Crystal form B of ABT-888, preparation method and applications thereof
A technology of ABT-888 and crystal form, applied in organic chemical methods, medical preparations containing active ingredients, pharmaceutical formulas, etc., can solve the problems of high operation requirements, complicated preparation process, poor solubility, etc., and achieve low cost , simple operation, and the effect of improving solubility
Active Publication Date: 2015-12-09
CRYSTAL PHARMATECH CO LTD
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Problems solved by technology
Among the two crystal forms, the solubility of crystal form 1 is relatively good, but crystal form 1 needs to react with the acid or diacid salt of ABT-888 with a base, and the crystal form 1 mixed with one or more than one solvent can be made by deprotonation reaction. ABT-888 is obtained by crystallization or recrystallization in the form of solid, semi-solid, wax or oil. The preparation process is relatively complicated and the requirements for operation are also high.
Although the preparation of crystal form 2 is relatively simple, it can be obtained by completely dissolving ABT-888 in methanol, then concentrating at 35°C, and drying to constant weight, but its solubility is poor
Method used
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Embodiment 1
[0029] Dissolve 21.8 mg of the free base of the compound of formula I in 1.5 mL of methanol and volatilize at room temperature (25±1° C.) to obtain solid crystals, labeled as sample 1.
Embodiment 2
[0031] 20.7 mg of the free base of the compound of formula I was dissolved in 1.0 mL of methanol, and volatilized at room temperature (25±1° C.) to obtain solid crystals, labeled as sample 2.
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Abstract
The present invention relates to a crystal form B of ABT-888, a preparation method and applications thereof, wherein the characteristic peaks exist in the X-ray powder diffraction spectrum (CuK[alpha] radiation) of the crystal form B when the 2[theta] value is 9.4+ / -0.2 DEG, 17.3+ / -0.2 DEG, and 22.8+ / -0.2 DEG. The preparation method comprises: dissolving ABT-888 free alkali in methanol, and naturally volatilizing at a room temperature to obtain the crystal form B. Compared with the existing crystal form, the crystal form B has characteristics of high solubility, simple preparation process and good stability, and provides important significance for improvement of treatment effects of metastatic breast cancer, colon cancer, metastatic melanoma and brain tumor and reduction of drug loading.
Description
technical field [0001] The present invention relates to crystal form B of 2-[(2R)-2-methyl-2-pyrrolidinyl]-1H-benzimidazole-7-carboxamide and a preparation method thereof. Background technique [0002] 2-[(2R)-2-methyl-2-pyrrolidinyl]-1H-benzimidazole-7-carboxamide (compound shown in formula I), also known as ABT-888 (veliparib), is manufactured by Abbott ( A new type of highly selective PARP inhibitor developed by Abbvie). In vivo and in vitro experiments have shown that ABT-888 has a significant inhibitory effect on PARP activity, and has achieved remarkable effects in the treatment of metastatic breast cancer, colon cancer, metastatic melanoma and brain tumors. At present, the combined application of ABT-888 and whole brain radiotherapy for the treatment of metastatic brain tumors has entered the phase I clinical stage, and the treatment of metastatic breast cancer, colon cancer and metastatic melanoma has also entered the phase II clinical stage, and it is used in combi...
Claims
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Patent Type & Authority Applications(China)
IPC IPC(8): C07D403/04A61K31/4184A61P35/00
CPCC07B2200/13C07D403/04A61K31/4184
Inventor 陈敏华张炎锋刘凯张晓宇
Owner CRYSTAL PHARMATECH CO LTD
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