SU925248A3 - Способ получени 3-замещенных карбониламинофениловых эфиров N-(2-пропинил)-карбаниловой кислоты - Google Patents
Способ получени 3-замещенных карбониламинофениловых эфиров N-(2-пропинил)-карбаниловой кислоты Download PDFInfo
- Publication number
- SU925248A3 SU925248A3 SU802901453A SU2901453A SU925248A3 SU 925248 A3 SU925248 A3 SU 925248A3 SU 802901453 A SU802901453 A SU 802901453A SU 2901453 A SU2901453 A SU 2901453A SU 925248 A3 SU925248 A3 SU 925248A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- ics
- ric
- compounds
- propinyl
- carbonylaminophenyl
- Prior art date
Links
- -1 3-substituted carbonylaminophenyl esters Chemical class 0.000 title claims description 12
- 238000000034 method Methods 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 5
- 241000196324 Embryophyta Species 0.000 claims abstract 4
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 2
- 238000002360 preparation method Methods 0.000 claims abstract 2
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000013543 active substance Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
- VLNHDKDBGWXJEE-GYHUNEDQSA-N 5'-guanidinonaltrindole Chemical compound N1([C@@H]2CC=3C4=C(C(=CC=3)O)O[C@H]3C=5NC6=CC=C(C=C6C=5C[C@]2(O)[C@]34CC1)NC(=N)N)CC1CC1 VLNHDKDBGWXJEE-GYHUNEDQSA-N 0.000 claims 1
- 101100291030 Arabidopsis thaliana GNTI gene Proteins 0.000 claims 1
- 229920000742 Cotton Polymers 0.000 claims 1
- 244000299507 Gossypium hirsutum Species 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- 244000061456 Solanum tuberosum Species 0.000 claims 1
- 235000002595 Solanum tuberosum Nutrition 0.000 claims 1
- 240000006694 Stellaria media Species 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 235000021307 Triticum Nutrition 0.000 claims 1
- 244000098338 Triticum aestivum Species 0.000 claims 1
- 240000008042 Zea mays Species 0.000 claims 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 235000005822 corn Nutrition 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 241001233957 eudicotyledons Species 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 239000013067 intermediate product Substances 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 230000001902 propagating effect Effects 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 244000045561 useful plants Species 0.000 claims 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 230000006378 damage Effects 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792913975 DE2913975A1 (de) | 1979-04-05 | 1979-04-05 | N-(2-propinyl)-carbanilsaeure-(3-alkoxy- und alkylthiocarbonylamino-phenyl)-ester, verfahren zur herstellung dieser verbindungen sowie diese enthaltende selektive herbizide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU925248A3 true SU925248A3 (ru) | 1982-04-30 |
Family
ID=6067686
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU802901453A SU925248A3 (ru) | 1979-04-05 | 1980-03-28 | Способ получени 3-замещенных карбониламинофениловых эфиров N-(2-пропинил)-карбаниловой кислоты |
Country Status (35)
| Country | Link |
|---|---|
| JP (1) | JPS5819672B2 (es) |
| AR (1) | AR224521A1 (es) |
| AT (1) | AT365896B (es) |
| AU (1) | AU535374B2 (es) |
| BE (1) | BE882627A (es) |
| BG (1) | BG34897A3 (es) |
| BR (1) | BR8002009A (es) |
| CA (1) | CA1125301A (es) |
| CH (1) | CH645344A5 (es) |
| CS (1) | CS209949B2 (es) |
| DD (1) | DD149996A5 (es) |
| DE (1) | DE2913975A1 (es) |
| EG (1) | EG14317A (es) |
| ES (1) | ES8107172A1 (es) |
| FI (1) | FI800832A7 (es) |
| FR (1) | FR2453142A1 (es) |
| GB (1) | GB2049672B (es) |
| GR (1) | GR67206B (es) |
