(19)
(11)EP 3 889 136 A1

(12)EUROPEAN PATENT APPLICATION
published in accordance with Art. 153(4) EPC

(43)Date of publication:
06.10.2021 Bulletin 2021/40

(21)Application number: 19888746.5

(22)Date of filing:  17.10.2019
(51)International Patent Classification (IPC): 
C07D 209/18(2006.01)
A61P 35/00(2006.01)
A61K 31/404(2006.01)
(52)Cooperative Patent Classification (CPC):
A61K 31/404; A61P 35/00; C07D 209/18
(86)International application number:
PCT/CN2019/111624
(87)International publication number:
WO 2020/108154 (04.06.2020 Gazette  2020/23)
(84)Designated Contracting States:
AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR
Designated Extension States:
BA ME
Designated Validation States:
KH MA MD TN

(30)Priority: 28.11.2018 CN 201811434915

(71)Applicants:
  • Luoxin Pharmaceutical (Shanghai) Co., Ltd.
    China (Shanghai) Pilot Free Trade Zone Pudong New Area Shanghai 201210 (CN)
  • Shandong Luoxin Pharmaceutical Group Stock Co., Ltd.
    Shandong 276017 (CN)

(72)Inventors:
  • HE, Huijun
    Shanghai 200131 (CN)
  • SHI, Shenyi
    Shanghai 200131 (CN)
  • LU, Jianyu
    Shanghai 200131 (CN)
  • DING, Charles Z.
    Shanghai 200131 (CN)
  • HU, Lihong
    Shanghai 200131 (CN)
  • SHI, Bin
    Shanghai 201210 (CN)
  • YANG, Wenqian
    Shanghai 201210 (CN)
  • DONG, Jiaqiang
    Shanghai 201210 (CN)
  • WANG, Tie-Lin
    Shanghai 201210 (CN)

(74)Representative: Haseltine Lake Kempner LLP 
Redcliff Quay 120 Redcliff Street
Bristol BS1 6HU
Bristol BS1 6HU (GB)

  


(54)SALT FORM OF ESTROGEN RECEPTOR DOWNREGULATOR, CRYSTALLINE FORM THEREOF, AND PREPARATION METHOD THEREFOR


(57) Provided are a salt form of an estrogen receptor down-regulator, a crystalline form thereof, and a preparation method therefor.




Description


[0001] This application claims priority to Chinese patent application CN201811434915.8 filed on November 28, 2018. The contents of which are incorporated herein by its entirety.

Technical Field



[0002] The present disclosure relates to salt forms of estrogen receptor down-regulator, crystalline forms thereof, and processes of preparation therefor, and the use of the salt and crystal forms in the preparation of a drug for treating breast cancer.

Background arts



[0003] According to the statistics of WHO, breast cancer has become the second most prevalent cancer in the world and has the highest incidence among women. After years of research, the role of the estrogen-estrogen receptor signaling pathway in breast cancer development has already been identified; and the estrogen receptor (ER) has also been developed into the most important biomarker for breast cancer. Taking estrogen receptor expression as a discriminative index, breast cancer can be divided into estrogen receptor-positive breast cancer and estrogen receptor-negative breast cancer; wherein estrogen receptor-positive breast cancer accounts for more than 70% of the total number of breast cancer patients.

[0004] Endocrine Therapy (ET) targeting the estrogen-estrogen receptor signaling pathway in breast cancer cells has become the first choice for treating estrogen receptor-positive breast cancer because of its minimal harm and significant effect. Endocrine therapy mainly includes the following three treatment methods: ovarian suppression therapy, aromatase inhibitor (AI), and selective estrogen receptor modulator (SERM). Due to its unsatisfactory efficacy and low patient satisfaction, the ovarian suppression therapy is less commonly used than the other two treatment methods. Early aromatase inhibitors (first and second generation) had low target selectivity and large toxic and side effects. After many years of research, the third-generation aromatase inhibitors have been widely used since their selectivity has been greatly improved, which solved the problem of the early aromatase inhibitors. Among them, letrozole and the like have been used as first-line drugs for the treatment of estrogen receptor-positive breast cancer. Selective estrogen receptor modulators (SERMs) directly act on estrogen receptors to block this signaling pathway, which has a significant effect and a long history of application. Among them, tamoxifen is the most representative selective estrogen receptor modulator. As a first-line drug recommended for priority use, tamoxifen has shown significant clinical efficacy in the prevention and treatment of estrogen receptor-positive breast cancer.

[0005] Although the aromatase inhibitor letrozole and the selective estrogen receptor modulator tamoxifen have shown good efficacy in the treatment of estrogen receptor-positive breast cancer, with the application of the two types of drugs, the drug resistance problem of estrogen receptor-positive breast cancer to aromatase inhibitors and selective estrogen receptor modulators has also become increasingly prominent. A large amount of studies has shown that the resistance mechanisms of breast cancer to these two hormone therapies are not exactly the same. For aromatase inhibitors, the estrogen receptor can be mutated accordingly. The mutated estrogen receptor can maintain an excited conformation in the absence of estrogen, allowing it to continue to perform the receptor function to promote breast cancer cell proliferation. The resistance mechanism of breast cancer cells to the selective estrogen receptor modulator tamoxifen is complex and diverse. First, breast cancer cells can compensate for the loss of function of estrogen receptor activation functional domain-2 (AF-2) caused by tamoxifen through activating the function of estrogen receptor activation functional domain-1 (AF-1). At the same time, breast cancer cells can adjust the structure or concentration of the estrogen receptor co-activator to adapt to the conformation of the estrogen receptor bound to tamoxifen, resulting in the recovery of the function of the estrogen receptor, thereby producing drug resistance.

[0006] Selective estrogen receptor down-regulator (SERD) has shown its unique superiority in the treatment of breast cancer resistant to the above two hormone therapies. Mechanistically, selective estrogen receptor down-regulators antagonize the function of estrogen receptor, which can greatly accelerate the ubiquitination degradation of estrogen receptors in breast cancer cells (normal or mutated) and completely block estrogen/estrogen receptor signaling pathway, thereby achieving the purpose of inhibiting the growth and proliferation of normal or drug-resistant breast cancer cells. Studies have shown that selective estrogen receptor down-regulators can effectively inhibit the proliferation of hormone-resistant breast cancer cells. Fulvestrant, which is the only commercially available selective estrogen receptor down-regulator, has shown good effects in the treatment of hormone-resistant breast cancer, confirming the unique advantages of selective estrogen receptor down-regulators. However, fulvestrant itself has many problems. First, because of its poor PK properties, fulvestrant shows zero oral bioavailability; meanwhile, fulvestrant has a higher blood clearance. For these two reasons, this drug can only be administered by intramuscular injection. However, due to its strong lipophilic structure, fulvestrant administered by intramuscular injection also has serious problems in terms of tissue distribution. Therefore, the development of selective estrogen receptor down-regulators with oral bioavailability is an urgent medical requirement.

