Patent Application
20210340142
The present invention relates to salt forms and crystalline forms of 6-(2-chloro-3,5-dimethoxyphenyl)-N-(4-(4-morpholinopiperidin-1-yl)phenyl)-[1,2,4]triazolo[4′,3′:1,6]pyrido[2,3-d]pyrimidin-2-amine, methods of preparing the crystalline forms, pharmaceutical compositions comprising such crystalline forms, use of the new crystalline forms and the pharmaceutical compositions as FGFR inhibitor, and methods of using the new crystalline forms and the pharmaceutical compositions for treating FGFR-mediated diseases.
Protein kinases are enzymes that catalyze the phosphorylation of proteins, in most instances, the phosphorylation occurs on the serine (ser), threonine (thr) and tyrosine (tyr) residues of the protein. Many aspects of cell life processes (eg. cell growth, differentiation, proliferation, cell cycle and survival) are dependent on the activity of protein kinase. Furthermore, many diseases (eg. cancer and inflammation) are associated with the abnormal activity of protein kinase.
It has been found that Protein Tyrosine Kinase (PTK) have more than 100 family members so far, which play an important role in regulating cell differentiation, growth and proliferation. According to the structure of PTK, it can be divided into two types: receptor type PTK and non-receptor type PTK. The former is also known as transmembrane PTK, and the latter is also known as intracellular PTK.
Fibroblast growth factor receptors (FGFR) which belongs to a member of receptor tyrosine kinase (RTK) superfamily has become one of the targets for global pharmaceutical companies developing novel anti-tumor drugs. FGFR involves in the modulation of cell proliferation, apoptosis, migration, neovascularization and other processes. Due to its wide range of uses, FGFR and other RTK are regulated strictly in normal circumstances. In the tumor, such as breast cancer, bladder cancer, prostate cancer (currently developed indications), FGFR activation mutation or the over expression of ligand/receptor lead to its continuous activation, which is not only closely related to tumor occurrence, development, poor prognosis, but also plays a vital role in tumor angiogenesis, tumor invasion and metastasis. Therefore, FGFR is recognized as an important candidate for targeted cancer therapies, and the development of FGFR small molecular inhibitors has received more and more attention gradually.
The activation and transduction of fibroblast growth factor (FGFs): FGFs can initiate autophosphorylation of FGFRs on tyrosine residues of key activation loops in tyrosine kinase domain, which results in the transition of the tyrosine kinase domain from an inactive state to an activated state. (Bae J H, Schlessinger J. Molecules and Cells, 2010, 29(5): 443-448). The activated tyrosine kinase domain in FGFRs will phosphorylate other tyrosine residues progressively along the FGFRs-binding adaptor molecule at the substrate binding site. Phosphorylation of tyrosine residues in the C-terminal region of FGFRs enables phosphatase Cy (PLCT) to be absorbed and activated, Which catalyzesthe conversion of phosphatidylinositol diphosphate (PIP2) to diglyceride (DAG) and triphosphate Alcohol (IP3). (Dailey L, Ambrostti D, Mansukhani A, et al. Cytokine & Growth Factor Reviews, 2005, 16(2), 233-247). Activated FGFR Phosphorylation Substrate 2 (FRS2) is capable of absorbing the Growth Factor Receptor Binding Protein 2 (GRB2) adaptor molecule.
FGFs signal can be transmitted to the Ras mitogen-activated protein kinase (Ras-MAPK) or PI3 kinase-protein kinase B (PI3K-AKT) signaling pathway via FRS2 and GRB2, and transmitted to protein kinase C (PKC) or protein kinase D (PKD) signaling pathway through PLC7 and DAG Kinase, and transmitted to the calcium ion release cascade pathway through PLC7 and IP3. FGFs-induced Ras-MAPK activation involves in cell proliferation, whereas FGFs-induced PI3K-AKT activation involves in cell survival.
FGFs signal participates in various aspects of tumor biology, such as anti-apoptosis, angiogenesis, Epithelial to Mesenchymal Transition (EMT), and invasion, etc. Targeted therapy of FGFRs has become the topical issues in the field of clinical oncology, and small molecule compounds designed and developed to fit the ATP binding POCket in the tyrosine kinase domain have been used in cancer therapy.
In human cancer cells with abnormal activation of FGFRs and anti-apoptotic potential, inhibition of FGFs signaling can reduce the load of cancer cells while inhibiting angiogenesis, and FGFR inhibitors can enhance the sensitivity of cancer cells against conventional anticancer drugs (such as 5-fluorouracil, irinotecan, paclitaxel, etc.). With the deepen understanding of FGFs signal networks and the intensive study of the mechanisms of action of FGFs and FGFRs, FGFR inhibitors with strong specificity and good therapeutic effects will be developed, therefore FGFR-targeted drugs may used to treat tumors will have extremely broad prospects.
Polymorphs of a particular organic pharmaceutical compound may have different physical properties, such as solubility, hygroscopicity and stability, due to their distinct three-dimensional crystal structures. However, it is generally not possible to predict whether a particular organic compound will form different crystalline forms, let alone predict the structure and properties of the crystalline forms themselves. Exploring new crystalline or polymorphic forms of a pharmaceutically useful compound provides a new opportunity for improving the overall characteristics of a pharmaceutical product and at the same time expands the variety of materials available to formulation scientists when designing. The discovery of new crystal forms of useful compounds has expanded the material variety for formulation design, which is obviously advantageous.
The present invention relates to the salt form of 6-(2-chloro-3,5-dimethoxyphenyl)-N-(4-(4-morpholinopiperidin-1-yl)phenyl)-[1,2,4]triazolo[4′,3′:1,6]pyrido[2,3-d]pyrimidin-2-amine represented by Formula I, and the substantially pure crystalline form of each salt form.
The Salt Form of the Compound of Formula I
In some embodiments, one acid and compound I form a corresponding salt. These salt-type compounds can exist in various physical forms. For example, it can be solutions, suspensions or solid forms. In some embodiments, the salt-type compound is in solid form. When in a solid form, the compound may be amorphous, crystalline or a mixture thereof. The salt forms formed by compound I and nine acids are exemplarily listed as follows. The nine acids are maleic acid, methanesulfonic acid, benzenesulfonic acid, hydrochloric acid, phosphoric acid, L-tartaric acid, L-malic acid, citric acid and fumaric acid.
Exemplary Examples of the Crystalline Forms of Each Salt Form of the Compound Represented by Structural Formula I are as Follows:
The present invention provides a preferable crystalline form of the maleate salt of compound of formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 5.6°±0.2°, 8.4°±0.2°, 11.2°±0.2°, 22.6°±0.2° and 28.3°±0.2°. For convenience, it is called maleate salt crystalline form 1 in the present invention.
The present invention provides another preferable crystalline form of the maleate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 5.9°±0.2. For convenience, it is called maleate salt crystalline form 2 in the present invention.
The present invention provides a preferable crystalline form of the methanesulfonate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 4.7°±0.2°, 9.4°±0.2° and 14.1°±0.2°. For convenience, it is called methanesulfonate salt crystalline form 1 in the present invention.
The present invention provides another preferable crystalline form of the methanesulfonate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 3.9°±0.2°, 15.7°±0.2° and 20.4°±0.2°. For convenience, it is called methanesulfonate salt crystalline form 2 in the present invention.
The present invention provides a preferable crystalline form of the benzenesulfonic acid (besylate) salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 4.5°±0.2°, 18.1°±0.2°, 20.4°±0.2° and 21.5°±0.2°. For convenience, it is called besylate salt crystalline form 1 in the present invention.
The present invention provides another preferable crystalline form of the besylate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 4.0°±0.2°, 4.9°±0.2°, 6.9°±0.2° and 18.4°±0.2°. For convenience, it is called besylate salt crystalline form 2 in the present invention.
The present invention provides a preferable crystalline form of the hydrochloride salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 4.2°±0.2°, 4.7°±0.2° and 6.9°±0.2°. For convenience, it is called hydrochloride salt crystalline form 1 in the present invention.
The present invention provides a preferable crystalline form of the phosphate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 7.5°±0.2°, 15.1°±0.2°, 16.4°±0.2°, 18.9°±0.2° and 26.8°±0.2°. For convenience, it is called phosphate salt crystalline form 1 in the present invention.
The present invention provides a preferable crystalline form of the L-tartrate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 7.6°±0.2°, 18.8°±0.2° and 27.3°±0.2°. For convenience, it is called L-tartrate salt crystalline form 1 in the present invention.
The present invention provides a preferable crystalline form of the L-malate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 3.6°±0.2°, 7.4°±0.2° and 18.8°±0.2°. For convenience, it is called L-malate salt crystalline form 1 in the present invention.
The present invention provides a preferable crystalline form of the citrate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 3.5°±0.2°, 7.3°±0.2° and 18.7°±0.2°. For convenience, it is called citrate salt crystalline form 1 in the present invention.
The present invention provides a preferable crystalline form of the fumarate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 5.5°±0.2°, 5.7°±0.2° and 19.3°±0.2°. For convenience, it is called fumarate salt crystalline form 1 in the present invention.
The present invention provides another preferable crystalline form of the fumarate salt of compound represented by structural formula I, the X-ray powder diffraction pattern of this crystalline form comprises characteristic peaks with diffraction angles 2θ of 4.5°±0.2°. For convenience, it is called fumarate salt crystalline form 2 in the present invention.
The X-ray powder diffraction patterns are all measured by Kalpha line of the Cu target.
