CRYSTAL FORM OF MALEATE OF TYROSINE KINASE INHIBITOR AND PREPARATION METHOD THEREFOR

Abstract

Provided are a crystal form of a maleate of a tyrosine kinase inhibitor and a preparation method therefor. Specifically, provided are I crystal form, a II crystal form, a III crystal form, a IV crystal form and a V crystal form of the compound as shown in formula (I) and a preparation method therefor. The new crystal form has a good stability, thereby making same better to use in clinical treatments.

##STR00001##

Claims

1. A crystal form of a compound represented by formula (I), wherein: the crystal form is a crystal form I which has an X-ray powder diffraction pattern spectrum comprising characteristic peaks at 2θ angles of 6.57, 8.12, 9.76, 10.77, 14.98, 15.89, 20.97, 21.64, 22.06 and 22.61, the crystal form is a crystal form II which has an X-ray powder diffraction pattern spectrum comprising characteristic peaks at 2θ angles of 6.340, 9.030, 10.232, 11.503, 18.282, 19.399, 20.865 and 21.558, the crystal form is a crystal form III which has an X-ray powder diffraction pattern spectrum comprising characteristic peaks at 2θ angles of 6.291, 6.547, 8.561, 9.908, 10.401, 17.381, 19.326 and 23.741, the crystal form is a crystal form IV which has an X-ray powder diffraction pattern spectrum comprising characteristic peaks at 2θ angles of 5.638, 9.417, 11.054, 12.386, 15.218, 15.639, 17.074 and 18.369, or the crystal form is a crystal form V which has an X-ray powder diffraction pattern spectrum comprising characteristic peaks at 2θ angles of 5.469, 5.477, 6.512, 10.376, 11.593, 18.241, 19.386, 21.028 and 22.286, ##STR00005##

2. The crystal form of the compound represented by formula (I) as defined in claim 1, wherein the crystal form is crystal form I.

3. The crystal form of the compound represented by formula (I) as defined in claim 2, which has an X-ray powder diffraction pattern spectrum as shown in FIG. 1.

4. The crystal form of the compound represented by formula (I) as defined in claim 1, wherein the crystal form is crystal form II.

5. The crystal form of the compound represented by formula (I) as defined in claim 1, wherein the crystal form is crystal form III.

6. The crystal form of the compound represented by formula (I) as defined in claim 1, wherein the crystal form is crystal form IV.

7. The crystal form of the compound represented by formula (I) as defined in claim 6, which has an X-ray powder diffraction pattern spectrum comprising characteristic peaks at 2θ angles of 5.638, 8.268, 8.772, 9.417, 11.054, 12.386, 13.739, 15.218, 15.639, 16.312, 17.074, 18.369, 19.152, 20.439, 21.907, 22.307, 22.779, 23.414, 24.146, 24.837, 25.384, 25.852, 26.426, 26.774, 28.685, 29.782, 31.620 and 32.482.

8. The crystal form of the compound represented by formula (I) as defined in claim 6, which has an X-ray powder diffraction pattern spectrum is as shown in FIG. 7.

9. The crystal form of the compound represented by formula (I) as defined in claim 1, wherein the crystal form is crystal form V.

10. The crystal form of the compound represented by formula (I) as defined in claim 1, wherein the error range of the 2θ angle is ±0.2.

11. A pharmaceutical composition prepared by mixing one or more of the crystal form of the compound represented by formula (I) as defined in claim 1 with one or more pharmaceutically acceptable carriers, diluents or excipients.

12. A pharmaceutical composition comprising one or more of the crystal form of the compound represented by formula (I) as defined in claim 1 and one or more pharmaceutically acceptable carriers, diluents or excipients.

