CRYSTAL FORM OF BENZIMIDAZOLE-2-ONE COMPOUND, SOLVATE THEREOF, CRYSTAL FORM OF SOLVATE THEREOF, AND PREPARATION METHOD THEREOF

Abstract

A crystal form of compound 1, a solvate thereof, a crystal form of the solvate thereof, and a preparation method therefor. Further comprised is an application of the crystal forms in the preparation of a medicament for treating diseases related to TNFα.

##STR00001##

Claims

1. A crystal form A of compound 1, which has an X-ray powder diffraction pattern having characteristic diffraction peaks at 2θ angles of: 11.91±0.20°, 19.36±0.20°, and 23.17±0.20° ##STR00008##

2. The crystal form A of compound 1 according to claim 1, wherein the X-ray powder diffraction pattern has characteristic diffraction peaks at 2θ angles of: 11.26±0.20°, 11.91±0.20°, 12.91±0.20°, 14.27±0.20°, 19.36±0.20°, 22.26±0.20°, 23.17±0.20°, and 24.97±0.20°.

3. The crystal form A of compound 1 according to claim 2, wherein the X-ray powder diffraction pattern has characteristic diffraction peaks at 2θ angles of: 11.26±0.20°, 11.91±0.20°, 12.91±0.20°, 14.27±0.20°, 15.83±0.20°, 17.53±0.20°, 19.36±0.20°, 20.33±0.20°, 22.26±0.20°, 23.17±0.20°, 24.97±0.20°, and 26.50±0.20°.

4. The crystal form A of compound 1 according to claim 3, wherein the X-ray powder diffraction pattern has characteristic diffraction peaks at 2θ angles of: 11.26°, 11.91°, 12.91°, 14.27°, 15.83°, 17.53°, 19.36°, 20.33°, 22.26°, 22.59°, 23.17°, 24.97°, 26.50°, and 29.46°.

5. The crystal form A of compound 1 according to claim 4, wherein the XRPD pattern is as shown in FIG. 1.

6. The crystal form A of compound 1 according to claim 1, which has a differential scanning calorimetry curve having an onset of an endothermic peak at 147.0±3.0° C.

7. (canceled)

8. The crystal form A of compound 1 according to claim 1, which has a thermogravimetric analysis curve having a weight loss of up to 0.70% at 140.0±3.0° C.

9. (canceled)

10. A solvate represented by formula (I-1) ##STR00009## wherein n is selected from 0.1˜1.5.

11. The solvate according to claim 10, wherein n is selected from 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.1, 1.2, 1.3, 1.4, and 1.5.

12. The solvate according to claim 11, wherein n is 0.5.

13. A crystal form B of a solvate represented by formula (I-1-1), which has an X-ray powder diffraction pattern having characteristic diffraction peaks at 2θ angles of: 6.84±0.20°, 8.90±0.20°, and 23.00±0.20° ##STR00010##

14. The crystal form B of the solvate according to claim 13, wherein the X-ray powder diffraction pattern has characteristic diffraction peaks at 2θ angles of: 6.84±0.20°, 8.90±0.20°, 11.27±0.20°, 12.75±0.20°, 16.15±0.20°, 17.54±0.20°, 22.06±0.20°, and 23.00±0.20°.

15. The crystal form B of the solvate according to claim 14, wherein the X-ray powder diffraction pattern has characteristic diffraction peaks at 2θ angles of: 6.84±0.20°, 8.90±0.20°, 11.27±0.20°, 12.75±0.20°, 16.15±0.20°, 17.54±0.20°, 19.17±0.20°, 19.70±0.20°, 20.41±0.20°, 22.06±0.20°, 23.00±0.20°, and 25.95±0.20°.

16. The crystal form B of the solvate according to claim 15, wherein the X-ray powder diffraction pattern has characteristic diffraction peaks at 2θ angles of: 6.84°, 8.90°, 11.27°, 12.75°, 13.29°, 14.94°, 16.15°, 17.54°, 17.93°, 19.17°, 19.70°, 20.41°, 20.79°, 22.06°, 22.72°, 23.00°, 23.86°, 25.95°, 27.82°, 28.45°, 30.14°, and 32.87°.

17. The crystal form B of the solvate according to claim 16, wherein the XRPD pattern is as shown in FIG. 5.

18. The crystal form B of the solvate according to claim 13, which has a differential scanning calorimetry curve having an onset of an endothermic peak at 77.5±3.0° C.

19. (canceled)

20. The crystal form B of the solvate according to claim 13, which has a thermogravimetric analysis curve having a weight loss of up to 10.46% at 80.0±3.0° C.

21. (canceled)

22. A method of treating a disease related to TNFα in a subject in need thereof, comprising administering to the subject the crystal form A of compound 1 according to claim 1.

