NO116250B - - Google Patents
Info
- Publication number
- NO116250B NO116250B NO157554A NO15755465A NO116250B NO 116250 B NO116250 B NO 116250B NO 157554 A NO157554 A NO 157554A NO 15755465 A NO15755465 A NO 15755465A NO 116250 B NO116250 B NO 116250B
- Authority
- NO
- Norway
- Prior art keywords
- nitro
- furyl
- imidazo
- dihydro
- thiadiazine
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 5
- 239000011707 mineral Substances 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 4
- 230000000845 anti-microbial effect Effects 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- QVUZWDCOZDRQDD-UHFFFAOYSA-N 1-aminoimidazolidine-2-thione Chemical compound NN1CCNC1=S QVUZWDCOZDRQDD-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000588724 Escherichia coli Species 0.000 description 2
- 241000191967 Staphylococcus aureus Species 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000186810 Erysipelothrix rhusiopathiae Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 241000588915 Klebsiella aerogenes Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 241000607142 Salmonella Species 0.000 description 1
- 241000193985 Streptococcus agalactiae Species 0.000 description 1
- 241000193996 Streptococcus pyogenes Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- HMKCSFHWMJHMTG-UHFFFAOYSA-N bis(furan-2-yl)methanone Chemical compound C=1C=COC=1C(=O)C1=CC=CO1 HMKCSFHWMJHMTG-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- -1 halogen hydrogen salt Chemical class 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- IAIWVQXQOWNYOU-FPYGCLRLSA-N nitrofural Chemical class NC(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 IAIWVQXQOWNYOU-FPYGCLRLSA-N 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US358656A US3277082A (en) | 1964-04-09 | 1964-04-09 | 6, 7-dihydro-3-(5-nitro-2-furyl) imidazo[2, 1-b]-1, 3, 4-thiadiazine and salts thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO116250B true NO116250B (pt) | 1969-02-24 |
Family
ID=23410533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO157554A NO116250B (pt) | 1964-04-09 | 1965-04-06 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3277082A (pt) |
| AT (1) | AT248425B (pt) |
| BE (1) | BE662274A (pt) |
| BR (1) | BR6568571D0 (pt) |
| CH (1) | CH443326A (pt) |
| DE (1) | DE1620071A1 (pt) |
| DK (1) | DK106974C (pt) |
| ES (1) | ES311004A1 (pt) |
| FR (2) | FR1590062A (pt) |
| GB (1) | GB1088472A (pt) |
| IL (1) | IL23143A (pt) |
| NL (2) | NL6504296A (pt) |
| NO (1) | NO116250B (pt) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH457458A (de) * | 1965-12-29 | 1968-06-15 | Agripat Sa | Verfahren zur Herstellung von Tetrahydro-1,3,5-thiadiazin-2-thionen und ihre Verwendung als Mikrobizide |
| DE3702757A1 (de) * | 1987-01-30 | 1988-08-11 | Hoechst Ag | Neue imidazo- und triazolo-thiadiazine, verfahren zu ihrer herstellung, die sie enthaltenden arzneimittel und ihre verwendung, sowie einige bei der herstellung der genannten verbindungen gebildete zwischenprodukte |
-
0
- NL NL123292D patent/NL123292C/xx active
- BE BE662274D patent/BE662274A/xx unknown
-
1964
- 1964-04-09 US US358656A patent/US3277082A/en not_active Expired - Lifetime
-
1965
- 1965-03-11 IL IL23143A patent/IL23143A/en unknown
- 1965-03-25 ES ES0311004A patent/ES311004A1/es not_active Expired
