METHOD FOR PREPARING N-ACETYL-D-GALACTOSAMINE TRIPOLYMER PRECURSOR

Abstract

Disclosed is a method for preparing an N-acetyl-D-galactosamine tripolymer precursor. In the preparation of the tripolymer precursor, a compound 4 is prepared by the following steps: adding a compound 3, a 4 molecular sieve powder, and a reaction solvent into a reactor; inflating and changing protective gas for 3 times; stirring; firstly adding an enol, followed by slowly dropping trimethylsilyl trifluoromethanesulfonate; after a reaction, quenching the reaction with an alkali solution; and performing extraction, separating liquid, washing, drying, filtration, etc., so as to obtain the compound 4. According to the present disclosure, the problems of various production processes, more times of column chromatography for purification of products accompanied by lower yields in the prior art are solved.

Claims

1. A method for preparing an N-acetyl-D-galactosamine tripolymer precursor, and the method comprises: ##STR00025## ##STR00026## ##STR00027## wherein n represents an integer ranging from 2 to 6, and m represents an integer ranging from 1 to 20, wherein a method for preparing a compound 4 comprises: adding a compound 3, a 4 molecular sieve powder, and a reaction solvent into a reactor at a room temperature; performing stirring at an inert gas atmosphere; firstly, adding an enol, followed by slowly dropping trimethylsilyl trifluoromethanesulfonate; after a reaction, quenching the reaction with an alkali solution; filtering to remove the 4 molecular sieve powder, washing the organic phase with saturated salt solution for three times, removing the solvent in vacuo; performing recrystallization with a non-polar organic solvent; and performing filtration with suction to obtain a filter cake, that is, the compound 4, ##STR00028## wherein the reaction solvent is selected from any one of dichloromethane, 1,2-dichloroethane, trichloromethane, and tetrachloromethane; the inert gas is selected from either nitrogen gas or argon gas; the alkali solution is selected from any one of sodium bicarbonate, sodium carbonate, potassium bicarbonate, potassium carbonate, sodium methoxide and sodium ethoxide; and the non-polar organic solvent is selected from any one or more of n-pentane, n-hexane, cyclohexane, cyclopentane, petroleum ether, heptane, and tetrahydrofuran, and wherein a method for preparing a compound 5 comprises: adding the compound 4 and the organic solvent into a reactor at the room temperature, followed by stirring; slowly adding a NaIO.sub.4 solution, and followed by stirring; adding RuCl.sub.2, followed by stirring; and evaporating under reduced pressure to obtain the compound 5: ##STR00029##

2. The method for preparing an N-acetyl-D-galactosamine tripolymer precursor according to claim 1, wherein a method for preparing a compound 11 comprises: adding a monobenzyl alkanedioate into dimethylformamide at the room temperature; adding O-benzotriazole-tetramethyluronium hexafluophosphate and N,N-diisopropylethylamine in sequence, followed by stirring; adding a compound 10, followed by stirring; removing dimethylformamide in vacuo; dissolving a residue in dichloromethane; washing the organic phase; performing drying with sodium sulfate, followed by filtration and evaporating under reduced pressure; and purifying the crude product by silica gel column chromatography to obtain the compound 11: ##STR00030##

3. (canceled)

4. The method for preparing an N-acetyl-D-galactosamine tripolymer precursor according to claim 1, wherein a method for preparing a compound 12 comprises: dissolving the compound 11 in a reaction solvent at the room temperature; adding a palladium-carbon, followed by stirring in a hydrogen atmosphere; and performing post-treatment to obtain the compound 12, and ##STR00031## wherein the reaction solvent is methanol.

5. (canceled)

6. The method for preparing an N-acetyl-D-galactosamine tripolymer precursor according to claim 1, wherein n represents 4, and m represents 9.