The present invention further provides preferable embodiments of maleate salt crystalline form 1:
Preferably, the X-ray powder diffraction pattern of maleate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 5.6°±0.2°, 8.4°±0.2°, 11.2°±0.2°, 17.0°±0.2°, 19.7°±0.2°, 22.6°±0.2°, 25.4°±0.2°, 28.3°±0.2°.
Preferably, the X-ray powder diffraction pattern of maleate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 5.6°±0.2°, 8.4°±0.2°, 11.2°±0.2°, 17.0°±0.2°, 19.7°±0.2°, 22.6°±0.2°, 23.3°±0.2°, 25.4°±0.2°, 28.3°±0.2°.
Preferably, the X-ray powder diffraction pattern of maleate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 5.6°±0.2°, 8.4°±0.2°, 11.2°±0.2°, 14.0°±0.2°, 17.0°±0.2°, 19.7°±0.2°, 22.6°±0.2°, 23.3°±0.2°, 25.4±0.2°, 28.3°±0.2°.
Preferably, the X-ray powder diffraction pattern of maleate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 5.6°±0.2°, 8.4°±0.2°, 11.2°±0.2°, 15.3°±0.2°, 15.9°±0.2°, 17.0°±0.2°, 17.5°±0.2°, 18.5°±0.2°, 19.7°±0.2°, 22.6°±0.2°, 23.3°±0.2° 25.4°±0.2°, 26.3°±0.2°, 27.5°±0.2° and 28.3°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of maleate salt crystalline form 1 is shown in Table 1.
Preferably, the X-ray powder diffraction pattern of maleate salt crystalline form 1 is approximately as shown in
Preferably, the X-ray powder diffraction pattern of maleate salt crystalline form 1 is approximately as shown in
Further, maleate salt crystalline form 1 has a differential scanning calorimetry (DSC) thermogram substantially as shown in
Further, the maleate salt crystalline form 1 has a thermal gravimetric analysis (TGA) thermogram substantially as shown in
The present invention further provides preferable embodiments of maleate salt crystalline form 2:
Preferably, the X-ray powder diffraction pattern of maleate salt crystalline form 2 comprises characteristic peaks with diffraction angles 2θ of 5.9°±0.2°, 11.7°±0.2°, 17.6°±0.2°, 20.6°±0.2° and 23.5°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of maleate salt crystalline form 2 is shown in Table 2.
Preferably, the X-ray powder diffraction pattern of maleate salt crystalline form 2 is approximately as shown in
Further, maleate salt crystalline form 2 has a differential scanning calorimetry (DSC) thermogram substantially as shown in
Further, maleate salt crystalline form 2 has a thermal gravimetric analysis (TGA) thermogram substantially as shown in
The present invention further provides an amorphous form of maleate salt of the compound of formula I, the amorphous form has an X-ray powder diffraction pattern shown in
The present invention further provides preferable embodiments of methanesulfonate salt crystalline form 1:
Preferably, the X-ray powder diffraction pattern of methanesulfonate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 4.7°±0.2°, 9.4°±0.2°, 10.7°±0.2°, 12.1°±0.2°, 14.1°±0.2° and 19.0°±0.2°.
Preferably, the X-ray powder diffraction pattern of methanesulfonate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 4.7°±0.2°, 9.4°±0.2°, 10.7°±0.2°, 12.1°±0.2°, 14.1°±0.2°, 16.3°±0.2°, 16.8°±0.2° and 19.0°±0.2°.
Preferably, the X-ray powder diffraction pattern of methanesulfonate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 4.7°±0.2°, 9.4°±0.2°, 10.7°±0.2°, 12.1°±0.2°, 14.1°±0.2°, 16.3°±0.2°, 16.8°±0.2°, 19.0°±0.2°, 21.1°±0.2°, 21.4°±0.2°, 23.9°±0.2° and 28.2°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of methanesulfonate salt crystalline form 1 is shown in Table 3.
Preferably, the X-ray powder diffraction pattern of methane sulfonate salt crystalline form 1 is approximately as shown in
Further, the solubility of methanesulfonate salt crystalline form 1 in water at 25° C. is about 1.0 mg/mL.
Further, methanesulfonate salt crystalline form 1 has a hot-stage XRD pattern substantially as shown in
Further, methanesulfonate salt crystalline form 1 has a thermal gravimetric analysis (TGA) thermogram substantially as shown in
Further, methanesulfonate salt crystalline form 1 has a differential scanning calorimetry (DSC) thermogram substantially as shown in
Further, methanesulfonate salt crystalline form 1 has a 1H-NMR spectrum substantially as shown in
The present invention further provides preferable embodiments of methanesulfonate salt crystalline form 2:
Preferably, the X-ray powder diffraction pattern of methanesulfonate salt crystalline form 2 comprises characteristic peaks with diffraction angles 2θ of 3.9°±0.2°, 4.8°±0.2°, 6.5°±0.2°, 13.0°±0.2°, 13.9°±0.2°, 15.7°±0.2° and 20.4°±0.2°.
Preferably, the X-ray powder diffraction pattern of methanesulfonate salt crystalline form 2 comprises characteristic peaks with diffraction angles 2θ of 3.9°±0.2°, 4.8°±0.2°, 6.5°±0.2°, 8.0°±0.2°, 11.9°±0.2°, 12.4°±0.2°, 13.0°±0.2°, 13.9°±0.2°, 15.7°±0.2°, 16.4°±0.2°, 18.7°±0.2°, 19.6°±0.2°, 19.8°±0.2°, 20.4°±0.2°, 21.6°±0.2°, 22.4°±0.2°, 23.7°±0.2° and 24.6°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of methanesulfonate salt crystalline form 2 is shown in Table 4.
Preferably, the X-ray powder diffraction pattern of methanesulfonate salt crystalline form 2 is approximately as shown in
Further, the solubility of the methanesulfonate salt crystalline form 2 in water at 25° C. is about 5.0 mg/mL.
Further, methanesulfonate salt crystalline form 2 has a hot-stage XRD pattern substantially as shown in
Further, methanesulfonate salt crystalline form 2 has a thermal gravimetric analysis (TGA) thermogram substantially as shown in
Further, methanesulfonate salt crystalline form 2 has a differential scanning calorimetry (DSC) thermogram substantially as shown in
Further, methanesulfonate salt crystalline form 2 has a 1H-NMR spectrum substantially as shown in
The present invention further provides preferable embodiments of besylate salt crystalline form 1:
Preferably, the X-ray powder diffraction pattern of besylate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 4.5°±0.2°, 7.9°±0.2°, 12.5°±0.2°, 12.9°±0.2°, 18.1°±0.2°, 20.4°±0.2° and 21.5°±0.2°.
Preferably, the X-ray powder diffraction pattern of besylate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 4.5°±0.2°, 6.3°±0.2°, 7.9°±0.2°, 9.0°±0.2°, 12.5°±0.2°, 12.9°±0.2°, 13.9°±0.2°, 15.7°±0.2°, 16.3°±0.2°, 18.1°±0.2°, 18.9°±0.2°, 19.3°±0.2°, 20.4°±0.2°, 21.5°±0.2°, 24.3°±0.2° and 26.2°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of besylate salt crystalline form 1 is shown in Table 5.
Preferably, the X-ray powder diffraction pattern of besylate salt crystalline form 1 is approximately as shown in
Further, the solubility of the besylate salt crystalline form 1 in water at 25° C. is about 0.08 mg/mL.
Further, besylate salt crystalline form 1 is analyzed by differential scanning calorimetry, the onset temperature of endothermic peak of besylate salt crystalline form 1 is about 224° C., and the peak temperature is about 234° C.
Further, besylate salt crystalline form 1 is analyzed by thermal gravimetric analysis, it shows that besylate salt crystalline form 1 has a weight loss of about 3.8% before 120° C.
Further, besylate salt crystalline form 1 has a 1H-NMR spectrum substantially as shown in
The present invention further provides preferable embodiments of besylate salt crystalline form 2:
Preferably, the X-ray powder diffraction pattern of besylate salt crystalline form 2 comprises characteristic peaks with diffraction angles 2θ of 4.0°±0.2°, 4.5°±0.2°, 4.9°±0.2°, 6.9°±0.2°, 14.4°±0.2°, 14.7°±0.2°, 18.4°±0.2° and 24.1°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of besylate salt crystalline form 2 is shown in Table 6.
Preferably, the X-ray powder diffraction pattern of besylate salt crystalline form 2 is approximately as shown in
Further, the solubility of besylate salt crystalline form 2 in water at 25° C. is about 1.0 mg/mL.
Further, the thermal gravimetric analysis shows that besylate salt crystalline form 2 has a weight loss of about 7.80% before 120° C.
Further, besylate salt crystalline form 2 has a differential scanning calorimetry (DSC) thermogram substantially as shown in
Further, besylate salt crystalline form 2 has a 1H-NMR spectrum as shown in
The present invention further provides preferable embodiments of hydrochloride salt crystalline form 1:
Preferably, the X-ray powder diffraction pattern of hydrochloride salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 4.2°±0.2°, 4.7°±0.2°, 6.9°±0.2°, 9.3°±0.2°, 12.1°±0.2°, 14.0°±0.2°, 14.6°±0.2°, 15.6°±0.2° and 19.7°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of hydrochloride salt crystalline form 1 is shown in Table 7.
