Complex of glucose derivative and proline, crystal, preparation method and use

Abstract

Disclosed are a complex of glucose derivative and proline, a crystal, a preparation method and a use. In an X-ray powder diffraction diagram of the eutectic crystal when the diffraction angle is 2θ, characteristic diffraction peaks comprise 4.339, 11.499, 12.835, 13.921, 15.294, 16.212, 16.804, 17.154, 18.335, 19.274, 19.982, 22.710, 23.218, 24.885, 27.940, 29.612 and 30.313, and the 2θ error range is ±0.1. The method comprises: mixing a compound A solution with an L-proline solution, and performing cooling and crystallization. The present invention further provides a of the crystal in medicine preparation. The eutectic crystal in the present invention features high water-solubility, low hygroscopicity and high stability, and is suitable for manufacturing a variety of preparations. ##STR00001##

Claims

1. A eutectic crystal of a complex represented by formula I formed by a glucose derivative and L-proline, wherein the complex is composed of compound A represented by formula A and L-proline, and wherein the molar ratio of compound A to L-proline in the complex is 1:2; ##STR00009## and wherein an X-ray powder diffraction diagram of the eutectic crystal, when the diffraction angle is 2θ and under Cu-Kα1 radiation, shows characterized peaks at: 4.339±0.1, 15.294±0.1, 16.804±0.1, 18.335±0.1, 19.274±0.1, 19.982±0.1, 23.218±0.1 and 24.885±0.1; or 4.339±0.1, 11.499±0.1, 12.835±0.1, 13.921±0.1, 15.294±0.1, 16.212±0.1, 16.804±0.1, 17.154±0.1, 18.335±0.1, 19.274±0.1, 19.982±0.1, 22.710±0.1, 23.218±0.1, 24.885±0.1, 27.940±0.1, 29.612±0.1 and 30.313±0.1.

2. The eutectic crystal of claim 1, wherein an X-ray powder diffraction diagram of the eutectic crystal shows characterized peaks at 4.339±0.1, 15.294±0.1, 16.804±0.1, 18.335±0.1, 19.274±0.1, 19.982±0.1, 23.218±0.1 and 24.885±0.1 when the diffraction angle is 2θ and under Cu-Kα1 radiation.

3. The eutectic crystal of claim 1, wherein an X-ray powder diffraction diagram of the eutectic crystal shows characterized peaks at 4.339±0.1, 11.499±0.1, 12.835±0.1, 13.921±0.1, 15.294±0.1, 16.212±0.1, 16.804±0.1, 17.154±0.1, 18.335±0.1, 19.274±0.1, 19.982±0.1, 22.710±0.1, 23.218±0.1, 24.885±0.1, 27.940±0.1, 29.612±0.1 and 30.313±0.1 when the diffraction angle is 2θ and under Cu-Kα1 radiation.

4. A preparation method for preparing the eutectic crystal of claim 1, comprising the following steps: mixing a solution containing compound A and a solvent with a solution containing L-proline and a solvent at a temperature of from 30° C.-80° C., cooling the resulting mixture and crystallizing the resulting cooled mixture; wherein the solvent in the solution containing compound A is selected from the group consisting of acetone, ethyl acetate and acetonitrile; and wherein the solvent in the solution containing L-proline is 95% aqueous ethanol.

5. The preparation method of claim 4, further comprising, before mixing with the solution containing L-proline, filtering the solution containing compound A with a microporous membrane, and then mixing the resulting filtrate containing compound A with the solution containing L-proline; wherein the microporous membrane is a nylon membrane with a pore size of 0.45 μm.

6. The preparation method of claim 4, wherein the mixing of the solution containing compound A with the solution containing L-proline is at a temperature of 55° C.-65° C.

7. The preparation method of claim 4, wherein the concentration of compound A in the solution containing compound A is 25 mg/mL-400 mg/mL; and the amount of the 95% aqueous ethanol in the solution containing L-proline is 90 mg/mL-120 mg/mL relative to the mass of L-proline in the solution containing L-proline.