23. A method of treating a disease related to TNFα in a subject in need thereof, comprising administering to the subject the solvate according to claim 10.

24. A method of treating a disease related to TNFα in a subject in need thereof, comprising administering to the subject the crystal form B of the solvate according to claim 13.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0065] FIG. 1 is an XRPD pattern of the crystal form A of compound 1 with Cu-Kα radiation.

[0066] FIG. 2 is a DSC curve of the crystal form A of compound 1.

[0067] FIG. 3 is a TGA curve of the crystal form A of compound 1.

[0068] FIG. 4 is a DVS curve of the crystal form A of compound 1.

[0069] FIG. 5 is an XRPD pattern of the crystal form B of compound 1 with Cu-Kα radiation.

[0070] FIG. 6 is a DSC curve of the crystal form B of compound 1.

[0071] FIG. 7 is a TGA curve of the crystal form B of compound 1.

DETAILED DESCRIPTION OF THE INVENTION

[0072] In order to better understand the content of the present disclosure, the present disclosure is further illustrated below in conjunction with specific examples, but the specific examples are not intended to limit the content of the present disclosure.

Example 1: Preparation of Amorphous Form of Compound 1

[0073] ##STR00005##

Step 1: Synthesis of Compound 4

[0074] Compound 2 (15.00 g, 94.29 mmol) was dissolved in N,N-dimethylformamide (150 mL) at room temperature under nitrogen atmosphere, and compound 3 (25.77 g, 94.29 mmol) and potassium carbonate (19.55 g, 141.43 mmol) were then added in sequence. The reaction mixture was heated to 70° C. and reacted with stirring for 16 hours. After the reaction was completed, the mixture was cooled to room temperature. Saturated brine (400 mL) was added, and the mixture was extracted with ethyl acetate (200 mL×3). The organic phases were combined, washed with saturated brine (200 mL×3), dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to remove the solvent. The resulting residue was purified by column chromatography (eluent: ethyl acetate/petroleum ether=0:1 to 2:3, volume ratio) to give the title compound 4. .sup.1HNMR (400 MHz, CDCl.sub.3) δ: 8.52 (d, J=6.5 Hz, 1H), 7.90 (dd, J=8.9, 3.0 Hz, 1H), 7.20-7.15 (m, 1H), 6.96-6.93 (m, 1H), 6.90-6.85 (m, 2H), 6.82-6.78 (m, 1H), 5.20-5.15 (m, 1H), 4.09-4.01 (m, 2H), 3.86 (s, 3H), 3.65 (dd, J=14.7, 8.1 Hz, 1H), 3.48 (dd, J=14.7, 4.8 Hz, 1H), 2.80 (s, 3H), 1.45 (t, J=6.9 Hz, 3H).

Step 2: Synthesis of Compound 5

[0075] Compound 4 (16.00 g, 38.79 mmol) was dissolved in a mixed solvent of ethanol (128 mL) and ethyl acetate (32 mL) at room temperature under nitrogen atmosphere, and wet palladium on carbon (5.00 g, purity: 10%) was then added. The atmosphere was replaced 3 times with hydrogen gas, and the reaction mixture was stirred to react at room temperature under hydrogen atmosphere (30 psi) for 16 hours. After the reaction was completed, the reaction mixture was filtered, and the filter cake was washed with ethyl acetate (100 mL×3). The filtrate was concentrated under reduced pressure to remove the solvent. The resulting residue was purified by column chromatography (eluent: ethyl acetate/petroleum ether=0:1 to 3:2, volume ratio) to give the title compound 5. .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ: 7.07 (d, J=1.2 Hz, 1H), 6.91-6.84 (m, 2H), 6.36 (dd, J=10.8, 2.9 Hz, 1H), 6.30 (dd, J=8.6, 5.8 Hz, 1H), 6.09 (td, J=8.6, 2.9, 1H), 4.99 (s, 2H), 4.96 (d, J=9.3 Hz, 1H), 4.74 (td, J=9.4, 3.8 Hz, 1H), 4.02-3.96 (m, 2H), 3.73-3.67 (m, 4H), 3.39-3.36 (m, 1H), 3.01 (s, 3H), 1.30 (t, J=7.0 Hz, 3H).

