I; a compound of the Formula H-2-3 is prepared from a compound of the Formula H-2-1 and a compound of the Formula H-2-2 in the presence of a third solvent and an alkaline, a compound of the Formula H-2-5 is prepared by a reaction of a compound of the Formula H-2-3 and a compound of the Formula H-2-4 in the presence of a fourth solvent and an acid, and a compound of the Formula H-2-6 is obtained by reacting a compound of the Formula H-2-5 with R.sup.1H or an acid addition salt thereof in the presence of a fifth solvent and a reducing agent; and optionally, an optically pure target product is prepared by a chiral resolution.

12. A pharmaceutical composition, comprising a therapeutically effective amount of the compound of Formula I, I-1, I-2, II, II-1, III, III-1, IV, IV-1, V, or VI, or a pharmaceutically acceptable salt of the compound, wherein preferably, the pharmaceutical composition further comprises one or more pharmaceutically acceptable carriers; preferably, the pharmaceutical composition is administered orally, for example, the pharmaceutical composition is in a form of tablets, capsules, or a solution; and preferably, the pharmaceutical composition is administered parenterally in a form of a sterile aqueous solution, a suspension, or a lyophilized powder.

13. A method of a use of a compound of Formula I, I-1, I-2, II, II-1, III, III-1, IV, IV-1, V, or VI, or a pharmaceutically acceptable salt of the compound in a preparation of a drug for preventing and/or treating diseases or disease conditions mediated by AXL protein kinase; and preferably, the diseases or disease conditions mediated by the AXL protein kinase comprise autoimmune diseases.

14. A method for preventing and/or treating diseases or disease conditions mediated by AXL protein kinase, comprising: administering a compound of Formula I, I-1, I-2, II, II-1, III, III-1, IV, IV-1, V, or VI, or a pharmaceutically acceptable salt of the compound, or the pharmaceutical composition according to claim 12 to an individual in need; and preferably, the diseases or disease conditions mediated by the AXL protein kinase comprise autoimmune diseases.

15. The compound of the Formula I or the pharmaceutically acceptable salt of the compound according to claim 4, wherein R.sup.3 is selected from the group consisting of deuterium, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxyl ##STR00522##  wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by hydroxyl, halogen, cyano, C.sub.1-3 alkoxyl, or 4-7 membered heterocycloalkyl.

16. The compound of the Formula II or the pharmaceutically acceptable salt of the compound according to claim 6, wherein R.sup.a is deuterium, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, ##STR00523## wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by one or more deuterium, halogen, or cyano.

17. The compound of the Formula II or the pharmaceutically acceptable salt of the compound according to claim 6, wherein R.sup.a is deuterium, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, ##STR00524## wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by one or more deuterium, halogen, or cyano.

18. The compound of the Formula IV or the pharmaceutically acceptable salt of the compound according to claim 8, wherein R.sup.b is deuterium, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, ##STR00525##  wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by one or more deuterium, halogen, or cyano.

19. The compound of the Formula IV or the pharmaceutically acceptable salt of the compound according to claim 8, wherein R.sup.b is deuterium, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxyl, ##STR00526## wherein the C.sub.1-6 alkyl or the C.sub.1-6 alkoxyl is optionally substituted by one or more deuterium, halogen, or cyano.

Description

DETAIL OF THE DESCRIPTION

[0603] The preparation methods of the compounds of the present invention are described in more detail below, but these specific preparation methods do not constitute any limitation on the scope of the present invention. In addition, reaction conditions such as reactants, solvents, alkali, amounts of compounds used, reaction temperature, reaction time, etc. are not limited to the following examples. The compounds of the present invention can also be conveniently prepared by combining various synthetic methods described in this description or known in the art, and such combinations can be easily performed by a person skilled in the art.

Part I Preparation

Preparation Example 1 7-amino-2-methylisoindolin-1-one

[0604] ##STR00293##

[0605] a) Preparation of 2-methyl-7-nitroisoindolin-1-one

[0606] 7-nitroisoindolin-1-one (450 mg) is dissolved in N,N-dimethyl formamide (15 mL), added with potassium carbonate (690 mg) and methyl iodide (430 mg), and then stirred and stands overnight at room temperature; the reaction solution is poured into water, extracted with ethyl acetate and then purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (300 mg). MS(ESI+): 193.02 (M+H).

[0607] b) Preparation of 7-amino-2-methylisoindolin-1-one

[0608] 2-methyl-7-nitroisoindolin-1-one (300 mg) is dissolved in methanol (30 mL), added with palladium charcoal (30 mg) and hydrazine hydrate (438 mg), and then stirred at room temperature for 6 h. The reaction solution is filtered with diatomite, concentrated to dryness and then purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (245 mg). MS(ESI+): 162.98 (M+H).

Preparation Example 2 N-(2-aminophenyl) methanesulfonamide

[0609] ##STR00294##

[0610] O-phenylenediamine (500 mg), triethylamine (1403 mg) and 10 mL of anhydrous dichloromethane are added to a reaction flask. After all of them are dissolved, the mixture is added dropwise with a dichloromethane solution of methanesulfonyl chloride (1095 mg) at 0° C. After the addition is completed, the temperature is gradually raised to room temperature and the reaction is performed for 12 h. After the reaction is completed, the reaction solution is quenched with 1 ml of methanol. The pH of the system is adjusted to 8 with 1M hydrochloric acid. The system is then concentrated to dryness to obtain a crude product. The crude product is purified by column chromatography (dichloromethane/methanol=20:1) to obtain 505 mg of the title compound. MS(ESI+): 187.1 (M+H).

Preparation Example 3 3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-amine

[0611] ##STR00295##

a) Synthesis of 7-nitro-3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

[0612] 7-nitro-2,3,4,5-tetrahydro-1H-benzo[D]azepine (1920 mg), tetrahydropyran-4-one (1100 mg) and acetic acid (1110 mg) are dissolved in 30 ml of methanol, stirred for 1 h, and added with sodium triacetoxyborohydride (3180 mg) in batches to react overnight, and then filtered. The filtrate is concentrated to dryness, and purified by column chromatography (dichloromethane/methanol=20:1) to obtain 1380 mg of the title compound. MS(ESI+): 277.2 (M+H).

b) Synthesis of 3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-amine

[0613] 7-nitro-3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine (1380 mg) is dissolved in 50 ml of methanol, added with 10% palladium charcoal (150 mg) under the protection of nitrogen, added dropwise with 80% hydrazine hydrate (2 ml) and reacted to release gas. After 3 hours of reaction, the reactant is filtered. The mother liquor is concentrated to dryness under reduced pressure to obtain 1200 mg of the title compound. MS(ESI+): 247.2 (M+H).

Preparation Example 4 2-amino-5-cyano-N-methylbenzamide

[0614] ##STR00296##

[0615] 2-amino-5-cyano-N-methylbenzoic acid (500 mg), methylamine solution (6.2 mmol, 3.1 ml), 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (2.36 g) and N,N-diisopropylethylamine (1.2 g) are dissolved in N,N-dimethylformamide (15 mL) and stirred at room temperature for 4 h. The reaction solution is diluted with 80 mL of ethyl acetate and washed with a saturated sodium chloride aqueous solution (50 mL×3). An organic layer is taken and concentrated to dryness to obtain the title compound (550 mg). MS(ESI+): 176.1 (M+H).

Preparation Example 5 2-amino-N-methyl-5-(trifluoromethyl)benzamide

[0616] ##STR00297##

[0617] 2-amino-5-(trifluoromethyl)benzoic acid (100 mg), methylamine (31 mg), N,N-dimethylformamide (5 ml), N,N-diisopropylethylamine (194 mg), and 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (285 mg) are added at 0° C. After the addition, the mixture is transferred to room temperature and reacted for 2.0 h. After the reaction is completed, the reactant is added with 20 ml of water and then separated. The organic layers are extracted with ethyl acetate, merged, and dried with anhydrous sodium sulfate. A solvent is removed by rotary evaporation under reduced pressure. The reactant is purified by column chromatography (petroleum ether/ethyl acetate=3/1) to obtain 76 mg of the title compound. MS(ESI+): 219.1 (M+H).

Preparation Example 6 2-amino-5-chloro-N-methylbenzamide

[0618] ##STR00298##

[0619] 2-amino-5-chloro-benzoic acid (250 mg), 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (665 mg) and N,N-diisopropylethylamine (377 mg) are sequentially added to a reaction flask, dissolved with 10 mL of anhydrous N,N-dimethylformamide, activated at room temperature for 10 min, then slowly added dropwise with a tetrahydrofuran solution of methylamine (1.75 mmol, 0.9 mL), and reacted for 1 h at room temperature after the addition is completed. After the reaction is completed, the reaction solution is added with 100 mL of ethyl acetate, and washed with a saturated sodium chloride solution for three times. Organic phases are merged, and concentrated to dryness under reduced pressure to obtain 495 mg of the crude title compound. MS(ESI+): 185.1 (M+H).

Preparation Example 7 N-(2-aminophenyl)cyclopropanesulfonamide

[0620] ##STR00299##

[0621] O-phenylenediamine (500 mg), triethylamine (1403 mg) and 10 mL of anhydrous dichloromethane are added to a reaction flask. After all of them are dissolved, the mixture is added dropwise with cyclopropanesulfonyl chloride (715 mg) at 0° C. After the addition is completed, the temperature is gradually raised to room temperature and the reaction is performed for 12 h. After the reaction is completed, the reaction solution is quenched with 1 ml of methanol. The pH of the system is adjusted to 8 with 1M hydrochloric acid and then concentrated to dryness to obtain a crude product. The crude product is purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (1.094 g). MS(ESI+): 213.1 (M+H).

Preparation Example 8 4-amino-2-methoxyl-N-methylnicotinamide

[0622] ##STR00300##

[0623] 4-amino-2-methoxynicotinamide (1680 mg), 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (4180 mg) and N,N-diisopropylethylamine (2580 mg) are dissolved in N,N-dimethylformamide (15 mL), added with 2M methylamine solution (5 mL) and stirred at room temperature for 1 h. After the reaction is completed, the reaction solution is poured into 30 mL of water, and extracted with ethyl acetate (15 mL×3). An organic layer is taken and concentrated to dryness, and purified by column chromatography to obtain the title compound (900 mg). MS(ESI+): 182.1 (M+H).

Preparation Example 9 4-amino-6-methoxyl-N-methylnicotinamide

[0624] ##STR00301##

[0625] 4-amino-6-methoxynicotinamide (1680 mg), 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (4180 mg) and N,N-diisopropylethylamine (2580 mg) are dissolved in N,N-dimethylformamide (15 mL), added with 2M methylamine solution (5 mL, 10 mmol) and stirred at room temperature for 1 h. After the reaction is completed, the reaction solution is poured into 30 mL of water, and extracted with ethyl acetate (15 ml×3). An organic layer is taken and concentrated to dryness, and purified by column chromatography to obtain a yellow oily substance (560 mg). MS(ESI+): 182.1 (M+H).

Preparation Example 10 6-amino-N-methylquinoxaline-5-carboxamide

[0626] ##STR00302##

[0627] a) Preparation of N,N-bis(tert-butoxycarbonyl)-5-bromoquinoxaline-6-amine (2)

[0628] 6-amino-5-bromoquinoxaline (1.0 g), 4-dimethylaminopyridine (0.05 g), and di-tert butyl carbonate (2.24 g) are dissolved in tetrahydrofuran (25 mL) and stirred at 40° C. for 4 h. The reaction solution is poured into 50 mL of water and diluted, and then extracted with ethyl acetate (50 ml×3). An organic layer is taken and concentrated to dryness, and purified by column chromatography (dichloromethane/methanol=40:1) to obtain the title compound (1.5 g). MS(ESI+): 424.1 (M+H).

[0629] b) Preparation of tert-butyl 6-((tert-butoxycarbonyl)amino)quinoxaline-5-carboxylate

[0630] N,N-bis(tert-butoxycarbonyl)-5-bromoquinoxaline-6-amine (500 mg) is dissolved in tetrahydrofuran (20 mL). After the temperature is cooled to −78° C., n-butyllithium (0.74 mL) is added under the protection of nitrogen, and the reaction ends after 30 min. The reaction solution is quenched by adding 5 mL of saturated ammonium chloride solution, and the tetrahydrofuran layer is taken and concentrated to dryness to obtain the title compound (320 mg). MS(ESI+): 346.2 (M+H).

[0631] c) Preparation of 6-aminoquinoxaline-5-carboxylic acid tert-butyl 6-((tert-butoxycarbonyl)amino)aminoquinoxaline-5-carboxylate (100 mg) is dissolved in dichloromethane (5 mL), added with trifluoroacetic acid (164 mg) and reacted at room temperature for 8 h. After the reaction is completed, the reactant is purified by column chromatography (dichloromethane/methanol=40:1) to obtain the title compound (40 mg). MS(ESI+): 290.1 (M+H).

[0632] d) Preparation of 6-amino-N-methylquinoxaline-5-carboxamide

[0633] 6-aminoquinoxaline-5-carboxylic acid (40 mg), 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (161 mg) and N,N-diisopropylethylamine (54 mg) are dissolved in N,N-dimethylformamide (5 mL), added with 2M methylamine solution (0.21 mL, 0.42 mmol) and then stirred at room temperature for 1 h. After the reaction is completed, the reaction solution is poured into 30 mL of water and extracted with ethyl acetate (15 mL×3). The organic layer is taken and concentrated to dryness, and purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (28 mg). MS(ESI+): 203.1 (M+H).

Preparation Example 11 (2-amino-5-fluorophenyl)dimethylphosphine oxide

[0634] ##STR00303##

[0635] A compound 4-fluoro-2-iodoaniline (2.0 g), dimethyl phosphine oxide (0.79 g), potassium phosphate (2.14 g), tris(dibenzalacetone) dipalladium (0.153 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.097 g) are dissolved in DMF (15 mL), heated to 100° C. under the protection of nitrogen and reacted for 16 h. The reaction solution is cooled and filtered. The filtrate is spin-dried, and added with 1M hydrochloric acid solution (30 mL) to adjust the pH to 1 to 2. Insoluble substances are removed by suction filtration. The filtrate is washed with dichloromethane (30 mL×2). An aqueous phase is taken, added with a saturated sodium bicarbonate solution to adjust the pH to 8 to 9, and then extracted with dichloromethane (50 mL×3). The dichloromethane is spin-dried to obtain a crude product. The crude product is slurried with 30 mL of an ethyl acetate and petroleum ether (5:1) mixed solvent to obtain the title product (1.1 g). MS(ESI+): 188.08 (M+H).

Preparation Example 12 (2-amino-5-chlorophenyl) dimethyl phosphine oxide

[0636] ##STR00304##

[0637] 4-chloro-2-iodoaniline (1 g), dimethylphosphine oxide (368 mg), potassium phosphate (996 mg), tris(dibenzalacetone) dipalladium (366 mg), 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (232 mg), and N,N-dimethylformamide/water (3:1, 10 ml) are sequentially added to a reaction flask. Nitrogen replacement is performed for 5 times. The reaction is performed in an oil bath at 100° C. for 3 h. After the reaction is completed, the solvent is removed by rotary evaporation under reduced pressure, and purified by column chromatography (dichloromethane/methanol=20/1) to obtain 685 mg of the title product. MS(ESI+): 204.1 (M+H).

Preparation Example 13 (2-amino-5-methylphenyl) dimethyl phosphine oxide

[0638] ##STR00305##

[0639] 2-iodo-4-methylaniline (1 g), dimethyl phosphine oxide (505 mg), palladium acetate (97 mg), 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (249 mg), potassium phosphate (1.35 g), 15 mL of N,N-dimethylformamide and 3 mL of water are sequentially added to a reaction flask, dissolved, heated to 110° C. under the protection of nitrogen and reacted for 3 h. After the reaction is completed, the temperature is cooled to room temperature. Insoluble inorganic salts and catalysts are removed by filtration. The filtrate is concentrated under reduced pressure and diluted with 30 mL of water. The pH is adjusted to 2 with 1M hydrochloric acid. Insoluble substances are removed by filtration. The filtrate is washed with dichloromethane and an aqueous layer is separated. The aqueous layer is adjusted to the pH of 9 with 1M sodium hydroxide solution and then extracted with dichloromethane. An organic phase is separated, dried with anhydrous sodium sulfate, filtered by suction, and concentrated to dryness under reduced pressure to obtain 1.6 g of the title product. MS(ESI+): 184.07 (M+H).

Preparation Example 14 (2-amino-5-cyanophenyl) dimethyl phosphine oxide

[0640] ##STR00306##

[0641] A compound 4-cyano-2-iodoaniline (0.98 g), dimethyl phosphine oxide (0.376 g), potassium phosphate (1.02 g), tris(dibenzalacetone) dipalladium (0.073 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.046 g) are dissolved in N,N-dimethylformamide (10 mL), heated to 100° C. under the protection of nitrogen and reacted for 16 h. The reaction solution is cooled and filtered. The filtrate is concentrated to dryness, and added with 1M hydrochloric acid solution (30 mL) to adjust the pH to 1 to 2. Insoluble substances are removed by suction filtration. The filtrate is washed with dichloromethane (30 mL×2). A water phase is taken, added with a saturated sodium bicarbonate solution to adjust the pH to 8 to 9, then extracted with dichloromethane (50 mL×3), and concentrated to dryness to obtain the title product (0.7 g). MS(ESI+): 195.08 (M+H).

Preparation Example 15 (2-amino-5-methoxyphenyl)dimethyl phosphine oxide

[0642] ##STR00307##

[0643] A compound 4-methoxyl-2-iodoaniline (1.0 g), dimethyl phosphine oxide (0.376 g), potassium phosphate (1.02 g), tris(dibenzalacetone) dipalladium (0.073 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.046 g) are dissolved in N,N-dimethylformamide (10 mL), heated to 100° C. under the protection of nitrogen and reacted for 16 h. The reaction solution is cooled and filtered. The filtrate is concentrated to dryness, and added with 1M hydrochloric acid solution (30 mL) to adjust the pH to 1 to 2. Insoluble substances are removed by suction filtration. The filtrate is washed with dichloromethane (30 mL×2). A water phase is taken, added with a saturated sodium bicarbonate solution to adjust the pH to 8 to 9, then extracted with dichloromethane (50 mL×3), and concentrated to dryness to obtain the title product (0.7 g). MS(ESI+): 200.8 (M+H).

Preparation Example 16 (2-aminophenyl)bis(methyl-d.SUB.3.) phosphine oxide

[0644] ##STR00308##

[0645] a) Preparation of bis(methyl-d.sub.3) phosphine oxide

[0646] Magnesium chips (3.6 g) are added into a three-necked reaction flask. Nitrogen replacement is performed for three times. 30 ml of anhydrous ether is then added, cooled to −10° C., and stirred. Iodomethane-d.sub.3 (20 g) is diluted with 30 ml of ether and slowly dropwise added into the reaction flask. A reflux reaction is performed for 3 h after dropping. After the reflux reaction is completed, the temperature is cooled to 0° C. 20 ml of diethyl ether diluent of diethyl phosphite (6.35 g) is slowly dropwise added, and then quenched with a cold saturated potassium carbonate aqueous solution (19.2 g, 20 ml). Generated solid is removed by filtration. The filter cake is washed twice with ethanol, and the filtrate is concentrated at −0.8 Mpa and 50° C. The solid is removed by filtration again, and the filtrate is the title product (12 g).

[0647] b) Preparation of (2-aminophenyl)bis(methyl-d.sub.3) phosphine oxide

[0648] 2-iodoaniline (2.19 g), bis(methyl-d.sub.3)phosphine oxide (1.68 g), potassium phosphate (3.17 g), palladium acetate (916 mg), 4,5-bisdiphenyl phosphine-9,9-dimethylxanthene (578 mg), 15 ml of N,N-dimethylformamide and 3 ml of water are sequentially added to a 100 ml three-necked flask. Nitrogen replacement is performed for 3 times. The reaction is then performed at 110° C. for 3 h. After the reaction is completed, the reactant is spin-dried under reduced pressure, and purified by silica-gel column chromatography (dichloromethane/methanol=20:1) to obtain 1.3 g of the title product. MS(ESI+): 176.1 (M+H).

Preparation Example 17 (2-amino-5-fluorophenyl)bis(methyl-d.SUB.3.) phosphine oxide

[0649] ##STR00309##

[0650] 4-fluoro-2-iodoaniline (1.18 g), bis(methyl-d.sub.3) phosphine oxide (1.68 g), potassium phosphate (2.12 g), palladium acetate (92 mg), 4,5-bisdiphenyl phosphine-9,9-dimethylxanthene (58 mg), 15 ml of N,N-dimethylformamide and 3 ml of water are sequentially added to a 100 ml three-necked flask. Nitrogen replacement is performed for 3 times. The reaction is then performed at 110° C. for 3 h. After the reaction is completed, the solid is removed by filtration, the filtrate is concentrated to dryness under reduced pressure, and 15 ml of 2M hydrochloric acid is added to the residues to precipitate a yellow solid, and insoluble substances are removed by suction filtration. After an aqueous phase is washed twice with 15 ml of dichloromethane, the aqueous phase is added with a saturated potassium carbonate solution to adjust the pH to 10, and then extracted twice with 15 ml of dichloromethane. An organic phase is concentrated to dryness to obtain the title compound (1 g). MS(ESI+): 193.1 (M+H).

Preparation Example 18 (4-amino-1,3-phenylene)bis(dimethyl phosphine oxide)

[0651] ##STR00310##

[0652] 2,4-diiodoaniline (2 g), dimethyl phosphine oxide (1.6 g), potassium phosphate (2.12 g), palladium acetate (92 mg), 4,5-bisdiphenyl phosphine-9,9-dimethylxanthene (58 mg) and 15 ml of N,N-dimethylformamide are sequentially added to a 100 ml three-necked flask. Nitrogen replacement is performed for 3 times. The reaction is then performed at 110° C. for 5 h. After the reaction is completed, the solid is removed by filtration, the filtrate is concentrated to dryness under reduced pressure, and 3 ml of 2M hydrochloric acid is added to the residues to precipitate a yellow solid, and insoluble substances are removed by suction filtration. After an aqueous phase is washed twice with 15 ml of dichloromethane, and the aqueous phase is added with a saturated potassium carbonate solution to adjust the pH to 7. The aqueous phase is concentrated to dryness, and purified by column chromatography (dichloromethane/methanol=20:1, v/v) to obtain the title compound (1.4 g). MS(ESI+): 246.1 (M+H).

Preparation Example 19 (2-amino-5-difluoromethoxyphenyl)dimethyl phosphine oxide

[0653] ##STR00311##

[0654] A compound 4-difluoromethoxyl-2-iodoaniline (1.0 g), dimethyl phosphine oxide (0.366 g), potassium phosphate (1.00 g), tris(dibenzalacetone) dipalladium (0.073 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.046 g) are dissolved in N,N-dimethylformamide (10 mL), heated to 100° C. under the protection of nitrogen and reacted for 16 h. The reaction solution is cooled and filtered. The filtrate is concentrated to dryness, and added with 1M hydrochloric acid solution (30 mL) to adjust the pH to 1 to 2. Insoluble substances are removed by suction filtration. The filtrate is washed with dichloromethane (30 mL×2). A water phase is taken, added with a saturated sodium bicarbonate solution to adjust the pH to 8 to 9, then extracted with dichloromethane (50 mL×3), and concentrated to dryness to obtain the title product (0.7 g). MS(ESI+): 235.2 (M+H).

Preparation Example 20 (2-amino-5-(1H-tetrazol-1-yl)phenyl)dimethyl phosphine oxide

[0655] ##STR00312##

1) 2-iodo-4-(1H-tetrazol-1-yl)aniline

[0656] A compound 4-(1H-tetrazol-1-yl)aniline (0.97 g) is dissolved in glacial acetic acid (30 ml), stirred and cooled at 0° C., added with N-iodosuccinimide (1.57 g) in batches, and reacted for 15 min. Then, water (100 ml) and ethyl acetate (150 ml) are added to the reaction solution, added with a potassium carbonate solid to adjust the pH to 9, and separated to obtain an organic phase. The organic phase is then washed with water (100 ml). The organic phase is concentrated to dryness to obtain 1.8 g of the title product.

[0657] 2) (2-amino-5-(1H-tetrazol-1-yl)phenyl)dimethyl phosphine oxide

[0658] A compound 2-iodo-4-(1H-tetrazol-1-yl)aniline (1.68 g), dimethyl phosphine oxide (0.685 g), potassium phosphate (2.48 g), tris(dibenzalacetone) dipalladium (0.267 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.338 g) are dissolved in N,N-dimethylformamide (30 mL), heated to 100° C. under the protection of nitrogen, and reacted for 8 h. The reaction solution is cooled and filtered. The filtrate is concentrated to dryness, and added with 2M hydrochloric acid solution (30 mL) to adjust the pH to 2 to 3. Insoluble substances are removed by suction filtration. The filtrate is added with potassium carbonate to adjust the pH to 9, and then extracted with ethyl acetate (100 mL×3). The organic phase is concentrated to dryness to obtain the title compound (0.3 g). MS(ESI+): 238.2 (M+H).

Preparation Example 21 3-(tetrahydrofuran-3-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-amine

[0659] ##STR00313##

1) 7-nitro-3-(tetrahydrofuran-3-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

[0660] Dichloromethane (40 ml) is added to a 100 ml reaction flask, and added with 7-nitro-2,3,4,5-tetrahydro-1H-benzo[d]heterocyclic nitrogen (1.9 g), dihydrofuran-3(2H)-one (0.86 g) and acetic acid (1.1 g) under stirring at room temperature, and then stirred for 1 h. Then sodium triacetoxyborohyride (4.2 g) is added in batches, and stirred and stands overnight at room temperature. After the reaction is completed, a sodium hydroxide solution (100 ml, 1 M) is added for quenching. Then, liquid separation is performed. A dichloromethane phase is concentrated to dryness under reduced pressure, and the obtained residue is purified by silica-gel column chromatography (dichloromethane:methanol=20:1 v/v) to obtain 2.5 g of the title product.

2) 3-(tetrahydrofuran-3-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-amine

[0661] Methanol (40 ml) is added to a 100 ml reaction flask. Nitrogen replacement is performed for three times. Hydrazine hydrate (10 ml, 80% w/w) and palladium charcoal (0.25 g, 10% w/w) are sequentially added under stirring at room temperature, and stirred for 1 h. The mixture is then filtered. The mother liquor is concentrated to dryness under reduced pressure, and the obtained residue is purified by silica-gel column chromatography (dichloromethane:methanol=20:1 v/v) to obtain 1.5 g of the title product. MS(ESI+): 233.2 (M+H).

Preparation Example 22 (2-amino-5-trifluoromethoxyphenyl)dimethyl phosphine oxide

[0662] ##STR00314##

[0663] A compound 4-trifluoromethoxyl-2-iodoaniline (1.0 g), dimethyl phosphine oxide (0.366 g), potassium phosphate (1.00 g), tris(dibenzalacetone) dipalladium (0.073 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.046 g) are dissolved in N,N-dimethylformamide (10 mL), heated to 100° C. under the protection of nitrogen and reacted for 16 h. The reaction solution is cooled and filtered. The filtrate is concentrated to dryness, and added with 1M hydrochloric acid solution (30 mL) to adjust the pH to 1 to 2. Insoluble substances are removed by suction filtration. The filtrate is washed with dichloromethane (30 mL×2). A water phase is taken, added with a saturated sodium bicarbonate solution to adjust the pH to 8 to 9, then extracted with dichloromethane (50 mL×3), and concentrated to dryness to obtain the title product (0.7 g). MS(ESI+): 254.1 (M+H).

Preparation Example 23 (2-amino-5-cyclopropylphenyl)dimethyl phosphine oxide

[0664] ##STR00315##

1) 2-iodo-4-cyclopropylaniline

[0665] A compound 4-cyclopropylaniline (1.0 g) is dissolved in glacial acetic acid (30 ml), stirred and cooled at 0° C., added with N-iodosuccinimide (1.57 g) in batches, and reacted for 15 min. Then, water (100 ml) and ethyl acetate (150 ml) are added to the reaction solution, added with a potassium carbonate solid to adjust the pH to 9, and separated to obtain an organic phase. The organic phase is then washed with water (100 ml). The organic phase is concentrated to dryness to obtain 1.2 g of the title product.

[0666] 2) (2-amino-5-cyclopropylphenyl)dimethyl phosphine oxide

[0667] A compound 2-iodo-4-cyclopropylaniline (1.2 g), dimethyl phosphine oxide (0.685 g), potassium phosphate (2.48 g), tris(dibenzalacetone) dipalladium (0.267 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.338 g) are dissolved in N,N-dimethylformamide (30 mL), heated to 100° C. under the protection of nitrogen, and reacted for 8 h. The reaction solution is cooled and filtered. The filtrate is concentrated to dryness, and added with 2M hydrochloric acid solution (30 mL) to adjust the pH to 2 to 3. Insoluble substances are removed by suction filtration. The filtrate is added with potassium carbonate to adjust the pH to 9, and then extracted with ethyl acetate (100 mL×3). An organic phase is concentrated to dryness to obtain the title compound (0.3 g). MS(ESI+): 210.1 (M+H).

Preparation Example 24 (2-amino-5-isopropoxyphenyl)dimethyl phosphine oxide

[0668] ##STR00316##

1) 2-iodo-4-isopropoxyaniline

[0669] A compound 4-isopropoxyaniline (1.0 g) is dissolved in glacial acetic acid (30 ml), stirred and cooled at 0° C., added with N-iodosuccinimide (1.57 g) in batches, and reacted for 15 min. Then, water (100 ml) and ethyl acetate (150 ml) are added to the reaction solution, added with a potassium carbonate solid to adjust the pH to 9, and separated to obtain an organic phase. The organic phase is then washed with water (100 ml). The organic phase is concentrated to dryness to obtain 1.2 g of the title product.

[0670] 2) (2-amino-5-isopropoxyphenyl)dimethyl phosphine oxide

[0671] A compound 2-iodo-4-isopropoxyaniline (1.2 g), dimethyl phosphine oxide (0.685 g), potassium phosphate (2.48 g), tris(dibenzalacetone) dipalladium (0.267 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.338 g) are dissolved in N,N-dimethylformamide (30 mL), heated to 100° C. under the protection of nitrogen, and reacted for 8 h. The reaction solution is cooled and filtered. The filtrate is concentrated to dryness, and added with 2M hydrochloric acid solution (30 mL) to adjust the pH to 2 to 3. Insoluble substances are removed by suction filtration. The filtrate is added with potassium carbonate to adjust the pH to 9, and then extracted with ethyl acetate (100 mL×3). The organic phase is concentrated to dryness to obtain the title compound (0.3 g). MS(ESI+): 226.1 (M+H).

Preparation Example 25 (2-amino-4-methoxyl-5-fluorophenyl)dimethyl phosphine oxide

[0672] ##STR00317##

[0673] A compound 2-bromo-4-fluoro-5-methoxyaniline (2 g), dimethyl phosphine oxide (0.85 g), potassium phosphate (2.48 g), palladium acetate (0.10 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.266 g) are dissolved in N,N-dimethylformamide (40 mL), heated to 120° C. under the protection of nitrogen, and reacted for 48 h. The reaction solution is concentrated to dryness, and the residue is purified by silica-gel column chromatography (dichloromethane/methanol=40:1 v/v) to obtain the title compound (0.5 g). MS(ESI+): 218.1 (M+H).

Preparation Example 26 (2-amino-5-fluoro-6-chlorophenyl) dimethyl phosphine oxide

[0674] ##STR00318##

[0675] A compound 2-iodo-3-chloro-4-fluoroaniline (1.5 g), dimethyl phosphine oxide (0.24 g), potassium phosphate (0.65 g), palladium acetate (0.06 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.09 g) are dissolved in N,N-dimethylformamide (30 mL), heated to 120° C. under the protection nitrogen, and reacted for 2 h. The reaction solution is concentrated to dryness, and the residue is purified by silica-gel column chromatography (dichloromethane/methanol=10:1 v/v) to obtain the title compound (0.35 g). MS(ESI+): 222.1 (M+H).

Preparation Example 27 (2-amino-5-fluoro-6-chlorophenyl) dimethyl phosphine oxide

[0676] ##STR00319##

a) N-(4-fluoro-3-methoxyphenyl)-2,2-dimethylpropionamide

[0677] 4-fluoro-3-methoxyaniline (5 g) and triethylamine (3.94 g) are added to dichloromethane (100 mL) in the atmosphere of nitrogen at room temperature, and then added dropwise with 2,2-dimethylpropionyl chloride (4.27 g) under stirring. The resulting mixture is stirred for 1 h. The reactant is quenched by adding water (100 mL) at room temperature and extracted with dichloromethane (3×100 mL). The merged organic layer is dried with anhydrous sodium sulfate. After filtration, the filtrate is concentrated under reduced pressure. The residue is purified by silica-gel column chromatography and eluted with petroleum ether:ethyl acetate=(1:1 v/v) to obtain the title product (7.7 g). MS(ESI+): 226.1 (M+H).

b) N-(4-fluoro-2-iodo-3-methoxyphenyl)-2,2-dimethylpropionamide

[0678] N-(4-fluoro-3-methoxyphenyl)-2,2-dimethylpropionamide (1 g) is added to tetrahydrofuran (20 mL), and added dropwise with n-butyllithium (0.71 g) at 0° C. in the atmosphere of nitrogen. The resulting mixture is stirred at 0° C. in the atmosphere of nitrogen for 2 h. At −78° C., iodine (1.41 g, dissolved in 10 mL of tetrahydrofuran) is added dropwise to the above mixture for 30 min. The resulting mixture is stirred for another 2 h at −78° C. The reaction is quenched by adding a saturated aqueous ammonium chloride solution (10 mL) at 0° C. The resulting mixture is extracted with ethyl acetate (3×100 mL). The merged organic layer is dried with anhydrous sodium sulfate. After filtration, the filtrate is concentrated under reduced pressure. The residue is purified by silica-gel column chromatography and eluted with petroleum ether:ethyl acetate=(1:1 v/v) to obtain the title product (1.3 g). MS(ESI+): 218.1 (M+H).

c) N-[2-(dimethylphosphoryl)-4-fluoro-3-methoxyphenyl]-2,2-dimethylpropionamide

[0679] A compound N-(4-fluoro-2-iodo-3-methoxyphenyl)-2,2-dimethylpropionamide (0.55 g), dimethyl phosphine oxide (0.15 g), potassium phosphate (1.0 g), palladium acetate (0.04 g) and 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (0.18 g) are dissolved in N,N-dimethylformamide (10 mL), heated to 120° C. in the atmosphere of nitrogen, and reacted for 2 h. The reaction solution is concentrated to dryness, and the residue is purified by silica-gel column chromatography (dichloromethane/methanol=10:1 v/v) to obtain the title compound (0.31 g). MS(ESI+): 302.1 (M+H).