[0007] WO2012037411A2 reported an oral selective estrogen receptor down-regulator ARN-810, and a phase II clinical trial of this molecule in the treatment of ER-positive breast cancer is ongoing. According to reports [J.Med.Chem.2015,58 (12), 4888-4904], the important pharmacophore of the molecule is the indazole structure on the left side of the molecule, and the nitrogen atoms in the indazole structure bind to the estrogen receptor as a hydrogen bond acceptor.



[0008] WO2017162206A1 reports a series of orally selective estrogen receptor down-regulation, including the preparation and biological activity of compound 1-8 (Example 8 in WO2017162206A1):


Content of the present invention



[0009] The present invention provides a compound of formula (I),



[0010] The present invention also provides a crystal form A of the compound of formula (I), wherein the X-ray powder diffraction pattern under Cu-Kα radiation has characteristic diffraction peaks at the following 2θ angles: 5.52± 0.2°, 13.68± 0.2°, 19.98± 0.2°, 20.80± 0.2°, 22.02± 0.2°, 22.44± 0.2°, 24.94± 0.2° and 26.96± 0.2°,



[0011] In some embodiments of the present invention, the crystal form A, has nine or more than nine, ten or more than ten, or eleven or more than eleven characteristic diffraction peaks in the X-ray powder diffraction pattern under Cu-Kα radiation at the 2θ angles selected from the group consisting of 5.52±0.2°, 13.68±0.2°, 18.86±0.2°, 19.98±0.2°, 20.80±0.2°, 21.62±0.2°, 22.02±0.2°, 22.44±0.2°, 23.34±0.2°, 24.94±0.2°, 26.96±0.2° and 28.42±0.2°.

[0012] In some embodiments of the present invention, the X-ray powder diffraction pattern of the crystal form A under Cu-Kα radiation is shown in FIG. 1.

[0013] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form A is shown in Table 1.
Table 1. Analysis data of the XRPD pattern of the crystal form A of the compound of formula (I)
No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)
1 5.519 16.0002 891 84.0 21 23.341 3.808 377 35.5
2 10.023 8.8181 138 13.0 22 24.939 3.5676 413 38.9
3 10.483 8.4319 169 15.9 23 25.957 3.4298 156 14.7
4 10.962 8.0646 306 28.8 24 26.96 3.3045 755 71.1
5 11.739 7.5328 259 24.4 25 27.561 3.2338 322 30.3
6 12.419 7.1213 283 26.6 26 28.038 3.1798 202 19.0
7 13.68 6.468 581 54.7 27 28.419 3.138 409 38.5
8 15.401 5.7486 208 19.6 28 29.454 3.0301 63 5.9
9 16.239 5.4539 114 10.8 29 29.863 2.9895 98 9.2
10 16.973 5.2196 165 15.5 30 30.459 2.9324 129 12.2
11 17.579 5.041 113 10.6 31 31.062 2.8769 123 11.5
12 18.241 4.8596 194 18.3 32 31.638 2.8258 47 4.4
13 18.859 4.7018 374 35.2 33 32.499 2.7528 186 17.5
14 19.181 4.6234 201 18.9 34 33.841 2.6467 88 8.3
15 19.979 4.4405 573 54.0 35 34.643 2.5872 36 3.4
16 20.482 4.3327 598 56.4 36 35.035 2.5591 47 4.4
17 20.802 4.2667 605 57.0 37 36.013 2.4918 42 3.4
18 21.618 4.1075 373 35.1 38 37.44 2.4001 69 4.0
19 22.019 4.0335 655 61.7 39 38.058 2.3625 93 6.5
20 22.437 3.9593 1061 100.0          


[0014] In some embodiments of the present invention, the differential scanning calorimetric curve of the crystal form A has an endothermic peak at 239.46°C±3°C.

[0015] In some embodiments of the present invention, the differential scanning calorimetric curve pattern of the crystal form A is shown in FIG. 2.

[0016] The present invention also provides a crystal form B of the compound of formula (I), wherein the X-ray powder diffraction pattern under Cu-Kα radiation has characteristic diffraction peaks at the following 2θ angles: 5.68 ± 0.2°, 12.36 ± 0.2°, 19.24 ± 0.2°, 19.86 ± 0.2°, 20.62 ± 0.2°, 21.64 ± 0.2°, 22.68 ± 0.2° and 24.96 ± 0.2°.

[0017] In some embodiments of the present invention, the crystal form B has nine or more than nine, ten or more than ten, or eleven or more than eleven characteristic diffraction peaks in the X-ray powder diffraction pattern under Cu-Kα radiation at the 2θ angle selected from the group consisting of 5.68 ± 0.2°, 12.36 ± 0.2°, 13.42 ± 0.2°, 19.24 ± 0.2°, 19.86 ± 0.2°, 20.62 ± 0.2°, 21.64 ± 0.2°, 22.68 ± 0.2°, 24.96 ± 0.2°, 26.38 ± 0.2°, 27.44 ± 0.2° and 30.62± 0.2°.

[0018] In some embodiments of the present invention, the X-ray powder diffraction pattern of the crystal form B under Cu-Kα radiation is shown in FIG. 3.

[0019] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form B is shown in Table 2.
Table 2. Analysis data of the XRPD pattern of the crystal form B of the compound of formula (I)
No.2θ Angle (°)d-spacing (Å)Inte nsityRelative intensity (%)No2θ Angle (°)d-spacing (Å)Intensi tyRelative intensity (%)
1 5.677 15.5537 459 73.3 18 24.959 3.5648 397 63.4
2 9.756 9.0589 103 16.5 19 25.240 3.5257 222 35.4
3 11.315 7.8134 53 8.5 20 26.378 3.3760 278 44.4
4 12.363 7.1538 352 56.2 21 27.059 3.2926 66 10.6
5 13.420 6.5923 315 50.4 22 27.438 3.2480 249 39.8
6 14.798 5.9815 68 10.9 23 28.098 3.1732 79 12.6
7 15.406 5.7470 41 6.6 24 28.482 3.1313 93 14.9
8 16.481 5.3744 62 9.9 25 29.483 3.0272 66 10.6
9 17.281 5.1273 128 20.5 26 30.002 2.9760 127 20.3
10 17.721 5.0009 146 23.3 27 30.622 2.9171 267 42.6
11 18.898 4.6920 253 40.5 28 31.080 2.8752 219 34.9
12 19.239 4.6096 432 68.9 29 33.402 2.6804 41 6.6
13 19.860 4.4668 481 76.7 30 34.198 2.6199 51 8.1
14 20.619 4.3041 422 67.3 31 34.985 2.5627 79 12.7
15 21.641 4.1032 626 100.0 32 38.698 2.3249 49 7.8
16 22.681 3.9173 390 62.2 33 39.020 2.3065 67 10.6
17 23.258 3.8213 98 15.6 / / / / /


[0020] The present invention also provides a compound of formula (II),



[0021] The present invention also provides a crystal form C of the compound of formula (II), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 4.