Step 3: Synthesis of Amorphous Form of Compound 1

[0076] Compound 5 (12.2 g, 31.90 mmol) was dissolved in ethyl acetate (120 mL) at room temperature, and carbonyldiimidazole (15.52 g, 95.70 mmol) was then added. The reaction mixture was stirred to react at room temperature for 16 hours. After the reaction was completed, the reaction mixture was cooled to room temperature, and 1 M diluted hydrochloric acid (5 mL) and water (50 mL) were added. The mixture was extracted with ethyl acetate (80 mL×3). The organic phases were combined, washed with saturated brine (50 mL×2), dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to remove the solvent. The resulting residue was isolated by column chromatography (eluent: ethyl acetate/petroleum ether=0:1 to 3:2, volume ratio), purified by preparative HPLC (mobile phase: acetonitrile/water, neutral system), and then lyophilized in vacuum to give the title compound 1, which is amorphous. MS-ESI m/z: 409.0 [M+H].sup.+; .sup.1H NMR (400 MHz, CD.sub.3OD) δ: 7.11-7.08 (m, 2H), 7.06-7.04 (m, 1H), 6.93 (d, J=8.4 Hz, 1H), 6.83 (dd, J=8.5, 2.4 Hz, 1H), 6.79-6.74 (m, 1H), 6.00 (dd, J=10.5, 3.9 Hz, 1H), 4.58 (dd, J=14.8, 10.8 Hz, 1H), 4.08-3.96 (m, 3H), 3.80 (s, 3H), 2.94 (s, 3H), 1.35 (t, J=7.0 Hz, 3H).

Example 2: Preparation of Crystal Form a of Compound 1

[0077] ##STR00006##

Step 1: Synthesis of Compound 4

[0078] Compound 2 (200.05 g, 1.26 mol) was dissolved in N,N-dimethylacetamide (2000 mL) at 20° C.-30° C., and then compound 3 (516.45 g, 1.89 moL) was added. Diisopropylethylamine (325.00 g, 2.52 mol) was slowly added dropwise to the above solution (over a period of about 20 minutes). After the addition was completed, the reaction mixture was heated to 110° C.-120° C. and stirred to react at 110° C.-120° C. for 16 hours. After the reaction was completed, the reaction solution was cooled to 15° C., and then slowly poured into an ice water (10500 mL). A large amount of solids precipitate out. The mixture was filtered, and the filter cake was washed with ethanol (200 mL). The filter cake was collected and the solvent was removed under reduced pressure. Sample was added to ethanol (1500 mL), and the mixture was slurried with stirring at 15° C. for 16 hours. The slurry was filtered, and the filter cake was washed with ethanol (200 mL). The filter cake was dried under reduced pressure to remove the solvent to give the title compound 4. .sup.1HNMR (400 MHz, CDCl.sub.3) δ: 8.52 (d, J=6.5 Hz, 1H), 7.90 (dd, J=8.9, 3.0 Hz, 1H), 7.20-7.15 (m, 1H), 6.96-6.93 (m, 1H), 6.90-6.85 (m, 2H), 6.82-6.78 (m, 1H), 5.20-5.15 (m, 1H), 4.09-4.01 (m, 2H), 3.86 (s, 3H), 3.65 (dd, J=14.7, 8.1 Hz, 1H), 3.48 (dd, J=14.7, 4.8 Hz, 1H), 2.80 (s, 3H), 1.45 (t, J=6.9 Hz, 3H).

Step 2: Synthesis of Compound 5

[0079] Compound 4 (122.83 g, 0.30 mol) was dissolved in a mixed solvent of dichloromethane (500 mL) and ethyl acetate (500 mL) at 20° C.-25° C. under nitrogen atmosphere, and wet palladium on carbon (7.50 g, purity: 10%) was then added. The atmosphere was replaced 3 times with hydrogen gas, and the reaction mixture was stirred to react at 25° C.-35° C. under hydrogen atmosphere (25-35 psi) for 16 hours (Four batches of raw materials were reacted in parallel and processed in combination). After the reaction was completed, four batches of reaction solution were combined, and filtered through Celite. The filter cake was washed with dichloromethane (200 mL). The filtrate was rotary-evaporated to dryness under reduced pressure to give a crude product. The crude product was added to ethanol (3200 mL), and the mixture was heated to 78° C. and stirred at 78° C. for 1 hour (until the reaction mixture became completely clear). The heating was stopped, and the mixture was allowed to slowly cool to 20° C. with stirring. The mixture was stirred at 20° C. for another 12 hours. During the stirring, a large amount of solids precipitated out. The reaction mixture was filtered, and the filter cake was washed with ethanol (200 mL). The filter cake was collected, and rotary-evaporated to dryness under reduced pressure to give a product (406.15 g). 329.50 g of the product was weighed and dissolved in dichloromethane (2000 mL). The mixture was purified by column chromatography (eluent: dichloromethane/methanol=1:0, volume ratio) to give compound 5. .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ: 7.07 (d, J=1.2 Hz, 1H), 6.91-6.84 (m, 2H), 6.36 (dd, J=10.8, 2.9 Hz, 1H), 6.30 (dd, J=8.6, 5.8 Hz, 1H), 6.09 (td, J=8.6, 2.9, 1H), 4.99 (s, 2H), 4.96 (d, J=9.3 Hz, 1H), 4.74 (td, J=9.4, 3.8 Hz, 1H), 4.02-3.96 (m, 2H), 3.73-3.67 (m, 4H), 3.39-3.36 (m, 1H), 3.01 (s, 3H), 1.30 (t, J=7.0 Hz, 3H).

