SYNTHESIS METHOD AND APPLICATION OF METFORMIN HYDROCHLORIDE

Abstract

The present invention belongs to the field of pharmaceutical synthesis, disclosing a synthetic process and application of metformin hydrochloride, which is to take dicyandiamine and dimethylamine, after dissolving in lower alcohol, adding sodium alkoxide, mixing evenly and gradually raising the temperature for condensation reaction, after the reaction ends, adding hydrochloric acid to adjust the pH to acidic, that is, metformin hydrochloride as described. The synthetic process of metformin hydrochloride provided in this invention, reduces the energy consumption during the reaction, reduces the production cost, and reduces the difficulty of product purification. The present invention is applicable to the synthesis of metformin hydrochloride, the as synthesized metformin hydrochloride is used to prepare metformin hydrochloride sustained release tablets.

Claims

1. A synthetic method of metformin hydrochloride, The synthesis is to take dicyandiamine and dimethylamine dissolved in lower alcohol, add sodium alkoxide, after mixing evenly gradually raising the temperature for condensation reaction, after the end of the reaction, after adding hydrochloric acid to adjust the pH to acidic, that is, to obtain the said metformin hydrochloride, the reaction formula is: ##STR00004##

2. A synthetic method of metformin hydrochloride as recited in claim 1, The described gradual raising temperature was 5° C. lifting per 10 min interval, the highest raising of the reaction temperature was up to 80° C., and the lowest raising temperature of the reaction temperature was 20° C.

3. A synthetic method of metformin hydrochloride as recited in claim 2, The lower alcohols are methanol, ethanol, propanol or glycol; The sodium alkoxide is sodium methoxide or sodium ethoxide.

4. A synthetic method of metformin hydrochloride as recited in claim 1, The reaction temperature for the condensation reaction ranged from 40 to 80° C. and the reaction time ranged from 2 to 5 h.

5. A synthetic method of metformin hydrochloride as recited in claim 1, The dicyandiamide to dimethylamine molar ratio was 1:1˜1.3; The molar ratio of sodium alkoxide to dicyandiamide was 2˜2.8:1; The pH adjustment is utilizing hydrochloric acid to adjust the pH value to 1˜3.

6. One application of the synthetic process of metformin hydrochloride according to claim 1, the synthetic procedure described is for the synthesis of metformin hydrochloride; The as synthesized metformin hydrochloride was used to prepare metformin hydrochloride sustained release tablets.

7. A synthetic method of metformin hydrochloride as recited in claim 3, The reaction temperature for the condensation reaction ranged from 40 to 80° C. and the reaction time ranged from 2 to 5 h.

8. A synthetic method of metformin hydrochloride as recited in claim 2, The dicyandiamide to dimethylamine molar ratio was 1:1˜1.3; The molar ratio of sodium alkoxide to dicyandiamide was 2˜2.8:1; The pH adjustment is utilizing hydrochloric acid to adjust the pH value to 1˜3.

9. A synthetic method of metformin hydrochloride as recited in claim 3, The dicyandiamide to dimethylamine molar ratio was 1:1˜1.3; The molar ratio of sodium alkoxide to dicyandiamide was 2˜2.8:1; The pH adjustment is utilizing hydrochloric acid to adjust the pH value to 1˜3.

10. One application of the synthetic process of metformin hydrochloride according to claim 2, the synthetic procedure described is for the synthesis of metformin hydrochloride; The as synthesized metformin hydrochloride was used to prepare metformin hydrochloride sustained release tablets.

11. One application of the synthetic process of metformin hydrochloride according to claim 3, the synthetic procedure described is for the synthesis of metformin hydrochloride; The as synthesized metformin hydrochloride was used to prepare metformin hydrochloride sustained release tablets.

12. One application of the synthetic process of metformin hydrochloride according to claim 4, the synthetic procedure described is for the synthesis of metformin hydrochloride; The as synthesized metformin hydrochloride was used to prepare metformin hydrochloride sustained release tablets.

13. One application of the synthetic process of metformin hydrochloride according to claim 5, the synthetic procedure described is for the synthesis of metformin hydrochloride; The as synthesized metformin hydrochloride was used to prepare metformin hydrochloride sustained release tablets.

Description

BRIEF DESCRIPTION OF THE FIGURES

[0024] The invention is further detailed below in combination with the drawings and specific examples.