13. A method for preparing the crystal form of the compound represented by formula (I) as defined in claim 2, wherein the method comprising: mixing and slurring the compound represented by formula (I) with a solvent and filtering the crystals obtained, the solvent is selected from one or more of water and tetrahydrofuran; or mixing the compound represented by formula (I) with a solvent to volatilize and crystallize, and the solvent is one or more selected from ethanol, isopropanol, n-propanol, acetone, acetonitrile, 2-butanone, dimethyl sulfoxide, nitromethane, propylene glycol methyl ether, isoamylol and acetophenone; or mixing the compound represented by formula (II) with maleic acid and a solvent to precipitate a solid and filtering the crystals obtained, the solvent is one or more selected from isopropanol, water, and dichloromethane, preferably a mixed solvent of isopropanol/water or dichloromethane, ##STR00006##

14. A method for preparing crystal form of the compound represented by formula (I) as defined in claim 4, wherein the method comprising: mixing and slurring a crystal form of the compound of formula (I) with tetrahydrofuran and filtering the crystals obtained, preferably, the crystal form of the compound represented by formula (I) is crystal form I.

15. A method for preparing the crystal form of the compound represented by formula (I) as defined in claim 5, wherein the method comprising: mixing the compound represented by formula (II) with maleic acid and acetone to precipitate a solid, and filtering the crystals obtained, ##STR00007##

16. A method for preparing the crystal form of the compound represented by formula (I) as defined in claim 6, the method comprising: mixing the compound represented by formula (II) with maleic acid and a solvent to precipitate a solid, and filtering the crystals obtained, the solvent can be one or more selected from n-propanol, isopropyl acetate, 2-butanone, isopropanol, and ethanol, preferably ethanol, ##STR00008##

17. A method for preparing the crystal form of the compound represented by formula (I) as defined in claim 9, the method comprising: mixing the compound represented by formula (II) with maleic acid and a solvent to precipitate a solid, filtering the crystals obtained, the solvent can be 1,4-dioxane and/or tetrahydrofuran, ##STR00009##

18. A method for preparing a pharmaceutical composition comprising the compound represented by formula (I) or the pharmaceutically acceptable salt thereof, wherein the method comprises mixing one or more of the crystal form of the compound represented by formula (I) as defined in claim 1 with one or more pharmaceutically acceptable carriers, diluents or excipients.

19. A method for the treatment and/or prevention of a disease or a condition related to a protein kinase, wherein the protein kinase is selected from EGFR receptor tyrosine kinase or HER-2 receptor tyrosine kinase, the disease or condition is preferably cancer, and the cancer is preferably lung cancer, breast cancer, epidermal squamous cell carcinoma or gastric cancer, wherein the method comprises administering to a patient in need thereof the pharmaceutical composition of claim 11.

20. The crystal form of the compound represented by formula (I) as defined in claim 2, which has an X-ray powder diffraction pattern spectrum comprising characteristic peaks at 2θ angles of 6.57, 8.12, 9.76, 10.77, 12.42, 13.11, 14.47, 14.98, 15.28, 15.89, 16.29, 16.49, 17.13, 17.46, 18.92, 19.56, 19.83, 20.29, 20.97, 21.64, 22.06, 22.61, 22.99, 24.00, 24.60, 25.62, 26.46, 27.30, 27.99, 29.05, 30.19, 30.69, 31.90, 33.88 and 36.07.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0050] FIG. 1 is the XRPD pattern spectrum of the I crystal form of the compound represented by formula (I);

[0051] FIG. 2 is a DSC pattern spectrum of the I crystal form of the compound represented by formula (I);

[0052] FIG. 3 is the XRPD pattern spectrum of the II crystal form of the compound represented by formula (I);

[0053] FIG. 4 is a DSC pattern spectrum of the II crystal form of the compound represented by formula (I);

[0054] FIG. 5 is the XRPD pattern spectrum of the III crystal form of the compound represented by formula (I);

[0055] FIG. 6 is a DSC pattern spectrum of the III crystal form of the compound represented by formula (I);

[0056] FIG. 7 is the XRPD pattern spectrum of the IV crystal form of the compound represented by formula (I);

[0057] FIG. 8 is a DSC pattern spectrum of the IV crystal form of the compound represented by formula (I);

[0058] FIG. 9 is the XRPD pattern spectrum of the V crystal form of the compound represented by formula (I);

[0059] FIG. 10 is a DSC pattern spectrum of the V crystal form of the compound represented by formula (I);

[0060] FIG. 11 is the XRPD pattern spectrum of the amorphous compound represented by formula (I).