Step 3: Synthesis of Crystal Form A of Compound 1

[0080] Compound 5 (175.09 g, 0.46 mol) was dissolved in acetone (1800 mL) at 20° C. under nitrogen atmospheres, and then carbonyldiimidazole (163.32 g, 1.01 mol) was added. The reaction mixture was stirred to react at 15° C.-25° C. for 16 hours. After the completion of the reaction, the reaction mixture was directly concentrated under reduced pressure, and the resulting residue was dissolved in ethyl acetate (1000 mL). The mixture was washed with 1 M diluted hydrochloric acid (1000 mL×2), water (1000 mL×2), and then saturated brine (1000 mL). The organic phase was dried with anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to remove the solvent. The resulting residue was added to ethanol (360 mL), stirred for 30 minutes, and then filtered. The filter cake was washed with ethanol (100 mL). The filter cake was collected, and the solvent was removed under reduced pressure to give a product. After the product was obtained, the product was added to a mixed solvent of ethanol (150 mL) and ethyl acetate (150 mL). The reaction mixture was heated to 78° C. and stirred at 78° C. until the reaction solution became clear. The heating was stopped, and the reaction solution was allowed to naturally cool to 20° C. with stirring. The stirring was continued for another 12 hours. Solids precipitated out during the stirring. The mixture was filtered, and the filter cake was washed with ethanol (50 mL×2). The filter cake was collected, and the solvent was removed under reduced pressure to give a product. After the product was obtained, the product was added to a mixed solvent of ethanol (60 mL) and ethyl acetate (60 mL). The reaction mixture was stirred at 20° C. for 2 hours, and then filtered. The filter cake was washed with ethanol (10 mL). The filter cake was collected, and the solvent was removed under reduced pressure. The filter cake was then dried in vacuum for 6 hours (temperature: 40-45° C., pressure: —0.08 MPa) to give the title crystal form A of compound 1. MS-ESI m/z: 409.0 [M+H].sup.+; .sup.1H NMR (400 MHz, CD.sub.3OD) δ: 7.11-7.08 (m, 2H), 7.06-7.04 (m, 1H), 6.93 (d, J=8.4 Hz, 1H), 6.83 (dd, J=8.5, 2.4 Hz, 1H), 6.79-6.74 (m, 1H), 6.00 (dd, J=10.5, 3.9 Hz, 1H), 4.58 (dd, J=14.8, 10.8 Hz, 1H), 4.08-3.96 (m, 3H), 3.80 (s, 3H), 2.94 (s, 3H), 1.35 (t, J=7.0 Hz, 3H).

Example 3: Preparation of Crystal Form A of Compound 1

[0081] About 175 mg of amorphous compound 1 was added to 1.0 ml of ethanol, and dissolved with ultrasound. The mixture was further subjected to ultrasound, and a large amount of white solid precipitated out. The suspension was stirred at room temperature for 3 hours, and then centrifuged to give a solid, which was the crystal form A of compound 1.

Example 4: Preparation of Crystal Form B of the Solvate of Compound 1

[0082] ##STR00007##

[0083] About 24 mg of amorphous compound 1 was added to 0.2 ml of m-xylene, and the suspension was stirred at room temperature for about 2 days. The mixture was separated by centrifugation to give a solid, which was the crystal form B. .sup.1H NMR (400 MHz, CDCl.sub.3) δ: 8.21 (s, 1H), 7.15 (dd, J=7.4, 7.4 Hz, 0.5H), 7.03 (dd, J=2.3 Hz, 1H), 7.02 (dd, J=8.3, 2.3 Hz, 1H), 7.00-6.97 (m, 2.5H), 6.84-6.78 (m, 3H), 5.76 (dd, J=9.5, 4.2 Hz, 1H), 4.71 (dd, J=14.8, 9.5 Hz, 1H), 4.06 (q, J=7.0 Hz, 2H), 3.84 (dd, J=15.1, 4.8 Hz, 1H), 3.84 (s, 3H), 2.78 (s, 3H), 2.32 (s, 3H), 1.44 (t, J=7.0 Hz, 3H).

Assay Example 1: Study on the Hygroscopicity of Crystal Form a of Compound 1

[0084] Assay Materials:

[0085] SEM Advantage-1 Dynamic Vapor Sorption Apparatus.

[0086] Assay Method:

[0087] 10-30 mg of crystal form A of compound 1 was weighed and placed in a DVS sample pan for assaying.

[0088] Results of the Assay:

[0089] DVS curve of crystal form A of compound 1 was as shown in FIG. 4, ΔW=0.05%.

