http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-104808-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/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-277 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-76 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/A01N43-82 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-277 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-06 |
| filingDate | 2016-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b18aa29e050d3799734e3e668bffc241 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44e715c25f0ef116010198799eba5722 |
| publicationDate | 2017-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-104808-A1 |
| titleOfInvention | CYCLIC AMIDAS REPLACED AS HERBICIDES |
| abstract | In addition, compositions containing the compounds of formula (1) and methods for controlling unwanted vegetation are described; The methods comprise bringing the unwanted vegetation or its environment into contact with an effective amount of a compound or a composition of the present. Claim 1: A compound selected from formula (1), N-oxides and salts thereof, wherein: A is a saturated, partially unsaturated or completely unsaturated chain containing from 2 to 3 selected atoms of up to 3 carbon atoms, up to 1 O atom, up to 1 S atom and up to 2 N atoms, where up to 2 carbon members are independently selected from C (= O) and C (= S), and the sulfur atom member is selected from S (= O) ᵘ (= NR⁸) ᵛ; that chain is optionally substituted with up to 5 substituents independently selected from R¹⁵ in carbon atoms and R¹⁶ in nitrogen atoms; Q¹ is a phenyl ring or a naphthalenyl ring system; each ring or ring system is optionally substituted with up to 5 substituents independently selected from R⁷; or a 5- to 6-membered heteroaromatic ring or an 8 to 10-membered heteroaromatic bicyclic ring system; Each ring or ring system contains ring members selected from carbon atoms and from 1 to 4 heteroatoms independently selected from up to 2 O atoms, up to 2 S atoms and up to 4 N atoms, where up to 3 ring members that are carbon are independently selected from C (= O) and C (= S), and ring members that are sulfur atoms are independently selected from S (= O) ᵘ (= NR⁸) ᵛ; each ring or ring system is optionally substituted with up to 5 substituents independently selected from R⁷ in ring members that are carbon atoms and selected from R⁹ in ring members that are nitrogen atoms; Q² is a phenyl ring or a naphthalenyl ring system; each ring or ring system is optionally substituted with up to 5 substituents independently selected from R¹⁰; or a 5- to 6-membered