8. The preparation method of claim 4, wherein the molar ratio of L-proline in the solution containing L-proline to compound A in the solution containing compound A is in the range of from 1:1 to 2:1; the mixing of the solution containing compound A with the solution containing L-proline is by vortex mixing, magnetic mixing or turbulence mixing; the mixing of the solution containing compound A with the solution containing L-proline lasts for 1-30 mins; and the cooling results in cooling to a temperature between 10° C. and less than 30° C.

9. The preparation method of claim 4, wherein the cooling is conducted at a rate of 1-20° C./h.

10. The preparation method of claim 9, wherein the cooling is conducted at a rate of 5-10° C./h.

11. The preparation method of claim 4, wherein the cooling and crystallizing are carried out under stirring.

Description

DESCRIPTION OF FIGURES

(1) FIG. 1 is the X-ray powder diffraction diagram of the eutectic crystal of the complex formed by compound A and L-proline in effect example 1.

(2) FIG. 2 is the X-ray powder diffraction diagram of compound A in effect example 1.

(3) FIG. 3 is the polarizing light microscope photos of the eutectic crystal of the complex formed by compound A and L-proline in effect example 2.

(4) FIG. 4 is the polarizing light microscope photos of compound A in effect example 2.

(5) FIG. 5 is the dynamic vapor sorption isotherm of the eutectic crystal of the complex formed by compound A and L-proline in effect example 3.

(6) FIG. 6 is the dynamic vapor sorption isotherm of compound A in effect example 3.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

(7) The following embodiments further illustrate the present invention, but the present invention is not limited thereto.

(8) When an experimental condition is not specified in the following examples, conventional methods and conditions can be used, or can be selected from the product manual.

(9) Compound A in the following example could be prepared with a prior method, such as the method disclosed in WO2012/109996.

Example 1 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(10) Compound A (25.0 mg) was dissolved in acetone (1 mL) and heated to 30° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 30° C. An equimolar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (53.4 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 5 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 10° C./h under stirring, meanwhile a large amount of white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane once. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product.

Example 2 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(11) Compound A (25.0 mg) was dissolved in acetone (1 mL) and heated to 35° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 35° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (106.8 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 10 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 15° C./h under stirring, meanwhile a large amount of white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane twice. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product.

Example 3 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(12) Compound A (25.0 mg) was dissolved in acetonitrile (1 mL) and heated to 30° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 30° C. An equimolar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (53.4 μL) was added slowly under magnetic stirring. The solution turned turbid after 10 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 10° C./h under stirring, meanwhile a large amount of white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane once. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product.

Example 4 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(13) Compound A (25.0 mg) was dissolved in acetonitrile (1 mL) and heated to 45° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 45° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (106.8 μL) was added slowly under magnetic stirring. The solution turned turbid after 15 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 15° C./h under stirring, meanwhile a large amount of white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane twice. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product.

Example 5 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(14) Compound A (25.0 mg) was dissolved in ethyl acetate (1 mL) and heated to 40° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 35° C. An equimolar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (53.4 μL) was added slowly under magnetic stirring. The solution turned turbid after 10 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 10° C./h under stirring, meanwhile a large amount of white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane once. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product.

Example 6 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(15) Compound A (25.0 mg) was dissolved in ethyl acetate (1 mL) and heated to 45° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 45° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (106.8 μL) was added slowly under magnetic stirring. The solution turned turbid after 15 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 15° C./h under stirring, meanwhile a large amount of white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane twice. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product.

Example 7 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(16) Compound A (100.4 mg) was dissolved in acetone (0.5 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (429 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 20 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 5° C./h under stirring, meanwhile white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (46.9 mg, yield 31.3%).

Example 8 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(17) Compound A (250.4 mg) was dissolved in acetone (1 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (1088 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 15 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 5° C./h under stirring, meanwhile white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (331.8 mg, yield 88.8%).

Example 9 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(18) Compound A (250.9 mg) was dissolved in acetone (1 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (1090 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 25 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 5° C./h under stirring, meanwhile white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (271.0 mg, yield 72.5%).

Example 10 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(19) Compound A (250.9 mg) was dissolved in acetone (1 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (1090 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 25 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 5° C./h under stirring, meanwhile white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (271.0 mg, yield 72.5%).