[0680] d) (2-amino-5-fluoro-6-methoxyphenyl)dimethyl phosphine oxide

[0681] N-[2-(dimethylphosphoryl)-4-fluoro-3-methoxyphenyl]-2,2-dimethylpropionamide (290 mg) is added to hydrochloric acid (6M, 6 mL), and stirred at 100° C. in the atmosphere of nitrogen and stands overnight. The mixture is neutralized to pH=8 with a saturated sodium carbonate aqueous solution. An aqueous layer is extracted with dichloromethane (3×5 mL). The merged organic layer is dried with anhydrous sodium sulfate. After filtration, the filtrate is concentrated under reduced pressure to obtain the title product (170 mg). MS(ESI+): 218.1 (M+H).

Example 1 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N,N-dimethyl benzenesulfonamide

[0682] ##STR00320##

[0683] a) Preparation of 2-((2,5-dichloropyrimidin-4-yl)amino)-N,N-dimethyl benzenesulfonamide

[0684] 10 ml of anhydrous N,N-dimethylformamide, 2-amino-N,N-dimethyl benzenesulfonamide (200 mg), and 2,4,5-trichloropyrimidine (183 mg) are sequentially added to a reaction flask, added with sodium hydride (120 mg, 60%) at 0° C., and reacted at 0° C. for 3 h. After the reaction is completed, 20 ml of water is added for quenching. The reaction solution is extracted with 20 ml of ethyl acetate. The organic phase is concentrated to dryness. The crude product is purified by column chromatography (petroleum ether/ethyl acetate=20/1) to obtain the title compound (223 mg).

[0685] b) Preparation of (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N,N-dimethyl benzenesulfonamide N-butanol (10 ml), 2-((2,5-dichloropyrimidin-4-yl)amino)-N,N-dimethyl benzenesulfonamide (223 mg), 0.25 ml of trifluoroacetic acid, and (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (115 mg) are sequentially added to a reaction flask, and reacted at 110° C. for 5 h. After the reaction is completed, the reactant is concentrated to dryness. The residue is added with 20 ml of ethyl acetate, and then washed with 1M aqueous sodium hydroxide solution (10 ml) for three times. The organic phase is concentrated to dryness, and purified by column chromatography (dichloromethane/methanol=20/1) to obtain the title compound (180 mg).

[0686] .sup.1H NMR (400 MHz, CDCl.sub.3) δ 9.43 (s, 1H), 8.54 (dd, J=8.4, 1.1 Hz, 1H), 8.12 (s, 1H), 7.87 (dd, J=8.0, 1.6 Hz, 1H), 7.56 (m, J=8.7, 7.4, 1.6 Hz, 1H), 7.31 (d, J=6.5 Hz, 2H), 7.24 (d, J=8.2 Hz, 1H), 7.13 (s, 1H), 7.04 (d, J=8.8 Hz, 1H), 3.36-3.15 (m, 5H), 2.87 (m, 1H), 2.75 (m, 9H), 2.38 (m, 2H), 2.09-1.92 (m, 4H), 1.57 (m, 2H). MS(ESI+): 541.2 (M+H).

Example 2 (S)-3-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N,N-dimethyl benzenesulfonamide

[0687] ##STR00321##

[0688] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 3-amino-N,N-dimethyl benzenesulfonamide.

[0689] .sup.1H NMR (400 MHz, CDCl.sub.3) δ8.59 (s, 1H), 8.10 (s, 1H), 8.02 (ddd, J=5.5, 3.5, 2.3 Hz, 1H), 7.93-7.88 (m, 1H), 7.56-7.49 (m, 2H), 7.31 (s, 1H), 7.24 (dd, J=8.0, 2.3 Hz, 1H), 7.19 (s, 1H), 7.02 (d, J=8.0 Hz, 1H), 3.36-3.11 (m, 5H), 2.85 (m, 1H), 2.73 (m, 9H), 2.35 (m, 2H), 2.08-1.92 (m, 4H), 1.55 (m, 2H). MS(ESI+): 541.2 (M+H).

Example 3 (S)-4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N,N-dimethyl benzenesulfonamide

[0690] ##STR00322##

[0691] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 4-amino-N,N-dimethyl benzenesulfonamide.

[0692] .sup.1H NMR (400 MHz, CDCl.sub.3) δ8.11 (s, 1H), 7.87-7.79 (m, 2H), 7.73 (d, J=8.6 Hz, 2H), 7.47 (d, J=2.2 Hz, 1H), 7.41 (d, J=12.3 Hz, 2H), 7.13 (dd, J=8.1, 2.3 Hz, 1H), 7.04 (d, J=8.1 Hz, 1H), 3.48-3.14 (m, 5H), 2.85 (m, 1H), 2.71 (m, 9H), 2.44 (m, 2H), 2.04 (m, 4H), 1.56 (m, 2H). MS(ESI+): 541.2 (M+H).

Example 4 (S)-5-chloro-N.SUP.2.-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)-N.SUP.4.-(2-(pyrrolidin-1-ylsulfo)phenyl)pyrimidine-2,4-diamine

[0693] ##STR00323##

[0694] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 1-(2-aminophenylsulfone)pyrrolidine.

[0695] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 9.43 (s, 1H), 9.32 (s, 1H), 8.52 (s, 1H), 8.27 (s, 1H), 7.88 (dd, J=8.0, 1.5 Hz, 1H), 7.75-7.61 (m, 1H), 7.36 (dd, J=12.0, 4.7 Hz, 2H), 7.28 (d, J=7.9 Hz, 1H), 6.99 (d, J=8.2 Hz, 1H), 3.14 (t, J=6.7 Hz, 5H), 2.89 (s, 6H), 2.73-2.59 (m, 2H), 2.05 (s, 2H), 1.79 (s, 4H), 1.73-1.57 (m, 4H), 1.45 (s, 2H). MS(ESI+): 567.2 (M+H).

Example 5 (S)-5-chloro-N.SUP.2.-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)-N.SUP.4.-(3-(pyrrolidin-1-ylsulfo)phenyl)pyrimidine-2,4-diamine

[0696] ##STR00324##

[0697] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 3-(1-pyrrolylsulfonyl)aniline.

[0698] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 9.27 (s, 1H), 9.19 (s, 1H), 8.24 (t, J=8.3 Hz, 1H), 8.19 (s, 1H), 7.89 (d, J=1.7 Hz, 1H), 7.55 (ddd, J=11.0, 7.8, 4.7 Hz, 2H), 7.38 (d, J=1.8 Hz, 1H), 7.25 (d, J=8.0 Hz, 1H), 6.94 (d, J=8.2 Hz, 1H), 3.17 (t, J=6.7 Hz, 5H), 3.04-2.76 (m, 6H), 2.65-2.54 (m, 2H), 2.06 (s, 2H), 1.80 (s, 4H), 1.69-1.58 (m, 4H), 1.42 (s, 2H). MS(ESI+): 567.2 (M+H).

Example 6 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)(pyrrolidin-1-yl)methanone

[0699] ##STR00325##

[0700] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-aminophenyl)(pyrrolidin-1-yl)methanone.

[0701] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 9.67 (s, 1H), 9.27 (s, 1H), 8.32 (d, J=8.2 Hz, 1H), 8.17 (s, 1H), 7.56 (d, J=7.6 Hz, 1H), 7.45 (dd, J=8.2, 4.7 Hz, 2H), 7.30 (d, J=8.0 Hz, 1H), 7.19 (t, J=7.5 Hz, 1H), 6.97 (d, J=8.2 Hz, 1H), 3.50-3.41 (m, 5H), 2.84 (s, 6H), 2.59 (d, J=10.1 Hz, 2H), 2.03 (s, 2H), 1.81 (m, 8H), 1.45 (s, 2H). MS(ESI+): 531.3 (M+H).

Example 7 (S)-3-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N,N-dimethylfuran-2-carboxamide

[0702] ##STR00326##

[0703] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 3-amino-N,N-dimethylfuran-2-carboxamide.

[0704] .sup.1H NMR (400 MHz, CDCl.sub.3) δ10.67 (s, 1H), δ 8.04 (s, 1H), 7.55 (d, J=2.0 Hz, 1H), 7.49-7.32 (m, 3H), 7.23 (dd, J=8.0, 2.3 Hz, 1H), 7.07 (d, J=8.1 Hz, 1H), 3.46-3.11 (m, 10H), 2.95-2.68 (m, 5H), 2.40 (m, 2H), 2.03 (m, 4H), 1.60 (m, 2H). MS(ESI+): 495.2 (M+H).

Example 8 (S)-5-chloro-4-(2-isopropoxyl)anilino-2-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine

[0705] ##STR00327##

[0706] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-(1-methylethoxyl)aniline.

[0707] .sup.1H NMR (400 MHz, CDCl.sub.3) δ 8.47 (d, J=8.1 Hz, 1H), 8.05 (d, J=3.6 Hz, 2H), 7.42 (s, 1H), 7.30 (s, 1H), 7.16 (s, 1H), 7.04 (dd, J=17.9, 8.1 Hz, 2H), 6.93 (dd, J=15.4, 7.8 Hz, 2H), 4.70-4.54 (m, 1H), 3.54-3.00 (m, 5H), 2.96-2.68 (m, 4H), 2.38 (m, 2H), 2.03 (m, 4H), 1.55 (m, 2H), 1.41 (m, 6H). MS(ESI+): 492.2 (M+H).

Example 9 (S)-4-(benzo[d][1,3]dioxo-4-yl)-5-chloro-2-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine

[0708] ##STR00328##

[0709] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 4-amino-1,3-benzodioxole.

[0710] .sup.1H NMR (400 MHz, CDCl.sub.3) δ 8.04 (s, 1H), 7.51 (d, J=8.3 Hz, 1H), 7.36 (d, J=2.4 Hz, 1H), 7.29 (s, 1H), 7.25-7.19 (m, 1H), 7.00 (d, J=7.8 Hz, 2H), 6.83 (t, J=8.1 Hz, 1H), 6.71 (d, J=7.7 Hz, 1H), 5.99-0.93 (m, 2H), 3.56-3.05 (m, 5H), 2.85 (m, 1H), 2.71 (m, 3H), 2.37 (m, 2H), 2.03 (m, 4H), 1.60-1.47 (m, 2H). MS(ESI+): 478.2 (M+H).

Example 10 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide

[0711] ##STR00329##

[0712] a) (2-((2,5-dichloropyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide

[0713] 10 ml of anhydrous N,N-dimethylformamide, (2-aminophenyl)dimethyl phosphine oxide (169 mg), and 2,4,5-trichloropyrimidine (183 mg) are sequentially added to a reaction flask, added with sodium hydride (120 mg, 60%) at 0° C., and reacted at 0° C. for 3 h. After the reaction is completed, 20 ml of water is added for quenching. The reaction solution is extracted with 20 ml of ethyl acetate. The organic phase is concentrated to dryness. The crude product is purified by column chromatography (petroleum ether/ethyl acetate=20/1) to obtain the title compound (200 mg).

[0714] b) (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide

[0715] 10 ml of N-butanol, (2-((2,5-dichloropyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide (158 mg), p-toluenesulfonic acid monohydrate (190 mg), (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (115 mg) are sequentially added to a reaction flask, and reacted at 110° C. for 5 h. After the reaction is completed, the reactant is concentrated to dryness. The residue is added with 20 ml of ethyl acetate, and then washed with 1M aqueous sodium hydroxide solution (10 ml) for three times. The organic phase is concentrated to dryness, and purified by column chromatography (dichloromethane/methanol=20/1) to obtain the title compound (115 mg).

[0716] .sup.1H NMR (400 MHz, CDCl.sub.3) δ 10.88 (s, 1H), 8.62-8.54 (m, 1H), 8.08 (s, 1H), 7.51-7.43 (m, 1H), 7.37 (d, J=2.3 Hz, 1H), 7.31 (m, 2H), 7.22 (s, 1H), 7.15 (m, 1H), 7.04 (d, J=8.1 Hz, 1H), 3.45-3.19 (m, 5H), 2.91-2.68 (m, 4H), 2.37 (m, 2H), 2.02 (m, 4H), 1.84 (m, 6H), 1.56 (m, 2H). MS(ESI+): 510.2 (M+H).

Example 11 (S)-2-(3-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)acetonitrile

[0717] ##STR00330##

[0718] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 3-aminobenzeneacetonitrile.

[0719] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 9.17 (s, 1H), 8.91 (s, 1H), 8.28 (s, 1H), 8.16 (d, J=17.6 Hz, 1H), 7.68 (t, J=10.8 Hz, 1H), 7.60 (s, 1H), 7.37 (t, J=7.9 Hz, 1H), 7.29 (d, J=8.0 Hz, 1H), 7.12 (d, J=7.8 Hz, 1H), 6.98-6.88 (m, 1H), 4.03 (m, 2H), 2.84 (s, 1H), 2.66 (s, 4H), 2.39 (m, 4H), 1.91 (s, 2H), 1.72 (s, 4H), 1.46 (s, 2H). MS(ESI+): 473.2 (M+H).

Example 12 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylbenzamide

[0720] ##STR00331##

[0721] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-N-methylbenzamide.

[0722] .sup.1H NMR (400 MHz, Chloroform-d) δ 11.02 (s, 1H), 8.74-8.48 (m, 1H), 8.08 (s, 1H), 7.51 (dd, J=8.0, 1.5 Hz, 1H), 7.43 (ddd, J=8.7, 7.3, 1.5 Hz, 1H), 7.36 (d, J=2.3 Hz, 1H), 7.26-7.22 (m, 1H), 7.14-6.93 (m, 3H), 6.55 (m, 1H), 3.11 (m, 4H), 3.02 (m, 3H), 2.85 (m, 2H), 2.77-2.66 (m, 3H), 2.30 (m, 2H), 1.95 (m, 4H), 1.51 (m, 2H). MS(ESI+): 491.2 (M+H).

Example 13 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)benzamide

[0723] ##STR00332##

[0724] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-benzamide.

[0725] .sup.1H NMR (400 MHz, CDCl.sub.3) δ 11.18 (s, 1H), 8.67 (dd, J=8.4, 1.1 Hz, 1H), 8.08 (s, 1H), 7.60 (dd, J=7.9, 1.6 Hz, 1H), 7.47 (ddd, J=8.7, 7.3, 1.6 Hz, 1H), 7.39 (d, J=2.3 Hz, 1H), 7.28 (d, J=2.4 Hz, 1H), 7.18-7.08 (m, 2H), 7.04 (d, J=8.1 Hz, 1H), 3.48-3.12 (m, 5H), 2.93-2.65 (m, 5H), 2.38-2.02 (m, 7H), 1.56 (m, 2H). MS(ESI+): 477.2 (M+H).

Example 14 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methyl benzenesulfonamide

[0726] ##STR00333##

[0727] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-N-methyl benzenesulfonamide.

[0728] .sup.1H NMR (400 MHz, CDCl.sub.3) δ 8.06 (s, 1H), 7.53 (d, J=2.3 Hz, 1H), 7.49 (dd, J=8.2, 1.6 Hz, 1H), 7.24-7.11 (m, 3H), 7.03 (s, 1H), 6.59 (dd, J=8.2, 1.1 Hz, 1H), 6.47 (ddd, J=8.2, 7.1, 1.1 Hz, 1H), 5.02 (s, 1H), 3.57 (s, 3H), 3.35-3.04 (m, 5H), 2.95 (m, 2H), 2.77 (m, 2H), 2.37 (m, 2H), 2.01-1.93 (m, 4H), 1.62 (m, 2H). MS(ESI+): 527.2 (M+H).

Example 15 (S)-2-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)propan-2-ol

[0729] ##STR00334##

[0730] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-(2-aminophenyl)propan-2-ol.

[0731] .sup.1H NMR (400 MHz, CDCl.sub.3) δ 9.96 (s, 1H), 8.25 (dd, J=8.1, 1.4 Hz, 1H), 8.02 (s, 1H), 7.31 (m, 4H), 7.08 (m, 2H), 7.00 (d, J=7.8 Hz, 1H), 3.41-3.08 (m, 5H), 2.96-2.63 (m, 5H), 2.34 (m, 2H), 1.99 (m, 4H), 1.70 (s, 6H), 1.58-1.44 (m, 2H). MS(ESI+): 492.2 (M+H).

Example 16 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluorobenzamide

[0732] ##STR00335##

[0733] a) 2-((2,5-dichloropyrimidin-4-yl)amino)-5-fluoro-benzamide 2,4,5-trichloropyrimidine (1.33 mmol), 2-amino-5-fluoro-benzamide (1.1 mmol) and tetrahydrofuran (10 mL) are added into a 100 mL three-necked flask, stirred and cooled to −20° C., added dropwise with a tetrahydrofuran solution of lithium hexamethyldisilazide (1.65 mmol, 1 mol/L), heated naturally to room temperature and reacted for 8 h. After the reaction is completed, the resolution solution is quenched with a saturated ammonium chloride solution, and extracted with 30 mL of ethyl acetate and 30 mL of water.

[0734] An organic phase is dried with anhydrous sodium sulfate and concentrated to dryness under reduced pressure to obtain the title compound (470 mg). MS(ESI+): 300.9 (M+H).

[0735] b) (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluorobenzamide

[0736] 2-((2,5-dichloropyrimidin-4-yl)amino)-5-fluoro-benzamide (0.9 mmol), (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (1.08 mmol), tris(dibenzylideneacetone) dipalladium (0.09 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamine)-biphenyl (0.27 mmol), cesium carbonate (1.8 mmol), 2-methyltetrahydrofuran (10 mL) and water (5 mL) are added to a 50 mL three-necked flask. Nitrogen protection is performed. The reaction is then performed at 76° C. for 24 h. The aqueous phase is extracted with 30 mL of ethyl acetate, and an organic layer is concentrated to dryness under reduced pressure, and purified with silica-gel column chromatography to obtain 28 mg of the title compound.

[0737] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.59 (s, 1H), 9.35 (s, 1H), 8.76 (s, 1H), 8.35 (s, 1H), 8.25 (s, 1H), 7.88 (s, 1H), 7.69 (dd, J=9.7, 3.0 Hz, 1H), 7.43 (d, J=1.9 Hz, 1H), 7.38-7.28 (m, 2H), 7.04 (d, J=8.2 Hz, 1H), 2.96-2.71 (m, 7H), 2.68-2.55 (m, 2H), 2.08 (br, 2H), 1.78 (br, 4H), 1.47 (br, 2H). MS(ESI+): 495.2 (M+H).

Example 17 (S)-5-chloro-N.SUP.4.-(2-(5-methyloxazol-2-yl)phenyl)-N.SUP.2.-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine

[0738] ##STR00336##

[0739] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-(5-methyl-2-oxazolyl)aniline.

[0740] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.50 (s, 1H), 9.37 (s, 1H), 8.95 (d, J=7.3 Hz, 1H), 8.26 (s, 1H), 7.99 (dd, J=7.9, 1.3 Hz, 1H), 7.48-7.39 (m, 2H), 7.35 (d, J=8.0 Hz, 1H), 7.25-7.15 (m, 2H), 7.02 (d, J=8.1 Hz, 1H), 2.96-2.80 (m, 2H), 2.69-2.54 (m, 7H), 2.43 (s, 3H), 1.92 (br, 2H), 1.71 (br, 4H), 1.52 (br, 2H). MS(ESI+): 515.2 (M+H).

Example 18 (S)—N.SUP.4.-(2-(1H-imidazol-2-yl)phenyl)-5-chloro-N.SUP.2.-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine

[0741] ##STR00337##

[0742] a) Preparation of N-(2(1H-imidazol-2-yl)phenyl)-2,5-dichloropyrimidin-4-amine

[0743] 2-(1H-imidazol-2-yl)aniline (200 mg) and 2,4,5-trichloropyrimidine (200 mg), and N,N-diisopropylethylamine (390 mg) are sequentially added to a reaction flask, and reacted in an oil bath at 80° C. for 5.0 h. After the reaction is completed, water (50 ml) is added. The aqueous layer is extracted with ethyl acetate (5 ml*3). Organic layers are merged, dried with anhydrous sodium sulfate, concentrated under reduced pressure to dryness, and purified by column chromatography (petroleum ether/ethyl acetate=5/1) to obtain the title compound (152 mg).

[0744] b) Preparation of 2,5-dichloro-N-(2-(1-(tetrahydro-2H-pyran-2-yl)-1H-imidazol-2-yl)phenyl)pyrimidin-4-amine

[0745] N-(2-(1H-imidazol-2-yl)phenyl)-2,5-dichloropyrimidin-4-amine (150 mg), dihydropyran (84 mg), p-toluenesulfonic acid (19 mg), and ethyl acetate (10 ml) are sequentially added to a reaction flask. The reaction is performed at 50° C. for 3.5 h. After the reaction is completed, the organic layer is washed with saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated to dryness under reduced pressure. The crude product is purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (120 mg).

[0746] c) Preparation of 5-chloro-N.sup.2—((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)-N.sup.4-(2-(1-(tetrahydro-2H-pyran-2-yl)-1H-imidazol-2-yl)phenyl)pyrimidine-2,4-diamine

[0747] (2,5-dichloro-N-(2-(1-(tetrahydro-2H-pyran-2-yl)-1H-imidazol-2-yl)phenyl)pyrimidine-4-amine) (120 mg), 5((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine) (185 mg), tris(dibenzylideneacetone) dipalladium(0)(48 mg), 2-dicyclohexylphosphino-2′-(N,N-dimethylamine)-biphenyl(20 mg), cesium carbonate (460 mg), and N,N-dimethylformamide (9 ml) are sequentially added to a reaction flask. Nitrogen replacement is performed for five times. A microwave reaction is performed at 130° C. for 1 h. After the reaction is completed, the solid is removed by suction filtration, and the filter cake is washed with dichloromethane. Organic layers are merged, dried with anhydrous sodium sulfate, and concentrated under reduced pressure to dryness. The crude product is purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (95 mg).

[0748] d) Preparation of (S)—N.sup.4-(2-(1H-imidazol-2-yl)phenyl)-5-chloro-N.sup.2-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine

[0749] 5-chloro-N.sup.2—((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)-N.sup.4-(2-(1-(tetrahydro-2H-pyran-2-yl)-1H-imidazol-2-yl)phenyl)pyrimidine-2,4-diamine (95 mg), camphorsulfonic acid (187 mg), and dichloromethane/methanol (5 ml: 5 ml) are sequentially added to a reaction flask, and stirred and stands overnight at room temperature. After the reaction is completed, water is added for extraction. The organic phase is dried with anhydrous sodium sulfate. The solid substance obtained by drying under reduced pressure. The solid substance is purified by silica-gel column chromatography to obtain the title compound (15 mg).

[0750] .sup.1H NMR (400 MHz, CDCl.sub.3) δ 12.17 (s, 1H), 8.75-8.58 (m, 2H), 8.07 (s, 1H), 7.58 (dd, J=7.9, 1.3 Hz, 1H), 7.35 (d, J=2.0 Hz, 1H), 7.32-7.28 (m, 1H), 7.25-7.14 (m, 3H), 7.11 (d, J=7.7 Hz, 1H), 7.01-6.94 (m, 2H), 3.06 (s, 4H), 2.71 (m, 5H), 2.23 (m, 4H), 1.56-1.48 (m, 2H), 1.45 (s, 2H). MS(ESI+): 500.2 (M+H).

Example 19 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluoro-N-methylhenzamide

[0751] ##STR00338##

[0752] a) Preparation of 2-((2,5-dichloropyrimidin-4-yl)amino)-5-fluoro-N-methyl-benzamide

[0753] 2,4,5-trichloropyrimidine (1.2 mmol), 2-amino-5-fluoro-N-methyl-benzamide (1.0 mmol) and tetrahydrofuran (10 mL) are added into a 100 mL three-necked flask, added dropwise with lithium hexamethyldisilazide (2.5 mmol) at −20° C., heated to room temperature after dropping, and stirred for 8 h. After the reaction of the raw materials is completed, the reaction is stopped. A saturated ammonium chloride solution is added for quenching. 30 mL of ethyl acetate and 30 mL of water are added to the reaction solution, stirred and extracted. The aqueous layer is extracted again with 30 mL of ethyl acetate. Organic phases are merged, washed sequentially with water and saturated sodium chloride solution, and dried with anhydrous sodium sulfate. After filtration, the filtrate is concentrated under reduced pressure to dryness to obtain the title compound (250 mg).

[0754] b) Preparation of (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluoro-N-methylbenzamide

[0755] 2-((2,5-dichloropyrimidin-4-yl)amino)-5-fluoro-N-methyl-benzamide (0.38 mmol), (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (0.38 mmol), tris(dibenzylideneacetone) dipalladium (0.04 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamine)-biphenyl (0.12 mmol), cesium carbonate (0.76 mmol), 2-methyltetrahydrofuran (10 mL) and water (5 mL) are added to a 50 mL three-necked flask. Nitrogen protection is performed. The reaction is then performed at 76° C. for 24 h. The aqueous phase is extracted with 30 mL of ethyl acetate, and an organic layer is concentrated to dryness, and purified with silica-gel column chromatography to obtain the title compound (53 mg).

[0756] .sup.1H NMR (400 MHz, DMSO-d6) δ 11.31 (s, 1H), 9.31 (s, 1H), 8.82 (d, J=4.6 Hz, 1H), 8.75-8.66 (m, 1H), 8.20 (s, 1H), 7.62 (dd, J=9.6, 3.0 Hz, 1H), 7.41 (d, J=2.0 Hz, 1H), 7.36-7.26 (m, 2H), 7.01 (d, J=8.2 Hz, 1H), 2.96-2.76 (m, 5H), 2.70-2.53 (m, 7H), 1.93 (m, 2H), 1.72 (br, 4H), 1.51 (m, 2H). MS(ESI+): 509.1 (M+H).

Example 20 (S)-4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylnicotinamide

[0757] ##STR00339##

[0758] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 4-amino-N-methylnicotinamide. MS(ESI+): 492.2 (M+H).

Example 21 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylnicotinamide

[0759] ##STR00340##

[0760] a) Preparation of ethyl 2-((2,5-dichloropyrimidin-4-yl)amino)nicotinate

[0761] Sodium hydride (130.83 mg) is added at 0° C. to a N,N dimethylformamide solution (15 mL) in which ethyl 2-aminonicotinate (543.59 mg) is dissolved. The reaction mixture is stirred for 20 min. 2,3,5-trichloropyrimidine (500 mg) is added at 0° C. The reaction mixture is stirred at 0° C. for 3 h. The reaction solution is poured into water (100 mL), and extracted with ethyl acetate (100 mL). The organic phase is washed with a saturated sodium chloride solution (100 mL*3), dried with anhydrous sodium sulfate, and concentrated to dryness under reduced pressure. The crude product is purified by silica-gel column chromatography (petroleum ether:ethyl acetate=1:1) to obtain the title compound (0.2 g).

[0762] b) Preparation of ethyl (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)nicotinate

[0763] (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (220.68 mg) and p-toluenesulfonic acid (219.97 mg) are added at 20° C. to a dimethylsulfoxide solution (10 ml) in which ethyl 2-((2,5-dichloropyrimidine-4-yl)amino)nicotinate (200 mg) is dissolved. The reaction mixture is stirred in microwaves at 150° C. for 1 h. The reaction solution is poured into water (100 mL), and then extracted with dichloromethane (100 mL). The organic phase is washed with a saturated sodium chloride solution (100 mL*3), and spin-dried with anhydrous sodium sulfate. The product is purified by silica-gel plate chromatography (dichloromethane:methanol=10:1) to obtain the title compound (0.2 g).

[0764] c) Preparation of (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)nicotinic acid

[0765] Ethyl (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)nicotinate (200 mg) is dissolved in methanol (10 mL) at 20° C., and added with sodium hydroxide (78.89 mg) and water (1 mL). The reaction mixture is stirred at 80° C. for 3 h. The reaction solution is concentrated to dryness to obtain the title compound (0.15 g).

[0766] d) Preparation of (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methyl nicotinamide

[0767] A 2M methylaminotetrahydrofuran solution (0.18 mL) and diisopropylethylamine (121.43 mg) are added at 20° C. to N,N dimethylformamide (5 mL) in which (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino) nicotinic acid (150 mg) is dissolved. The reaction mixture is stirred for 2 min. 2-(7-benzotriazole oxide)-N,N,N′,N′-tetramethylurea hexafluorophosphate (142.89 mg) is added. The reaction mixture is stirred at 20° C. for 3 h. The reaction solution is poured into water (100 mL), and then extracted with dichloromethane (100 mL). The organic phase is washed with a saturated sodium chloride solution (100 mL*3), dried with anhydrous sodium sulfate, and concentrated to dryness. The product is purified by silica-gel plate chromatography (dichloromethane:methanol=10:1) to obtain the title compound (20 mg).

[0768] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ11.37 (s, 1H), 9.35 (s, 1H), 9.02 (s, 1H), 8.59 (s, 1H), 8.27 (s, 1H), 8.24 (s, 1H), 7.89 (s, 1H), 7.44 (s, 1H), 7.24 (s, 1H), 6.96-7.05 (m, 1H), 3.17 (d, J=4.8 Hz, 1H), 2.70-2.98 (m, 9H), 1.97-2.16 (m, 2H), 1.77 (m, 4H), 1.41-1.56 (m, 2H), 1.24 (d, J=6.0 Hz, 2H). MS(ESI+): 492.2 (M+H).

Example 22 (S)-5-chloro-N.SUP.4.-(2-(isopropylsulfo)phenyl)-N.SUP.2.-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine

[0769] ##STR00341##

[0770] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-(isopropylsulfonyl)aniline.

[0771] .sup.1H NMR (400 MHz, CDCl.sub.3) δ 9.59 (s, 1H), 8.62-8.54 (m, 1H), 8.14 (s, 1H), 7.92 (d, J=6.9 Hz, 1H), 7.60 (t, J=7.4 Hz, 1H), 7.28 (d, J=9.1 Hz, 3H), 7.10-6.92 (m, 2H), 3.24 (dd, J=13.4, 6.6 Hz, 1H), 3.07 (m, 4H), 2.96-2.88 (m, 1H), 2.89-2.67 (m, 4H), 1.97 (m, 4H), 1.56 (m, 4H), 1.30 (t, J=11.9 Hz, 6H). MS(ESI+): 540.2 (M+H).

Example 23 (S)-5-chloro-N.SUP.4.-(2-(methylsulfonyl)phenyl)-N.SUP.2.-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine

[0772] ##STR00342##

[0773] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-(methylsulfonyl)aniline.

[0774] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 9.37 (m, 2H), 8.49 (d, J=7.4 Hz, 1H), 8.24 (m, 1H), 7.94 (d, J=7.9 Hz, 1H), 7.73 (t, J=7.8 Hz, 1H), 7.48-7.35 (m, 2H), 7.30 (d, J=7.9 Hz, 1H), 7.00 (d, J=8.1 Hz, 1H), 3.27 (s, 3H), 3.10 (m, 4H), 2.62 (m, 3H), 2.50 (m, 2H), 2.17 (m, 2H), 1.85 (m, 4H), 1.41 (d, J=8.1 Hz, 2H). MS(ESI+): 512.2 (M+H).

Example 24 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-cyclopropyl benzenesulfonamide

[0775] ##STR00343##

[0776] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-N-cyclopropyl benzenesulfonamide.

[0777] .sup.1H NMR (400 MHz, DMSO-d6) δ 9.43 (s, 1H), 9.28 (s, 1H), 8.49 (d, J=8.3 Hz, 1H), 8.27 (s, 2H), 7.87 (td, J=8.3, 1.6 Hz, 1H), 7.65 (ddd, J=8.6, 7.3, 1.7 Hz, 1H), 7.47 (d, J=2.3 Hz, 1H), 7.40-7.26 (m, 2H), 7.01 (d, J=8.1 Hz, 1H), 3.10 (s, 4H), 2.81 (dd, J=14.4, 7.6 Hz, 1H), 2.63 (s, 3H), 2.14 (tt, J=6.8, 3.5 Hz, 3H), 1.86 (d, J=6.4 Hz, 4H), 1.42 (s, 2H), 0.54-0.26 (m, 5H). MS(ESI+): 553.2 (M+H).

Example 25 (S)—N.SUP.4.-(2-(1H-1,2,4-triazol-5-yl)phenyl)-5-chloro-N.SUP.2.-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine

[0778] ##STR00344##

[0779] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-(1H-1,2,4-thiazol-5-yl)aniline.

[0780] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.48 (s, 1H), 9.34 (s, 1H), 8.82 (d, J=8.5 Hz, 1H), 8.69 (s, 1H), 8.22 (d, J=3.2 Hz, 2H), 8.15 (dd, J=7.9, 1.6 Hz, 1H), 7.46 (d, J=2.2 Hz, 1H), 7.45-7.30 (m, 2H), 7.21 (t, J=7.5 Hz, 1H), 7.03 (d, J=8.1 Hz, 1H), 2.84 (s, 7H), 2.61 (t, J=12.6 Hz, 2H), 2.05 (s, 2H), 1.77 (s, 4H), 1.49 (s, 2H). MS(ESI+): 501.2 (M+H).

Example 26 (S)-5-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylthiazole-4-carboxamide

[0781] ##STR00345##

[0782] a) Preparation of ethyl 5-((2,5-dichloropyrimidin-4-yl)amino)thiazole-4-carboxylate

[0783] ethyl 5-aminothiazole-4-carboxylate (1.27 mmol), 2,4,5-trichloropyrimidine (1.90 mmol) and tetrahydrofuran (10 mL) are added to a 100 mL single-necked flask. The mixture is stirred and cooled (the external temperature is −20° C.). Next, sodium hydride (3.8 mmol) is added to the reaction solution in batches. The reaction solution is gradually heated to room temperature and stirred for 8 h. After the reaction of the raw materials is completed, the reaction is stopped. A saturated ammonium chloride solution is added for quenching. 30 mL of ethyl acetate and 30 mL of water are added to the reaction solution, stirred and extracted. The aqueous layer is extracted again with 30 mL of ethyl acetate. Organic phases are merged, washed sequentially with water and saturated sodium chloride solution, and dried with anhydrous sodium sulfate. After filtration, the filtrate is concentrated to dryness to obtain the title compound (236 mg).

[0784] b) Preparation of ethyl (S)-5-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)thiazole-4-carboxylate

[0785] ethyl 5-((2,5-dichloropyrimidin-4-yl)amino)thiazole-4-carboxylate (0.31 mmol), (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (0.34 mmol), n-butanol (4 mL) and trifluoroacetic acid (0.1 mL) are added to a 10 mL microwave tube. After nitrogen protection, microwave reaction is performed at 120° C. for 2 h. The reactant is concentrated to dryness to obtain the title compound (196 mg).

[0786] MS(ESI+): 513.1 (M+H).

[0787] c) Preparation of (S)-5-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)thiazole-4-carboxylic acid

[0788] Ethyl (S)-5-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl]-amino)pyrimidin-4-yl)amino)thiazole-4-carboxylate (0.38 mmol), methanol (5 mL) and tetrahydrofuran (5 mL) are added to a 50 mL three-necked flask and stirred. A lithium hydroxide solution is added dropwise, stirred and stands overnight. After the reaction is completed, the reactant is desolvatized to dryness. 3 mL of water and 2N hydrogen chloride are added to the concentrated residue to adjust the pH to about 2 and freeze-dried to obtain the title compound. Proceed to the next step directly.