heteroaromatic ring or an 8 to 10-membered heteroaromatic bicyclic ring system; Each ring or ring system contains ring members selected from carbon atoms and from 1 to 4 heteroatoms independently selected from up to 2 O atoms, up to 2 S atoms and up to 4 N atoms, where up to 3 ring members that are carbon are independently selected from C (= O) and C (= S), and ring members that are sulfur atoms are independently selected from S (= O) ᵘ (= NR⁸) ᵛ; each ring or ring system is optionally substituted with up to 5 substituents independently selected from R¹⁰ in ring members that are carbon atoms and selected from R¹¹ in ring members that are nitrogen atoms; Y¹ and Y² are, each independently, O, S or NR¹²; J is -CR²R³-; or -CR²R³-CR²ᵃR³ᵃ- where the entity -CR²R³- is directly connected to the N; R¹ is H, hydroxy, amino, cyano, formyl, C₃₋₈ alkylcarbonylalkyl, -C (C₁₋₄ alkyl) = NO (C₁₋₄ alkyl), -C (O) NH₂, C₁₋₆ alkyl, C₁₋₆ haloalkyl , C₂₋₆ alkenyl, C₃₋₆ alkynyl, C₂₋₆ cyanoalkyl, C₃₋₆ cycloalkyl, C₄₋₈ cycloalkylalkyl, C₂₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₂₋₈ haloalkenyl alkyl, C₂₋₈ alkylthioalkyl , Cul alkylsulfinylalkyl, C₂₋₈ alkylsulfonylalkyl, C₂₋₈ alkylcarbonyl, C₂₋₈ haloalkylcarbonyl, C₅₋₁₀ cycloalkylcarbonyl, C₂₋₈ alkoxycarbonyl, C₄₋₁₀ haloalkoxycarbonyl, C₄₋₁₀ cycloalkoxycarbonyl , C₂₋₈ alkylaminocarbonyl, C₃₋₁₀ dialkylaminocarbonyl, C₄₋₁₀ cycloalkylaminocarbonyl, C₁₋₆ alkoxy, C₁₋₆ haloalkyl, C₃₋₈ cycloalkylthio, alkyl lsulfinyl C₁₋₆, haloalkylsulfinyl C₁₋₆, cycloalkylsulfinyl C₃₋₈, alkylsulfonyl C₁₋₆, haloalkylsulfonyl C₁₋₆, cycloalkylsulfonyl C₃₋₈, alkylaminosulfonyl C₁₋₆, dialkylaminosulfonyl C₂₋₈, trialkylsilyl C₃₋₁₀; or arylcarbonyl, arylalkenyl alkyl, arylcarbonylalkyl or -CPh = N-O (C₁₋₄ alkyl), each optionally substituted in ring members with up to 5 substituents independently selected from R¹³; or G¹; R² and R³ are each independently H, halogen, hydroxyl, C₁₋₄ alkyl, C₁₋₄ haloalkyl or C₁₋₄ alkoxy; or R² and R³ are considered together with the carbon atom to which they are attached to form a C₃₋₇ cycloalkyl ring; R²ᵃ and R³ᵃ are each independently H, halogen or C₁₋₄ alkyl; or R²ᵃ and R³ᵃ are considered together with the carbon atom to which they are attached to form a C₃₋₇ cycloalkyl ring; each R⁴ is, independently, H, halogen, hydroxyl, C₁₋₄ alkoxy or C₁₋₄ alkyl; each R⁵ is independently H, halogen, hydroxyl, C₁₋₄ alkoxy, cyano or C₁₋₄ alkyl; R⁶ is H, hydroxyl, amino, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₂₋₆ alkenyl, C₃₋₆ alkynyl, C₂₋₈ alkoxyalkyl, C₂₋₈ alkoxyalkyl alkyl, C halo alkylthioalkyl, C₂ alkylsulfinyl alkyl ₋₈, Cils alkylsulfonylalkyl, C₂₋₈ alkylcarbonyl, C₂₋₈ haloalkylcarbonyl, C₄₋₁₀ cycloalkylcarbonyl, C₂₋₈ haloalkoxycarbonyl, C₄₋₁₀ cycloalkoxycarbonyl, C₂₋₈ alkylaminocarbonyl, C₄ dialkylaminocarbonyl, C₄ cycloalkylaminocarbonyl ₋₁₀, C₁₋₆ alkoxy, C₁₋₆ alkylthio, C₁₋₆ haloalkylthio, C₃₋₈ cycloalkylthio, C₁₋₆ haloalkylsulfinyl, C₃₋₈ cycloalkylsulfinyl, C₁₋₆ alkylsulfonyl, C₁₋₆ haloalkylsulfonyl, C₃ cycloalkylsulfonyl ₋₈, C₁₋₆ alkylaminosulfonyl, C₂₋₈ dialkylaminosulfonyl or C₃₋₁₀ trialkylsilyl; or G¹; each R⁷ is independently halogen, hydroxyl, cyano, nitro, C₁₋₈ alkyl, C₂₋₈ cyanoalkyl, C₁₋₈ cyanoalkoxy, C₁₋₈ haloalkyl, C₂₋₈ alkenyl, C₂₋₈ haloalkenyl, C₂₋₈ alkynyl, haloalkynyl C₂₋₈, C₁₋₈ nitroalkyl, C₂₋₈ nitroalkenyl, C₂₋₈ alkoxyalkyl, C₃₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₃₋₈ cycloalkyl, C₃₋₈ halocycloalkyl, C₄₋₁₀ cycloalkylalkyl, C₄₋₁₀ alkylcycloalkyl, alkoxy C₁₋₈, C halo haloalkoxy, C₂₋₈ alkenyloxy, C₂₋₈ haloalkenyloxy, C₃₋₈ alkynyloxy, C₃₋₈ haloalkyloxy, C₃₋₈ alkylthio, C halo haloalkylthio, C₁₋₈ alkylsulfinyl, haloalkylsulfinyl C₁₋₈, C₁₋₈ alkylsulfonyl, C₁₋₈ haloalkylsulfonyl, hydroxy, formyl, C₂₋₈ alkylcarbonyl, C₂₋₈ alkylcarbonyloxy, C₁₋₈ alkylsulfonyloxy, C₁₋₈ haloalkylsulfonyloxy, amino, C₁₋₄ alkylamino, C₂₋₄ dialkylamino, formylamino, C₂₋₄ alkylcarbonylamino, -SF₅, -SCN, C₄₋₁₀ cycloalkylalkoxy, C₄₋₁₀ cycloalkylalkyl, C₂₋₈ alkenyloxy, C₂₋₈ haloalkenyloxy, C₂₋₈ alkoxyalkoxy, C₂₋₈ alkylthioalkyl, C₂₋₈ alkylsulfinylalkyl, C₂₋₈ alkylsulfonylalkyl, C₁₋₈ alkylsulfonyloxy, C halo haloalkylsulfonyloxy, C₃₋₈ alkylthio, C₁₋₈ haloalkylthio, C₁₋₈ alkylsulfinyl, C₁₋₈ haloalkyl C₁₋₈ alkylsulfonyl, or C₁₋₈ haloalkylsulfonyl, C₂₋₈ alkynyl, C₂₋₈ haloalkynyl, C₂₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₂₋₈ haloalkoxyalkoxy, C₁₋₈ haloalkoxyalkyl, C₃₋₈ haloalkyl , C₂₋₈ alkylcarbonyloxy, C₂₋₈ haloalkylcarbonyloxy, C₃₋₁₂ trialkylsilyl, trimethylsilylmethyl or trimethylsilylmethoxy; or G²; or R¹⁷ON = CR¹⁷ᵃ-, (R¹⁸) ₂C = NO, (R¹⁹) ₂NN = CR¹⁷ᵃ-, (R¹⁸) ₂C = NNR²⁰ᵃ-, R²⁰N = CR¹⁷ᵃ-, (R¹⁸) ₂C = N-, R¹⁷ON = CR¹⁷ᵃC (R²³ᵇ) ₂- or (R¹⁸) ₂C = NOC (R²⁴ᵃ) ₂-, where the double bond that projects to the right indicates the point of connection to Q¹; or two adjacent R⁷s are considered in conjunction with the carbon atoms to which they are attached to form a C₃₋₇ cycloalkyl ring; each R¹⁰ is independently halogen, hydroxyl, cyano, nitro, C₁₋₈ alkyl, C₂₋₈ cyanoalkyl, C₁₋₈ cyanoalkoxy, C₁₋₃ haloalkyl, C₂₋₈ alkenyl, C₂₋₈ haloalkenyl, C₂₋₈ alkynyl, haloalkynyl C₂₋₈, C₁₋₈ nitroalkyl, C₂₋₈ nitroalkenyl, C₂₋₈ alkoxyalkyl, C₃₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₃₋₈ cycloalkyl, C₃₋₈ halocycloalkyl, C₄₋₁₀ cycloalkylalkyl, C₄₋₁₀ alkylcycloalkyl, alkoxy