SU730302A3 - Способ получени метил-3-(2хиноксалинилметилен) карбазат - диоксида - Google Patents
Способ получени метил-3-(2хиноксалинилметилен) карбазат - диоксида Download PDFInfo
- Publication number
- SU730302A3 SU730302A3 SU742013770A SU2013770A SU730302A3 SU 730302 A3 SU730302 A3 SU 730302A3 SU 742013770 A SU742013770 A SU 742013770A SU 2013770 A SU2013770 A SU 2013770A SU 730302 A3 SU730302 A3 SU 730302A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dioxide
- carbazate
- quinoxalinylmethylene
- methyl
- acetal
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 7
- OVGGLBAWFMIPPY-UHFFFAOYSA-N methyl N-[(1,4-dioxidoquinoxaline-1,4-diium-2-yl)methylideneamino]carbamate Chemical compound C1=CC=CC2=[N+]([O-])C(C=NNC(=O)OC)=C[N+]([O-])=C21 OVGGLBAWFMIPPY-UHFFFAOYSA-N 0.000 title 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 5
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims abstract 4
- 150000002923 oximes Chemical class 0.000 claims abstract 2
- 150000007659 semicarbazones Chemical class 0.000 claims abstract 2
- 150000003584 thiosemicarbazones Chemical class 0.000 claims abstract 2
- -1 2-quinoxalinylmethylene Chemical group 0.000 claims description 6
- 239000003377 acid catalyst Substances 0.000 claims description 5
- WFJRIDQGVSJLLH-UHFFFAOYSA-N methyl n-aminocarbamate Chemical compound COC(=O)NN WFJRIDQGVSJLLH-UHFFFAOYSA-N 0.000 claims description 4
- 239000012442 inert solvent Substances 0.000 claims description 3
- OWIUPIRUAQMTTK-UHFFFAOYSA-M n-aminocarbamate Chemical compound NNC([O-])=O OWIUPIRUAQMTTK-UHFFFAOYSA-M 0.000 claims description 3
- CWGBFIRHYJNILV-UHFFFAOYSA-N (1,4-diphenyl-1,2,4-triazol-4-ium-3-yl)-phenylazanide Chemical compound C=1C=CC=CC=1[N-]C1=NN(C=2C=CC=CC=2)C=[N+]1C1=CC=CC=C1 CWGBFIRHYJNILV-UHFFFAOYSA-N 0.000 claims 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 150000007857 hydrazones Chemical class 0.000 abstract 2
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical compound ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 abstract 1
- 239000002904 solvent Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 150000001241 acetals Chemical class 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- KCYQCRLROQUKQT-UHFFFAOYSA-N (benzylideneamino)carbamic acid Chemical class OC(=O)NN=CC1=CC=CC=C1 KCYQCRLROQUKQT-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Fodder In General (AREA)
- Plural Heterocyclic Compounds (AREA)
- Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34980573A | 1973-04-10 | 1973-04-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU730302A3 true SU730302A3 (ru) | 1980-04-25 |
Family
ID=23374042
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU742013770A SU730302A3 (ru) | 1973-04-10 | 1974-03-29 | Способ получени метил-3-(2хиноксалинилметилен) карбазат - диоксида |
Country Status (27)
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5135625Y2 (enrdf_load_stackoverflow) * | 1971-03-30 | 1976-09-02 | ||
| JPS4984830U (enrdf_load_stackoverflow) * | 1972-11-09 | 1974-07-23 | ||
| JPS49100338U (enrdf_load_stackoverflow) * | 1972-12-20 | 1974-08-29 | ||
| IT1078991B (it) * | 1977-05-26 | 1985-05-08 | Erregierre Ind Chim Spa | Processo per la preparazione del carbometossi idrazone,della 2-formilchinossalina-1,4-di-n-ossido |
| JPS5487994U (enrdf_load_stackoverflow) * | 1977-12-02 | 1979-06-21 | ||
| DK141708B (da) * | 1978-04-20 | 1980-05-27 | Rasmussen Holding As V Kann | Manøvrerings- og låsegreb til vinduer. |
-
1974
- 1974-03-11 SE SE7403236A patent/SE407219B/xx not_active IP Right Cessation
- 1974-03-15 GB GB1170674A patent/GB1462424A/en not_active Expired
- 1974-03-18 IL IL44434A patent/IL44434A/en unknown
- 1974-03-19 AU AU66828/74A patent/AU477279B2/en not_active Expired
- 1974-03-26 YU YU00834/74A patent/YU39151B/xx unknown
- 1974-03-26 NL NL7404044A patent/NL7404044A/xx unknown
- 1974-03-27 IT IT49751/74A patent/IT1056058B/it active
- 1974-03-28 JP JP3402874A patent/JPS5333596B2/ja not_active Expired
- 1974-03-29 FI FI978/74A patent/FI59405C/fi active
- 1974-03-29 CH CH446274A patent/CH603599A5/xx not_active IP Right Cessation
- 1974-03-29 IE IE00686/74A patent/IE39110B1/xx unknown
- 1974-03-29 FR FR7411526A patent/FR2225429B1/fr not_active Expired
- 1974-03-29 DK DK174874AA patent/DK140756B/da not_active IP Right Cessation
- 1974-03-29 SU SU742013770A patent/SU730302A3/ru active
- 1974-03-29 HU HUPI412A patent/HU170050B/hu unknown
- 1974-03-29 NO NO741133A patent/NO141851C/no unknown
- 1974-03-30 ES ES424803A patent/ES424803A1/es not_active Expired
- 1974-03-30 RO RO7478252A patent/RO71311A/ro unknown
- 1974-04-01 PL PL1974170010A patent/PL94963B1/pl unknown
- 1974-04-01 AR AR253076A patent/AR210723A1/es active
- 1974-04-01 DD DD177605A patent/DD110875A5/xx unknown
- 1974-04-01 CA CA196,545A patent/CA1018977A/en not_active Expired
- 1974-04-01 CS CS742332A patent/CS212276B2/cs unknown
- 1974-04-01 ZA ZA00742052A patent/ZA742052B/xx unknown
-
1976
- 1976-03-23 PH PH18245A patent/PH11135A/en unknown
-
1977
- 1977-09-22 HK HK488/77A patent/HK48877A/xx unknown
-
1978
- 1978-12-30 MY MY14/78A patent/MY7800014A/xx unknown
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