7. The method for preparing an N-acetyl-D-galactosamine tripolymer precursor according to claim 1, wherein a method for preparing the compound 3 comprises: adding and dissolving a compound 2 into a reaction solvent at the room temperature, followed by stirring; adding trimethylsilyl trifluoromethanesulfonate, followed by heating to 40-65 DEG C and stirring; then quenching the reaction by adding an alkali; performing drying, filtration and evaporation on an extracted organic phase under reduced pressure to obtain the compound 3, and wherein the reaction solvent is selected from any one of dichloromethane, 1,2-dichloroethane, trichloromethane, and tetrachloromethane; and the alkali in the quenching the reaction by adding an alkali is selected from any one of diaminopropane, trimethylamine, triethylamine, tripropylamine, triisopropylamine, tributylamine, triisobutylamine, tri-sec-butylamine, tri-n-pentylamine, methoxyethylamine, and ethoxyethylamine; ##STR00032##

8. The method for preparing an N-acetyl-D-galactosamine tripolymer precursor according to claim 4, wherein a method for preparing the compound 2 comprises: adding a compound 1 into solvent at the room temperature, followed by stirring; adding an acetylating agent and a deacid reagent, followed by stirring; removing the solvent in vacuo; and then adding a recrystallization solvent, followed by filtration and drying, to obtain the compound 2, and ##STR00033## wherein the acetylating agent is acetic anhydride; the deacid reagent is selected from any one of sodium acetate, the triethylamine and isopropylamine; and the recrystallization solvent is selected from any one of a C.sub.1-C.sub.10 alcohol and a mixed liquor of various C.sub.1-C.sub.10 alcohols.

9. The method for preparing an N-acetyl-D-galactosamine tripolymer precursor according to claim 1, wherein a method for preparing a compound 9 comprises: dissolving a compound 8 and a compound 5 in a reaction solvent at the room temperature, followed by stirring; adding N-methylimidazole and N,N,N,N-tetramethylchlofmainiumhexafluophosphate, followed by stirring in a sealed condition; after the reaction, diluting the mixture with water, and extracting with dichloromethane for three times; washing the organic phase with saturated salt solution; performing drying with anhydrous sodium sulfate, filtration, and evaporating under reduced pressure; and purifying a crude product by the silica gel column chromatography to obtain the compound 9, and ##STR00034## wherein n represents 4.

10. The method for preparing an N-acetyl-D-galactosamine tripolymer precursor according to claim 1, wherein a method for preparing a compound 7 comprises: dissolving a compound 6 in a reaction solvent in an inert gas atmosphere at the room temperature followed by stirring; adding N-(tert-butyloxycarbonyl)-1,3-diaminopropane; reducing the reaction temperature to 0 DEG C; adding 1-hydroxybenzotriazole and O-benzotriazole-tetramethylurea hexafluorophosphate during stirring, followed by adding N,N-diisopropylethylamine dropwise; slowly raising the reaction temperature to the room temperature and continuing to stir overnight; adding water, followed by extracting the mixture for three times with ethyl acetate; washing the combined organic phase with an inorganic alkali saturated solution, water, an acid aqueous solution, water and saturated salt solution in sequence; and performing drying with the anhydrous sodium sulfate, followed by filtration and evaporating under reduced pressure to obtain the compound 7, and ##STR00035## wherein the inert gas is selected from either nitrogen gas or argon gas; the reaction solvent is selected from any one or more of ethyl ether, diisopropyl ether, tetrahydrofuran, 1,4-dioxane, and 1,2-dimethoxy-ethane; and the inorganic alkali is selected from any one of sodium carbonate, potassium carbonate, sodium bicarbonate, trisodium phosphate, disodium hydrogen phosphate, potassium carbonate, potassium bicarbonate, tripotassium orthophosphate, and potassium hydrogen phosphate.

11. A preparation method of a compound 4 for preparing an N-acetyl-D-galactosamine tripolymer precursor, and the preparation method comprises: adding a compound 3, a 4 molecular sieve powder, and a reaction solvent into a reactor at the room temperature; performing stirring at an inert gas atmosphere; firstly adding an enol, followed by slowly dropping trimethylsilyl trifluoromethanesulfonate; after a reaction, quenching the reaction with an alkali solution; filtering to remove 4 molecular sieve powder, washing the organic phase with saturated salt solution for three times; removing the solvent in vacuo; performing recrystallization with a non-polar organic solvent; and performing filtration with suction to obtain a filter cake, that is, the compound 4, and ##STR00036## wherein n represents 4; the reaction solvent is selected from any one of dichloromethane, 1,2-dichloroethane, trichloromethane and tetrachloromethane; the inert gas is selected from either nitrogen gas or argon gas; the alkali solution is selected from any one of sodium bicarbonate, sodium carbonate, potassium bicarbonate, potassium carbonate, sodium methoxide, and sodium ethoxide; and the non-polar organic solvent is selected from any one or more of n-pentane, n-hexane, cyclohexane, cyclopentane, petroleum ether, heptane, and tetrahydrofuran.