C₁₋₈, C halo haloalkoxy, C₂₋₈ alkenyloxy, C₂₋₈ haloalkenyloxy, C₃₋₈ alkynyloxy, C₃₋₈ haloalkyloxy, C₃₋₈ alkylthio, C halo haloalkylthio, C₁₋₈ alkylsulfinyl, haloalkylsulfinyl C₁₋₈, C₁₋₈ alkylsulfonyl, C₁₋₈ haloalkylsulfonyl, hydroxy, formyl, C₂₋₈ alkylcarbonyl, C₂₋₈ alkylcarbonyloxy, C₁₋₈ alkylsulfonyloxy, C₁₋ haloalkylsulfonyloxy , amino, C₁₋₄ alkylamino, C₂₋₄ dialkylamino, formylamino, C₂₋₄ alkylcarbonylamino, -SF₅, -SCN, C₄₋₁₀ cycloalkylalkoxy, C₄₋₁₀ cycloalkylalkyl, C₂₋₈ alkenyloxy, C₂₋₈ haloalkenyloxy, C₂₋₈ alkoxyalkoxy , C₂₋₈ alkylthioalkyl, C₂₋₈ alkylsulfinyl alkyl, C₂₋₈ alkylsulfonylalkyl, C₂₋₈ alkylsulfonyloxy, C halo haloalkylsulfonyloxy, C₃₋₈ alkylthio, C₁₋₈ haloalkylthio, C₁₋₈ alkylsulfinyl, C₁₋₈ haloalkyl , C₁₋₈ alkylsulfonyl, C₁₋₈ haloalkylsulfonyl, C₂₋₈ alkynyl, C₂₋₈ haloalkynyl, C₂₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₂₋₈ haloalkoxyalkoxy, C₁₋₈ haloalkoxyalkyl, C₃₋₈ haloalkyl , C₂₋₈ alkylcarbonyloxy, C₂₋₈ haloalkylcarbonyloxy, C₃₋₁₂ trialkylsilyl, trimethylsilylmethyl or trimethylsilylmethoxy; or G²; or R¹⁷ON = CR¹⁷ᵃ-, (R¹⁸) ₂C = NO-, (R¹⁹) ₂NN = CR¹⁷ᵃ-, (R¹⁸) ₂C = NNR²⁰ᵃ-, R²⁰N = CR¹⁷ᵃ-, (R¹⁸) ₂C = N-, R¹⁷ON = CR¹⁷ᵃC (R²³ᵇ) ₂ - or (R¹⁸) ₂C = NOC (R²⁴ᵃ) ₂-, where the double link that projects to the right indicates the connection point to Q²; or two adjacent R¹⁰s are considered in conjunction with the carbon atoms to which they are attached to form a C₃₋₇ cycloalkyl ring; each R⁸ is independently H, cyano, C₂₋₃ alkylcarbonyl or C₂₋₃ haloalkylcarbonyl; each R⁹ and R¹¹ is, independently, cyano, C₁₋₃ alkyl, C₂₋₃ alkenyl, C₂₋₃ alkynyl, C₃₋₆ cycloalkyl, C₂₋₃ alkoxyalkyl, C₁₋₃ alkoxy, C₂₋₃ alkylcarbonyl, C₂₋₃ alkoxycarbonyl, C₂₋₃ alkylaminoalkyl or C₃₋₄ dialkylaminoalkyl; each R¹² is independently H, cyano, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, - (C = O) CH₃ or - (C = O) CF₃; each G¹ is, independently, phenyl, phenylmethyl, pyridinylmethyl, phenylcarbonyl, phenoxy, phenylethynyl, phenylsulfonyl, phenylcarbonylalkyl, 2-, 3- or 4-pyridinyloxy or a 5- or 6-membered heteroaromatic ring; each is optionally substituted on the annular members with up to 5 substituents independently selected from R¹³; each G² is, independently, phenyl, phenylmethyl, pyridinylmethyl, phenylcarbonyl, phenylcarbonylalkyl, phenoxy, phenylethynyl, phenylsulfonyl, 2-, 3- or 4-pyridinyloxy or a 5- or 6-membered heteroaromatic ring; each is optionally substituted on the annular members with up to 5 substituents independently selected from R¹⁴; each R¹³ and R¹⁴ is independently halogen, cyano, hydroxyl, amino, nitro, CHO, -C (= O) OH, -C (= O) NH₂, -SO₂NH₂, C₁₋₆ alkyl, C₁₋₆ haloalkyl, alkenyl C₂₋₆, C₂₋₆ alkynyl, C₂₋₈ alkylcarbonyl, C₂₋₈ haloalkylcarbonyl, C₂₋₈ alkoxycarbonyl, C₄₋₁₀ cycloalkoxycarbonyl, C₂₋₈ alkylaminocarbonyl, C₃₋₁₀ dialkylaminocarbonyl, C₁₋₆ alkoxy, haloalkoxy C₁₋₆, Ccar alkylcarbonyloxy, C₁₋₆ alkylthio, C₁₋₆ haloalkylthio, C₁₋₆ alkylsulfinyl, C₁₋₆ haloalkylsulfinyl, C₁₋₆ alkylsulfonyl, C₁₋₆ haloalkylsulfonyl, C₂₋₈ alkylaminosulfonyl, Cquila dialkylaminosulfonyl, trialkylsilyl C₃₋₁₀, C₁₋₆ alkylamino, C₂₋₈ dialkylamino, C₂₋₈ alkylcarbonylamino, C₁₋₆ alkylsulfonylamino, phenyl, pyridinyl or thienyl; each R¹⁵ is independently halogen, cyano, hydroxyl, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₂₋₄ alkoxyalkyl, C₂₋₄ alkylcarbonyl, C₂₋₄ alkoxycarbonyl, C₃₋ cycloalkyl ₆ or C₄₋₈ cycloalkylalkyl; or two adjacent R¹⁵s are considered in conjunction with the carbon atom (s) to which they are attached to form a C₃₋₇ cycloalkyl ring; each R¹⁶ is, independently, cyano, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₄ alkoxy, C₂₋₄ alkylcarbonyl, C₂₋₄ alkoxycarbonyl or C₃₋₆ cycloalkyl; each R¹⁷ is, independently, H, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₄₋₈ cycloalkylalkyl, C₁₋₆ haloalkyl, Cque alkynyl, C₂₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₂ alkylthioalkyl ₋₈, C-alkylsulfinylalkyl, C₂₋₈ alkylsulfonylalkyl, C₂₋₈ alkylcarbonyl, C₂₋₈ haloalkylcarbonyl, C₂₋₈ alkoxycarbonyl, C₄₋₁₀ haloalkoxycarbonyl, C₄₋₁₀ cycloalkoxycarbonyl, C₂₋₈ alkylaminocarbonyl, C₃ dialkylaminocarbonyl ₋₁₀, C₄₋₁₀ cycloalkylaminocarbonyl, C₁₋₆ alkylsulfinyl, C₁₋₆ haloalkylsulfinyl, C₃₋₈ cycloalkylsulfinyl, C₁₋₆ alkylsulfonyl, C₃₋₈ haloalkylsulfonyl, C₁₋₆ cycloalkylsulfonyl, or C₃ dialkylaminosulfonyl or C₃ trialkylsilyl ₋₁₀; or G¹; each R¹⁷ᵃ is, independently, H, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₄₋₈ cycloalkylalkyl, C₁₋₆ haloalkyl, Cque alkynyl, C₂₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₂ alkylthioalkyl ₋₈, C-alkylsulfinylalkyl, C₂₋₈ alkylsulfonylalkyl, C₁₋₆ alkoxy, C₁₋₆ alkylthio, C₁₋₆ haloalkylthio, C₃₋₈ cycloalkylthio or C₃₋₁₀ trialkylsilyl; or G¹; each R¹⁸ is independently H, hydroxyl, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₄₋₈ cycloalkylalkyl, C₁₋₆ haloalkyl, C₂₋₆ alkynyl, C₃₋₆ alkynyl, C₂₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₂₋₈ alkylthioalkyl, C₂₋₈ alkyl alkylsilyl alkyl, C₂₋₈ alkylsulfonylalkyl, C₂₋₈ alkylcarbonyl, C₂₋₈ haloalkylcarbonyl, C₂₋₈ alkoxycarbonyl, C₂₋₈ haloalkoxycarbonyl, C₄₋₁₀ cycloalkoxycarbonyl, C₂₋₈ alkylaminocarbonyl C₃₋₁₀ dialkylaminocarbonyl, C₄₋₁₀ cycloalkylaminocarbonyl, C₁₋₆ alkoxy, C₁₋₆ alkylthio, C₃₋₈ haloalkylthio, C₁₋₆ alkylsulfinyl, C₁₋₆ haloalkylsulfinyl, C₃₋₈ cycloalkylsulfinyl, C₁₋₆ alkylsulfonyl, C₁₋₆ haloalkylsulfonyl, C₃₋₈ cycloalkylsulfonyl, C₁₋₆ alkylaminosulfonyl, C₂₋₈ dialkylaminosulfonyl ot C₃₋₁₀-rialkylsilyl; or G¹; each R¹⁹ is, independently, H, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₄₋₈ cycloalkylalkyl, C₁₋₆ haloalkyl, Cque alkynyl, C₂₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₂ alkylthioalkyl ₋₈, C-alkylsulfinylalkyl, C₂₋₈ alkylsulfonylalkyl, C₂₋₈ alkylcarbonyl, C₂₋₈ haloalkylcarbonyl, C₂₋₈ alkoxycarbonyl, C₄₋₁₀ haloalkoxycarbonyl, C₄₋₁₀ cycloalkoxycarbonyl, C₂₋₈ alkylaminocarbonyl, C₃ dialkylaminocarbonyl ₋₁₀, C₄₋₁₀ cycloalkylaminocarbonyl, C₁₋₆ alkoxy, C₁₋₆ alkylsulfinyl, C₁₋₆ haloalkylsulfinyl, C₃₋₈ cycloalkylsulfonyl, C₁₋₆ alkylsulfonyl, C₁₋₆ haloalkylsulfonyl, C₁₋₆ cycloalkylsulfonyl, C₂ alkylaminosulfonyl, C₂ dialkylaminosulfonyl ₋₈ or trialkylsilyl C₃₋₁₀; or G¹; each R²⁰ is independently H, hydroxyl, amino, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₄₋₈ cycloalkylalkyl, C₁₋₆ haloalkyl, C₂₋₆ alkenyl, C₃₋₆ alkynyl, C₂₋₈ alkoxyalkyl, C₂₋ haloalkoxyalkyl ₈, alkylthioalkyl C₂₋₈, alkylsulfinylalkylC₂₋₈, alkylsulfonylalkylC₂₋₈, alkylcarbonyl C₂₋₈, haloalkylcarbonyl C₂₋₈, cycloalkylcarbonyl C₄₋₁₀, alkoxycarbonyl C₂₋₈, haloalkoxycarbonyl C₂₋₈, cycloalkoxycarbonyl C₄₋₁₀, alkylaminocarbonyl C₂₋ ₈, dialkylaminocarbonyl C₃₋₁₀, cycloalkylaminocarbonyl C₄₋₁₀, alkoxy C₁₋₆, alkylsulfinyl C₁₋₆, haloalkylsulfinyl C₁₋₆, cycloalkylsulfinyl C₃₋₈, alkylsulfonyl C₁₋₆, haloalkylsulfonyl C₁₋₆, cycloalkylsulfonyl C₃₋₈, alkylaminosulfonyl C₁₋ ₆, Cquila dialkylaminosulfonyl or C₃₋₁₀ trialkylsilyl; or G¹; each R²⁰ᵃ is, independently, H, C₁₋₆ alkyl, Cal cycloalkyl, C₄₋₈ cycloalkylalkyl, C halo haloalkyl, Cque alkynyl, C₂₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₂ alkylthioalkyl ₋₈, Cul alkylsulfinylalkyl, C₂₋₈ alkylsulfonylalkyl, C₁₋₆ alkoxy or C₃₋₁₀ trialkylsilyl; G or G¹; each R²³ᵇ is independently H, halogen, cyano, hydroxyl, C₁₋₄ alkyl, C₃₋₈ cycloalkyl, C₄₋₈ cycloalkylalkyl, C₁₋₄ haloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, C₂₋₄ alkoxyalkyl, alkylcarbonyl C₂₋₄, C₂₋₄ alkoxycarbonyl or C₃₋₆ cycloalkyl; each R²⁴ᵃ is independently H, C₁₋₄ alkyl, C₃₋₈ cycloalkyl, C₄₋₈ cycloalkylalkyl, C₁₋₄ haloalkyl, C alco alkoxy, C₁₋₄ haloalkoxy, C₂₋₄ alkoxyalkyl, C₂₋₄ alkylcarbonyl, C₂ alkoxycarbonyl ₋₄ or C₃₋₆ cycloalkyl; and each u and v are independently 0, 1 or 2 in each instance of S (= O) ᵘ (= NR⁸) ᵛ, provided that the sum of u and v is 0, 1 or 2; provided that A is S and Q¹ is unsubstituted phenyl, Q² is different from unsubstituted phenyl. |
| priorityDate | 2015-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 50.