[0022] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form C is shown in Table 3.
Table 3. Analysis data of the XRPD pattern of the crystal form C of the compound of formula (II)
No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)
1 6.476 13.6374 325 34.6 20 24.980 3.5618 217 23.1
2 11.021 8.0219 518 55.1 21 25.460 3.4957 154 16.4
3 11.777 7.5081 100 10.6 22 26.022 3.4215 290 30.8
4 12.106 7.3051 42 4.5 23 26.361 3.3782 465 49.4
5 12.920 6.8463 138 14.7 24 27.156 3.2811 558 59.4
6 13.997 6.3222 508 54.1 25 27.962 3.1883 174 18.5
7 15.427 5.7389 92 9.8 26 28.222 3.1596 369 39.2
8 15.797 5.6054 222 23.7 27 28.619 3.1166 244 26.0
9 16.557 5.3497 149 15.9 28 30.803 2.9004 304 32.4
10 17.282 5.1271 237 25.2 29 31.120 2.8716 247 26.3
11 17.561 5.0460 285 30.3 30 31.759 2.8153 139 14.8
12 18.238 4.8605 123 13.1 31 32.080 2.7878 132 14.0
13 18.721 4.7362 596 63.4 32 33.422 2.6789 144 15.3
14 19.579 4.5305 786 83.6 33 33.880 2.6437 71 7.6
15 20.361 4.3581 586 62.3 34 34.858 2.5718 59 6.3
16 21.221 4.1833 298 31.7 35 35.800 2.5062 53 5.6
17 22.138 4.0121 940 100.0 36 36.804 2.4401 46 4.9
18 24.018 3.7021 763 81.2 37 38.760 2.3213 54 5.7
19 24.334 3.6547 190 20.2 / / / / /


[0023] The present invention also provides a compound of formula (III),



[0024] The present invention also provides a crystal form D of the compound of formula (III), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 5.

[0025] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form D is shown in Table 4.
Table 4. Analysis data of the XRPD pattern of the crystal form D of the compound of formula (III)
No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)No.2θ Angle (°)d-spacing (Å)Intens ityRelative intensity (%)
1 5.798 15.2301 346 29.5 17 24.021 3.7017 210 17.9
2 9.7 9.1108 95 8.1 18 24.532 3.6257 239 20.4
3 10.033 8.8092 235 20.1 19 25.406 3.503 123 10.5
4 11.475 7.705 142 12.1 20 26.288 3.3873 300 25.6
5 12.265 7.2103 238 20.3 21 26.623 3.3455 539 46
6 13.271 6.6661 651 55.5 22 27.964 3.188 344 29.4
7 14.433 6.1318 120 10.2 23 28.657 3.1125 177 15.1
8 16.525 5.36 215 18.3 24 29.661 3.0094 169 14.4
9 17.866 4.9607 167 14.2 25 30.69 2.9108 93 7.9
10 18.378 4.8234 121 10.3 26 31.059 2.8771 63 5.4
11 19.149 4.6311 860 73.4 27 31.491 2.8385 71 6.1
12 19.901 4.4578 88 7.5 28 32.009 2.7938 223 19
13 20.396 4.3505 1082 92.3 29 33.249 2.6923 160 13.7
14 20.845 4.258 355 30.3 30 33.604 2.6647 99 8.4
15 21.416 4.1456 501 42.7 31 38.144 2.3574 91 7.8
16 22.797 3.8975 1172 100 32 38.632 2.3287 58 4.9


[0026] The present invention also provides a crystal form E of the compound of formula (III), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 6.

[0027] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form E is shown in Table 5.
Table 5. Analysis data of the XRPD pattern of the crystal form E of the compound of formula (III)
No.2θ Angle (°)d-spacing (Å)Intensi tyRelative intensity (%)No.2θ Angle (°)d-spacing (Å)Intensi tyRelative intensity (%)
1 4.896 18.0349 88 7.9 13 21.375 4.1535 232 28.9
2 9.679 9.1306 69 6.2 14 22.602 3.9307 199 17.8
3 10.373 8.5209 337 30.2 15 23.631 3.7619 112 10
4 11.788 7.5012 72 6.5 16 24.04 3.6987 205 18.4
5 12.54 7.0531 122 10.9 17 25.064 3.5499 195 17.5
6 13.324 6.6395 84 7.5 18 26.011 3.4228 135 12.1
7 14.377 6.1558 431 38.6 19 28.122 3.1705 153 13.7
8 15.717 5.6338 521 46.7 20 28.458 3.1338 304 27.2
9 17.22 5.1453 154 13.8 21 30.074 2.969 125 11.2
10 17.967 4.9329 76 6.8 22 30.763 2.9041 70 6.3
11 19.326 4.5891 206 18.5 23 31.631 2.8263 145 13
12 20.944 4.2381 1116 100 24 33.189 2.6971 90 8.1


[0028] The present invention also provides a compound of formula (IV),



[0029] The present invention also provides a crystal form F of the compound of formula (IV),wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 7.

[0030] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form F is shown in Table 6.
Table 6. Analysis data of the XRPD pattern of the crystal form F of the compound of formula (IV)
No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)No.2θ Angle (°)d-spacing (Å)Intensi tyRelative intensity (%)
1 5.102 17.3079 350 39.2 16 19.801 4.48 434 48.7
2 6.9 12.8008 368 41.3 17 20.41 4.3477 269 30.2
3 7.785 11.3466 892 100 18 21.017 4.2234 146 16.4
4 10.827 8.165 376 42.2 19 22.305 3.9825 172 19.3
5 11.359 7.7833 68 7.6 20 22.852 3.8883 343 38.5
6 11.869 7.45 345 38.7 21 24.095 3.6904 178 20
7 12.461 7.0973 73 8.2 22 24.888 3.5746 138 15.5
8 13.23 6.6868 241 27 23 25.243 3.5251 229 25.7
9 13.606 6.5026 587 65.8 24 26.227 3.395 221 24.8
10 14.078 6.2855 710 79.6 25 26.821 3.3213 108 12.1
11 14.866 5.9543 84 9.4 26 27.334 3.26 198 22.2
12 16.664 5.3156 227 25.4 27 28.931 3.0836 97 10.9
13 17.393 5.0944 114 12.8 28 29.297 3.046 72 8.1
14 18.04 4.9132 158 17.7 29 30.841 2.8968 67 7.5
15 19.287 4.5983 236 26.5 30 34.874 2.5705 71 8


[0031] The present invention also provides a crystal form G of the compound of formula (IV),wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 8.