12. A preparation method of a compound 5 for preparing an N-acetyl-D-galactosamine tripolymer precursor, and the preparation method comprises: adding a compound 4 and an organic solvent into a reactor at the room temperature, followed by stirring; slowly adding a NaIO.sub.4 solution, followed by stirring; adding RuCl.sub.2, followed by stirring; and evaporating under reduced pressure to obtain the compound 5, and ##STR00037## wherein n represents 4.

13. The method for preparing an N-acetyl-D-galactosamine tripolymer precursor according to claim 2, wherein n represents 4, and m represents 9.

14. The method for preparing an N-acetyl-D-galactosamine tripolymer precursor according to claim 4, wherein n represents 4, and m represents 9.

Description

SPECIFIC EMBODIMENTS

[0031] The technical solutions of the present disclosure will be described clearly and completely below. Obviously, the examples described are only a part of examples of the present disclosure rather than all examples. Based on the examples of the present disclosure, all other examples obtained by those ordinary skilled in the art without creative efforts fall within the scope of protection of the present disclosure.

Example 1

[0032] (1) A method for synthesizing a compound 2 as an intermediate product includes the following steps.

##STR00014##

[0033] Galactosamine (10.012 g, 46.38 mmol) and dichloromethane (DCM, 100 mL) are added into a reactor in sequence and stirred at a room temperature, then triethylamine (35.13 g, 34.78 mmol) and acetic anhydride (35.48 g, 34.78 mmol) are added into the reactor separately, followed by performing stirring overnight, and thin-layer chromatography (TLC) (DCM:MeOH=5:1) is performed to monitor the reaction.

[0034] After the reaction, the reaction solution is evaporated under reduced pressure, followed by adding methanol and performing stirring for 2 h to perform crystallization, then filtration is performed, and a filter cake is washed with a small amount of methanol, thereby obtaining a white solid, that is, the compound 2 (mass: 20.670 g, yield: 95%).

[0035] Nuclear magnetic data characterization is as follows:

[0036] .sup.1H NMR (400 MHz, CDCl.sub.3): 5.70 (d, J=8.7 Hz, 1H), 5.37 (s, 2H), 5.08 (dd, J=11.2, 3.1 Hz, 1H), 4.45 (dd, J=20.0, 9.2 Hz, 1H), 4.14 (ddd, J=25.1, 11.3, 6.7 Hz, 2H), 4.02 (t, J=6.4 Hz, 1H), 2.17 (s, 3H), 2.13 (s, 3H), 2.05 (s, 3H), 2.02 (s, 3H), 1.94 (s, 3H).

[0037] (2) A method for synthesizing a compound 3 as an intermediate product includes the following steps.

##STR00015##

[0038] The compound 2 (6.001 g, 15.41 mmol) and 1,2-dichloroethane (60 mL) are added into a reactor in sequence and stirred at the room temperature, then trimethylsilyl trifluoromethanesulfonate (TMSOTf) (3.767 g, 16.95 mmol) are dropped into the reaction solution slowly, after dropping, the temperature is raised to 55 DEG C and stirring is performed for 1 h, and the TLC (DCM:MeOH=20:1) is performed to monitor the reaction.

[0039] After the reaction, the reaction solution is evaporated under reduced pressure to obtain the compound 3 (mass: 5.021 g, yield: 98%).

[0040] Nuclear magnetic data characterization is as follows:

[0041] .sup.1H NMR (400 MHz, CDCl.sub.3): 5.92 (d, J=6.8 Hz, 1H), 5.39 (t, J=3.0 Hz, 1H), 4.84 (dd, J=7.4, 3.3 Hz, 1H), 4.21-4.16 (m, 1H), 4.13 (dd, J=11.1, 6.9 Hz, 1H), 4.04 (dd, J=11.1, 5.8 Hz, 1H), 3.9-3.88 (m, 1H), 2.05 (s, 3H), 2.00 (s, 6H), 1.98 (d, J=0.9 Hz, 3H).

[0042] (3) A method for synthesizing a compound 4 as an intermediate product includes the following steps

##STR00016##

[0043] An untreated compound 3 (5.021 g, 15.18 mmol), a 4 molecular sieve powder (MS, 5.011 g) and 1,2-dichloroethane (35 mL) are added into a reactor in sequence at the room temperature, followed by inflating and changing nitrogen gas three times and performing stirring for 5 minutes, 5-hexen-1-ol (1.680 g, 16.77 mmol) is added firstly, and then TMSOTf (1.687 g, 7.592 mmol) is dropped into the reactor slowly in 10 minutes, and after dropping, the TLC (DCM:MeOH=20:1) is performed immediately to monitor the reaction.

