http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0149974-A2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D279-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D265-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-32 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D279-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N25-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-84 |
| filingDate | 1984-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a870a4e9f7b708656769d95693bd0a56 |
| publicationDate | 1985-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0149974-A2 |
| titleOfInvention | Means for protecting cultured plants against the phytotoxic effect of herbicides |
| abstract | The acylamide derivatives of formula I below are suitable as antidotes, "antidotes" or "safeners" to protect crop plants from the phytotoxic action of herbicides. Cultures are preferably millet, cereals, rice, corn and soybeans, and herbicides are chloroacetanilides and thiol carbamates.n n n X Sauerstoff, Schwefel, -SO- oder -SO 2 -, R 1 C 1 -C 6 -Halogenalkyl, C 1 -C 6 -Cyanalkyl oder C 2 -C e -Halogenalkenyl, R 2 und R 5 unabhängig voneinander Wasserstoff, C i -C 4 -Alkyl, C 1 -C 4 -Halogenalkyl, C 2 -C 4 -Alkenyl, C 2 -C 4 -Alkinyl oder C 2 -C 4 -Alkoxyalkyl, R 3 und R 4 unabhängig voneinander Wasserstoff, C 2 -C 4 -Alkenyl, C 2 -C 4 -Alkinyl, Cyan, C 2 -C 4 -Alkoxyalkyl, -COOR 8 , -CO-NR g R 10 oder unsubstituiertes oder durch Halogen, Cyan oder -CO-A substituiertes C 1 -C 4 -Alkyl, R 6 und R 7 unabhängig voneinander Wasserstoff, Halogen, C 1 -C 4 -Alkyl, C l -C 4 -Alkoxy, C 1 -C 4 -Hafogenalkyl oder C,-C 4 -Halogenalkoxy, A C 1 -C 4 -Alkyl, C 2 -C 4 -Alkenyl, C 1 -C 4 -Alkoxy, C 3 -C 4 -Alkenyloxy, C 3 -C 4 -Alkinyloxy oder -NR 11 R 12 , R 8 , R 10 und R 12 unabhängig voneinander Wasserstoff, C 1 -C 4 -Alkyl, C 3 -C 4 -Alkenyl, C 3 -C 4 -Alkinyl oder C 3 -C 4 -Alkoxyalkyl und R 9 und R" unabhängig voneinander Wasserstoff, C 1 -C 4 -Alkyl, C 3 -C 4 -Alkenyl, C 1 -C 4 -Alkoxy, C 3 -C 4 -Alkinyl oder C 3 -C 4 -Alkoxyalkyl bedeuten, wobei auch R 9 und R 10 sowie R" und R 12 zusammen mit dem sie bindenden Stickstoffatom einen 5- bis 6-gliedrigen gesättigten Heterocyclus bilden können, der als Ringglied gegebenenfalls ein Sauerstoff- oder Schwefelatom oder eine -NH-oder -N(C 1 -C 4 -Alkyl)-Brücke enthalten kann. The acylamide derivatives correspond to formula I. wherein X oxygen, sulfur, -SO- or -SO 2 -, R 1 C 1 -C 6 haloalkyl, C 1 -C 6 cyanoalkyl or C 2 -C e haloalkenyl, R 2 and R 5 independently of one another are hydrogen, C i -C 4 alkyl, C 1 -C 4 haloalkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl or C 2 -C 4 alkoxyalkyl, R 3 and R 4 are independently hydrogen, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, cyano, C 2 -C 4 alkoxyalkyl, -COOR 8 , -CO-NR g R 10 or unsubstituted or by Halogen, cyano or -CO-A substituted C 1 -C 4 alkyl, R 6 and R 7 independently of one another are hydrogen, halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -hafogenalkyl or C, -C 4 -haloalkoxy, AC 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 1 -C 4 alkoxy, C 3 -C 4 alkenyloxy, C 3 -C 4 alkynyloxy or -NR 11 R 12 , R 8 , R 10 and R 12 independently of one another are hydrogen, C 1 -C 4 alkyl, C 3 -C 4 alkenyl, C 3 -C 4 alkynyl or C 3 -C 4 alkoxyalkyl and R 9 and R "independently of one another are hydrogen, C 1 -C 4 alkyl, C 3 -C 4 alkenyl, C 1 -C 4 alkoxy, C 3 -C 4 alkynyl or C 3 -C 4 alkoxyalkyl, where too R 9 and R 10 and R "and R 12 together with the nitrogen atom which binds them can form a 5- to 6-membered saturated heterocycle which, as a ring member, optionally contains an oxygen or sulfur atom or an -NH-or -N (C 1 - C 4 alkyl) bridge can contain. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-102007012168-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8420570-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021245008-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8895471-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0685157-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0616770-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2065374-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2065373-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007050425-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7741317-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1836894-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9426108-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6569806-B1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7563749-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2289310-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5556828-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8754234-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5541148-A |
| priorityDate | 1983-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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