![]() Method of producing thermally stable crystalline sulfuric acid-additive salts of 7-/-alpha-(2-aminot
专利摘要:
The invention relates to heterocyclic compounds, in particular to the preparation of a thermally stable crystalline addition salt with 7- [α- (2-aminothiazol-4-yl) -α- (Z) methoxyiminoacetamido] -3 - [(1-methyl -1-pyrrolidinio) -methyl] -3-cephem-4-carboxylate, having a diffraction X-ray lattice, removed for powder on a copper tube with a nickel filter (CU: NI) with specific values of interplanar spacing D and relative intensities 1 / 1 °, which can be used in medicine. The goal is to develop a method for obtaining a new crystalline form of a cephalosporin antibiotic. The production of the target product is carried out by the reaction of amphoteric 7- [α- (2-aminothiazol-4-yl) -α- (Z) -methoxyiminoacetamido] -3 - [(1-methyl-1-pyrrolidinio) methyl] -3-cephem- 4-carboxylate with a concentration of 100-200 mg / ml with H 2 SO 4 (1-2 mol. Eq.) In an aqueous medium. The crystallization of the desired product from the reaction mixture is then initiated and recovered. 1 tab. 公开号:SU1516013A3 申请号:SU864027914 申请日:1986-08-04 公开日:1989-10-15 发明作者:А.Каплан Муррей;В.Худима Томас;А.Липпер Роберт 申请人:Бристоль-Мейерз Компани (Фирма); IPC主号:
专利说明:
1.5 g of amphoteric ions are slowly added to 10 ml of energetically stirred 1 N, sulfuric acid solution (1.59 mol eq) at 20-26 ° C. A solution is obtained. Then, the crystallization is initiated by means of a seed using a crystalline sulfuric acid addition salt, and the crystalline mass is held in the form of a slurry for 0.5 h. Next, the crystals are separated by vacuum filtration, washed with 3 ml of acetone: water (1: 1 by volume) and two servings of 5 ml of acetone; then vacuum sugoku is performed at 40-50 ° overnight, The yield is 1.3 g of the sulfuric acid addition salt. Elemental analysis Calculated,%: C 39-, 44; And 4.53; N 14.52; S -16.62; - not detected . Found,%: C 38.91; H 4.57; N 14.64; S 16.71; 1.42. Example 2. Obtaining additive sulfuric acid, 1.5 g of amphoteric ions are dissolved in 5 ml of water; B, the resulting solution is added with stirring 5 ml of 1 M solution of HjiSO4. Then, the crystallization is initiated by priming the crystalline acid addition salt, then the crystals are incubated in hplame for 0.5 h. Then the crystals are separated by vacuum filtration, washed with 3 ml of a mixture of acetone: water (1: 1 by volume) and two portions 5 ml of acetone; then dried under vacuum at 40-50 ° C overnight. The yield is 1.3 g of the sulfuric acid addition salt. X-ray diffraction grating of crystalline sulfate salt (- (2-aminothiazol-4-yl) -o / - (E) -methoxyminoacetamido D-3 (1-methyl-1-pyrrolidino) -methyl -: Z-cepham-4- the carboxylate prepared according to examples 1 and 2 was determined using a diffractometer for powdered Rigaku materials using a copper tube, a nickel filter and a sample contained in a glass cup as x-ray targets. The scan rate was 2 / min in the field of change from four 40, while mechanically recording 0 five 0 five 0 five 0 five The diagram was drawn in order to fix the angles with the maximum diffraction. On the basis of these data, the intervals (d) and relative intensities (1/1 °) were determined. These data are given below, d-intercept | А 1/1 °,% 9,20100 6.8950 5.5028 5.0922 4.5038 4,4144 4.1964 3.7838 3.6444 3.3925 3.3131 3.1547 Example 3. The study of stability at elevated temperatures. The thermal stability was determined by storing the compositions in dry containers at different temperatures, and the change in efficiency was determined using HPLC, The results are presented in the table. (The increase in efficiency is indicated by a plus sign in front of a number; a loss of efficiency of less than 10% for 2-4 weeks at 45-56 C generally indicates a decrease in efficiency of less than 10% for 2-3 years with room temperature) Example 4, Testing physical mixtures. Physical mixtures were obtained from a crystalline sulfuric acid addition salt with trisodium orthophosphate, sodium bicarbonate, L (+) - lysine and L () - arginine. The bases were added in such proportions as to ensure that the pH of the mixture was diluted with water until amphoteric ions activity was 250 mg / kg (as determined by HPLC) in the following limits: trisodium orthophosphate (pH 6.0); sodium bicarbonate (pH 6.0); Lr - (- f) - lysine (pH 6.0); L - (+) - arginine (pH 6.0 /, Injection compositions of wages using sterile water to bring amphoter5 activity 1516013, 6 ions up to 250 mg / ml, which op-d, A Determined by HPLC, Difficulties. 9.20 100 with solubility was not 50 Injections were performed (at a dose of 100 mg / kg) 5.50 28 by intramuscular method to rabbits, 5.09 22 while the pain was 4.50 38 allowable limits. Minimum4,44 A4 pain sensations observed at 4,19 63 the use of a composition containing ar-S 3.78 38 ginin, 3.64 4A
权利要求:
Claims (1) [1] Claim 3 3,39 25 The method of obtaining thermally Sta-3,31 31 bil crystalline additive3,15, 47 salts with sulfuric acid. - (2-ami-15 characterized in that notiazol-4-yl) -o (- (2) -methoxyimino-in the aquatic environment of amphotsrgay 7-CC / - (2-acetamido-3- (1-methyl-1-pyrrolidi-aminothia-4-yl) (7) -methoxyimino -methyl-3-cephem-4-carboxylate, noacetamido / -3-C (1 -methyl-1-pyroreuting the following. X-lidinio-methyl-3-cephem-4-carboxygen diffraction grating, taken for powder 20 lats with a concentration of 100-200 mg / ml on a copper tube with a nickel filter (Cu: Ni) with the following values of interplanar distances d and relative intensities Comparative data on thermal stability of amorphous and crystalline additive salt with sulfuric acid Loss Form at storage (%) at a temperature, ° С 4556 100 week days 112G41b ll2 | 4 1 Amphoteric ions 3751 71 - 57 - - 100 H ZO-salt 2.43 +5 1.4 5 + 3 O 0-10 Up to + 5 + 6 + 6 Compiled by Z. Latypova Editor L. Veselovska Tehred A. Kravchuk Corrector L. Patay - .. ",.". ".-.----" ...------- .------ ------------------ I Order 6299/59 Circulation 352Subscription BHHHTPi State Committee for Inventions and Discoveries at the State Committee on Science and Technology of the USSR 113035, Moscow, Zh-35, 4/5 Raushsk nab. Production and publishing plant Patent, Uzhgorod, st. Gagarin, 101 enter into interaction with sulfuric acid, taken in an amount of 1–2 mol eq, then initiate the crystallization of the target product from the reaction mixture and isolate it.