[0090] Conclusion:

[0091] Crystal form A of compound 1 had a hygroscopic weight gain of 0.05% at 25° C. and 80% RH, which was less than 0.2%, showing no or almost no hygroscopicity.

Assay Example 2: Stability Assay of Crystal Form A of Compound 1 in Different Solvents

[0092] 17 aliquots of crystal form A of compound 1 were weighed (about 15 mg per aliquot), and an appropriate amount of a single or mixed solvent in the Table below was added, respectively. The suspension was stirred at room temperature or 50° C. for 2 weeks. Solids were collected by centrifugation, and detected by XRPD for the crystal form status. The results were shown in Table 3.

TABLE-US-00004 TABLE 3 Stability assay of crystal form A of compound 1 in different solvents Status (after 2 Crystal No. Solvent (volume ratio) Temperature weeks) form 1 Methyl tert-butyl ether Room Suspension A temperature 2 Toluene Room Suspension A temperature 3 Water Room Suspension A temperature 4 Acetone:toluene (2:1) Room Suspension A temperature 5 Ethyl acetate:m-xylene (2:1) Room Suspension A temperature 6 Acetonitrile:water (3:1) Room Suspension A temperature 7 Dichloromethane:m-xylene (1:1) Room Suspension A temperature 8 Isopropanol:water (98:2) Room Suspension A temperature 9 Isopropanol:water (95:5) Room Suspension A temperature 10 Isopropanol:water (92:8) Room Suspension A temperature 11 Isopropanol:water (85:5) Room Suspension A temperature 12 2-Methyltetrahydrofuran:n-octane 50° C. Suspension A (4:1) 13 Ethanol:water (3:1) 50° C. Suspension A 14 1,4-Dioxane:n-heptane (1:1) 50° C. Suspension A 15 Methyl isobutyl ketone:n-hexane 50° C. Suspension A (2:1) 16 2-Butanol:m-xylene (2:1) 50° C. Suspension A 17 Dimethyl sulfoxide:water (2:1) 50° C. Suspension A

[0093] Conclusion: Crystal form A of compound 1 had good stability in solvents such as methyl tert-butyl ether, toluene, water, and a mixed solvent of alcohol and water.

Assay Example 3: Solid Stability Assay of Crystal Form a of Compound 1 at High Temperature, High Humidity and Strong Light Conditions

[0094] According to “Guidelines for Stability Assay of APIs and Preparations” (Chinese Pharmacopoeia 2015 Edition, Volume IV, General Principles 9001), crystal form A of compound 1 was assayed for stability at high temperature (60° C., open), high humidity (room temperature/92.5% relative humidity, open) and strong light (5000±500 Lux, 90 μw/cm.sup.2, sealed).

[0095] 1.5 g of crystal form A of compound 1 was weighed, placed in an open watch glass, and spread into a thin layer. The samples placed under high temperature and high humidity conditions were placed in a desiccator for inspection, and samples were taken on the 5.sup.th, 10.sup.th, and 30.sup.th days for assaying. The assay results were compared with the initial assay results on day 0. The samples placed under strong light condition were covered with a quartz glass cover, and samples were taken on the 5.sup.th and 10.sup.th days for assaying. The assay results were compared with the initial assay results on day 0. The assay results were shown in Table 4 below.

TABLE-US-00005 TABLE 4 Results of solid stability assay of crystal form A of compound 1 under high temperature, high humidity, and strong light conditions Sampling Total Assay conditions time point Appearance Content impurity — Day 0 White 99.5% 0.33% powder High temperature Day 5 White 101.3% 0.32% (60° C., open) powder Day 10 White 100.3% 0.32% powder Day 30 White 99.2% 0.33% powder High humidity Day 5 White 101.1% 0.32% (room temperature/ powder 92.5% relative Day 10 White 100.3% 0.32% humidity, open) powder Day 30 White 99.5% 0.33% powder Strong light (5000 ± Day 5 White 100.4% 0.33% 500 Lux, 90 powder μw/cm.sup.2, sealed) Day 10 White 100.7% 0.33% powder

[0096] Conclusion: Crystal form A of compound 1 had good stability under high temperature, high humidity, or strong light condition.

Assay Example 4: Solid Stability Assay of Crystal Form a of Compound 1 Under Accelerated Condition

[0097] According to “Guidelines for Stability Assay of APIs and Preparations” (Chinese Pharmacopoeia 2015 Edition, Volume IV, General Principles 9001), crystal form A of compound 1 was assayed for stability under accelerated condition of high temperature and high humidity (40° C./75% relative humidity, sealed).

[0098] 1.5 g of crystal form A of compound 1 was weighed and placed in a double-layer low-density polyethylene bag. Each layer of low-density polyethylene bag was sealed by buckling, respectively, and then the double-layer low-density polyethylene bag was placed in an aluminum foil bag and heat-sealed. Samples were taken on the 1.sup.st, 2.sup.nd, 3.sup.rd and 6.sup.th months for assaying, and the assay results were compared with the initial assay results on day 0. The assay results were shown in Table 5 below.