[0044] After the reaction, 20 mL of dichloromethane is added into the reaction solution, followed by quenching the reaction with a small amount of a sodium bicarbonate saturated solution, filtration is performed with diatomite, and an organic phase is separated. The organic phase is washed with saturated salt solution, followed by drying with anhydrous sodium sulfate and filtration, filtrate is evaporated under reduced pressure to obtain an oily matter, and then n-hexane is added, followed by stirring, and crystallization occurs to obtain a solid with faint yellow, that is, the compound 4 (mass: 5.635 g, yield: 86%).

[0045] Nuclear magnetic data characterization is as follows:

[0046] .sup.1H NMR (400 MHz, CDCl.sub.3): 5.78-5.62 (m, 2H), 5.26 (dt, J=11.1, 3.5 Hz, 2H), 5.00-4.83 (m, 2H), 4.65 (d, J=8.4 Hz, 1H), 4.15-4.01 (m, 2H), 3.93-3.77 (m, 3H), 3.43 (dt, J=9.6, 6.8 Hz, 1H), 2.07 (s, 3H), 1.98 (s, 4H), 1.93 (s, 3H), 1.88 (s, 3H), 1.53 (dq, J=12.6, 6.5 Hz, 2H), 1.43-1.29 (m, 2H).

[0047] (4) A method for synthesizing a compound 5 as an intermediate product includes the following steps.

##STR00017##

[0048] The compound 4 (5.005 g, 11.04 mmol), dichloromethane (15 mL), and acetonitrile (15 mL) are mixed uniformly, and are added into a reactor and stirred at the room temperature, a NaIO.sub.4 solution formed by dissolving NaIO.sub.4 (9.961 g, 46.57 mmol) in 25 mL of deionized water is slowly added into a reaction solution, followed by stirring for 15 min, RuCl.sub.2 (0.04 g, 0.2328 mmol) is added into a reaction solution, followed by stirring for 1 h, and the TLC (DCM:MeOH=10:1) is performed to monitor the reaction.

[0049] After the reaction, 20 mL of water is added into a reaction solution, followed by slowly adding a saturated NaHCO.sub.3 solution to adjust a pH value of the reaction solution to 7.5, an aqueous phase is washed twice with dichloromethane, and the aqueous phase is retained. Then, a citric acid solution is dropped slowly into the aqueous phase until the pH value is 3, the aqueous phase is extracted twice with dichloromethane, and the organic phase is retained. Finally, the organic phase is washed twice with saturated salt solution, followed by removing the aqueous phase, 3% of NaS solution is added into the organic phase, followed by stirring until the color of the organic phase turn to yellow, and the organic phase is separated, and evaporation is performed under reduced pressure to obtain the compound 5 (mass: 4.276 g, yield: 82%).

[0050] Nuclear magnetic data characterization is as follows:

[0051] .sup.1H NMR (400 MHz, CDCl.sub.3): 5.72 (d, 1H, J=8.5 Hz), 5.35 (d, 1H, J=3.5 Hz), 5.26 (dd, 1H, J=3.5 Hz, 11.5 Hz), 4.67 (d, 1H, J=8.5 Hz), 4.17 (dd, 1H, J=6.5 Hz, 11.5 Hz), 4.12 (dd, 1H, J=6.5 Hz, 11.5 Hz), 4.00 (dt, 1H, J=8.5 Hz, 11.5 Hz), 3.92 (m, 2H), 3.53 (m, 1 H), 2.39 (m, 2H), 2.15 (s, 3H), 2.05 (s, 3H), 2.01 (s, 3H), 1.97 (s, 3H), 1.71 (m, 2H), 1.65 (m, 2H).

[0052] (5) A method for synthesizing a compound 7 as an intermediate product includes the following steps.

##STR00018##

[0053] A compound 6 (3.613 g, 7.442 mmol), tetrahydrofuran (THF, 18 mL) and N-(tert-butoxycarbonyl)-1,3-diaminopropane (4.211 g, 24.17 mmol) are added into a reactor, a reaction solution is cooled to 0 DEG C, and hydroxybenzotriazole (HOBT, 3.511 g, 25.98 mmol) and benzotriazole-tetramethylurea hexafluorophosphate (HBTU, 8.712 g, 22.97 mmol) are added during stirring. Then, N,N-diisopropylethylamine (DIEA, 5.921 g, 45.81 mmol) is added dropwise, the reaction temperature is raised to the room temperature slowly, and a reaction solution is stirred contentiously overnight.