Preferably, the X-ray powder diffraction pattern of hydrochloride salt crystalline form 1 is approximately as shown in
Further, the solubility of hydrochloride salt crystalline form 1 in water at 25° C. is about 1.25 mg/mL.
Further, the differential scanning calorimetry analysis shows that the onset temperature of endothermic peak of the hydrochloride salt crystalline form 1 is about 216° C., and the peak temperature is about 223° C.
Further, the thermal gravimetric analysis shows that hydrochloride salt crystalline form 1 has a weight loss of about 8.8% before 120° C.
The present invention further provides preferable embodiments of phosphate salt crystalline form 1:
Preferably, the X-ray powder diffraction pattern of phosphate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 7.5°±0.2°, 12.6°±0.2°, 15.1°±0.2°, 16.4°±0.2°, 18.1°±0.2°, 18.3°±0.2°, 18.9°±0.2°, 19.4°±0.2°, 21.4°±0.2°, 22.2°±0.2° and 26.8°±0.2°.
Preferably, the X-ray powder diffraction pattern of phosphate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 7.5°±0.2°, 9.2°±0.2°, 9.5°±0.2°, 10.4°±0.2°, 12.6°±0.2°, 13.0°±0.2°, 13.8°±0.2°, 14.5°±0.2°, 15.1°±0.2°, 16.4°±0.2°, 18.1°±0.2°, 18.3°±0.2°, 18.9°±0.2°, 19.4°±0.2°, 20.1°±0.2°, 21.4°±0.2°, 22.2°±0.2°, 23.3°±0.2°, 23.6°±0.2°, 25.3°±0.2°, 25.6°±0.2°, 26.0°±0.2°, 26.8°±0.2° and 28.1°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of phosphate salt crystalline form 1 is shown in Table 8.
Preferably, the X-ray powder diffraction pattern of phosphate salt crystalline form 1 is approximately as shown in
Further, the solubility of phosphate salt crystalline form 1 in water at 25° C. is about 0.1 mg/mL.
Further, the thermal gravimetric analysis shows that phosphate salt crystalline form 1 has a weight loss of about 4.0% before 120° C.
Further, phosphate salt crystalline form 1 has a differential scanning calorimetry (DSC) thermogram substantially as shown in
The present invention further provides preferable embodiments of L-tartrate salt crystalline form 1:
Preferably, the X-ray powder diffraction pattern of L-tartrate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 3.6°±0.2°, 7.1°±0.2°, 7.6°±0.2°, 18.8°±0.2°, 19.4°±0.2° and 27.3°±0.2°.
Preferably, the X-ray powder diffraction pattern of the L-tartrate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 3.6°±0.2°, 7.1°±0.2°, 7.6°±0.2°, 9.0°±0.2°, 13.1°±0.2°, 14.6°±0.2°, 15.2°±0.2°, 18.8°±0.2°, 19.4°±0.2°, 20.9°±0.2°, 21.4°±0.2°, 22.1°±0.2°, 23.6°±0.2° and 27.3°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of L-tartrate salt crystalline form 1 is shown in Table 9.
Preferably, the X-ray powder diffraction pattern of L-tartrate salt crystalline form 1 is approximately as shown in
Further, the solubility of L-tartrate salt crystalline form 1 in water at 25° C. is about 0.08 mg/mL.
Further, the differential scanning calorimetry analysis shows the onset temperature of endothermic peak of the L-tartrate salt crystalline form 1 is about 201° C., and the peak temperature is about 213° C.
Further, the thermal gravimetric analysis shows that L-tartrate salt crystalline form 1 has a weight loss of about 2.7% before 120° C.
Further, L-tartrate salt crystalline form 1 has a 1H-NMR spectrum substantially as shown in
The present invention further provides preferable embodiments of the L-malate salt crystalline form 1:
Preferably, the X-ray powder diffraction pattern of L-malate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 3.6°±0.2°, 7.4°±0.2°, 18.8°±0.2° and 27.2°±0.2°.
Preferably, the X-ray powder diffraction pattern of L-malate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 3.6°±0.2°, 7.4°±0.2°, 9.0°±0.2°, 10.5°±0.2°, 13.0°±0.2°, 15.1°±0.2°, 18.8°±0.2° and 27.2°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of L-malate salt crystalline form 1 is shown in Table 10.
Preferably, the X-ray powder diffraction pattern of L-malate salt crystalline form 1 is approximately as shown in
Further, the solubility of L-malate salt crystalline form 1 in water at 25° C. is about 0.25 mg/mL.
Further, the thermal gravimetric analysis shows that L-malate salt crystalline form 1 has a weight loss of about 3.3%.
Further, L-malate salt crystalline form 1 has a differential scanning calorimetry (DSC) thermogram substantially as shown in
Further, L-malate salt crystalline form 1 has a 1H-NMR spectrum substantially as shown in
The present invention further provides preferable embodiments of citrate salt crystalline form 1:
Preferably, the X-ray powder diffraction pattern of citrate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 3.5°±0.2°, 7.3°±0.2°, 12.5°±0.2°, 14.9°±0.2°, 18.7°±0.2°, 21.0°±0.2° and 26.8°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of citrate salt crystalline form 1 is shown in Table 11.
Preferably, the X-ray powder diffraction pattern of citrate salt crystalline form 1 is approximately as shown in
Further, the solubility of citrate salt crystalline form 1 in water at 25° C. is about 0.08 mg/mL.
Further, the differential scanning calorimetry analysis shows the onset temperature of endothermic peak of the citrate salt crystalline form 1 is about 164° C., and the peak temperature is about 188° C.
Further, the thermal gravimetric analysis shows that citrate salt crystalline form 1 has a weight loss of about 2.2% before 120° C.
Further, citrate salt crystalline form 1 has a 1H-NMR spectrum substantially as shown in
The present invention further provides preferable embodiments of fumarate salt crystalline form 1:
Preferably, the X-ray powder diffraction pattern of fumarate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 5.5°±0.2°, 5.7°±0.2°, 17.0°±0.2°, 19.3°±0.2° and 22.2°±0.2°.
Preferably, the X-ray powder diffraction pattern of fumarate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 5.5°±0.2°, 5.7°±0.2°, 17.0°±0.2°, 19.3°±0.2°, 22.2°±0.2°, 23.5°±0.2° and 27.0°±0.2°.
Preferably, the X-ray powder diffraction pattern of fumarate salt crystalline form 1 comprises characteristic peaks with diffraction angles 2θ of 5.5°±0.2°, 5.7°±0.2°, 10.8°±0.2°, 13.6°±0.2°, 16.1°±0.2°, 17.0°±0.2°, 18.2°±0.2°, 19.3°±0.2°, 20.3°±0.2°, 22.2°±0.2°, 23.5°±0.2°24.9°±0.2° and 27.0°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of fumarate salt crystalline form 1 is shown in Table 12.
Preferably, the X-ray powder diffraction pattern of fumarate salt crystalline form 1 is approximately as shown in
The present invention further provides preferable embodiments of fumarate salt crystalline form 2:
Preferably, the X-ray powder diffraction pattern of fumarate salt crystalline form 2 comprises characteristic peaks with diffraction angles 2θ of 4.5°±0.2°, 9.0°±0.2° and 13.4°±0.2°.
More preferably, the main data of the X-ray powder diffraction pattern of fumarate salt crystalline form 2 is shown in Table 13.
Preferably, the X-ray powder diffraction pattern of fumarate salt crystalline form 2 is approximately as shown in
Further, the solubility of fumarate salt crystalline form 2 in water at 25° C. is less than 0.05 mg/mL.
Further, the differential scanning calorimetry analysis shows the onset temperature of endothermic peak of the fumarate salt crystalline form 2 is about 182° C., and the peak temperature is about 194° C.
Further, the thermal gravimetric analysis shows that fumarate salt crystalline form 2 has a weight loss of about 3.2% before 120° C.
Further, fumarate salt crystalline form 2 has a 1H-NMR spectrum substantially as shown in
According to the present invention, the purity of the maleate salt crystalline form 1, maleate salt crystalline form 2, methanesulfonate salt crystalline form 1, methanesulfonate salt crystalline form 2, besylate salt crystalline form 1, besylate salt crystalline form 2, hydrochloride salt crystalline form 1, phosphate salt crystalline form 1, L-tartrate salt crystalline form 1, L-malate salt crystalline form 1, citrate salt crystalline form 1, fumarate salt crystalline form 1 and fumarate salt crystalline form 2 are preferably greater than 50%, for example, greater than 85%, greater than 99%, or greater than 99.5%.
The present invention further provides methods of preparing the compound of Formula I and the salt forms thereof, which include maleate salt crystalline form 1, maleate salt crystalline form 2, methanesulfonate salt crystalline form 1, methanesulfonate salt crystalline form 2, besylate salt crystalline form 1, besylate salt crystalline form 2, hydrochloride salt crystalline form 1, phosphate salt crystalline form 1, L-tartrate salt crystalline form 1, L-malate salt crystalline form 1, citrate salt crystalline form 1, fumarate salt crystalline form 1 and fumarate salt crystalline form 2.