TABLE-US-00006 TABLE 5 Results of solid stability assay of crystal form A of compound 1 under accelerated condition (40° C./75% relative humidity, sealed) Crystal Assay Sampling Total form condition time point Appearance Content impurity (XRPD) — Day 0 White 99.5% 0.33% A powder 40° C./75% Month 1 White 99.5% 0.32% Not relative powder detected humidity, Month 2 White 99.4% 0.33% Not sealed powder detected Month 3 White 99.2% 0.33% A powder Month 6 White 99.5% 0.33% A powder

[0099] Conclusion: Crystal form A of compound 1 had good stability under accelerated condition of 40° C./75% relative humidity.

Assay Example 5: Solid Stability Assay of Crystal Form A of Compound 1 Under Long-Term Condition

[0100] According to “Guidelines for Stability Assay of APIs and Preparations” (Chinese Pharmacopoeia 2015 Edition, Volume IV, General Principles 9001), crystal form A of compound 1 was assayed for stability under long-term condition (25° C./60% relative humidity, sealed).

[0101] 1.5 g of crystal form A of compound 1 was weighed and placed in a double-layer low-density polyethylene bag. Each layer of low-density polyethylene bag was sealed by buckling, respectively, and then the double-layer low-density polyethylene bag was placed in an aluminum foil bag and heat-sealed. Samples were taken on the 3.sup.rd and 6.sup.th months for assaying, and the assay results were compared with the initial assay results on day 0. The assay results were shown in Table 6 below.

TABLE-US-00007 TABLE 6 Results of solid stability assay of crystal form A of compound 1 under long-term condition (25° C./60% relative humidity, sealed) Crystal Assay Sampling Total form Condition time point Appearance Content impurity (XRPD) — Day 0 White 99.5% 0.33% A powder 25° C./60% Month 3 White 99.0% 0.34% A relative powder humidity, Month 6 White 99.5% 0.33% A sealed powder

[0102] Conclusion: Crystal form A of compound 1 had good stability under long-term condition of 25° C./60% relative humidity.

Assay Example 1: Inhibitory Activity of Compound 1 on Phosphodiesterase 4B Subtype (PDE4B Enzyme)

[0103] The biological assay was based on fluorescence polarization measurement of AMP/GMP expression, that is, tracing binding of AMP/GMP antibody to indicate the activity of the enzyme.

[0104] Agents:

[0105] Buffer solution for the assay: 10 mM trihydroxymethyl aminomethane-hydrochloric acid buffer solution (Tris-HCl) (pH 7.5), 5 mM MgCl.sub.2, 0.01% polyoxyethylene lauryl ether (Brij 35), 1 mM dithiothreitol (DTT), and 1% DMSO.

[0106] Enzyme: Recombinant human PDE4B (Genebank Accession Number NM_002600; amino acid 305 terminal) was expressed with baculovirus in Sf9 insect cells using N-terminal GST tag. MW=78 kDa.

[0107] Enzyme substrate: 1 μM cAMP

[0108] Detection: Transcreener® AMP2/GMP2 antibody and AMP2/GMP2 AlexaFluor633 tracing.

[0109] Procedures: [0110] 1. Dissolving the recombinant human PDE4B enzyme and enzyme substrate (1 μM cAMP) in freshly prepared assay buffer, respectively; [0111] 2. Transferring the above PDE4B enzyme buffer solution to reaction wells; [0112] 3. Adding compound 1 dissolved with 100% DMSO to reaction wells with the PDE4B enzyme buffer solution via acoustic technology (echo 550 nanoliter range) and incubating at room temperature for 10 min; [0113] 4. Then, adding the enzyme substrate buffer solution to the above reaction wells to initiate reaction; [0114] 5. Incubating at room temperature for 1 h; [0115] 6. Adding the detection mixture (Transcreener® AMP2/GMP2 antibody and AMP2/GMP2 AlexaFluor633 tracing) to terminate the reaction and incubating with slow mixing for 90 min. The range of fluorescence polarization determination was Ex/Em=620/688.

[0116] Data Analysis:

[0117] The fluorescence polarization signal was converted into nM based on AMP/GMP standard curve and % enzyme activity calculated by Excel software relative to the DMSO control. The curve was fitted with GraphPad Prism (drawing medical icons).

TABLE-US-00008 TABLE 7 Results of in vitro screening assay of compound 1 disclosed herein Compound IC.sub.50 (nM)* Compound 1 26.2 *Average in triplicate.

[0118] Conclusion:

[0119] Compound 1 exhibited excellent in vitro activity of inhibiting phosphodiesterase 4B subtype (PDE4B).

