http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-118613-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e445efbdd9771acb62e05c2c3cfb6ed2 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01P3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-82 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D271-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D419-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D419-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-836 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-06 |
| filingDate | 2020-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d71b123aceb865381682964099a187c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d90f7a2d4d657545cd1537a38b140fe1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_218bf9aa78dae8e4fc95c3c500435223 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a2f60deb74d842e280bb1b953c6098e2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_29371fc936ba36c48ecb9ee4558aa6ab http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b11c625f162cd8f2a701f2ad847731fe http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_35ca3ce754c5c29d23dbc30d01ba1ac5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f910544dfd29045377da54f16037e4e0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de83929b736d00ba08d1b6a8b17a926f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_caf04d2842fcbed0a63585c0bb8fa19d |
| publicationDate | 2021-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-118613-A1 |
| titleOfInvention | OXADIAZOLE COMPOUNDS TO CONTROL OR PREVENT PHYTOPATHOGENIC FUNGI |
| abstract | Claim 1: A compound of formula (1), wherein R¹ is C₁₋₃-haloalkyl; W is O or S; L¹ is a direct bond, or is selected from the group consisting of -CR²R³-, -C (= W¹) -, -CR²R³C (= W¹) -, -O-, -S (= O) ₀₋₂- , and -NR⁴ᵃ-, where W¹ is O or S; the expression "-" at the beginning and end of the group indicates the point of attachment to either the oxidazole ring or A; k is an integer ranging from 0 to 4; A is a fused or unfused 3- to 10-membered carbocyclic or heterocyclic ring; wherein, A is optionally substituted with one or more identical or different groups from RA; RA is selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, SF₅, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃₋₈-cycloalkyl, C₃₋ ₈-cycloalkylalkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy-C₁₋₄-alkyl, C₁₋₆-hydroxyalkyl, C₂₋₆-haloalkenyl, C₂₋₆-haloalkynyl, C₃₋₈-halocycloalkyl, C₁₋₆- alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-halo6alkoxycarbonyl, C₁₋₆-alkylthio, C₁₋₆-haloalkylthio, C₁₋₆-haloalkylsulfinyl, C₁₋₆-haloalkylsulfonyl, C₁₋₆-alkylsulfinyl, C₁₋₆-alkylsulfonyl, C₁₋₆-alkylamino, C₁₋₆-dialkylamino, C₃₋₈-cycloalkylamino, C₁₋₆-alkyl-C₃₋₈-cycloalkylamino, C₁₋₆-alkylcarbonyl, C₁₋₆-alkoxycarbonyl, C₁₋₆-alkylaminocarbonyl, C₁₋ ₆-dialkylaminocarbonyl, C₁₋₆-alkoxycarbonyloxy, C₁₋₆-alkylaminocarbonyloxy, C₁₋₆-dialkylaminocarbonyloxy and a 3- to 6-membered carbocyclic or heterocyclic ring; wherein, a 3- to 6-membered carbocyclic or heterocyclic ring may be optionally substituted with one or more identical or different substituent groups selected from the group consisting of halogen, cyano, nitro, hydroxy, C₁₋₆-alkyl , C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkylalkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxyalkyl, C₁₋₆-hydroxyalkyl, C₂₋₆-haloalkenyl, C₂ ₋₆-haloalkynyl, C₃₋₆-halocycloalkyl, C₁₋₆-alkoxy, C₁₋₆-alkylthio, C₁₋₆-haloalkylthio, C₁₋₆-haloalkylsulfinyl, C₁₋₆-haloalkylsulfonyl, C₁₋₆-alkylsulfinyl, C₁₋₆ -alkylsulfonyl, C₁₋₆-alkylamino, di-C₁₋₆-alkylamino, C₃₋₆-cycloalkylamino, C₁₋₆-alkyl-C₃₋₆-cycloalkylamino, C₁₋₆-alkylcarbonyl, C₁₋₆-alkoxycarbonyl, C₁₋₆ -alkylaminocarbonyl, di-C₁₋₆-alkylaminocarbonyl, C₁₋₆-alkoxycarbonyloxy, C₁₋₆-alkylaminocarbonyloxy and di-C₁₋₆-alkylaminocarbonyloxy; L² and L⁴ are a direct bond or are independently selected from the group consisting of -O-, -S (= O) ₀₋₂-, -NR¹⁰-, -C (= O) -, -C (= S ) -, a compound of the group of