Wherein, the compound of Formula I can be prepared by the following route:
Wherein, the preparation methods of maleate salt crystalline form 1 are as follows:
The compound of Formula I was added into acetone/water, stirred at 60° C., the system was not clear, maleic acid was dissolved in water and added dropwise to the above suspension system, stirred to obtain a clear solution, and continued stirring for about 2 minutes until a solid was precipitated, stirring was continued at 60° C. for 30 minutes, naturally cooled to room temperature and stirred for 4 days, filtered under reduced pressure, the solid was dried in vacuo for 24 hours to obtain maleate salt crystalline form 1; or,
After the amorphous of maleate crystalline form 1 was added into dimethyl sulfoxide/ethanol, dimethyl sulfoxide/acetone, dimethyl sulfoxide/butanone, dimethyl sulfoxide/ethyl acetate, dimethyl sulfoxide/acetonitrile, trifluoroethanol/butanone, trifluoroethanol/methyl tert-butyl ether, trifluoroethanol/isopropyl acetate, trifluoroethanol/acetonitrile, water/methanol, water/ethanol, water/isopropanol, water/acetone or water/acetonitrile, the temperature was warmed up to 60° C. to obtain a clear solution, filtered and stirred in a ice-salt bath. The solids were precipitated, and centrifuged immediately to obtain maleate crystalline Form 1. If there was no solid precipitated, stirred overnight at 4° C. or the solution was evaporated out at room temperature to precipitated a solid, which was maleate crystalline form 1.
Wherein, the preparation methods of maleate salt crystalline form 2 are as follows:
Maleate salt crystalline form 1 was added into dimethyl sulfoxide and placed in a tetrahydrofuran system at room temperature, diffused and stand to crystallization, maleate salt crystalline form 2 was obtained; or, Maleate salt crystalline form 1 was added into dimethyl sulfoxide/tetrahydrofuran, stirred at 60° C. to clear, filtered, and the filtrate was stirred to precipitate a yellow solid, which was centrifuged at room temperature and dried under vacuum to obtain maleate salt crystalline form 2.
Wherein, the preparation methods of amorphous are as follows:
Maleate salt crystalline form 1 was added into trifluoroethanol/dichloromethane and stirred in a water bath at 60° C. for 10 minutes. The system was not clear, the suspension was concentrated to dryness under reduced pressure at 40° C. to obtain a dark yellow solid, which was amorphous of the maleate salt crystalline form 1.
Wherein, the preparation method of methanesulfonate salt crystalline form 1 is as follows:
Compound of Formula I was added acetone and water sequentially, stirred at 60° C. in a water bath, the system was not clear, methanesulfonic acid was dissolved in water and added dropwise to the above suspension system, a clear solution was obtained. The clear solution was stirred at room temperature for 30 minutes, there was no precipitation, acetone was added dropwise and then a large amount of solids were precipitated, continued stirring at room temperature for 3 days, filtrated under reduced pressure, dried under vacuum at room temperature for 24 hours to obtain methanesulfonate salt crystalline form 1.
Wherein, the preparation method of methanesulfonate salt crystalline form 2 is as follows:
Compound of Formula I was added into acetone and water, stirred to clear at 60° C. in a water bath, methanesulfonic acid was dissolved in acetone, and added dropwise to the above clear system, there was no precipitation, and stirring was continued at 60° C. for 30 minutes, there was no precipitation. The mixture was naturally cooled to room temperature, stirred for 2 days, filtered under reduced pressure, and dried under vacuum at room temperature for 24 hours to obtain methanesulfonate salt crystalline form 2.
Wherein, the preparation method of besylate salt crystalline form 1 is as follows:
Compound of Formula I was added acetone, stirred at 60° C. in a water bath, the system was not clear, benzenesulfonic acid was dissolved in water and added dropwise to the above suspension system at room temperature, the system was still not clear, continued stirring at room temperature for 5 days, filtrated under reduced pressure, dried under vacuum at room temperature for 24 hours, and benzenesulfonate salt crystalline form 1 was obtained.
Wherein, the preparation method of besylate salt crystalline form 2 is as follows:
Compound of Formula I was added acetone and water sequentially, stirred to clear at 60° C. in a water bath, benzenesulfonic acid was dissolved in acetone, and added dropwise to the above clear system, there was no precipitation, stirring was continued at 60° C. for 30 minutes, there was still no precipitation, naturally cooled to room temperature, stirred for 2 days to precipitate, filtered under reduced pressure, dried under vacuum at room temperature for 24 hours to obtain benzenesulfonate salt crystalline form 2.
Wherein, the preparation method of hydrochloride salt crystalline form 1 is as follows:
Compound of Formula I was added into acetone to disperse, stirred for 10 minutes at 50° C. in a water bath, and then water was added, most of which was clear, concentrated hydrochloric acid was dissolved in water and added dropwise to the above suspension system, a large amount of white precipitate were precipitated, continued stirring for 30 minutes, naturally cooled to room temperature, stirred overnight, and continued stirring for 1 day, filtered under reduced pressure, dried under vacuum at 45° C. for 3 hours to obtain hydrochloride salt crystalline form 1.
Wherein, the preparation method of phosphate salt crystalline form 1 is as follows:
Compound of Formula I was added acetone, stirred at 60° C. in a water bath, the system was not clear, 85% phosphoric acid was dissolved in water and added dropwise to the suspension system at room temperature, the system was not clear, continued stirring at room temperature for 5 days, filtrated under reduced pressure, dried under vacuum at room temperature for 24 hours, to obtain phosphate salt crystalline form 1.
Wherein, the preparation method of L-tartrate salt crystalline form 1 is as follows:
Compound of Formula I was added isopropanol, stirred at 60° C. for 10 minutes, the system was not clear, L-tartaric acid was dissolved in water, and added dropwise to the above suspension system, the system became clear after stirring, stirring was continued for 30 minutes, and then isopropanol was added dropwise, there was no precipitation, stirring was continued for 30 minutes, there was no precipitation, naturally cooled to room temperature, stirred overnight, precipitated solid, filtrated under reduced pressure, dried under vacuum at 45° C. for 3 hours to obtain L-tartrate salt crystalline form 1.
Wherein, the preparation method of L-malate salt crystalline form 1 is as follows:
Compound of Formula I was added isopropanol to disperse, stirred at 60° C. for 10 minutes, the system was not clear, L-malic acid was dissolved in water, and added dropwise to the above suspension system, the system became clear after stirring, and stirring was continued for 10 minutes, and then isopropanol was added dropwise, there was no precipitation, stirring was continued for 30 minutes, there was still no precipitation, naturally cooled to room temperature, stirred overnight, precipitated solids, filtrated under reduced pressure, filter cake was rinsed with isopropanol and methyl tert-butyl ether 3 times, dried under vacuum at 45° C. for 3 hours to obtain L-malate salt crystalline form 1.
Wherein, the preparation method of citrate salt crystalline form 1 is as follows:
Compound of Formula I was added into isopropanol to disperse, stirred at 60° C. for 10 minutes, the system was not clear, citric acid was dissolved in water, and added dropwise to the above suspension system, the system became clear after stirring, stirring was continued for 30 minutes, and then isopropanol was added dropwise, there was no precipitation, stirring was continued for 30 minutes, there was still no precipitation, naturally cooled to room temperature, stirred overnight, precipitated solids, filtrated under reduced pressure, filter cake was rinsed with isopropanol and methyl tert-butyl ether 3 times, dried under vacuum at 45° C. for 3 hours to obtain citrate salt crystalline form 1.
Wherein, the preparation method of fumarate salt crystalline form 1 is as follows:
Compound of Formula I was added tetrahydrofuran, stirred to clear at 60° C., fumaric acid was dissolved in tetrahydrofuran, and added dropwise to the clear system at room temperature, there was no precipitation, continued stirring for 4 days, precipitated solids, centrifuged, dried under vacuum at room temperature for 4 hours to obtain fumarate salt crystalline form 1.
Wherein, the preparation method of fumarate salt crystalline form 2 is as follows:
Compound of Formula I was added into isopropanol to disperse, stirred at 60° C. for 10 minutes, the system was not clear, fumaric acid was dissolved in water, and added dropwise to the above suspension system, the system became clear after stirring, stirring was continued for 30 minutes, there was no precipitation, naturally cooled to room temperature and stirred overnight to precipitate a solid, continued stirring at room temperature for 1 day, filtrated under reduced pressure, dried under vacuum at 45° C. for 3 hours to obtain L-tartrate fumarate salt crystalline form 2.
The present invention further provides a pharmaceutical composition comprising a therapeutically effective amount of the salt form or the crystalline form of the present invention, and a pharmaceutically acceptable excipient, adjuvant or carrier. In the above mentioned composition, the weight ratio of the salt form or the crystalline form to the excipient, adjuvant or carrier can be within the range of 0.0001 to 10.
Secondly, the present invention also provides preferable embodiments of the above mentioned pharmaceutical composition.
Preferably, the pharmaceutical composition comprises a therapeutically effective amount of the salt form or the crystalline form of the present invention, in combination with at least one other active ingredient.
Preferably, the pharmaceutical composition is used in an oral administration.
Preferably, the pharmaceutical composition is used in a tablet or a capsule.
Preferably, the pharmaceutical composition comprises 0.01 wt %-99 wt % of the crystalline form of the present invention.
Preferably, the pharmaceutical composition comprises 0.05 wt %-50 wt % of the crystalline form of the present invention.
Preferably, the pharmaceutical composition comprises 0.1 wt %-30 wt % of the crystalline form of the present invention
The present invention further provides the use of the crystalline form or the pharmaceutical composition in the preparation of a medicament.
The present invention further provides preferable embodiments of the use:
Preferably, the use is treating, preventing, delaying or arresting the occurrence or progression in cancer or cancer metastasis.
Preferably, the use is the preparation of the medication for treating diseases mediated by FGFR.
Preferably, the disease is cancer.