[0032] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form G is shown in Table 7.
Table 7. Analysis data of the XRPD pattern of the crystal form G of the compound of formula (IV)
No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)
1 4.57 19.3182 195 44.5 12 19.901 4.4576 105 24
2 6.021 14.6669 161 36.8 13 21.079 4.2112 152 34.7
3 6.962 12.6869 438 100 14 22.301 3.983 142 32.4
4 7.33 12.0502 172 39.3 15 24.792 3.5883 157 35.8
5 11.055 7.9966 141 32.2 16 25.913 3.4355 95 21.7
6 12.207 7.2446 272 62.1 17 26.386 3.375 96 21.9
7 12.719 6.9543 369 84.2 18 26.861 3.3164 69 15.8
8 16.863 5.2533 101 23.1 19 28.811 3.0962 72 16.4
9 17.955 4.9363 74 16.9 20 29.684 3.0071 73 16.7
10 18.93 4.6841 156 35.6 21 31.477 2.8398 76 17.4
11 19.324 4.5894 75 17.1 22 33.411 2.6797 59 13.5


[0033] The present invention also provides a compound of formula (V),



[0034] The present invention also provides a crystal form H of the compound of formula (V), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 9.

[0035] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form H is shown in Table 8.
Table 8. Analysis data of the XRPD pattern of the crystal form H of the compound of formula (V)
No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)
1 6.566 13.4503 197 31.3 12 20.686 4.2904 283 44.9
2 7.69 11.4875 167 26.5 13 21.494 4.1307 206 32.7
3 10.478 8.4359 66 10.5 14 22.836 3.8911 435 69
4 11.961 7.3932 80 12.7 15 23.744 3.7441 278 44.1
5 12.599 7.02 248 39.4 16 25.105 3.5442 229 36.3
6 15.224 5.8149 491 77.9 17 26.643 3.343 230 36.5
7 16.369 5.4108 152 24.1 18 28.536 3.1254 293 46.5
8 16.879 5.2484 119 18.9 19 29.643 3.0112 69 11
9 17.551 5.0489 630 100 20 30.824 2.8984 151 24
10 18.557 4.7775 126 20 21 32.6 2.7444 56 8.9
11 19.837 4.472 106 16.8 22 34.099 2.6272 69 11


[0036] The present invention also provides a crystal form I of the compound of formula (V), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 10.

[0037] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form H is shown in Table 9.
Table 9. Analysis data of the XRPD pattern of the crystal form I of the compound of formula (V)
No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)
1 5.157 17.1214 110 26.3 11 19.939 4.4493 213 51
2 8.102 10.903 221 52.9 12 20.529 4.3228 298 71.3
3 11.155 7.9256 108 25.8 13 20.823 4.2623 151 36.1
4 11.807 7.4894 176 42.1 14 21.83 4.068 77 18.4
5 12.205 7.2456 84 20.1 15 23.073 3.8516 417 99.8
6 12.789 6.916 62 14.8 16 23.744 3.7442 78 18.7
7 14.492 6.1071 243 58.1 17 24.533 3.6255 147 35.2
8 14.945 5.923 171 40.9 18 25.816 3.4481 158 37.8
9 17.651 5.0205 418 100 19 26.265 3.3902 119 28.5
10 18.813 4.7129 237 56.7 20 27.687 3.2192 224 53.6


[0038] The present invention also provides a crystal form J of the compound of formula (V), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 11.

[0039] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form J is shown in Table10.
Table 10. Analysis data of the XRPD pattern of the crystal form J of the compound of formula (V)
No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)
1 5.03 17.5537 118 41.3 12 19.602 4.525 216 75.5
2 7.569 11.671 199 69.6 13 20.431 4.3432 209 73.1
3 8.005 11.0357 125 43.7 14 21.688 4.0942 73 25.5
4 11.638 7.5975 183 64 15 21.986 4.0395 96 33.6
5 13.073 6.7665 286 100 16 22.444 3.958 111 38.8
6 13.547 6.531 137 47.9 17 22.894 3.8813 146 51
7 14.375 6.1566 106 37.1 18 24.832 3.5826 76 26.6
8 14.869 5.9532 129 45.1 19 25.522 3.4873 115 40.2
9 16.464 5.3796 102 35.7 20 25.939 3.4322 120 42
10 17.825 4.9719 204 71.3 21 27.509 3.2397 88 30.8
11 19.127 4.6362 181 63.3 / / / / /


[0040] The present invention also provides a compound of formula (VI),



[0041] The present invention also provides a crystal form K of the compound of formula (VI), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 12.

[0042] In some embodiments of the present invention, the analysis data of the XRPD pattern of the crystal form K is shown in Table 11.
Table 11. Analysis data of the XRPD pattern of the crystal form K of the compound of formula (VI)
No.2θ Angle (°)d-spacing (Å)IntensityRelative intensity (%)No.2θ Angle (°)d-spacing (Å)Inte nsityRelative intensity (%)
1 5.935 14.8801 194 19.9 17 22.975 3.8677 616 63.1
2 6.763 13.0593 126 12.9 18 23.288 3.8164 570 58.3
3 11.219 7.8806 609 62.3 19 23.922 3.7168 536 54.9
4 12.009 7.3638 196 20.1 20 24.965 3.5637 703 72
5 13.035 6.7864 218 22.3 21 26.128 3.4077 226 23.1
6 13.564 6.5229 92 9.4 22 27.705 3.2172 366 37.5
7 14.627 6.0511 162 16.6 23 28.355 3.1449 128 13.1
8 15.164 5.8378 371 38 24 29.145 3.0614 374 38.3
9 16.031 5.524 977 100 25 29.8 2.9956 109 11.2
10 16.621 5.3292 244 25 26 30.482 2.9301 87 8.9
11 17.451 5.0777 433 44.3 27 30.941 2.8877 72 7.4
12 17.807 4.977 551 56.4 28 32.223 2.7757 90 9.2
13 18.671 4.7484 846 86.6 29 33.584 2.6663 103 10.5
14 20.132 4.4071 666 68.2 30 36.224 2.4778 57 5.8
15 21.039 4.2191 267 27.3 31 38.159 2.3565 57 5.8
16 22.403 3.9652 382 39.1 32 38.91 2.3127 69 7.1


[0043] The present invention also provides uses of the compounds or the crystal forms mentioned above in manufacturing a medicament for treating the breast cancer.