Example 11 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(20) Compound A (100.7 mg) was dissolved in acetone (0.5 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (433 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 25 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 5° C./h under stirring, meanwhile white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (93.6 mg, yield 64.4%).

Example 12 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(21) Compound A (100.8 mg) was dissolved in acetone (0.5 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (433 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 25 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 5° C./h under stirring, meanwhile white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (107.8 mg, yield 71.4%).

Example 13 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(22) Compound A (200.4 mg) was dissolved in acetone (1.2 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (856 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 25 minutes magnetic stirring, and then the mixture was cooled quickly with an ice-bath for 10 mins and white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product.

Example 14 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(23) Compound A (272.3 mg) was dissolved in acetone (3.6 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (1164 μL) was added slowly under magnetic stirring. The solution turned turbid and white solid began to precipitate after 10 minutes magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 5° C./h under stirring, meanwhile white precipitate appeared. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (327.8 mg, yield 80.6%).

Example 15 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(24) Compound A (400.6 mg) was dissolved in acetone (4.8 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (1712 μL) was added slowly under magnetic stirring. The solution turned turbid after 10 minutes magnetic stirring and a lot of white solid precipitated after another 0.5 min, and then the mixture was cooled down to room temperature at a rate of 20° C./h under magnetic stirring. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (461 mg, yield 77.1%).

Example 16 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(25) Compound A (589 mg) was dissolved in acetone (7.068 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (2977 μL) was added slowly under magnetic stirring. The solution turned turbid after 1 minute magnetic stirring and a lot of white solid began to precipitate, and then the mixture was cooled down to room temperature at a rate of 20° C./h under magnetic stirring. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product.

Example 17 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(26) Compound A (407.52 mg) was dissolved in acetone (4.8 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (1742 μL) was added slowly under magnetic stirring. The solution turned turbid after 1 minute magnetic stirring and a lot of white solid began to precipitate after another 1 minute, and then the mixture was cooled down to room temperature at a rate of 10° C./h under magnetic stirring. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (476.75 mg, yield 78.4%).

Example 18 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(27) Compound A (410.5 mg) was dissolved in acetone (4.8 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (1754 μL) was added slowly under magnetic stirring. The solution turned turbid after 1 minute magnetic stirring and a lot of white solid began to precipitate after another 1 min, and then the mixture was cooled down to room temperature at a rate of 10° C./h under magnetic stirring. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (445.98 mg, yield 72.8%).

Example 19 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(28) Compound A (404.52 mg) was dissolved in acetone (4.8 mL) and heated to 55° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 55° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (1729 μL) was added slowly under magnetic stirring. The solution turned turbid after 1 minute magnetic stirring and a lot of white solid began to precipitate, and then the mixture was cooled down to room temperature at a rate of 20° C./h under magnetic stirring. The precipitated white solid was isolated from the suspension via vacuum filtration, and rinsed with n-heptane three times. The product was then placed in a vacuum oven and dried under reduced pressure at 40° C. to obtain the final product (437.95 mg, yield 72.6%).

Comparative Example 1 Preparation of the Eutectic Crystal of the Complex Formed by Compound A and L-Proline

(29) Compound A (102.0 mg) was dissolved in isopropyl alcohol (0.5 mL) and heated to 80° C. with magnetic stirring until compound A fully dissolved. The solution was filtered with a 0.45 μm microporous membrane (nylon membrane) and the filtrate was placed on a heater at 80° C. A 2-fold molar ratio of 1 mol/L a solution containing L-proline in 95% aqueous ethanol (436 μL) was added slowly under magnetic stirring. The solution was clear after 1 h magnetic stirring, and then the mixture was cooled down to room temperature at a rate of 10° C./h under magnetic stirring. The solution turned turbid and little amount of white solid began to precipitate after stirring for 12 hours at room temperature. However, the mixture became clear when stirring stopped and small amount of oil was observed floating on the surface of the solution. There was no solid observed after the mixture was stored at 4° C. for 12 hours.

(30) From the above comparative example 1, the eutectic crystal of the complex formed by compound A and L-proline could not be obtained if isopropyl alcohol was used as a solvent for dissolving compound A, even other conditions strictly followed the previously described preparation method in the present invention. It proved that the solvent for dissolving compound A was a key factor for the preparation method. The solvent should be not only a good solvent for dissolving compound A, but also a solvent miscible with 95% aqueous ethanol.