[0789] d) Preparation of (S)-5-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylthiazole-4-carboxamide

[0790] (S)-5-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo [7]annulen-2-yl)amino)pyrimidin-4-yl)amino)thiazole-4-carboxylic acid (0.16 mmol), a tetrahydrofuran solution of methylamine (0.24 mmol), triethylamine (0.32 mmol) and N,N-dimethyl formamide (5 mL) are added to a 50 mL single-necked flask and stirred at room temperature. Then, a BOP reagent (0.32 mmol) is then added and reacted for 1 h. After the reaction is completed, 30 mL of water and 30 mL of ethyl acetate are added, stirred and extracted. The organic layer is concentrated to dryness, and purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (37 mg).

[0791] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.10 (s, 1H), 9.44 (s, 1H), 8.71 (s, 1H), 8.57 (d, J=4.8 Hz, 1H), 8.32 (s, 1H), 7.47 (s, 1H), 7.33 (d, J=7.3 Hz, 1H), 7.12 (d, J=8.1 Hz, 1H), 3.06-2.97 (m, 2H), 2.89-2.60 (m, 10H), 2.24 (br, 2H), 1.87 (s, 4H), 1.50 (br, 2H). MS(ESI+): 498.1 (M+H).

Example 27 (S)-3-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylisoniamide

[0792] ##STR00346##

[0793] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 3-aminoisonicotinate.

[0794] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ9.98 (s, 1H), 9.47 (s, 1H), 8.46 (d, J=5.0 Hz, 1H), 8.25-8.38 (m, 2H), 7.85 (d, J=4.8 Hz, 1H), 7.40 (s, 1H), 7.25-7.32 (m, 1H), 6.98 (d, J=8.1 Hz, 1H), 3.91 (s, 3H), 2.81-2.93 (m, 2H), 2.89-2.60 (m, 7H), 1.81-1.96 (m, 2H), 1.65-1.77 (m, 4H), 1.44-1.59 (m, 2H). MS(ESI+): 493.2 (M+H).

Example 28 (S)-7-((5-chloro-2-(((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino))pyrimidin-4-yl)amino)-2-methylisoindolin-1-one

[0795] ##STR00347##

[0796] a) Preparation of 7-((2,5-dichloropyrimidin-4-yl)amino)-2-methylisoindolin-1-one

[0797] 7-amino-2-methylisoindolin-1-one (50 mg) and 2,4,5-trichloropyrimidine (113 mg) are dissolved in tetrahydrofuran (5 mL), cooled to −20° C., and then added with sodium hydride (37.2 mg). The reaction ends after 3 h. The reaction solution is poured into ice water for quenching, and then extracted with ethyl acetate. The ethyl acetate phase is concentrated to dryness and purified by column chromatography (dichloromethane/methanol=40:1) to obtain the title compound (65 mg). MS(ESI+): 308.96 (M+H).

[0798] b) Preparation of (S)-7-((5-chloro-2-(((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino))pyrimidin-4-yl)amino)-2-methylisoindolin-1-one 7-((2,5-dichloropyrimidin-4-yl)amino)-2-methylisoindolin-1-one (55 mg) and (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (41 mg) are dissolved in n-butanol (5 mL), added with trifluoroacetic acid (0.5 mL), heated under the protection of nitrogen at 120° C., and reacted for 8 h. After the reaction is completed, the reaction solution is added with 2 mL of saturated sodium bicarbonate solution. The organic phase is taken and concentrated to dryness, and purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (75 mg).

[0799] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.67 (s, 1H), 9.41 (s, 1H), 8.73 (d, J=8.3 Hz, 1H), 8.25 (s, 1H), 7.53-7.41 (m, 2H), 7.34 (d, J=8.2 Hz, 1H), 7.21 (d, J=7.5 Hz, 1H), 7.05 (d, J=8.1 Hz, 1H), 4.49 (s, 2H), 3.09 (s, 3H), 2.97-2.81 (m, 2H), 2.69-2.56 (m, 7H), 1.97 (s, 2H), 1.80-1.66 (m, 4H), 1.53 (s, 2H). MS(ESI+): 503.3 (M+H).

Example 29 (S)-7-((5-chloro-2-(((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino))pyrimidin-4-yl)amino)isoindolin-1-one

[0800] ##STR00348##

[0801] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 7-amino-isoindolin-1-one.

[0802] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.72 (s, 1H), 9.44 (s, 1H), 8.81 (s, 1H), 8.74 (d, J=8.3 Hz, 1H), 8.24 (d, J=8.5 Hz, 2H), 7.49 (d, J=7.0 Hz, 1H), 7.36 (d, J=7.7 Hz, 1H), 7.21 (d, J=7.5 Hz, 1H), 7.07 (d, J=8.1 Hz, 1H), 4.41 (s, 2H), 2.93-2.75 (m, 7H), 2.73-2.60 (m, 2H), 2.07 (s, 2H), 1.77 (d, J=6.0 Hz, 4H), 1.50 (s, 2H). MS(ESI+): 489.1 (M+H).

Example 30 (S)—N-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)methanesulfonamide

[0803] ##STR00349##

[0804] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with N-(2-aminophenyl) methanesulfonamide.

[0805] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 9.25 (s, 1H), 8.63 (s, 1H), 8.24 (s, 1H), 8.16 (s, 1H), 7.96 (d, J=6.9 Hz, 1H), 7.46-7.34 (m, 3H), 7.31-7.12 (m, 2H), 6.91 (d, J=8.1 Hz, 1H), 3.01-2.72 (m, 8H), 2.59 (d, J=11.3 Hz, 4H), 2.08 (s, 2H), 1.80 (s, 4H), 1.41 (s, 2H). MS(ESI+): 527.2 (M+H).

Example 31 2-((5-chloro-2-((3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]aza-7-yl)amino)pyrimidin-4-yl)amino)-N-methylbenzamide

[0806] ##STR00350##

[0807] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-N-methylbenzamide.

[0808] (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine in step b) is replaced with 3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-amine to obtain the target product.

[0809] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.58 (s, 1H), 9.35 (s, 1H), 8.74 (dd, J=12.7, 7.1 Hz, 2H), 8.16 (d, J=7.2 Hz, 1H), 7.76 (d, J=7.8 Hz, 1H), 7.52-7.41 (m, 2H), 7.35 (d, J=8.0 Hz, 1H), 7.15 (t, J=7.6 Hz, 1H), 7.01 (d, J=8.1 Hz, 1H), 3.89 (d, J=8.1 Hz, 4H), 2.91-2.59 (m, 12H), 1.63 (d, J=11.6 Hz, 2H), 1.52 (dt, J=11.8, 8.0 Hz, 2H). MS(ESI+): 507.2 (M+H).

Example 32 2-((5-chloro-2-((3-cyclopentyl-2,3,4,5-tetrahydro-1H-benzo(d)aza-7-yl)amino)pyrimidine-4-yl)amino)-N-methylbenzamide

[0810] ##STR00351##

[0811] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-N-methylbenzamide.

[0812] (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine in step b) is replaced with 3-cyclopentyl-2,3,4,5-tetrahydro-1H-benzo[d]aza-7-amine to obtain the target product.

[0813] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.60 (s, 1H), 9.39 (s, 1H), 8.75 (dd, J=11.5, 6.7 Hz, 2H), 8.24-8.19 (m, 1H), 7.76 (d, J=7.9 Hz, 1H), 7.48 (d, J=9.1 Hz, 2H), 7.40 (d, J=8.0 Hz, 1H), 7.15 (t, J=7.5 Hz, 1H), 7.04 (d, J=8.0 Hz, 1H), 3.18 (s, 1H), 2.96-2.75 (m, 11H), 1.88 (s, 2H), 1.62 (d, J=26.3 Hz, 2H), 1.51 (s, 4H). MS(ESI+): 491.2 (M+H).

Example 33 (S)-3-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylpicolinamide

[0814] ##STR00352##

[0815] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 3-amino-N-methyl-2-pyridine carboxamide. MS(ESI+): 492.2 (M+H).

Example 34 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-cyano-N-methylbenzamide

[0816] ##STR00353##

[0817] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-5-cyano-N-methylbenzamide.

[0818] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.98 (s, 1H), 9.47 (s, 1H), 8.97 (d, 2H), 8.28 (d, J=9.4 Hz, 1H), 8.24 (d, J=2.0 Hz, 1H), 7.83 (dd, J=8.8, 2.0 Hz, 1H), 7.42 (d, J=2.2 Hz, 1H), 7.30 (d, J=8.4 Hz, 1H), 7.04 (d, J=8.1 Hz, 1H), 2.90 (m, 1H), 2.83 (m, 4H), 2.63 (d, J=6.2 Hz, 3H), 2.56 (m, 4H), 1.93 (s, 2H), 1.71 (m, 4H), 1.52 (s, 2H). MS(ESI+): 516.1 (M+H).

Example 35 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methyl-5-(trifluoromethyl)benzamide

[0819] ##STR00354##

[0820] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-N-methyl-5-(trifluoromethyl)benzamide.

[0821] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.92 (s, 1H), 9.48 (s, 1H), 9.01 (m, 2H), 8.30 (s, 1H), 8.16 (d, J=7.6 Hz, 1H), 7.74 (d, J=8.9 Hz, 1H), 7.52 (d, J=1.5 Hz, 1H), 7.34 (d, J=8.1 Hz, 1H), 7.08 (d, J=8.2 Hz, 1H), 3.10 (s, 3H), 2.84 (d, J=4.4 Hz, 3H), 2.78-2.57 (m, 4H), 2.33 (s, 2H), 2.18 (s, 2H), 1.85 (s, 4H), 1.46 (s, 2H). MS(ESI+): 559.2 (M+H).

Example 36 (S)-5-chloro-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylbenzamide

[0822] ##STR00355##

[0823] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-5-chloro-N-methylbenzamide.

[0824] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.51 (s, 1H), 9.39 (s, 1H), 8.89 (d, J=4.5 Hz, 1H), 8.74 (d, J=8.7 Hz, 1H), 8.22 (d, J=10.7 Hz, 1H), 7.84 (d, J=2.5 Hz, 1H), 7.56-7.43 (m, 2H), 7.32 (d, J=7.9 Hz, 1H), 7.05 (d, J=8.2 Hz, 1H), 2.98 (m, 5H), 2.81 (d, J=4.5 Hz, 5H), 2.70-2.57 (m, 2H), 2.12 (s, 2H), 1.81 (s, 4H), 1.47 (s, 2H). MS(ESI+): 525.1 (M+H).

Example 37 (S)-2-((5-chloro-2-(((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino))pyrimidin-4-yl)amino)-5-methoxyl-N-methylbenzamide

[0825] ##STR00356##

[0826] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-5-methoxyl-N-methylbenzamide.

[0827] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.13 (s, 1H), 9.26 (s, 1H), 8.75 (d, J=4.5 Hz, 1H), 8.54 (d, J=8.7 Hz, 1H), 8.15 (s, 1H), 7.45 (d, J=1.8 Hz, 1H), 7.33-7.27 (m, 2H), 7.04 (dd, J=9.1, 2.9 Hz, 1H), 7.00 (d, J=8.2 Hz, 1H), 3.83 (s, 3H), 2.89-2.71 (m, 10H), 2.62-2.52 (m, 2H), 2.00 (br, 2H), 1.75 (br, 4H), 1.49 (br, 2H). MS(ESI+): 521.2 (M+H).

Example 38 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-(2-methoxyethyl)benzamide

[0828] ##STR00357##

[0829] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-N-(2-methoxyethyl)benzamide. MS(ESI+): 535.1 (M+H).

Example 39 2-((5-chloro-2-((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-(tetrahydrofuran-3-yl)benzamide

[0830] ##STR00358##

[0831] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-N-(tetrahydro-3-furyl)benzamide. MS(ESI+): 547.2 (M+H).

Example 40 (S)-5-chloro-N.SUP.4.-(2-(morpholinmethyl)phenyl)-N.SUP.2.-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine

[0832] ##STR00359##

[0833] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-(morpholin-4-methyl)aniline.

[0834] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.06 (s, 1H), 9.28 (s, 1H), 8.33-8.10 (m, 2H), 7.49 (s, 1H), 7.38-7.21 (m, 3H), 7.08 (t, J=7.3 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 3.61 (d, J=9.2 Hz, 6H), 3.10-2.75 (m, 6H), 2.67 (s, 1H), 2.59 (t, J=11.9 Hz, 2H), 2.40 (s, 4H), 2.09 (s, 2H), 1.79 (s, 4H), 1.44 (s, 2H). MS(ESI+): 533.2 (M+H).

Example 41 (S)—N-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)cyclopropanesulfonamide

[0835] ##STR00360##

[0836] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with N-(2-aminophenyl)cyclopropanesulfonamide.

[0837] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 9.27 (s, 1H), 8.56 (s, 1H), 8.18 (d, J=13.3 Hz, 1H), 7.98 (d, J=7.6 Hz, 1H), 7.48-7.36 (m, 2H), 7.31 (t, J=7.1 Hz, 1H), 7.24 (t, J=6.9 Hz, 2H), 6.92 (d, 1H), 3.02 (s, 6H), 2.78 (m, 1H), 2.57 (m, 3H), 2.09 (m, 2H), 1.82 (m, 4H), 1.40 (m, 2H), 0.84 (m, Hz, 4H). MS(ESI+): 553.2 (M+H).

Example 42 (S)-4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methyl-2-oxo-1,2-dihydropyridine-3-carboxamide

[0838] ##STR00361##

[0839] According to the preparation method of Example 1, 2-amino-, -dimethylbenzenesulfonamide in step a) is replaced with 4-amino-6-methoxyl-N-methylnicotinamide. This product is a demethyl byproduct of Preparation Example 44.

[0840] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.30 (s, 1H), 11.98 (s, 1H), 10.69 (d, 1H), 9.53 (s, 1H), 8.36 (s, 1H), 8.14 (d, 1H), 7.44 (m, 2H), 7.29 (d, 1H), 7.04 (d, 1H), 2.92-2.83 (m, 5H), 2.68-2.33 (m, 7H), 1.86 (m, 2H), 1.69 (m, 4H), 1.54 (m, 2H). MS(ESI+): 508.2 (M+H).

Example 43 (S)-4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-6-methoxyl-N-methylnicotinamide

[0841] ##STR00362##

[0842] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 4-amino-6-methoxyl-N-methylnicotinamide.

[0843] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.63 (s, 1H), 8.36 (s, 1H), 8.30 (d, 2H), 7.36 (m, 2H), 7.13 (d, 1H), 6.98 (d, 1H), 6.26 (s, 1H), 4.00 (s, 3H), 3.07 (s, 3H), 2.90 (m, 4H), 2.74 (m, 2H), 2.50 (s, 2H), 1.87 (m, 3H), 1.69 (m, 4H), 1.54 (m, 2H). MS(ESI+): 522.3 (M+H).

Example 44 (S)-4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-2-methoxyl-N-methylnicotinamide

[0844] ##STR00363##

[0845] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 4-amino-2-methoxyl-N-methylnicotinamide.

[0846] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.21 (s, 1H), 9.48 (s, 1H), 8.65 (d, 1H), 8.53 (m, 1H), 8.32 (s, 1H), 8.12 (d, 1H), 7.44 (m, 1H), 7.33 (d, 1H), 7.04 (d, 1H), 3.96 (s, 3H), 3.98-2.83 (m, 6H), 2.40-2.61 (m, 5H), 1.85 (m, 3H), 1.69 (m, 4H), 1.54 (m, 2H). MS(ESI+): 522.3 (M+H).

Example 45 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-hydroxyl-N-methylbenzamide

[0847] ##STR00364##

[0848] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-5-hydroxyl-N-methylbenzamide.

[0849] .sup.1HNMR (400 MHz, DMSOd.sub.6)δ10.85 (s, 1H), 9.57 (s, 1H), 9.22 (s, 1H), 8.63 (d, J=4.6 Hz, 1H), 8.38 (d, J=8.8 Hz, 1H), 8.12 (s, 1H), 7.45 (s, 1H), 7.32 (d, J=7.3 Hz, 1H), 7.10 (d, J=2.7 Hz, 1H), 6.02-6.91 (m, 2H), 3.00-2.70 (m, 7H), 2.65-2.56 (m, 2H), 2.14-1.94 (m, 2H), 1.78 (s, 4H), 1.58-1.43 (m, 2H), 1.23 (s, 3H). MS(ESI+): 507.3 (M+H).

Example 46 2-((5-chloro-2-((3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]aza-7-yl)amino)pyrimidin-4-yl)amino)-5-fluoro-N-methylbenzamide

[0850] ##STR00365##

[0851] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 2-amino-5-fluoro-N-methylbenzamide.

[0852] (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine in step b) is replaced with 3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-amine to obtain the target product. .sup.1HNMR (400 MHz, DMSO-d.sub.6)δ11.31 (s, 1H), 9.32 (s, 1H), 8.82 (s, 1H), 8.65 (s, 1H), 8.19 (s, 1H), 7.63 (d, 1H), 0.39 (d, 1H), 7.30 (d, 2H), 7.00 (d, 1H), 3.87 (m, 2H), 3.87 (m, 2H), 2.81-2.78 (m, 5H), 2.70 (m, 3H), 2.65 (m, 4H), 1.63-1.56 (m, 2H), 1.54-1.45 (m, 2H). MS(ESI+): 525.2 (M+H).

Example 47 (S)-(6-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)quinoxalin-5-yl)dimethyl phosphine oxide

[0853] ##STR00366##

[0854] a) Preparation of 5-iodoquinoxaline-6-amine

[0855] Quinoxaline-6-amine (2900 mg) is dissolved in a mixture solution of 50 ml of dichloromethane and 80 ml of saturated sodium bicarbonate, added dropwise with iodine chloride (3900 mg) at 0° C., and reacted for 1 h. Liquid separation is then performed. The organic phase is subjected to rotary evaporation under reduced pressure. The resulting crude product is purified by silica-gel column chromatography to obtain the title compound (3 g).

[0856] b) Preparation of (6-aminoquinoxalin-5-yl)dimethyl phosphine oxide

[0857] 5-iodoquinoxaline-6-amine (2710 mg), dimethyl phosphine oxide (780 mg), potassium phosphate (3180 mg), palladium acetate (112 mg), 4,5-bisdiphenyl phosphine-9,9-dimethylxanthene (518 mg), 30 ml of N,N-dimethylformamide and 6 ml of water are sequentially added to a 100 ml three-necked flask. Nitrogen replacement is performed for 3 times. The reaction is then performed at 120° C. for 24 h. After the reaction is completed, 200 ml of dichloromethane and 100 ml of water are added. Liquid separation is performed. The resulting organic phase is filtered, concentrated under reduced pressure to dryness, and purified by reverse-phase column chromatography (acetonitrile/water) to obtain the title compound (1.3 g).

[0858] c) Preparation of 6-((2,5-dichloropyrimidin-4-yl)amino)quinoxalin-5-yl)dimethyl phosphine oxide

[0859] (6-aminoquinoxalin-5-yl)dimethyl phosphine oxide (183 mg) and 2,4,5-trichloropyrimidine (221 mg) are dissolved in THF (5 mL), cooled to −20° C., and then added with sodium hydride (80 mg, 60%). The mixture is transfered to room temperature after 30 min and continued to react for 5 h. The reaction solution is quenched by adding 5 mL of saturated ammonium chloride solution, and then extracted with 10 mL of ethyl acetate. The organic phase is concentrated to dryness, and purified by silica-gel column chromatography to obtain the title compound (120 mg).

[0860] d) Preparation of (S)-(6-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)quinoxalin-5-yl)dimethyl phosphine oxide

[0861] 6-((2,5-dichloropyrimidin-4-yl)amino)quinoxalin-5-yl)dimethyl phosphine oxide (25 mg) and (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (16.5 mg) are dissolved in n-butanol (3 mL), added with trifluoroacetic acid (0.3 mL), and reacted at 120° C. for 4 h. The reaction solution is neutralized by adding 2M sodium hydroxide solution (2 mL), and separated. The aqueous phase is extracted with ethyl acetate. The organic phases are merged, and concentrated to dryness and purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (35 mg).

[0862] .sup.1H NMR (400 MHz, CDCl3) δ 12.78 (d, J=3.0 Hz, 1H), 9.17 (dd, J=9.6, 4.1 Hz, 1H), 8.83-8.65 (m, 2H), 8.17 (d, J=2.6 Hz, 1H), 8.09 (d, J=9.5 Hz, 1H), 7.36-7.28 (m, 2H), 7.07 (d, J=8.2 Hz, 2H), 3.09 (m, 4H), 2.89 (m, 1H), 2.82-2.60 (m, 4H), 2.33 (m, 2H), 2.20-2.03 (m, 6H), 1.96 (m, 4H), 1.55 (m, 2H). MS(ESI+): 562.2 (M+H).

Example 48 (S)-6-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylquinoxaline-5-carboxamide

[0863] ##STR00367##

[0864] a) Preparation of 6-((2,5-dichloropyrimidin-4-yl)amino)-N-methylquinoxaline-5-carboxamide

[0865] 6-amino-N-methylquinoxaline-5-carboxamide (25 mg) and 2,4,5-trichloropyrimidine (68 mg) are dissolved in tetrahydrofuran (5 mL), cooled to −20° C., and then added with sodium hydride (15 mg). The mixture is transferred to room temperature after 30 min and continued to react for 5 h. The reaction solution is quenched by adding 5 mL of saturated ammonium chloride solution. A tetrahydrofuran layer is taken. The aqueous phase is extracted with ethyl acetate. The organic phases are merged, and concentrated to dryness and purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (27 mg). MS: ½[M+H].sup.+: 175.1.

[0866] b) Preparation of (S)-6-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-N-methylquinoxaline-5-carboxamide

[0867] 6-((2,5-dichloropyrimidin-4-yl)amino)-N-methylquinoxaline-5-carboxamide (25 mg) and (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (16.5 mg) are dissolved in n-butanol (3 mL), added with trifluoroacetic acid (0.3 mL), and reacted at 120° C. for 4 h. The reaction solution is neutralized by adding 2M sodium hydroxide solution (2 mL), and separated. The aqueous phase is extracted with ethyl acetate. The organic phases are merged, and concentrated to dryness and purified by column chromatography (dichloromethane/methanol=20:1) to obtain the title compound (1.5 mg). MS(ESI+): 543.3 (M+H).

Example 49 7-((5-chloro-2-((3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]aza-7-yl)amino)pyrimidin-4-yl)amino)-2-methylisoindolin-1-one

[0868] ##STR00368##

[0869] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with 7-amino-2-methylisoindolin-1-one.

[0870] (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine in step b) is replaced with 3-(tetrahydro-2H-pyran-4-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-amine to obtain the target product.

[0871] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.67 (s, 1H), 9.45 (s, 1H), 8.25 (s, 1H), 7.48 (d, J=8.3 Hz, 2H), 7.36 (dd, J=8.1, 2.2 Hz, 1H), 7.21 (d, J=7.5 Hz, 1H), 7.14-7.07 (m, 1H), 7.06 (s, 1H), 4.49 (s, 2H), 3.90 (dd, J=11.0, 4.1 Hz, 2H), 3.28 (td, J=11.7, 2.0 Hz, 3H), 3.09 (s, 3H), 2.89-2.74 (m, 8H), 1.75-1.60 (m, 2H), 1.54 (qd, J=11.9, 4.4 Hz, 2H). MS(ESI+): 519.2 (M+H).

Example 50 (2-((5-chloro-2-(((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)(imino)(methyl)-λ.SUP.6.-sulfanone

[0872] ##STR00369##

[0873] a) Preparation of 2-(methylthio)aniline

[0874] At 0° C., titanium trichloride (5 ml) is added dropwise to a tetrahydrofuran (5 ml) solution of 2-nitrobenzene sulfide (169 mg), and after dropping, transferred to room temperature and reacted for 4.0 h. After the reaction is completed, the reactant is added with sodium hydroxide (2M) to adjust the pH to 9. The organic layers are extracted with ethyl acetate, merged, and dried with anhydrous sodium sulfate. A solvent is removed by rotary evaporation under reduced pressure to obtain the title compound (125 mg). MS(ESI+): 140.1 (M+H).

[0875] b) Preparation of 2,5-dichloro-N-(2-(methylthio)phenyl)pyrimidin-4-amine

[0876] At 0° C., sodium hydride (72 mg) is added to an N,N-dimethylformamide (3 ml) solution of 2-aminoanisole (120 mg), stirred for 10 min and added with 2,4,5-trichloropyrimidine (329 mg), and then transferred to room temperature and reacted for 3.0 h. After the reaction is completed, the reactant is quenched with 1 ml of ammonium chloride. Liquid separation is performed. Organic layers are extracted with ethyl acetate, merged, and dried with anhydrous sodium sulfate. A solvent is removed by rotary evaporation under reduced pressure. The reactant is purified by column chromatography (petroleum ether/ethyl acetate=50/1) to obtain the title compound (65 mg). MS(ESI+): 286.2 (M+H).

[0877] c) Preparation of tert-butyl (2,5-dichloropyrimidin-4-yl)(2-(methylthio)phenyl) carbamate

[0878] Di-tert-butyl dicarbonate (99 mg) and 4-dimethylaminopyridine (14 mg) are added to a dichloromethane (3 ml) solution of 2,5-dichloro-N-(2-(methylthio)phenyl)pyrimidin-4-amine (65 mg), and reacted at room temperature for 2 h. After the reaction is completed, the solvent is removed by rotary evaporation under reduced pressure. The resulting product is purified by column chromatography (petroleum ether/ethyl acetate=20:1) to obtain the title product (72 mg). MS(ESI+): 386.1 (M+H).

[0879] d) Preparation of tert-butyl (2,5-dichloropyrimidin-4-yl)(2-(S-methylsulfonimidoyl)phenyl) carbamate

[0880] Ammonium acetate (57 mg) and iodobenzene diacetate (122 mg) are added to an ethanol (3 ml) solution of tert-butyl (2,5-dichloropyrimidin-4-yl)(2-(methylthio)phenyl) carbamate (72 mg), and reacted at room temperature for 2 h. After the reaction is completed, the solvent is removed by rotary evaporation under reduced pressure. The crude product is purified by column chromatography (petroleum ether/ethyl acetate=20/1) to obtain the title product (55 mg). MS(ESI+): 417.1 (M+H).

[0881] e) Preparation of tert-butyl (2,5-dichloropyrimidin-4-yl)(2-(S-methyl-N-(2,2,2-trifluoroacetyl)sulfonimidoyl)phenyl) carbamate Trifluoroacetic acid (55 mg), 4-dimethylaminopyridine (2 mg) and triethylamine (33 mg) are added to a dichloromethane (3 ml) solution of tert-butyl(2,5-dichloropyrimidin-4-yl)(2-(S-methylsulfonimido)phenyl)carbamate (55 mg), and reacted at room temperature for 3.0 h. After the reaction is completed, a solvent is removed by rotary evaporation under reduced pressure. The crude product is purified by column chromatography (petroleum ether/ethyl acetate=20/1) to obtain the title compound (42 mg). MS(ESI+): 513.1 (M+H).

f) N-((2-((5-chloro-2-(((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)(methyl)(oxo)-λ.SUP.6.-sulfonamidoyl)-2,2,2-trifluoroacetamide

[0882] (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (28 mg) and trifluoroacetic acid (0.1 ml) are added to a n-butanol (3 ml) solution of tert-butyl(2,5-dichloropyrimidin-4-yl)(2-(S-methyl-N-(2,2,2-trifluoroacetyl)sulfonimide)phenyl)carbamate (42 mg), and reacted in microwaves at 120° C. for 2.0 h. After the reaction is completed, a solvent is removed by rotary evaporation under reduced pressure to obtain the title compound (25 mg). MS(ESI+): 607.1 (M+H).

[0883] g) (2-((5-chloro-2-((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)(imino)(methyl)-λ.sup.6-sulfanone

[0884] N-((2-((5-chloro-2-((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)(methyl)(oxo)-λ.sup.6-sulfonamidoyl)-2,2,2-trifluoroacetamide, ethanol (3 ml) and potassium carbonate (41 mg) are sequentially added to a reaction flask, and reacted at room temperature for 3 h. After the reaction is completed, a solvent is removed by rotary evaporation under reduced pressure. The resulting product is purified by silica-gel column chromatography to obtain the title product (6 mg).

[0885] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.82 (s, 1H), 9.39 (s, 1H), 8.66 (d, J=8.3 Hz, 1H), 8.26 (s, 1H), 7.93 (dd, J=7.9, 1.6 Hz, 1H), 7.71-7.58 (m, 1H), 7.46-7.26 (m, 3H), 7.00 (d, J=8.2 Hz, 1H), 5.15 (s, 1H), 3.12 (s, 4H), 2.85 (s, 3H), 2.67 (m, 3H), 2.33 (m, 2H), 2.04-1.88 (m, 2H), 1.72 (m, 4H), 1.58-1.43 (m, 2H). MS(ESI+): 511.3 (M+H).

Example 51 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluorophenyl)dimethyl phosphine oxide

[0886] ##STR00370##

[0887] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-fluorophenyl)dimethyl phosphine oxide.

[0888] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.84 (s, 1H), 9.28 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.8, 3.1 Hz, 1H), 7.41-7.29 (m, 2H), 7.26 (dd, J=8.2, 2.2 Hz, 1H), 6.97 (d, J=8.2 Hz, 1H), 2.84 (m, 2H), 2.56 (s, 7H), 1.87 (s, 2H), 1.81 (s, 3H), 1.78 (s, 3H), 1.70 (s, 4H), 1.50 (s, 2H). MS(ESI+): 528.2 (M+H).

Example 52 (S)-(5-chloro-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluorophenyl)dimethyl phosphine oxide

[0889] ##STR00371##

[0890] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-chlorophenyl) dimethyl phosphine oxide.

[0891] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.12 (s, 1H), 9.33 (s, 1H), 8.57 (s, 1H), 8.19 (s, 1H), 7.69 (dd, J=13.7, 2.4 Hz, 1H), 7.49 (dd, J=9.0, 2.4 Hz, 1H), 7.42 (d, J=2.1 Hz, 1H), 7.25 (d, J=8.1 Hz, 1H), 6.99 (d, J=8.1 Hz, 1H), 3.17 (s, 2H), 2.95-2.75 (m, 2H), 2.64-2.53 (m, 5H), 1.91 (s, 2H), 1.84 (s, 3H), 1.80 (s, 3H), 1.71 (s, 4H), 1.52 (s, 2H). MS(ESI+): 544.2 (M+H).

Example 53 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-methylphenyl) dimethyl phosphine oxide

[0892] ##STR00372##

[0893] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide.

[0894] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.92 (s, 1H), 9.25 (s, 1H), 8.39 (s, 1H), 8.14 (s, 1H), 7.55-7.37 (m, 2H), 7.29 (ddd, J=14.0, 8.1, 2.1 Hz, 2H), 6.96 (d, J=8.2 Hz, 1H), 2.96-2.76 (m, 2H), 2.70-2.54 (m, 4H), 2.44 (s, 3H), 2.34 (s, 3H), 1.89 (d, J=11.2 Hz, 2H), 1.78 (s, 3H), 1.74 (s, 3H), 1.70 (s, 4H), 1.51 (s, 2H). MS(ESI+): 524.2 (M+H).

Example 54 (S)-4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-3-(dimethylphosphoryl)benzonitrile

[0895] ##STR00373##

[0896] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-cyanophenyl) dimethyl phosphine oxide.

[0897] .sup.1H NMR (400 MHz, DMSO-d6) δ 11.72 (s, 1H), 9.43 (s, 1H), 8.85 (s, 1H), 8.26 (s, 1H), 8.17-8.09 (m, 1H), 7.83 (d, J=9.0 Hz, 1H), 7.40 (s, 1H), 7.27 (d, J=8.2 Hz, 1H), 7.02 (d, J=8.1 Hz, 1H), 2.88 (s, 2H), 2.66 (m, 1H), 2.51 (s, 4H), 2.32 (p, J=1.8 Hz, 2H), 2.00 (s, 2H), 1.86 (s, 3H), 1.84 (s, 3H), 1.68 (s, 4H), 1.52 (s, 2H). MS(ESI+): 535.3 (M+H).

Example 55 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-methoxyphenyl)dimethyl phosphine oxide

[0898] ##STR00374##

[0899] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-methoxyphenyl)dimethyl phosphine oxide.

[0900] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.53 (s, 1H), 9.21 (s, 1H), 8.27 (d, J=6.9 Hz, 1H), 8.12 (s, 1H), 7.38 (d, J=2.3 Hz, 1H), 7.23 (dd, J=8.1, 2.2 Hz, 1H), 7.16 (dd, J=14.4, 3.0 Hz, 1H), 7.09 (dd, J=9.1, 2.9 Hz, 1H), 6.93 (d, J=8.1 Hz, 1H), 3.82 (s, 3H), 2.83 (m, 2H), 2.55 (d, J=6.1 Hz, 4H), 2.47-2.4 (m, 3H), 1.87 (m, 2H), 1.77 (s, 3H), 1.74 (s, 3H), 1.68 (d, J=6.2 Hz, 4H), 1.50 (s, 2H). MS(ESI+): 540.2 (M+H).

Example 56 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)bis(methyl-d.SUB.3.) phosphine oxide

[0901] ##STR00375##

[0902] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-aminophenyl)bis(methyl-d.sub.3) phosphine oxide.

[0903] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.11 (s, 1H), 9.28 (s, 1H), 8.57 (d, J=6.1 Hz, 1H), 8.17 (s, 1H), 7.60 (ddd, J=13.9, 7.7, 1.6 Hz, 1H), 7.49 (t, J=7.9 Hz, 1H), 7.39 (d, J=2.3 Hz, 1H), 7.31 (dd, J=8.1, 2.3 Hz, 1H), 7.19 (td, J=7.6, 2.0 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 4.20-3.94 (m, 1H), 3.17 (d, J=4.8 Hz, 2H), 2.87 (s, 2H), 2.53 (s, 4H), 1.85 (s, 2H), 1.73-1.64 (m, 4H), 1.51 (s, 2H). MS(ESI+): 516.3 (M+H).

Example 57 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluorophenyl)bis(methyl-d.SUB.3.) phosphine oxide

[0904] ##STR00376##

[0905] According to the preparation method of Example 1,2-amino-N—N-dimethylbenzenesulfonamide in step a) is replaced with (2-amino-5-fluorophenyl)bis(methyl-d.sub.3) phosphine oxide.

[0906] .sup.1H NMR (400 MHz, DMSO-d6) δ 10.80 (s, 1H), 9.27 (s, 1H), 8.49 (s, 1H), 8.16 (s, 1H), 7.52 (ddd, J=14.0, 8.7, 3.1 Hz, 1H), 7.39- 7.30 (m, 2H), 7.26 (dd, J=8.1, 2.2 Hz, 1H), 6.97 (d, J=8.2 Hz, 1H), 2.93-2.66 (m, 2H), 2.62-2.53 (m, 7H), 1.88 (d, J=2.2 Hz, 2H), 1.68 (q, J=3.9 Hz, 4H), 1.44 (s, 2H). MS(ESI+): 534.2 (M+H).