[0054] After the reaction, 40 mL of water is added into a reaction mixture firstly, followed by transferring into a separatory funnel containing 80 mL of ethyl acetate, and extraction and liquid separation are performed to separate an organic phase. The organic phase is washed with 20 mL of 10% NaHCO3 aqueous solution, 20 mL of water, 40 mL of 10% citric acid solution, 20 mL of water, and 20 mL of salt solution in sequence, and dried with anhydrous sodium sulfate, and the solvent and volatile matters are removed in vacuo to obtain an oily liquid with faint yellow, that is, the compound 7 (mass: 6.944 g, yield: 94%).

[0055] Nuclear magnetic data characterization is as follows:

[0056] .sup.1H NMR (400 MHz, CDCl.sub.3): 7.40-7.30 (m, 5H); 6.87 (m, 3H); 5.55 (s, 1H); 5.19 (t, J=5.8 Hz, 3H); 5.01 (s, 2H); 3.64 (s, 6H); 3.62 (t, J=6.0 Hz, 6H); 3.25 (m, 6H); 3.09 (m, 6H); 2.42 (t, J=6.0 Hz, 6H); 1.59 (m, 6H); 1.41 (s, 27H).

[0057] (6) A method for synthesizing a compound 8 as an intermediate product includes the following steps.

##STR00019##

[0058] The compound 7 (6.031 g, 6.415 mmol) and 45 mL of trifluoroacetic acid are dissolved in 280 mL of DCM at the room temperature, and stirred for 30 minutes.

[0059] After the reaction, the reaction solution is diluted with methylbenzene (300 mL), evaporated under reduced pressure, and the two steps are repeated three times to obtain a pale red oily matter, that is, trifluoroacetates (mass: 6.207 g, yield: 99%) of the compound 8.

[0060] Nuclear magnetic data characterization is as follows: none.

[0061] (7) A method for synthesizing a compound 9 as an intermediate product includes the following steps.

##STR00020##

[0062] The trifluoroacetates (1.823 g, 1.86 mmol) of the compound 8 and the compound 5 (5.086 g, 11.34 mmol) are dissolved in 30 mL of acetonitrile, N-methylimidazole (NM, 2.876 g, 35.03 mmol), N,N,N,N-tetramethylchlofmainiumhexafluophosphate (TCFH, 3.489 g, 12.43 mmol) are added in sequence, and stirring is performed overnight in a sealed condition at the room temperature. After the reaction, dichloromethane (30 mL) is added into the reaction solution, an organic phase is washed with saturated salt solution, followed by drying with anhydrous sodium sulfate, evaporated under reduced pressure, and the crude product is purified by the silica gel column chromatography, and dichloromethane and methanol are used as an eluent, thereby obtaining a white solid, that is, the compound 9 (mass: 2.943 g, yield: 81%).

[0063] Nuclear magnetic data characterization is as follows:

[0064] .sup.1H NMR (400 MHz, DMSO-d.sub.6): 7.87-7.76 (m, 6H); 7.71 (t, J=5.7 Hz, 3H); 7.37-7.25 (m, 5H); 6.52 (brs, 1H); 5.20 (d, J=3.4 Hz); 5.00-4.92 (m, 5H); 4.47 (d, J=8.5 Hz, 3H); 4.06-3.97 (m, 9H); 3.86 (dt, J=8.8, 11.1 Hz, 3H); 3.69 (dt, J=5.6, 9.9 Hz, 3H); 3.53 (t, J=6.4 Hz, 6H); 3.47 (s, 6H); 3.39 (dt, J=6.4, 9.9 Hz, 3H); 3.07-2.97 (m, 12H); 2.26 (t, J=6.4 Hz, 6H); 2.09 (s, 9H); 2.03 (t, J=7.0 Hz, 6H); 1.98 (s, 9H); 1.88 (s, 9H); 1.76 (s, 9H); 1.58-1.35 (m, 18H).

[0065] (8) A method for synthesizing a compound 10 as an intermediate product includes the following steps.