Effect Example 1 Identification of X-Ray Powder Diffraction

(31) 1. Samples: Eutectic crystal of the complex formed by compound A and L-proline prepared in example 1-19 and compound A.

(32) 2. Parameters of X-ray powder diffraction: A Cu-Kα.sub.1 source (=1.54056 angstrom); Operating Voltage: 40 kV; Operating Current: 40 mA; Detector: PSD Detector; Scans Angle: 4-40 degrees (2-theta); Step value: 0.05°; Scanning Speed: 0.5 sec/step.

(33) 3. Experimental result

(34) The X-ray powder diffraction diagram of the eutectic crystal of the complex formed by compound A and L-proline prepared in example 1-19 is shown in FIG. 1. It can be seen from FIG. 1 that the diffraction peaks of the eutectic crystal of the complex formed by compound A and L-proline were selected from the following peaks: diffraction angle 2θ=4.339, 11.499, 12.835, 13.921, 15.294, 16.212, 16.804, 17.154, 18.335, 19.274, 19.982, 22.710, 23.218, 24.885, 27.940, 29.612 and 30.313 degrees. Peaks corresponding to marked numerals in FIG. 1 are shown in Table 1:

(35) TABLE-US-00001 TABLE 1 Peak number 2θ value 1 4.339 2 11.499 3 12.835 4 13.921 5 15.294 6 16.212 7 16.804 8 17.154 9 18.335 10 19.274 11 19.982 12 22.710 13 23.218 14 24.885 15 27.940 16 29.612 17 30.313

(36) The X-ray powder diffraction diagram of starting material compound A is shown in FIG. 2. It can be seen from FIG. 2 that there is no obvious diffraction peaks in the X-ray powder diffraction diagram of starting material compound A, which means that starting material compound A is amorphous.

Effect Example 2 Polarized Light Microscopy

(37) 1. Samples: Eutectic crystal of the complex formed by compound A and L-proline prepared in example 1-19 and compound A.

(38) 2. Parameters of Polarized light microscopy: Eyepiece 10×, Objective 10×.

(39) 3. Experimental result

(40) The polarizing light microscope photo of the eutectic crystal of the complex formed by compound A and L-proline prepared in example 1-19 is shown in FIG. 3. It can be seen from FIG. 3 that the eutectic crystal has obvious birefringence and shows a crystal habit of irregular particle. The particle size distributes in the range from 10 μm to 50 μm.

(41) The polarizing light microscope photo of starting material compound A is shown in FIG. 4. Compound A has no birefringence phenomenon and is in irregular glass state.

(42) It can be seen from above comparison that comparing with the amorphous compound A, the eutectic crystal of the complex formed by compound A and L-proline of the present invention with a particle form has better stability and is conducive to the process for pharmaceutical preparation.

Effect Example 3 Dynamic Vapor Sorption Test

(43) 1. Samples: Eutectic crystal of the complex formed by compound A and L-proline prepared in example 1-19 and compound A.

(44) 2. Parameters of dynamic vapor sorption test: The instrument: a dynamic moisture absorption analyzer (DVS Advantage, Surface Measurement System Ltd); Experimental temperature: 25° C.; Adsorption range: 0-95% relative humidity; Step interval: 5% relative humidity; Balance standard of weight gain: less than 0.01% weight change in 5 minutes; Longest time of balance: 120 minutes.

(45) 3. Experimental result

(46) The dynamic vapor sorption isotherm of the eutectic crystal of the complex formed by compound A and L-proline prepared in example 1-19 is shown in FIG. 5. It can be seen in FIG. 5 that when an initial mass is 10.2006 mg and relative humidity is increased from 0% to 85% RH, L-proline eutectic crystal absorbs moisture slowly and the moisture absorbed is only 2.174%, while RH is 95%, the weight increased finally is about 9.967%, which indicates that the eutectic crystal of the complex formed by compound A and L-proline is not very sensitive to moisture under normal conditions. In FIG. 5, Y axis is the weight gain percentage of the sample against its dry weight. In FIG. 5, relative humidity is defined as the ratio of the vapor pressure of water in air to the saturated vapor pressure of water.