Technical effects



[0044] Compared with the free acid form of the compound 1-8 reported in WO2017162206A1, the solubility of the compound of formula (I) of the present invention and the crystal form thereof in water is nearly hundredfold improved; in the solubility test of biological media, the solubility of the compound of formula (I) and the crystal form thereof has also been significantly improved; in in vivo pharmacokinetic studies, the compound of formula (I) and the crystal form thereof exhibited superior properties, and the amount of exposure in the organism was significantly increased. These good properties of the compound of formula (I) and the crystal form thereof make it more conducive to the preparation of medicines, benefit patients, and meet clinical needs.

Definitions and explanations



[0045] Unless otherwise indicated, the following terms and phrases used herein are intended to have the following meanings. A particular term or phrase should not be considered uncertain or unclear without a special definition, but should be understood according to its ordinary meaning. When a trade name appears herein, it is intended to refer to its corresponding product or its active ingredient.

[0046] The intermediate compounds of the present invention can be prepared by a variety of synthetic methods well known to those skilled in the art, including the following specific embodiments, the embodiments formed by combining them with other chemical synthesis methods, and equivalent alternatives well known to those skilled in the art, preferred embodiments include, but are not limited to, the embodiments of the present invention.

[0047] The chemical reactions of the specific embodiments of the present invention are performed in suitable solvents, and the solvents must be suitable for the chemical changes of the present invention and the reagents and materials required for the same. In order to obtain the compounds of the present invention, it is sometimes necessary for those skilled in the art to modify or select the synthetic steps or reaction schemes based on the existing embodiments.

[0048] The present invention will be described in detail below through embodiments, which do not imply any limitation to the present invention.

[0049] All solvents used in the present invention are commercially available and can be used without further purification.

[0050] The present invention uses the following abbreviations: MW stands for microwave; r.t. stands for room temperature; aq stands for aqueous solution; DCM stands for dichloromethane; THF stands for tetrahydrofuran; DMSO stands for dimethyl sulfoxide; NMP stands for N-methylpyrrolidone; EtOAc stands for ethyl acetate; EtOH stands for ethanol; MeOH stands for methanol; dioxane stands for dioxane; HOAc stands for acetic acid; Boc stands for tert-butoxycarbonyl, Cbz stands for benzyloxycarbonyl, both of Boc and Cbz are amine protecting groups; Boc2O stands for di-tert-butyl dicarbonate; DIPEA stands for ethyldiisopropylamine; TEA or Et3N stands for triethylamine; BnNH2 stands for benzylamine; PMBNH2 stands for p-methoxybenzylamine; KOAc stands for potassium acetate; NaOAc stands for sodium acetate; Cs2CO3 stands for cesium carbonate; K2CO3 stands for potassium carbonate; NaHCO3 stands for sodium bicarbonate; Na2SO4 stands for sodium sulfate; pyridine stands for pyridine; NaOH stands for sodium hydroxide; TEA or Et3N stands for triethylamine; NaH stands for sodium hydrogen; LiHMDS stands for lithium bis(trimethylsilyl)amide; i-PrMgBr stands for isopropylmagnesium bromide; t-BuOK stands for potassium t-butoxide; t-BuONa stands for sodium t-butoxide; Pd2(dba)3 stands for tris(dibenzylideneacetone)dipalladium; Pd(PPh3)4 stands for tetrakis(triphenylphosphine)palladium; Pd(dppf)Cl2CH2Cl2 stands for 1,1'-bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex; Pd(OAc)2 stands for palladium acetate; Pd(PPh3)2Cl2 stands for palladium bis(triphenylphosphine)dichloride; Pd(PPh3)3Cl stands for stands for rhodium tris(triphenylphosphine)chloride; Pd(OH)2 stands for palladium hydroxide; Xantphos stands for 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; Xphos stands for 2-(dicyclohexylphosphino)-2',4',6'-tri-iso-propyl-1,1'-biphenyl; BINAP stands for (±)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl; Xantphos stands for 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; Xphos-Pd-G1 stands for chloro(2-dicyclohexylphosphino-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2'-aminoethyl) phenyl]palladium(II); Xphos-PD-G2 stands for chloro(2-dicyclohexylphosphino-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2'-amino-1,1'-b iphenyl)]palladium(II); Xphos-Pd-G3 stands for methanesulfonato(2-dicyclohexylphosphino-2',4',6'-tri-iso-propyl-1,1'-biphenyl)(2'-a mino-1,1'-biphenyl-2-yl)palladium(II); I2 stands for iodine; LiCl stands for lithium chloride; HCl stands for hydrochloric acid; maleic acid stands for maleic acid.

[0051] Compounds are named by hand or Chemdraw® software, and commercially available compounds use the supplier catalog names thereof.

X-Ray Powder Diffractometer (XRPD) method



[0052] Instrument model: Bruker D8 advance X-ray diffractometer.

[0053] Test method: about 10-20mg sample was used for XRPD detection.

[0054] X-ray Tube: Cu, Kα, (λ=1.54056 Ǻ).

[0055] X-ray tube voltage: 40 kV, X-ray tube current: 40 mA.

[0056] Divergence slit: 0.60 mm.

[0057] Detector slit: 10.50 mm.

[0058] Anti-scattering slit: 7.10 mm.

[0059] Scanning range: 3-40 deg or 4-40 deg.

[0060] Step diameter: 0.02 deg.

[0061] Step length: 0.12 seconds.

[0062] Rotation speed of sample tray: 15 rpm.

Differential Scanning Calorimeter (DSC) method



[0063] Instrument model: TA Q2000 differential scanning calorimeter.

[0064] Test method: samples (about 1 mg) were sealed in DSC aluminum pans for testing, and heated at a heating rate of 10°C/min from room temperature to 250°C (or 280°C), at a flow rate of 50 mL/min N2.

Thermal Gravimetric Analyzer (TGA) method



[0065] Instrument model: TA Q5000 thermal gravimetric analyzer.

