DE2100685C2 - Verfahren zur Herstellung von reinen 4-Amino-5-halogen-pyridazonen-(6) - Google Patents
Verfahren zur Herstellung von reinen 4-Amino-5-halogen-pyridazonen-(6)Info
- Publication number
- DE2100685C2 DE2100685C2 DE19712100685 DE2100685A DE2100685C2 DE 2100685 C2 DE2100685 C2 DE 2100685C2 DE 19712100685 DE19712100685 DE 19712100685 DE 2100685 A DE2100685 A DE 2100685A DE 2100685 C2 DE2100685 C2 DE 2100685C2
- Authority
- DE
- Germany
- Prior art keywords
- amino
- parts
- chloro
- compound
- extraction
- 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
- 238000000034 method Methods 0.000 title claims description 8
- 238000002360 preparation method Methods 0.000 title claims description 3
- -1 trifluoromethylphenyl radical Chemical class 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 18
- 238000000605 extraction Methods 0.000 description 15
- 238000000926 separation method Methods 0.000 description 13
- 239000002904 solvent Substances 0.000 description 12
- 238000002844 melting Methods 0.000 description 11
- 230000008018 melting Effects 0.000 description 11
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229960004132 diethyl ether Drugs 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 239000000575 pesticide Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000001640 fractional crystallisation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 235000016068 Berberis vulgaris Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 241001233037 catfish Species 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- NPOMSUOUAZCMBL-UHFFFAOYSA-N dichloromethane;ethoxyethane Chemical compound ClCCl.CCOCC NPOMSUOUAZCMBL-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with 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
- C07D237/22—Nitrogen and oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712100685 DE2100685C2 (de) | 1971-01-08 | 1971-01-08 | Verfahren zur Herstellung von reinen 4-Amino-5-halogen-pyridazonen-(6) |
| CH1585871A CH562807A5 (en:Method) | 1971-01-08 | 1971-10-29 | |
| CS10572A CS172940B2 (en:Method) | 1971-01-08 | 1972-01-07 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712100685 DE2100685C2 (de) | 1971-01-08 | 1971-01-08 | Verfahren zur Herstellung von reinen 4-Amino-5-halogen-pyridazonen-(6) |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2100685A1 DE2100685A1 (en) | 1972-07-20 |
| DE2100685C2 true DE2100685C2 (de) | 1983-09-22 |
Family
ID=5795396
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19712100685 Expired DE2100685C2 (de) | 1971-01-08 | 1971-01-08 | Verfahren zur Herstellung von reinen 4-Amino-5-halogen-pyridazonen-(6) |
Country Status (3)
| Country | Link |
|---|---|
| CH (1) | CH562807A5 (en:Method) |
| CS (1) | CS172940B2 (en:Method) |
| DE (1) | DE2100685C2 (en:Method) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1096594B (it) * | 1978-06-22 | 1985-08-26 | Oxon Italia Spa | Procedimento per ottenere 5-amino-4-cloro-2-fenil-3(2h)-pirid azinone esente da 5-cloro-4amino-2-fenil-3(2h)-pirida zionone da miscele dei due isomeri ed applicazione quale erbicida selettivo del prodotto ottenuto |
| WO1981001288A1 (en) * | 1979-10-31 | 1981-05-14 | Koege Kemisk Vaerk | Method for producing 4-chloro-5-amino-2-phenyl-3(2h)-pyridazinone from 4,5-dichloro-2-phenyl-3(2h)-pyridazinone and ammonia |
| US7968287B2 (en) | 2004-10-08 | 2011-06-28 | Medical Research Council Harvard University | In vitro evolution in microfluidic systems |
| CA2636855C (en) | 2006-01-11 | 2016-09-27 | Raindance Technologies, Inc. | Microfluidic devices and methods of use in the formation and control of nanoreactors |
| US9562837B2 (en) | 2006-05-11 | 2017-02-07 | Raindance Technologies, Inc. | Systems for handling microfludic droplets |
| EP3335782B1 (en) | 2006-05-11 | 2020-09-09 | Bio-Rad Laboratories, Inc. | Microfluidic devices |
| WO2008097559A2 (en) | 2007-02-06 | 2008-08-14 | Brandeis University | Manipulation of fluids and reactions in microfluidic systems |
| WO2008130623A1 (en) | 2007-04-19 | 2008-10-30 | Brandeis University | Manipulation of fluids, fluid components and reactions in microfluidic systems |
| US12038438B2 (en) | 2008-07-18 | 2024-07-16 | Bio-Rad Laboratories, Inc. | Enzyme quantification |
| EP2315629B1 (en) | 2008-07-18 | 2021-12-15 | Bio-Rad Laboratories, Inc. | Droplet libraries |
| EP3415235A1 (en) | 2009-03-23 | 2018-12-19 | Raindance Technologies Inc. | Manipulation of microfluidic droplets |
| US10351905B2 (en) | 2010-02-12 | 2019-07-16 | Bio-Rad Laboratories, Inc. | Digital analyte analysis |
