DE1795209C3 - Verfahren zur Herstellung von 7-Aminocephalosporansäure aus einem Cephalosporin C-Zinkkomplex in Gegenwart von Silylierungsmitteln - Google Patents
Verfahren zur Herstellung von 7-Aminocephalosporansäure aus einem Cephalosporin C-Zinkkomplex in Gegenwart von SilylierungsmittelnInfo
- Publication number
- DE1795209C3 DE1795209C3 DE1795209A DE1795209A DE1795209C3 DE 1795209 C3 DE1795209 C3 DE 1795209C3 DE 1795209 A DE1795209 A DE 1795209A DE 1795209 A DE1795209 A DE 1795209A DE 1795209 C3 DE1795209 C3 DE 1795209C3
- Authority
- DE
- Germany
- Prior art keywords
- cephalosporin
- minutes
- zinc complex
- preparation
- aminocephalosporanic acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- HSHGZXNAXBPPDL-HZGVNTEJSA-N 7beta-aminocephalosporanic acid Chemical compound S1CC(COC(=O)C)=C(C([O-])=O)N2C(=O)[C@@H]([NH3+])[C@@H]12 HSHGZXNAXBPPDL-HZGVNTEJSA-N 0.000 title claims description 13
- 238000000034 method Methods 0.000 title claims description 8
- 239000003795 chemical substances by application Substances 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title claims 2
- TVMXJQZBKOMFQK-OOARYINLSA-L zinc;(6r,7r)-3-(acetyloxymethyl)-7-[[(5r)-5-amino-5-carboxylatopentanoyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chemical compound [Zn+2].S1CC(COC(=O)C)=C(C([O-])=O)N2C(=O)[C@@H](NC(=O)CCC[C@@H](N)C([O-])=O)[C@@H]12 TVMXJQZBKOMFQK-OOARYINLSA-L 0.000 title description 7
- HOKIDJSKDBPKTQ-GLXFQSAKSA-N cephalosporin C Chemical compound S1CC(COC(=O)C)=C(C(O)=O)N2C(=O)[C@@H](NC(=O)CCC[C@@H](N)C(O)=O)[C@@H]12 HOKIDJSKDBPKTQ-GLXFQSAKSA-N 0.000 claims description 14
- 238000001816 cooling Methods 0.000 claims description 8
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 claims description 8
- 239000011701 zinc Substances 0.000 claims description 8
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- -1 imide chloride Chemical class 0.000 claims description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052725 zinc Inorganic materials 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 230000007062 hydrolysis Effects 0.000 claims description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 150000003512 tertiary amines Chemical class 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 2
- 239000011260 aqueous acid Substances 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 238000003776 cleavage reaction Methods 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 230000007017 scission Effects 0.000 claims description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 45
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 33
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 30
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 22
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 11
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 235000019253 formic acid Nutrition 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000005051 trimethylchlorosilane Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 3
- 125000004185 ester group Chemical group 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229930186147 Cephalosporin Natural products 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- PQLVXDKIJBQVDF-UHFFFAOYSA-N acetic acid;hydrate Chemical compound O.CC(O)=O PQLVXDKIJBQVDF-UHFFFAOYSA-N 0.000 description 2
- 229940124587 cephalosporin Drugs 0.000 description 2
- 150000001780 cephalosporins Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 125000006239 protecting group Chemical group 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- OLRJXMHANKMLTD-UHFFFAOYSA-N silyl Chemical compound [SiH3] OLRJXMHANKMLTD-UHFFFAOYSA-N 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- 238000002211 ultraviolet spectrum Methods 0.000 description 2
- NDVMCQUOSYOQMZ-UHFFFAOYSA-N 2,2-bis(trimethylsilyl)acetamide Chemical compound C[Si](C)(C)C(C(N)=O)[Si](C)(C)C NDVMCQUOSYOQMZ-UHFFFAOYSA-N 0.000 description 1
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- JOOMLFKONHCLCJ-UHFFFAOYSA-N N-(trimethylsilyl)diethylamine Chemical compound CCN(CC)[Si](C)(C)C JOOMLFKONHCLCJ-UHFFFAOYSA-N 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- QFFVPLLCYGOFPU-UHFFFAOYSA-N barium chromate Chemical compound [Ba+2].[O-][Cr]([O-])(=O)=O QFFVPLLCYGOFPU-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- OSQPUMRCKZAIOZ-UHFFFAOYSA-N carbon dioxide;ethanol Chemical compound CCO.O=C=O OSQPUMRCKZAIOZ-UHFFFAOYSA-N 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- HVCRTPRIKAOFRG-UHFFFAOYSA-N n-methyl-2-trimethylsilylacetamide Chemical compound CNC(=O)C[Si](C)(C)C HVCRTPRIKAOFRG-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003797 solvolysis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1896—Compounds having one or more Si-O-acyl linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cephalosporin Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1232967 | 1967-09-01 | ||