Example 58 Preparation of Compounds 58-1 to 58-4

[0907] ##STR00377##

[0908] a) (2-((2,5-dichloropyrimidin-4-yl)amino)-5-fluorophenyl)dimethyl phosphine oxide

[0909] Compounds (2-amino-5-fluorophenyl)dimethyl phosphine oxide (1.1 g) and 2,4,5-trichloropyrimidine (1.18 g) are dissolved in N,N-dimethylformamide (15 mL), added with N,N-diisopropylethylamine (1.52 g), heated to 70° C., and reacted for 5 h. The reaction solution is diluted with 50 mL of water. The diluted solution is extracted with ethyl acetate (80 mL×3). An ethyl acetate layer is washed for three times with a saturated sodium chloride solution (50 mL×3). The organic layer is dried with anhydrous sodium sulfate and concentrated to dryness to obtain a crude product. The crude product is slurried with ethanol (20 mL) to obtain the title compound (1.08 g). MS(ESI+): 334.06 (M+H).

[0910] b) 2-((5-chloro-4-((2-(dimethylphosphoryl)-4-fluorophenyl)amino)pyrimidin-2-yl)amino)-5,6,8,9-tetrahydro-7H-benzo[7]annulen-7-one

[0911] N,N-dimethylformamide (5 ml), 2-amino-5,6,8,9-tetrahydrobenzo[7]annulen-7-one (200.00 mg) and 2,5-dichloro-N-[2-(dimethylphosphoryl)-4-fluorophenyl]pyrimidin-4-amine (343.20 mg) are added to a reaction flask, and added with a 1,4-dioxane solution (80.00 mg) of 4M hydrochloric acid under stirring under the protection of nitrogen. The reaction mixture is irradiated with microwave radiation at 130° C. for 10 min, concentrated under reduced pressure, and diluted with N,N-dimethylformamide (5 ml). The precipitated solid is collected by filtration and washed with petroleum ether/ethyl acetate (5:1) (2×5 mL) to obtain filtrate of the title product. The filtrate is concentrated under reduced pressure to 5 ml. A preparation solution phase is purified by column chromatography (column: XBridge Prep OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 25% B to 65% B within 10 min; UV detection wavelength: 220 nm; product retention time: 7.53 min) to obtain the pure title product (100 mg). MS(ESI+): 473.05 (M+H).

[0912] c) Preparation of Compounds 58-1, 58-2, 58-3 and 58-4

[0913] 2-azabicyclo[3.1.0]hexane hydrochloride (75.87 mg) and magnesium sulfate (101.81 mg) are stirred and mixed, add to dichloromethane (5 mL), and added with triethylamine (85.59 mg) at room temperature in the atmosphere of nitrogen. 2-[(5-chloro-4-[[2-(dimethylphosphoryl)-4-fluorophenyl]amino]pyrimidin-2-yl)amino]-5,6,8,9-tetrahydrobenzo[7]annulen-7-one (100.00 mg) is added to the mixture after stirring for 10 min, and stirred at 35° C. for 1 h. Sodium cyanoborohydride (39.87 mg) is added to the mixture, and stirred at 35° C. for 3 h. The resulting mixture is filtered, and a filter cake is washed with dichloromethane (3×10 mL). The mother liquor is concentrated under reduced pressure, and the resulting residue is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, and mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 25% B to 65% B, 10 min; detection wavelength: 220 nm; isomer mixture retention time: 8.62 min) to obtain the title product (a mixture of four isomers).

[0914] Chiral resolution is performed by chiral liquid chromatography (Chiralpak IA, 2×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (10 mM ammonia-methanol), and mobile phase B: ethanol; flow rate: 18 ml/min; gradient: 50% B within 16 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.).

[0915] Isomer 58-1 (12.2 mg) having a chiral HPLC retention time of 1.96 min.

[0916] .sup.1H NMR (400 MHz, DMSO-d.sub.6): δ 10.84 (s, 1H), 9.27 (s, 1H), 8.50 (d, J=8.4 Hz, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.7, 3.0 Hz, 1H), 7.38 (d, J=2.3 Hz, 1H), 7.39-7.30 (m, 1H), 7.26 (d, J=8.0 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 2.95-2.82 (m, 3H), 2.71-2.65 (m, 1H), 2.48-2.41 (m, 2H), 2.26 (t, J=6.6 Hz, 1H), 1.99-1.84 (m, 3H), 1.82 (s, 3H), 1.80 (s, 1H), 1.78 (s, 3H), 1.77-1.71 (m, 1H), 1.69-1.62 (m, 1H), 1.47 (s, 1H), 1.35 (s, 1H), 0.62 (q, J=4.2, 3.6 Hz, 1H), 0.09 (q, J=5.6 Hz, 1H). MS(ESI+): 540.15 (M+H).

[0917] Isomer 58-2 (10.6 mg) having a chiral HPLC retention time of 3.58 min.

[0918] .sup.1H NMR (400 MHz, DMSO-d.sub.6): δ 10.83 (s, 1H), 9.27 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=14.0, 8.8, 3.0 Hz, 1H), 7.39-7.30 (m, 2H), 7.27 (d, J=7.9 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 2.91 (t, J=8.3 Hz, 2H), 2.85-2.78 (m, 1H), 2.68 (s, 1H), 2.46 (s, 2H), 2.26 (t, J=6.6 Hz, 1H), 1.86 (s, 3H), 1.80 (d, J=13.7 Hz, 8H), 1.70-1.63 (m, 1H), 1.46 (s, 1H), 1.34 (s, 1H), 0.61 (d, J=6.8 Hz, 1H), 0.09 (q, J=5.6 Hz, 1H). MS(ESI+): 540.15 (M+H).

[0919] Isomer 58-3 (12.7 mg) having a chiral HPLC retention time of 1.39 min.

[0920] .sup.1H NMR (400 MHz, DMSO-d.sub.6): δ 10.82 (s, 1H), 9.27 (s, 1H), 8.49 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.8, 3.0 Hz, 1H), 7.39-7.30 (m, 2H), 7.30-7.23 (m, 1H), 6.98 (d, J=8.1 Hz, 1H), 2.96-2.87 (m, 2H), 2.78 (s, 1H), 2.68 (s, 1H), 2.46 (s, 2H), 2.26 (t, J=6.6 Hz, 1H), 1.99-1.85 (m, 3H), 1.80 (d, J=13.7 Hz, 8H), 1.65 (s, 1H), 1.48 (s, 1H), 1.35 (s, 1H), 0.62 (s, 1H), 0.09 (d, J=8.0 Hz, 1H). MS(ESI+): 540.15 (M+H).

[0921] Isomer 58-4 (12.2 mg) having a chiral HPLC retention time of 1.58 min.

[0922] .sup.1H NMR (400 MHz, DMSO-d.sub.6): δ 10.84 (s, 1H), 9.27 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=14.0, 8.8, 3.1 Hz, 1H), 7.41-7.30 (m, 2H), 7.26 (d, J=7.8 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 2.94-2.82 (m, 3H), 2.69 (s, 1H), 2.46 (s, 3H), 2.05-1.84 (m, 3H), 1.80 (d, J=13.7 Hz, 8H), 1.66 (s, 1H), 1.47 (s, 1H), 1.36 (s, 1H), 0.63 (s, 1H), 0.10 (s, 1H). MS(ESI+): 540.15 (M+H).

Example 59 Preparation of Compounds 59-1 and 59-2

[0923] ##STR00378##

[0924] According to the preparation method of Example 58, 2-azabicyclo[3.1.0]hexane hydrochloride in step b) is replaced with 3-azabicyclo[3.1.0]hexane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, and mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 25B to 65B, 10 min; detection wavelength: 220 nm; isomer mixture retention time: 8.62 min) to obtain a mixture of isomers.

[0925] Chiral resolution is performed on the mixture of isomers by chiral liquid chromatography (CHIRALPAK IF, 2×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethanolamine), and mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 20% B within 21 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[0926] isomer 59-1 (16.8 mg) having a chiral HPLC retention time of 8.10 min.

[0927] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ10.83 (s, 1H), 9.26 (s, 1H), 8.49 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.7, 3.0 Hz, 1H), 7.33 (dq, J=8.7, 3.0 Hz, 2H), 7.26 (dd, J=8.2, 2.2 Hz, 1H), 6.96 (d, J=8.1 Hz, 1H), 2.95-2.80 (m, 4H), 2.39 (s, 3H), 2.31-2.21 (m, 1H), 1.81 (s, 3H), 1.78 (s, 3H), 1.77-1.61 (m, 2H), 1.51 (s, 2H), 1.38 (s, 2H), 1.24 (s, 1H), 0.60 (q, J=3.7 Hz, 1H), 0.31 (s, 1H). MS(ESI+): 540.15 (M+H)

[0928] Isomer 59-2 (15.3 mg) having a chiral HPLC retention time of 10.29 min.

[0929] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.83 (s, 1H), 9.26 (s, 1H), 8.49 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.7, 3.0 Hz, 1H), 7.33 (dq, J=8.8, 3.1 Hz, 2H), 7.26 (dd, J=8.2, 2.3 Hz, 1H), 6.96 (d, J=8.1 Hz, 1H), 2.89 (m, 4H), 2.43 (m, 3H), 2.26 (t, J=6.7 Hz, 1H), 1.81 (s, 3H), 1.78 (s, 4H), 1.76-1.72 (m, 1H), 1.69-1.61 (m, 1H), 1.51 (s, 2H), 1.38 (s, 2H), 0.59 (q, J=3.7 Hz, 1H), 0.31 (s, 1H). MS(ESI+): 540.15 (M+H)

Example 60 Preparation of Compounds 60-1 and 60-2

[0930] ##STR00379##

[0931] According to the preparation method of Example 58, 2-azabicyclo[3.1.0]hexane hydrochloride in step b) is replaced with 2-azabicyclo[2.1.1]hexane hydrochloride. The crude product is purified b

[0932] y reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, and mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 25% B-65% B, 10 min; detection wavelength: 220 nm; isomer mixture retention time: 8.62 min) to obtain an isomer mixture.

[0933] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IG, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (10 mM ammonia-methanol), and mobile phase B: ethanol; flow rate: 20 ml/min;

[0934] gradient: 20% B within 10 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[0935] isomer 60-1 (28.7 mg) having a chiral HPLC retention time of 1.67 min.

[0936] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.84 (s, 1H), 9.27 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=14.0, 8.8, 3.1 Hz, 1H), 7.39-7.30 (m, 2H), 7.27 (dd, J=8.2, 2.3 Hz, 1H), 6.97 (d, J=8.2 Hz, 1H), 3.65 (d, J=6.5 Hz, 1H), 2.85 (d, J=37.1 Hz, 2H), 2.73-2.62 (m, 3H), 2.57 (d, J=14.5 Hz, 3H), 1.92 (d, J=12.8 Hz, 2H), 1.82 (s, 3H), 1.78 (s, 3H), 1.61 (s, 2H), 1.48-1.20 (m, 4H). MS(ESI+): 540.15 (M+H)

[0937] Isomer 60-2 (27.7 mg) having a chiral HPLC retention time of 2.31 min.

[0938] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.84 (s, 1H), 9.27 (s, 1H), 8.51 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.8, 3.0 Hz, 1H), 7.41-7.30 (m, 2H), 7.27 (dd, J=8.1, 2.2 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 3.65 (d, J=6.5 Hz, 1H), 2.86 (m, 2H), 2.74-2.62 (m, 3H), 2.57 (d, J=14.5 Hz, 3H), 1.92 (d, J=14.3 Hz, 2H), 1.82 (s, 3H), 1.78 (s, 3H), 1.61 (d, J=4.3 Hz, 2H), 1.48-1.21 (m, 4H). MS(ESI+): 540.15 (M+H)

Example 61 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-hydroxyphenyl)dimethyl phosphine oxide

[0939] ##STR00380##

[0940] (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-methoxyphenyl)dimethyl phosphine oxide (140 mg) and dichloromethane (10 mL) are added to a 25 mL single-necked flask and stirred. The temperature is then cooled to −20° C. Boron tribromide (150 mg) is added dropwise to the reaction solution. After the addition is completed, the temperature gradually rises to room temperature and the reaction solution is stirred and stands overnight. The temperature is then cooled to −20° C., sodium bicarbonate is added dropwise to obtain a saturated solution, and the saturated solution is extracted with dichloromethane (10 mL). The organic layers are merged, concentrated to dryness, and purified by silica-gel column chromatography (dichloromethane:methanol=20: v/v) to obtain 16 mg of the title product.

[0941] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ10.19 (s, 1H), 9.69 (s, 1H), 9.17 (s, 1H), 8.07 (d, J=16.1 Hz, 2H), 7.37 (d, J=2.3 Hz, 1H), 7.28-7.16 (m, 1H), 7.03 (dd, J=14.3, 2.9 Hz, 1H), 6.95 (dd, J=8.9, 2.8 Hz, 1H), 6.90 (d, J=8.2 Hz, 1H), 2.82 (m, 2H), 2.55 (m, 4H), 2.44 (d, J=12.7 Hz, 3H), 1.84 (s, 2H), 1.70 (s, 3H), 1.69 (s, 4H), 1.67 (s, 3H), 1.50 (s, 2H). MS(ESI+): 526.2 (M+H).

Example 62 Preparation of Compounds 62-1 and 62-2

[0942] ##STR00381##

[0943] According to the preparation method of Example 58, 2-azabicyclo[3.1.0]hexane hydrochlroide in step c) is replaced with 5-azaspiro[2.4]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, and mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 25% B-55% B, 8 min; detection wavelength: 254/220 nm) to obtain 60 mg of an isomer mixture.

[0944] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (CHIRALPAK IC, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (10 mM ammonia-methanol), and mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 50% B within 12 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[0945] Isomer 62-1 (27.2 mg) having a HPLC retention time of 7.9 min.

[0946] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ10.84 (s, 1H), 9.27 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (m, 1H), 7.39-7.29 (m, 2H), 7.27 (d, J=8.1 Hz, 1H), 6.97 (d, J=8.2 Hz, 1H), 2.88 (m, 2H), 2.73 (m, 2H), 2.48 (m, 2H), 2.43 (m, 2H), 1.90-1.68 (m, 11H), 1.50 (s, 2H), 0.51 (m, 4H). MS(ESI+): 554.2 (M+H)

[0947] Isomer 62-2 (28.2 mg) having a HPLC retention time of 9.8 min.

[0948] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ 10.84 (s, 1H), 9.27 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.7, 3.1 Hz, 1H), 7.39-7.30 (m, 2H), 7.27 (dd, J=7.9, 2.0 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 2.87 (s, 2H), 2.73 (t, J=6.8 Hz, 2H), 2.59 (s, 2H), 2.51-2.41 (m, 2H), 1.92-1.68 (m, 11H), 1.50 (s, 2H), 0.56-0.45 (m, 4H). MS(ESI+): 554.2 (M+H)

Example 63 Preparation of Compounds 63-1, 63-2, 63-3 and 63-4

[0949] ##STR00382##

[0950] According to the preparation method of Example 58, 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 2-oxa-5-azabicyclo[2.2.1]heptane hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: Xselect CSH-OBD column 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 20% B-53% B within 8 min; wavelength: 210 nm; retention time: 7.02 min) to obtain a white mixture of four isomers.

[0951] The mixture of four isomers is purified by a chiral high-performance liquid chromatography column (IC column: CHIRALPAK ID, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (10 mM ammonia-methanol), and mobile phase B: ethanol; flow rate: [0952] 20 ml/min; gradient: 10% B within 27 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[0953] isomer 63-1 (20 mg) having a HPLC retention time of 13.5 min.

[0954] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.83 (s, 1H), 9.26 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (t, J=11.4 Hz, 1H), 7.35 (s, 2H), 7.30-7.23 (m, 1H), 6.96 (d, J=8.2 Hz, 1H), 4.33 (s, 1H), 3.89 (d, J=7.5 Hz, 1H), 3.69 (s, 1H), 3.55 (s, 1H), 3.44 (s, 2H), 2.99 (d, J=9.3 Hz, 1H), 2.87 (s, 2H), 2.68 (s, 1H), 2.33 (m, 1H), 1.80 (m, 8H), 1.72 (d, J=9.4 Hz, 1H), 1.61 (m, 1H), 1.40 (m, 2H). MS(ESI+): 556.2 (M+H);

[0955] isomer 63-2 (14.7 mg) having a HPLC retention time of 16.8 min.

[0956] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.83 (s, 1H), 9.26 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (m, 1H), 7.35 (m, 2H), 7.29-7.24 (m, 1H), 6.96 (d, J=8.2 Hz, 1H), 4.33 (s, 1H), 3.89 (d, J=7.5 Hz, 1H), 3.69 (s, 1H), 3.55 (s, 2H), 2.99 (m, 1H), 2.87 (m, 2H), 2.68 (m, 2H), 2.33 (m, 1H), 1.80 (m, 8H), 1.72 (m, 1H), 1.61 (m, 1H), 1.40 (m, 2H). MS(ESI+): 556.2 (M+H); and a mixture (42 mg) of the isomer 63-3 and the isomer 63-4;

[0957] the mixture of the isomer 63-3 and the isomer 63-4 is purified by chiral liquid chromatography (column: Chiralpak IC, 2×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (10 mM ammonia-methanol), mobile phase B: isopropanol; flow rate: 20 ml/min; gradient: 30% B within 21 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.)) again to obtain:

[0958] isomer 63-3 (14.7 mg) having a HPLC retention time of 9.2 min.

[0959] .sup.1H NMR: (400 MHz, DMSO-d.sub.6, ppm): δ 10.84 (s, 1H), 9.26 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.57-7.47 (m, 1H), 7.39-7.24 (m, 3H), 6.97 (m, 1H), 4.33 (m, 1H), 3.90 (m, 1H), 3.69 (m, 1H), 3.53 (m, 1H), 3.00 (m, 1H), 2.86 (s, 3H), 2.70 (m, 2H), 2.33 (m, 1H), 1.80 (m, 8H), 1.72 (m, 1H), 1.61 (m, 1H), 1.40 (m, 2H). MS(ESI+): 556.2 (M+H);

[0960] isomer 63-4 (15 mg) having a HPLC retention time of 18.9 min.

[0961] .sup.1H NMR: (400 MHz, DMSO-d.sub.6, ppm): δ 10.84 (s, 1H), 9.26 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (m, 1H), 7.39-7.22 (m, 3H), 6.97 (d, J=8.2 Hz, 1H), 4.33 (d, J=2.1 Hz, 1H), 3.89 (m, 1H), 3.71-3.67 (m, 1H), 3.53 (m, 1H), 3.00 (m, 1H), 2.87 (m, 2H), 2.70 (m, 1H), 2.55 (m, 2H), 2.33 (m, 1H), 1.80 (m, 8H), 1.72 (m, 1H), 1.61 (m, 1H), 1.39 (m, 2H). MS(ESI+): 556.2 (M+H).

Example 64 Preparation of (2-((5-chloro-2-(((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)(methyl)(methylimino)-λ.SUP.6.-sulfanone

[0962] ##STR00383##

a) 2-(Methylthio)nitrobenzene

[0963] 1-fluoro-2-nitrobenzene (1.4 g), isopropanol (15 ml), and sodium thiomethoxide (2.1 g) are sequentially added to a reaction flask, and reacted for 3 h at room temperature. After the reaction is completed, the reaction solution is cooled to 0° C., and filtered by suction. The filter cake is washed with water (10 ml*2), and dried to obtain 1.62 g of the title product.

[0964] b) Preparation of imino(methyl)(2-nitrophenyl)-λ.sup.6-sulfanone

[0965] A compound 2-methylthionitrobenzene (400 mg), ethanol (15 ml), iodobenzenediacetic acid (1.5 g), and ammonium acetate (0.74 g) are sequentially added to a reaction flask, and reacted at room temperature for 2 h. After the reaction is completed, a solvent is removed by concentration under reduced pressure, and purified by silica-gel column chromatography (dichloromethane/methanol=50/1 v/v) to obtain 374 mg of the title product.

[0966] c) Preparation of methyl(methylimino)(2-nitrophenyl)-λ.sup.6-sulfanone

[0967] Imino(methyl)(2-nitrophenyl)-λ.sup.6-sulfanone (370 mg), N,N-dimethylformamide (2 ml), and sodium hydride (89 mg, 60% w/w) are sequentially added to a reaction flask, added dropwise with iodomethane (315 mg), and reacted at room temperature for 1 h. After the reaction is completed, a solvent is removed by concentration under reduced pressure, and purified by silica-gel column chromatography (dichloromethane/methanol=50/1 v/v) to obtain 289 mg of the title product.

[0968] d) Preparation of (2-aminophenyl)(methyl)(methylimino)-λ.sup.6-sulfanone

[0969] Titanium trichloride (6 ml) is added dropwise to a tetrahydrofuran (5 ml) solution of methyl(methylimino)(2-nitrophenyl)-λ.sup.6-sulfanone (235 mg) under an ice bath condition, gradually heated to room temperature and reacted for 2 h. After the reaction is completed, the reaction solution is neutralized by adding dropwise 2M sodium hydroxide to weak alkaline and filtered by suction. The filter cake is washed with ethyl acetate (10 ml*3). The organic layers are merged, dried and then concentrated to obtain 182 mg of the title product.

[0970] e) Preparation of (2-((2,5-dichloropyrimidin-4-yl)amino)phenyl)(methyl)(methylimino)-λ.sup.6-sulfanone

[0971] At 0° C., 2,4,5-trichloropyrimidine (217 mg), (2-aminophenyl)(methyl)(methylimino)-λ.sup.6-sulfanone (182 mg), N, N-dimethylformamide (5 ml), and sodium hydride (48 mg, 60% w/w) are sequentially added to a reaction flask. The mixture is gradually heated to room temperature and reacted for 2 h. After the reaction is completed, the reaction solution is quenched with a saturated ammonium chloride solution and separated. The aqueous phase is extracted with ethyl acetate. The organic layers are merged, dried with anhydrous sodium sulfate, concentrated, and purified by silica-gel column chromatography (dichloromethane/methanol=20/1 v/v) to obtain 170 mg of the title product.

[0972] f) (2-((5-chloro-2-(((S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)(methyl)(methylimino)-λ.sup.6-sulfanone

[0973] (2-((2,5-dichloropyrimidin-4-yl)amino)phenyl)(methyl)(methylimino)-λ.sup.6-sulfanone (170 mg), N, N-dimethylformamide (5 ml), (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (118 mg), and p-toluenesulfonic acid monohydrate (194 mg) are sequentially added to a reaction flask, and reacted in 400 W microwaves at 120° C. for 1 h. After the reaction is completed, a solvent is removed by concentration under reduced pressure, and purified by silica-gel column chromatography (dichloromethane/methanol=20:1 v/v) to obtain 46 mg of the title product.

[0974] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.83 (s, 1H), 9.39 (s, 1H), 8.75 (d, J=6.8 Hz, 1H), 8.26 (s, 1H), 7.89 (dd, J=7.9, 1.5 Hz, 1H), 7.64 (t, J=7.9 Hz, 1H), 7.40 (s, 1H), 7.32 (t, J=7.6 Hz, 2H), 7.00 (d, J=8.1 Hz, 1H), 3.18 (s, 3H), 2.88 (s, 2H), 2.71 (s, 3H), 2.67-2.52 (m, 7H), 1.92 (s, 2H), 1.71 (s, 4H), 1.51 (s, 2H). MS(ESI+): 525.2 (M+H).

Example 65 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-3-fluoro-5-methylphenyl) dimethyl phosphine oxide

[0975] ##STR00384##

[0976] According to the preparation method of Example 47, quinoxaline-6-amine in step a) is replaced with 2-fluoro-4-methylaniline.

[0977] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ8.96 (s, 1H), 7.52 (d, J=12.2 Hz, 1H), 7.42 (d, J=10.7 Hz, 1H), 7.22 (s, 1H), 6.98 (d, J=8.1 Hz, 1H), 6.74 (dd, J=13.7, 8.0 Hz, 2H), 6.29 (d, J=28.4 Hz, 1H), 2.85-2.67 (m, 2H), 2.42 (d, J=12.2 Hz, 7H), 1.89 (s, 2H), 1.80 (s, 2H), 1.68 (d, J=6.1 Hz, 4H), 1.62 (s, 3H), 1.59 (s, 3H), 1.45 (s, 2H). MS(ESI+): 542.2 (M+H).

Example 66 2-((5-chloro-2-((3-(tetrahydrofuran-3-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-yl)amino)pyrimidin-4-yl)amino)-5-fluorophenyl)dimethyl phosphine oxide

[0978] ##STR00385##

[0979] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-fluorophenyl)dimethyl phosphine oxide.

[0980] (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine in step b) is replaced with 3-(tetrahydrofuran-3-yl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-amine to obtain the target product.

[0981] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.87 (s, 1H), 9.31 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.56-7.49 (m, 1H), 7.37-7.28 (m, 3H), 6.98 (d, J=7.9 Hz, 1H), 3.86-3.71 (m, 3H), 3.67-3.47 (m, 3H), 3.22 (br, 1H), 2.85-2.68 (m, 5H), 2.64-2.57 (m, 2H), 1.01-1.94 (m, 1H), 1.81 (s, 3H), 1.78 (s, 3H). MS(ESI+): 530.1 (M+H).

Example 67 Preparation of Compounds 67-1 and 67-2

[0982] ##STR00386##

[0983] According to the preparation method of Example 58, 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 6,6-difluoro-3-azabicyclo[3.1.0]hexane hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: Xselect CSH-OBD column 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 40% B-70% B within 8 min; wavelength: 254/220 nm) to obtain 200 mg of a mixture of two isomers.

[0984] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (IC column: CHIRALPAK IC, 2×25 cm (filler 5 μm); mobile phase A: n-hexane (10 mM ammonia-methanol), and mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 30% B within 12 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[0985] isomer 67-1 (91 mg, 36.98%) having a HPLC retention time of 11.2 min:

[0986] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.84 (s, 1H), 9.27 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (m, 1H), 7.38-7.29 (m, 2H), 7.27 (d, J=8.2 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 3.31 (s, 3H), 3.03 (m, 2H), 2.84 (m, 4H), 2.32 (m, 2H), 1.80 (m, 6H), 1.74 (m, 2H), 1.55 (m, 2H). MS(ESI+): 576.2 (M+H).

[0987] Isomer 67-2 (93.4 mg, 37.96%) having a HPLC retention time of 8.6 min:

[0988] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm):δ 10.84 (s, 1H), 9.27 (s, 1H), 8.50 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.8, 3.1 Hz, 1H), 7.38-7.29 (m, 2H), 7.27 (d, J=7.9 Hz, 1H), 6.97 (d, J=8.2 Hz, 1H), 3.31 (s, 3H), 3.03 (m, 2H), 2.84 (m, 4H), 2.32 (m, 2H), 1.80 (m, 6H), 1.74 (m, 2H), 1.55 (m, 2H). MS(ESI+): 576.2 (M+H).

Example 68 Preparation of Compounds 68-1 and 68-2

[0989] ##STR00387##

[0990] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) with 6,6-difluoro-3-azabicyclo[3.1.0]hexane hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: Xselect CSH-OBD column 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 45% B-75% B within 8 min; wavelength: 210 nm; retention time of isomer mixture: 6.57 min) to obtain a mixture of two isomers.

[0991] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IE, 2×25 cm (filler 5 μm); mobile phase A: n-hexane (10 mM ammonia-methanol), and mobile phase B: ethanol; flow rate: 15 ml/min; gradient: 50% B within 25 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) isomer 68-1 (85 mg) having a HPLC retention time of 19.4 min were obtained:

[0992] .sup.1H NMR: (400 MHz, DMSO-d.sub.6, ppm): δ 10.86 (s, 1H), 9.24 (s, 1H), 8.38 (s, 1H), 8.15 (s, 1H), 7.43 (d, J=15.2 Hz, 2H), 7.29 (m, 2H), 6.96 (m, 1H), 3.41 (s, 3H), 3.05 (s, 2H), 2.86 (m, 4H), 2.34 (m, 5H), 1.76 (m, 8H), 1.54 (m 2H). MS(ESI+): 572.2 (M+H).

[0993] Isomer 68-2 (85 mg) having a HPLC retention time of 14.9 min were obtained:

[0994] .sup.1H NMR: (400 MHz, DMSO-d.sub.6, ppm): δ 10.83 (s, 1H), 9.22 (s, 1H), 8.37 (s, 1H), 8.14 (d, J=0.7 Hz, 1H), 7.47-7.36 (m, 2H), 7.28 (m, 2H), 6.96 (m, 1H), 3.50 (s, 3H), 3.03 (m, 2H), 2.85 (m, 4H), 2.34 (m, 5H), 1.76 (m, 8H), 1.55 (m, 2H). MS(ESI+): 572.2 (M+H).

Example 69 Preparation of Compounds 69-1 and 69-2

[0995] ##STR00388##

[0996] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 5-azaspiro[2.4]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, and mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 45% B-75% B, 8 min; detection wavelength: 210 nm; retention time: 6.57 min) to obtain 60 mg of an isomer mixture.

[0997] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IF, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (10 mM ammonia-methanol), and mobile phase B: ethanol;

[0998] flow rate: 15 ml/min;

[0999] gradient: 30% B within 24 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1000] isomer 69-1 (76 mg) having a HPLC retention time of 10.8 min.

[1001] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.93 (s, 1H), 9.26 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.49-7.38 (m, 2H), 7.34-7.23 (m, 2H), 6.97 (d, J=8.1 Hz, 1H), 3.31 (s, 5H), 2.84 (m, 4H), 2.34 (s, 3H), 2.01-1.88 (m, 1H), 1.77 (m, 9H), 1.47 (m, 2H), 0.53 (m, 4H). MS(ESI+): 550.2 (M+H). Isomer 69-2 (90 mg) having a HPLC retention time of 19.6 min.

[1002] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.93 (s, 1H), 9.26 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.49-7.38 (m, 2H), 7.34-7.23 (m, 2H), 6.97 (d, J=8.1 Hz, 1H), 3.31 (m, 5H), 2.84 (m, 4H), 2.34 (s, 3H), 2.01-1.88 (m, 1H), 1.77 (m, 9H), 1.47 (m, 2H), 0.53 (m, 4H). MS(ESI+): 550.2 (M+H).

Example 70 Preparation of Compounds 70-1 and 70-2

[1003] ##STR00389##

[1004] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 2-azabicyclo[2.1.1]hexane hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: Xselect CSH-OBD column 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 10% B-40% B within 10 min; wavelength: 254/220 nm) to obtain 160 mg of a mixture of two isomers.

[1005] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IG, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (10 nM ammonia-methanol solution), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 30% B within 11 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1006] isomer 70-1 (mg) having a HPLC retention time of 6.5 min.

[1007] .sup.1H-NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.50-7.36 (m, 2H), 7.30 (ddd, J=10.8, 8.2, 2.1 Hz, 2H), 6.98 (d, J=8.1 Hz, 1H), 3.70 (s, 1H), 2.86 (d, J=35.4 Hz, 2H), 2.72 (dt, J=6.5, 3.0 Hz, 3H), 2.64-2.53 (m, 3H), 2.34 (s, 3H), 1.92 (d, J=18.7 Hz, 2H), 1.77 (d, J=13.5 Hz, 6H), 1.64 (s, 2H), 1.54-1.19 (m, 4H). MS(ESI+): 536.2 (M+H).

[1008] Isomer 70-2 (mg) having a HPLC retention time of 9.2 min;

[1009] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.44 (dd, J=12.6, 2.2 Hz, 2H), 7.30 (ddd, J=11.0, 8.1, 2.2 Hz, 2H), 6.98 (d, J=8.1 Hz, 1H), 3.70 (s, 1H), 2.89 (s, 2H), 2.77-2.65 (m, 3H), 2.65-2.54 (m, 3H), 2.34 (s, 3H), 1.92 (d, J=18.1 Hz, 2H), 1.77 (d, J=13.5 Hz, 6H), 1.64 (s, 2H), 1.54-1.21 (m, 4H). MS(ESI+): 536.2 (M+H).

Example 71 Preparation of Compounds 71-1 and 71-2

[1010] ##STR00390##

[1011] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-azabicyclo[3.1.0]hexane hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: Xselect CSH-OBD column 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 35% B-85% B within 8 min; wavelength: 254/220 nm) to obtain 140 mg of a mixture of two isomers.

[1012] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IE, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 18 ml/min; gradient: 20% B within 17 min, isogradient; detection wavelength: 220/254 nm and column temperature: 25° C.) to obtain:

[1013] isomer 71-1 (45.8 mg) having a HPLC retention time of 12.4 min:

[1014] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.90 (s, 1H), 9.24 (s, 1H), 8.37 (d, J=5.8 Hz, 1H), 8.15 (s, 1H), 7.47-7.37 (m, 2H), 7.28 (m, 2H), 6.95 (d, J=8.2 Hz, 1H), 3.32 (s, 2H), 2.95 (d, J=8.3 Hz, 2H), 2.87 (s, 2H), 2.42-2.36 (m, 3H), 2.34 (s, 3H), 1.76 (m, 8H), 1.52 (s, 2H), 1.38 (s, 2H), 0.60 (m, 1H), 0.32 (m, 1H). MS(ESI+): 536.2 (M+H).

[1015] Isomer 71-2 (46.2 mg) having a HPLC retention time of 14.5 min:

[1016] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.90 (s, 1H), 9.24 (s, 1H), 8.38 (s, 1H), 8.15 (s, 1H), 7.47-7.37 (m, 2H), 7.34-7.22 (m, 2H), 6.95 (d, J=8.1 Hz, 1H), 3.33 (s, 2H), 2.95 (d, J=8.3 Hz, 2H), 2.90-2.82 (m, 2H), 2.40 (s, 3H), 2.34 (s, 3H), 1.76 (m, 8H), 1.52 (m, 2H), 1.41-1.35 (m, 2H), 0.60 (m, 1H), 0.32 (m, 1H). MS(ESI+): 536.2 (M+H).

Example 72 Preparation of Compounds 72-1, 72-2, 72-3 and 72-4

[1017] ##STR00391##

[1018] According to the preparation method of Example 58, 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 2-oxa-5-azabicyclo[2.2.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 25% B-50% B, 8 min; detection wavelength: 254/220 nm) to obtain 275 mg of an isomer mixture.

[1019] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IG, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (10 mM ammonia-methanol), mobile phase B: ethanol;

[1020] flow rate: 20 ml/min; gradient: 15% B within 45 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1021] isomer 72-1 (36.4 mg) having a HPLC retention time of 1.67 min.

[1022] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): (400 MHz, DMSO-d.sub.6, ppm): δ 10.90 (s, 1H), 9.24 (s, 1H), 8.40 (dd, J=8.6, 4.4 Hz, 1H), 8.15 (s, 1H), 7.47-7.38 (m, 2H), 7.29 (ddd, J=12.4, 8.3, 2.2 Hz, 2H), 6.96 (d, J=8.1 Hz, 1H), 4.33 (t, J=1.9 Hz, 1H), 3.90 (d, J=7.5 Hz, 1H), 3.70 (s, 1H), 3.59-3.50 (m, 1H), 2.99 (dd, J=9.6, 1.8 Hz, 1H), 2.86 (s, 2H), 2.71 (s, 1H), 2.53 (s, 1H), 2.48 (s, 1H), 2.34 (s, 4H), 1.83-1.71 (m, 9H), 1.65-1.58 (m, 1H), 1.54-1.27 (m, 2H). MS(ESI+): 552 (M+H).