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0061] Hereinafter, the present disclosure will be explained in more detail with the embodiments, the embodiments of the present disclosure are only used to illustrate the technical solutions of the present disclosure, and do not limit the essence and scope of the present disclosure.

[0062] Experimental conditions of the equipment used in the test:

[0063] 1. Differential Scanning calorimeter (DSC)

[0064] Instrument model: Mettler Toledo DSC 1 STAR.sup.e System

[0065] Purge gas: nitrogen

[0066] Heating rate: 10.0° C./min

[0067] Temperature range:40-250° C.

[0068] 2. Differential Scanning calorimeter (DSC)

[0069] Instrument model: Mettler Toledo DSC 3+

[0070] Purge gas: nitrogen

[0071] Heating rate: 10.0° C./min

[0072] Temperature range:25-300° C.

[0073] 3. X-ray Powder Diffraction (XRPD)

[0074] Instrument model: BRUKER D8 DISCOVERY X-ray powder deiffractometer

[0075] Ray: monochrome Cu-Kα ray (λ=1.5406)

[0076] Scanning mode: θ/2θ, Scanning range: 5-48°

[0077] Voltage: 40 KV, current: 40 mA

[0078] 4. X-ray Powder Diffraction (XRPD)

[0079] Instrument model: BRUKER D8 Focus X-ray powder deiffractometer

[0080] Ray: monochrome Cu-Kα ray (λ=1.5406)

[0081] Scanning mode: θ/2θ, Scanning range:2-40°

[0082] Voltage: 40 KV, current: 40 mA

[0083] Among them, the 2θ data with 2 decimal places is measured by BRUKER D8 Focus X-ray powder diffractometer.

EMBODIMENT 1

[0084] According to the method described in Embodiment 1 in CN102675287A, 0.5 g of the compound represented by formula (II) was added to obtain the amorphous form of the compound represented by formula (I), and its X-ray diffraction pattern spectrum is shown in FIG. 11.

EMBODIMENT 2

[0085] 5.0 g of the amorphous compound represented by formula (I) was placed in a reaction flask, 50 mL of purified water was added thereto and the mixture was slurried and converted to crystals, then filtered with suction, the filter cake was washed with a small amount of purified water, and dried at 40° C. to obtain the I crystal form of the compound represented by formula (I). Its X-ray diffraction pattern spectrum is shown in FIG. 1, and its DSC pattern spectrum is shown in FIG. 2, the characteristic peak positions are shown in the following table:

TABLE-US-00001 TABLE 1 characteristic peak positions of the I crystal form Number of 2θ d I the peaks [°] [Å] [%] Peak 1 6.57 13.449 83.5 Peak 2 8.12 10.874 69.1 Peak 3 9.76 9.052 26.0 Peak 4 10.77 8.207 19.5 Peak 5 12.42 7.119 7.0 Peak 6 13.11 6.748 21.8 Peak 7 14.47 6.117 30.0 Peak 8 14.98 5.911 55.1 Peak 9 15.28 5.794 32.9 Peak 10 15.89 5.572 47.7 Peak 11 16.29 5.436 17.6 Peak 12 16.49 5.371 20.0 Peak 13 17.13 5.173 10.6 Peak 14 17.46 5.076 10.3 Peak 15 18.92 4.686 12.4 Peak 16 19.56 4.535 23.6 Peak 17 19.83 4.474 22.1 Peak 18 20.29 4.373 13.4 Peak 19 20.97 4.233 43.2 Peak 20 21.64 4.103 31.2 Peak 21 22.06 4.027 100.0 Peak 22 22.61 3.930 42.5 Peak 23 22.99 3.865 22.2 Peak 24 24.00 3.704 48.2 Peak 25 24.60 3.615 23.8 Peak 26 25.62 3.475 96.8 Peak 27 26.46 3.366 67.5 Peak 28 27.30 3.264 18.1 Peak 29 27.99 3.186 20.4 Peak 30 29.05 3.071 8.7 Peak 31 30.19 2.958 17.8 Peak 32 30.69 2.910 14.2 Peak 33 31.90 2.803 13.3 Peak 34 33.88 2.644 9.7 Peak 35 36.07 2.488 4.7