| EP4484577A3 (en) | 2010-02-12 | 2025-03-26 | Bio-Rad Laboratories, Inc. | Digital analyte analysis |
| US9399797B2 (en) | 2010-02-12 | 2016-07-26 | Raindance Technologies, Inc. | Digital analyte analysis |
| US9366632B2 (en) | 2010-02-12 | 2016-06-14 | Raindance Technologies, Inc. | Digital analyte analysis |
| EP2622103B2 (en) | 2010-09-30 | 2022-11-16 | Bio-Rad Laboratories, Inc. | Sandwich assays in droplets |
| EP3412778A1 (en) | 2011-02-11 | 2018-12-12 | Raindance Technologies, Inc. | Methods for forming mixed droplets |
| EP2675819B1 (en) | 2011-02-18 | 2020-04-08 | Bio-Rad Laboratories, Inc. | Compositions and methods for molecular labeling |
| WO2012167142A2 (en) | 2011-06-02 | 2012-12-06 | Raindance Technolgies, Inc. | Enzyme quantification |
| US8658430B2 (en) | 2011-07-20 | 2014-02-25 | Raindance Technologies, Inc. | Manipulating droplet size |
| US11901041B2 (en) | 2013-10-04 | 2024-02-13 | Bio-Rad Laboratories, Inc. | Digital analysis of nucleic acid modification |
| US9944977B2 (en) | 2013-12-12 | 2018-04-17 | Raindance Technologies, Inc. | Distinguishing rare variations in a nucleic acid sequence from a sample |
| US10647981B1 (en) | 2015-09-08 | 2020-05-12 | Bio-Rad Laboratories, Inc. | Nucleic acid library generation methods and compositions |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1105232B (de) * | 1958-11-21 | 1961-04-20 | Basf Ag | Mittel zur Beeinflussung des Pflanzen-wachstums |
| AT260943B (de) * | 1965-05-26 | 1968-03-25 | Pavel Dipl Ing Rapos | Verfahren zur Gewinnung von reinem 5-Amino-4-chlor-2-phenylpyridazin-3-on |
-
1971
- 1971-01-08 DE DE19712100685 patent/DE2100685C2/de not_active Expired
- 1971-10-29 CH CH1585871A patent/CH562807A5/xx not_active IP Right Cessation
-
1972
- 1972-01-07 CS CS10572A patent/CS172940B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE2100685A1 (en) | 1972-07-20 |
| CS172940B2 (en:Method) | 1977-01-28 |
| CH562807A5 (en:Method) | 1975-06-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2100685C2 (de) | Verfahren zur Herstellung von reinen 4-Amino-5-halogen-pyridazonen-(6) | |
| DE2338257A1 (de) | Verfahren zur herstellung n-substituierter lactame | |
| DE1643146A1 (de) | Verfahren zur Herstellung von epsilon-Caprolactonen und bzw. oder 6-Formyloxycapronsaeuren | |
| DE2263247C3 (de) | Verfahren zur Reinigung von Anthrachinon | |
| DE2453529A1 (de) | Verfahren zur herstellung von nitronaphthalinen | |
| DE1493977A1 (de) | Verfahren zur Herstellung von Hydrochinon aus p-Dialkylbenzol-bis-hydroperoxyden | |
| DE2148717A1 (de) | Verfahren zur Reinigung von Lactamen | |
| DE2558399C3 (de) | Verfahren zur Herstellung von 3,6-Dichlorpicolinsäure | |
| DE2647499C2 (de) | Verfahren zur kontinuierlichen Herstellung von Acetoacetamiden | |
| DE1263743B (de) | Verfahren zur Herstellung von substituierten Acetamiden | |
| DE2708388A1 (de) | Verfahren zur herstellung von 4,4'- dihydroxydiphenylsulfon | |
| DE68905673T2 (de) | Verfahren zur Ausscheidung von 2,6-Dimethylnaphthalin. | |
| EP0423679A2 (de) | Verfahren zur Herstellung von 5-(Carbamoyl)-5H-dibenz[b,f]azepin | |
| EP0014406B1 (de) | Verfahren zur Abtrennung von Selen, Selenverbindungen, Schwefel und/oder Schwefelverbindungen aus diese Elemente bzw. Verbindungen aufweisenden Urethanen | |
| DE19757530C2 (de) | Verfahren zur Isolierung von Carbazol sowie Herstellung von 9,10-Dihydroanthracen aus Rohanthracen | |
| EP0043031B1 (de) | Verfahren zur Gewinnung von reinen Anilin-Verbindungen | |
| DE1768130C3 (de) | lsocyan-diphenyl(-thio)-äther sowie Verfahren zu ihrer Herstellung und deren Verwendung zur Bekämpfung von Akariden | |
| DE932065C (de) | Verfahren zur Trennung von Desoxycholsaeure-Cholsaeure-Gemischen | |
| DE2354325A1 (de) | Verfahren zur herstellung von alkalisalzen des carbazols | |
| EP0086745A1 (de) | Verfahren zur Herstellung einer sehr reinen Handelsform von 4,2',4'-Trichlor-2-hydroxydiphenyläther | |
| DE2646955A1 (de) | Verfahren zur gewinnung von adipinsaeuredimethylester, alpha-methylglutarsaeuredimethylester und aethylbernsteinsaeurediester aus solche enthaltenden reaktionsgemischen | |
| DE2935775A1 (de) | Verfahren zur herstellung von 4-nitroso-diphenylamin | |
| DE1095841B (de) | Verfahren zur Herstellung alkylsubstituierter Hydrazine | |
| EP0634411A1 (de) | Verfahren zur Herstellung von 8-(4'-(4"-(Pyrimidin-2'''-yl)-piperazin-1"-yl)-butyl)-8-aza-spiro(4,5) decan-7,9-dion und von dessen Hydrochloriden hoher Reinheit | |
| DE1030351B (de) | Verfahren zur Gewinnung von ª‰-Naphthol |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8330 | Complete disclaimer |