INTERMEDIATE COMPOUNDS USED FOR PREPARING BRIVARACETAM, PREPARATION METHODS FOR INTERMEDIATE COMPOUNDS, AND USE

Abstract

The present disclosure provides intermediates used for preparing Brivaracetam, a preparation method and a use thereof, including an intermediate compound A and an intermediate compound B and a preparation method thereof, as well as a synthetic route for using the intermediate compound B to prepare Brivaracetam. The present technical solution can obtain high-quality and high-optical purity Brivaracetam and intermediates thereof, the proportion of Brivaracetam among the four optical isomers being greater than 99.5%. In addition, neither silica gel column for separation and purification nor expensive chiral high performance liquid chromatography for resolution is required, thereby avoiding cumbersome separation and purification steps, also avoiding waste of raw materials, reducing the production cost and making it more suitable for industrial production.

Claims

1. An intermediate compound A, wherein a structural formula of the intermediate compound A is shown in Formula II: ##STR00010## wherein R.sub.1 is selected from one of vinyl or ethynyl.

2. A preparation method of the intermediate compound A of claim 1, comprising reacting a compound of which the structural formula is shown in Formula I with an unsaturated hydrocarbon metallic reagent, to obtain the intermediate compound with the structural formula of Formula II, wherein the reaction route is as follows: ##STR00011## wherein R.sub.1 is selected from one of vinyl or ethynyl.

3. The preparation method according to claim 2, further comprising one or more of the following: the reaction is carried out under a copper-containing catalyst; the copper-containing catalyst is selected from a combination of any one or more of cuprous chloride, cuprous bromide, cuprous iodide, cuprous cyanide or copper trifluorosulfonate; the molar ratio of the copper-containing catalyst to the compound of Formula I is (0.01-2):1; the reaction temperature is −78° C. to 35° C.

4. An intermediate compound B, wherein a structural formula of the intermediate compound B is shown in Formula IV: ##STR00012##

5. A preparation method of the intermediate compound B of claim 4, comprising the following steps: a) subjecting an intermediate compound of Formula II to deesterification reaction to obtain a compound with a structural formula of Formula III, wherein the reaction route is as follows: ##STR00013## b) subjecting the compound with the structural formula of Formula III to hydrogenation reduction to obtain a compound with a structural formula of Formula IV, wherein the reaction route is as follows: ##STR00014## wherein R.sub.1 is selected from one of vinyl or ethynyl.

6. The preparation method according to claim 5, wherein step a) further comprises one or more of the following: the intermediate compound of Formula II is subjected to deesterification reaction with lithium bromide; the molar ratio of the intermediate compound of Formula II to lithium bromide is 1:(1.0-1.5); the reaction temperature is 90-160° C.

7. The preparation method according to claim 5, wherein step b) further comprises one or more of the following: the hydrogenation reduction of the compound with the structural formula of Formula III is conducted in the presence of a catalyst to obtain the compound with the structural formula of Formula IV; the reaction temperature is 30-60° C.; the mass ratio of the catalyst to the compound with the structural formula of Formula III is 5%-10%.

8. A use of the intermediate compound B of claim 4 in the preparation of Brivaracetam.

9. The use according to claim 8, comprising reacting the compound with the structural formula of Formula IV with (S)-2-aminobutanamide to obtain Brivaracetam, wherein the synthetic route is as follows: ##STR00015##

10. The use according to claim 9, comprising one or more of the following: the molar ratio of the compound with the structural formula of Formula IV to (S)-2-aminobutanamide or an acceptable salt thereof is 1:(1.0-1.5); the reaction temperature is 60-110° C.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0045] FIG. 1 is a diagram showing the preparation route of the intermediate compound II according to an embodiment of the present disclosure;

[0046] FIG. 2 is a diagram showing the preparation route of the compound with the structural formula of Formula III according to an embodiment of the present disclosure;

[0047] FIG. 3 is a diagram showing the preparation route of the compound with a structural formula of Formula IV;

[0048] FIG. 4 is a diagram showing the preparation route of Brivaracetam;

[0049] FIG. 5 shows the chiral mapping of the intermediate compound II according to an embodiment of the present disclosure;

[0050] FIG. 6 shows the chiral mapping of the intermediate compound IV according to an embodiment of the present disclosure;

[0051] FIG. 7 shows the chiral mapping of Brivaracetam according to an embodiment of the present disclosure.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0052] The implementation of the present disclosure will be illustrated through the following specific examples. Other advantages and effects of the present disclosure can be readily appreciated by those skilled in the art from the content disclosed in this specification. The present disclosure can also be implemented or applied through other different specific embodiments. Various details in this specification can also be modified or changed in various ways based on different viewpoints and applications without departing from the spirit of the present disclosure.