EMBODIMENT 3

[0086] 50 mg of the amorphous compound represented by formula (I) was placed in a reaction flask, 1 mL of tetrahydrofuran was added, the mixture was slurried and converted to crystals, then filtered with suction, and dried at 40° C. to obtain the I crystal form of the compound represented by formula (I).

EMBODIMENT 4

[0087] Approximately 10 mg of the I crystal form of the compound represented by formula (I) was placed in a reaction flask, and 40 μL of ethanol was added for dissolution, the mixture was stirred at room temperature, and volatilized to crystallize to obtain the I crystal form of the compound represented by formula (I).

EMBODIMENT 5

[0088] Approximately 20 mg of the compound represented by formula (II) was weighed and 4 mg of maleic acid was added thereto, 90% IPA/H.sub.2O 200 μL was added at room temperature and stirred for dissolution, the stirring was continued and solids were precipitated, the mixture was then centrifuged, and the solid sample was dried in vacuum to obtain I crystal form of the compound represented by formula (I).

EMBODIMENT 6

[0089] 500 μL of tetrahydrofuran was added to about 10 mg of I crystal form of the compound represented by formula (I), the mixture was slurried at room temperature, centrifuged, and the solid part was dried in vacuum to obtain the II crystal form of the compound represented by formula (I). Its X-ray diffraction pattern spectrum is shown in FIG. 3, the DSC pattern spectrum is shown in FIG. 4, and the characteristic peak positions are shown in the table below:

TABLE-US-00002 TABLE 2 characteristic peak positions of the II crystal form Number of 2θ d I the peaks [°] [Å] [%] Peak 1 6.340 13.92901 100.0 Peak 2 9.030 9.78560 28.1 Peak 3 10.232 8.63810 26.2 Peak 4 11.503 7.68685 58.5 Peak 5 12.629 7.00355 7.1 Peak 6 13.637 6.48824 8.2 Peak 7 14.526 6.09317 9.4 Peak 8 16.170 5.47718 18.4 Peak 9 17.639 5.02414 16.1 Peak 10 18.282 4.84890 21.0 Peak 11 19.399 4.57199 89.3 Peak 12 20.865 4.25396 25.0 Peak 13 21.558 4.11881 20.9 Peak 14 22.078 4.02300 9.9 Peak 15 22.616 3.92835 7.2 Peak 16 23.562 3.77274 28.7 Peak 17 24.479 3.63346 23.0 Peak 18 25.801 3.45026 24.9 Peak 19 27.601 3.22924 9.3 Peak 20 28.139 3.16862 9.2 Peak 21 29.671 3.00846 8.1 Peak 22 31.893 2.80374 13.7 Peak 23 33.887 2.64321 2.8

EMBODIMENT 7

[0090] Approximately 20 mg of the compound represented by formula (II) was weighed and 4 mg of maleic acid was added thereto, then 200 μL of acetone was added and stirred for dissolution at room temperature, the stirring was continued, and solids were precipitated, the mixture was centrifuged, and the solid sample was dried in vacuum to obtain the III crystal form of the compound represented by formula (I). Its X-ray diffraction pattern spectrum is shown in FIG. 5, the DSC pattern spectrum is shown in FIG. 6, and the characteristic peak positions are shown in the table below:

TABLE-US-00003 TABLE 3 characteristic peak positions of the III crystal form Number of 2θ d I the peaks [°] [Å] [%] Peak 1 4.864 18.15286 12.6 Peak 2 5.516 16.00949 8.7 Peak 3 6.291 14.03761 43.9 Peak 4 6.547 13.48974 100.0 Peak 5 8.068 10.94991 8.0 Peak 6 8.561 10.31997 29.6 Peak 7 9.908 8.92036 14.9 Peak 8 10.401 8.49865 30.3 Peak 9 11.603 7.62067 36.5 Peak 10 13.267 6.66808 14.9 Peak 11 13.819 6.40329 19.5 Peak 12 14.725 6.01129 14.1 Peak 13 16.270 5.44375 12.4 Peak 14 17.381 5.09798 23.6 Peak 15 18.398 4.81836 4.8 Peak 16 19.326 4.58904 31.9 Peak 17 20.125 4.40876 8.2 Peak 18 21.040 4.21905 18.2 Peak 19 21.498 4.13015 10.5 Peak 20 22.250 3.99231 4.6 Peak 21 23.741 3.74469 31.3 Peak 22 24.426 3.64129 10.8 Peak 23 25.795 3.45105 19.1 Peak 24 26.765 3.32819 5.5 Peak 25 28.530 3.12612 11.2 Peak 26 31.815 2.81042 11.7

EMBODIMENT 8

[0091] Approximately 20 mg of the compound represented by formula (II) was weighed and 4 mg of maleic acid was added thereto, then 200 μL of ethanol was added and stirred at room temperature for dissolution, the stirring was continued and solids were precipitated, the mixture was slurried at room temperature, then centrifuged, the solid sample was dried in vacuum to obtain the IV crystal form of the compound represented by formula (I). Its X-ray diffraction pattern spectrum is shown in FIG. 7, the DSC pattern spectrum is shown in FIG. 8, and the characteristic peak positions are shown in the table below:

TABLE-US-00004 TABLE 4 characteristic peak positions of the IV crystal form Number of 2θ d I the peaks [°] [Å] [%] Peak 1 5.638 15.66303 15.5 Peak 2 8.268 10.68476 2.8 Peak 3 8.772 10.07253 5.0 Peak 4 9.417 9.38383 17.1 Peak 5 11.054 7.99762 50.0 Peak 6 12.386 7.14073 26.7 Peak 7 13.739 6.44002 12.0 Peak 8 15.218 5.81732 22.3 Peak 9 15.639 5.66189 42.8 Peak 10 16.312 5.42975 4.6 Peak 11 17.074 5.18907 31.0 Peak 12 18.369 4.82595 40.1 Peak 13 19.152 4.63046 12.9 Peak 14 20.439 4.34161 9.2 Peak 15 21.907 4.05396 6.9 Peak 16 22.307 3.98207 12.9 Peak 17 22.779 3.90071 26.5 Peak 18 23.414 3.79636 100.0 Peak 19 24.146 3.68285 16.5 Peak 20 24.837 3.58196 3.2 Peak 21 25.384 3.50594 36.5 Peak 22 25.852 3.44352 11.9 Peak 23 26.426 3.37005 45.6 Peak 24 26.774 3.32706 17.7 Peak 25 28.685 3.10956 37.1 Peak 26 29.782 2.99752 6.5 Peak 27 31.620 2.82733 4.0 Peak 28 32.482 2.75427 7.5

EMBODIMENT 9

[0092] Approximately 20 mg of the compound represented by formula (II) was weighted and 4 mg of maleic acid was added thereto, then 400 μL of 1,4-dioxane was added and the temperature was raised to 50° C. for reaction, after the completion of the reaction, the mixture was centrifuged and the solid sample was dried in vacuum to obtain the V crystal form of the compound represented by formula (I). Its X-ray diffraction pattern spectrum is shown in FIG. 9, the DSC pattern spectrum is shown in FIG. 10, the characteristic peak positions are shown in the table below.