| CH883268A CH517119A (de) | 1967-09-01 | 1968-06-14 | Neues Verfahren zur Herstellung von 7-Aminocephalosporansäure |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE1795209A1 DE1795209A1 (de) | 1971-12-30 |
| DE1795209B2 DE1795209B2 (de) | 1979-07-12 |
| DE1795209C3 true DE1795209C3 (de) | 1980-03-13 |
Family
ID=25703829
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1795209A Expired DE1795209C3 (de) | 1967-09-01 | 1968-08-23 | Verfahren zur Herstellung von 7-Aminocephalosporansäure aus einem Cephalosporin C-Zinkkomplex in Gegenwart von Silylierungsmitteln |
| DE1795868A Expired DE1795868C3 (de) | 1967-09-01 | 1968-08-23 | Verfahren zur Herstellung von 7-Aminocephalosporansäure aus Cephalosporin C oder seinen Salzen in Gegenwart von Silylierungsmitteln |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1795868A Expired DE1795868C3 (de) | 1967-09-01 | 1968-08-23 | Verfahren zur Herstellung von 7-Aminocephalosporansäure aus Cephalosporin C oder seinen Salzen in Gegenwart von Silylierungsmitteln |
Country Status (13)
| Country | Link |
|---|---|
| JP (3) | JPS524557B1 (da) |
| AT (1) | AT299447B (da) |
| BE (1) | BE720185A (da) |
| CH (1) | CH517119A (da) |
| CS (1) | CS159748B2 (da) |
| DE (2) | DE1795209C3 (da) |
| DK (1) | DK144701C (da) |
| ES (1) | ES357714A2 (da) |
| GB (1) | GB1244191A (da) |
| IT (1) | IT1045676B (da) |
| NL (1) | NL166263C (da) |
| SE (1) | SE364285B (da) |
| YU (2) | YU35259B (da) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54164550U (da) * | 1978-05-10 | 1979-11-17 | ||
| IL63942A (en) * | 1981-09-27 | 1988-07-31 | Zwi Schwartz | Beverage bag provided with rigid hanging means |
| JPH0420652A (ja) * | 1990-05-15 | 1992-01-24 | Tooma:Kk | 木質タイル |
| US7591219B2 (en) | 2004-05-26 | 2009-09-22 | Pamela Saha | Disposable combined squeezer/stirrer/dispenser/brewer device |
| US7849785B1 (en) | 2005-05-18 | 2010-12-14 | Pamela Saha | Disposable combined squeezer/stirrer/dispenser/brewer device with bottom cup |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK118506B (da) * | 1963-02-18 | 1970-08-31 | Ciba Geigy | Fremgangsmåde til fremstilling af 7-aminocephalosporansyre eller estere deraf. |
-
1968
- 1968-06-14 CH CH883268A patent/CH517119A/de not_active IP Right Cessation
- 1968-08-23 DE DE1795209A patent/DE1795209C3/de not_active Expired
- 1968-08-23 DE DE1795868A patent/DE1795868C3/de not_active Expired
- 1968-08-26 GB GB40708/68A patent/GB1244191A/en not_active Expired
- 1968-08-29 YU YU2024/68A patent/YU35259B/xx unknown
- 1968-08-30 DK DK419368A patent/DK144701C/da not_active IP Right Cessation
- 1968-08-30 ES ES357714A patent/ES357714A2/es not_active Expired
- 1968-08-30 NL NL6812413.A patent/NL166263C/xx not_active IP Right Cessation
- 1968-08-30 AT AT845268A patent/AT299447B/de not_active IP Right Cessation
- 1968-08-30 BE BE720185D patent/BE720185A/xx unknown
- 1968-08-30 SE SE11670/68A patent/SE364285B/xx unknown
- 1968-08-30 IT IT39408/68A patent/IT1045676B/it active
- 1968-08-30 JP JP43061852A patent/JPS524557B1/ja active Pending
- 1968-09-02 CS CS6177A patent/CS159748B2/cs unknown
-
1974
- 1974-07-01 JP JP49074387A patent/JPS5233119B1/ja active Pending
- 1974-07-11 YU YU1952/74A patent/YU36735B/xx unknown
-
1976
- 1976-02-07 JP JP51011862A patent/JPS525520B1/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| YU36735B (en) | 1984-08-31 |
| AT299447B (de) | 1972-06-26 |
| JPS524557B1 (da) | 1977-02-04 |
| JPS525520B1 (da) | 1977-02-14 |
| JPS5233119B1 (da) | 1977-08-26 |
| BE720185A (da) | 1969-02-28 |
| YU35259B (en) | 1980-10-31 |
| NL6812413A (da) | 1969-03-04 |
| DK144701B (da) | 1982-05-17 |
| YU202468A (en) | 1980-04-30 |
| DE1795209A1 (de) | 1971-12-30 |
| YU195274A (en) | 1982-06-18 |
| ES357714A2 (es) | 1970-04-01 |
| NL166263B (nl) | 1981-02-16 |
| DE1795868C3 (de) | 1981-11-12 |
| NL166263C (nl) | 1981-07-15 |
| IT1045676B (it) | 1980-06-10 |
| CH517119A (de) | 1971-12-31 |
| GB1244191A (en) | 1971-08-25 |
| DK144701C (da) | 1982-10-11 |
| DE1795209B2 (de) | 1979-07-12 |
| DE1795868B1 (de) | 1981-01-08 |
| CS159748B2 (da) | 1975-01-31 |
| SE364285B (da) | 1974-02-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OI | Miscellaneous see part 1 | ||
| OI | Miscellaneous see part 1 | ||
| OI | Miscellaneous see part 1 | ||
| C3 | Grant after two publication steps (3rd publication) |