[1023] Isomer 72-2 (56.8 g) having a HPLC retention time of 6.119 min.

[1024] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): (400 MHz, DMSO-d.sub.6, ppm): δ 10.90 (s, 1H), 9.25 (s, 1H), 8.39 (dd, J=9.0, 4.5 Hz, 1H), 8.15 (s, 1H), 7.43 (dd, J=14.2, 2.2 Hz, 2H), 7.29 (ddd, J=13.1, 8.3, 2.2 Hz, 2H), 6.96 (d, J=8.1 Hz, 1H), 4.33 (t, J=1.9 Hz, 1H), 3.90 (d, J=7.5 Hz, 1H), 3.70 (s, 1H), 3.53 (dd, J=7.6, 1.7 Hz, 1H), 3.01 (dd, J=9.6, 1.8 Hz, 1H), 2.86 (s, 2H), 2.72 (d, J=8.8 Hz, 1H), 2.57 (d, J=11.9 Hz, 1H), 2.47 (d, J=15.3 Hz, 1H), 2.33 (s, 4H), 1.76 (d, J=13.5 Hz, 9H), 1.65-1.58 (m, 1H), 1.39 (s, 2H). MS(ESI+): 552 (M+H).

[1025] Isomer 72-3 (60.3 g) having a HPLC retention time of 7.224 min.

[1026] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.92-10.87 (m, 1H), 9.24 (s, 1H), 8.40 (d, J=7.6 Hz, 1H), 8.15 (s, 1H), 7.47-7.38 (m, 2H), 7.29 (ddd, J=11.7, 8.3, 2.1 Hz, 2H), 6.96 (d, J=8.1 Hz, 1H), 4.33 (s, 1H), 3.90 (d, J=7.5 Hz, 1H), 3.70 (s, 1H), 3.54 (d, J=7.4 Hz, 1H), 2.99 (dd, J=9.5, 1.6 Hz, 1H), 2.90-2.83 (m, 2H), 2.72 (d, J=8.5 Hz, 1H), 2.55 (d, J=8.1 Hz, 1H), 2.48 (s, 1H), 2.34 (s, 4H), 1.76 (d, J=13.5 Hz, 9H), 1.62 (d, J=9.3 Hz, 1H), 1.39 (s, 2H). MS(ESI+): 552 (M+H)

[1027] Isomer 72-4 (32.2 mg) having a HPLC retention time of 9.412 min.

[1028] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): (400 MHz, DMSO-d.sub.6, ppm): δ 10.89 (s, 1H), 9.24 (s, 1H), 8.39 (dd, J=8.3, 4.3 Hz, 1H), 8.15 (s, 1H), 7.43 (dd, J=14.4, 2.1 Hz, 2H), 7.29 (ddd, J=14.3, 8.3, 2.2 Hz, 2H), 6.96 (d, J=8.1 Hz, 1H), 4.34 (t, J=2.0 Hz, 1H), 3.90 (d, J=7.5 Hz, 1H), 3.71 (s, 1H), 3.54 (dd, J=7.6, 1.7 Hz, 1H), 3.01 (dd, J=9.6, 1.8 Hz, 1H), 2.86 (s, 2H), 2.73 (d, J=8.6 Hz, 1H), 2.61-2.54 (m, 1H), 2.47 (s, 1H), 2.36 (d, J=9.2 Hz, 4H), 1.76 (d, J=13.5 Hz, 9H), 1.66-1.59 (m, 1H), 1.39 (s, 2H). MS(ESI+): 552 (M+H).

Example 73 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-methylpyridin-3-yl)dimethyl phosphine oxide

[1029] ##STR00392##

[1030] According to the preparation method of Example 47, quinoxaline-6-amine in step a) is replaced with 2-amino-5-methylpyridine.

[1031] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 9.32 (s, 1H), 8.47 (s, 1H), 7.95 (d, J=13.2 Hz, 1H), 7.66 (s, 1H), 7.37 (dd, J=7.9, 2.3 Hz, 1H), 7.11 (t, J=7.8 Hz, 1H), 7.40 (s, 1H), 6.96 (t, J=8.3 Hz, 2H), 2.75 (d, J=8.1 Hz, 1H), 2.36 (s, 3H), 2.29 (s, 2H), 1.97 (s, 3H), 1.91-2.52 (m, 3H), 1.79 (s, 2H), 1.75 (s, 4H), 1.46 (s, 2H). MS(ESI+): 525.4 (M+H).

Example 74 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(trifluoromethyl)phenyl)dimethyl phosphine oxide

[1032] ##STR00393##

[1033] According to the preparation method of Example 47, quinoxaline-6-amine in step a) is replaced with 4-trifluoromethylaniline.

[1034] .sup.1H NMR (400 MHz, DMSO-d6, ppm):δ 9.74 (s, 1H), 9.31 (s, 1H), 8.18 (s, 1H), 7.70 (dd, J=11.5, 4.3 Hz, 1H), 7.59 (dd, J=7.5, 3.0 Hz, 1H), 7.10 (t, J=8.5 Hz, 2H), 7.06 (d, J=7.6 Hz, 1H), 6.81 (d, J=7.9 Hz, 1H), 2.83 (s, 7H), 2.62 (s, 2H), 2.04 (s, 2H), 1.88 (d, J=13.8 Hz, 6H), 1.77 (s, 4H), 1.49 (dd, J=14.1, 3.7 Hz, 2H). MS(ESI+): 578.2 (M+H).

Example 75 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(difluoromethoxyl)phenyl)dimethyl phosphine oxide

[1035] ##STR00394##

[1036] According to the preparation method of Example 10, (2-aminophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-difluoromethoxyphenyl)dimethyl phosphine oxide.

[1037] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm) δ 10.96 (s, 1H), 9.30 (s, 1H), 8.55 (s, 1H), 8.28 (s, 0.5H), 8.18 (s, 1H), 7.52-7.45 (m, 1H), 7.44 (d, J=2.9 Hz, 0.25H), 7.39 (d, J=2.3 Hz, 1H), 7.34-7.23 (m, 2H), 7.09 (s, 0.25H), 6.98 (d, J=8.1 Hz, 1H), 2.87-2.80 (m, 2H), 2.65 (s, 7H), 1.91 (s, 2H), 1.82 (s, 3H), 1.79 (s, 3H), 1.72 (q, J=3.2 Hz, 4H), 1.51 (s, 2H). MS(ESI+): 576.2 (M+H).

Example 76 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(trifluoromethoxyl)phenyl)dimethyl phosphine oxide

[1038] ##STR00395##

[1039] According to the preparation method of Example 10, (2-aminophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-trifluoromethoxyphenyl)dimethyl phosphine oxide.

[1040] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.18 (s, 1H), 9.35 (s, 1H), 8.66 (s, 1H), 8.22 (d, J=8.9 Hz, 1H), 7.66 (d, J=14.0 Hz, 1H), 7.52-7.37 (m, 2H), 7.30 (d, J=7.3 Hz, 1H), 7.00 (d, J=8.1 Hz, 1H), 2.77 (d, J=75.5 Hz, 7H), 2.57 (d, J=11.6 Hz, 2H), 2.06 (s, 2H), 1.91-1.69 (m, 10H), 1.49 (s, 2H). MS(ESI+): 594.2 (M+H).

Example 77 (S)-4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-3-(dimethylphosphoryl)-N-methylbenzamide

[1041] ##STR00396##

[1042] According to the preparation method in step b) to step d) of Example 47, 5-iodoquinoxaline-6-amine in step b) is replaced with 4-amino-3-iodo-N-methylbenzamide. 1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ9.38 (s, 1H), 8.72 (s, 1H), 8.51 (q, J=4.5 Hz, 1H), 8.29 (s, 1H), 8.09-7.88 (m, 2H), 7.47 (d, J=2.3 Hz, 1H), 7.29 (d, J=8.2 Hz, 1H), 7.02 (d, J=8.1 Hz, 1H), 2.82 (d, J=4.5 Hz, 5H), 2.76 (s, 5H), 2.58 (t, J=12.8 Hz, 2H), 2.01 (s, 2H), 1.87 (s, 3H), 1.83 (s, 3H), 1.76 (d, J=5.9 Hz, 4H), 1.49 (s, 2H). MS(ESI+): 567.2 (M+H).

Example 78 (S)-4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-3-(dimethylphosphoryl)benzamide

[1043] ##STR00397##

[1044] (S)-4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-3-(dimethylphosphoryl)benzonitrile (120 mg), 2N sodium hydroxide (2 ml) and ethanol (10 mL) are added to a 30 mL microwave tube. The microwave reaction is performed at 150° C. for 4 h under the protection of nitrogen, and then stopped. The reaction solution is concentrated to dryness, and the residue is purified by silica-gel column chromatography to obtain 40 mg of the title product.

[1045] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.35 (s, 1H), 9.35 (s, 1H), 8.59 (s, 1H), 8.21 (s, 1H), 8.09-7.92 (m, 2H), 7.45 (s, 1H), 7.25 (s, 1H), 7.01 (d, J=8.0 Hz, 1H), 3.39 (s, 2H), 2.91-2.55 (m, 9H), 2.08 (br, 2H), 1.87-1.71 (m, 10H), 1.52 (br, 2H). MS(ESI+): 553.2 (M+H).

Example 79 (S)-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(dimethylphosphoryl)-N-methylbenzamide

[1046] ##STR00398##

[1047] According to the preparation method in step b) to step d) of Example 47, 5-iodoquinoxaline-6-amine in step b) is replaced with 2-amino-5-bromo-N-methylbenzamide.

[1048] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ9.41 (s, 1H), 8.95 (q, J=4.6 Hz, 1H), 8.84 (d, J=8.6 Hz, 1H), 8.26 (d, J=2.2 Hz, 2H), 8.07 (d, J=11.5 Hz, 1H), 7.79 (t, J=9.8 Hz, 1H), 7.49 (d, J=2.3 Hz, 1H), 7.26 (s, 1H), 7.03 (d, J=8.1 Hz, 1H), 2.84 (d, J=4.4 Hz, 5H), 2.71 (s, 5H), 2.57 (s, 2H), 1.98 (s, 2H), 1.81-1.70 (m, 7H), 1.68 (d, J=1.9 Hz, 3H), 1.53 (s, 2H). MS(ESI+): 567.2 (M+H).

Example 80 (S)-(5-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-2-methylpyridin-4-yl)dimethyl phosphine oxide

[1049] ##STR00399##

[1050] According to the preparation method in step b) to step d) of Example 47, 5-iodoquinoxaline-6-amine in step b) is replaced with 4-iodo-6-methylpyridin-3-amine.

[1051] .sup.1H NMR (400 MHz, CDCl.sub.3, ppm):δ 8.86 (dd, J=8.8, 5.5 Hz, 1H), 8.44 (s, 1H), 8.06 (s, 1H), 7.44 (s, 1H), 7.34 (dd, J=8.1, 2.3 Hz, 1H), 7.29 (s, 1H), 7.13 (dd, J=8.7, 2.0 Hz, 1H), 7.06 (d, J=8.1 Hz, 1H), 3.40 (m, 2H), 3.28 (m, 3H), 2.87 (m, 1H), 2.78 (m, 3H), 2.52 (s, 3H), 2.41 (m, 2H), 2.04 (m, 4H), 1.87 (m, 6H), 1.65-1.51 (m, 2H). MS(ESI+): 525.1 (M+H).

Example 81 (S)-(3-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-6-methylpyridin-2-yl)dimethyl phosphine oxide

[1052] ##STR00400##

[1053] According to the preparation method in step b) to step d) of Example 47, 5-iodoquinoxaline-6-amine in step b) is replaced with 4-iodo-6-methylpyridin-3-amine.

[1054] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm) δ 9.37 (s, 1H), 8.97 (s, 1H), 8.29 (s, 1H), 8.20 (s, 1H), 7.42 (d, J=2.3 Hz, 1H), 7.32 (td, J=5.4, 2.6 Hz, 2H), 7.04 (d, J=8.1 Hz, 1H), 2.93 (m, 4H), 2.74 (m, 1H), 2.63 (m, 2H), 2.51 (m, 5H), 2.12 (m, 2H), 1.78 (m, 10H), 1.49 (m, 2H). MS(ESI+): 525.1 (M+H).

Example 82 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(trifluoromethyl)pyridin-3-yl)dimethyl phosphine oxide

[1055] ##STR00401##

[1056] According to the preparation method of Example 47, quinoxaline-6-amine in step a) is replaced with 5-trifluoromethylpyridinediamine.

[1057] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 9.47 (s, 1H), 8.85 (s, 1H), 8.39 (dd, J=13.3, 2.5 Hz, 1H), 8.33 (s, 1H), 8.25 (s, 1H), 7.60- 7.49 (m, 2H), 6.97 (d, J=8.1 Hz, 1H), 2.84 (m, 2H), 2.70 (m, 5H), 1.89 (m, 8H), 1.73 (m, 4H), 1.49 (m, 2H). MS(ESI+): 579.2 (M+H).

Example 83 Preparation of Compounds 83-1 and 83-2

[1058] ##STR00402##

[1059] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-difluoromethoxyphenyl)dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 2-azabicyclo[2.1.1]hexane hydrochloride.

[1060] The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 15% B-47% B within 8 min; wavelength: 254/220 nm; and column temperature: 25° C.) to obtain 87 mg of a mixture of two isomers.

[1061] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IC, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 20% B within 12 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1062] isomer 83-1 (23.8 mg) having a HPLC retention time of 6.4 min:

[1063] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ 10.96 (s, 1H), 9.28 (s, 1H), 8.56 (s, 1H), 8.18 (s, 1H), 7.50-7.42 (m, 1.25H), 7.40 (d, J=2.3 Hz, 1H), 7.34-7.23 (m, 2.5H), 7.08 (s, 0.25H), 6.98 (d, J=8.1 Hz, 1H), 3.68 (s, 1H), 2.90 (s, 2H), 2.76-2.63 (m, 2H), 2.58 (s, 2H), 1.92 (s, 2H), 1.81 (d, J=13.7 Hz, 6H), 1.63 (s, 2H), 1.35 (d, J=4.0 Hz, 4H), 1.24 (s, 2H). MS(ESI+): 588.2 (M+H).

[1064] Isomer 83-2 (23.8 mg) having a HPLC retention time of 10.4 min:

[1065] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ10.96 (s, 1H), 9.28 (s, 1H), 8.56 (s, 1H), 8.18 (s, 1H), 7.50-7.43 (m, 1H), 7.40 (d, J=2.3 Hz, 0.25H), 7.32-7.25 (m, 2.5H), 7.08 (s, 0.25H), 6.98 (d, J=8.2 Hz, 1H), 3.71 (s, 1H), 2.89 (s, 2H), 2.75-2.69 (m, 2H), 2.58 (d, J=11.5 Hz, 2H), 2.05-1.86 (m, 2H), 1.81 (d, J=13.7 Hz, 6H), 1.64 (s, 2H), 1.35 (d, J=4.6 Hz, 4H), 1.24 (s, 2H). MS(ESI+): 588.2 (M+H).

Example 84 Preparation of Compounds 84-1 and 84-2

[1066] ##STR00403##

[1067] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-difluoromethoxyphenyl)dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-6-azabicyclo[3.1.1]heptane hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 17% B-45% B within 12 min; isomer mixture retention time: 11.57 min; wavelength: 254/220 nm; column temperature: 250° C.) to obtain a mixture of two isomers.

[1068] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IG, 2×25 cm (filler 5 μm); mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 50% B within 18 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1069] isomer 84-1 (24 mg) having a HPLC retention time of 12.1 min:

[1070] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ 10.94 (s, 1H), 9.29 (s, 1H), 8.54 (s, 1H), 8.18 (s, 1H), 7.54-7.06 (m, 5H), 6.97 (d, J=8.1 Hz, 1H), 4.13 (dd, J=10.6, 2.8 Hz, 2H), 3.58 (d, J=10.9 Hz, 2H), 3.52 (d, J=6.0 Hz, 2H), 3.11 (s, 1H), 2.80 (t, J=11.1 Hz, 1H), 2.65 (s, 3H), 2.40-2.29 (m, 1H), 1.80 (d, J=13.6 Hz, 8H), 1.68 (d, J=7.8 Hz, 1H), 1.09 (s, 2H). MS(ESI+): 604.2 (M+H).

[1071] Isomer 84-2 (23 mg) having a HPLC retention time of 15.5 min:

[1072] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.94 (s, 1H), 9.29 (s, 1H), 8.54 (s, 1H), 8.18 (s, 1H), 7.54-7.06 (m, 5H), 6.97 (d, J=8.1 Hz, 1H), 4.13 (dd, J=10.6, 2.8 Hz, 2H), 3.58 (d, J=10.9 Hz, 2H), 3.52 (d, J=6.0 Hz, 2H), 3.11 (s, 1H), 2.80 (t, J=11.1 Hz, 1H), 2.65 (s, 3H), 2.40-2.29 (m, 1H), 1.80 (d, J=13.6 Hz, 8H), 1.68 (d, J=7.8 Hz, 1H), 1.09 (s, 2H). MS(ESI+): 604.2 (M+H).

Example 85 Preparation of Compounds 85-1 and 85-2

[1073] ##STR00404##

[1074] According to the preparation method of Example 58, (2-amino-5-fluorophenyl) dimethyl phosphinc oxide in step a) is replaced with (2-amino-5-difluoromethoxyphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride. The crude product is purified by recversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD, C18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acctonitrilc (0.1% formic acid): flow rate: 60 mL/min; gradient: 20% B-60% B, 8 min: detection wavelength: 220 nm; isomer mixture retention time: 6.12 min; and column temperature: 25° C.) to obtain 75 mg of isomer mixture.

[1075] Chiral resolution is performed on the isomer mixture by cliiral liquid chromatography (column: CHIRALPAK IF, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% dicthyiamine), mobile phase B: ethanol: flow rate: 20 ml/min: gradient: 30% B within 23 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain: isomer 85-1 (22.3 mg) having a HPLC retention time of 16.0 min.

[1076] .sup.1H NMR (400 MHz, DMSO-.sub.6, ppm): δ 10.95 (s, 1H), 9.27 (s, 1H), 8.55 (s, 1H). 8.18 (d, J=1.1 Hz, 1H), 7.51-7.42 (m, 1.3H), 7.39 (s, 1H), 7.34-6.98 (m, 2.5H), 7.07 (s, 0.3H), 6.96(d, J=8.0 Hz, 1H), 3.63-3.53 (m, 2H), 3.45 (d, J=10.2 Hz, 2H), 3.06 (s, 2H), 2.51-2.39 (m, 3H) 1.81 (m, 7H), 1.79- 1.64 (m, 5H), 1.63-1.25 (m, 3H), 1.24 (s, 1H), MS(ESI+): 618.2 (M+H).

[1077] Isomer 85-2 (22.0 mg) having a HPLC retention time of 20.2 min.

[1078] .sup.1H NMR (400 MHz, DMSO-.sub.6, ppm): δ 10.95 (s, 1H), 9.27 (s, 1H), 8.55 (s, 1H), 8.18 (s, 1H), 7.52-7.42 (m, 1H), 7.39 (d, J=2.2 Hz, 1H), 7.33-7.06 (m, 3H), 7.08 (s, 0.4H), 6.97 (d, J=8.1 Hz, 1H), 3.57 (s, 2H), 3.45 (d, J=10.2 Hz, 2H), 3.05 (s, 2H), 2.51 (s, 3H), 1.82 (m, 7H), 1.79-1.67 (m, 5H), 1.67-1.39 (m, 3H), 1.24 (s, 1H), MS(ESI+): 618.2 (M+H).

Example 86 Compounds 86-1 and 86-2

[1079] ##STR00405##

[1080] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-cyanophenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 2-azabicyclo[2.1.1]hexane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (0.05% hydrochloric acid); mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 50B-500B, 8 min; detection wavelength: 210 nm; isomer mixture retention time: 6.02 min) to obtain 70 mg of an isomer mixture.

[1081] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IG, 3 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate; gradient: 50% B within 21 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1082] isomer 86-1 (24.8 mg) having a HPLC retention time of 14.6 min.

[1083] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.74 (s, 1H), 9.44 (s, 1H), 8.87 (s, 1H), 8.27 (s, 1H), 8.13 (d, J=13.8 Hz, 1H), 7.84 (d, J 8.9 Hz, 1H), 7.42 (s, 1H), 7.30 (d, J=7.7 Hz, 1H), 7.04 (d, J=8.1 Hz, 1H), 3.73 (s, 1H), 3.02-2.76 (m, 3H), 2.73 (s, 2H), 2.58 (d, J=11.4 Hz, 2H), 2.00 (d, J=14.2 Hz, 2H), 1.87 (m, 7H), 1.62 (m, 2H), 1.36 (s, 3H), 1.24 (s, 1H). MS(ESI+): 547.2 (M+H).

[1084] Isomer 86-2 (24.9 mg) having a HPLC retention time of 18.4 min.

[1085] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.74 (s, 1H), 9.45 (s, 1H), 8.88 (s, 1H), 8.27 (s, 1H), 8.14 (dd, J=13.9, 2.0 Hz, 1H), 7.85 (d, J=9.0 Hz, 1H), 7.43 (d, J=2.3 Hz, 1H), 7.38-7.21 (m, 1H), 7.06 (d, J=8.1 Hz, 1H), 3.81 (s, 1H), 2.81 (d, J=48.5 Hz, 5H), 2.62 (s, 2H), 2.06 (d, J=18.6 Hz, 2H), 1.87 (d, J=13.8 Hz, 7H), 1.66 (d, J=51.2 Hz, 2H), 1.54-1.27 (m, 4H). MS(ESI+): 547.2 (M+H).

Example 87 Compounds 87-1 and 87-2

[1086] ##STR00406##

[1087] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-cyanophenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-6-azabicyclo[3.1.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (0.05% hydrochloric acid); mobile phase B: acetonitrile; flow rate: 60 m/min; gradient: 5% B-30% B, 8 min; detection wavelength:

[1088] 210 nm; isomer mixture retention time: 7.05 min; column temperature: 25° C.) to obtain an isomer mixture.

[1089] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IG, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 30% B within 21 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1090] isomer 87-1 (23 mg) having a HPLC retention time of 16.4 min.

[1091] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.71 (s, 1H), 9.44 (s, 1H), 8.84 (s, 1H), 8.27 (s, 1H), 8.13 (dd, J=13.9, 2.0 Hz, 1H), 7.88-7.76 (m, 1H), 7.42 (d, J=2.3 Hz, 1H), 7.33-7.23 (m, 1H), 7.04 (d, J=8.2 Hz, 1H), 4.15 (d, J=10.6 Hz, 2H), 3.59 (d, J=10.8 Hz, 4H), 3.14 (s, 1H), 2.88-2.75 (m, 1H), 2.67 (d, J=13.8 Hz, 3H), 2.36 (s, 1H), 1.87 (d, J=13.7 Hz, 8H), 1.69 (d, J=7.7 Hz, 1H), 1.11 (s, 2H). MS(ESI+): 563.2 (M+H).

[1092] Isomer 87-2 (23.5 mg) having a HPLC retention time of 18.9 min.

[1093] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ 11.71 (s, 1H), 9.44 (s, 1H), 8.85 (s, 1H), 8.27 (s, 1H), 8.13 (dd, J=13.9, 2.0 Hz, 1H), 7.84 (dd, J=9.1, 2.0 Hz, 1H), 7.42 (d, J=2.3 Hz, 1H), 7.35-7.25 (m, 1H), 7.04 (d, J=8.1 Hz, 1H), 4.15 (d, J=10.6 Hz, 2H), 3.60 (d, J=11.6 Hz, 4H), 3.15 (s, 1H), 2.88-2.77 (m, 1H), 2.69 (s, 3H), 2.37 (s, 1H), 1.87 (d, J=13.7 Hz, 8H), 1.70 (s, 1H), 1.11 (s, 2H). MS(ESI+): 563.2 (M+H).

Example 88 Compounds 88-1 and 88-2

[1094] ##STR00407##

[1095] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-cyanophenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate aqueous solution), mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 20% B-60% B, 6 min; detection wavelength: 220 nm; column temperature: 25° C.) to obtain 65 mg of an isomer mixture.

[1096] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IA, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate; gradient: 50% B within 16 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1097] isomer 88-1 (22.6 mg) having a HPLC retention time of 9.55 min.

[1098] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.71 (s, 1H), 9.44 (s, 1H), 8.84 (s, 1H), 8.27 (s, 1H), 8.13 (dd, J=13.9, 2.0 Hz, 1H), 7.88-7.76 (m, 1H), 7.42 (d, J=2.3 Hz, 1H), 7.33-7.23 (m, 1H), 7.04 (d, J=8.2 Hz, 1H), 4.15 (d, J=10.6 Hz, 2H), 3.59 (d, J=10.8 Hz, 4H), 3.14 (s, 1H), 2.88-2.75 (m, 1H), 2.67 (d, J=13.8 Hz, 3H), 2.36 (s, 1H), 1.87 (m, 8H), 1.69 (d, J=7.7 Hz, 1H), 1.11 (s, 2H). MS(ESI+): 577.2 (M+H).

[1099] Isomer 88-2 (23.5 mg) having a HPLC retention time of 12.7 min.

[1100] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.71 (s, 1H), 9.44 (s, 1H), 8.85 (s, 1H), 8.27 (s, 1H), 8.13 (dd, J=13.9, 2.0 Hz, 1H), 7.84 (dd, J=9.1, 2.0 Hz, 1H), 7.42 (d, J=2.3 Hz, 1H), 7.35-7.25 (m, 1H), 7.04 (d, J=8.1 Hz, 1H), 4.15 (d, J=10.6 Hz, 2H), 3.60 (d, J=11.6 Hz, 4H), 3.15 (s, 1H), 2.88-2.77 (m, 1H), 2.69 (s, 3H), 2.37 (s, 1H), 1.87 (m, 8H), 1.70 (s, 1H), 1.11 (s, 2H). MS(ESI+): 577.2 (M+H).

Example 89 Compounds 89-1 and 89-2

[1101] ##STR00408##

[1102] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-6-azabicyclo[3.1.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 m/min; gradient: 15% B-50% B, 8 min; detection wavelength: 220 nm; isomer mixture retention time: 8.1 min; column temperature: 25° C.) to obtain 92 mg of an isomer mixture.

[1103] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IF, 5 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min;

[1104] gradient: 25% B within 15 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1105] isomer 89-1 (21.7 mg) having a HPLC retention time of 13.7 min.

[1106] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.93 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.48-7.31 (m, 2H), 7.30-7.28 (m, 2H), 6.98 (d, J=8.2 Hz, 1H), 4.15 (d, J=10.8 Hz, 2H), 3.56 (d, J=22.1 Hz, 3H), 3.13 (s, 2H), 2.78 (d, J=8.0 Hz, 1H), 2.66 (s, 3H), 2.33 (s, 4H), 1.77 (d, J=13.5 Hz, 9H), 1.09 (s, 2H). MS(ESI+): 552.2 (M+H).

[1107] Isomer 89-2 (21.1 mg) having a HPLC retention time of 19.5 min.

[1108] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ 10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (dd, J=11.5, 4.3 Hz, 1H), 7.43 (dd, J=14.1, 2.1 Hz, 1H), 7.30 (t, J=7.5 Hz, 2H), 6.98 (d, J=8.1 Hz, 1H), 4.15 (d, J=10.7 Hz, 1H), 3.59 (s, 3H), 3.21 (s, 2H), 2.78 (s, 2H), 1.88 (d, J=13.8 Hz, 3H), 2.33 (s, 4H), 1.76 (dd, J=13.7, 1.1 Hz, 2H). MS(ESI+): 552.2 (M+H).

Example 90 Compounds 90-1 and 90-2

[1109] ##STR00409##

[1110] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 m/min; gradient: 25% B-60% B, 8 min; detection wavelength: 220 nm; isomer mixture retention time: 5.15 min) to obtain 63 mg of an isomer mixture.

[1111] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IA, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 30% B within 20 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1112] isomer 90-1 (29.5 mg) having a HPLC retention time of 13.7 min.

[1113] 1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.92 (s, 1H), 9.23 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.50-7.34 (m, 2H), 7.29 (dd, J=16.0, 8.4 Hz, 2H), 6.96 (d, J=8.1 Hz, 1H), 3.58 (d, J=7.4 Hz, 2H), 3.47 (s, 2H), 3.30 (s, 4H), 3.04 (s, 2H), 2.34 (s, 4H), 1.77 (d, J=13.5 Hz, 12H), 1.58 (s, 2H). MS(ESI+): 566.2 (M+H).

[1114] Isomer 90-2 (20.2 mg) having a HPLC retention time of 16.6 min.

[1115] 1H NMR (400 MHz, DMSO-d.sub.6, ppm) δ 10.92 (s, 1H), 9.23 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.47-7.35 (m, 2H), 7.29 (dd, J=15.5, 8.3 Hz, 2H), 6.96 (d, J=8.1 Hz, 1H), 3.58 (d, J=9.9 Hz, 2H), 3.47 (s, 2H), 3.31 (s, 4H), 3.04 (s, 2H), 2.34 (s, 4H), 1.77 (d, J=13.5 Hz, 12H), 1.59 (s, 2H). MS(ESI+): 566.2 (M+H).

Example 91 Compounds 91-1 and 91-2

[1116] ##STR00410##

[1117] According to the preparation method of Example 58, 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxo-6-azabicyclo[3.1.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 15% B-52% B, 8 min; detection wavelength: 220 nm) to obtain 70 mg of an isomer mixture.

[1118] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (CHIRALPAK IA, 5 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 20% B within 29 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1119] isomer 91-1 (25.5 mg) having a HPLC retention time of 17.9 min.

[1120] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm) δ 10.87 (s, 1H), 9.28 (s, 1H), 8.52 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.8, 3.0 Hz, 1H), 7.33 (dt, J=18.0, 6.2 Hz, 3H), 6.98 (d, J=8.1 Hz, 1H), 4.15 (d, J=10.8 Hz, 2H), 3.56 (m, 3H), 3.13 (s, 2H), 2.78 (d, J=9.6 Hz, 1H), 2.67 (s, 3H), 2.37 (s, 1H), 1.80 (m, 9H), 1.08 (s, 2H). MS(ESI+): 556.2 (M+H).

[1121] Isomer 91-2 (30.3 mg) having a HPLC retention time of 24.2 min.

[1122] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm) δ 10.87 (s, 1H), 9.28 (s, 1H), 8.52 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=13.9, 8.8, 3.0 Hz, 1H), 7.33 (dt, J=18.0, 6.2 Hz, 3H), 6.98 (d, J=8.1 Hz, 1H), 4.15 (d, J=10.8 Hz, 2H), 3.56 (m, 3H), 3.13 (s, 2H), 2.78 (d, J=9.6 Hz, 1H), 2.67 (s, 3H), 2.37 (s, 1H), 1.80 (m, 9H), 1.08 (s, 2H). MS(ESI+): 556.2 (M+H).

Example 92 Compounds 92-1 and 92-2

[1123] ##STR00411##

[1124] According to the preparation method of Example 58, 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 15% B-50% B, 8 min; detection wavelength: 220 nm) to obtain 130 mg of an isomer mixture.

[1125] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (CHIRALPAK IF, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min; gradient: 30% B within 20 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1126] isomer 92-1 (28.9 mg) having a HPLC retention time of 3.65 min.

[1127] .sup.1H NMR (400 MHz, DMSO-d6, ppm) δ 10.86 (s, 1H), 9.26 (s, 1H), 8.51 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=14.0, 8.8, 3.1 Hz, 1H), 7.39-7.21 (m, 3H), 6.97 (d, J=8.1 Hz, 1H), 3.57 (d, J=10.1 Hz, 2H), 3.45 (d, J=10.0 Hz, 2H), 3.30 (s, 4H), 3.04 (s, 2H), 2.41 (d, J=20.5 Hz, 1H), 1.90-1.56 (m, 14H). MS(ESI+): 570.2 (M+H).

[1128] Isomer 92-2 (28.9 mg) having a HPLC retention time of 4.85 min.

[1129] .sup.1H NMR (400 MHz, DMSO-d6, ppm) δ 10.86 (s, 1H), 9.26 (s, 1H), 8.51 (s, 1H), 8.17 (s, 1H), 7.53 (ddd, J=14.0, 8.8, 3.1 Hz, 1H), 7.39-7.31 (m, 2H), 7.27 (d, J=8 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 3.57 (d, J=10.1 Hz, 2H), 3.45 (d, J=10.0 Hz, 2H), 3.30 (s, 4H), 3.04 (s, 2H), 2.41 (d, J=20.5 Hz, 1H), 1.90-1.56 (m, 14H). MS(ESI+): 570.2 (M+H).

Example 93 Compounds 93-1 and 93-2

[1130] ##STR00412##

[1131] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-chlorophenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-6-azabicyclo[3.1.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 20% B-55% B, 8 min; detection wavelength: 220 nm) to obtain 60 mg of an isomer mixture.

[1132] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IE, 3 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min; gradient: 50% B within 32 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1133] isomer 93-1 (23.7 mg) having a HPLC retention time of 23.7 min.

[1134] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.11 (s, 1H), 9.31 (s, 1H), 8.57 (s, 1H), 8.19 (s, 1H), 7.69 (dd, J=13.6, 2.6 Hz, 1H), 7.49 (dd, J=9.0, 2.6 Hz, 1H), 7.41 (d, J=2.3 Hz, 1H), 7.30-7.23 (m, 1H), 6.99 (d, J=8.1 Hz, 1H), 4.14 (d, J=10.6 Hz, 2H), 3.63-3.51 (m, 4H), 3.13 (s, 1H), 2.80 (t, J=11.3 Hz, 1H), 2.66 (s, 3H), 2.36 (d, J=6.9 Hz, 1H), 1.82 (d, J=13.7 Hz, 8H), 1.68 (d, J=7.8 Hz, 1H), 1.23-1.01 (m, 2H). MS(ESI+): 572.2 (M+H).

[1135] Isomer 93-2 (22.3 mg) having a HPLC retention time of 27.9 min.

[1136] .sup.1H HNMR (400 MHz, DMSO-d6, ppm):δ 11.11 (s, 1H), 9.31 (s, 1H), 8.57 (s, 1H), 8.19 (s, 1H), 7.69 (dd, J=13.6, 2.6 Hz, 1H), 7.49 (dd, J=9.0, 2.6 Hz, 1H), 7.41 (d, J=2.3 Hz, 1H), 7.30-7.23 (m, 1H), 6.99 (d, J=8.1 Hz, 1H), 4.14 (d, J=10.6 Hz, 2H), 3.63 (d, J=11.6 Hz, 4H), 3.13 (s, 1H), 2.80-2.77 (m, 1H), 2.66 (s, 3H), 2.36 (s, 1H), 1.82 (d, J=13.7 Hz, 8H), 1.68 (s, 1H), 1.11 (s, 2H). MS(ESI+): 572.2 (M+H).