TABLE-US-00005 TABLE 5 characteristic peak positions of the V crystal form Number of 2θ d I the peaks [°] [Å] [%] Peak 1 5.469 16.14750 36.4 Peak 2 5.477 16.12122 37.8 Peak 3 6.512 13.56204 100.0 Peak 4 10.376 8.51906 15.8 Peak 5 11.593 7.62717 32.2 Peak 6 13.220 6.69166 5.0 Peak 7 14.708 6.01819 6.1 Peak 8 15.600 5.67590 7.8 Peak 9 16.492 5.37076 6.0 Peak 10 18.241 4.85972 20.0 Peak 11 19.386 4.57517 25.7 Peak 12 21.028 4.22145 26.2 Peak 13 22.286 3.98581 21.6 Peak 14 22.747 3.90608 10.1 Peak 15 23.758 3.74218 15.8 Peak 16 24.693 3.60252 4.0 Peak 17 25.509 3.48913 13.2 Peak 18 25.926 3.43386 21.8 Peak 19 26.563 3.35304 3.2 Peak 20 27.837 3.20233 8.2 Peak 21 29.792 2.99653 3.8 Peak 22 30.727 2.90746 4.3 Peak 23 32.086 2.78729 5.8

[0093] EMBODIMENT 10

[0094] The stability of the I crystal form of the compound represented by formula (I) was investigated. The purity of the crystal form was detected by Agilent1200 DAD high performance liquid chromatography system, and Waters symmetry C18, (250*4.6 mm, 5 μm) was used as the detection column, mobile phase: sodium dihydrogen phosphate/ACN/H.sub.2O, detection wavelength: 261 nm.

TABLE-US-00006 TABLE 6 Experimental results of the influencing factors for the I crystal form and amorphous from of the compound represented by formula (I) sample/ Time RH RH purity % (day) illumination 40° C. 75% 90% I crystal form 0 99.56 99.56 99.56 99.56 5 99.35 99.55 99.53 99.53 10 99.29 99.51 99.53 99.54 30 99.00 99.43 99.52 99.51 amorphous 0 99.31 99.31 99.31 99.31 5 98.04 99.21 99.35 95.76 10 96.65 99.13 99.33 94.05 30 93.48 98.57 99.09 85.09

[0095] It can be seen from the table that after long-term storage, I crystal form has good physical and chemical stability; while the amorphous form has poor stability under illumination, high temperature and high humidity conditions.

EMBODIMENT 11

[0096] The stability of the I and IV crystal form of the compound represented by formula (I) was investigated. The purity of the crystal forms was detected by Thermo Ultimate3000DAD high-performance liquid chromatography system, and Waters symmetry C18, (250*4.6 mm, 5 μm) was used as the detection chromatographic column, mobile phase: sodium dihydrogen phosphate/ACN/H.sub.2O, detection wavelength: 261 nm.

TABLE-US-00007 TABLE 7 Experimental results of the influencing factors for the I and IV crystal form of the compound represented by formula (I) sample/ Time RH RH purity % (day) illumination 40° C. 60° C. 75% 90% I crystal form 0 99.83 99.83 99.83 99.83 99.83 5 99.68 99.78 99.64 99.81 99.81 10 99.59 99.77 99.51 99.81 99.82 30 99.29 99.69 99.24 99.68 99.82 IV crystal form 0 99.94 99.94 99.94 99.94 99.94 5 99.92 99.92 99.83 99.93 99.93 10 99.92 99.93 99.77 99.94 99.94 30 99.85 99.85 99.50 99.94 99.93

[0097] Although the specific embodiments of the present disclosure have been described above, those skilled in the art should understand that these are only examples, various changes or modifications can be made to these embodiments without departing from the principle and essence of the present invention. Therefore, the protection scope of the present disclosure is defined by the appended claims.