[0025] FIG. 1 is the ion chromatogram of metformin hydrochloride A1 as synthesized in example 1 of the present invention.

SPECIFICALLY IMPLEMENTED

[0026] The preferred examples of the invention are illustrated below in combination with the drawings. It is understood that the preferred examples described here are intended solely to illustrate and understand the invention and are not intended to qualify the invention.

Example 1 a Synthetic Procedure for Metformin Hydrochloride A1

[0027] The present example provides a synthetic method of metformin hydrochloride A1, which is synthesized by weighing 16.8 g dicyandiamine added to 50 ml methanol dissolved, after stirring evenly, 9.1 g dimethylamine added, after stirring dissolved, 27 g sodium methoxide added, ramped 5° C. every ten minutes to the reaction temperature of 30° C., incubated and stirred for 5 h, a small amount of the reaction liquid was taken after 5 h, diluted and the reaction progress was monitored using ion chromatography, The ion peak of dicyandiamide disappeared and a new peak appeared, and the molecular weight was 130.17 (M+), this peak was the ion peak of metformin, that is, the end of the reaction, after the end of the reaction, concentrated methanol to dryness, the remaining material cooled to room temperature, 50 ml of purified water was added dropwise, 15 ml of hydrochloric add at a concentration of 38% was added to adjust the pH to 3, after mixing and stirring, another 200 ml of ethyl acetate was added, after mixing and stirring for 20 min, Layering on standing, recovery of concentrated organic phase, drying over anhydrous sodium sulfate, which can be used for the next synthesis; The obtained aqueous phase, distilled under reduced pressure until the volume of the remaining solution was one-fifth of the volume of the original aqueous phase, and the temperature of the remaining solution was reduced to room temperature, 180 mL concentration of 80% ethanol was added, mixed evenly, stop stirring, put in a freezer, low temperature crystal removal, and filtered under an ice water bath, the cake was dissolved again into 20 ml of purified water, 100 g of activated carbon was added, stirred for 10 min decolorization, After filtration, the cake was cleaned with 20 ml of purified water, 120 ml of ethanol at a concentration of 80% was added again, and after mixing was homogeneous, the crystal was crystallized at low temperature for 7 h, filtered, and the cake was dried, that is, 31.7 g of metformin hydrochloride A1 was obtained in 96.3% yield. Its reaction formula is:

##STR00003##

[0028] A small amount of dried metformin A1 hydrochloride was taken, diluted by dissolving in acetonitrile, and examined by ion chromatography, the purity of metformin A1 hydrochloride was 99.1%, and the obtained ion chromatogram was shown in FIG. 1.

Example 2˜4 Synthetic Procedure for Metformin Hydrochloride A2˜A4

[0029] Examples 2˜4 provide metformin hydrochloride A2˜A4 is synthesized essentially the same as example 1 except only part of the process parameters are different, and the specific process parameters are shown in Table 1.

TABLE-US-00001 TABLE 1 table of specific process parameters of metformin hydrochloride A2~A4 Examples process parameters 2 3 4 Lower alcohols (ml) Ethanol   60   Propanol 100     Glycol     80 Sodium alkoxide (g) Sodium methoxide 8.1 30.24   Ethanolic sodium 17.3   32.91 Condensation reaction Temperature (° C.) 40 65 80 Time (h) 4 2 3 Dicyandiamide to dimethylamine molar ratio 1:1.18 1:1.24 1:1.3 Molar ratio of sodium alkoxide to dicyandiamide 2:1 2.8:1 2.42:1 Reaction pH 2.4 3 1.3 The resulting metformin Marked serial number A2 A3 A4 hydrochloride Yield (%) 94.5 93.2 92.8 Purity (%) 98.9 99.4 99.0

[0030] All other parameters are identical to example 1.

Synthesis of Metformin Hydrochloride by the Melt to Ratio 1 Method

[0031] Weighed 16.8 g dicyandiamine and 16.2 g dimethylamine hydrochloride into the reaction vessel, heated to 210° C., after reaction 2 h, samples were sent for inspection, the obtained test results appeared in the same position and the same molecular weight absorption peak of metformin hydrochloride in example 1, but the test map contains more impurity peaks, after the treatment of metformin hydrochloride in 82.1% yield, 95.4% purity.