| HU (1) | HU181764B (es) |
| IL (1) | IL59736A (es) |
| IN (1) | IN154011B (es) |
| IT (1) | IT1148780B (es) |
| MA (1) | MA18803A1 (es) |
| MX (1) | MX6017E (es) |
| NL (1) | NL8001638A (es) |
| PH (1) | PH17275A (es) |
| PL (1) | PL123694B1 (es) |
| PT (1) | PT71032A (es) |
| RO (1) | RO79220A (es) |
| SE (1) | SE8002183L (es) |
| SU (1) | SU925248A3 (es) |
| TR (1) | TR20575A (es) |
| YU (1) | YU76180A (es) |
| ZA (1) | ZA802032B (es) |
| ZW (1) | ZW7980A1 (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6014760U (ja) * | 1983-07-09 | 1985-01-31 | フランスベッド株式会社 | マツトレス装置 |
| JPS6074668U (ja) * | 1983-10-28 | 1985-05-25 | フランスベッド株式会社 | マツトレス |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2413933A1 (de) * | 1974-03-20 | 1975-09-25 | Schering Ag | Diurethane mit selektiver herbizider wirkung |
| DE2557552C2 (de) * | 1975-12-18 | 1984-12-20 | Schering AG, 1000 Berlin und 4709 Bergkamen | Diurethane und herbizide Mittel, enthaltend diese Verbindungen als Wirkstoffe |
| DE2650796A1 (de) * | 1976-11-03 | 1978-05-11 | Schering Ag | Diurethane, verfahren zur herstellung dieser verbindungen sowie diese enthaltendes selektives herbizides mittel |
| DE2651526A1 (de) * | 1976-11-09 | 1978-05-18 | Schering Ag | Diurethane, verfahren zur herstellung dieser verbindungen sowie diese enthaltendes selektives herbizides mittel |
-
1979
- 1979-04-05 DE DE19792913975 patent/DE2913975A1/de not_active Withdrawn
-
1980
- 1980-03-18 FI FI800832A patent/FI800832A7/fi not_active Application Discontinuation
- 1980-03-19 NL NL8001638A patent/NL8001638A/nl not_active Application Discontinuation
- 1980-03-19 YU YU00761/80A patent/YU76180A/xx unknown
- 1980-03-20 SE SE8002183A patent/SE8002183L/ not_active Application Discontinuation
- 1980-03-25 IN IN217/DEL/80A patent/IN154011B/en unknown
- 1980-03-26 CH CH238480A patent/CH645344A5/de not_active IP Right Cessation
- 1980-03-27 CS CS802160A patent/CS209949B2/cs unknown
- 1980-03-28 SU SU802901453A patent/SU925248A3/ru active
- 1980-03-28 PT PT71032A patent/PT71032A/pt unknown
- 1980-03-31 IL IL59736A patent/IL59736A/xx unknown
- 1980-03-31 MX MX808729U patent/MX6017E/es unknown
- 1980-03-31 GB GB8010810A patent/GB2049672B/en not_active Expired
- 1980-04-01 CA CA348,942A patent/CA1125301A/en not_active Expired
- 1980-04-01 BR BR8002009A patent/BR8002009A/pt unknown
- 1980-04-02 GR GR61616A patent/GR67206B/el unknown
- 1980-04-02 BG BG047214A patent/BG34897A3/xx unknown
- 1980-04-02 AT AT0180680A patent/AT365896B/de not_active IP Right Cessation
- 1980-04-02 ES ES490256A patent/ES8107172A1/es not_active Expired
- 1980-04-02 AR AR280534A patent/AR224521A1/es active
- 1980-04-03 IT IT21168/80A patent/IT1148780B/it active
- 1980-04-03 PL PL1980223231A patent/PL123694B1/pl unknown
- 1980-04-03 BE BE0/200112A patent/BE882627A/fr not_active IP Right Cessation
- 1980-04-03 ZA ZA00802032A patent/ZA802032B/xx unknown
- 1980-04-03 HU HU80818A patent/HU181764B/hu unknown
- 1980-04-03 AU AU57150/80A patent/AU535374B2/en not_active Ceased
- 1980-04-03 DD DD80220215A patent/DD149996A5/de unknown
- 1980-04-03 TR TR20575A patent/TR20575A/xx unknown
- 1980-04-03 ZW ZW79/80A patent/ZW7980A1/xx unknown
- 1980-04-04 RO RO80100727A patent/RO79220A/ro unknown
- 1980-04-04 JP JP55043644A patent/JPS5819672B2/ja not_active Expired
- 1980-04-04 FR FR8007670A patent/FR2453142A1/fr active Granted
- 1980-04-04 MA MA18998A patent/MA18803A1/fr unknown
- 1980-04-05 EG EG207/80A patent/EG14317A/xx active
- 1980-04-07 PH PH23863A patent/PH17275A/en unknown
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