Example 94 Compounds 94-1 and 94-2

[1137] ##STR00413##

[1138] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-chlorophenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 25% B-65% B, 8 min; detection wavelength: 254 nm; column temperature: 25° C.) to obtain 65 mg of an isomer mixture.

[1139] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (CHIRALPAK IA, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min; gradient: 50% B within 14 min, isogradient; detection wavelength: 254 nm; column temperature: 25° C.) to obtain:

[1140] isomer 94-1 (25.1 mg) having a HPLC retention time of 1.85 min.

[1141] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.10 (s, 1H), 9.30 (s, 1H), 8.56 (s, 1H), 8.19 (s, 1H), 7.69 (dd, J=13.6, 2.5 Hz, 1H), 7.49 (dd, J=9.1, 2.5 Hz, 1H), 7.40 (d, J=2.2 Hz, 1H), 7.27-7.20 (m, 1H), 6.98 (d, J=8.1 Hz, 1H), 3.58 (d, J=10.1 Hz, 2H), 3.45 (d, J=10.2 Hz, 2H), 3.28 (s, 4H), 3.04 (s, 2H), 2.39 (s, 1H), 1.82 (m, 12H), 1.77 (s, 2H). MS(ESI+): 586 (M+H).

[1142] Isomer 94-2 (23.4 mg) having a HPLC retention time of 2.73 min.

[1143] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.10 (s, 1H), 9.30 (s, 1H), 8.56 (s, 1H), 8.19 (s, 1H), 7.69 (dd, J=13.6, 2.5 Hz, 1H), 7.49 (dd, J=9.1, 2.5 Hz, 1H), 7.40 (d, J=2.2 Hz, 1H), 7.27-7.20 (m, 1H), 6.98 (d, J=8.1 Hz, 1H), 3.58 (d, J=10.1 Hz, 2H), 3.45 (d, J=10.2 Hz, 2H), 3.28 (s, 4H), 3.04 (s, 2H), 2.39 (s, 1H), 1.82 (m, 12H), 1.77 (s, 2H). MS(ESI+): 586 (M+H).

Example 95 Preparation of Compounds 95-1 and 95-2

[1144] ##STR00414##

[1145] According to the preparation method of Example 58, 2-azabicyclo[3.1.0]hexane hydrochloride in step b) is replaced with 3-azabicyclo[3.1.0]hexane-6-carbonitrile. The crude product is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 30% B-68% B, 8 min; detection wavelength: 220 nm; isomer mixture retention time: 7.85 min) to obtain an isomer mixture.

[1146] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IF, 5 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min;

[1147] gradient: 20% B within 17.5 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1148] isomer 95-1 (21.7 mg) having a HPLC retention time of 13.4 min.

[1149] .sup.1H NMR (400 MHz, DMSO-d6, ppm) δ 10.82 (s, 1H), 9.25 (s, 1H), 8.49 (s, 1H), 8.16 (s, 1H), 7.53 (ddd, J=13.9, 8.8, 3.1 Hz, 1H), 7.38-7.30 (m, 2H), 7.26 (d, J=2.2 Hz, 1H), 6.96 (d, J=8.1 Hz, 1H), 3.06 (d, J=10.1 Hz, 2H), 2.43 (d, J=9.0 Hz, 2H), 2.15 (s, 2H), 1.87 (s, 2H), 1.79 (d, J=13.7 Hz, 1H), 1.73-1.45 (m, 2H). MS(ESI+): 565.2 (M+H).

[1150] Isomer 95-2 (21.1 mg) having a HPLC retention time of 16.2 min.

[1151] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.82 (s, 1H), 9.25 (s, 1H), 8.49 (s, 1H), 8.16 (s, 1H), 7.53 (ddd, J=14.0, 8.7, 3.0 Hz, 1H), 7.37-7.29 (m, 2H), 7.26 (dd, J=8.1, 2.2 Hz, 1H), 6.96 (d, J=8.2 Hz, 1H), 3.07-2.97 (m, 2H), 2.94-2.69 (m, 2H), 2.54 (s, 1H), 2.43 (d, J=9.0 Hz, 4H), 2.15 (t, J=2.6 Hz, 2H), 1.87 (t, J=3.2 Hz, 1H), 1.79 (d, J=13.6 Hz, 6H), 1.73 (s, 2H), 1.45 (d, J=16.2 Hz, 2H). MS(ESI+): 565.2 (M+H).

Example 96 Preparation of Compounds 96-1 and 96-2

[1152] ##STR00415##

[1153] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-chlorophenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-azabicyclo[3.1.0]hexane-6-carbonitrile. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 45% B-85% B, 8 min; detection wavelength: 254 nm) to obtain 58 mg of an isomer mixture.

[1154] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IA, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 30% B within 37 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1155] isomer 96-1 (17.4 mg) having a HPLC retention time of 23 min.

[1156] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.10 (s, 1H), 9.30 (s, 1H), 8.55 (s, 1H), 8.19 (s, 1H), 7.69 (dd, J=13.6, 2.5 Hz, 1H), 7.48 (dd, J=9.0, 2.6 Hz, 1H), 7.39 (d, J=2.3 Hz, 1H), 7.27-7.20 (m, 1H), 6.97 (d, J=8.2 Hz, 1H), 3.03 (d, J=9.2 Hz, 2H), 2.83 (s, 2H), 2.54 (s, 1H), 2.43 (d, J=9.0 Hz, 4H), 2.15 (d, J=2.7 Hz, 2H), 1.82 (m, 9H), 1.49 (s, 2H). MS(ESI+): 581.2 (M+H).

[1157] Isomer 96-2 (23.1 mg) having a HPLC retention time of 30.8 min.

[1158] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.10 (s, 1H), 9.30 (s, 1H), 8.55 (s, 1H), 8.19 (s, 1H), 7.69 (dd, J=13.6, 2.5 Hz, 1H), 7.48 (dd, J=9.0, 2.6 Hz, 1H), 7.39 (d, J=2.3 Hz, 1H), 7.27-7.20 (m, 1H), 6.97 (d, J=8.2 Hz, 1H), 3.03 (d, J=9.2 Hz, 2H), 2.83 (s, 2H), 2.54 (s, 1H), 2.43 (d, J=9.0 Hz, 4H), 2.15 (d, J=2.7 Hz, 2H), 1.87 (s, 1H), 1.82 (d, J=13.7 Hz, 6H), 1.77-1.64 (m, 2H) 1.49 (s, 2H). MS(ESI+): 581.2 (M+H).

Example 97 Compounds 97-1 and 97-2

[1159] ##STR00416##

[1160] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-cyanophenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-azabicyclo[3.1.0]hexane-6-carbonitrile. The crude product is purified by reversed-phase high-performance liquid chromatography (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 m/min; gradient: 45% B-75% B, 10 min; detection wavelength: 220 nm; isomer mixture retention time: 8.72 min) to obtain 48 mg of an isomer mixture.

[1161] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IF, 3 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min;

[1162] gradient: 10% B within 26 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1163] isomer 97-1 (20 mg) having a HPLC retention time of 16.2 min.

[1164] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.72 (s, 1H), 9.42 (s, 1H), 8.85 (s, 1H), 8.27 (s, 1H), 8.13 (dd, J=13.8, 2.0 Hz, 1H), 7.90-7.77 (m, 1H), 7.38 (d, J=2.3 Hz, 1H), 7.29 (d, J=8.1 Hz, 1H), 7.02 (d, J=8.1 Hz, 1H), 3.03 (dd, J=9.3, 2.9 Hz, 2H), 2.86 (s, 2H), 2.69-2.66 (m, 1H), 2.44 (d, J=9.2 Hz, 4H), 2.15 (d, J=2.8 Hz, 2H), 1.87 (d, J=13.7 Hz, 7H), 1.75 (s, 2H), 1.49 (s, 2H). MS(ESI+): 572.2 (M+H).

[1165] Isomer 97-2 (20.2 mg) having a HPLC retention time of 23 min.

[1166] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.72 (s, 1H), 9.42 (s, 1H), 8.85 (s, 1H), 8.27 (s, 1H), 8.13 (dd, J=14.0, 2.0 Hz, 1H), 7.83 (d, J=9.0 Hz, 1H), 7.38 (d, J=2.2 Hz, 1H), 7.32-7.25 (m, 1H), 7.02 (d, J=8.1 Hz, 1H), 3.03 (d, J=9.1 Hz, 2H), 2.84 (s, 2H), 2.69-2.66 (m, 1H), 2.44 (d, J=9.0 Hz, 4H), 2.15 (d, J=2.7 Hz, 2H), 1.87 (d, J=13.8 Hz, 7H), 1.75 (s, 2H), 1.49 (s, 2H). MS(ESI+): 572.2 (M+H).

Example 98 Compounds 98-1 and 98-2

[1167] ##STR00417##

[1168] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-azabicyclo[3.1.0]hexane-6-carbonitrile. The crude product is purified by reversed-phase high-performance liquid chromatography (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 m/min; gradient: 50% B-66% B, 10 min; detection wavelength: 220 nm; isomer mixture retention time: 8.72 min) to obtain 63 mg of an isomer mixture.

[1169] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IF, 3 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min;

[1170] gradient: 20% B within 27 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1171] isomer 98-1 (20.5 mg) having a HPLC retention time of 19.1 min.

[1172] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.92 (s, 1H), 9.23 (s, 1H), 8.39 (s, 1H), 8.15 (s, 1H), 7.47-7.37 (m, 2H), 7.34-7.24 (m, 2H), 6.95 (d, J=8.1 Hz, 1H), 3.03 (d, J=9.2 Hz, 2H), 2.83 (s, 2H), 2.69-2.66 (m, 1H), 2.44 (d, J=9.2 Hz, 4H), 2.34 (s, 3H), 2.16 (s, 2H), 1.88 (s, 1H), 1.77 (d, J=13.5 Hz, 8H), 1.49 (s, 2H). MS(ESI+): 561.2 (M+H).

[1173] Isomer 98-2 (20.4 mg) having a HPLC retention time of 25.1 min.

[1174] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.92 (s, 1H), 9.24 (s, 1H), 8.39 (s, 1H), 8.15 (d, J=2.2 Hz, 1H), 7.47-7.37 (m, 2H), 7.34-7.24 (m, 2H), 6.95 (d, J=8.3 Hz, 1H), 3.02 (d, J=9.3 Hz, 2H), 2.93-2.74 (m, 3H), 2.34 (s, 4H), 2.21 (s, 3H), 2.16 (s, 2H), 1.88 (s, 1H), 1.84-1.66 (m, 8H), 1.49 (s, 2H). MS(ESI+): 561.2 (M+H).

Example 99 Compounds 99- and 99-2

[1175] ##STR00418##

[1176] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-difluoromethoxyphenyl)dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-azabicyclo[3.1.0]hexane-6-carbonitrile. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 m/min; gradient: 35% B-64% B, 10 min; detection wavelength: 220 nm; isomer mixture retention time: 9.6 min) to obtain an isomer mixture.

[1177] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IE, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min;

[1178] gradient: 10% B within 24 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1179] isomer 99-1 (22.5 mg) having a HPLC retention time of 14.3 min.

[1180] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.96 (s, 1H), 9.27 (s, 1H), 8.55 (s, 1H), 8.18 (s, 1H), 7.49-7.42 (m, 1H), 7.37 (d, J=2.3 Hz, 1H), 7.29 (d, J=8.6 Hz, 2H), 7.26-7.20 (m, 1H), 6.96 (d, J=8.1 Hz, 1H), 3.03 (d, J=9.2 Hz, 2H), 2.84 (s, 2H), 2.55 (s, 1H), 2.42 (d, J=9.2 Hz, 4H), 2.16 (t, J=2.6 Hz, 2H), 1.87 (s, 1H), 1.81 (d, J=13.6 Hz, 6H), 1.71 (s, 2H), 1.50 (s, 2H). MS(ESI+): 613.2 (M+H).

[1181] Isomer 99-2 (22.4 mg) having a HPLC retention time of 21.25 min.

[1182] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.96 (s, 1H), 9.27 (s, 1H), 8.55 (s, 1H), 8.18 (s, 1H), 7.49-7.42 (m, 1H), 7.37 (d, J=2.3 Hz, 1H), 7.32-7.21 (m, 3H), 6.96 (d, J=8.1 Hz, 1H), 3.03 (d, J=9.2 Hz, 2H), 2.84 (s, 2H), 2.55 (s, 1H), 2.42 (d, J=9.2 Hz, 4H), 2.15 (d, J=2.6 Hz, 2H), 1.87 (s, 1H), 1.81 (d, J=13.7 Hz, 6H), 1.71 (s, 2H), 1.51 (s, 2H). MS(ESI+):613.2 (M+H).

Example 100 Preparation of Compounds 100-1 and 100-2

[1183] ##STR00419##

[1184] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-trifluoromethoxyphenyl)dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-6-azabicyclo[3.1.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 30% B-60% B, 8 min; detection wavelength: 220 nm) to obtain 70 mg of an isomer mixture.

[1185] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IG, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 30% B within 25 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1186] isomer 100-1 (18.4 mg) having a HPLC retention time of 17.1 min.

[1187] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.15 (s, 1H), 9.32 (s, 1H), 8.65 (s, 1H), 8.21 (s, 1H), 7.66 (dd, J=13.8, 2.9 Hz, 1H), 7.46 (d, J=12.0 Hz, 1H), 7.40 (d, J=4.0 Hz, 1H), 7.27 (d, J=8.0 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 4.13 (dd, J=10.5, 5.5 Hz, 2H), 3.67-3.46 (m, 4H), 3.12 (s, 1H), 2.91-2.77 (m, 1H), 2.67 (d, J=11.1 Hz, 3H), 2.35 (d, J=7.1 Hz, 1H), 1.85-1.78 (m, 8H), 1.65 (d, J=8 Hz, 1H), 1.10 (s, 2H). MS(ESI+): 622.2 (M+H).

[1188] Isomer 100-2 (18.2 mg) having a HPLC retention time of 22.4 min.

[1189] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.15 (s, 1H), 9.32 (s, 1H), 8.65 (s, 1H), 8.21 (s, 1H), 7.66 (dd, J=13.8, 2.9 Hz, 1H), 7.46 (d, J=12.0 Hz, 1H), 7.40 (d, J=4.0 Hz, 1H), 7.27 (d, J=8.0 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 4.13 (dd, J=10.5, 5.5 Hz, 2H), 3.67-3.46 (m, 4H), 3.12 (s, 1H), 2.91-2.77 (m, 1H), 2.67 (d, J=11.1 Hz, 3H), 2.35 (d, J=7.1 Hz, 1H), 1.85-1.78 (m, 8H), 1.65 (d, J=8 Hz, 1H), 1.10 (s, 2H). MS(ESI+): 622.2 (M+H).

Example 101 Compounds 101-1 and 101-2

[1190] ##STR00420##

[1191] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-trifluoromethoxyphenyl)dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 40% B-70% B, 8 min; detection wavelength: 220 nm) to obtain 63 mg of an isomer mixture.

[1192] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IG, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 30% B within 23 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1193] isomer 101-1 (23.8 mg) having a HPLC retention time of 15.3 min.

[1194] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.16 (s, 1H), 9.30 (s, 1H), 8.65 (s, 1H), 8.21 (s, 1H), 7.66 (dd, J=13.9, 2.8 Hz, 1H), 7.44 (d, J=12.0 Hz, 1H), 7.37 (s, 1H), 7.24 (d, J=7.9 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 3.58 (d, J=10.1 Hz, 2H), 3.45 (d, J=10.2 Hz, 2H), 3.30 (s, 2H), 3.07 (s, 2H), 2.47-2.30 (m, 2H), 1.85 (s, 7H), 1.82 (s. 4H), 1.76-1.65 (m, 4H). MS(ESI+): 636.2 (M+H).

[1195] Isomer 101-2 (18.6 mg) having a HPLC retention time of 19.7 min.

[1196] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.16 (s, 1H), 9.30 (s, 1H), 8.65 (s, 1H), 8.21 (s, 1H), 7.66 (dd, J=13.9, 2.8 Hz, 1H), 7.44 (d, J=12.0 Hz, 1H), 7.37 (s, 1H), 7.24 (d, J=7.9 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 3.58 (d, J=10.1 Hz, 2H), 3.45 (d, J=10.2 Hz, 2H), 3.30 (s, 2H), 3.07 (s, 2H), 2.47-2.30 (m, 2H), 1.85 (s, 7H), 1.82 (s. 4H), 1.76-1.65 (m, 4H). MS(ESI+): 636.2 (M+H).

Example 102 Compounds 102-1 and 102-2

[1197] ##STR00421##

[1198] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-trifluoromethoxyphenyl)dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 3-azabicyclo[2.1.1]hexane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 20% B-60% B, 8 min; detection wavelength: 254 nm) to obtain 75 mg of an isomer mixture.

[1199] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IG, 3 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: n-hexane (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 20% B within 20 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1200] isomer 102-1 (18.6 mg) having a HPLC retention time of 15.7 min.

[1201] .sup.1H NMR (400 MHz, DMSO-d6, ppm):δ 11.16 (s, 1H), 9.31 (s, 1H), 8.66 (s, 1H), 8.21 (s, 1H), 7.66 (dd, J=13.9, 2.8 Hz, 1H), 7.45 (d, J=9.3 Hz, 1H), 7.40 (d, J=2.2 Hz, 1H), 7.26 (d, J=8.2 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 3.73-3.57 (m, 1H), 2.90 (s, 2H), 2.68 (d, J=18.6 Hz, 3H), 2.55 (s, 3H), 1.83 (d, J=13.7 Hz, 8H), 1.61 (s, 2H), 1.34 (s, 4H). MS(ESI+): 606.05 (M+H).

[1202] Isomer 102-2 (18.7 mg) having a HPLC retention time of 18.3 min.

[1203] .sup.1H NMR (400 MHz, DMSO-d6, ppm):δ 11.16 (s, 1H), 9.31 (s, 1H), 8.66 (s, 1H), 8.21 (s, 1H), 7.66 (dd, J=13.9, 2.9 Hz, 1H), 7.45 (d, J=9.5 Hz, 1H), 7.40 (d, J=2.2 Hz, 1H), 7.29-7.23 (m, 1H), 6.98 (d, J=8.1 Hz, 1H), 3.65 (s, 1H), 2.90 (s, 2H), 2.68 (d, J=19.3 Hz, 3H), 2.55 (s, 3H), 1.83 (d, J=13.7 Hz, 8H), 1.63 (d, J=15.2 Hz, 2H), 1.34 (s, 4H). MS(ESI+): 606.10 (M+H).

Example 103 Compounds 103-1 and 103-2

[1204] ##STR00422##

[1205] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-trifluoromethoxyphenyl)dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (1R,4R)-2-oxa-5-azabicyclo[2.2.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD chromatographic column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 m/min; gradient: 30% B-65% B, 8 min; detection wavelength: 220 nm; isomer mixture retention time: 6.65 min) to obtain 70 mg of an isomer mixture.

[1206] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IG, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine); mobile phase B: ethanol; flow rate: [1207] 20 ml/min;

[1208] gradient: 10% B within 21 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1209] isomer 103-1 (21.2 mg) having a HPLC retention time of 13.5 min.

[1210] .sup.1H-NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.14 (s, 1H), 9.30 (s, 1H), 8.65 (d, J=9.3 Hz, 1H), 8.20 (s, 1H), 7.65 (dd, J=13.8, 2.9 Hz, 1H), 7.44 (dd, J=8.4, 2.6 Hz, 1H), 7.38 (d, J=2.3 Hz, 1H), 7.26 (dd, J=8.0, 2.3 Hz, 1H), 6.97 (d, J=8.2 Hz, 1H), 4.33 (t, J 1.9 Hz, 1H), 3.89 (d, J=7.5 Hz, 1H), 3.71-3.66 (m, 1H), 3.53 (dd, J=7.6, 1.6 Hz, 1H), 2.99 (dd, J=9.5, 1.8 Hz, 1H), 2.87 (s, 2H), 2.69 (d, J=6.9 Hz, 1H), 2.55 (s, 1H), 2.46 (s, 1H), 2.32 (d, J=9.5 Hz, 1H), 1.83 (d, J=13.8 Hz, 8H), 1.72 (dd, J=9.3, 2.1 Hz, 1H), 1.65-1.58 (m, 1H), 1.55-1.28 (m, 2H). MS(ESI+): 622.2 (M+H).

[1211] Isomer 103-2 (21.7 mg) having a HPLC retention time of 17.8 min.

[1212] .sup.1H NMR (400 MHz, DMSO-d6, ppm):δ 11.11 (s, 1H), 9.29 (s, 1H), 8.63 (t, J 6.6 Hz, 1H), 8.20 (s, 1H), 7.65 (dd, J=13.9, 2.8 Hz, 1H), 7.45 (dd, J=9.2, 2.8 Hz, 1H), 7.39 (d, J=2.3 Hz, 1H), 7.25 (dd, J=8.0, 2.3 Hz, 1H), 6.96 (d, J=8.1 Hz, 1H), 4.33 (t, J 2.0 Hz, 1H), 3.89 (d, J=7.5 Hz, 1H), 3.68 (d, J=2.1 Hz, 1H), 3.53 (dd, J=7.5, 1.6 Hz, 1H), 2.99 (dd, J=9.6, 1.8 Hz, 1H), 2.88 (s, 2H), 2.68 (dt, J=14.3, 7.9 Hz, 1H), 2.59-2.52 (m, 1H), 2.48 (s, 1H), 2.33 (d, J=9.4 Hz, 1H), 1.83 (d, J=13.7 Hz, 8H), 1.72 (dd, J=9.4, 2.1 Hz, 1H), 1.61 (dd, J=9.4, 2.4 Hz, 1H), 1.43 (s, 2H). MS(ESI+): 622.2 (M+H).

Example 104 Compounds 104-1 and 104-2

[1213] ##STR00423##

[1214] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-trifluoromethoxyphenyl)dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD chromatographic column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 m/min; gradient: 30% B-65% B, 8 min; detection wavelength: 220 nm; isomer mixture retention time: 6.65 min) to obtain 75 mg of an isomer mixture.

[1215] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK ID, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine); mobile phase B: ethanol; flow rate: [1216] 20 ml/min;

[1217] gradient: 10% B within 24 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1218] isomer 104-1 (21.6 mg) having a HPLC retention time of 11.4 min.

[1219] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.29 (s, 1H), 9.51 (s, 1H), 8.66 (s, 1H), 8.24 (d, J=1.4 Hz, 1H), 7.68 (dd, J=13.8, 2.9 Hz, 1H), 7.53-7.47 (m, 1H), 7.39 (q, J=7.9, 6.3 Hz, 2H), 7.06 (t, J=8.3 Hz, 1H), 4.64 (dd, J=41.1, 26.0 Hz, 2H), 4.22 (t, J=9.7 Hz, 1H), 3.66 (dd, J=18.8, 9.5 Hz, 1H), 3.53-3.28 (m, 2H), 3.18 (d, J=11.4 Hz, 1H), 2.85-2.66 (m, 4H), 2.27 (s, 2H), 2.17 (t, J=9.6 Hz, 1H), 2.08 (d, J=11.1 Hz, 1H), 1.84 (d, J=13.7 Hz, 6H), 1.66-1.49 (m, 1H), 1.42 (p, J=11.7 Hz, 1H). MS(ESI+): 622.1 (M+H).

[1220] Isomer 104-2 (22.8 mg) having a HPLC retention time of 21.3 min.

[1221] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):11.15 (s, 1H), 9.30 (s, 1H), 8.65 (s, 1H), 8.20 (s, 1H), 7.65 (dd, J=13.8, 2.8 Hz, 1H), 7.47-7.42 (m, 1H), 7.39 (d, J=2.2 Hz, 1H), 7.26 (dd, J=8.2, 2.3 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 4.33 (t, J=2.0 Hz, 1H), 3.90 (d, J=7.5 Hz, 1H), 3.69 (d, J=2.2 Hz, 1H), 3.53 (dd, J=7.6, 1.7 Hz, 1H), 2.99 (dd, J=9.4, 1.8 Hz, 1H), 2.88 (s, 2H), 2.69 (d, J=7.1 Hz, 1H), 2.55 (s, 2H), 2.32 (d, J=9.5 Hz, 1H), 1.83 (d, J=13.7 Hz, 8H), 1.73 (d, J=2.1 Hz, 1H), 1.65-1.58 (m, 1H), 1.56-1.33 (m, 2H). MS(ESI+): 622.1 (M+H).

Example 105 Compounds 105-1 and 105-2

[1222] ##STR00424##

[1223] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-chlorophenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (1R,4R)-2-oxa-5-azabicyclo[2.2.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD chromatographic column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 mL/min; gradient: 3% B-73/B, 6 min; detection wavelength: 220 nm; isomer mixture retention time: 7.05 min) to obtain 70 mg of an isomer mixture.

[1224] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IF, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine); mobile phase B: ethanol; flow rate: 15 ml/min;

[1225] gradient: 30% B within 18 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1226] isomer 105-1 (26.4 mg) having a HPLC retention time of 11.7 min.

[1227] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.10 (s, 1H), 9.31 (s, 1H), 8.56 (s, 1H), 8.19 (s, 1H), 7.69 (dd, J=13.6, 2.6 Hz, 1H), 7.49 (dd, J=9.0, 2.5 Hz, 1H), 7.41 (d, J=2.3 Hz, 1H), 7.28-7.21 (m, 1H), 6.99 (d, J=8.1 Hz, 1H), 4.34 (d, J=2.5 Hz, 1H), 3.90 (d, J=7.5 Hz, 1H), 3.70 (s, 1H), 3.54 (dd, J=7.5, 1.6 Hz, 1H), 3.01 (dd, J=9.4, 1.8 Hz, 1H), 2.88 (s, 2H), 2.71 (s, 1H), 2.64-2.54 (m, 2H), 2.34 (d, J=9.3 Hz, 1H), 1.82 (d, J=13.7 Hz, 8H), 1.73 (d, J=9.9 Hz, 1H), 1.62 (d, J=8.6 Hz, 1H), 1.41 (s, 2H). MS(ESI+): 572.10 (M+H).

[1228] Isomer 105-2 (23.0 mg) having a HPLC retention time of 16.0 min.

[1229] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.09 (s, 1H), 9.30 (s, 1H), 8.56 (s, 1H), 8.19 (s, 1H), 7.69 (dd, J=13.6, 2.5 Hz, 1H), 7.50 (dd, J=9.0, 2.5 Hz, 1H), 7.41 (d, J=2.3 Hz, 1H), 7.24 (dd, J=7.7, 1.9 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 4.33 (t, J 1.9 Hz, 1H), 3.90 (d, J=7.4 Hz, 1H), 3.71 (s, 1H), 3.54 (dd, J=7.5, 1.6 Hz, 1H), 3.00 (dd, J=9.5, 1.8 Hz, 1H), 2.85 (d, J=31.5 Hz, 2H), 2.71 (s, 1H), 2.55 (s, 2H), 2.34 (d, J=9.4 Hz, 1H), 1.82 (d, J=13.7 Hz, 8H), 1.73 (d, J=9.1 Hz, 1H), 1.66-1.59 (m, 1H), 1.43 (s, 2H). MS(ESI+): 572.10 (M+H).

Example 106 Compounds 106-1 and 106-2

[1230] ##STR00425##

[1231] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-chlorophenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: Xselect CSH OBD column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile; flow rate: 60 m/min; gradient: 3% B-73% B, 6 min; detection wavelength: 220 nm; isomer mixture retention time: 7.05 min) to obtain 80 mg of an isomer mixture.

[1232] Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK IF, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine); mobile phase B: ethanol; flow rate: 15 ml/min;

[1233] gradient: 30% B within 18 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1234] isomer 106-1 (25.6 mg) having a HPLC retention time of 11.7 min.

[1235] .sup.1H NMR (400 MHz, DMSO-d6, ppm):δ 11.10 (s, 1H), 9.31 (s, 1H), 8.56 (s, 1H), 8.20 (s, 1H), 7.69 (dd, J=13.7, 2.6 Hz, 1H), 7.50 (dd, J=9.0, 2.5 Hz, 1H), 7.42 (d, J=2.3 Hz, 1H), 7.25 (dd, J=8.0, 2.2 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 4.41-4.30 (m, 1H), 3.91 (d, J=7.6 Hz, 1H), 3.72 (s, 1H), 3.60-3.50 (m, 1H), 3.01 (d, J=9.4 Hz, 1H), 2.80 (d, J=61.2 Hz, 3H), 2.54 (s, 2H), 2.37-2.33 (m, 1H), 1.82 (d, J=13.7 Hz, 8H), 1.74 (d, J=9.3 Hz, 1H), 1.63 (d, J=9.3 Hz, 1H), 1.43 (s, 2H). MS(ESI+): 572.10 (M+H).

[1236] Isomer 106-2 (27.9 mg) having a HPLC retention time of 16.0 min.

[1237] .sup.1H NMR (400 MHz, DMSO-d6, ppm):δ 11.10 (s, 1H), 9.31 (s, 1H), 8.56 (s, 1H), 8.20 (s, 1H), 7.69 (dd, J=13.7, 2.6 Hz, 1H), 7.50 (dd, J=9.0, 2.5 Hz, 1H), 7.42 (d, J=2.3 Hz, 1H), 7.25 (dd, J=8.0, 2.2 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 4.41-4.30 (m, 1H), 3.91 (d, J=7.6 Hz, 1H), 3.72 (s, 1H), 3.60-3.50 (m, 1H), 3.01 (d, J=9.4 Hz, 1H), 2.80 (d, J=61.2 Hz, 3H), 2.54 (s, 2H), 2.37-2.33 (m, 1H), 1.82 (d, J=13.7 Hz, 8H), 1.74 (d, J=9.3 Hz, 1H), 1.63 (d, J=9.3 Hz, 1H), 1.43 (s, 2H). MS(ESI+): 572.10 (M+H).

Example 107 Preparation of (S)-(4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)pyridin-3-yl)dimethyl phosphine oxide

[1238] ##STR00426##

[1239] a) Preparation of 2,5-dichloro-N-(3-iodopyridin-4-yl)pyrimidin-4-amine

[1240] 2,4,5-trichloropyrimidine (200 mg), 3-iodopyridine-4-amine (254 mg), and tetrahydrofuran (10 ml) are sequentially added to a reaction flask, added dropwise with lithium bis(trimethylsilyl)amide (2.2 ml, 1M) at −10° C., and reacted for 1 h. After the reaction is completed, the mixture is quenched by adding a saturated ammonium chloride solution (5 ml), and extracted with ethyl acetate (5 ml*2). After the solution is separated, the organic layers are merged, and dried with anhydrous sodium sulfate. The organic phase is concentrated to dryness. The residue is purified by silica-gel column chromatography (mobile phase: dichloromethane/methanol=50/1) to obtain 216 mg of the title product.

[1241] b) Preparation of (S)-5-chloro-N.sup.4-(3-iodopyridin-4-yl)-N.sup.2-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine

[1242] A compound 2,5-dichloro-N-(3-iodopyridin-4-yl)pyrimidin-4-amine (176 mg), (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (110 mg), n-butanol (5 ml), and trifluoroacetic acid (0.1 ml) are sequentially added to a reaction flask, and reacted in 400 W microwaves at 120° C. for 5 h. After the reaction is completed, the reactant is concentrated to dryness, and purified by column chromatography (mobile phase: dichloromethane/methanol=50/1) to obtain 86 mg of the title product.

[1243] c) Preparation of (S)-(4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)pyridin-3-yl)dimethyl phosphine oxide

[1244] (S)-5-chloro-N.sup.4-(3-iodopyridin-4-yl)-N.sup.2-(7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)pyrimidine-2,4-diamine (40 mg), dimethyl phosphine oxide (11 mg), potassium phosphate (22 mg), palladium acetate (2 mg), 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (4 mg), and N,N-dimethylformamide (10 ml) are sequentially added to a reaction flask, heated to 100° C. in the atmosphere of nitrogen, and reacted for 3 h. After the reaction is completed, the reactant is concentrated to dryness, and purified by silica-gel column chromatography (dichloromethane/methanol=20:1 v/v) to obtain 40 mg of the title product.

[1245] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 9.49 (s, 1H), 8.77 (s, 1H), 8.67 (d, J=8.4 Hz, 1H), 8.47 (d, J=5.6 Hz, 1H), 8.28 (s, 1H), 8.22 (s, 1H), 7.43 (s, 1H), 7.34 (d, J=7.0 Hz, 1H), 7.07 (d, J=8.1 Hz, 1H), 2.83 (s, 7H), 2.62 (s, 2H), 2.04 (s, 2H), 1.88 (d, J=13.8 Hz, 6H), 1.77 (s, 4H), 1.49 (dd, J=14.1, 3.7 Hz, 2H). MS(ESI+): 511.2 (M+H).

Example 108 (S)-(4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-1,3-phenylene)bis(dimethyl phosphine oxide)

[1246] ##STR00427##

[1247] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (4-amino-1,3-phenylene)bis(dimethyl phosphine oxide).

[1248] .sup.1H NMR (400 MHz, CDCl.sub.3): δ8.81 (ddd, J=8.7, 4.0, 2.4 Hz, 1H), 7.81 (ddd, J=13.7, 11.4, 1.9 Hz, 1H), 7.74-7.67 (m, 1H), 7.63-7.54 (m, 1H), 7.33 (dd, J=14.2, 2.3 Hz, 2H), 7.17-7.11 (m, 2H), 7.03 (d, J=8.1 Hz, 1H), 3.19 (m, 4H), 2.91-2.78 (m, 2H), 2.71 (m, 2H), 2.32 (m, 4H), 2.01 (m, 4H), 1.91 (s, 3H), 1.88 (s, 3H), 1.77 (s, J=1.7 Hz, 3H), 1.74 (s, J=1.7 Hz, 3H), 1.61 (m, 2H). MS(ESI+): 586.3 (M+H).

Example 109 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(1H-tetrazol-1-yl)phenyl)dimethyl phosphine oxide

[1249] ##STR00428##

[1250] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-(1H-tetrazol-1-yl)phenyl)dimethyl phosphine oxide.

[1251] .sup.1H NMR (400 MHz, CDCl.sub.3): δ 11.23 (s, 1H), 9.47 (s, 1H), 8.91 (dd, J=8.9, 4.4 Hz, 1H), 8.15 (s, 1H), 7.81-7.66 (m, 2H), 7.43 (d, J=2.3 Hz, 1H), 7.20-7.08 (m, 2H), 7.04 (d, J=8.1 Hz, 1H), 3.13 (m, 4H), 2.89-2.84 (m, 1H), 2.78-2.64 (m, 4H), 2.33 (m, 2H), 2.02 (m, 4H), 1.96 (s, 3H), 1.93 (s, 3H), 1.66 (m, 2H). MS(ESI+): 578.2 (M+H).

Example 110 (S)-(5-bromo 2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide

[1252] ##STR00429##

[1253] a) (2-amino-5-bromophenyl)dimethyl phosphine oxide

[1254] An intermediate 4-bromo-2-iodoaniline (1.5 g), dimethyl phosphine oxide (500 mg), tris(dibenzylideneacetone) dipalladium (480 mg), 4,5-bis(diphenylphosphine)-9,9-dimethylxanthene (900 mg), triethylamine (101 mg) and dioxane (30 mL) are added to a 100 mL single-necked bottle. The reaction solution is placed at 60° C., and reacted for 3 h under the protection of nitrogen. The reaction solution is concentrated to dryness, and the residue is purified by silica-gel column chromatography (dichloromethane/methanol=20:1 v/v) to obtain 927 mg of the title product.

