http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-102544-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_173bc2c63b34988699010ba05e5b1376 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 |
| filingDate | 2015-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_68b76864009951cd4820ee4b5329fd54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5baf676b47ebedb7e496fe0ff34dcaa2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51975fd44471f1e0d6074a90ebe6207b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a95039a607698e5000f32e203166b888 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c019df3686152c92cb46154e57da1f5d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d78aad0a34a3fc4ce8e6701945fe2bda http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3a9c65480da271eb574d8985347dc4d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4bd1028dab78cfa06efe40bebb51afa7 |
| publicationDate | 2017-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-102544-A1 |
| titleOfInvention | COMPOUNDS DERIVED FROM DIHYDROHYDANTOINE AS HERBICIDES |
| abstract | The application refers to dihydromidantoin derivatives. In addition, it refers to processes and intermediates for preparing compounds of formula (1), herbicidal compositions comprising these compounds and methods for using these compounds in order to control or inhibit plant growth. Claim 1: A compound of formula (1) wherein X is selected from S and O; A is a remainder of formula (2) or (3); Rᵇ is selected from C₁₋₆ alkyl substituted with one or more groups independently selected from hydroxyl, halogen, cyano and C₁₋₆ alkoxy and, when R¹ or R² is C₂₋₆ alkynyl or one of R¹ or R² is C₂ or C₃ alkyl and the other is not H, or R¹ and R² together form an annular structure as described below, Rᵇ can also be C₁₋₆ alkyl; Rᶜ is selected from hydrogen, halogen, cyano, C₁₋₆ alkyl and C₁₋₆ haloalkyl; R¹ is selected from hydrogen, C₁₋₆ alkyl optionally substituted with NR¹⁰R¹¹, C₁₋₃ haloalkyl, C₁₋₆ alkoxy and C₂₋₆ alkynyl; where R¹⁰ and R¹¹ are independently selected from hydrogen, C₁₋₆ alkyl and C₁₋₆ haloalkyl; R² is selected from hydrogen, hydroxy, halogen, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₁₋₆ alkoxy, C₁₋₆ haloalkyl, C₁₋₆ haloalkoxy, (C₁₋₆ alkoxy) - (C₁ alkyl ₋₆) and the group -NR¹²R¹³, where R¹² and R¹³ are independently selected from hydrogen and C₁₋₆ alkyl, or R¹ and R², together with the nitrogen and carbon atoms to which they are attached, form a 3-7 ring saturated or partially unsaturated members optionally comprising 1 to 3 heteroatoms independently selected from S, O and N and optionally substituted with 1 to 3 groups independently selected from hydroxyl, = O, C₁₋₆ alkyl and C₁₋₆ haloalkyl; R³ is selected from halogen, hydroxyl, -NR⁵R⁶ or any of the moieties of the group of formulas (4); R⁵ and R⁶ are independently selected from hydrogen, C₁₋₂₀ alkyl, C₁₋₂₀ haloalkyl, C₂₋₂₀ alkenyl and C₂₋₂₀ alkynyl, or R⁵ and R⁶, together with the carbon atoms to which they are attached, form a ring of 3-6 saturated or partially unsaturated members optionally comprising 1 to 3 heteroatoms independently selected from S, O and N and optionally substituted with 1 to 3 groups independently selected from halogen and C₁₋₆ alkyl; R⁷ and R⁸ are independently selected from hydrogen, C₂₋₆ alkyl, C₁₋₆ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, a C₅₋₁₀ heteroaryl group which can be mono- or bicyclic comprising from 1 to 4 independently selected heteroatoms between N, O and S and optionally substituted with 1 to 3 groups independently selected from halogen, C₁₋₃ alkyl, C₁₋₃ haloalkyl and C₁₋₃ alkoxy, a C₆₋₁₀ aryl group optionally substituted with 1 to 3 groups selected independently between halogen, nitro, cyano, C₁₋₃ alkyl, C₁₋₃ alkoxy, C₁₋₃ haloalkyl and C₁₋₃ haloalkoxy, or R⁷ and R⁸ together with the atoms to which they are attached form a saturated 3-6 membered ring or partially unsaturated optionally comprising 1 to 3 heteroatoms independently selected from S, O and N and optionally substituted with 1 to 3 groups independently selected and between halogen or C₁₋₆ alkyl; R⁹ is selected from C₁₋₆ alkyl or benzyl optionally substituted with 1 to 3 groups independently selected from halogen, nitro, cyano, C₁₋₃ alkyl, C₁₋₃ alkoxy, C₁₋₃ haloalkyl and C₁₋₃ haloalkoxy; or a salt or N-oxide form thereof, with the following conditions (i) when R¹ is methyl, A is the rest of the formula (2), if Rᵇ is Ciano cyanoalkyl or C₁₋₆ haloalkyl, then R² is not C₁₋₄ alkoxy or (C₁₋₄ alkoxy) - (C₁₋₄ alkyl); (ii) when R¹ is C₁₋₃ alkyl, R² is hydrogen, hydroxyl, methyl or allyl, Rᵇ is not C₁₋₆ alkyl substituted by halogen or C₁₋₆ alkoxy; (iii) when R¹ is C₁₋₃ alkyl, R² is H, A is the remainder of formula (2), then Rᵇ is not C₁₋₆ alkyl substituted by halogen. |
| priorityDate | 2014-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 33.