GB1325581A - 3-methyl-2-quinoxalinecarboxamide-di-n-oxides - Google Patents
3-methyl-2-quinoxalinecarboxamide-di-n-oxidesInfo
- Publication number
- GB1325581A GB1325581A GB3348970A GB3348970A GB1325581A GB 1325581 A GB1325581 A GB 1325581A GB 3348970 A GB3348970 A GB 3348970A GB 3348970 A GB3348970 A GB 3348970A GB 1325581 A GB1325581 A GB 1325581A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- piperazinyl
- reacting
- formula
- methyl
- 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
- 125000000217 alkyl group Chemical group 0.000 abstract 16
- 150000001875 compounds Chemical class 0.000 abstract 5
- 125000004193 piperazinyl group Chemical group 0.000 abstract 5
- -1 sulphamoyl Chemical group 0.000 abstract 5
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 abstract 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 4
- 150000001412 amines Chemical class 0.000 abstract 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 2
- GZFAINXKJDVGFY-UHFFFAOYSA-N 3-methyl-4-oxido-1-oxoquinoxalin-1-ium-2-carboxylic acid Chemical class C1=CC=CC2=[N+]([O-])C(C)=C(C(O)=O)[N+]([O-])=C21 GZFAINXKJDVGFY-UHFFFAOYSA-N 0.000 abstract 2
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- CCMJPJQJSXHJSU-UHFFFAOYSA-N 1-azido-2-nitro-4-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=CC=C1N=[N+]=[N-] CCMJPJQJSXHJSU-UHFFFAOYSA-N 0.000 abstract 1
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- ATXBGHLILIABGX-UHFFFAOYSA-N 2-nitro-4-(trifluoromethyl)aniline Chemical compound NC1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O ATXBGHLILIABGX-UHFFFAOYSA-N 0.000 abstract 1
- HEESYTZYPZVWPI-UHFFFAOYSA-N 3-piperazin-1-yl-2-[(2-piperazin-1-ylacetyl)amino]propanamide Chemical compound N1(CCNCC1)CC(=O)NC(C(=O)N)CN1CCNCC1 HEESYTZYPZVWPI-UHFFFAOYSA-N 0.000 abstract 1
- PABPOXAAUYKNEJ-UHFFFAOYSA-N 4-piperazin-1-ylbutanamide Chemical compound NC(=O)CCCN1CCNCC1 PABPOXAAUYKNEJ-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 150000001718 carbodiimides Chemical class 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000012954 diazonium Substances 0.000 abstract 1
- 150000001989 diazonium salts Chemical class 0.000 abstract 1
- 125000005594 diketone group Chemical group 0.000 abstract 1
- 150000002081 enamines Chemical class 0.000 abstract 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 150000004885 piperazines Chemical class 0.000 abstract 1
- 150000003252 quinoxalines Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000001117 sulphuric acid Substances 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
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/116—Heterocyclic compounds
- A23K20/137—Heterocyclic compounds containing two hetero atoms, of which at least one is nitrogen
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K50/00—Feeding-stuffs specially adapted for particular animals
- A23K50/30—Feeding-stuffs specially adapted for particular animals for swines
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Animal Husbandry (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Birds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US84377569A | 1969-07-22 | 1969-07-22 | |
| US84381069A | 1969-07-22 | 1969-07-22 | |
| US655070A | 1970-01-28 | 1970-01-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1325581A true GB1325581A (en) | 1973-08-01 |
Family
ID=27358146
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3348970A Expired GB1325581A (en) | 1969-07-22 | 1970-07-09 | 3-methyl-2-quinoxalinecarboxamide-di-n-oxides |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE753582A (enrdf_load_stackoverflow) |
| DE (1) | DE2035480A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2059542B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1325581A (enrdf_load_stackoverflow) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4012512A (en) * | 1972-09-05 | 1977-03-15 | Ciba-Geigy Corporation | Animal feeds containing quinoxaline-di-n-oxide derivatives |
| CN112805312A (zh) * | 2018-08-21 | 2021-05-14 | 亨茨曼国际有限公司 | 用于pir/pur泡沫生产的催化剂 |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3644360A (en) * | 1970-05-05 | 1972-02-22 | Pfizer | 3-substituted methylquinoxaline-2-carboxamide-1 4-dioxides |
| CH575213A5 (enrdf_load_stackoverflow) * | 1972-09-05 | 1976-05-14 | Ciba Geigy Ag | |
| US4225584A (en) * | 1977-12-10 | 1980-09-30 | Henkel Kommanditgesellschaft Auf Aktien | Animal feeds containing a mixture of nitrovin, carbadox or olaquindox and proteolytic enzymes |
| IT7869686A0 (it) * | 1978-11-24 | 1978-11-24 | Loranze Torino A | Procedimento di preparazione di 2metil 3 bidrossietilcarbamollchinossalina i.4 di n ossido puroed altri composti ad esso simili |
| AT379805B (de) * | 1981-11-06 | 1986-03-10 | Ind Quimica Agropecuaria S A | Verfahren zur herstellung einer chinoxalinverbindung |
| JPS62132870A (ja) * | 1985-12-04 | 1987-06-16 | Chisso Corp | Ｎ−（２−ヒドロキシエチル）−２−メチル−３−カルボン酸アミド−キノキサリン−１，４−ジ−ｎ−オキシドの精製法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3398141A (en) * | 1966-01-12 | 1968-08-20 | Research Corp | Quinoxaline-di-nu-oxides |
| DE1670937C3 (de) * | 1967-10-04 | 1979-08-30 | Bayer Ag, 5090 Leverkusen | 2-Halogenmethyl-3-carbonsäureamidochinoxalin-di-N-oxide-( 1.4) |
| DE1670935C3 (de) * | 1967-10-04 | 1975-12-04 | Bayer Ag, 5090 Leverkusen | 2-Methyl-3-carbonsäureamidochinoxalin-1,4-dl-N-oxide, ein Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende antibakterielle Mittel |
-
1970
- 1970-07-09 GB GB3348970A patent/GB1325581A/en not_active Expired
- 1970-07-16 BE BE753582D patent/BE753582A/xx not_active IP Right Cessation
- 1970-07-17 FR FR7026396A patent/FR2059542B1/fr not_active Expired
- 1970-07-17 DE DE19702035480 patent/DE2035480A1/de active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4012512A (en) * | 1972-09-05 | 1977-03-15 | Ciba-Geigy Corporation | Animal feeds containing quinoxaline-di-n-oxide derivatives |
| CN112805312A (zh) * | 2018-08-21 | 2021-05-14 | 亨茨曼国际有限公司 | 用于pir/pur泡沫生产的催化剂 |
Also Published As
| Publication number | Publication date |
|---|---|
| BE753582A (fr) | 1974-01-18 |
| FR2059542A1 (enrdf_load_stackoverflow) | 1971-06-04 |
| FR2059542B1 (enrdf_load_stackoverflow) | 1975-11-28 |
| DE2035480A1 (de) | 1971-02-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |