DD143160A5 - Verfahren zur herstellung von 3-chlor-4h-1,2,6-thiadiazin-4-onen - Google Patents
Verfahren zur herstellung von 3-chlor-4h-1,2,6-thiadiazin-4-onen Download PDFInfo
- Publication number
- DD143160A5 DD143160A5 DD78212567A DD21256778A DD143160A5 DD 143160 A5 DD143160 A5 DD 143160A5 DD 78212567 A DD78212567 A DD 78212567A DD 21256778 A DD21256778 A DD 21256778A DD 143160 A5 DD143160 A5 DD 143160A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- alkyl
- group
- general formula
- thiadiazin
- chloro
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 37
- ZKHPZXACANWNKQ-UHFFFAOYSA-N 3,5-dichloro-1,2,6-thiadiazin-4-one Chemical compound ClC1=NSN=C(Cl)C1=O ZKHPZXACANWNKQ-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 4
- 150000001342 alkaline earth metals Chemical class 0.000 claims abstract description 3
- -1 naphthoxy Chemical group 0.000 claims description 68
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 8
- 125000005843 halogen group Chemical group 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- BIUUKZJGENGHDB-UHFFFAOYSA-N 3-chloro-1,2,6-thiadiazin-4-one Chemical class ClC1=NSN=CC1=O BIUUKZJGENGHDB-UHFFFAOYSA-N 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000004442 acylamino group Chemical group 0.000 claims 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 239000003513 alkali Substances 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 description 12
- 230000005764 inhibitory process Effects 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
- 241000233866 Fungi Species 0.000 description 9
- 239000000203 mixture Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 229920001817 Agar Polymers 0.000 description 6
- 239000008272 agar Substances 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000003032 phytopathogenic effect Effects 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 241000896222 Erysiphe polygoni Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 230000002538 fungal effect Effects 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 230000001408 fungistatic effect Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- MGAXYKDBRBNWKT-UHFFFAOYSA-N (5-oxooxolan-2-yl)methyl 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OCC1OC(=O)CC1 MGAXYKDBRBNWKT-UHFFFAOYSA-N 0.000 description 1
- XLHUBROMZOAQMV-UHFFFAOYSA-N 1,4-benzosemiquinone Chemical group [O]C1=CC=C(O)C=C1 XLHUBROMZOAQMV-UHFFFAOYSA-N 0.000 description 1
- UGRMITBWUVWUEB-UHFFFAOYSA-N 1-$l^{1}-oxidanyl-3-methylbenzene Chemical group CC1=CC=CC([O])=C1 UGRMITBWUVWUEB-UHFFFAOYSA-N 0.000 description 1
- QDKWLJJOYIFEBS-UHFFFAOYSA-N 1-fluoro-4-$l^{1}-oxidanylbenzene Chemical group [O]C1=CC=C(F)C=C1 QDKWLJJOYIFEBS-UHFFFAOYSA-N 0.000 description 1
- PKPISMMHAZJUNS-UHFFFAOYSA-N 3-chloro-5-phenoxy-1,2,6-thiadiazin-4-one Chemical compound O=C1C(Cl)=NSN=C1OC1=CC=CC=C1 PKPISMMHAZJUNS-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241000213004 Alternaria solani Species 0.000 description 1
- 241001450781 Bipolaris oryzae Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000395107 Cladosporium cucumerinum Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 241000427940 Fusarium solani Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- 241001518731 Monilinia fructicola Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000233622 Phytophthora infestans Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000918584 Pythium ultimum Species 0.000 description 1
- 241000813090 Rhizoctonia solani Species 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 125000005281 alkyl ureido group Chemical group 0.000 description 1
- 239000012496 blank sample Substances 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
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 244000000010 microbial pathogen Species 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- CFPLEOLETMZLIB-UHFFFAOYSA-M sodium;4-chlorophenolate Chemical compound [Na+].[O-]C1=CC=C(Cl)C=C1 CFPLEOLETMZLIB-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 230000004763 spore germination Effects 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 125000004953 trihalomethyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/782,860 US4097594A (en) | 1977-03-30 | 1977-03-30 | Mono-5-substituted-3-chloro-4H-1,2,6-thiadiazin-4-one antifungal agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD143160A5 true DD143160A5 (de) | 1980-08-06 |
Family
ID=25127411
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD78212567A DD143160A5 (de) | 1977-03-30 | 1978-03-30 | Verfahren zur herstellung von 3-chlor-4h-1,2,6-thiadiazin-4-onen |