类似技术:
公开号 | 公开日 | 专利标题 SU1516013A3|1989-10-15|Method of producing thermally stable crystalline sulfuric acid-additive salts of 7-/-alpha-|-alpha-|-methoxyiminoacetamido/-3-/|-methyl/-3-cephem-4-carboxylate US4910301A|1990-03-20|Cefepime cephalosporin salts RU1787158C|1993-01-07|Method of cephem compound or theirs additive salts with acids synthesis CS244940B2|1986-08-14|Production method of /s/-epimeres of esters of 7beta-malonamido -7alfa-methoxy-3-tetrazolythiomethyl-1-dethia-loxa-3-cefem-4-carboxyl acid KR910000420B1|1991-01-25|Process for preparing crystalline cephem-acid addition salts CS258143B2|1988-07-15|Method of crystalline solavate production AU621040B2|1992-03-05|Crystallized cephem-acid addition salts, and a process for the preparation thereof AU2006300882B2|2012-05-03|Crystalline sodium salt of cephalosporin antibiotic US4727070A|1988-02-23|3-Propenzl cephalosporin isomer separation process and derivative US5409918A|1995-04-25|Crystalline cephem acid addition salts and process for their preparation US5244891A|1993-09-14|Injectable compositions of cefepime dihydrochloride hydrate US4994451A|1991-02-19|Cephalosporin salts and injectable compositions JPS60120886A|1985-06-28|Crystal of cephemcarboxylic acid sodium salt SU925251A3|1982-04-30|Process for producing d-configuration crystalline form of sesquisalt of sodium 7beta-[alpha-carboxy-alpha-| acetamido-7-alpha-methoxy-3-| thiomethyl-2-oxadethia-3-cefem-4-carboxyate EP0166580A2|1986-01-02|Improvements in or relating to ceftazidime US4124762A|1978-11-07|7-[|phenyl]acetamido-cephalosporin derivatives IE48572B1|1985-03-06|Production of sodium cefamandole SU571187A3|1977-08-30|Method of obtaining derivatives of 2-aminomethyl-4,6-digahaloidophenol derivatives KR820000142B1|1982-02-20|Process for preparing novel penicillin and cephalosporin derivatives PL51904B1|1966-06-25|
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引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 JPS55151588A|1979-05-14|1980-11-26|Takeda Chem Ind Ltd|Preparation of cephalosporin salt crystal| US4406899A|1982-03-04|1983-09-27|Bristol-Myers Company|Cephalosporins| CA1213882A|1982-03-04|1986-11-12|Jun Okumura|Cephalosporins| US4525473A|1983-03-30|1985-06-25|Bristol-Myers Company|Cephalosporins| DE3419015A1|1984-05-22|1985-11-28|Bayer Ag, 5090 Leverkusen|METHOD FOR PRODUCING CEPHALOSPORINES| GB8424692D0|1984-10-01|1984-11-07|Glaxo Group Ltd|Chemical compounds| GB2165245B|1984-10-01|1988-05-25|Glaxo Group Ltd|Chemical compounds|US4883868A|1984-12-27|1989-11-28|Banyu Pharmaceutical Co., Ltd.|7-amino-3-methyl-3-cephem derivatives| US4959469A|1984-12-27|1990-09-25|Banyu Pharmaceutical Company, Ltd.|Crystalline cephalosporin compounds| US4910301A|1985-08-05|1990-03-20|Bristol-Myers Company|Cefepime cephalosporin salts| US5244891A|1985-08-05|1993-09-14|Bristol-Myers Squibb Company|Injectable compositions of cefepime dihydrochloride hydrate| US4808617A|1985-12-18|1989-02-28|Bristol-Myers Company|Lyophilized or precipitated cephalosporin zwitterion and salt combination| KR950010084B1|1987-06-25|1995-09-06|반유세이야꾸 가부시끼가이샤|The preparing process for crystallic cephal sporin compounds| JPH02101081A|1988-10-08|1990-04-12|Meiji Seika Kaisha Ltd|Crystalline dihydrochloride of cephalosporin derivative and production thereof| CA2011116C|1989-03-06|1999-11-16|Murray A. Kaplan|Lyophilized bmy-28142 dihydrochloride for parenteral use| CA2101571A1|1992-09-08|1994-03-09|Elizabeth A. Garofalo|Crystalline dihydrate of a cephalosporin dihydrate salt and injectable compositions thereof| EP0638573A1|1993-08-10|1995-02-15|Lucky Ltd.|Crystalline hydrates of cephalosporin and process for preparation thereof| ES2298850T3|2003-12-23|2008-05-16|Sandoz Gmbh|PROCESS FOR THE PRODUCTION OF INTERMEDIATES TO USE IN THE SYNTHESIS OF CEPHALOSPORINE.| WO2008056221A2|2006-11-06|2008-05-15|Orchid Chemicals & Pharmaceuticals Limited|Crystalline sulfate salt of cephalosporin antibiotic| DE102012101680A1|2012-02-29|2013-08-29|Aicuris Gmbh & Co. Kg|Pharmaceutical preparation containing an antiviral dihydroquinazoline derivative|
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