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Crystal form of deuterated osimertinib pharmaceutical salt and preparation method thereof

A medicinal salt and deuterated technology, applied in the field of medicine, can solve the problems of undisclosed compound crystal form, hygroscopicity, solubility physicochemical data, other crystal forms and stability data of unreported compounds, etc., to improve bioavailability and The effect of drug safety, improvement of drug production quality, and high solubility

Inactive Publication Date: 2020-06-16
GUANGZHOU BOJI MEDICINE SERVICES
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Chinese patent CN104140418A discloses 2-(2,4,5-substituted aniline) pyrimidine derivatives and their uses, through the selective deuteration of Osimertinib, the compound (structure shown in formula I ~ formula V) or its pharmaceutically acceptable The salt or solvate of the compound improves the pharmacokinetic properties of the drug and reduces the toxicity of the drug; however, the specific physical and chemical data such as the crystal form, hygroscopicity, and solubility of the compound are not disclosed, and other crystal forms and stability data of the compound are not reported.

Method used

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  • Crystal form of deuterated osimertinib pharmaceutical salt and preparation method thereof
  • Crystal form of deuterated osimertinib pharmaceutical salt and preparation method thereof
  • Crystal form of deuterated osimertinib pharmaceutical salt and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] Embodiment 1: Preparation of crystalline form I of deuterated Osimertinib pharmaceutical salt

[0039] This embodiment is used to prepare the crystal form I of the deuterated Osimertinib medicinal salt shown in formula VI, comprising the following steps: dissolving 2.00 g of deuterated Osimertinib in a 20ml mixed solvent (volume ratio of ethanol, acetone and isobutyl acetate 1:2:1.5), heated to 45°C, added methanesulfonic acid aqueous solution (0.46g methanesulfonic acid dissolved in 3ml water) to the solution at a flow rate of 0.2ml / min, stirred for 2h after addition, cooled to 5°C, The cooling rate is 10°C per hour. Subsequently, stand for crystallization for 3 h, and then filter, and vacuum-dry the filter cake at room temperature for 10 h to obtain 2.20 g of a yellow solid with a yield of 92%. Its X-ray powder diffraction pattern is as figure 1 shown.

[0040] Thermogravimetric analyzer (model: NETZSCH TG 209) thermal weight loss of crystalline form I of deuterated ...

Embodiment 2

[0041] Embodiment 2: Preparation of crystalline form I of deuterated Osimertinib pharmaceutical salt

[0042] This embodiment is used to prepare the crystal form I of the deuterated Osimertinib medicinal salt shown in formula VI, comprising the following steps: dissolving 4.00 g of deuterated Osimertinib in a 20ml mixed solvent (volume ratio of ethanol, acetone and isobutyl acetate 1:1:2), heated to 30°C, added methanesulfonic acid aqueous solution (1.14g methanesulfonic acid dissolved in 9ml water) to the solution at a flow rate of 0.1ml / min, stirred for 2h after addition, cooled to 0°C, The cooling rate is 10°C per hour. Subsequently, the crystallization was allowed to stand for 4 hours, and then filtered, and the filter cake was vacuum-dried at room temperature for 14 hours to obtain 4.28 g of a yellow solid with a yield of 90%. The X-ray powder diffraction spectrum obtained by measuring the crystalline form I of the deuterated Osimertinib pharmaceutical salt obtained by u...

Embodiment 3

[0043] Embodiment 3: Preparation of crystalline form I of deuterated Osimertinib pharmaceutical salt

[0044] This embodiment is used to prepare the crystal form I of the deuterated Osimertinib medicinal salt shown in formula VI, comprising the following steps: dissolving 4.00 g of deuterated Osimertinib in a 32ml mixed solvent (volume ratio of ethanol, acetone and isobutyl acetate 1:1.2:1), heated to 50°C, added methanesulfonic acid aqueous solution (0.76g methanesulfonic acid dissolved in 6ml water) into the solution at a flow rate of 0.1ml / min, stirred for 2h after addition, cooled to 10°C, The cooling rate is 10°C per hour. Subsequently, the crystallization was allowed to stand for 2 h, and then filtered, and the filter cake was vacuum-dried at room temperature for 10 h to obtain 4.23 g of a yellow solid with a yield of 89%. The X-ray powder diffraction spectrum obtained by measuring the crystalline form I of the deuterated Osimertinib pharmaceutical salt obtained by usin...

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Abstract

The invention relates to a compound crystal form and a preparation method thereof, in particular to a crystal form I of a deuterated osimertinib pharmaceutical salt as well as a preparation method andapplication thereof. An X-ray powder diffraction pattern of the crystal form represented by a 2theta angle has characteristic diffraction peaks at positions of 5.49 + / -0.2 degrees, 6.42 + / -0.2 degrees, 11.01 + / -0.2 degrees, 11.61 + / -0.2 degrees, 12.46 + / -0.2 degrees, 13.42 + / -0.2 degrees, 14.22 + / -0.2 degrees and 15.58 + / -0.2 degrees. The crystal form is not easy to absorb moisture, has higher solubility, better stability, better fluidity and preparation processability, and has important significance in preparation of EGFR tyrosine kinase inhibitor drugs. The invention also discloses the preparation method of the crystal form I of the deuterated osimertinib pharmaceutical salt, and the crystal form I obtained by the preparation method has higher purity and higher yield.

Description

technical field [0001] The invention belongs to the technical field of medicine, and in particular relates to a crystal form of a medicinal salt of deuterated osimertinib and a preparation method thereof. Background technique [0002] In my country, more than 730,000 new lung cancer patients are diagnosed every year, which is the malignant tumor with the highest morbidity and mortality. About 30% to 40% of non-small cell lung cancer patients in China have EGFR mutations, and patients with EGFR mutations who have received EGFR-TKI drugs (such as gefitinib, erlotinib, and icotinib) Among them, about two-thirds of patients will develop drug resistance due to the T790M mutation, leading to re-progression of the disease, and patients urgently need new treatment options. [0003] Osimertinib (generic name Osimertinib, hereinafter referred to as this) is the third-generation oral, irreversible and selective EGFR mutation inhibitor developed by AstraZeneca. Approved tumor drug for...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D403/04C07C303/32C07C309/04
CPCC07D403/04C07C303/32C07C309/04C07B2200/13C07B2200/05
Inventor 马仁强田玉婷陆静云
Owner GUANGZHOU BOJI MEDICINE SERVICES
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