##STR00021##

[0066] The compound 9 (1.012 g, mmol) is dissolved in 10 mL of methanol at the room temperature, and 0.1 g of 5% palladium-carbon is added into the reaction solution, followed by inflating and changing hydrogen gas three times and stirring for 4 h.

[0067] After the reaction, filtration is performed with diatomite, a filter cake is washed with a small amount of methanol, and the filtrate is concentrated in vacuo to obtain the compound 10 (mass: 1.012 g, yield: 99%).

[0068] Nuclear magnetic data characterization:

[0069] .sup.1H NMR (400 MHz, DMSO-d.sub.6): 7.88 (t, J=5.5 Hz, 3H); 7.82 (d, J=9.2 Hz, 3H); 7.76 (t, J=5.6 Hz, 3H); 5.20 (d, J=3.4 Hz, 3H); 4.95 (dd, J=3.4, 11.2 Hz, 3H); 4.47 (d, J=8.5 Hz, 3H); 4.07-3.97 (m,9H); 3.86 (dt, J=8.9, 11.0 Hz, 3H); 3.69 (dt, J=5.9, 9.8 Hz, 3H); 3.63 (t, J=6.3 Hz, 6H); 3.48-3.34 (m, 9H); 3.03 (q, J=6.6 Hz, 12H); 2.33 (t, J=6.2 Hz, 6H); 2.09 (s, 9H); 2.03 (t, J=7.1 Hz, 6H); 1.99 (s, 9H); 1.89 (s, 9H); 1.76 (s, 9H); 1.56-1.38 (m,18H).

[0070] (9) A method for synthesizing a compound 11 as an intermediate product includes the following steps.

##STR00022##

[0071] Monobenzyl dodecanoate (0.125 g, 0.393 mmol) is dissolved in 4 mL of diisopropylethylamine (DMF) at the room temperature, HBTU (0.164 g, 0.4324 mmol) and DIEA (0.2050 mL, 1.174 mmol) are added in sequence, and stirring is performed for a few minutes. Then, 2 mL of a DMF solution containing the compound 10 (0.751 g, 5.24 mmol) is added, and stirring is performed overnight.

[0072] After the reaction, the reaction solution is concentrated in vacuo, residues are dissolved in 20 mL of DCM, and the organic phase is washed with saturated NaHCO.sub.3 solution and water in sequence, followed by drying with anhydrous Na.sub.2SO.sub.4, filtration, and concentrating in vacuo. Finally, silica gel column chromatography is performed (3-15% MeOH/DCM gradient elution), and concentration in vacuo is performed to obtain a white solid, that is, the compound 11 (mass: 0.608 g, yield: 75%).

[0073] Nuclear magnetic data characterization is as follows:

[0074] .sup.1H NMR (400 MHz, DMSO-d.sub.6): 7.86-7.77 (m, 6H, NH); 7.72 (t, J=5.7 Hz, 3H); 7.39-7.28 (m, 5H); 6.97 (s, 1H); 5.20 (d, J=3.4 Hz, 3H); 5.07 (s, 2H); 4.95 (dd, J=3.4, 11.2 Hz, 3H); 4.47 (d, J=8.5 Hz, 3H); 4.07-3.96 (m, 9H); 3.86 (dt, J=8.9, 11.2 Hz); 3.69 (dt, J=5.9, 9.9 Hz, 3H); 3.60-3.45 (m, 12H); 3.39 (dt, J=6.3, 9.9 Hz, 3H); 3.08-2.95 (m, 12H); 2.32 (t, J=7.4 Hz, 2H); 2.26 (t, J=6.3 Hz, 6H); 2.09 (s, 9H), 2.03 (t, J=7.0 Hz, 8H); 1.98 (s, 9H); 1.88 (s, 9H), 1.76 (s, 9H); 1.56-1.36 (m, 22H); 1.28-1.14 (m, 12H).

[0075] (10) A method for synthesizing a compound 12 as an intermediate product includes the following steps.

##STR00023##

[0076] The compound 11 (1.000 g, 0.500 mmol), 10 mL of methanol and 5% of palladium-carbon (0.100 g) are added, followed by inflating and changing hydrogen gas three times, and stirring is performed overnight.

[0077] After the reaction, the reaction solution is filtered with diatomite, a filter cake is washed with a small amount of methanol, and the filtrate is concentrated in vacuo to obtain a white solid, that is, the compound 12 (mass: 0.960 g, yield: 96%).