Preferably, the cancer is selected from breast cancer, multiple myeloma, bladder cancer, endometrial cancer, stomach cancer, cervical cancer, rhabdomyosarcoma, non-small cell lung cancer, small cell lung cancer, pleomorphic lung cancer, ovarian cancer, esophageal cancer, melanoma, colorectal cancer, Hepatocellular carcinoma, head and neck tumors, intracranial tumors, hepatobiliary duct cell carcinoma, myelodysplastic syndrome, malignant glioma, prostate cancer, thyroid cancer, Schwann cell tumor, lung squamous cell carcinoma, lichenoid Keratosis, synovial sarcoma, skin cancer, pancreatic cancer, testicular cancer and liposarcoma.
Preferably, the use is to be an FGFR inhibitor.
Preferably, in the above-mentioned use, the FGFR contains FGFR1, FGFR2, FGFR3 or FGFR4.
The present invention also provides a method for administering to treatment subject a therapeutically effective amount of at least any one crystalline form or pharmaceutical composition to treating and/or preventing diseases mediated by FGFR.
Preferably, in the above-mentioned method, the FGFR contains FGFR1, FGFR2, FGFR3 or FGFR4.
Preferably, in the above-mentioned method, the disease mediated by FGFR is cancer.
Preferably, in the above-mentioned method, the cancer is selected from breast cancer, multiple myeloma, bladder cancer, endometrial cancer, stomach cancer, cervical cancer, rhabdomyosarcoma, non-small cell lung cancer, small cell lung cancer, pleomorphic lung cancer, ovarian cancer, esophageal cancer, melanoma, colorectal cancer, Hepatocellular carcinoma, head and neck tumors, intracranial tumors, hepatobiliary duct cell carcinoma, myelodysplastic syndrome, malignant glioma, prostate cancer, thyroid cancer, Schwann cell tumor, lung squamous cell carcinoma, lichenoid Keratosis, synovial sarcoma, skin cancer, pancreatic cancer, testicular cancer and liposarcoma.
The present invention also provides a method for treating cancer, comprising administering a therapeutically effective amount of at least any one crystalline form or pharmaceutical composition to treatment subject, and the cancer is breast cancer multiple myeloma, bladder cancer, endometrial cancer, stomach cancer, cervical cancer, rhabdomyosarcoma, non-small cell lung cancer, small cell lung cancer, pleomorphic lung cancer, ovarian cancer, esophageal cancer, melanoma, colorectal cancer, Hepatocellular carcinoma, head and neck tumors, intracranial tumors, hepatobiliary duct cell carcinoma, myelodysplastic syndrome, malignant glioma, prostate cancer, thyroid cancer, Schwann cell tumor, lung squamous cell carcinoma, lichenoid Keratosis, synovial sarcoma, skin cancer, pancreatic cancer, testicular cancer or liposarcoma.
Preferably, in the above-mentioned method, the treatment subject is human.
All the crystalline forms of the invention are substantially pure.
As used herein, the term “substantially pure” means that the content of the crystalline form is not less than 85%, preferably not less than 95%, more preferably not less than 99%.
In present invention, the term “substantially” and “approximately” used in “has a X-ray powder diffraction pattern substantially as shown in
Those skilled in the art will understand that due to the changes in sample purity, sample preparation and measurement conditions (such as heating rate), the DSC measurement data may be undergo small changes. It's should be understood that alternative melting point readings may be given by other types of instruments or by using other conditions which is different from those described below. Thus, the endothermic diagrams cited in the present invention are not regarded as absolute values, and such measurement errors will be considered when interpreting the DSC date.
The term “therapeutically effective amount” as herein used, refers to the amount of a compound that, when administered to a subject for treating a disease, or at least one of the clinical symptoms of a disease or disorder, is sufficient to affect such treatment for the disease, disorder, or symptom. The “therapeutically effective amount” can vary with the compound, the disease, disorder, and/or symptoms of the disease or disorder, severity of the disease, disorder, and/or symptoms of the disease or disorder, the age of the subject to be treated, and/or the weight of the subject to be treated. An appropriate amount in any given instance can be apparent to those skilled in the art or can be determined by routine experiments. In the case of combination therapy, the “therapeutically effective amount” refers to the total amount of the combination objects for the effective treatment of a disease, a disorder or a condition.
The salt form or crystalline form of this invention can be combined as the active ingredient, and mixed with the pharmaceutical carrier to form the pharmaceutical composition. The carrier may take a wide variety of forms depending on the form of preparation desired for administration, e.g., oral or parenteral (including intravenous).
Thus, the pharmaceutical compositions of the present invention can be presented as discrete units suitable for oral administration such as capsules, cachets or tablets each containing a predetermined amount of the active ingredient. Further, the compositions can be presented as a powder, as granules, as a solution, as a suspension in an aqueous liquid, as a non-aqueous liquid, as an oil-in-water emulsion, or as a water-in-oil liquid emulsion. In addition to the common dosage forms set out above, the salt form or crystalline form of this invention may also be administered by controlled release means and/or delivery devices. The compositions may be prepared by any of the methods of pharmacy. In general, such methods include a step of bringing into association the active ingredient with the carrier that constitutes one or more necessary ingredients. In general, the compositions are prepared by uniformly and intimately admixing the active ingredient with liquid carriers or finely divided solid carriers or both. The product can then be conveniently shaped into the desired presentation.
“Pharmaceutically acceptable carrier” refers to a conventional pharmaceutical carrier suitable for the desired pharmaceutical preparation, for example: diluents and excipients such as water, various organic solvents, etc.; such as starch, pregelatinized starch, sucrose, Fillers such as dextrin, mannitol, lactose, spray-dried lactose, microcrystalline cellulose, silicified microcrystalline cellulose, inorganic salts, etc.; such as starch syrup, dextrin, powdered sugar, syrup, mucilage, polyethylene glycol, Cellulose derivatives, alginate, gelatin, hydroxypropyl cellulose, copovidone and polyvinylpyrrolidone (PVP); wetting agents such as distilled water, ethanol and glycerin; such as dry starch, low substitution Disintegrants of hydroxypropyl cellulose, hydroxypropyl starch, agar, calcium carbonate, sodium bicarbonate, crospovidone, croscarmellose sodium, sodium carboxymethyl starch, etc.; such as quaternary ammonium compounds, Amino acid ethylamine derivatives, acetoacetates, β-dicarboxylic acid esters, aromatic acidic compounds, aliphatic acidic compounds, etc. absorption enhancers; such as sodium cetyl sulfate, sodium stearyl sulfate, dioctyl sulfate Sodium sulfosuccinate, sodium lauryl sulfonate, benzalkonium bromide, benzalkonium chloride, domefen, lecithin, cetyl alcohol, sodium lauryl sulfate, tween and spaan, etc. Surfactants; such as polyethylene glycol, carbomer, cellulose derivatives, glycerin gelatin, polyvinyl alcohol, cocoa butter, synthetic or fully synthetic fatty acid glycerides, polyvinyl alcohol 40 stearate, petrolatum, solid Paraffin, liquid paraffin, simethicone, lanolin, beeswax, and dolphin and other drug-carrying bases; absorption carriers such as kaolin and bentonite; such as talc, micronized silica gel, silicon dioxide, hydrogenated vegetable oil, dodecyl Lubricants such as magnesium sulfate, sodium lauryl sulfate, stearic acid, calcium stearate, magnesium stearate, sodium stearyl fumarate and polyethylene glycol. In addition, other pharmaceutically acceptable auxiliary materials can be added to the pharmaceutical composition, such as antioxidants, coloring agents, preservatives, pH regulators, hardeners, emulsifiers, propellants, dispersants, stabilizers, thickeners, Complexing agents, buffers, penetration enhancers, polymers, fragrances, sweeteners and dyes. Preferably, excipients suitable for the desired dosage form and desired mode of administration are used.
The term “disease” or “disorder” or “condition” refers to any disease, discomfort, illness, symptoms or indications.
Unless otherwise specified, the detection instrument information and detection method parameters used in the present invention are as follows:
The present invention is further exemplified, but not limited, by the following examples that illustrate the invention. In the examples of the present invention, unless expressly stated, the technique or method is a conventional technique or method in the art.
API: Active Pharmaceutical Ingredients;
ATCC: American Type Culture Collection;
DCM: dichloromethane;
13C-NMR: 13C Nuclear Magnetic Resonance;
DMSO: dimethyl sulfoxide;
h: hour;
1H-NMR: 1H Nuclear Magnetic Resonance;
HPLC: High Performance Liquid Chromatography;
LC/MS: Liquid Chromatography-Mass Spectrometry;
m-CPBA: meta-chloroperoxybenzoic acid;
min: minute;
PO: oral administration;
RH: Relative Humidity;
RRT: Relative Retention Time;
TFA: trifluoroacetic acid;
TGA: thermogravimetric analysis;
UPLC: Ultra Performance Liquid Chromatography;
XRD: X-ray powder diffraction.
500 g of compound M1-1, 651 g of TEA and 782 ml of ammonia (25%) were dissolved in 2.4 L of THF, stirred at RT for 12 hrs. The reaction mixture was diluted with water, extracted with EA, washed with water, dried over anhydrous Na2SO4, and concentrated under reduced pressure to obtain 450 g of compound M1-2 with a yield of 98.3%. It was used directly in the next step without purification.
LC-MS[M+H+]214.
Under nitrogen protection at −20° C., 570 ml of LiAlH4 (2.5N, suspended in THF) was added dropwise with stirring to a mixture of 250 g of compound M1-2 dissolved in 2 L THF, the reaction mixture was stirred at −10° C. for 3 hrs, 50 ml of water was added to terminate the reaction, below 15° C., 50 ml of 15% NaOH solution was added under stirring, and then 150 ml of water was added. The mixture was filtered, the filter cake was washed with EA, the filtrate was collected and concentrated under reduced pressure to obtain 180 g of compound M1-3 with a yield of 89.7%, it was used directly in the next step without purification.
LC-MS [M+H+] 172.1.
A mixture of 320 g M1-3, 1465 g MnO2 and 3 L DCM was stirred at RT for 12 hrs, filtered, the filter cake was washed with DCM, the filtrate was collected and concentrated under reduced pressure to obtain 261 g of M1 with a yield of 82.5%, it was used directly in the next reaction without purification.
A mixture of 16.77 g a-1, 11.17 g M1, 27.33 g K2CO3 and 150 ml DMF was stirred at 110° C. for 12 hrs. The reaction mixture was cooled to RT, poured into ice water, filtered, the filter cake was washed with water and dried under reduced pressure to obtain 17.21 g of compound a-2 as a yellow solid, it was used directly in the next step without purification.
LC-MS [M+H+] 363.1.
16.75 g of compound a-1 was dissolved in 50 ml of acetic acid, stirred at RT, 15.97 g of NaNO2 was added in portions, the reaction mixture was stirred at 70° C. for 3 hrs, cooled to RT, poured into ice water, filtered, the filter cake was washed with water, and dried under reduced pressure to obtain 15.21 g of compound a-3 as light yellow solid.
LC-MS [M+H+] 364.0.
A mixture of 2.71 g of compound a-3 and 50 ml of phosphorus oxychloride was stirred at 100° C. for 3 hrs, the reaction solution was concentrated to remove most of the phosphorus oxychloride, and the residue was quenched with ice water. The pH was adjusted to 8 with saturated NaHCO3, the mixture was extracted with EA, washed with saturated sodium chloride, dried over anhydrous Na2SO4, and concentrated under reduced pressure to obtain 3.01 g of compound a-4 as a white solid, which was used directly in the next step without purification.
A mixture of 500 mg of compound a-4, 818 mg of hydrazine hydrate (80%) and 25 ml of ethanol was refluxed for 2 hrs, concentrated under reduced pressure to obtain 520 mg of crude compound a-5 as a yellow solid, which was used directly in the next step without purification.
LC-MS [M+H+] 378.1.
A mixture of 520 mg of compound a-5 and 25 ml of formic acid was refluxed for 1 h, the reaction mixture was diluted with water, filtered, and the filter cake was washed with water to obtain 310 mg of compound A as a pale yellow solid with a yield of 58%.
LC-MS [M+H+] 388.1.
Compound A (100.01 g), DCM (2000 mL) and TFA (130 mL) was sequentially added into a 10 L three-neck flask with stirring, and stirring was continued until the system was clear. The reaction system was cooled to 0° C. to −5° C., m-CPBA was dissolved in ethyl acetate and then added dropwise to the above reaction system, the addition was completed after 30 minutes, and the temperature was maintained at 0° C. to 5° C. for 1.5 hours. The reaction was monitored by thin layer chromatography (DCM:methanol=15:1), and sampled for LC-MS to detected the completion. 103.98 g of anhydrous sodium sulfite was dissolved in 2600 mL of water and added dropwise to the reaction system to quench the reaction. After 10 minutes, the dripping is completed, stand still and separate. 1000 mL of water was added to the organic phase, stirred for 5 min, stand still and separate. The organic phase was concentrated under reduced pressure. The obtained residue was added 1000 mL of ethyl acetate and slurried for 1 h, and filtered. The filter cake was added 1000 mL of anhydrous methanol and slurried for 1 hour and filtered. The filter cake was dried under vacuum at 45° C. for 14 hours to obtain 78.57 g of light yellow solid B with a yield of 75.4%.
Compound B (77.52 g), sec-butanol (1550 mL), compound C (60.21 g) and TFA (39 mL) were sequentially added into a 10 L three-necked flask with stirring, and start heating to warm to reflux for 6 hours, the reaction was monitored by thin layer chromatography (DCM:methanol=15:1), and sampled for LC-MS to detected the completion. After cooling, the reaction system was concentrated under reduced pressure, and the concentrated residue was added to 1162 mL of anhydrous methanol and slurried for 30 min to 1 h, and filtered. The filter cake was added 775 mL of anhydrous methanol and slurried for 10 to 30 minutes, and filtered. The filter cake was sampled for UPLC to test purity. The filter cake was added anhydrous methanol (1077 mL), DCM (5385 mL) and TFA (179 mL), stirred to dissolve and filter. 428.10 g of anhydrous potassium carbonate was dissolved in 4200 mL of water, added dropwise to the filtrate, stirred, and the pH was adjusted to alkaline, stand still and separated. The organic phase was concentrated under reduced pressure, and the obtained solid was added 898 mL of anhydrous methanol and slurried for 1 h, and filtered. The filter cake was dried under vacuum at 45° C. for 12 hours to obtain 105.36 g of the compound of Formula I with a yield of 91.3%.
4.0 g of the compound of Formula I was added 200 mL of acetone and 36 mL of water, stirred at 60° C., the system was not clear, 2.318 g of maleic acid was dissolved in 4.0 mL of water, and added dropwise to the above suspension system, the system was stirred to dissolve and stirring was continued for about 2 minutes, the solid was precipitated, continued stirring at 60° C. for 30 minutes, naturally cooled to RT, stirred for 4 days, filtered under reduced pressure, and dried in vacuo at room temperature for 24 hours to obtain 5.336 g of maleate salt crystalline form 1 of the compound of Formula I.
40.03 g of the compound of Formula I was added into 800 mL of anhydrous methanol, 400 mL of water was added, and the temperature was raised to 50° C. 8.50 g of maleic acid was dissolved in 40 mL of water and added dropwise to the above reaction system. The system was gradually dissolved and filtered while hot. The filtrate was transferred to a 5 L three-necked flask, 1200 mL of anhydrous methanol was added with stirring, and the temperature was raised to 50° C. 14.69 g of maleic acid was dissolved in 60 mL of water and added dropwise to the reaction system. After the dropwise addition, the reaction was naturally cooled and stirred overnight. Filtered and the filter cake was rinsed with anhydrous methanol. The filter cake was dried under vacuum at 60° C. for 20 hours to obtain 53.27 g of light yellow solid, which is maleate salt crystalline form 1 of the compound of Formula I, and the yield was 96.0%.
About 10 mg of maleate saltmaleate saltmaleate salt crystalline form 1 was added into 0.1 mL of dimethyl sulfoxide, and placed in a tetrahydrofuran system at room temperature for diffusion and standing for crystallization, and the maleate salt crystalline form 2 was obtained.
About 10 mg of maleate salt crystalline form 1 was sequentially added 0.1 mL of dimethyl sulfoxide and 5.0 mL of tetrahydrofuran, stirred to clear at 60° C., filtered, and the filtrate was placed in an ice-salt bath and stirred to precipitate a yellow solid, centrifuged at room temperature and dried under vacuum, to obtain the maleate salt crystalline form 2 was obtained.
400 mg of the compound of Formula I was sequentially added 20 mL of acetone and 2 mL of water, stirred at 60° C. in a water bath, the system was not clear, 70.35 mg of methanesulfonic acid was dissolved in 2.0 mL of water, and added dropwise to the above suspension system, and then the system was clear. The system was removed to room temperature and stirred for 30 minutes, there was no precipitation, 20 mL of acetone was added dropwise to the system, and then a large amount of solid was precipitated, continued stirring at room temperature for 3 days, filtered under reduced pressure, and dried under vacuum at room temperature for 24 hours to obtain 342 mg of methanesulfonate salt crystalline form 1.
200 mg of the compound of Formula I was added 10 mL of acetone and 2 mL of water, stirred to clear at 60° C. in a water bath, 96 mg of methanesulfonic acid was dissolved in 0.2 mL of acetone, and added dropwise to the above clear system, there was no precipitation, stirring was continued at 60° C. for 30 minutes, there was no precipitation, naturally cooled to room temperature, stirred for 2 days, filtered under reduced pressure, and dried under vacuum at room temperature for 24 hours to obtain 160 mg of methanesulfonate salt crystalline form 2.
100 mg of the compound of Formula I was added 20 mL of acetone, stirred at 60° C. in a water bath, the system was not clear, 28.94 mg of benzenesulfonic acid was dissolved in 1.0 mL of water and added dropwise to the above suspension system at room temperature, the system was still not clear, continued stirring at room temperature for 5 days, filtered under reduced pressure, and dried under vacuum at room temperature for 24 hours to obtain 54 mg of besylate salt crystalline form 1.
200 mg of the compound of Formula I was added 10 mL of acetone and 2.0 mL of water sequentially, stirred to clear at 60° C. in a water bath, 158 mg of benzenesulfonic acid was dissolved in 0.2 mL of acetone, and added dropwise to the above clear system, there was still precipitation, the stirring was continued at 60° C. for 30 minutes, there was still no precipitation, naturally cooled to room temperature, stirred for 2 days, solid was precipitated, filtered under reduced pressure and dried under vacuum at room temperature for 24 hours to obtain 141 mg of besylate salt crystalline form 2.
