SU784770A3 - Способ получени анилидов циклопропанкарбоновой кислоты - Google Patents
Способ получени анилидов циклопропанкарбоновой кислоты Download PDFInfo
- Publication number
- SU784770A3 SU784770A3 SU782621101A SU2621101A SU784770A3 SU 784770 A3 SU784770 A3 SU 784770A3 SU 782621101 A SU782621101 A SU 782621101A SU 2621101 A SU2621101 A SU 2621101A SU 784770 A3 SU784770 A3 SU 784770A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- anilide
- furyl
- oxoperhydro
- acid
- cyclopropanecarboxylic acid
- Prior art date
Links
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 title claims description 54
- 238000000034 method Methods 0.000 title claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 2
- 239000001257 hydrogen Substances 0.000 claims abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 2
- -1 trimethylphenyl Chemical group 0.000 claims description 26
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 3
- 239000003153 chemical reaction reagent Substances 0.000 claims description 2
- 230000003902 lesion Effects 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims 1
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 1
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 claims 1
- 150000003931 anilides Chemical class 0.000 claims 1
- 125000004802 cyanophenyl group Chemical group 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 6
- ZOOSILUVXHVRJE-UHFFFAOYSA-N cyclopropanecarbonyl chloride Chemical compound ClC(=O)C1CC1 ZOOSILUVXHVRJE-UHFFFAOYSA-N 0.000 abstract description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- OCHYJSATRBHPLB-UHFFFAOYSA-N n-phenylcyclopropanecarboxamide Chemical class C1CC1C(=O)NC1=CC=CC=C1 OCHYJSATRBHPLB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
- 239000002689 soil Substances 0.000 description 5
- 239000013543 active substance Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 241000233866 Fungi Species 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000017074 necrotic cell death Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000233639 Pythium Species 0.000 description 2
- 235000021536 Sugar beet Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 235000021537 Beetroot Nutrition 0.000 description 1
- 101100115207 Dictyostelium discoideum culA gene Proteins 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 241000219094 Vitaceae Species 0.000 description 1
- 241000219095 Vitis Species 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 230000009514 concussion Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 235000021021 grapes Nutrition 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D307/32—Oxygen atoms
- C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/16—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D309/28—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D309/30—Oxygen atoms, e.g. delta-lactones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (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)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2724786A DE2724786C2 (de) | 1977-05-27 | 1977-05-27 | Cyclopropancarbonsäure-[N-(2-oxoperhydro-3-furyl)-anilide], Verfahren zu ihrer Herstellung sowie diese Verbindungen enthaltende fungizide Mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU784770A3 true SU784770A3 (ru) | 1980-11-30 |
Family
ID=6010435
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU782621101A SU784770A3 (ru) | 1977-05-27 | 1978-05-26 | Способ получени анилидов циклопропанкарбоновой кислоты |
| SU782621053A SU727107A3 (ru) | 1977-05-27 | 1978-05-26 | Фунгицидное средство |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU782621053A SU727107A3 (ru) | 1977-05-27 | 1978-05-26 | Фунгицидное средство |
Country Status (39)
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4440780A (en) * | 1979-06-01 | 1984-04-03 | Chevron Research Company | Fungicidal 3-(N-acyl-N-arylamino)-and 3-(N-thionoacyl-N-arylamino)-gamma-butyrolactones and gamma-thiobutyrolactones |
| EP0016985A1 (de) * | 1979-03-16 | 1980-10-15 | F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft | Substituierte Anilide, Verfahren zu deren Herstellung, fungicide Mittel enthaltend solche Verbindungen sowie Verwendung solcher Verbindungen bzw. Mittel zur Bekämpfung von Pflanzenfungi |
| DE2920435A1 (de) * | 1979-05-19 | 1980-12-04 | Basf Ag | 2-aminopropanalacetale, verfahren zu ihrer herstellung, ihre anwendung als fungizide und verfahren zur herstellung von substituierten anilinen |
| US4599351A (en) * | 1981-08-14 | 1986-07-08 | Chevron Research Company | Fungicidal 3-(N-acyl-N-arylamino) lactones |
| JPS61186735U (enExample) * | 1985-05-14 | 1986-11-21 |
-
1977
- 1977-05-27 DE DE2724786A patent/DE2724786C2/de not_active Expired
-
1978
- 1978-04-24 FI FI781264A patent/FI68397C/fi not_active IP Right Cessation
- 1978-05-09 YU YU1102/78A patent/YU40192B/xx unknown
- 1978-05-11 MX MX787079U patent/MX5224E/es unknown
- 1978-05-12 CA CA303,250A patent/CA1108161A/en not_active Expired
- 1978-05-15 PH PH21136A patent/PH15700A/en unknown
- 1978-05-16 IL IL54719A patent/IL54719A/xx unknown
- 1978-05-18 TR TR20568A patent/TR20568A/xx unknown
- 1978-05-18 NL NL7805404A patent/NL7805404A/xx not_active Application Discontinuation
- 1978-05-23 PT PT68075A patent/PT68075B/pt unknown
- 1978-05-23 CY CY1163A patent/CY1163A/en unknown
- 1978-05-23 GB GB21326/78A patent/GB1603730A/en not_active Expired
- 1978-05-24 AR AR272308A patent/AR220710A1/es active
- 1978-05-24 PL PL1978207069A patent/PL110646B1/pl unknown
- 1978-05-24 ES ES470195A patent/ES470195A1/es not_active Expired
- 1978-05-24 EG EG333/78A patent/EG13373A/xx active
- 1978-05-24 IE IE1029/78A patent/IE46923B1/en unknown
- 1978-05-24 JP JP6212278A patent/JPS53147061A/ja active Granted
- 1978-05-24 AT AT380578A patent/AT360803B/de not_active IP Right Cessation
- 1978-05-25 LU LU79711A patent/LU79711A1/de unknown
- 1978-05-25 IT IT23774/78A patent/IT1096326B/it active
- 1978-05-25 RO RO7894166A patent/RO75072A/ro unknown
- 1978-05-25 SE SE7805994A patent/SE442868B/sv not_active IP Right Cessation
- 1978-05-25 CS CS783406A patent/CS203192B2/cs unknown
- 1978-05-25 DD DD78205587A patent/DD136093A5/xx unknown
- 1978-05-26 NO NO781838A patent/NO149430C/no unknown
- 1978-05-26 HU HU78SCHE646A patent/HU184201B/hu unknown
- 1978-05-26 BR BR7803382A patent/BR7803382A/pt unknown
- 1978-05-26 ZA ZA00783036A patent/ZA783036B/xx unknown
- 1978-05-26 FR FR7815747A patent/FR2392019A1/fr active Granted
- 1978-05-26 SU SU782621101A patent/SU784770A3/ru active
- 1978-05-26 BG BG039862A patent/BG28688A3/xx unknown
- 1978-05-26 GR GR56344A patent/GR72966B/el unknown
- 1978-05-26 DK DK233878A patent/DK233878A/da not_active Application Discontinuation
- 1978-05-26 CH CH580678A patent/CH633784A5/de not_active IP Right Cessation
- 1978-05-26 BE BE188101A patent/BE867556A/xx not_active IP Right Cessation
- 1978-05-26 SU SU782621053A patent/SU727107A3/ru active
- 1978-05-26 AU AU36529/78A patent/AU520353B2/en not_active Expired
-
1982
- 1982-10-28 KE KE3241A patent/KE3241A/xx unknown
-
1983
- 1983-12-30 MY MY210/83A patent/MY8300210A/xx unknown
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