[0053] It should be noted that the process equipment or devices not specifically indicated in the following examples are all conventional equipment or devices in the art.

[0054] In addition, it should be understood that, the one or more method steps mentioned in the present disclosure does not exclude that there may be other method steps before and after the combined steps or other method steps may be inserted between these explicitly mentioned steps, unless otherwise stated. It should also be understood that, the combined connection relationship between one or more equipment/devices mentioned in the present disclosure does not exclude that there may be other equipment/devices before and after the combined equipment/devices or other equipment/devices may be inserted between the two explicitly mentioned equipment/devices, unless otherwise stated. In addition, unless otherwise stated, the numbering of the method steps is only a convenient tool for identifying the method steps, and is not intended to limit the order of the method steps or to limit the applicable scope of the present disclosure, and the change or adjustment of their relative relationship, if there is no substantial change to the technical content, should also be considered as the applicable scope of the present disclosure.

[0055] In the exemplary embodiment of the present disclosure, Brivaracetam is synthesized through the route as shown in FIG. 1, of which the specific steps are as follows.

(1) Preparation of Intermediate Compound II

[0056] Under the protection of N2, into a mechanically stirred 10 L three-necked flask was slowly added a mixed solution of vinyl magnesium bromide and tetrahydrofuran (1 M, 10.6 L, 10.6 mol) and cooled to −40° C., into which was slowly added cuprous iodide (896 g, 4.7 mol) while controlling the temperature not exceeding −35° C. Upon the completion of addition, they were stirred at −45 to −35° C. for 2.0 hours, and then the compound with the structural formula of I (1.0 kg, 5.88 mol) and tetrahydrofuran (3.0 L) were dropwise added within 2.5 hours. While controlling the temperature not exceeding 35° C., they were reacted for 0.5 hours after dropwise addition. The reaction solution was slowly added into saturated ammonium chloride solution (5.0 L) and stirred for layering. The aqueous phase was extracted with methyl tert-butyl ether (2×1.0 L), the methyl tert-butyl ether layers were combined and concentrated to get yellow oil, 1.02 kg, and the yield was 88.4%.

[0057] The chiral analysis method for the product intermediate compound II in this step is as follows:

Model: LC-10A

Column: YMC Amylose-SA 4.6*250 mm 5 um

[0058] Mobile phase: ethanol:n-hexane=5:95 (VN)
Detection wavelength: 214 nm
Flow rate: 0.8 ml/min
Isocratic elution: 35 min.

[0059] NMR characterization results of the product in step (1) are as follows: HNMR (400 MHz, CDCl.sub.3), ppm, d 5.67 (1H, m), 5.11 (2H, m), 4.46 (1H, dd, J=9.01 Hz and 7.60 Hz), 4.21 (2H, q, J=7.12 Hz), 3.92 (1H, dd, J=8.99 Hz and 7.52 Hz), 3.22 (1H, d, 8.40 Hz), 3.01 (1H, m), 2.26 (2H, m), 1.26 (3H, t, J=7.16 Hz).

(2) Preparation of the Compound with the Structural Formula of Formula III

[0060] Into a mechanically stirred 10.0 L three-necked flask were added the intermediate compound of Formula II prepared above (1.3 kg, 6.5 mol), DMF (6.5 L), water (234 mL), LiBr (677.43 g, 7.8 mol), and then heated to 140° C. to react for 12 hours. The reaction solution was dropwise added into saturated ammonium chloride (6.5 L), into which was then added methyl tert-butyl ether (2.6 L) and stirred for layering. The aqueous phase was extracted with methyl tert-butyl ether (2.6 L). The combined methyl tert-butyl ether was dried over anhydrous sodium sulfate and concentrated to get yellow oil, which was distilled in vacuum at reduced pressure (0.32 mmHg, Teb: 80-85° C.) to get white and transparent oil, that was the compound with the structural formula of Formula III, 455 g, and the yield was 55.0%.