200 mg of the compound of Formula I was added 10 mL of acetone to disperse, stirred at 50° C. in a water bath for 10 minutes, then 1.8 mL of water was added, most of it was dissolved, 101.09 mg of concentrated hydrochloric acid was dissolved in 0.2 mL of water and added dropwise to the above suspension system, a large amount of white solids were precipitated, stirring was continued for 30 minutes, and then naturally cooled to room temperature, stirred overnight, and continued stirring for 1 day, filtered under reduced pressure, dried under vacuum at 45° C. for 3 hours to obtain 158 mg of hydrochloride crystalline form 1.
100 mg of the compound of Formula I was added 20 mL of acetone, stirred at 60° C. in a water bath, the system was not clear, 21.10 mg of 85% phosphoric acid was dissolved in 1.0 mL of water and added dropwise to the above suspension system at room temperature, the system was still not clear, continued stirring for 5 days, filtered under reduced pressure, and dried under vacuum at room temperature for 24 hours to obtain 51 mg of phosphate salt crystalline form 1.
150 mg of the compound of Formula I was added 2.5 mL of isopropanol, stirred at 60° C. for 10 minutes, the system was not clear, 112 mg of L-tartaric acid was dissolved in 2.5 mL of water and added dropwise to the above suspension system, the system was stirred to clear, and continued stirring for 10 minutes, 7.5 mL isopropanol was added dropwise, there was no precipitation, stirring was continued for 30 minutes, there was still no precipitation, naturally cooled to room temperature, stirred overnight, a solid was precipitated, filtered under reduced pressure, and dried under vacuum at 45° C. for 3 hours to obtain 120 mg of L-tartrate salt crystalline form 1.
150 mg of the compound of Formula I was added 2.5 mL of isopropanol to disperse and stirred at 60° C. for 10 minutes, the system was not clear, 100 mg of L-malic acid was dissolved in 2.5 mL of water and added dropwise to the above suspension system, the system was stirred to clear, continued stirring for 10 minutes, 7.5 mL of isopropanol was added dropwise, there was no precipitation, continued stirring for 30 minutes, there was still no precipitation, naturally cooled to room temperature, stirred overnight, a solid was precipitated, filtrated under vacuum, filter cake was rinsed three times with isopropanol and methyl tert-butyl ether, dried under vacuum at 45° C. for 3 hours to obtain 120 mg of L-malate salt crystalline form 1.
150 mg of the compound of Formula I was added 2.5 mL of isopropanol to disperse and stirred at 60° C. for 10 minutes, the system was not clear, 144 mg of citric acid was dissolved in 2.5 mL of water and added dropwise to the above suspension system, the system was stirred to clear, continued stirring for 10 minutes, 7.5 mL isopropanol was added dropwise, there was no precipitation, continued stirring for 30 minutes, there was still no precipitation, naturally cooled to room temperature, stirred overnight, a solid was precipitated, filtrated under vacuum, filter cake was rinsed three times with isopropanol and methyl tert-butyl ether, and dried under vacuum at 45° C. for 3 hours to obtain 124 mg of L-malate salt crystalline form 1.
20 mg of the compound of Formula I was added 5.0 mL of tetrahydrofuran, stirred to clear at 60° C., 4.25 mg of fumaric acid was dissolved in 0.2 mL of tetrahydrofuran and added dropwise to the above solution system at room temperature, there was no precipitation, continued stirring at room temperature for 4 days, a solid was precipitated, centrifuged, and dried under vacuum at room temperature for 4 hours to obtain fumarate salt crystalline form 1.
150 mg of the compound of Formula I was added 2.5 mL of isopropanol to disperse and stirred at 60° C. for 10 minutes, the system was undissolved, 87 mg of fumaric acid was dissolved in 5 mL of water and added dropwise to the above suspension system, the system was stirred to clear, continued stirring for 30 minutes, there was no precipitation, naturally cooled to room temperature, stirred overnight, a solid was precipitated, stirring was continued for 1 day at RT, filtrated under vacuum, 5 filter cake was dried under vacuum at 45° C. for 3 hours to obtain 124 mg of fumarate salt crystalline form 2.
Two batches of samples of the compound represented by Formula I in different batch lots (batch numbers: 20180227-2 and 20180123) were obtained according to the preparation method provided in Example 1 of the present invention, and then obtained two batches of maleate salt crystalline form 1 in different batch lots according to the preparation method of Example 2, and characterized them separately, the XRD spectra are shown in
According to the XRD spectrum analysis data and the comparison chart in
The hygroscopicity of the sample (the sample is a variety of crystal forms shown in Table 26) was tested using dynamic vapor sorption (DVS) instrument, and the water uptake of the sample at 0% RH (relative humidity) to 80% RH was tested. The test results were shown in
It can be seen from the test results that the maleate crystalline form 1 has outstanding advantages in terms of hygroscopicity. Compared with the compound of structural formula I, the hygroscopicity of maleate crystalline form 1 is greatly reduced. Methanesulfonate crystalline form 1 also has obvious advantages, and other crystalline forms have relatively high hygroscopicity.
Samples and preparation of experimental: An appropriate amount of maleate salt crystalline form 1, methanesulfonate salt crystalline form 1 and the compound of Formula I were put in watch glasses, and then spread into a thin layer about 3-5 mm in thickness.
Experimental conditions: Under conventional (25° C., avoid light), high temperature (60° C., avoid light), high temperature and high humidity (40° C./75% RH, open and avoid light), light (25° C., 4500 lux±500 lux, open) and oxidation (40° C., container closure containing urea hydrogen peroxide, open and avoid light) conditions for 14 days.
Test items: Sampled on 0th day and 14th day, the XRD, TGA and HPLC were tested and compared, the test results on the 14th day were show in Table 27.
<1%
<1%
According to the Result Data:
(1) XRD detection showed that maleate salt crystalline form 1 had no significant change after 14 days under conventional, high temperature, high temperature and high humidity, light and oxidation conditions. The crystallinity of mesylate salt crystalline form 1 was decreased after 14 days under oxidizing conditions. The stability of crystalline form of the compound of Formula I was relatively low, and the specific XRD spectra were shown in
(2) TGA test showed that maleate salt crystalline form 1 had no significant change in weight loss after 14 days under conventional, high temperature, high temperature and high humidity, light and oxidation conditions, all the weight loss before 120° C. were less than 1%. The weight loss of mesylate salt crystalline form 1 was slightly increased after 14 days under oxidizing conditions. The specific TGA charts were shown in
(3) HPLC test results showed that the purity decrease of the main ingredient content of maleate salt crystalline form 1 was less than 0.1% after 14 days under conventional, high temperature, high temperature and high humidity conditions; the purity decrease of the main ingredient content was approximately 0.7% after 14 days under light condition; the purity decrease of the main ingredient content was about 5.3% after 14 days under oxidation condition; while the purity of the main ingredient content of the compound of Formula I and mesylate salt crystalline form 1 were significantly decreased under light condition.
After maleate salt crystalline form 2 was placed at room temperature for 1 day or heated to 120° C., the stability of crystalline form was tested by XRD, the specific test results were shown in
According to the test results, the crystallinity of maleate salt crystalline form 2 was significantly worse after 1 day at room temperature; after the temperature was raised to 120° C., the crystalline state of the maleate salt crystalline form 2 has changed, and part of it has transformed into maleate salt crystalline form 1.
Method: The inhibitory activity of the compound of Formula I against FGFR1, FGFR2, FGFR3, FGFR4 and KDR was tested by mobility shift assay (concentration of ATP is Km value).
Test Method:
Reagent: basic kinase buffer: 50 mM HEPES (pH 7.5); 0.0015% Brij-35
Stop buffer: 100 mM HEPES (pH 7.5); 0.0015% Brij-35; 0.2% Coating Reagent #3; 50 mM EDTA
Prepare compounds: dilute test compounds to specific concentration using 100% DMSO
Reaction process: 1) prepare 2.5× enzyme solution
Method 1: the growth inhibitory effect of the compound of Formula I on human tumor cell NCI-H1581 cultured in vitro was observed using CellTiter 96® AQueous One Solution cell proliferation assay kit method.
Test method: 18 μl of the cell suspension was added to a 96-well plate and placed in a CO2 incubator overnight. Tested compounds were dissolved in DMSO and subjected to a 3-fold gradient dilution for a total of 10 concentrations. 201 of the medium containing the test compound and DMSO was transferred to the corresponding cell wells respectively. Incubated in 5% CO2 at 37° C. for 144 hrs. 40 μl of CellTiter 96® AQueous One Solution cell proliferation assay reagent was added to detection board and was incubated in 5% CO2 at 37° C. for 2 hrs. The IC50 value was calculated by recording the light absorption value (OD490) at 490 nm using VICTOR TM X5 instrument.
Method 2: the growth inhibitory effect of the compound of Formula I on human tumor cell NCI-H1581 and SNU-16 cultured in vitro was observed using CellTiter Glo assay method.
Test method: the cells were added appropriate volume of whole medium to suspend. 100 μl of the cell suspension was added to a 96-well plate and placed in a CO2 incubator overnight. Tested compounds were dissolved in DMSO and subjected to a 3-fold gradient dilution for a total of 10 concentrations. Tested compound and DMSO reference materials were transferred to the corresponding wells containing 100 μl of medium respectively. Incubated in 5% CO2 at 37° C. for 96 hrs. 100 μl of CellTiter-Glo reagent was added to the assay plate and incubated for 10 min at room temperature to stabilize the luminescence signal. The IC50 value was calculated by recording the RLU (relative luminescence unit) using VICTOR TM X5 instrument.