[1255] b) (5-bromo-2-((2,5-dichloropyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide

[1256] An intermediate (2-amino-5-bromophenyl)dimethyl phosphine oxide (1.36 g), 2,4,5-trichloropyrimidine (1.3 g), N,N-dimethylformamide (15 mL) and N,N-diisopropylethylamine (600 mg) are placed in a 30 mL microwave tube under the protection of nitrogen. After the reaction solution is subjected to a microwave reaction at 110° C. for 1.5 h, the reaction is stopped. The reaction solution is concentrated to dryness, and the residue is slurried with 10 mL of methanol and filtered by suction to obtain 411 mg of the title product.

[1257] c) (S)-(5-bromo-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide

[1258] An intermediate (5-bromo-2-((2,5-dichloropyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide (120 mg), (S)-7-(pyrrolidine-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (69 mg), n-butanol (4 mL) and p-toluenesulfonic acid monohydrate (120 mg) are added to 10 mL microwave tube. The microwave reaction is performed at 120° C. for 1 h under the protection of nitrogen. The reaction solution is concentrated to dryness, and the residue is added with ethyl acetate (20 mL) and then washed with 2N sodium hydroxide (10 mL) for three times. The organic layer is concentrated to dryness, and the residue is purified by silica-gel column chromatography (dichloromethane/methanol=20:1 v/v) to obtain 200 mg of the title product.

[1259] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.11 (s, 1H), 9.31 (s, 1H), 8.49 (s, 1H), 8.19 (s, 1H), 7.79 (dd, J=13.5, 2.4 Hz, 1H), 7.60 (dd, J=9.0, 2.4 Hz, 1H), 7.43 (d, J=2.3 Hz, 1H), 7.22 (d, J=8.1 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 2.96-2.66 (m, 5H), 2.59-2.54 (m, 4H), 1.87 (s, 2H), 1.83 (s, 3H), 1.80 (s, 3H), 171-1.67 (m, 4H), 1.53 (br, 2H). MS(ESI+): 588.1 (M+H).

Example 111 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl-5-d)dimethyl phosphine oxide

[1260] ##STR00430##

[1261] An intermediate (S)-(5-bromo-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide (100 mg), deuterated methanol (0.5 mL), palladium acetate (4 mg), butyldi-1-adamantylphosphine (12 mg), potassium phosphate (72 mg) and toluene (4 mL) are added to a 25 mL single-necked bottle. The reaction solution is placed at 80° C., and reacted for 8 h under the protection of nitrogen. The reaction solution is desolventized to dryness. The reaction solution is concentrated to dryness. The residue is purified by silica-gel column chromatography (dichloromethane/methanol=20:1 v/v) to obtain 40 mg of the title product.

[1262] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.10 (s, 1H), 9.27 (s, 1H), 8.57 (s, 1H), 8.17 (s, 1H), 7.69-7.57 (m, 1H), 7.49 (d, J=8.6 Hz, 1H), 7.38 (s, 1H), 7.31 (d, J=8.6 Hz, 1H), 6.97 (d, J=8.0 Hz, 1H), 2.94-2.74 (m, 5H), 2.61-2.55 (m, 4H), 1.94-1.73 (m, 8H), 1.73-1.62 (s, 4H), 1.54-1.47 (m, 2H). MS(ESI+): 511.1 (M+H).

Example 112 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-cyclopropylphenyl)dimethyl phosphine oxide

[1263] ##STR00431##

[1264] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-cyclopropylphenyl)dimethyl phosphine oxide.

[1265] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.91 (s, 1H), 9.24 (s, 1H), 8.25 (s, 1H), 8.14 (s, 1H), 7.44 (d, J=2.3 Hz, 1H), 7.31 (dd, J=14.3, 2.2 Hz, 1H), 7.25 (dd, J=8.1, 2.3 Hz, 1H), 7.14 (dd, J=8.6, 2.2 Hz, 1H), 6.97 (d, J=8.2 Hz, 1H), 2.87 (m, 1H), 2.73 (m, 6H), 2.62-2.52 (m, 2H), 2.05-1.92 (m, 3H), 1.77 (m, 10H), 1.51 (s, 2H), 1.01-0.95 (m, 2H), 0.76-0.70 (m, 2H). MS(ESI+): 550.2 (M+H).

Example 113 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-6-methylphenyl) dimethyl phosphine oxide

[1266] ##STR00432##

[1267] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-6-methylphenyl) dimethyl phosphine oxide.

[1268] .sup.1H NMR (400 MHz, Chloroform-d) δ 11.96 (s, 1H), 8.38 (dd, J=8.5, 3.9 Hz, 1H), 8.06 (s, 1H), 7.40-7.33 (m, 1H), 7.31-7.27 (m, 2H), 7.01 (d, J=8.7 Hz, 1H), 6.93 (dd, J=7.5, 3.9 Hz, 1H), 6.84 (s, 1H), 2.93-2.72 (m, 6H), 2.66 (t, J=12.8 Hz, 2H), 2.46 (s, 3H), 2.17 (s, 2H), 1.98 (s, 3H), 1.94 (s, 3H), 1.86 (s, 5H), 1.57-1.50 (m, 2H). MS(ESI+): 524.2 (M+H).

Example 114 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(isopropyloxyl)phenyl dimethyl phosphine oxide

[1269] ##STR00433##

[1270] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-isopropyloxylphenyl)dimethyl phosphine oxide.

[1271] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.42 (s, 1H), 8.43 (dd, J=9.2, 5.1 Hz, 1H), 8.05 (s, 1H), 7.29 (d, J=7.8 Hz, 2H), 7.06-6.98 (m, 2H), 6.89 (s, 1H), 6.81 (dd, J=15.0, 2.9 Hz, 1H), 4.54 (p, J=6.0 Hz, 1H), 2.86 (s, 7H), 2.71-2.63 (m, 2H), 2.19 (s, 2H), 1.88 (d, J=6.2 Hz, 4H), 1.83 (s, 3H), 1.80 (s, 3H), 1.57 (s, 2H), 1.38 (s, 3H), 1.36 (s, 3H). MS(ESI+): 568.3 (M+H).

Example 115 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(methoxymethyl)phenyl)dimethylphosphine oxide

[1272] ##STR00434##

a) 2-iodo-4-(methoxymethyl)aniline

[1273] 4-(methoxymethyl)aniline (9 g), iodine (16.65 g) and sodium bicarbonate (16.53 g) are added to a dichloromethane (261 mL)/water (135 mL) solution, and stirred at 22° C. for 16 h. The reaction solution is quenched with saturated sodium thiosulfate (10 ml) at room temperature. The resulting mixture is extracted with dichloromethane (3×100 mL). The merged organic layer is then washed with a saturated aqueous sodium chloride solution (1×100 mL). The organic layer is then dried with anhydrous sodium sulfate. After filtration, the filtrate is concentrated under reduced pressure. The residue is purified by silica-gel column chromatography (petroleum ether:ethyl acetate=1:1 v/v) to obtain the title product (16 g). MS(ESI+): 264.0 (M+H).

[1274] b) (2-amino-5-(methoxymethyl)phenyl)dimethyl phosphine oxide

[1275] Dimethyl phosphine oxide (5.22 g) is added to N,N-dimethylformamide (224 mL) which was added with 2-iodo-4-(methoxymethyl)aniline (16 g, 60.82 mmol, 1.00 equivalent), potassium phosphate (14.20 g), palladium acetate (0.68 g) and 4,5-bisdiphenylphosphine-9,9-dimethylxanthene (1.76 g) in the atmosphere of nitrogen and stirred, reacted under stirring at 120° C. for 2 h. The mixture is cooled to room temperature. The mixture is filtered, and a filter cake is washed with N,N-dimethylformamide (3×5 mL). The filtrate is concentrated under reduced pressure. The residue is purified by silica-gel column chromatography (dichloromethane/methanol=20:1 v/v) to obtain the title product (12.9 g). MS(ESI+): 214.1 (M+H).

[1276] c) (2-((2,5-dichloropyrimidin-4-yl)amino)-5-(methoxymethyl)phenyl)dimethyl phosphine oxide

[1277] (2-((2,5-dichloropyrimidin-4-yl)amino)-5-(methoxymethyl)phenyl)dimethyl phosphine oxide (1.10 g), 2,4,5-trichloropyrimidine (1.23 g) and N,N-diisopropylethylamine (2.00 g) are added to N,N-dimethylformamide (22 mL) at room temperature, and stirred for 3 h. The resulting mixture is diluted with dichloromethane (30 mL). The reaction is quenched by adding water (10 ml) at 0° C. The resulting mixture is extracted with dichloromethane (3×50 mL). The merged organic layer is washed with saturated sodium chloride (1×50 mL) and dried with anhydrous sodium sulfate. After filtration, the filtrate is concentrated under reduced pressure. The residue is purified by silica-gel column chromatography (dichloromethane/methanol=20:1 v/v) to obtain the title product (1.28 g).

[1278] MS(ESI+): 360.0 (M+H).

[1279] d) (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(methoxymethyl)phenyl)dimethyl phosphine oxide

[1280] (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(methoxymethyl)phenyl)dimethylphosphine oxide (50.00 mg) and (S)-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-amine (31.98 mg) are added to isopropanol (2 mL), then added with a 1,4-dioxane solution (10 drops, 4M) of hydrogen chloride, and irradiated with microwaves at 130° C. for 3.5 h. The mixture is cooled to room temperature and concentrated under reduced pressure. The crude product is purified by reversed-phase high-performance liquid chromatography (column: YMC Actus Triart C18, 30*150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B:

[1281] acetonitrile; flow rate: 60 mL/min; gradient: 20% B to 50% B within 8 min; wavelength: 220 nm; retention time: 6.83 min; column temperature: 25° C.) to obtain the title product (20.2 mg).

[1282] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.07 (s, 1H), 9.26 (s, 1H), 8.52 (d, J=4.6 Hz, 1H), 8.17 (s, 1H), 7.53 (dd, J=14.0, 2.0 Hz, 1H), 7.44 (q, J 3.1 Hz, 2H), 7.26 (dd, J=8.1, 2.3 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 4.42 (s, 2H), 3.31 (s, 3H), 3.01-2.75 (m, 2H), 2.55 (s, 5H), 2.50 (s, 2H), 1.84 (s, 2H), 1.81 (s, 3H), 1.77 (s, 3H), 1.70 (q, J 3.6, 3.2 Hz, 4H), 1.54 (s, 2H). MS(ESI+): 554.2 (M+H).

Example 116 Compounds 116-1 and 116-2

[1283] ##STR00435##

a) 2-[(5-chloro-4-[[2-(dimethylphosphoryl)-4-(methoxymethyl)phenyl]amino]pyrimidin-2-yl)amino]-5,6,8,9-tetrahydrobenzo[7]annulen-7-one

[1284] (2-((2,5-dichloropyrimidin-4-yl)amino)-5-(methoxymethyl)phenyl)dimethyl phosphine oxide (1.10 g) and 2-amino-5,6,8,9-tetrahydrobenzo[7]annulen-7-one (0.54 g) are added to isopropanol (20 mL), then added with a 1,4-dioxane solution (10 drops, 4M) of hydrogen chloride, and irradiated with microwaves at 130° C. for 0.5 h. The mixture is then cooled to room temperature, and filtered, and the precipitated solid is collected and washed with isopropanol (1×10 mL) to obtain the title product (1 g). MS(ESI+): 499.2 (M+H).

[1285] b) (2-((2-((7-(2-azabicyclo[2.1.1]hexan-2-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)-5-chloropyrimidin-4-yl)amino)-5-(methoxymethyl)phenyl)dimethyl phosphine oxide

[1286] According to the preparation method in step c) of Example 58, 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 2-azabicyclo[2.1.1]hexane hydrochloride. The crude product is purified by reversed-phase high-performance liquid chromatography (column: XBridge-Prep-OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: 10 mmol/L ammonium bicarbonate aqueous solution, mobile phase B: acetonitrile (0.1% formic acid)); flow rate: 60 mL/min; gradient: 5% B-45% B, 8 min; detection wavelength: 220 nm; column temperature: 25° C.) to obtain an isomer mixture.

[1287] c) Chiral resolution is performed on the isomer mixture by chiral liquid chromatography (column: CHIRALPAK ID, 2 cm×25 cm, with a filler particle size of 5 μm; mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: [1288] 20 ml/min; gradient: 25% B within 13 min, isogradient; detection wavelength: 220/254 nm; column temperature: 25° C.) to obtain:

[1289] isomer 116-1 (47.4 mg) having a HPLC retention time of 8.6 min.

[1290] .sup.1H NMR (400 MHz, DMSO-d6, ppm):δ 11.10 (s, 1H), 9.31 (s, 1H), 8.56 (s, 1H), 8.20 (s, 1H), 7.69 (dd, J=13.7, 2.6 Hz, 1H), 7.50 (dd, J=9.0, 2.5 Hz, 1H), 7.42 (d, J=2.3 Hz, 1H), 7.25 (dd, J=8.0, 2.2 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 4.41-4.30 (m, 1H), 3.91 (d, J=7.6 Hz, 1H), 3.72 (s, 1H), 3.60-3.50 (m, 1H), 3.01 (d, J=9.4 Hz, 1H), 2.80 (d, J=61.2 Hz, 3H), 2.54 (s, 2H), 2.37-2.33 (m, 1H), 1.82 (d, J=13.7 Hz, 8H), 1.74 (d, J=9.3 Hz, 1H), 1.63 (d, J=9.3 Hz, 1H), 1.43 (s, 2H). MS(ESI+): 566.2 (M+H).

[1291] Isomer 116-2 (38.2 mg) having a HPLC retention time of 10.8 min.

[1292] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.07 (s, 1H), 9.27 (s, 1H), 8.53 (d, J=8.3 Hz, 1H), 8.18 (s, 1H), 7.54 (dd, J=14.0, 2.0 Hz, 1H), 7.45 (dt, J=5.0, 2.6 Hz, 2H), 7.27 (d, J=8.1 Hz, 1H), 6.98 (d, J=8.1 Hz, 1H), 4.43 (s, 2H), 3.66 (s, 1H), 3.32 (s, 3H), 2.89 (s, 2H), 2.75-2.62 (m, 3H), 2.52 (s, 2H), 2.50 (s, 1H), 1.91 (s, 2H), 1.79 (d, J=13.5 Hz, 6H), 1.62 (s, 2H), 1.34 (s, 4H). MS(ESI+): 566.2 (M+H).

Example 117 (S)-(4-chloro-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzoannulen-2-yl)amino)pyrimidin-4-yl)amino)-6-methylphenyl)dimethyl phosphine oxide

[1293] ##STR00436##

[1294] According to the preparation method of Example 115, 4-(methoxymethyl)aniline in step a) is replaced with 5-chloro-3-methylaniline.

[1295] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 12.11 (s, 1H), 9.30 (s, 1H), 8.29 (dd, J=6.2, 3.7 Hz, 1H), 8.17 (s, 1H), 7.40 (dd, J=8.1, 2.3 Hz, 1H), 7.22 (d, J=2.4 Hz, 1H), 7.12 (s, 1H), 6.97 (d, J=8.2 Hz, 1H), 2.87-2.76 (m, 2H), 2.68 (d, J=6.0 Hz, 4H), 2.62 (s, 1H), 2.54 (s, 2H), 2.45 (s, 3H), 1.93 (s, 2H), 1.90 (s, 3H), 1.87 (s, 3H), 1.78-1.66 (m, 4H), 1.47 (s, 2H). MS(ESI+): 558.1 (M+H).

Example 118 (S)-(4-chloro-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzoannulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluorophenyl)dimethyl phosphine oxide

[1296] ##STR00437##

[1297] According to preparation method (steps b˜d) of Example 115, 2-iodo-4-(methoxymethyl)aniline in step b) is replaced with 5-chloro-4-fluoro-2-iodoaniline.

[1298] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 11.09 (s, 1H), 9.36 (s, 1H), 8.70 (s, 1H), 8.20 (s, 1H), 7.73 (dd, J=13.7, 9.3 Hz, 1H), 7.36 (dd, J=8.1, 2.2 Hz, 1H), 7.26-7.22 (m, 1H), 7.01 (d, J=8.2 Hz, 1H), 2.92-2.75 (m, 3H), 2.70-2.64 (m, 4H), 2.59-2.53 (m, 2H), 1.93 (br, 2H), 1.83 (s, 3H), 1.80 (s, 3H), 1.72 (br, 4H), 1.49 (br, 2H). MS(ESI+): 562.1 (M+H).

Example 119 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)dimethyl phosphine oxide

[1299] ##STR00438##

[1300] (S)-(5-bromo-2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)phenyl)dimethyl phosphine oxide (50 mg), 2-oxo-6-azaspiro[3.3]heptane (18 mg), 2-bicyclohexylphosphino-2′,6′-diisopropoxybiphenyl (6 mg), tris(dibenzylideneacetone)dipalladium (6 mg), and cesium carbonate (55 mg) are added to 1,4-dioxane (5 ml) under the protection of nitrogen, and reacted at 100° C. for 3 h. After the reaction is completed, the solid is removed by suction filtration. The filter cake is washed twice with dichloromethane (10 ml×2). Organic layers are merged. The reaction solution is desolventized to dryness. The reaction solution is concentrated to dryness, and the residue is purified by silica-gel column chromatography (dichloromethane/methanol=20:1 v/v) to obtain 35 mg of the title product.

[1301] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ10.23 (s, 1H), 9.15 (s, 1H), 8.25 (s, 1H), 8.10-8.02 (m, 1H), 7.41 (d, J=2.3 Hz, 1H), 7.17 (d, J=8.1 Hz, 1H), 6.91 (d, J=8.2 Hz, 1H), 6.66-6.59 (m, 2H), 4.73 (s, 4H), 4.02 (s, 4H), 2.91-2.73 (m, 3H), 2.59 (br, 4H), 2.44-2.36 (m, 2H), 1.85 (br, 2H), 1.75-1.65 (m, 10H), 1.52 (br, 2H). MS(ESI+): 607.3 (M+H).

Example 120 Preparation of Compounds 120-1 and 120-2

[1302] ##STR00439##

[1303] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (3S)-pyrrolidine-3-carbonitrile hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 30% B-68% B within 8 min; wavelength: 254/220 nm) to obtain of a mixture of two isomers.

[1304] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IF, 5×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min; gradient: 20% B within 17.5 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1305] isomer 120-1 (20 mg) having a HPLC retention time of 13.4 min:

[1306] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.46-7.39 (m, 2H), 7.34-7.25 (m, 2H), 6.98 (d, J=8.2 Hz, 1H), 3.29-3.20 (m, 1H), 2.94-2.69 (m, 5H), 2.62-2.54 (m, 3H), 2.46 (s, 1H), 2.34 (s, 3H), 2.23-2.11 (m, 1H), 1.99-1.81 (m, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.52 (s, 2H). MS(ESI+): 549.2 (M+H).

[1307] isomer 120-2 (20 mg) having a HPLC retention time of 16.2 min:

[1308] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.93 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.47-7.39 (m, 2H), 7.35-7.25 (m, 2H), 6.98 (d, J=8.2 Hz, 1H), 3.23-3.25 (m, 1H), 2.95-2.70 (m, 5H), 2.57 (d, J=6.7 Hz, 4H), 2.34 (s, 3H), 2.23-2.11 (m, 1H), 2.00-1.81 (m, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.51 (s, 2H). MS(ESI+): 549.2 (M+H).

Example 121 Preparation of Compounds 121-1 and 121-2

[1309] ##STR00440##

[1310] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (3R)-3-fluoropyrrolidine hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 30% B-68% B within 8 min; wavelength:

[1311] 254/220 nm) to obtain of a mixture of two isomers.

[1312] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IF, 5×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min; gradient: 20% B within 17.5 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1313] isomer 121-1 (20 mg) having a HPLC retention time of 13.4 min:

[1314] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.51-7.38 (m, 2H), 7.35-7.22 (m, 2H), 6.98 (d, J=8.2 Hz, 1H), 5.20 (m, 1H), 2.99-2.69 (m, 5H), 2.57 (s, 2H), 2.45 (s, 2H), 2.34 (s, 3H), 2.09 (ddd, J=18.3, 14.3, 7.0 Hz, 1H), 1.91 (d, J=26.4 Hz, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.49 (s, 2H).

[1315] MS(ESI+): 542.2 (M+H).

[1316] Isomer 121-2 (20 mg) having a HPLC retention time of 16.2 min:

[1317] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.48-7.39 (m, 2H), 7.35-7.24 (m, 2H), 6.98 (d, J=8.1 Hz, 1H), 5.20 (d, J=56.2 Hz, 1H), 2.97-2.70 (m, 5H), 2.57 (s, 3H), 2.46 (s, 1H), 2.34 (s, 3H), 2.19- 2.04 (m, 1H), 1.87 (s, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.49 (s, 2H).

[1318] MS(ESI+): 542.2 (M+H).

Example 122 Preparation of Compounds 122-1 and 122-2

[1319] ##STR00441##

[1320] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (3S)-3-fluoropyrrolidine hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 20% B-58% B within 8 min; wavelength: 254/220 nm) to obtain a mixture of two isomers (63 mg).

[1321] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IE, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 19 ml/min; gradient: 35% B within 11 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1322] isomer 122-1 (15.2 mg) having a HPLC retention time of 5.9 min:

[1323] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.51-7.38 (m, 2H), 7.35-7.22 (m, 2H), 6.98 (d, J=8.2 Hz, 1H), 5.20 (m, 1H), 2.99-2.69 (m, 5H), 2.57 (s, 2H), 2.45 (s, 2H), 2.34 (s, 3H), 2.09 (ddd, J=18.3, 14.3, 7.0 Hz, 1H), 1.91 (d, J=26.4 Hz, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.49 (s, 2H). MS(ESI+): 542.2 (M+H).

[1324] Isomer 122-2 (20.2 mg) having a HPLC retention time of 9.0 min:

[1325] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.48-7.39 (m, 2H), 7.35-7.24 (m, 2H), 6.98 (d, J=8.1 Hz, 1H), 5.20 (d, J=56.2 Hz, 1H), 2.97-2.70 (m, 5H), 2.57 (s, 3H), 2.46 (s, 1H), 2.34 (s, 3H), 2.19- 2.04 (m, 1H), 1.87 (s, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.49 (s, 2H). MS(ESI+): 542.2 (M+H).

Example 123 Preparation of Compounds 123-1 and 123-2

[1326] ##STR00442##

[1327] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 2-oxo-6-azaspiro[3.4]octane oxalate. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 20% B-58% B within 8 min; wavelength: 254/220 nm) to obtain a mixture of two isomers (63 mg).

[1328] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IE, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 19 ml/min; gradient: 35% B within 12 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1329] isomer 123-1 (18.9 mg) having a HPLC retention time of 9.1 min:

[1330] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm):δ10.92 (s, 1H), 9.24 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.43 (d, J=14.8 Hz, 2H), 7.29 (dd, J=14.5, 8.4 Hz, 2H), 6.97 (d, J=8.1 Hz, 1H), 4.57-4.34 (m, 4H), 2.97-2.63 (m, 4H), 2.62-2.52 (m, 3H), 2.47 (s, 2H), 2.34 (d, J=3.1 Hz, 3H), 2.11-1.92 (m, 2H), 1.77 (d, J=13.5 Hz, 8H), 1.51 (s, 2H). MS(ESI+): 566.2 (M+H).

[1331] Isomer 123-2 (19.6 mg) having a HPLC retention time of 10.6 min:

[1332] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.92 (s, 1H), 9.24 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.53-7.40 (m, 2H), 7.29 (dd, J=14.4, 8.6 Hz, 2H), 6.97 (d, J=8.1 Hz, 1H), 4.68-4.30 (m, 4H), 2.98-2.64 (m, 4H), 2.62-2.53 (m, 3H), 2.42 (s, 2H), 2.34 (d, J=3.0 Hz, 3H), 2.03 (t, J=7.0 Hz, 2H), 1.77 (d, J=13.5 Hz, 8H), 1.52 (s, 2H). MS(ESI+): 566.2 (M+H).

Example 124 Preparation of Compounds 124-1 and 124-2

[1333] ##STR00443##

[1334] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (3R)-pyrrolidin-3-ol hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 10% B-45% B within 8 min; wavelength: 254/220 nm) to obtain a mixture of two isomers (71 mg).

[1335] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IE, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 25% B within 12 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1336] isomer 124-1 (15.7 mg) having a HPLC retention time of 7.9 min:

[1337] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.54-7.37 (m, 2H), 7.36-7.16 (m, 2H), 6.97 (d, J=8.1 Hz, 1H), 4.66 (s, 1H), 4.18 (s, 1H), 2.85 (d, J=29.2 Hz, 3H), 2.73-2.60 (m, 1H), 2.55 (s, 2H), 2.42 (d, J=40.0 Hz, 3H), 2.34 (s, 3H), 2.12-1.81 (m, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.52 (d, J=32.5 Hz, 3H). MS(ESI+): 540.2 (M+H).

[1338] Isomer 124-2 (18.3 mg) having a HPLC retention time of 10.0 min:

[1339] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.49-7.38 (m, 2H), 7.35-7.21 (m, 2H), 6.97 (d, J=8.1 Hz, 1H), 4.65 (d, J=4.6 Hz, 1H), 4.18 (s, 1H), 2.82 (dd, J=20.0, 11.6 Hz, 3H), 2.67 (dt, J=6.1, 3.1 Hz, 2H), 2.54 (s, 1H), 2.45 (s, 3H), 2.34 (s, 3H), 1.95 (dt, J=15.2, 7.6 Hz, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.53 (s, 3H). MS(ESI+): 540.2 (M+H).

Example 125 Preparation of Compounds 125-1 and 125-2

[1340] ##STR00444##

[1341] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (3S)-pyrrolidin-3-ol hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 15% B-60% B within 8 min; wavelength: 254/220 nm) to obtain a mixture of two isomers (56 mg).

[1342] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IE, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min; gradient: 30% B within 20 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1343] isomer 125-1 (21.1 mg) having a HPLC retention time of 13.2 min:

[1344] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.57-7.37 (m, 2H), 7.35-7.20 (m, 2H), 6.97 (d, J=8.1 Hz, 1H), 4.65 (d, J=4.6 Hz, 1H), 4.18 (s, 1H), 2.89 (s, 1H), 2.82 (d, J=9.3 Hz, 2H), 2.66 (s, 2H), 2.52 (s, 1H), 2.40 (d, J=9.6 Hz, 3H), 2.34 (s, 3H), 1.97 (dt, J 13.1, 7.0 Hz, 1H), 1.84 (s, 2H), 1.77 (d, J=13.5 Hz, 6H), 1.53 (d, J=30.2 Hz, 3H). MS(ESI+): 540.2 (M+H).

[1345] Isomer 125-2 (21.1 mg) having a HPLC retention time of 17.9 min:

[1346] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.48-7.37 (m, 2H), 7.34-7.22 (m, 2H), 6.97 (d, J=8.2 Hz, 1H), 4.65 (s, 1H), 4.26-4.10 (m, 1H), 2.89 (s, 1H), 2.82 (d, J=9.3 Hz, 2H), 2.66 (s, 2H), 2.52 (s, 1H), 2.40 (d, J=9.6 Hz, 3H), 2.34 (s, 3H), 1.97 (dt, J=13.1, 7.0 Hz, 1H), 1.84 (s, 2H), 1.77 (d, J=13.5 Hz, 6H), 1.52 (d, J=30.2 Hz, 3H). MS(ESI+): 540.2 (M+H).

Example 126 Preparation of Compounds 126-1 and 126-2

[1347] ##STR00445##

[1348] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (3R)-3-methoxypyrrolidine hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 10% B-55% B within 8 min; wavelength: 254/220 nm) to obtain a mixture of two isomers.

[1349] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IE, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 30% B within 20 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1350] isomer 126-1 (18.3 mg) having a HPLC retention time of 6.7 min:

[1351] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ 10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.43 (dd, J=13.4, 2.2 Hz, 2H), 7.29 (ddd, J=15.0, 8.4, 2.0 Hz, 2H), 6.97 (d, J=8.1 Hz, 1H), 3.86 (s, 1H), 3.18 (s, 3H), 2.95-2.72 (m, 3H), 2.69-2.58 (m, 1H), 2.55 (s, 1H), 2.46 (s, 4H), 2.34 (s, 3H), 2.04-1.80 (m, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.66 (s, 1H), 1.49 (s, 2H). MS(ESI+): 554.2 (M+H).

[1352] Isomer 126-2 (16.7 mg) having a HPLC retention time of 8.45 min:

[1353] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.40 (d, J=8.3 Hz, 1H), 8.15 (s, 1H), 7.49-7.39 (m, 2H), 7.35- 7.23 (m, 2H), 6.97 (d, J=8.1 Hz, 1H), 3.87 (s, 1H), 3.18 (s, 3H), 2.80 (s, 3H), 2.69-2.59 (m, 1H), 2.55 (s, 2H), 2.44 (s, 3H), 2.34 (s, 3H), 2.02-1.81 (m, 3H), 1.78 (s, 3H), 1.75 (s, 3H), 1.67 (s, 1H), 1.49 (s, 2H). MS(ESI+): 554.2 (M+H).

Example 127 Preparation of Compounds 127-1 and 127-2

[1354] ##STR00446##

[1355] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (3S)-3-methoxypyrrolidine hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 15% B-60% B within 8 min; wavelength: 254/220 nm) to obtain a mixture of two isomers (56 mg).

[1356] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IF, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 15 ml/min; gradient: 30% B within 20 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1357] isomer 127-1 (24.5 mg) having a HPLC retention time of 13.2 min:

[1358] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ 10.92 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.48-7.38 (m, 2H), 7.34-7.22 (m, 2H), 6.97 (d, J=8.2 Hz, 1H), 3.87 (s, 1H), 3.18 (s, 3H), 2.82 (q, J 14.8, 8.1 Hz, 3H), 2.64 (d, J=7.8 Hz, 1H), 2.54 (s, 2H), 2.44 (s, 3H), 2.34 (s, 3H), 2.03-1.80 (m, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.66 (s, 1H), 1.49 (s, 2H). MS(ESI+): 554.2 (M+H).

[1359] Isomer 127-2 (22.3 mg) having a HPLC retention time of 17.9 min:

[1360] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm):δ10.92 (s, 1H), 9.25 (s, 1H), 8.39 (s, 1H), 8.15 (s, 1H), 7.43 (dd, J=13.5, 2.2 Hz, 2H), 7.29 (ddd, J=14.9, 8.5, 2.0 Hz, 2H), 6.97 (d, J=8.1 Hz, 1H), 3.86 (dt, J 7.2, 3.6 Hz, 1H), 3.18 (s, 3H), 2.82 (q, J 14.8, 8.1 Hz, 3H), 2.64 (d, J=7.8 Hz, 1H), 2.54 (s, 2H), 2.44 (s, 3H), 2.34 (s, 3H), 2.03-1.80 (m, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.65 (t, J 11.1 Hz, 1H), 1.49 (s, 2H). MS(ESI+): 554.2 (M+H).

Example 128 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-cyclopropoxyphenyl)dimethyl phosphine oxide

[1361] ##STR00447##

[1362] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-cyclopropoxyphenyl)dimethyl phosphine oxide.

[1363] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ 10.56 (s, 1H), 9.22 (s, 1H), 8.32 (s, 1H), 8.13 (s, 1H), 7.38 (m, 1H), 7.32 (m, 3H), 6.94 (d, J=8.4 Hz, 1H), 3.93 (m, 1H), 2.87 (m, 2H), 2.53 (m, 4H), 2.42 (m, 3H), 1.83 (m, 2H), 1.77 (m, 3H), 1.73 (m, 3H) 1.69 (m, 4H), 1.53 (m, 2H), 0.82 (m, 2H), 0.70 (m, 2H). MS(ESI+): 566.2 (M+H).

Example 129 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluoro-4-methylphenyl)dimethyl phosphine oxide

[1364] ##STR00448##

[1365] According to the preparation method of Example 115, 4-(methoxymethyl)aniline in step a) is replaced with 4-fluoro-2-iodo-5-methylaniline.

[1366] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm):δ10.79 (s, 1H), 9.24 (s, 1H), 8.36 (s, 1H), 8.16 (s, 1H), 7.45 (dd, J=13.8, 9.5 Hz, 1H), 7.37 (dd, J=8.0, 2.3 Hz, 1H), 7.22 (s, 1H), 6.95 (d, J=8.1 Hz, 1H), 2.89 (s, 1H), 2.80 (s, 2H), 2.56-2.48 (m, 4H), 2.43 (d, J=9.4 Hz, 2H), 2.23 (s, 3H), 1.76 (d, J=13.6 Hz, 8H), 1.72-1.64 (m, 4H), 1.51 (s, 2H). MS(ESI+): 542.2 (M+H).

Example 130 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-4-methylphenyl)dimethyl phosphine oxide

[1367] ##STR00449##

[1368] According to the preparation method of Example 115, 4-(methoxymethyl)aniline in step a) is replaced with 2-iodo-5-methylaniline.

[1369] .sup.1H NMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.78 (s, 1H), 8.59 (s, 1H), 8.39-8.32 (m, 1H), 8.08 (s, 1H), 7.44 (dd, J=8.1, 2.3 Hz, 1H), 7.18 (s, 1H), 7.06-6.98 (m, 2H), 6.94 (dt, J=7.9, 2.0 Hz, 1H), 3.09 (s, 4H), 2.90-2.65 (m, 5H), 2.32 (s, 5H), 1.95 (t, J=3.9 Hz, 3H), 1.81 (d, J=13.1 Hz, 6H), 1.58-1.46 (m, 2H), 1.26 (p, J=7.7, 7.0 Hz, 1H). MS(ESI+): 524.2 (M+H).

Example 131 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-fluoro-4-methoxylphenyl)dimethyl phosphine oxide

[1370] ##STR00450##

[1371] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-4-methoxyl-5-fluorophenyl)dimethyl phosphine oxide. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: Xselect CSH-OBD column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 15% B-50% B within 8 min; wavelength: 254/220 nm) to obtain the title product (65 mg). The HPLC retention time is 7.65 min.

[1372] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.92 (s, 1H), 9.24 (s, 1H), 8.19 (s, 1H), 8.10 (dd, J=8.1, 4.1 Hz, 1H), 7.50 (dd, J=13.4, 11.5 Hz, 1H), 7.33 (d, J=2.4 Hz, 1H), 7.25 (dd, J=8.0, 2.3 Hz, 1H), 6.93 (d, J=8.1 Hz, 1H), 3.59 (s, 3H), 2.89 (s, 1H), 2.77 (s, 1H), 2.54 (s, 4H), 2.42 (s, 3H), 1.82 (s, 2H), 1.76 (d, J=13.6 Hz, 6H), 1.69 (d, J=6.3 Hz, 4H), 1.51 (s, 2H). MS(ESI+): 558.2 (M+H).