- 1965-04-01 GB GB13940/65A patent/GB1088472A/en not_active Expired
- 1965-04-02 DK DK171865AA patent/DK106974C/da active
- 1965-04-05 BR BR168571/65A patent/BR6568571D0/pt unknown
- 1965-04-05 NL NL6504296A patent/NL6504296A/xx unknown
- 1965-04-06 NO NO157554A patent/NO116250B/no unknown
- 1965-04-06 CH CH475865A patent/CH443326A/de unknown
- 1965-04-07 DE DE19651620071 patent/DE1620071A1/de active Pending
- 1965-04-07 AT AT319665A patent/AT248425B/de active
- 1965-04-08 FR FR1590062D patent/FR1590062A/fr not_active Expired
- 1965-06-11 FR FR20380A patent/FR4441M/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ES311004A1 (es) | 1965-10-01 |
| AT248425B (de) | 1966-07-25 |
| US3277082A (en) | 1966-10-04 |
| IL23143A (en) | 1968-12-26 |
| FR4441M (pt) | 1966-09-19 |
| NL123292C (pt) | |
| CH443326A (de) | 1967-09-15 |
| NL6504296A (pt) | 1965-10-11 |
| FR1590062A (pt) | 1970-04-13 |
| BR6568571D0 (pt) | 1973-08-07 |
| DK106974C (da) | 1967-04-10 |
| DE1620071A1 (de) | 1969-12-11 |
| BE662274A (pt) | |
| GB1088472A (en) | 1967-10-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1445154C3 (de) | 1,4-Dihydro-1,8-naphthyridinderi vate und ein Verfahren zu ihrer Herstellung | |
| DK164914B (da) | Fremgangsmaade til udvinding af vancomycin i form af et krystallinsk salt fra en vandig oploesning af vancomycin samt krystallinsk vancomycin-diphosphat opnaaet ved fremgangsmaaden | |
| US3632806A (en) | Novel n - pyridylmethylidene - homo-cysteine thiolactone compound and the preparation thereof | |
| DE3419012A1 (de) | Ss-lactamantibiotika, verfahren zu deren herstellung sowie ihre verwendung als arzneimittel oder wachstumsfoerderer in der tieraufzucht oder als antioxidantien | |
| NO116250B (pt) | ||
| JPS60126284A (ja) | ピリドンカルボン酸誘導体およびその塩 | |
| DE1667893A1 (de) | Neue Anthelminthica | |
| NO157554B (no) | Anordning for transport av sammenkjedede patroner fra et magasin til et automatvaapen, saerlig for bruk i kanontaarn. | |
| US3230214A (en) | Preparation of 6-aminoacylpenicillanic acids | |
| NO138026B (no) | Analogifremgangsm}te til fremstilling av terapeutisk aktive n-benzhydryl-n`-p-hydroksybenzylpiperaziner | |
| NO763600L (pt) | ||
| CH521374A (de) | Verfahren zur Herstellung von 7-(a-(4-Pyridylthio)-acetamido)- 3-cephem-4-carbonsäuren | |
| US3574201A (en) | 5-nitrofuryl-1,2,4-oxadiazine derivatives | |
| SU988814A1 (ru) | Соли оротовой кислоты и @ -аминокислот, предупреждающие развитие утомлени при физических нагрузках | |
| US2574155A (en) | Substituted amino-nitroheterocycles and methods of preparing the same | |
| SU306669A1 (ru) | Способ очистки эритромицина | |
| US4016272A (en) | Anthelmintic thiodiphenylamine cupric chloride complex salt | |
| NO147383B (no) | Fremgangsmaate for fremstilling av 2-(karbamoyl)-fenyl-2-acetoksybenzoat. | |
| Leigh | 664. N-alkyl derivatives of penicillin V | |
| US2594265A (en) | Xesije percy waijljs | |
| Elliott et al. | 20. Bacteriostasis in the amino-acid series. Part I. Derivatives of alanine | |
| US3660384A (en) | 5-(2-(5-nitro-2-furyl)vinyl)picolinohydroxamic acid | |
| NO161102B (no) | Lokkemat for gnagere omfattende foede og en gift. | |
| NO152436B (no) | Haarfargemiddel | |
| US4029768A (en) | Composition for application to the animal brain for synthesis of brain components involved in the learning process, and method |