NO134258B - - Google Patents
Download PDFInfo
- Publication number
- NO134258B NO134258B NO16709867A NO16709867A NO134258B NO 134258 B NO134258 B NO 134258B NO 16709867 A NO16709867 A NO 16709867A NO 16709867 A NO16709867 A NO 16709867A NO 134258 B NO134258 B NO 134258B
- Authority
- NO
- Norway
- Prior art keywords
- alkali metal
- ampicillin
- aminobenzylpenicillin
- methylene chloride
- solution
- Prior art date
Links
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 39
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 claims description 23
- 229910052783 alkali metal Inorganic materials 0.000 claims description 12
- -1 alkali metal salts Chemical class 0.000 claims description 12
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 159000000000 sodium salts Chemical class 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 230000001376 precipitating effect Effects 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 4
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 239000000706 filtrate Substances 0.000 claims description 3
- 238000001914 filtration Methods 0.000 claims description 3
- 150000001339 alkali metal compounds Chemical class 0.000 claims description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- 229960000723 ampicillin Drugs 0.000 description 11
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 8
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Substances [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 7
- 238000003756 stirring Methods 0.000 description 6
- 125000005270 trialkylamine group Chemical group 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 229930182555 Penicillin Natural products 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 235000009518 sodium iodide Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- MGAXYKDBRBNWKT-UHFFFAOYSA-N (5-oxooxolan-2-yl)methyl 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OCC1OC(=O)CC1 MGAXYKDBRBNWKT-UHFFFAOYSA-N 0.000 description 1
- NGHVIOIJCVXTGV-ALEPSDHESA-N 6-aminopenicillanic acid Chemical compound [O-]C(=O)[C@H]1C(C)(C)S[C@@H]2[C@H]([NH3+])C(=O)N21 NGHVIOIJCVXTGV-ALEPSDHESA-N 0.000 description 1
- NGHVIOIJCVXTGV-UHFFFAOYSA-N 6beta-amino-penicillanic acid Natural products OC(=O)C1C(C)(C)SC2C(N)C(=O)N21 NGHVIOIJCVXTGV-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- KLOHDWPABZXLGI-YWUHCJSESA-M ampicillin sodium Chemical class [Na+].C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C([O-])=O)(C)C)=CC=CC=C1 KLOHDWPABZXLGI-YWUHCJSESA-M 0.000 description 1
- 229960003311 ampicillin trihydrate Drugs 0.000 description 1
- 230000000721 bacterilogical effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 235000011132 calcium sulphate Nutrition 0.000 description 1
- 239000001175 calcium sulphate Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000012024 dehydrating agents Substances 0.000 description 1
- 150000005332 diethylamines Chemical class 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- RBKMMJSQKNKNEV-RITPCOANSA-N penicillanic acid Chemical compound OC(=O)[C@H]1C(C)(C)S[C@@H]2CC(=O)N21 RBKMMJSQKNKNEV-RITPCOANSA-N 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 150000002960 penicillins Chemical class 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB926066A GB1128235A (en) | 1966-03-03 | 1966-03-03 | Alkali metal salts of ª‡-aminobenzylpenicillin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO134258B true NO134258B (fr) | 1976-05-31 |
| NO134258C NO134258C (fr) | 1976-09-08 |
Family
ID=9868558
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO16709867A NO134258C (fr) | 1966-03-03 | 1967-03-02 |
Country Status (10)
| Country | Link |
|---|---|
| AT (1) | AT272517B (fr) |
| BE (1) | BE694859A (fr) |
| CH (1) | CH485770A (fr) |
| DK (1) | DK131290B (fr) |