[0066] Test method: samples (2 to 5 mg) were disposed in TGA platinum pans for testing. The samples were heated from room temperature to 300°C or 20% weight loss at 25 mL/min N2 with a heating rate of 10°C/min.

Brief Description of the Drawings



[0067] 

Fig.1 is an XRPD pattern of the crystal form A of the compound of formula (I).

Fig. 2 is a DSC pattern of the crystal form A of the compound of formula (I).

Fig. 3 is an XRPD pattern of the crystal form B of the compound of formula (I).

Fig. 4 is an XRPD pattern of the crystal form C of the compound of formula (II).

Fig. 5 is an XRPD pattern of the crystal form D of the compound of formula (III).

Fig. 6 is an XRPD pattern of the crystal form E of the compound of formula (III).

Fig. 7 is an XRPD pattern of the crystal form F of the compound of formula (IV).

Fig. 8 is an XRPD pattern of the crystal form G of the compound of formula (IV).

Fig. 9 is an XRPD pattern of the crystal form H of the compound of formula (V).

Fig. 10 is an XRPD pattern of the crystal form I of the compound of formula (V).

Fig. 11 is an XRPD pattern of the crystal form J of the compound of formula (V).

Fig. 12 is an XRPD pattern of the crystal form K of the compound of formula (VI).


Detailed description of the embodiment



[0068] In order to better understand the content of the present invention, the following Embodiments further illustrate the present invention, but the present invention is not limited.

Embodiment 1: Preparation for the Crystal Form A of the Compound of Formula (I)



[0069] Anhydrous methanol (4.9 L), choline aqueous solution (49.5% by weight, 467.60 g), and anhydrous methanol (0.12 L) were added to the reaction kettle successively and the temperature was adjusted to 25°C. Then a solution of compound 1-8 (1004.15 g) in anhydrous methanol (4.90 L) was added dropwise to the reaction kettle, and the temperature was controlled between 20-25°C. After the addition, the mixture was stirred at around 35°C for 5h before the termination of the heating and stirring. Ethyl acetate (10.04 L) was added to the reaction solution, followed by concentrating to constant weight at 40°C, and the process was repeated twice. Ethyl acetate (16.58 L) was added again, the mixture was heated to 79°C and refluxed for 42 hours, then the stirring stopped after the mixture was cooled down to room temperature. The mixture was filtered, and the filter cake was washed with ethyl acetate (3.00 L), collected and dried at ambient temperature (15-25 °C) for 19h. The filter cake was dried at 45-50°C and -0.8MPa for about 28h to obtain the crystal form A of the compound of formula (I).
1H NMR (400MHz, DMSO-d6) δ = 12.14 (br s, 1H), 7.53 - 7.45 (m, 1H), 7.45 - 7.41 (m, 1H), 7.41 - 7.33 (m, 1H), 7.31 - 7.22 (m, 1H), 7.22 - 7.08 (m, 5H), 7.02 - 6.89 (m, 3H), 6.25 (d, J=16.0 Hz, 1H), 3.94 - 3.77 (m, 2H), 3.47 - 3.41 (m, 2H), 3.13 (s, 9H), 2.49 - 2.31 (m, 2H), 0.88 (t, J=7.6 Hz, 3H)

Embodiment 2: Preparation for the Crystal Form B of the Compound of Formula (I)



[0070] At 20°C, hydroxycholine methanol solution (45% by weight, 1g) was added to compound 1-8 (1g) and ethyl acetate (10mL) and the mixture was stirred at 20°C for 16 hours to obtain a yellow solution, which became a yellow suspension due to gradual precipitation. The mixture was filtered and the filter cake was washed with ethyl acetate (5 mL×3) to obtain the crystal form B of the compound of formula (I) by drying in vacuum.
1H NMR (400MHz, DMSO-d6) δ = 11.88 (br s, 1H), 7.47 (d, J=8.4 Hz,1H), 7.41 (d, J=8.4 Hz,2H), 7.28 (d, J=8.4 Hz,1H), 7.20 - 7.08 (m, 5H), 6.98 - 6.90 (m, 3H), 6.26 (d, J=16.0 Hz, 1H), 3.88 - 3.80 (m, 2H), 3.45 - 3.38 (m, 2H), 3.11 (s, 9H), 2.47 - 2.35 (m, 2H), 0.87 (t, J=7.2 Hz, 3H)

Embodiment 3: Preparation for the Crystal Form C of the Compound of Formula (II)



[0071] 1g Compound 1-8 was dissolved in 10mL ethyl acetate and the mixture was stirred at 50°C for 30 min, hydroxycholine aqueous solution (50% by weight, 248.86 mg) was added at 50°C and the mixture was stirred at 50°C for 5h, then cooled to 20°C and stirred for 12h. Solids were precipitated, then filtered off, and the filter cake was washed with ethyl acetate (3 mL x 3) and concentrated to give 1.08g white solid of the crystal form C of the compound of formula (II).
1H NMR (400MHz, DMSO-d6) δ = 11.62 (br s, 1H), 7.49 (d, J=8.4 Hz,1H), 7.41 (d, J=8.4 Hz,2H), 7.32 - 7.25 (m, 3H), 7.20 - 7.08 (m, 4H), 6.97 (d, J=8.4 Hz,2H), 6.38 (d, J=16.0 Hz, 1H), 3.88 - 3.82 (m, 1H), 3.43 - 3.38 (m, 1H), 3.11 (s, 4.5H), 2.50 - 2.32 (m, 2H), 0.89 (t, J=7.6 Hz, 3H)

Embodiment 4: Preparation for the Crystal of the Compound of Formula (III)


1)Preparation for the Crystal Form D of the Compound of Formula (III)



[0072] 0.2g Free acid was dissolved in acetonitrile (2 mL) and the mixture was stirred at 50°C for 30 minutes, 55.48mg trometamol was added and the mixture was stirred at 50°C for 5 hours, then cooled to 25°C and stirred for 16 hours. Solids were precipitated, and then filtered off, the filter cake was washed with n-heptane (5 mL), and the solid was concentrated to obtain 145mg bright yellow solid.
1H NMR (400MHz, DMSO-d6) δ = 11.52 (br s, 1H), 7.49 (d, J=8.0 Hz,1H), 7.40 (d, J=8.0 Hz,2H), 7.32 - 7.23 (m, 3H), 7.22 - 7.10 (m, 4H), 6.97 (d, J=8.0 Hz,2H), 6.32 (d, J=15.6 Hz, 1H), 3.41 (s, 6H), 2.48 - 2.39 (m, 2H), 0.87 (t, J=7.6 Hz, 3H)

