http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-106521-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e70c0aeade92d7571d955d3b90ea06e |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-647 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-10 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-10 |
| filingDate | 2016-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fdd094cfe2f434202aace107ddf0eecb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_86e5c761bfc0c77fff064d683c9bbc66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_37b6cfbe1cbaad95791f8328af943859 |
| publicationDate | 2018-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-106521-A1 |
| titleOfInvention | PIRIDAZINONA HERBICIDES |
| abstract | Compounds that include all stereoisomers, N-oxides and salts thereof, agricultural compositions containing them and their use as herbicides are described. Claim 1: A compound of the formula (1), stereoisomers, N-oxides and salts thereof wherein R¹ is H, C₁₋₇ alkyl, C₃₋₈ alkylcarbonylalkyl, C₃₋₈ alkoxycarbonylalkyl, C₄₋₇ alkylcycloalkyl, C₃₋ alkenyl ₇, C₃₋₇ alkynyl, C₃₋₇ cycloalkyl, C₄₋₇ cycloalkylalkyl, C₂₋₃ cyanoalkyl, C₁₋₄ nitroalkyl, C₂₋₇ haloalkoxyalkyl, C₁₋₇ haloalkyl, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl ₇, C₁₋₇ alkoxy, benzyl or phenyl; or a saturated or partially saturated 5 or 6 membered heterocyclic ring containing selected carbon ring members and up to 1 O and 1 S; W is O or S; A is selected from the compounds of the group of formulas (2); G is G¹ or W¹G¹; W¹ is C₁₋₄ alkanediyl or C₂₋₄ alkenodiyl; G¹ is H, -C (= O) R⁷, -C (= S) R⁷, -CO₂R⁸, -C (= O) SR⁸, -S (O) ₂R⁷, -CONR⁹R¹⁰, -S (O) ₂NR⁹R¹⁰ or P ( = O) R¹¹; or C₁₋₄ alkyl, C₂₋₄ alkenyl, C₂₋₄ alkynyl, C₁₋₄ haloalkyl, C₂₋₄ haloalkenyl, C₂₋₄ haloalkynyl, C₁₋₄ alkoxyalkyl, C₃₋₆ cycloalkyl or C₄₋₇ cycloalkylalkyl; or a 5- or 6-membered heterocyclic ring; R² is H, halogen, -CN, -CHO, C₁₋₇ alkyl, C₃₋₈ alkylcarbonylalkyl, C alco alkoxycarbonylalkyl, C₂₋₇ alkylcarbonyloxy, C₄₋₇ alkylcycloalkyl, C₃₋₇ alkenyl, C₃₋ alkynyl ₇, C₁₋₄ alkylsulfinyl, C₁₋₄ alkylsulfonyl, C₁₋₄ alkylamino, C₂₋₈ dialkylamino, C₄₋₇ cycloalkylalkyl, C₂₋₃ cyanoalkyl, C₁₋₄ nitroalkyl, C₂₋₇ haloalkoxyalkyl, C₁₋ haloalkyl ₇, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl, C₁₋₇ alkoxy, C₁₋₅ alkylthio or C₂₋₃ alkoxycarbonyl; or phenyl optionally substituted by halogen, C₁₋₄ alkyl or C₁₋₄ haloalkyl; each X¹ is, independently, N or CR³; each X² is, independently, N or CR³; each X³ is, independently, N or CR³; each X⁴, X⁵ and X⁶ is, independently, N or CR⁴; each X⁷, X⁸, X⁹ and X¹⁰ is, independently, N or CR⁵; Y¹ is O, S or NR⁶; Y² is O, S or NR⁶; Y⁴ is O, S or NR⁶; each R³ is independently H, halogen, nitro, -CN, C₁₋₅ alkyl, C₂₋₅ alkenyl, C₂₋₅ alkynyl, C₃₋₅ cycloalkyl, C₄₋₅ cycloalkylalkyl, C₁₋₅ haloalkyl, C₃₋₅ haloalkenyl, C₃₋₅ haloalkynyl, C₂₋₅ alkoxyalkyl, C₁₋₅ alkoxy, C₁₋₅ haloalkoxy, C₁₋₄ alkylthio, C₁₋₄ alkylsulfinyl, C₁₋₄ alkylsulfonyl, C₁₋₅ haloalkylthio or C₂₋₅ alkoxycarbonyl; each R⁴ is independently H, halogen, nitro, -CN, C₁₋₅ alkyl, C₂₋₅ alkenyl, C₂₋₅ alkynyl, C₃₋₅ cycloalkyl, C₄₋₅ cycloalkylalkyl, C₁₋₅ haloalkyl, C₃₋₅ haloalkenyl, C₃₋₅ haloalkynyl, C₂₋₅ alkoxyalkyl, C₁₋₅ alkoxy, C₁₋₅ haloalkoxy, C₁₋₄ alkylthio, C₁₋₄ alkylsulfinyl, C₁₋₄ alkylsulfonyl, C₁₋₅ haloalkylthio or C₂₋₅ alkoxycarbonyl; each R⁵ is, independently, halogen, -CN, nitro, C₁₋₅ alkyl, C₂₋₅ alkenyl, C₂₋₅ alkynyl, C₃₋₅ cycloalkyl, C₄₋₅ haloalkyl, C₃₋₅ haloalkenyl, C₃ haloalkenyl ₋₅, C₂₋₅ alkoxyalkyl, C₁₋₅ alkoxy, C₁₋₅ haloalkoxy, C₁₋₅ alkylthio, C₁₋₅ haloalkylthio or C₂₋₅ alkoxycarbonyl; R⁶ is H, C₁₋₇ alkyl, C₂₋₇ alkenyl, C₂₋₇ alkynyl, C₃₋₇ cycloalkyl, C₄₋₇ cycloalkylalkyl, C₁₋₇ haloalkyl or C₂₋₇ alkoxyalkyl; R⁷ is C₁₋₇ alkyl, C₃₋₇ alkenyl, C₃₋₇ alkynyl, C₃₋₇ cycloalkyl, C₁₋₇ haloalkyl, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl, C₄₋₇ cycloalkylalkyl; or phenyl, benzyl or a 5-6 membered heterocyclic ring, wherein each phenyl, benzyl or heterocyclic ring is optionally substituted by halogen, C₁₋₄ alkyl or C₁₋₄ haloalkyl; R⁸ is C₁₋₇ alkyl, C₃₋₇ alkenyl, C₃₋₇ alkynyl, C₃₋₇ cycloalkyl, C₁₋₇ haloalkyl, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl, C₄₋₇ cycloalkylalkyl; or phenyl, benzyl or a 5-6 membered heterocyclic ring, wherein each phenyl, benzyl or heterocyclic ring is optionally substituted by halogen, C₁₋₄ alkyl or C₁₋₄ haloalkyl; R⁹ is C₁₋₇ alkyl, C₃₋₇ alkenyl, C₃₋₇ alkynyl, C₃₋₇ cycloalkyl, C₂₋₇ haloalkyl, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl, C₄₋₇ cycloalkylalkyl; or phenyl, benzyl, or a 5- to 6-membered heterocyclic ring, wherein each phenyl, benzyl or heterocyclic ring is optionally substituted by halogen, C₁₋₄ alkyl or C₁₋₄ haloalkyl; R¹⁰ is H, C₁₋₇ alkyl, C₂₋₇ alkenyl, C₂₋₇ alkynyl, C₃₋₇ cycloalkyl, C₄₋₇ cycloalkylalkyl, C₁₋₇ haloalkyl or C₂₋₇ alkoxyalkyl; and R¹¹ is C₁₋₇ alkyl or C₁₋₇ alkoxy; provided that i) when A is the remainder of formula A-3 and X² is CR³, then X³ is different from CR³; ii) when A is the remainder of formula A-3 and X³ is CR³, then X² is different from CR³; iii) when A is the remainder of formula A-4 and Y⁴ is O, S or NR⁶, then at least one of X⁷, X⁸, X⁹ and X¹⁰ is different from CR⁵; and iv) when R¹ is CH₃; G is H or C (= O) CH₃; R² is Cl or Br; then the rest of formula A-3 is different from 4-quinolinyl (5-Cl), 5-quinolinyl, 4-isoquinolinyl, 5-isoquinolinyl, 6-isoquinolinyl and 8-isoquinolinyl. |
| priorityDate | 2015-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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