GB1101820A - Novel polymethylene quinoxaline dioxides - Google Patents
Novel polymethylene quinoxaline dioxidesInfo
- Publication number
- GB1101820A GB1101820A GB50031/65A GB5003165A GB1101820A GB 1101820 A GB1101820 A GB 1101820A GB 50031/65 A GB50031/65 A GB 50031/65A GB 5003165 A GB5003165 A GB 5003165A GB 1101820 A GB1101820 A GB 1101820A
- Authority
- GB
- United Kingdom
- Prior art keywords
- quinoxaline
- mercapto
- cyclohepta
- cyclopenta
- tetrahydro
- 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
- -1 polymethylene quinoxaline Polymers 0.000 title abstract 6
- 125000003545 alkoxy group Chemical group 0.000 abstract 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 6
- 125000004414 alkyl thio group Chemical group 0.000 abstract 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 5
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 abstract 5
- 125000004423 acyloxy group Chemical group 0.000 abstract 4
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 229910052794 bromium Inorganic materials 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 3
- 230000003647 oxidation Effects 0.000 abstract 3
- 238000007254 oxidation reaction Methods 0.000 abstract 3
- 150000003252 quinoxalines Chemical class 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 abstract 3
- JARRIPGIULGTFR-UHFFFAOYSA-N 4-oxido-2,3-dihydro-1h-cyclopenta[b]quinoxalin-4-ium Chemical compound C1=CC=C2[N+]([O-])=C(CCC3)C3=NC2=C1 JARRIPGIULGTFR-UHFFFAOYSA-N 0.000 abstract 2
- NNHBECQTCHBZHZ-UHFFFAOYSA-N 5-oxido-7,8,9,10-tetrahydro-6h-cyclohepta[b]quinoxalin-5-ium Chemical compound C1CCCCC2=NC3=CC=CC=C3[N+]([O-])=C21 NNHBECQTCHBZHZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 230000001590 oxidative effect Effects 0.000 abstract 2
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 abstract 1
- ZAXOLBARZSUKTN-UHFFFAOYSA-N 11-oxido-7,8,9,10-tetrahydro-6h-cyclohepta[b]quinoxalin-5-ium 5-oxide Chemical compound O=[N+]1C2=CC=CC=C2N([O-])C2=C1CCCCC2 ZAXOLBARZSUKTN-UHFFFAOYSA-N 0.000 abstract 1
- ONSCFBYWENASQN-UHFFFAOYSA-N 2,3-dihydro-1h-cyclopenta[b]quinoxaline Chemical compound C1=CC=C2N=C(CCC3)C3=NC2=C1 ONSCFBYWENASQN-UHFFFAOYSA-N 0.000 abstract 1
- DRGGRKCCQQDHNB-UHFFFAOYSA-N 7,8,9,10-tetrahydro-6h-cyclohepta[b]quinoxaline Chemical compound C1CCCCC2=NC3=CC=CC=C3N=C21 DRGGRKCCQQDHNB-UHFFFAOYSA-N 0.000 abstract 1
- ZOQNRQZXPOIANN-UHFFFAOYSA-N 9-oxido-2,3-dihydro-1h-cyclopenta[b]quinoxalin-4-ium 4-oxide Chemical compound O=[N+]1C2=CC=CC=C2N([O-])C2=C1CCC2 ZOQNRQZXPOIANN-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract 1
- 150000008065 acid anhydrides Chemical class 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000002152 alkylating effect Effects 0.000 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 239000002775 capsule Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- SLOCIJOTBVAMAJ-UHFFFAOYSA-N cycloheptane-1,2-dione Chemical class O=C1CCCCCC1=O SLOCIJOTBVAMAJ-UHFFFAOYSA-N 0.000 abstract 1
- CIISBNCSMVCNIP-UHFFFAOYSA-N cyclopentane-1,2-dione Chemical class O=C1CCCC1=O CIISBNCSMVCNIP-UHFFFAOYSA-N 0.000 abstract 1
- 239000012024 dehydrating agents‎ Substances 0.000 abstract 1
- 239000003651 drinking water Substances 0.000 abstract 1
- 235000020188 drinking water Nutrition 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000007937 lozenge Substances 0.000 abstract 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 244000144977 poultry Species 0.000 abstract 1
- 230000009885 systemic effect Effects 0.000 abstract 1
- 239000003826 tablet Substances 0.000 abstract 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 abstract 1
- 210000001635 urinary tract Anatomy 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/50—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to ring nitrogen atoms
- C07D241/52—Oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Feed For Specific Animals (AREA)
- Fodder In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US46393265A | 1965-06-14 | 1965-06-14 | |
| US46393365A | 1965-06-14 | 1965-06-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1101820A true GB1101820A (en) | 1968-01-31 |
Family
ID=27040779
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB50031/65A Expired GB1101820A (en) | 1965-06-14 | 1965-11-24 | Novel polymethylene quinoxaline dioxides |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS4834632B1 (enrdf_load_stackoverflow) |
| BE (1) | BE682444A (enrdf_load_stackoverflow) |
| BR (1) | BR6680318D0 (enrdf_load_stackoverflow) |
| CH (1) | CH570383A5 (enrdf_load_stackoverflow) |
| DE (1) | DE1620134A1 (enrdf_load_stackoverflow) |
| FR (1) | FR6061M (enrdf_load_stackoverflow) |
| GB (1) | GB1101820A (enrdf_load_stackoverflow) |
-
1965
- 1965-11-24 GB GB50031/65A patent/GB1101820A/en not_active Expired
-
1966
- 1966-06-11 DE DE19661620134 patent/DE1620134A1/de active Pending
- 1966-06-13 BR BR180318/66A patent/BR6680318D0/pt unknown
- 1966-06-13 CH CH847866A patent/CH570383A5/de not_active IP Right Cessation
- 1966-06-13 FR FR65275A patent/FR6061M/fr not_active Expired
- 1966-06-13 BE BE682444D patent/BE682444A/xx unknown
-
1967
- 1967-05-04 JP JP42028171A patent/JPS4834632B1/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CH570383A5 (en) | 1975-12-15 |
| BE682444A (enrdf_load_stackoverflow) | 1966-12-13 |
| JPS4834632B1 (enrdf_load_stackoverflow) | 1973-10-22 |
| DE1620134A1 (de) | 1970-02-12 |
| FR6061M (enrdf_load_stackoverflow) | 1968-05-27 |
| BR6680318D0 (pt) | 1973-12-26 |
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