[0061] NMR characterization results of the product in this step are as follows: HNMR (400 MHz, CDCl.sub.3), ppm δ 5.73-5.64 (m, 1H), 5.16-5.06 (m, 2H), 4.45-4.36 (m, 1H), 4.00 (dd, J=9.0, 5.8 Hz, 1H), 2.70-2.58 (m, 2H), 2.30-2.19 (m, 3H).

(3) Preparation of the Compound with the Structural Formula of Formula IV

[0062] The compound with the structural formula of Formula III prepared above (100 g, 0.79 mol) was dissolved in methanol (1.0 L), into which was added 10% of palladium on carbon. Nitrogen replacement was performed for 3 times, and hydrogen replacement was performed for 2 times. The reaction was continued at 35° C. for 6 hours. Palladium on carbon was filtered out, and the reaction was concentrated to get white and transparent oil 96.5 g, the yield was: 95.0%, ee (percentage of enantiomeric excess)>99%, see FIG. 6.

[0063] The chiral analysis method for the product in this step is as follows:

Instrument: Agilent 7890A equipped with Auto sampler, solvent: n-heptane

[0064] Chromatographic conditions are:

Column: Lipodex E, 25 meters, 0.25 mm, 1 μm film thickness or equivalent Injector
Temperature of injector: 130° C.
Injection volume: 0.4 μL

Carrier gas: Nitrogen

[0065] Airflow: 1.0 mL/min
Split ratio: 20.0

Liner: Split

[0066] Times of needle washes: 3
Run time: 74 minutes
Diluent: n-heptane
Temperature programming:

TABLE-US-00001 Temperature.slope Temperature Retention time (° C.) (° C.) (min) 0 40 2 10 200 5

Detector: 220° C.

[0067] Hydrogen flow: 30 mL/min
Airflow: 300 mL/min
Makeup flow: 30 mL/min
Data sensitivity: 20 HZ/0.01 min.

[0068] NMR characterization results of the product in this step are as follows: HNMR (400 MHz, CDCl.sub.3), ppm 4.42 (tapp, J=8.0 Hz, 1H), 3.93 (tapp, J=8.0 Hz, 1H), 2.65-2.54 (m, 2H), 2.19 (dd, J=16.3, 7.3 Hz, 1H), 1.48-1.44 (m, 2H), 1.40-1.30 (m, 2H), 0.95 (t, J=7.1 Hz, 3H).

(4) Preparation of Brivaracetam

[0069] The compound with the structural formula of Formula IV prepared above (10 g, 0.078 mol) was dissolved in toluene (100 ml), into which were added (S)-2-aminobutanamide (11.9 g, 0.117 mol) and p-toluenesulfonic acid (1.34 g), heated to reflux to repel water, and reacted for 24 hours. It was added into 50 ml water, toluene was concentrated to get yellow oil. 5 ml isopropyl acetate and 25 ml methyl tert-butyl ether were added for crystallization to get 10 g white solid, the yield was: 60%, ee (percentage of enantiomeric excess)>99%, see FIG. 7.

[0070] The chiral analysis method for the product in this step is as follows:

Model: LC-10A

Column: CHIRAL AD-H 4.6*250 mm 5 um

[0071] Mobile phase: isopropanol:n-hexane=10:90 (VN)
Detection wavelength: 220 nm
Flow rate: 0.8 ml/min
Isocratic elution: 30 min.

[0072] NMR characterization results of the product in this step are as follows: HNMR (400 MHz, CDCl.sub.3) ppm, δ 6.17 (1H, s) δ 5.34 (1H, s), δ 4.37-4.42 (1H, m), δ 3.47-3.55 (1H, m), δ 2.99-3.03 (1H, m), δ 2.45-2.52 (1H, m), δ 2.27-2.36 (1H, m), δ 2.02-2.16 (1H, m), δ 1.87-1.99 (1H, m), δ 1.63-1.73 (1H, m), δ 1.34-1.45 (2H, m), δ 1.29-1.36 (2H, m), δ ppm 0.85-0.90 (6H, m).

[0073] The above embodiments only exemplarily illustrate the principle of the present disclosure and its efficacy, and are not intended to limit the present disclosure. Anyone familiar with this technology can modify or change the above embodiments without departing from the spirit and scope of the present disclosure. Therefore, all equivalent modifications or changes made by those with ordinary knowledge in the technical field without departing from the spirit and technical ideas disclosed in the present disclosure should still be covered by the claims of the present disclosure.