BE879666A - Nouvelles cephalosporines, leur preparation et compositions les contenant - Google Patents
Nouvelles cephalosporines, leur preparation et compositions les contenant Download PDFInfo
- Publication number
- BE879666A BE879666A BE0/197842A BE197842A BE879666A BE 879666 A BE879666 A BE 879666A BE 0/197842 A BE0/197842 A BE 0/197842A BE 197842 A BE197842 A BE 197842A BE 879666 A BE879666 A BE 879666A
- Authority
- BE
- Belgium
- Prior art keywords
- emi
- preparation
- compositions containing
- novel cephalosporins
- cephalosporins
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title description 3
- 229930186147 Cephalosporin Natural products 0.000 title description 2
- 229940124587 cephalosporin Drugs 0.000 title description 2
- 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 title 1
- 150000001875 compounds Chemical class 0.000 description 4
- 229930182555 Penicillin Natural products 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- 229940088710 antibiotic agent Drugs 0.000 description 2
- 150000002960 penicillins Chemical class 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 241000238876 Acari Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- -1 alkali metal salts Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001780 cephalosporins Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/587—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with aliphatic hydrocarbon radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms, said aliphatic radicals being substituted in the alpha-position to the ring by a hetero atom, e.g. with m >= 0, Z being a singly or a doubly bound hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cephalosporin Compounds (AREA)
Description
<EMI ID=1.1> compositions les contenant <EMI ID=2.1> <EMI ID=3.1> pénicillines. Dans certaines circonstances, souhaitable d'utiliser une céphalosporine qui fasse <EMI ID=4.1> <EMI ID=5.1> <EMI ID=6.1> <EMI ID=7.1> large spectre. - ' <EMI ID=8.1> <EMI ID=9.1> <EMI ID=10.1> <EMI ID=11.1> <EMI ID=12.1> antibiotiques type des céphalosporines dans les- <EMI ID=13.1> <EMI ID=14.1> <EMI ID=15.1> <EMI ID=16.1> <EMI ID=17.1> éventuellement substitué susmentionné est un radical <EMI ID=18.1> Quant ja;rla position 3, elle porte, parmi de nombreux . dès radicaux mono- <EMI ID=19.1> est oqu <EMI ID=20.1> -aucun <EMI ID=21.1> <EMI ID=22.1> <EMI ID=23.1> <EMI ID=24.1> <EMI ID=25.1> activité tout particulièrement avantageuse (décrite plus en détail dans la suite du présent mémoire). contre toute <EMI ID=26.1> <EMI ID=27.1> <EMI ID=28.1> <EMI ID=29.1> <EMI ID=30.1> <EMI ID=31.1> <EMI ID=32.1> par rapport au groupe car, Dans présent <EMI ID=33.1> structure comme suit : <EMI ID=34.1> <EMI ID=35.1> les conformes invention sont des isomères <EMI ID=36.1> <EMI ID=37.1> <EMI ID=38.1> <EMI ID=39.1> <EMI ID=40.1> <EMI ID=41.1> portée de l'invention s'étend aussi bien aux <EMI ID=42.1> Les composés suivant l'invention font <EMI ID=43.1> <EMI ID=44.1> <EMI ID=45.1> <EMI ID=46.1> <EMI ID=47.1> solubles (par exemple des sels métaux alcalins, <EMI ID=48.1> <EMI ID=49.1> <EMI ID=50.1> <EMI ID=51.1> M MOI, <EMI ID=52.1> <EMI ID=53.1> <EMI ID=54.1> <EMI ID=55.1> -carbone auquel ils sont attachés. <EMI ID=56.1> <EMI ID=57.1> <EMI ID=58.1> <EMI ID=59.1> <EMI ID=60.1> <EMI ID=61.1> <EMI ID=62.1> <EMI ID=63.1> <EMI ID=64.1> <EMI ID=65.1> <EMI ID=66.1> <EMI ID=67.1> <EMI ID=68.1> <EMI ID=69.1> sur un composé de la formule <EMI ID=70.1> <EMI ID=71.1> <EMI ID=72.1> <EMI ID=73.1> <EMI ID=74.1> <EMI ID=75.1> <EMI ID=76.1> <EMI ID=77.1> exemple, on peut nient chlorures <EMI ID=78.1> <EMI ID=79.1> . les réactifs en solution ou suspension. effectue avantageusement la réaction utilisant <EMI ID=80.1> <EMI ID=81.1> <EMI ID=82.1> <EMI ID=83.1> <EMI ID=84.1> <EMI ID=85.1> <EMI ID=86.1> <EMI ID=87.1> <EMI ID=88.1> <EMI ID=89.1> <EMI ID=90.1> <EMI ID=91.1> <EMI