Metformin Hydrochloride was Synthesized by the Vehicle to Ratio 2

[0032] Weigh 16.8 g dicyandiamine and 16.2 g dimethylamine hydrochloride into the reaction vessel, add toluene after dissolving, heat to 150° C., after reaction for 2 h, sample for inspection, the obtained detection results appear in the same position and the same molecular weight ion peak as the ion peak of metformin hydrochloride in example 1, but the measured purity is not high, dilute after injection into the liquid chromatograph detection, The solvent peak of toluene in the obtained spectra was obvious, after cooling, concentrating, adding anhydrous ethanol crystallization, filtering, sampling for inspection, the solvent peak of toluene in the obtained results still obvious, repeatedly washed with anhydrous ethanol 5 times, each wash with anhydrous ethanol 200 ml, the toluene solvent peak in the detection results disappeared, the purity of the obtained metformin hydrochloride was 98.3%, the yield was 91.3%.

Comparison of the Synthesis Conditions of Metformin Hydrochloride at Ratio 3 1{circle around ( )}

[0033] The synthetic process of metformin hydrochloride provided in this pair of ratios is essentially the same as example 1 except that the reaction temperature is different and the specific reaction temperature is shown in Table 2.

TABLE-US-00002 TABLE 2 synthetic reaction temperature table for metformin hydrochloride Reaction Purity Sequence Temperature (° C.) Yield (%) (%) Phenomenon 1  30 47.2 64.7 There was more residue of raw materials and almost no metformin hydrochloride in the detected spectra 2 180 80.3 94.5 Solvent reduction was rapid, side reactions increased, and impurity peaks increased in the detection profiles

Versus Synthetic Conditions for Ratio 4 Metformin Hydrochloride {circle around (2)}

[0034] The synthetic procedure for metformin hydrochloride as provided in this pair of ratios is essentially the same as example 1 except that the synthesis is carried out by heating directly (i.e., rapidly or at a rate of 1° C./min or higher) to 70° C. during the heating process, a large number of bubbles are generated in the reaction liquid, and part of the reaction liquid spills out from the mouth of the reaction vessel, meanwhile a thermometer shows that the reaction liquid has risen rapidly, After explosion-proof plate was added, the reaction was closed after 2 h, and after the reaction liquid was cooled and no more vigorous bubbling, samples were sent for examination, and no metformin hydrochloride was produced in the resulting patterns.

Preparation of Sustained Release Tablets of Metformin Hydrochloride for Application

[0035] Metformin hydrochloride sustained release tablets were prepared by randomly selecting one of the synthesized metformin hydrochloride A1˜A4 from examples 1 to 4, and the specific preparation was as follows:

1) Crushing Sieving

[0036] Metformin hydrochloride, sodium carboxymethyl cellulose were crushed through an 80 mesh sieve before dosing production; Hydroxypropyl methylcellulose k100m, microcrystalline cellulose, hydroxypropyl methylcellulose E5 through a 60 mesh sieve, the rest of the material was directly weighed for use.

2) Granulation

[0037] Mixing: add the sieved metformin hydrochloride, sodium carboxymethyl cellulose to the boiling dry granulator, fan set 35 Hz, do not open heat, and mix for 10 min.

[0038] Granulation: set the fan frequency to 35 Hz, inlet temperature 80.0° C., set the atomization pressure 0.35 MPa for the inner layer and 0.30 MPa for the outer layer (or 0.05 MPa larger for the inner layer but not less than 0.2 MPa for the outer layer), set the feed rate 300 R/min, and start the spray granulation when the material temperature reaches 45° C.±5° C. and lift it every 5 min for 25 R. When the feed frequency reaches 450 R/min, until the end of the water spray and the material temperature reaches 42.0±2° C. then the pan drops to observe the material granulation. The total amount of water spray used in granulation here was 85 kg.

[0039] Second spray: without turning on hot air, set the fan frequency at 40 Hz and the water supply frequency at 500 R/min to spray wet the material. The fan frequency determines the drying rate, and the supply frequency determines the spray rate. The total amount of water to be sprayed on the second time is ¼ ˜½ of the amount to be sprayed on mixing the pellets.

[0040] Mixing: draw ⅓ of the prescribed amount of hydroxypropyl methylcellulose k100m into a boiling dry granulator and mix to dry for 5-10 min.