Example 132 (S)-(2-chloro-6-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo [7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-3-fluorophenyl)dimethyl phosphine oxide

[1373] ##STR00451##

[1374] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (2-amino-5-fluoro-6-chlorophenyl)dimethyl phosphine oxide. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 15% B-55% B within 8 min; wavelength: 254/220 nm) to obtain the title product (28.3 mg). The HPLC retention time is 7.07 min.

[1375] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ12.20 (s, 1H), 9.28 (s, 1H), 8.65 (s, 1H), 8.18 (s, 1H), 7.53 (dd, J=9.4, 8.3 Hz, 1H), 7.35 (d, J=2.3 Hz, 1H), 7.29 (dd, J=8.2, 2.2 Hz, 1H), 6.99 (d, J=8.2 Hz, 1H), 2.87 (s, 2H), 2.55-2.53 (m, 4H), 2.49-2.29 (m, 3H), 2.04 (d, J=13.9 Hz, 6H), 1.86 (s, 2H), 1.69 (s, 4H), 1.52 (s, 2H). MS(ESI+): 562.2 (M+H).

Example 133 Compounds 133-1 and 133-2

[1376] ##STR00452##

[1377] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-cyclopropoxyphenyl)dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with 2-azabicyclo[2.1.1]hexane hydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 20% B-55% B within 8 min; wavelength: 254/220 nm) to obtain a mixture of two isomers (65 mg).

[1378] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IG, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 20 ml/min; gradient: 25% B within 9 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1379] isomer 133-1 (21.5 mg) having a HPLC retention time of 7.5 min:

[1380] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ 10.53 (s, 1H), 9.21 (s, 1H), 8.32 (s, 1H), 8.12 (s, 1H), 7.38 (d, J=2.3 Hz, 1H), 7.28-7.19 (m, 3H), 6.95 (d, J=8.1 Hz, 1H), 3.92 (tt, J 6.0, 2.9 Hz, 1H), 3.66 (d, J=6.5 Hz, 1H), 2.89 (s, 2H), 2.71 (dt, J 6.0, 2.8 Hz, 1H), 2.67 (s, 2H), 2.54 (s, 2H), 1.90 (s, 2H), 1.75 (d, J=13.5 Hz, 6H), 1.62 (s, 2H), 1.40-1.30 (m, 5H), 0.83 (tt, J 4.7, 2.4 Hz, 2H), 0.69 (p, J 3.7, 3.0 Hz, 2H). MS(ESI+): 578.2 (M+H).

[1381] Isomer 133-2 (21.8 mg) having a HPLC retention time of 11.2 min:

[1382] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm):δ10.55 (s, 1H), 9.21 (s, 1H), 8.32 (s, 1H), 8.13 (s, 1H), 7.39 (d, J=2.3 Hz, 1H), 7.29-7.19 (m, 3H), 6.95 (d, J=8.1 Hz, 1H), 3.92 (tt, J 6.0, 2.9 Hz, 1H), 3.66 (s, 1H), 2.89 (s, 2H), 2.74-2.64 (m, 3H), 2.56 (d, J=12.5 Hz, 2H), 1.89 (s, 2H), 1.75 (d, J=13.5 Hz, 6H), 1.62 (s, 2H), 1.37-1.30 (m, 5H), 0.82 (td, J=5.5, 4.6, 2.2 Hz, 2H), 0.69 (p, J 3.8, 3.0 Hz, 2H). MS(ESI+): 578.2 (M+H).

Example 134 (S)-(6-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-3-fluoro-2-methoxyphenyl)dimethyl phosphine oxide

[1383] ##STR00453##

[1384] According to the preparation method of Example 1, 2-amino-N,N-dimethyl benzenesulfonamide in step a) is replaced with (6-amino-3-fluoro-2-methoxyphenyl)dimethyl phosphine oxide. The crude product is purified by apreparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 15% B-60% B within 8 min; wavelength: 254/220 nm) to obtain the title product (26 mg). The HPLC retention time is 7.33 min.

[1385] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ12.06 (s, 1H), 9.27 (s, 1H), 8.45 (s, 1H), 8.15 (s, 1H), 7.43-7.27 (m, 3H), 7.01 (d, J=8.1 Hz, 1H), 4.01 (d, J=3.3 Hz, 3H), 2.89 (s, 2H), 2.54 (d, J=5.2 Hz, 4H), 2.44 (s, 3H), 1.84 (d, J=14.1 Hz, 8H), 1.70 (d, J=5.8 Hz, 4H), 1.53 (s, 2H). MS(ESI+): 558.2 (M+H).

Example 135 (S)-(6-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-3-fluoro-2-methylphenyl)dimethyl phosphine oxide

[1386] ##STR00454##

[1387] According to the preparation method of Example 47, 5-iodoquinoxaline-6-amine in step a) is replaced with 3-methyl-4-fluoroaniline. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: Xselect CSH-OBD column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 15% B-50% B within 8 min; wavelength: 254/220 nm) to obtain the title product (12.2 mg). The HPLC retention time is 7.65 min.

[1388] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ11.29 (s, 1H), 9.21 (s, 1H), 8.10 (d, J=20.0 Hz, 2H), 7.38-7.29 (m, 2H), 7.20 (dd, J=8.2, 2.2 Hz, 1H), 6.92 (d, J=8.2 Hz, 1H), 2.86 (s, 1H), 2.72 (s, 1H), 2.60 (s, 4H), 2.48 (s, 2H), 2.40 (d, J=2.8 Hz, 3H), 1.87 (d, J=13.4 Hz, 8H), 1.72 (d, J=5.9 Hz, 4H), 1.48 (s, 2H). MS(ESI+): 542.2 (M+H).

Example 136 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-4-cyano-5-methoxyphenyl)dimethyl phosphine oxide

[1389] ##STR00455##

[1390] According to the preparation method of Example 47, 5-iodoquinoxaline-6-amine in step a) is replaced with 3-cyano-4-methoxyaniline.

[1391] The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: YMC-Actus Triart C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 20% B-45% B within 8 min; wavelength: 254/220 nm) to obtain the title product (9.6 mg). The HPLC retention time is 6.95 min.

[1392] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ10.71 (s, 1H), 9.33 (s, 1H), 8.64 (s, 1H), 8.17 (s, 1H), 7.36 (d, J=60.0 Hz, 1H), 7.31 (d, J=4.0 Hz, 1H), 7.21 (s, 1H), 6.98 (d, J=8.1 Hz, 1H), 3.99 (s, 3H), 2.84 (d, J=16.5 Hz, 2H), 2.51-2.45 (m, 4H), 2.42 (s, 3H), 1.84-1.80 (m, 8H), 1.69 (p, J=2.9 Hz, 4H), 1.50 (s, 2H). MS(ESI+): 565.2 (M+H).

Example 137 Compounds 137-1 and 137-2

[1393] ##STR00456##

[1394] According to the preparation method of Example 58, (2-amino-5-fluorophenyl)dimethyl phosphine oxide in step a) is replaced with (2-amino-5-methylphenyl) dimethyl phosphine oxide, and 2-azabicyclo[3.1.0]hexane hydrochloride in step c) is replaced with (3R)-pyrrolidine-3-cyanohydrochloride. The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 20% B-65% B within 8 min; wavelength: 254/220 nm) to obtain a mixture of two isomers (50 mg).

[1395] The mixture of two isomers is purified by a chiral high-performance liquid chromatography column (column: CHIRALPAK IE, 2×25 cm (filler 5 μm); mobile phase A: methyl tert-butyl ether (0.1% diethylamine), mobile phase B: ethanol; flow rate: 19 ml/min; gradient: 30% B within 9 min, isogradient; detection wavelength: 220/254 nm; and column temperature: 25° C.) to obtain:

[1396] isomer 137-1 (10.5 mg) having a HPLC retention time of 6.7 min:

[1397] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm): δ 10.93 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.48-7.39 (m, 2H), 7.35-7.25 (m, 2H), 6.98 (d, J=8.1 Hz, 1H), 3.23 (s, 2H), 2.89-2.70 (m, 5H), 2.55 (d, J=6.3 Hz, 3H), 2.34 (s, 3H), 2.15 (td, J=8.9, 8.3, 5.2 Hz, 1H), 1.94-1.86 (m, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.51 (s, 2H).

[1398] Isomer 137-2 (10.6 mg) having a HPLC retention time of 7.8 min:

[1399] .sup.1HNMR (400 MHz, DMSO-d.sub.6, ppm):δ10.93 (s, 1H), 9.25 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 7.48-7.39 (m, 2H), 7.35-7.25 (m, 2H), 6.98 (d, J=8.1 Hz, 1H), 3.26-3.20 (m, 2H), 2.89-2.70 (m, 6H), 2.57 (d, J=6.3 Hz, 2H), 2.34 (s, 3H), 2.15 (td, J=8.9, 8.3, 5.2 Hz, 1H), 1.94-1.86 (m, 3H), 1.77 (d, J=13.5 Hz, 6H), 1.51 (s, 2H). MS(ESI+): 549.2 (M+H).

Example 138 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(2-hydroxypropan-2-yl)phenyl))dimethyl phosphine oxide

[1400] ##STR00457##

[1401] According to the preparation method of Example 47, 5-iodoquinoxaline-6-amine in step a) is replaced with 2-(4-aminophenyl)propan-2-ol.

[1402] The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 10% B-50% B within 8 min; wavelength: 254/220 nm) to obtain the title product (11 mg). The HPLC retention time is 6.73 min.

[1403] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ11.00 (s, 1H), 9.26 (s, 1H), 8.44 (s, 1H), 8.16 (s, 1H), 7.59 (t, J=11.7 Hz, 2H), 7.45 (s, 1H), 7.26 (d, J=8.0 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 5.12 (s, 1H), 2.90 (s, 6H), 1.85 (s, 3H), 1.79 (s, 3H), 1.76 (s, 3H), 1.70 (s, 5H), 1.57 (s, 3H), 1.46 (s, 6H). MS(ESI+): 568.2 (M+H).

Example 139 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(2-methoxypropan-2-yl)phenyl)dimethyl phosphine oxide

[1404] ##STR00458##

[1405] According to the preparation method of Example 47, 5-iodoquinoxaline-6-amine in step a) is replaced with 4-(2-methoxypropan-2-yl)aniline.

[1406] The crude product is purified by a preparative high-performance liquid phase under the following conditions (column: XBridge Prep OBD C.sub.18 column, 30×150 mm, with a filler particle size of 5 μm; mobile phase A: water (10 mmol/L ammonium bicarbonate), mobile phase B: acetonitrile; flow rate: 60 ml/min; gradient: 15% B-55% B within 8 min; wavelength: 254/220 nm) to obtain the title product (19.3 mg). The HPLC retention time is 6.42 min.

[1407] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ11.11 (s, 1H), 9.27 (s, 1H), 8.53 (d, J=7.0 Hz, 1H), 8.17 (s, 1H), 7.52-7.43 (m, 3H), 7.24 (d, J=8.3 Hz, 1H), 6.97 (d, J=8.1 Hz, 1H), 3.01 (s, 3H), 2.91 (s, 2H), 2.54 (d, J=5.2 Hz, 5H), 2.48 (s, 2H), 1.85 (s, 2H), 1.81 (d, J=13.5 Hz, 6H), 1.69 (s, 4H), 1.56 (s, 2H), 1.49 (s, 6H). MS(ESI+): 582.2 (M+H).

Example 140 (S)-1-(4-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-3-(dimethylphosphoryl)phenyl)cyclopropane-1-carbonitrile

[1408] ##STR00459##

[1409] According to the preparation method of Example 47, 5-iodoquinoxaline-6-amine in step a) is replaced with 1-(4-aminophenyl)cyclopropanecarbonitrile.

[1410] .sup.1HNMR (400 MHz, DMSO-d6, ppm):δ11.13 (s, 1H), 9.30 (s, 1H), 8.56 (s, 1H), 8.26 (s, 1H), 7.53 (dd, J=8.8, 2.3 Hz, 1H), 7.44 (d, J=2.3 Hz, 1H), 7.36 (dd, J=14.0, 2.4 Hz, 1H), 7.28-7.22 (m, 1H), 6.99 (d, J=8.2 Hz, 1H), 2.95-2.77 (m, 3H), 2.72-2.55 (m, 6H), 2.00-1.88 (m, 2H), 1.82 (s, 3H), 1.78 (s, 3H), 1.77-1.70 (m, 6H), 1.62-1.48 (m, 4H). MS(ESI+): 575.3 (M+H).

Example 141 (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino)pyrimidin-4-yl)amino)-5-(hydroxymethyl)phenyl)dimethyl phosphine oxide

[1411] ##STR00460##

[1412] Acetic acid (10 ml) and an acetic acid solution (1 ml, 30% w/w) of hydrogen bromide are added to (S)-(2-((5-chloro-2-((7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl]amino)pyrimidin-4-yl)amino)-5-methoxymethyl)dimethyl phosphine oxide (500 mg), and reacted hermetically at 100° C. for 16 h. after the reaction is completed, a 2N aqueous sodium hydroxide solution is added to adjust the pH=9, and a viscous solid was precipitated. The viscous solid is purified by column chromatography (dichloromethane:methanol=10:1 v/v) to obtain the title product (50 mg).

[1413] 1H NMR (400 MHz, Chloroform-d) δ 10.85 (s, 1H), 8.50 (dd, J=8.7, 4.4 Hz, 1H), 8.06 (s, 1H), 7.67 (s, 1H), 7.49 (d, J=8.7 Hz, 1H), 7.20-7.12 (m, 1H), 7.09-7.00 (m, 2H), 6.90 (dd, J=8.0, 2.4 Hz, 1H), 4.67 (d, J=4.9 Hz, 2H), 3.09 (m, 4H), 2.88 (dt, J=13.3, 6.7 Hz, 2H), 2.76-2.62 (m, 4H), 2.48 (m, 1H), 2.25 (m, 1H), 1.98 (q, J=3.9 Hz, 4H), 1.83 (dd, J=13.1, 4.3 Hz, 6H), 1.60 (d, J=11.1 Hz, 2H). MS(ESI+): 540.3 (M+H).

Part II Biological Activity Test

[1414] The specific structure of the positive drug 1 (BGB324) used in the activity test is as follows:

##STR00461##

[1415] The specific structure of the positive drug 2 (TP0903) is as follows:

##STR00462##

[1416] The above compounds are purchased from Shanghai Shenghong Biological Technology Co., Ltd.

Test 1: Inhibitory Activity of Compound Against AXL Kinase

1. Experimental Process

[1417] a) AXL enzyme (Carna, 08-107) configuration and addition: a 1×enzyme buffer (200 μL of Enzymatic buffer kinase 5×, 10 μL of 500 mM MgCl.sub.2, 10 μL of 100 mM DTT and 6.26 μL of 2500 nM SEB are added with 773.75 μL of H.sub.2O, and prepared into 1 ml of 1× enzyme buffer) is used. AXL enzyme is diluted from 33.33 ng/uL to 0.027 ng/μL (1.67×, final conc.=0.016 ng/uL), a BioTek (MultiFlo FX) automatic liquid dispenser is used, and 6 μL of enzyme solution having a 1.67-fold final concentration is added respectively to compound wells and positive control wells; and 6 μL of 1×Enzymatic buffer is added to negative control wells.

[1418] b) Compound preparation and addition: the compounds and positive drugs prepared in the examples are diluted from 10 mM to 100 μM by DMSO, and titrated with a compound titrator (Tecan, D300e). The titrated solution is automatically sprayed by the titrator to each well to reach a required concentration, wherein the first concentration is 1 μM, and after ½ log dilution, a total of 8 concentrations are obtained. The resulting mixture is centrifuged at 2500 rpm for 30 s and incubated at room temperature for 15 min.

[1419] c) Preparation and addition of ATP and substrate: ATP (Sigma, A7699) is diluted with 1× enzyme buffer from 10 mM to 75 μM (5×), and the final concentration is 15 μM; the substrate TK Substrate 3-biotin (Cisbio, 61TK0BLC) is diluted with 1× enzyme buffer from 500 μM to 5 μM (5×), andthe final concentration is 1; ATP and the substrate are mixed in equal volume to obtain a mixed solution; the mixed solution is added to each well at 4 μL by using a BioTek automatic dispenser; centrifuged at 2500 rpm for 30 s, and reacted at 25° C. for 45 min.

[1420] d) Pirparation and addition of detection reagent: Streptavidin-XL665 (Cisbio, 610SAXLG) is diluted with HTRF KinEASE detection buffer (cisbio) from 16.67 μM to 250 nM (4×), and the final concentration is 62.5 nM; TK Antibody-Cryptate (Cisbio) is diluted with HTRF KinEASE detection buffer (cisbio) from 100× to 5×, and the final concentration is 1×; XL665 and Antibody are mixed in equal volume; the mixed solution is added to each well at 10 μL by using the BioTek automatic dispenser, centrifuged at 2500 rpm for 30 s, and reacted at 25° C. for 1 h. After the reaction is completed, the resulting product is detected by a multi-function plate reader HTR1p

2. Data Analysis

[1421] GraphPad Prism 5 software log (inhibitor) vs. response-Variable slope is used to fit a dose-response curve to obtain the IC.sub.50 value of the compound to the inhibition of AXL kinase.

[1422] The calculation formula of the inhibition rate is as follows:

[00001]$\%\mathrm{Inhibition}=\frac{\mathrm{Conversion}\%\mathrm{\_max}-\mathrm{Conversion}\%\mathrm{\_sample}}{\mathrm{Conversion}\%\mathrm{\_max}-\mathrm{Conversion}\%\mathrm{\_min}}\times 100$

Conversion %_sample: a conversion rate reading of a sample;
Conversion %_min: a conversion rate reading in the absence of enzyme active wells;
Conversion %_max: a conversion rate reading in the absence of compound inhibition wells.

3. Experimental Results

[1423] The experimental results are shown in Table 1, where the IC.sub.50 of the compound is expressed as “<” (less than) a specific value, which means that the IC.sub.50 value is lower than a detection limit of the test used.

TABLE-US-00001 TABLE 1 IC.sub.50 data of AXL Inhibitory Inhibitory activity activity Title IC.sub.50 (nM) Title IC.sub.50 (nM) compound against compound against of example AXL of example AXL Example 1 0.33 Example 2 13.40 Example 3 23.58 Example 4 <0.11 Example 5 20.71 Example 6 <0.11 Example 7 7.74 Example 8 8.28 Example 9 21.86 Example 10 2.35 Example 11 8.18 Example 12 <0.11 Example 13 <0.11 Example 15 2.41 Example 16 0.12 Example 17 27.91 Example 18 0.19 Example 19 0.11 Example 20 1.93 Example 21 6.53 Example 22 0.11 Example 23 1.38 Example 24 <0.11 Example 25 0.62 Example 26 7.21 Example 27 19.03 Example 28 0.31 Example 29 0.34 Example 30 1.05 Example 31 0.80 Example 32 0.75 Example 33 5.15 Example 34 1.27 Example 35 1.21 Example 36 0.36 Example 37 0.18 Example 38 6.24 Example 39 2.59 Example 40 0.72 Example 41 2.08 Example 42 14.57 Example 43 9.87 Example 44 1.47 Example 45 0.50 Example 46 0.80 Example 47 1.72 Example 48 0.42 Example 49 9.85 Example 50 2.16 Example 51 2.60 Example 52 1.06 Example 53 1.86 Example 54 3.10 Example 55 3.14 Example 56 2.04 Example 57 6.27 Example 58 1.88 Example 58 6.45 Isomer 58-1 Isomer 58-2 Example 58 60.44 Example 58 78.55 Isomer 58-3 Isomer 58-4 Example 59 1.39 Example 59 86.45 Isomer 59-1 Isomer 59-2 Example 60 1.65 Example 60 106.65 Isomer 60-1 Isomer 60-2 Example 61 2.38 Example 62 49.05 Isomer 62-1 Example 62 1.12 Example 63 1.93 Isomer 62-2 Isomer 63-1 Example 63 61.66 Example 63 2.46 Isomer 63-2 Isomer 63-3 Example 63 57.04 Example 69 1.35 Isomer 63-4 Isomer 69-1 Example 69 44.72 Example 70 1.23 Isomer 69-2 Isomer 70-1 Example 71 0.26 Example 71 26.70 Isomer 71-1 Isomer 71-2 Example 72 1.02 Example 72 1.0 Isomer 72-1 Isomer 72-2 Example 79 1.05 Example 84 0.98 Isomer 84-1 Example 84 28.79 Example 85 0.73 Isomer 84-2 Isomer 85-1 Example 85 33.05 Example 86 30.34 Isomer 85-2 Isomer 86-1 Example 86 1.57 Example 87 0.53 Isomer 86-2 Isomer 87-1 Example 87 36.48 Example 88 39.43 Isomer 87-2 Isomer 88-1 Example 88 0.55 Example 89 0.77 Isomer 88-2 Isomer 89-1 Example 89 27.38 Example 90 0.57 Isomer 89-2 Isomer 90-1 Example 90 45.71 Example 91 1.56 Isomer 90-2 Isomer 91-1 Example 91 57.40 Example 92 1.42 Isomer 91-2 Isomer 92-1 Example 92 38.16 Example 93 1.08 Isomer 92-2 Isomer 93-1 Example 93 14.88 Example 94 0.68 Isomer 93-2 Isomer 94-1 Example 94 27.57 Example 100 1.00 Isomer 94-2 Isomer 100-1 Example 100 40.01 Example 101 1.20 Isomer 100-2 Isomer 101-1 Example 101 55.21 Example 102 1.16 Isomer 101-2 Isomer 102-1 Example 102 35.53 Example 103 1.34 Isomer 102-2 Isomer 103-1 Example 103 47.51 Example 104 1.33 Isomer 103-2 Isomer 104-1 Example 104 62.97 Example 105 0.86 Isomer 104-2 Isomer 105-1 Example 105 24.92 Example 106 0.71 Isomer 105-2 Isomer 106-1 Example 106 21.81 Example 110 1.70 Isomer 106-2 Example 111 1.81 Example 112 2.41 Example 113 1.28 Example 114 2.03 Example 115 4.89 Example 116 4.94 Isomer 116-1 Example 116 96.83 Example 117 1.78 Isomer 116-2 Example 118 5.45 Example 119 9.24 Example 120 4.01 Example 120 64.16 Isomer 120-1 Isomer 120-2 Example 121 3.21 Example 121 50.07 Isomer 121-1 Isomer 121-2 Example 122 1.87 Example 122 63.43 Isomer 122-1 Isomer 122-2 Example 123 2.04 Example 123 38.18 Isomer 123-1 Isomer 123-2 Example 124 8.05 Example 124 74.33 Isomer 124-1 Isomer 124-2 Example 125 4.11 Example 125 80.46 Isomer 125-1 Isomer 125-2 Example 126 4.87 Example 126 47.35 Isomer 126-1 Isomer 126-2 Example 127 3.43 Example 127 66.44 Isomer 127-1 Isomer 127-2 Example 128 1.82 Example 129 9.68 Example 130 12.28 Example 131 207.20 Example 132 2.36 Example 133 1.09 Isomer 133-1 Example 133 38.08 Example 134 0.85 Isomer 133-2 Example 135 1.35 Example 136 13.08 Example 137 6.38 Example 137 38.24 Isomer 137-1 Isomer 137-2 Example 138 5.29 Example 139 2.53 Example 140 2.91 Example 141 2.43 Positive drug 1 2.25 Positive drug 2 16.39 (BGB324) (TP0903)

Test 2: Detection of Proliferation Inhibition Activity of Compounds to Cells

1. Experimental Process

[1424] MV-4-11 (human myeloid monocytic leukemia cell line, culture medium: JIMDM+10% fetal bovine serum) is purchased from Cobioer Biosciences Co., Ltd and cultured in a 5% C.sub.02 incubator at 37° C. The cells in a logarithmic growth phase are plated in a 96-well plate at cell densities of 8000 cells/well, 6000 cells/well, 2000 cells/well, 2000 cells/well and 3000 cells/well, and a blank control group is set at the same time.

[1425] A compound to be tested and the positive drug are dissolved in dimethyl sulfoxide to prepare a 10 mM stock solution, which is then stored in −80° C. refrigerator for long-time storage. After the cells are plated for 24 h, the 10 mM compound stock solution is diluted with dimethyl sulfoxide to obtain a working solution having a 200-fold concentration (the highest concentration is 200 or 2000 μM, a 3-fold gradient, a total of 10 concentrations), and 3 μL of the working solution of each concentration is added to 197 μL of complete medium, and diluted into a working solution of 3-fold concentration. 50 μL of the working solution is then taken and added to a 100 μL cell culture medium (a final concentration of dimethyl sulfoxide is 0.5%, v/v), and two complex holes are set for each concentration. After 72 h of dosing treatment, 50 μl of CellTiter-Glo® (purchased from Promega) is added to each well. Fluorescence signals are measured on Envision (PerkinElmer) according to an operating procedure of the specification. GraphPad Prism 5 software log(inhibitor) vs. response-Variable slope is used to fit a dose-response curve, so as to obtain the IC.sub.50 value of the compound to the inhibition of cell-proliferation. The calculation formulation of the inhibition rate is as follows:

[00002]$\mathrm{Inhibition}\mathrm{rate}\%=\frac{\begin{array}{c}1-(\mathrm{Signal}\mathrm{value}\mathrm{of}\mathrm{subject}-\\ \mathrm{signal}\mathrm{value}\mathrm{of}\mathrm{blank}\mathrm{group})\end{array}}{\begin{array}{c}\mathrm{Signal}\mathrm{value}\mathrm{of}\mathrm{negative}\mathrm{control}\mathrm{group}-\\ \mathrm{signal}\mathrm{value}\mathrm{of}\mathrm{blank}\mathrm{group}\end{array}}\times 100\%$

wherein:
signal value of subject: a mean fluorescence signal of cell+medium+compound group;
signal value of blank group: a mean fluorescence signal of medium group (containing 0.5% DMSO);
signal value of negative control group: a mean fluorescence signal of cell+medium group (containing 0.5% DMSO).

2. Experimental Results

[1426] The experimental results are shown in Table 2:

TABLE-US-00002 TABLE 2 Anti-proliferative activity of compounds for MV4-11 cells Title compound IC.sub.50 of examples (MV4-11, nM) Example 1 6.83 Example 6 3.38 Example 10 5.49 Example 12 1.44 Example 13 0.64 Example 15 9.15 Example 16 0.97 Example 19 1.60 Example 20 5.96 Example 22 6.76 Example 23 7.11 Example 24 6.89 Example 25 3.23 Example 29 3.23 Example 30 2.64 Example 31 1.46 Example 32 1.98 Example 34 6.16 Example 36 5.12 Example 37 3.39 Example 39 6.40 Example 40 4.93 Example 41 4.28 Example 45 3.48 Example 46 1.63 Example 47 5.24 Example 49 8.30 Example 51 4.53 Example 52 5.32 Example 53 6.61 Example 61 7.10 Example 62 3.50 Isomer 62-2 Example 63 7.02 Isomer 63-1 Example 69 3.46 Isomer 69-1 Example 70 9.38 Isomer 70-1 Example 71 7.74 Isomer 71-1 Example 75 2.93 Example 76 7.98 Example 77 10.13 Example 81 3.13 Example 84 2.55 Isomer 84-1 Example 85 1.93 Isomer 85-1 Example 86 2.91 Isomer 86-2 Example 87 3.78 Isomer 87-1 Example 88 2.06 Isomer 88-2 Example 89 2.99 Isomer 89-1 Example 90 2.94 Isomer 90-1 Example 91 2.25 Isomer 91-1 Example 92 2.01 Isomer 92-1 Example 93 2.65 Isomer 93-1 Example 94 2.42 Isomer 94-1 Example 95 7.49 Isomer 95-1 Example 96 9.15 Isomer 96-1 Example 97 8.88 Isomer 97-1 Example 98 8.66 Isomer 98-1 Example 99 7.52 Isomer 99-1 Example 102 5.19 Isomer 102-1 Example 103 6.24 Isomer 103-1 Example 104 7.21 Isomer 104-1 Example 105 2.16 Isomer 105-1 Example 106 3.51 Isomer 106-1 Example 109 8.56 Example 115 6.97 Example 116 10.11 Isomer 116-1 Example 118 30.29 Example 120 6.88 Isomer 120-1 Example 121 3.90 Isomer 121-1 Example 122 3.59 Isomer 122-1 Example 123 3.03 Isomer 123-1 Example 125 4.36 Isomer 125-1 Example 133 5.42 Isomer 133-1 Example 134 3.63 Example 135 4.23 Example 138 41.26 Example 141 13.91 Positive drug 1 208.1 (BGB324) Positive drug 2 11.97 (TP0903)

Test 3: In-Vivo Efficacy of Compound for MV4-11

[1427] Inhibitory effects of a compound and a positive drug on the in-vivo tumor growth of a xenograft tumor model of a nude mouse on human acute monocytic leukemia cell MV-4-11 are tested.

1. Construction of Mouse Model

[1428] MV-4-11 cells in a logarithmic growth phase are harvested, resuspended after cell counting, and adjusted in cell concentration to 7.0×10.sup.7 cells/mL. The resuspended solution is injected into the right armpit of the nude mice subcutaneously. Each animal is inoculated with 200 μL (14×10.sup.6 cells) of the suspended solution to establish a MV-4-11 xenograft tumor model. Afer the tumor volume reaches 100-300 mm.sup.3, tumor-bearing mice in good health and similar tumor volume are selected.

2. Compound Configuration

[1429] The compound and the positive drug are vortexed with a suitable solvent and then ultrasonicated to completely dissolve the compound. Then, an appropriate volume of citric acid buffer is slowly added, and the mixed solution is vortexed to make the solution mixed uniformly to obtain administrative formulations having concentrations of 0.1, 0.5, and 1 mg-mL.sup.−1.

[1430] Solvent control group: PEG400 & citric acid buffer (20:80, v:v).

3. Animal Grouping and Administration

[1431] The modeled mice are randomly divided into groups (n=6), and administrated with the relevant compounds and positive drugs on the day of grouping. After 21 days or after the tumor volume of the solvent control group reaches 2000 mm.sup.3, the experiment is terminated (whichever reaches the index first), and the administration volume is 10 mL-kg.sup.−1. Both the compound and the positive drug are administered by gavage, once a day. After the experiment starts, the tumor diameter and animal body weight are measured twice a week, and the tumor volume is calculated.

4. Data Analysis

[1432]
The tumor volume(TV) calculation formula is: tumor volume(mm.sup.3)=l×w.sup.2/2,

wherein l represents a long diameter (mm) of the tumor; w represents a short diameter (mm) of the tumor.

The calculation formula of relative tumor volume(RTV) is: RTV=TV.sub.t/TV.sub.initial

wherein TV.sub.initial is the tumor volume measured at the time of grouping and first administration; TV.sub.t is the tumor volume at each measurement during administration.

The calculation formula of tumor growth inhibition rate TGI(%) is: TGI=100%×[1−(TV.sub.t(T)−TV.sub.initial(T))/(TV.sub.t(C)−TV.sub.initial(C))]

wherein TV.sub.t(T) represents the tumor volume of treatment group at each measurement; TV.sub.initial(T) represents the tumor volume of treatment group measured at the time of grouping and first administration; TV.sub.t(C) represents the tumor volume of solvent control group at each measurement; TV.sub.initial(C) represents the tumor volume of the solvent control group measured at the time of grouping and first administration.

The calculation formula of relative tumor proliferation rate (% T/C) is: % T/C=100%×(RTV.sub.T/RTV.sub.C)

wherein RTV.sub.T represents RTV of treatment group; RTV.sub.C represents RTV of solvent control group.

[1433] The test data is calculated and subjected to related statistical treatment with Microsoft Office Excel 2007 software.

5. Experimental Results

[1434] The experimental results are shown in Table 3:

TABLE-US-00003 TABLE 3 In-vivo efficacy of compounds for MV4-11 Tumor Relative Intragastric growth tumor administration inhibition proliferation dose rate rate Compound (mg/kg/d) (TGI %) (% T/C) Example 10 5 106 3.7 Example 18 5 71 37 Example 19 1 78 28 Example 28 5 104 5.9 Example 47 5 94 15 Example 53 5 79 31 Example 115 5 85 23 Positive drug 1 20 32 71 (BGB324) Positive drug 2 5 62 42 (TP0903) Notes: the experimental data in the table is relevant data obtained at the end of the experiment (the end of the experiment is defined as: the end of the experiment after 21 days or after the tumor volume of the solvent control group reaches 2000 mm.sup.3 (whichever comes first)).

Test 4: Pharmacokinetic Study of Compounds on ICR Mice

1. Formulation of Gavage Prescriptions for Compounds

[1435] Each compound is prepared with DMSO into a 10 mg/mL stock solution.

[1436] Preparation of mixed solvent: Tween 80: PEG400: Water=1:9:90 (v/v/v)

[1437] 450 μl of the compound DMSO stock solution with a concentration of 10 mg/nmL is accurately sucked into a glass bottle, and added with an appropriate volume of DMSO and mixed solvent, wherein a ratio of the solvent in the final formulation is DMSO: mixed solvent (v/v)=10:90. The mixed solution is vortexed (or ultrasonically treated), and dispersed uniformly to obtain 4.5 mL. administration test solutions with a concentration of 1 mg/nL, respectively.

2. Test Plan

[1438] Male 6-10 week old ICR mice (sourced from: Beijing Vital River Laboratory Animal Technology Co., Ltd.) are taken, 6 mice in each group. The mice are fasted overnight and fed 4 h after the administration. On the day of the experiment, the mice are administrated with 10 mg-kg.sup.1 of compound test solution by gavage. After administration, about 100 μL of blood is harvested from the orbits of the mice at 0 min, 5 mmn, 15 mmn, 30 min, 14 h 2 h, 4 h, 8 h, and 24 h, and placed in EDTA-K.sub.2 anticoagulant tubes. The whole blood sample is centrifuged at 1500 to 1600 g for 10 mm, and the plasma obtained by separation is stored in a refrigerator at −40 to −20° C. for biological sample analysis. The blood drug concentration is determined by an LC-MS/MS method.

3. Data Analysis and Results

[1439] A non-compartmental model in Pharsight Phoenix 7.0 is used to calculate pharmacokinetic parameters. The specific results are shown in 5 the table below.

TABLE-US-00004 TABLE 4 ICR mouse pharmacokinetic results of the compounds Cmax Tmax AUC.sub.0-24 T1/2 Compound (ng/mL) (h) (ng .Math. h/mL) (h) Example 10 349 0.25 1000 3.33 Example 18 249 2.00 2300 3.03 Example 19 342 1.00 3540 3.05 Example 28 226 8.00 3000 NR Example 47 69 1.00 307 2.06 Example 51 419 0.50 1070 2.17 Example 52 429 0.50 1150 2.42 Example 53 676 1.00 2200 1.81 Example 58 171 0.50 822 4.04 Isomer 58-1 Example 58 278 0.25 549 3.06 Isomer 58-2 Example 59 695 0.25 2380 2.90 Isomer 59-1 Example 60 572 0.50 857 1.55 Isomer 60-1 Example 115 324 2.17 1300 1.35 Positive drug 2 26.8 0.25 52.2 1.20 (TP-0903) NR: Not reported