2)Preparation for the Crystal Form E of the Compound of Formula (III)



[0073] 0.2g Free acid was dissolved in isopropanol (2 mL) and the mixture was stirred at 50°C for 30 minutes. 55.48mg Tristearin was added and the mixture was stirred at 50°C for 5 hours, then cooled to 25°C and stirred for 16 hours. The solution was kept clear and poured into a glass vial containing 20 mL n-heptane, then the mixture was filtered to obtain a viscous oil, and concentrated to obtain 103mg bright yellow solid diethylamine salt.
1H NMR (400MHz, DMSO-d6) δ = 11.50 (br s, 1H), 7.48 (d, J=8.0 Hz,1H), 7.40 (d, J=8.0 Hz,2H), 7.33 - 7.22 (m, 3H), 7.21 - 7.08 (m, 4H), 6.96 (d, J=8.0 Hz,2H), 6.31 (d, J=16.0 Hz, 1H), 3.38 (s, 6H), 2.50 - 2.39 (m, 2H), 0.88 (t, J=7.6 Hz, 3H)

Embodiment 5: Preparation for the Compound of Formula (IV)



[0074] 1)Preparation for the Crystal Form F of the Compound of Formula (IV) 0.2g Free acid was dissolved in acetone (2mL) and the mixture was stirred at 50°C for 30 mins, 33.50mg diethylamine was added and the mixture was stirred at 50°C for 5h, then cooled to 25°C and stirred for 16h. A large amount of white solid was precipitated, filtered off, and the filter cake was washed with acetone (2mL×3), and the filter cake was concentrated to obtain 161mg white solid.
1H NMR (400MHz, DMSO-d6) δ = 11.56 (br s, 1H), 7.51 (d, J=7.2 Hz,1H), 7.40 (d, J=7.6 Hz,2H), 7.31 - 7.28 (m, 3H), 7.20 - 7.10 (m, 4H), 6.96 (d, J=8.4 Hz,2H), 6.32 (d, J=16.0 Hz, 1H), 2.76 (d, J=7.2 Hz, 4H), 2.51 - 2.43 (m, 2H), 1.11 (d, J=7.2 Hz, 6H), 0.89 (t, J=7.6 Hz, 3H)

2)Preparation for the Crystal Form G of the Compound of Formula (IV)



[0075] 0.2g Free acid was dissolved in isopropanol (2mL) and the mixture was stirred at 50°C for 30 mins, 33.50mg diethylamine was added and the mixture was stirred at 50°C for 5h, then cooled to 25°C and stirred for 16h. A large amount of white solid was precipitated, filtered off, and the filter cake was washed with acetone (2mL×3), and the filter cake was concentrated to obtain 163mg white solid piperazine salt.
1H NMR (400MHz, DMSO-d6) δ = 11.56 (br s, 1H), 7.51 (d, J=7.2 Hz,1H), 7.40 (d, J=7.6 Hz,2H), 7.31 - 7.28 (m, 3H), 7.20 - 7.10 (m, 4H), 6.97 (d, J=8.0 Hz,2H), 6.33 (d, J=16.0 Hz, 1H), 2.76 (d, J=7.2 Hz, 4H), 2.51 - 2.43 (m, 2H), 1.11 (d, J=7.2 Hz, 6H), 0.89 (t, J=7.6 Hz, 3H)

Embodiment 6: Preparation for the Crystal of the Compound of Formula (V)


1)Preparation for the Crystal Form H of the Compound of Formula (V)



[0076] 0.2g Free acid was dissolved in acetone (2mL) and the mixture was stirred at 50°C for 30 mins, 39.45mg piperazine was added and the mixture was stirred at 50°C for 5h, then cooled to 25°C and stirred for 16h. A large amount of white solid was precipitated, filtered off, and the filter cake was washed with acetone (2mL×3), and the filter cake was concentrated to obtain white solids.
1H NMR (400MHz, DMSO-d6) δ = 11.55 (br s, 1H), 7.49 (d, J=8.0 Hz,1H), 7.43 - 7.37 (m, 2H), 7.31 - 7.29 (m, 3H), 7.19 - 7.11 (m, 4H), 6.96 (d, J=8.4 Hz,2H), 6.32 (d, J=15.6 Hz, 1H), 2.78 (s, 8H), 2.50 - 2.41 (m, 2H), 0.89 (t, J=7.6 Hz, 3H)

2)Preparation for the Crystal Form I of the Compound of Formula (V)



[0077] 0.2g Free acid was dissolved in acetonitrile (2mL) and the mixture was stirred at 50°C for 30 mins, 39.45mg piperazine was added and the mixture was stirred at 50°C for 5h, then cooled to 25°C and stirred for 16h. A large amount of white solid was precipitated, filtered off, and the filter cake was washed with acetone (2mL×3), and the filter cake was concentrated to obtain white solids.
1H NMR (400MHz, DMSO-d6) δ = 11.55 (br s, 1H), 7.49 (d, J=8.0 Hz,1H), 7.43 - 7.37 (m, 2H), 7.31 - 7.29 (m, 3H), 7.19 - 7.12 (m, 4H), 6.96 (d, J=8.0 Hz,2H), 6.32 (d, J=16.0 Hz, 1H), 2.78 (s, 8H), 2.50 - 2.41 (m, 2H), 0.89 (t, J=7.6 Hz, 3H)

3)Preparation for the Crystal Form J of the Compound of Formula (V)



[0078] 0.2g Free acid was dissolved in isopropanol (2mL) and the mixture was stirred at 50°C for 30 mins, 39.45mg piperazine was added and the mixture was stirred at 50°C for 5h, then cooled to 25°C and stirred for 16h. A large amount of white solid was precipitated, filtered off, and the filter cake was washed with acetone (2mL×3), and the filter cake was concentrated to obtain white solids.
1H NMR (400MHz, DMSO-d6) δ = 11.54 (br s, 1H), 7.50 (d, J=8.0 Hz,1H), 7.43 - 7.37 (m, 2H), 7.33 - 7.25 (m, 3H), 7.21 - 7.14 (m, 4H), 6.96 (d, J=8.4 Hz,2H), 6.33 (d, J=16.0 Hz, 1H), 2.76 (s, 8H), 2.50 - 2.35 (m, 2H), 0.89 (t, J=7.6 Hz, 3H)

Embodiment 7: Preparation for the Crystal Form K of the Compound of Formula (VI)



[0079] 0.2g Free acid was dissolved in acetonitrile (2mL) and the mixture was stirred at 50°C for 30 mins, 110.08mg benzathine was added and the mixture was stirred at 50°C for 5h, then cooled to 25°C and stirred for 16h. A large amount of white solid was precipitated, filtered off, and the filter cake was washed with acetonitrile (2mL×3), and the filter cake was concentrated to obtain white solids.
1H NMR (400MHz, DMSO-d6) δ = 11.53 (br s, 1H), 7.51 (d, J=7.2 Hz,1H), 7.45 - 7.05 (m, 19H), 7.01 - 6.98 (m, 2H), 6.39 (d, J=16.0 Hz, 1H), 3.73 (s, 4H), 2.66 (s, 4H), 2.50 - 2.42 (m, 2H), 0.91-0.89 (m, 3H)

Embodiment 8: Solubility Test



[0080] Assay materials: compound 1-8, crystal form A of the compound of the formula (I), water, FaSSIF (simulated pre-meal intestinal fluid), FeSSIF (simulated post-meal intestinal fluid).