Assay Example 2: Evaluation of In Vitro Inhibition of TNFα Production in Human Peripheral Blood Mononuclear Cells (hPBMC)

[0120] Purpose of the Assay:

Inhibitory activity of compound 1 on lipopolysaccharide (LPS)-induced TNFα production in human peripheral blood mononuclear cells.

[0121] Procedures:

[0122] 1. PBMC Assay

PBMC cells were inoculated into a 96-well plate of cell culture grade at a density of 100,000 cells/100 μL/well. The cell culture medium was RPMI-1640 supplemented with 10% serum. The plate was incubated in a 37° C., 5% CO.sub.2 incubator for 2 hours. 16.8 μL/well of the assay compound was added to the cells and then the cells were incubated in a 37° C., 5% CO.sub.2 incubator for 60 minutes. 16.8 μL/well of LPS was then added to the cells and the cells were incubated in a 37° C., 5% CO.sub.2 incubator for 18 hours. The final DMSO concentration was 0.1%.

[0123] 2. Gradient Dilution of Dose of Compound

In the first step, compound 1 was diluted from a stock concentration to 1.5 mM with 100% DMSO. In the second step, the diluted compound was used as the first point and serially diluted 3-fold with 100% DMSO for 9 points. In the third step, the compound was diluted 125-fold with a serum-free medium, at which time the concentration of DMSO was 0.8%. Then 16.8 μL of the compound diluted with the medium was transferred to a 100 μL cell plate.
The compound was added, and then the cell plate was placed in a 37° C., 5% CO.sub.2 incubator and incubated for 1 hour.

[0124] 3. Dilution of LPS

In the first step, LPS was diluted with ultrapure water to a stock concentration of 1 mg/mL. In the second step, the LPS with a stock concentration was diluted with a serum-free medium to 1 μg/mL. In the third step, the LPS was diluted 1666.666-fold with a serum-free medium. Then 16.8 μL of LPS diluted with the medium was transferred to 116.8 μL cell plate, at which time the final concentration of DMSO was 0.1%. LPS was added, and then the cell plate was placed in a 37° C., 5% CO.sub.2 incubator and incubated for 18 hours.

[0125] 4. ELISA Assay [0126] 1) TNF-α antibody was diluted in a coating solution to 1 times volume, and then added to a 96-well plate with high binding performance at 100 μL per well. The plate was sealed with a membrane and placed in a refrigerator at 4° C. for 18 hours. [0127] 2) 2000 mL of wash buffer was formulated to 1 times volume for use. [0128] 3) After the plate was coated overnight, the coating solution was poured out and the plate was washed 3 times with 300 μL of wash buffer per well. [0129] 4) After washing the plate, 200 μL of blocking buffer was added to each well, and the plate was sealed with a membrane. The plate was placed in an incubator at 25° C. and incubated for one hour. [0130] 5) The cell plate incubated for 18 hours was centrifuged in a centrifuge (temperature: 25° C., rotation speed: 2000 rpm, time: 10 minutes, speed increase: 9, speed decrease: 1). After centrifugation, 100 μL of cell supernatant per well was transferred to a 3599 cell plate, and the plate was then placed in a refrigerator at 4° C. for use. [0131] 6) The cell supernatant was diluted 40-fold with blocking buffer and placed in a refrigerator at 4° C. for use. Standard was formulated and also placed in a refrigerator at 4° C. for use. [0132] 7) After the blocking was completed, the blocking solution was poured out, and the plate was washed 3 times with 300 μL of wash buffer per well. [0133] 8) The diluted cell supernatant samples and standards were added to a ELISA plate. The plate was sealed with a membrane, and then placed in an incubator at 25° C. and incubated for two hours. [0134] 9) The liquid in the plate was poured out, and the plate was washed 5 times with 300 μL of wash buffer per well. [0135] 10) Antibody was prepared, and added to the plate at 100 μL/well. The plate was sealed with a sealing membrane, and then placed in an incubator at 25° C. and incubated for one hour. [0136] 11) The liquid in the plate was poured out, and the plate was washed 7 times with 300 μL of wash buffer per well. [0137] 12) Chromogenic solution was prepared, and added to the plate at 100 μL/well. The plate was then placed in an incubator at 25° C. and incubated in the dark for half an hour. [0138] 13) 50 μL of stop solution was added to each well, and the plate was then centrifuged (temperature: 25° C., rotation speed: 1000 rpm, time: 1 minute, speed increase: 9, speed decrease: 9). [0139] 14) The plate was read on Envision within 30 minutes after centrifugation, and a value obtained by subtracting the absorbance at 570 from the absorbance at 450 was set as the final original data for use.

[0140] 5. Data Processing

Inhibition rate was calculated based on original data according to the formula of:

Inhibition rate=(1−(original value−HPE average)/(ZPE average−HPE average))*100

wherein ZPE is: 0% inhibition (75 pg/mL LPS, 0.1% DMSO), and HPE is: 100% inhibition (without LPS, 0.1% DMSO).