[0041] Whole grain: charge prescribed amount of silica into the mass compartment for whole grain using a lifting flip integrator with a 1.5 mm screen installed by the whole grain, push the boiling dryer's bin under the dry integrator, tighten the 6 coupling screws of the coupling barrel cover and seal after tightening; After pushing the bin cart away, operating the elevator flips the bucket 180° and rises to the appropriate height. Advance the 1000 l mixing tank so that the mixing bucket outlet is aligned to the inlet of the dry homogenizer, the outlet of the dry homogenizer is aligned to the mixing tank orifice and secured with a hose. Start the pellet. Set the whole grain rotation rate at 10 Hz. Open the barrel lid outlet knob and perform a full pelletization. After the end of the whole pellet ejection, close the barrel cap outlet knob and stop the whole pellet.

3) Total Admixture

[0042] Open the mixer hopper cover and add the remaining prescribed amounts of hydroxypropyl methylcellulose k100m, hydroxypropyl methylcellulose E5, microcrystalline cellulose and magnesium stearate into the mass chamber, pour the whole completed pellets, close and pinch the hopper cover, set the mixing time to 25 min, the mixing speed to 10 R/min and press the blend button to start mixing. After mixing, the intermediate pellet was sent for inspection at the fill port sampling volume.

4) Press

[0043] Formulate the stress tablet weight according to the content of intermediate granules, install 19 mm*9 mm metformin hydrochloride sustained release tablets special shape punch for tableting, tablet hardness is controlled at 170n˜200N, friability should not exceed 0.8%.

5) Blister Packing

[0044] Select 8/plate or 10/plate molds for packaging. Collect the intermediate product, PVC and aluminum foil, install the forming mold, heat sealing mold, print mold, punch planting mold, set up the fully automatic high-speed blister packaging machine air pressure 0.6 MPa˜0.8 MPa, upper and lower forming mold temperature 120˜140° C., heat sealing temperature 200° C.˜240° C., 20˜45 Hz punch speed, for packaging, i.e., metformin hydrochloride sustained release tablets M.

[0045] Stability Test of Extended Release Form of Metformin Hydrochloride in Experimental Cases

[0046] According to the method of preparing metformin hydrochloride sustained release tablets provided in the application example, D1, D2 of the synthesized metformin hydrochloride sustained release tablets in ratios 1-2; Metformin hydrochloride sustained release tablets (Qingdao Yellow Hai Pharmaceutical Co., Ltd.) were procured as metformin hydrochloride sustained release tablets D3

[0047] Test methods: stability test inspections were performed with reference to the second part of the Chinese Pharmacopoeia, 2015

[0048] Test conditions:

[0049] Long term test temperature: 25±2° C.;

[0050] Long term test humidity: rh60±10%;

[0051] Long term trial study duration: 0, 3, 6, 9, 12, 18, 24 months

[0052] The test results are shown in Table 3.

TABLE-US-00003 TABLE 3 Table of results of stability test of sustained release tablets of metformin hydrochloride. Metformin Metformin Metformin Metformin hydrochloride hydrochloride hydrochloride hydrochloride sustained release sustained release sustained release sustained release tablets M tablets D1 tablets D2 tablets D3 Month Impurity content (%) Impurity content (%) Impurity content (%) Impurity content (%)  0 0.61 4.6 1.7 0.81  3 0.63 4.65 1.76 0.83  6 0.67 4.69 1.79 0.86  9 0.71 4.71 1.82 0.88 12 0.73 4.74 1.86 0.9 18 0.75 4.78 1.90 0.93 24 0.77 4.86 2.02 0.95 Total increment 0.16 0.26 0.32 0.14 of impurities (%)

[0053] Our results showed that metformin hydrochloride sustained-release tablets prepared from metformin hydrochloride by using the synthesis method provided in the present work exhibited a small impurity increment of only 0.16% during 24 months of standing, which was superior to metformin hydrochloride sustained-release tablets D1 and D2 and similar to the stability of commercially available metformin hydrochloride sustained-release tablets D3.

[0054] It is required that said above be used only for preferred examples of the invention and are not intended to restrict the invention, although the invention is elaborated with reference to the above examples, which for those skilled in the art can still be modified with respect to the technical schemes documented for each of the above examples, or with equivalent replacement for portions of the technical features there in. Any modifications, equivalent replacements, refinements, etc. made shall be included within the spirit and principles of the invention.