| ES (1) | ES337475A1 (fr) |
| FI (1) | FI51355C (fr) |
| FR (1) | FR1512943A (fr) |
| GB (1) | GB1128235A (fr) |
| NL (1) | NL155833C (fr) |
| NO (1) | NO134258C (fr) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1465694A (en) * | 1973-05-15 | 1977-02-23 | Beecham Group Ltd | Preparation of penicillin salts |
| US4024130A (en) * | 1975-03-31 | 1977-05-17 | Pfizer Inc. | Process for the manufacture of alkali metal salts of 6-[2-phenyl-2-(imidoylaminoalkanoylamino)acetamido]penicillanic acids |
-
1966
- 1966-03-03 GB GB926066A patent/GB1128235A/en not_active Expired
-
1967
- 1967-02-22 NL NL6702734A patent/NL155833C/xx not_active IP Right Cessation
- 1967-02-28 CH CH291667A patent/CH485770A/de not_active IP Right Cessation
- 1967-03-01 BE BE694859D patent/BE694859A/xx not_active IP Right Cessation
- 1967-03-02 FI FI60967A patent/FI51355C/fi active
- 1967-03-02 ES ES337475A patent/ES337475A1/es not_active Expired
- 1967-03-02 NO NO16709867A patent/NO134258C/no unknown
- 1967-03-02 AT AT201067A patent/AT272517B/de active
- 1967-03-02 FR FR97127A patent/FR1512943A/fr not_active Expired
- 1967-03-03 DK DK112567A patent/DK131290B/da unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL6702734A (fr) | 1967-09-04 |
| NL155833C (nl) | 1982-04-16 |
| FI51355C (fi) | 1976-12-10 |
| FR1512943A (fr) | 1968-02-09 |
| NO134258C (fr) | 1976-09-08 |
| DK131290C (fr) | 1975-11-17 |
| FI51355B (fr) | 1976-08-31 |
| AT272517B (de) | 1969-07-10 |
| NL155833B (nl) | 1978-02-15 |
| BE694859A (fr) | 1967-09-01 |
| CH485770A (de) | 1970-02-15 |
| DE1670191B2 (de) | 1975-10-09 |
| DK131290B (da) | 1975-06-23 |
| DE1670191A1 (de) | 1971-03-25 |
| GB1128235A (en) | 1968-09-25 |
| ES337475A1 (es) | 1968-03-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4912211A (en) | Method for producing pure crystalline antibiotic products | |
| NO167098B (no) | Modulaer beskyttelsesstruktur for undervannsinstallasjoner. | |
| US3980637A (en) | Production of amoxicillin | |
| NO174424B (no) | Fremgangsmaate for fremstilling av dinatrium-cefodizim | |
| NO135777B (fr) | ||
| US3697506A (en) | Crystalline alkali metal salts of {60 -carboxybenzylpenicillin and process therefor | |
| NO134258B (fr) | ||
| AU674021B2 (en) | Process for the preparation of sterile beta-lactam antibiotics | |
| US3579530A (en) | Process for the resolution of racemic tetramisole | |
| NO142914B (no) | Analogifremgangsmaate for fremstilling av terapeutisk virksomme cefalosporiner | |
| US3239507A (en) | Isoxazolylpenicillin derivatives | |
| US3230214A (en) | Preparation of 6-aminoacylpenicillanic acids | |
| KR0135979B1 (ko) | 모액으로부터의 항생물질 회수방법 및 그의 약학적으로 허용할 수 있는 신규한 염 | |
| US3856779A (en) | Process for the preparation of sodium salt of ampicillin | |
| NO138375B (no) | Analogifremgangsmaate til fremstilling av terapeutisk virksomme cefalosporinderivater | |
| EP0220925A1 (fr) | Procédé de préparation du sel de sodium de l'amoxycilline | |
| RU2382790C2 (ru) | Способ получения динатриевой соли гемигептагидрата 7-{[2-аминотиазол-4-ил)-2-син-метоксиимино]ацетамидо}-3-{[(2,5-дигидро-6-гидрокси-2-метил-5-оксо-1,2,4-триазин-3-ил)тио]метил}-3-цефем-4-карбоновой кислоты | |
| US3714154A (en) | Recovery of cephalothin salts | |
| US3926958A (en) | Preparation of penicillin salts | |
| US3594366A (en) | Process for the preparation of aminoalicyclic and aminoarylalicyclic penicillins | |
| DE1670191C3 (de) | Verfahren zur Herstellung von Alkalimetallsalzen des alpha-Aminobenzylpenicillins und seiner Epimeren | |
| US3448104A (en) | Betaine penicillin derivatives | |
| US3129217A (en) | Derivatives of 6-(9-anthramido) penicillanic acid | |
| US3798212A (en) | Resolution of benzodiazepine derivatives | |
| DK159822B (da) | Fremgangsmaade til fremstilling af penicillansyrederivater |