ID=92.1> <EMI ID=93.1> <EMI ID=94.1> <EMI ID=95.1> <EMI ID=96.1> <EMI ID=97.1> <EMI ID=98.1> <EMI ID=99.1> <EMI ID=100.1> <EMI ID=101.1> <EMI ID=102.1> <EMI ID=103.1> milieu non. aqueux qui comprend, préférence, -on <EMI ID=104.1> <EMI ID=105.1> <EMI ID=106.1> tant l'anion voulu, +se des composés formule <EMI ID=107.1> <EMI ID=108.1> <EMI ID=109.1> <EMI ID=110.1> <EMI ID=111.1> <EMI ID=112.1> <EMI ID=113.1> <EMI ID=114.1> <EMI ID=115.1> <EMI ID=116.1> <EMI ID=117.1> <EMI ID=118.1> <EMI ID=119.1> Pour 'utilisation titre matières <EMI ID=120.1> <EMI ID=121.1> <EMI ID=122.1> <EMI ID=123.1> On peut préparer les acides de formule <EMI ID=124.1> <EMI ID=125.1> <EMI ID=126.1> <EMI ID=127.1> (dans laquelle possède les signifierons, précitées ; <EMI ID=128.1> <EMI ID=129.1> <EMI ID=130.1> que <EMI ID=131.1> <EMI ID=132.1> <EMI ID=133.1> <EMI ID=134.1> <EMI ID=135.1> <EMI ID=136.1> <EMI ID=137.1> <EMI ID=138.1> <EMI ID=139.1> <EMI ID=140.1> <EMI ID=141.1> peuvent se préparer par acylation des composés <EMI ID=142.1> <EMI ID=143.1> <EMI ID=144.1> thiourée. <EMI ID=145.1> <EMI ID=146.1> <EMI ID=147.1> <EMI ID=148.1> <EMI ID=149.1> <EMI ID=150.1> <EMI ID=151.1> <EMI ID=152.1> <EMI ID=153.1> <EMI ID=154.1> <EMI ID=155.1> <EMI ID=156.1> <EMI ID=157.1> <EMI ID=158.1> une, minute. <EMI ID=159.1> <EMI ID=160.1> <EMI ID=161.1> <EMI ID=162.1> <EMI ID=163.1> <EMI ID=164.1> <EMI ID=165.1> <EMI ID=166.1> <EMI ID=167.1> <EMI ID=168.1> <EMI ID=169.1> ���'�.'�'â���-��� <EMI ID=170.1> les,- les séchés <EMI ID=171.1> <EMI ID=172.1> <EMI ID=173.1> <EMI ID=174.1> <EMI ID=175.1> <EMI ID=176.1> <EMI ID=177.1> <EMI ID=178.1> <EMI ID=179.1> <EMI ID=180.1> <EMI ID=181.1> <EMI ID=182.1> <EMI ID=183.1> exiger des doses quotidiennes supérieures. Les antibiotiques conformes présente <EMI ID=184.1> <EMI ID=185.1> tiques, par exemple des pénicillines d'autres . �e�s�.�.os�aa��z�es. La composition qui suit, illustre façon.. <EMI ID=186.1> <EMI ID=187.1> <EMI ID=188.1> <EMI ID=189.1> <EMI ID=190.1> <EMI ID=191.1> <EMI ID=192.1> <EMI ID=193.1> <EMI ID=194.1> <EMI ID=195.1>
Claims (1)
- <EMI ID=196.1> <EMI ID=197.1><EMI ID=198.1><EMI ID=199.1><EMI ID=200.1><EMI ID=201.1> <EMI ID=202.1><EMI ID=203.1> <EMI ID=204.1><EMI ID=205.1><EMI ID=206.1><EMI ID=207.1> <EMI ID=208.1>
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7842164 | 1978-10-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE879666A true BE879666A (fr) | 1980-04-28 |
Family
ID=10500627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE0/197842A BE879666A (fr) | 1978-10-27 | 1979-10-26 | Nouvelles cephalosporines, leur preparation et compositions les contenant |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS5559197A (fr) |
| AU (1) | AU529338B2 (fr) |
| BE (1) | BE879666A (fr) |
| ZA (1) | ZA795738B (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ZA806977B (en) * | 1979-11-19 | 1981-10-28 | Fujisawa Pharmaceutical Co | 7-acylamino-3-vinylcephalosporanic acid derivatives and processes for the preparation thereof |
| JPS584789A (ja) * | 1981-04-03 | 1983-01-11 | Fujisawa Pharmaceut Co Ltd | 新規セフエム化合物およびその製造法 |
| DE3279470D1 (en) * | 1981-04-03 | 1989-04-06 | Fujisawa Pharmaceutical Co | New cephem compounds, processes for their preparation, pharmaceutical compositions containing them and their starting compounds |
-
1979
- 1979-10-26 AU AU52239/79A patent/AU529338B2/en not_active Ceased
- 1979-10-26 JP JP13920779A patent/JPS5559197A/ja active Pending
- 1979-10-26 BE BE0/197842A patent/BE879666A/fr not_active IP Right Cessation
- 1979-10-26 ZA ZA00795738A patent/ZA795738B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZA795738B (en) | 1980-10-29 |
| JPS5559197A (en) | 1980-05-02 |
| AU5223979A (en) | 1980-05-01 |
| AU529338B2 (en) | 1983-06-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RE | Patent lapsed |
Owner name: GLAXO GROUP LTD Effective date: 19851031 |