[0081] Assay method: compound 1-8 and the crystal form A of the compound of formula (I) were weighed in four portions and added to a 4mL glass vial respectively, then 2mL biological vehicle (FaSSIF, FeSSIF) and purified water were added respectively, the mixtures were mixed uniformly and the magnets were added to the suspensions, the mixtures were placed on a magnetic stirring heater for stirring (at 37°C, protected from light). Samples were taken after 24h, and the sample solution was quickly centrifuged, and the supernatant was diluted suitable folds and its concentration was determined by HPLC.

[0082] Assay results: see Table 12.
Table 12 Solubility Comparison-solubility of different biological vehicle
Compounds to be testedBiological vehicle
H2O(mg/mL)*FaSSIF(mg/mL)*FeSSIF(mg/mL)*
compound I-8 0.008 0.117 0.440
Crystal Form A of the compound of formula (I) 0.870 1.650 3.590
"*": the solubility of the crystal form A of the compound of formula (I) was calculated based on the free acid.


[0083] Experiment conclusion: compared with compound 1-8, the solubility of the crystal form A of the compound of formula (I) has been significantly improved.

Embodiment 9: In vivo PK experiments



[0084] Assay materials: beagle dogs, three dogs per group, two groups in total (administered by compound 1-8 and crystal form A of the compound of formula (I) respectively)

[0085] Assay methods: the animals in each group were administered with corresponding compounds by orally gavage once, and blood samples were collected before and 2h (±2min), 4h (±5min), 6h (±5min), 8h (±5min), 12h (±5min), and 24h (±10min) after the administration. The samples were detected by LC-MS/MS, and AUC, Cmax, and Tmax parameters were calculated by employing WinNonlin version 6.4.

[0086] Assay results: see Table 13.
Tables 13.
ParametersCompound 1-8Crystal Form A of the compound of formula (I)
P.O. dose (mg/kg) 300 300
Cmax (nM) 43467 75167
Tmax (h) 6 9.3
AUC0-last (nM.h) 613021 1309787
MRT0-last (h) 10.6 13.3


[0087] Assay conclusion: The crystal form A of the compound of formula (I) has good pharmacokinetic properties.


Claims

1. A compound of formula (I),


 
2. A crystal form A of the compound of formula (I), wherein the X-ray powder diffraction pattern under Cu-Kα radiation has characteristic diffraction peaks at the following 2θ angles: 5.52± 0.2°, 13.68± 0.2°, 19.98± 0.2°, 20.80± 0.2°, 22.02± 0.2°, 22.44± 0.2°, 24.94± 0.2° and 26.96± 0.2°,


 
3. The crystal form A of claim 2, wherein the X-ray powder diffraction pattern under Cu-Kα radiation has nine or more than nine, ten or more than ten, or eleven or more than eleven characteristic diffraction peaks at the 2θ angles selected from the group consisting of 5.52±0.2°, 13.68±0.2°, 18.86±0.2°, 19.98±0.2°, 20.80±0.2°, 21.62±0.2°, 22.02±0.2°, 22.44±0.2°, 23.34±0.2°, 24.94±0.2°, 26.96±0.2° and 28.42±0.2°.
 
4. The crystal form A of claim 3, wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 1.
 
5. The crystal form A of any one of claims 2 to 4, wherein the differential scanning calorimetric curve has an endothermic peak at 239.46°C±3°C.
 
6. The crystal form A of claim 5, wherein the differential scanning calorimetric curve pattern is shown in FIG. 2.
 
7. A crystal form B of the compound of formula (I), wherein the X-ray powder diffraction pattern under Cu-Kα radiation has characteristic diffraction peaks at the following 2θ angles: 5.68 ± 0.2°, 12.36 ± 0.2°, 19.24 ± 0.2°, 19.86 ± 0.2°, 20.62 ± 0.2°, 21.64 ± 0.2°, 22.68 ± 0.2° and 24.96 ± 0.2°.
 
8. The crystal form B of claim 7, wherein the X-ray powder diffraction pattern under Cu-Kα radiation has nine or more than nine, ten or more than ten, or eleven or more than eleven characteristic diffraction peaks at the 2θ angles selected from the group consisting of 5.68 ± 0.2°, 12.36 ± 0.2°, 13.42 ± 0.2°, 19.24 ± 0.2°, 19.86 ± 0.2°, 20.62 ± 0.2°, 21.64 ± 0.2°, 22.68 ± 0.2°, 24.96 ± 0.2°, 26.38 ± 0.2°, 27.44 ± 0.2° and 30.62± 0.2°.
 
9. The crystal form B of claim 8, wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 3.
 
10. A compound of formula (II),


 
11. A crystal form C of the compound of formula (II), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 4.
 
12. A compound of formula (III),


 
13. A crystal form D of the compound of formula (III), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 5.
 
14. A crystal form E of the compound of formula (III), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 6.
 
15. A compound of formula (IV),


 
16. A crystal form F of the compound of formula (IV), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 7.
 
17. A crystal form G of the compound of formula (IV), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 8.
 
18. A compound of formula (V),


 
19. A crystal form H of the compound of formula (V), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 9.
 
20. A crystal form I of the compound of formula (V), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 10.
 
21. A crystal form J of the compound of formula (V), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 11.
 
22. A compound of formula (VI),


 
23. A crystal form K of the compound of formula (VI), wherein the X-ray powder diffraction pattern under Cu-Kα radiation is shown in FIG. 12.
 
24. Use of the compound or the crystal form of any one of claims 1 to 23 in the preparation of a medicament for treating breast cancer.
 




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Cited references

REFERENCES CITED IN THE DESCRIPTION



This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.

Patent documents cited in the description




Non-patent literature cited in the description