The test results showed that the IC50 values of the compound of Formula I on NCI-H1581 cells and SNU-16 cells were 2.0 nM and <1 nM respectively.
Reagent: DMSO, polyethylene glycol-15-hydroxystearate (Solutol), saline.
Animals: BALB/C-nude strains nude mice: SPF animals, weighing 18-22 g, female, provided by Vitrallihua Experimental Animal Technology Co., Ltd. Fed with SPF feed, freely drink distilled water.
Human cancer cell line: NCI-H1581 human non-small cell lung cancer cell line, provided by Shanghai Ruizhi Chemical Research Co., Ltd.
Method of tumor transplantation assay: The NCI-H1581 cell line was inoculated subcutaneously into the right axilla of BALB/C nude mice with an amount of 1×107/100 μL/cell in an ultra-clean bench under sterile operation. After 10 days, the tumors were grown and touched (about 100-200 mm3). The animals were randomly divided into groups of 6 animals and each was weighted and labeled. The experimental group was intragastrically administered the compound of Formula I once a day. Nude mice were kept in a room with a temperature of 20-22° C., relative humidity of 40-60%, and the shielding system was supplemented by the environment of a clean laminar flow cabinet. The subcutaneous tumor volume was measured with a caliper every 3-4 days since the experiment started, and the tumor growth curve was drawn to calculate the tumor inhibition rate. The test results were statistically analyzed using GraphPad Prism 5 software, and the experimental data are shown in
Reagent: MSO, polyethylene glycol-15-hydroxystearate (Solutol), saline.
Animals: BALB/C-nude strains nude mice: SPF animals, weighing 18˜22 g, female, provided by Vitrallihua Experimental Animal Technology Co., Ltd. Fed with SPF feed, freely drink distilled water.
Human cancer cell line: SNU-16 human non-small cell lung cancer cell line, provided by ATCC, batch number was CRL-5974™.
Method of tumor transplantation assay: The SNU-16 cell line was inoculated into the right back of BALB/C nude mice with an amount of 0.2 mL (3×106 pcs+Matrigel)/one mouse in an ultra-clean bench under sterile operation, and when the average tumor volume reached 151 mm3, the drug was administered in groups. The animals were randomly divided into groups of 6 animals, each was weighted and labeled. The positive group was intragastrically administered JNJ42756493 once a day. The experimental group was intragastrically administered the compound of Formula I once a day. Nude mice were kept in a room temperature of 20-22° C., relative humidity of 40-60%, and the shielding system was supplemented by the environment of a clean laminar flow cabinet. The subcutaneous tumor volume was measured with a caliper twice a week after the experiment, and the tumor growth curve was drawn to calculate the tumor inhibition rate. The test results were statistically analyzed using GraphPad Prism 5 software, and the experimental data are shown in
Drugs and reagents: 6-(2-chloro-3,5-dimethoxyphenyl)-N-(4-(4-morpholinopiperidin-1-yl)phenyl)-[1,2,4]triazolo[4′, 3′:1,6]pyrido[2,3-d]pyrimidin-2-amine (compound of Formula I), and maleate salt crystalline form 1 of the compound of Formula I used in this study were grounded to fine particles. The material content (purity) was not less than 99.0%.
Experimental animals: SD rats were randomly divided into the compound of Formula I group and maleate salt crystalline form 1 group, each group including three male rats.
Pharmaceutical preparation: each compound was prepared into a clear solution in 10% DMSO/10% Solutol/80% Water solution, the final concentration of each compound was 1 mg/mL.
Administration and sample collection: each suspension was orally administered to fasted SD rats with a dose volume of 10 mL/kg and an administration dose of 10 mg/kg. The blood samples were collected in EDTA-K pre-anticoagulantion tubes before administration (0 h) and at 0.25 h, 0.5 h, 1 h, 2 h, 4 h, 7 h and 24 h after administration. The plasma was separated from the samples by centrifugation at 4000 rpm for 10 minutes at 4° C. The plasma was collected and stored at −80° C. for analysis.
The samples were analyzed by AB4000 API LC/MS combined with HPLC. Under liquid chromatography conditions, a phenomenex C18 2.6 u (50×2.1 mm) column was used as the stationary phase, acetonitrile-water and 0.1% formic acid were used as the mobile phase, and the injection volume was 10 μL. The PK data of the compound of Formula I and its maleate salt crystalline Form 1 were shown in Table 29 and
Drugs and reagents: 6-(2-chloro-3,5-dimethoxyphenyl)-N-(4-(4-morpholinopiperidin-1-yl)phenyl)-[1,2,4]triazolo[4′,3′:1,6]pyrido[2,3-d]pyrimidin-2-amine (compound of Formula I) and salt forms thereof which include malate salt crystalline form, tartrate salt crystalline form, phosphate salt crystalline form, methanesulfonate salt crystalline form, hydrochloride salt crystalline form, fumarate salt crystalline form, citrate salt crystalline form, besylate salt crystalline form used in this study were ground to fine particles. The material content (purity) was not less than 99.0%.
Experimental animals: SD rats were randomly divided into the compound of Formula I group and each salt crystalline form of the compound of Formula I group, each group including three male rats.
Pharmaceutical preparation: each compound was prepared in purified water, wherein, the mesylate salt crystalline form, hydrochloride salt crystalline form and besylate salt crystalline form were prepared into a clear solution, the malate salt crystalline form, tartrate salt crystalline form, phosphate salt crystalline form, fumarate salt crystalline form, citrate salt crystalline form and sulfate salt crystalline form were prepared into a suspension, and final concentration of each compound was 0.5 mg/mL.
Administration and sample collection: each suspension was orally administered to fasted SD rats with a dose volume of 10 mL/kg and an administration dose of 10 mg/kg. The blood samples were collected in EDTA-K pre-anticoagulantion tubes before administration (0 h) and at 0.25 h, 0.5 h, 1 h, 2 h, 4 h, 7 h and 24 h after administration. The plasma was separated from the samples by centrifugation at 4000 rpm for 10 minutes at 4° C. The plasma was collected and stored at −80° C. for analysis.
The samples were analyzed by AB4000 API LC/MS combined with HPLC. Under liquid chromatography conditions, a phenomenex C18 2.6 u (50×2.1 mm) column was used as the stationary phase, acetonitrile-water and 0.1% formic acid were used as the mobile phase, and the injection volume was 10 μL. The PK data of the compound of Formula I and its salt crystalline Form were shown in Table 30. The absorption value of the tartrate salt crystalline form of the compound of Formula I was higher than that of other compound.
1the compound of Formula I
2L- malate salt crystalline form 1 of the compound of Formula I
3L-tartrate salt crystalline form 1 of the compound of Formula I
4phosphate salt crystalline form 1 of the compound of Formula I
5methanesulfonate salt crystalline form 1 of the compound of Formula I
6hydrochloride salt crystalline form 1 of the compound of Formula I
7fumarate salt crystalline form 1 of the compound of Formula I
8citrate salt crystalline form 1 of the compound of Formula I
9besylate salt crystalline form 1 of the compound of Formula I
The formulation was shown in the following table:
1The unit content of the active ingredient has been adjusted according to the salinity coefficient
2 The API described here specifically refers to maleate salt crystalline form 1 of the compound of Formula I.
The preparation process of the capsule was described as follows:
Sieved API manually or using a crushing equipment equipped with a suitable sieve mesh size before added.
Weighed the sieved API, mannitol and crospovidone, and then transferred them to a square cone mixer for blending.
Magnesium stearate was weighed and added into the square cone mixer to continue blending.
The 5 mg size was filled with No. 2 gelatin capsule shell, the 2 mg size was filled with No. 3 gelatin capsule shell, and the 0.5 mg size was filled with No. 4 gelatin capsule shell.
This product was packaged in oral solid drug pharmaceutically acceptable high-density polyethylene bottle and oral solid drug pharmaceutically acceptable polypropylene/low-density polyethylene moisture-proof combination cover, the packaged product was stored at room temperature.
The formulation was shown in the following table:
1The unit content of the active ingredient has been adjusted according to the salinity coefficient
2The API described here specifically refers to maleate salt crystalline form 1 of the compound of Formula I.
The preparation process of the capsule was as follows:
1) API sieving
Sieved API manually or using a crushing equipment equipped with a suitable sieve mesh size before added.
2) Blending
Weighed the sieved API, microcrystalline cellulose, spray dried lactose and crospovidone, and then transferred them to a square cone mixer for blending.
3) Final blending
Magnesium stearate was weighed and added into the square cone mixer to continue blending.
4) Capsule filling
The 5 mg size was filled with No. 2 gelatin capsule shell, the 2 mg size was filled with No. 3 gelatin capsule shell, and the 0.5 mg size was filled with No. 4 gelatin capsule shell.
5) Package
This product was packaged in oral solid drug pharmaceutically acceptable high-density polyethylene bottle and oral solid drug pharmaceutically acceptable polypropylene/low-density polyethylene moisture-proof combination cover, the packaged product was stored at room temperature.
The exemplary embodiments of the present invention have been described above. However, the technical solution of the present invention should not be limited to this. Those skilled in the art should understand that any modification, equivalent replacement, improvement, etc. made within the spirit and principle scope of the present invention should fall within the scope of protection of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| PCT/CN2018/102549 | Aug 2018 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2019/102720 | 8/27/2019 | WO | 00 |