[0078] Nuclear magnetic data characterization is as follows:

[0079] .sup.1H NMR (400 MHz, DMSO-d.sub.6): 11.93 (brs, 1H); 7.91-7.81 (m, 6H); 7.72 (t, J=5.6 Hz, 3H); 6.96 (s, 1H); 5.20 (d, J=3.4, 3H); 4.96 (dd, J=3.4, 11.2 Hz, 3H); 4.48 (d, J=8.4; 3H); 4.05-3.97 (m, 9H); 3.86 (dt, J=8.8, 11.0 Hz, 3H); 3.69 (dt, J=6.0, 9.9 Hz, 3H); 3.57-3.47 (m, 12H); 3.40 (dt, J=6.3, 9.9 Hz, 3H); 3.07-2.98 (m,12H); 2.27 (t, J=6.4 Hz, 6H); 2.17 (t, J=7.4 Hz, 2H); 2.09 (s, 9H); 2.03 (t, J=7.2 Hz, 8H); 1.98(s, 9H); 1.89 (s, 9H); 1.76 (s, 9H); 1.55-1.37 (m, 22H); 1.27-1.16 (m, 12H).

[0080] (11) A method for synthesizing a compound 13 as an intermediate product includes the following steps.

##STR00024##

[0081] The compound 12 (0.631 g, 0.314 mmol), DMF (6.3 mL), and DMA (0.110 g, 0.795 mmol) are added into a reactor, and stirring is performed at 0 DEG C. 2,2,2-pentafluorophenyl trifluoroacetate (0.133 g, 0.477 mmol) is dropped into the reaction solution slowly, and after dropping, the temperature is raised to the room temperature, followed by stirring for 3 h.

[0082] After the reaction, the reaction solution is concentrated in vacuo; and then the silica gel column chromatography is performed to obtain a white solid, that is, the compound 13 (mass: 0.424 g; yield 62%).

[0083] Nuclear magnetic data characterization is as follows:

[0084] .sup.1H NMR (400 MHz, DMSO-d.sub.6): 7.71-7.80 (m, 9H), 6.98 (s, 1H), 5.22 (d, J=3.3 Hz, 3H), 4.99 (dd, J=11.1 Hz, 3.3 Hz, 3H), 4.50 (d, J=8.4 Hz, 3H), 4.02 (s, 9H), 3.82-3.92 (m, 3H), 3.69-3.74 (m, 3H), 3.52-3.56 (m, 16H), 3.39-3.44 (m, 3H), 3.03 (s, 12H), 2.75-2.79 (m, 2H), 2.28 (t, J=6.3 Hz, 6H), 2.00-2.10 (m, 26H), 1.89 (s, 9H), 1.77 (s, 9H), 1.64-1.68 (m, 2H), 1.25-1.53 (m, 28H).

Example 2

[0085] Example 2 is basically the same as Example 1, and differs from Example 1 in that the method for synthesizing the compound 3 as an intermediate product includes:

[0086] adding the compound 2 (1.028 g, 2.64 mmol) and 1,2-dichloroethane (10 mL) into a reactor in sequence and stirring the mixture at a room temperature; then dropping TMSOTf (0.646 g, 2.90 mmol) into a reaction solution slowly; after the dropping, raising the temperature to 40 DEG C, and performing stirring; and TLC (DCM:MeOH=20:1) is performed to monitor the reaction. After the reaction, the reaction solution is concentrated in vacuo to obtain the compound 3 (mass: 0.842 g, yield: 97%).

Example 3

[0087] Example 3 is basically the same as Example 1, and differs from Example 1 in that the method for synthesizing the compound 3 as an intermediate product includes:

[0088] adding a compound 2 (10.225 g, 26.26 mmol) and 1,2-dichloroethane (100 mL) into a reactor in sequence and stirring the mixture at a room temperature; then dropping TMSOTf (6.421 g, 28.89 mmol) into a reaction solution slowly; after the dropping, raising the temperature to 65 DEG C and performing stirring; and performing TLC (DCM:MeOH=20:1) to monitor the reaction. After the reaction, the reaction solution is concentrated in vacuo to obtain the compound 3 (mass: 8.216 g, yield: 95%).

[0089] While the present disclosure has been described in detail through the above preferred Examples, it should be recognized that the above description should not be considered as a limitation to the present disclosure. Various modifications and alternatives to the present disclosure will be apparent to those skilled in the art upon reading the foregoing. Accordingly, the scope of protection of the present disclosure should be defined by the attached claims.