(47) The dynamic vapor sorption isotherm of compound A is shown in FIG. 6. It can be seen in FIG. 6 that when an initial mass is 10.3109 mg and relative humidity is 50%, the moisture absorption rate of compound A significantly accelerates, the moisture absorbed is about 4.8%, and it keeps absorbing moisture rapidly, the weight increased finally is 14.72% when the relative humidity reaches 95% RH. Thus, compound A is sensitive to moisture. In FIG. 6, Y axis is the weight gain percentage of the sample against its dry weight. In FIG. 6, relative humidity is defined as the ratio of the vapor pressure of water in air to the saturated vapor pressure of water.

(48) It can be seen from above comparison that the eutectic crystal of the complex formed by compound A and L-proline of the present invention has low hygroscopicity, which shows obvious advantages.

Effect Example 4 Solubility Test

(49) 1. Samples: Eutectic crystal of the complex formed by compound A and L-proline prepared in example 1-19 and compound A.

(50) 2. Solubility test method: 2-3 mg sample was accurately weighed and put into a small vial, the right amount of ultra-pure water was added to make a target concentration of 2.0 mg/mL, the vial was rotated for 18 hrs at 25° C. till no changes of solubility, HPLC was used to determine the drug concentration, the solubility of the drug was calculated by preparing standard curve.

(51) HPLC measurement condition: Instrument: Agilent 1200 HPLC; Chromatographic column: Zorbax SB-C8 (3.5 μm, 4.6×75 mm), SN: USEB009791; Mobile phase A: 10 mmol/L aqueous ammonium acetate solution (0.77 g of ammonium acetate was mixed evenly with 1 L of Milli-Q water), Mobile phase B: Acetonitrile, Mobile phase A: Mobile phase B=65:35 (v:v); Column temperature: 25° C.; Wave length: 220 nm; Sampling volume: 10 μL; Flow velocity: 1 mL/min; Detection time: 5 min, t.sub.0=0.65 min, t.sub.R=2.7 min, K′=3.15 (capacity factor, this value should be greater than 2), tailing factor=1.1.

(52) 3. Experimental result

(53) TABLE-US-00002 TABLE 2 solubility of Eutectic crystal of the compound A and L-proline in different aqueous medium Target Solubility concen- pH measured Mass Volume tration Visual (after by HPLC Medium (mg) (mL) (mg/mL) solubility filtration) (mg/mL) Water 2.113 1.056 2.000 clear 7.941 1.94 0.1N 1.882 0.941 2.000 clear 0.975 1.91 HCl pH 2 1.724 0.862 2.000 clear 1.963 1.93 pH 4 2.162 1.080 2.000 clear 4.610 1.93 pH 6 1.977 0.988 2.000 clear 6.481 1.93 pH 8 1.714 0.857 2.000 clear 8.060 1.93 SGF 1.638 0.819 2.000 clear 2.871 1.85 SIF- 1.758 0.879 2.000 clear 6.533 1.98 Fasted SIF-Fed 2.057 1.028 2.000 clear 4.956 2.08

(54) TABLE-US-00003 TABLE 3 solubility of compound A in different aqueous medium Target Solubility concen- pH measured Mass Volume tration Visual (after by HPLC Medium (mg) (mL) (mg/mL) solubility filtration) (mg/mL) Water 3.102 1.552 2.000 clear 8.540 1.68 0.1N 3.190 1.596 2.000 clear 2.182 1.56 HCl pH 2 2.952 1.476 2.000 clear 2.151 1.61 pH 4 3.298 1.648 2.000 clear 5.094 1.64 pH 6 2.802 1.400 2.000 clear 6.180 1.64 pH 8 3.194 1.596 2.000 clear 8.020 1.57 SGF 2.634 1.316 2.000 clear 2.178 1.91 SIF- 2.776 1.388 2.000 clear 6.146 2.04 Fasted SIF-Fed 3.433 1.716 2.000 clear 5.099 1.92
Wherein, SGF refers to manual mode gastric juice, SIF-Fasted refers to simulation intestinal juice (before meal), SIF-Fed refers to simulation intestinal juice (after meal).