[0141] Data analysis was performed with XLfit statistical software. IC50 was calculated by the following method: the concentration and the inhibition rate (%) of the assayed compound was plotted using a 4-parameter logistic dose-response equation, and the compound concentration required for 50% inhibition (IC50) was determined.

TABLE-US-00009 TABLE 8 Results of inhibitory activity of compound 1 disclosed herein on TNFα production in hPBMC Compound IC.sub.50 (nM)* Compound 1 63.92 *Average in triplicate.

[0142] Conclusion:

[0143] Compound 1 exhibited excellent in vitro activity of inhibiting TNFα production in hPBMC.

Assay Example 3: In Vivo Model of PMA-Induced Ear Edema in CD-1 Mice

[0144] Purpose of the Assay:

[0145] Inflammatory edema, also known as tissue edema, is edema caused by accumulation of exudate caused by inflammation in interstices of tissues. An obvious inflammatory response mediated by protein kinase C (PKC) can be caused when administered topically to ears of mice with phorbol 12-myristate 13-acetate (PMA), thereby triggering a series of symptoms similar to human atopic dermatitis (AD). In the process of preclinical evaluation of candidate compounds for the treatment of AD, an animal model of PMA-induced ear edema in mice is usually used to evaluate the effectiveness.

[0146] The purpose of this assay was to investigate the therapeutic effect of compound 1 on the model of PMA-induced ear edema in CD-1 mice, so as to provide preclinical pharmacodynamic information for subsequent clinical studies.

[0147] Assay Method:

[0148] 1. Preparation of PMA

[0149] 1 mL of acetone was added to completely dissolve 1 mg of PMA, and then 800 μL of mother liquor was pipetted and added to 2400 μL of acetone to prepare 0.25 mg/mL PMA.

[0150] 2. Induction by PMA

[0151] CD-1 mice were sorted according to ear thickness and body weight. After removing four mice that were significantly different from the mean, the remaining mice were randomly divided into a normal control group including 6 mice and treatment groups (10 mice in each treatment group). 10 μL of PMA with a concentration of 0.25 mg/mL was applied to the front and back sides of the right ear of each mouse.

[0152] The induction did not need to be performed on mice in the normal control group.

[0153] 3. Administration and Dosage Design

[0154] The mice in the first group were normal mice, and these mice will not be treated in any way; the mice in the second group were given a vehicle; and the mice in the third group, the fourth group, and the fifth group were given compound 1 at a dose of 0.1 mg/ear, 0.3 mg/ear, and 1 mg/ear, respectively. Drugs were applied to the right ear of the mice 30 minutes before and 15 minutes after PMA induction, respectively.

TABLE-US-00010 TABLE 9 Grouping and dosage design in the assay Route of Dosage Frequency of Groups Assay drug Quantity administration mg/ear administration G1 Normal group 6 NA NA NA G2 Vehicle group 10 Application NA BID G3 Compound 1 10 Application 0.1 BID G4 Compound 1 10 Application 0.3 BID G5 Compound 1 10 Application 1 BID Note: NA represents “not available”; and BID represents “dosing twice a day”.

[0155] 4. Determination of Incidence Index of Ear Edema

[0156] Measurement and sampling: Ten hours after PMA induction, the mice were anesthetized and the thickness of the right ear was measured. After measuring the thickness of the right ear, the mouse was immediately euthanized, and the ear piece was collected and weighed.

[0157] 5. Statistical Processing

[0158] The assay data was expressed as mean±standard error of mean (Mean±SEM), and the degree of ear swelling and ear weight were analyzed by one-way analysis of variance (One-way ANOVA), wherein p<0.05 was considered a significant difference.

[0159] Results of the Assay:

[0160] By measuring at the time point of 10 hours after PMA induction, the ear thickness increased by 0.300-0.400 mm, which was much higher than the normal swelling range (−0.010 to 0.002 mm), and the ear weight increased by 28.8 mg on average, indicating that the ear edema model was established successfully.

[0161] Assay compound 1 can significantly reduce the edema degree of ear edema mice at the 10-hour point at three doses of 0.1 mg/ear, 0.3 mg/ear, and 1 mg/ear, and showed a good dose-effect relationship, wherein the inhibition rates of ear edema were 22%, 39%, and 88%, respectively, and the inhibition rates of ear weight gain were 39%, 46%, and 85%, respectively (compared with the vehicle control group, all p values were less than 0.0001).

[0162] Conclusion:

[0163] In the three dose groups of 0.1, 0.3 and 3 mg/ear, compound 1 had a significant improvement effect on the symptoms of PMA-induced ear edema, can significantly inhibit ear weight gain, and showed a good dose-effect relationship in all the three dose groups.