| DD78204488A DD137654A5 (de) | 1977-03-30 | 1978-03-30 | Fungizide mittel |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD78204488A DD137654A5 (de) | 1977-03-30 | 1978-03-30 | Fungizide mittel |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4097594A (da) |
| JP (1) | JPS53121775A (da) |
| AR (1) | AR220703A1 (da) |
| AU (1) | AU3450878A (da) |
| BE (1) | BE865394A (da) |
| BR (1) | BR7801933A (da) |
| DD (2) | DD143160A5 (da) |
| DE (1) | DE2813732A1 (da) |
| DK (1) | DK138178A (da) |
| ES (1) | ES468320A1 (da) |
| FR (1) | FR2385328A1 (da) |
| GB (1) | GB1574576A (da) |
| IE (1) | IE46684B1 (da) |
| IL (1) | IL54323A0 (da) |
| IT (1) | IT1096166B (da) |
| LU (1) | LU79343A1 (da) |
| NL (1) | NL7803308A (da) |
| PH (1) | PH14582A (da) |
| PL (2) | PL109247B1 (da) |
| SU (1) | SU828966A3 (da) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4497807A (en) * | 1978-03-31 | 1985-02-05 | E. I. Du Pont De Nemours And Company | Thiadiazinone plant disease control agents |
| US4143138A (en) * | 1978-05-08 | 1979-03-06 | Fmc Corporation | 3-chloro-5-(optionally substituted heterocycloxy)-4h-1,2,6-thiadiazin-4-one antifungal agents |
| ES2045545T3 (es) * | 1988-09-30 | 1994-01-16 | Ciba Geigy Ag | Biocidas para la proteccion de materiales y para sistemas acuosos. |
| SK283351B6 (sk) | 1992-01-29 | 2003-06-03 | Basf Aktiengesellschaft | Karbamáty a fungicídne prostriedky s ich obsahom |
| CA2146701A1 (en) * | 1994-04-11 | 1995-10-12 | Takashi Fujita | Heterocyclic compounds having anti-diabetic activity, their preparation and their use |
| US20030018514A1 (en) * | 2001-04-30 | 2003-01-23 | Billet Bradford E. | Predictive method |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3629250A (en) * | 1969-07-14 | 1971-12-21 | Minnesota Mining & Mfg | Fungicidal benzothiadiazine-2 3-dioxides |
| US3860713A (en) * | 1970-01-02 | 1975-01-14 | Betz Laboratories | Slime controlling compositions and their use |
| US3760076A (en) * | 1970-03-12 | 1973-09-18 | Ici Ltd | Combating pests with benzothiadiozines |
| DE2105687C2 (de) * | 1971-02-08 | 1981-09-24 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von 3-substituierten 2,1,3-Benzothiadiazin-4-on-2,2-dioxiden |
| DE2619090A1 (de) * | 1976-05-03 | 1977-11-17 | Celamerck Gmbh & Co Kg | 1.2.6-thiadiazinone, ihre herstellung und ihre verwendung |
-
1977
- 1977-03-30 US US05/782,860 patent/US4097594A/en not_active Expired - Lifetime
-
1978
- 1978-03-22 IL IL54323A patent/IL54323A0/xx unknown
- 1978-03-22 IE IE570/78A patent/IE46684B1/en unknown
- 1978-03-28 BE BE186339A patent/BE865394A/xx unknown
- 1978-03-28 AU AU34508/78A patent/AU3450878A/en active Pending
- 1978-03-28 JP JP3491578A patent/JPS53121775A/ja active Pending
- 1978-03-28 PH PH20937A patent/PH14582A/en unknown
- 1978-03-29 NL NL7803308A patent/NL7803308A/xx not_active Application Discontinuation
- 1978-03-29 DK DK138178A patent/DK138178A/da not_active IP Right Cessation
- 1978-03-29 FR FR7809159A patent/FR2385328A1/fr not_active Withdrawn
- 1978-03-29 GB GB12252/78A patent/GB1574576A/en not_active Expired
- 1978-03-29 BR BR7801933A patent/BR7801933A/pt unknown
- 1978-03-29 ES ES468320A patent/ES468320A1/es not_active Expired
- 1978-03-29 AR AR271594A patent/AR220703A1/es active
- 1978-03-29 IT IT21743/78A patent/IT1096166B/it active
- 1978-03-30 LU LU79343A patent/LU79343A1/xx unknown
- 1978-03-30 PL PL1978205689A patent/PL109247B1/pl unknown
- 1978-03-30 DD DD78212567A patent/DD143160A5/de unknown
- 1978-03-30 PL PL1978215855A patent/PL113019B1/pl unknown
- 1978-03-30 DD DD78204488A patent/DD137654A5/xx unknown
- 1978-03-30 DE DE19782813732 patent/DE2813732A1/de not_active Withdrawn
-
1979
- 1979-01-03 SU SU792706053A patent/SU828966A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| PL109247B1 (en) | 1980-05-31 |
| LU79343A1 (fr) | 1978-11-03 |
| BR7801933A (pt) | 1978-11-28 |
| US4097594A (en) | 1978-06-27 |
| DD137654A5 (de) | 1979-09-19 |
| PL205689A1 (pl) | 1979-01-29 |
| FR2385328A1 (fr) | 1978-10-27 |
| BE865394A (fr) | 1978-09-28 |
| AR220703A1 (es) | 1980-11-28 |
| IE46684B1 (en) | 1983-08-24 |
| IE780570L (en) | 1978-09-30 |
| IL54323A0 (en) | 1978-06-15 |
| SU828966A3 (ru) | 1981-05-07 |
| DE2813732A1 (de) | 1978-10-12 |
| ES468320A1 (es) | 1979-09-16 |
| AU3450878A (en) | 1979-10-04 |
| IT1096166B (it) | 1985-08-17 |
| PL113019B1 (en) | 1980-11-29 |
| NL7803308A (nl) | 1978-10-03 |
| PH14582A (en) | 1981-09-24 |
| IT7821743A0 (it) | 1978-03-29 |
| DK138178A (da) | 1978-10-01 |
| JPS53121775A (en) | 1978-10-24 |
| GB1574576A (en) | 1980-09-10 |
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