formulas (2), NR¹⁰- (C = W²) -NR¹⁰-, -NR¹⁰-S (= O) ₀₋₂-NR¹⁰-, - (C = W²) -NR¹⁰-NR¹⁰- , -S (= O) ₀₋₂-NR¹⁰-NR¹⁰-, -NR¹⁰-NR¹⁰- (C = W²) -, -NR¹⁰-NR¹⁰-S (= O) ₀₋₂-, -NR¹⁰- (C = W² ) -NR¹⁰-NR¹⁰-, -NR¹⁰-S (= O) ₀₋₂-NR¹⁰-NR¹⁰-, -NR¹⁰-NR¹⁰- (C = W²) -NR¹⁰-, -NR¹⁰-NR¹⁰-S (= O) ₀₋ ₂-NR¹⁰-, -O (C = W²) -NR¹⁰- and -NR¹⁰- (C = W²) -O-; X is a direct bond or -NR¹⁰-, or -O-, or -S (O) ₀₋₂-, or -C (= NOR¹¹) -; k is an integer ranging from 0 to 4; the expressions "-", "#" and "*" indicate a point of connection on both sides; W² is O or S; L³ is a direct bond or is selected from the group consisting of -CR¹⁶R¹⁷-, -CR¹⁶R¹⁷C (= O) -, -C (= O) -, -C (= S) -, -O-, -S ( = O) ₀₋₂-, -S (O) ₀₋₁ (= NR¹⁰) -, -S (= N-CN) -, -S (= N-NO₂) -, -S (= N-COR¹⁶) -, -S (= N-COOR¹¹) -, -S (= N- (S (= O) ₂R¹²)) -, -NR¹⁰-, -NR¹⁰ (C (= O)) O- and -CR¹⁶ (= N )OR-; R¹⁶ and R¹⁷ are independently selected from the group consisting of hydrogen, halogen, cyano, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃ ₋₈-cycloalkyl, C₁₋₆-alkylthio, C₃₋₈-cycloalkenyl, phenyl-C₁₋₆-alkyl, heteroaryl-C₁₋₆-alkyl, phenyl, naphthyl and a mono or bicyclic carbocyclic ring or an aromatic heterocyclic ring of 3 to 10 membered saturated and partially unsaturated, wherein the members of the heteroaryl ring of the heteroaryl-C₁₋₆-alkyl and the heterocyclic ring include C, N, O and S (O) ₀₋₂ and the members of the C ring of the carbocyclic ring or the heterocyclic ring can be replaced by one or more C (= O) and C (= S); and wherein R¹⁶ and R¹⁷ are independently unsubstituted or substituted with one or more identical or different R¹⁶ᵃ and R¹⁷ᵃ groups, respectively; R¹⁶ᵃ and R¹⁷ᵃ are independently selected from the group consisting of halogen, cyano, nitro, hydroxy, sulfanyl, amino, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁ ₋₆-alkylthio, C₁₋₆-haloalkylthio, C₃₋₈-cycloalkyl, amino-C₁₋₆-alkyl, di-C₁₋₆-alkylamino, NHSO₂-C₁₋₆-alkyl, -C (= O) -C₁₋ ₆-alkyl, C (= O) -C₁₋₆-alkoxy, C₁₋₆-alkylsulfonyl, hydroxy-C₁₋₆-alkyl, -C (= O) -NH₂, C (= O) -NH (C₁₋₆ -alkyl), C₁₋₆-alkylthio-C₁₋₆-alkyl, C₁₋₆-alkylamino-C₁₋₆-alkyl, di-C₁₋₆-alkylamino-C₁₋₆-alkyl, aminocarbonyl-C₁₋₆-alkyl and C₁₋₆-alkoxy-C₁₋₆-alkyl; or R¹⁶ and R¹⁷ together with the atoms to which they are attached form C (= O) or a vinyl group or a 3- to 7-membered monocyclic saturated heterocyclic ring or a carbocyclic ring, wherein the members of the heterocyclic ring include C , N, O and S (O) ₀₋₂; and wherein the vinyl group, heterocyclic ring, or carbocyclic ring is unsubstituted or substituted with one or more identical or different R¹⁶ᵇ and R¹⁷ᵇ, wherein R¹⁶ᵇ and R¹⁷ᵇ are independently selected from the group consisting of halogen, cyano, nitro, hydroxy, sulfanyl, amino, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-alkylthio, C₁₋₆-haloalkylthio, C₃₋₈- cycloalkyl, SO₂-C₁₋₆-alkyl, NHSO₂-C₁₋₆-alkyl, -C (= O) -C₁₋₆-alkyl, C (= O) -C₁₋₆-alkoxy, C₁₋₆-alkylsulfonyl, SO₂ -C₆H₄CH₃ and SO₂-aryl; R¹⁰ and R¹¹ are independently selected from the group consisting of hydrogen, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₁₋₆-alkoxy, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkenyl , C₃₋₆-cycloalkyl-C₁₋₆-alkyl, phenyl-C₁₋₆-alkyl, phenyl, pyridinayl, C (= O) - (C₁₋₆-alkyl), C (= O) - (C₁₋₆- alkoxy) and -N (R¹⁰ᵃ) ₂; wherein R¹⁰ᵃ is independently selected from the group consisting of hydrogen, OH, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkenyl, C₁₋ ₆-alkoxy, C₁₋₆-alkoxy-C₁₋₆-alkyl and C₁₋₆-alkylthio; R¹⁰ and R¹¹ are independently unsubstituted or substituted with an identical or different radical selected from the group consisting of halogen, hydroxy, oxo, cyano, C₁₋₆-alkyl, C₁₋₆-alkoxy, and C₃₋₆-cycloalkyl ; R¹² is selected from the group consisting of hydrogen, NRᵍRʰ; wherein, Rᵍ and Rʰ independently represent hydrogen, hydroxy, cyano, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, or C₃₋₈-cycloalkyl; (C = O) -Rⁱ, where Rⁱ represents hydrogen, halogen, cyano, C₁₋₄-alkyl, C₂₋₄-alkenyl, C₂₋₄-alkynyl, C₁₋₄-haloalkyl, C₂₋₄-haloalkenyl, C₂₋₄-haloalkynyl, C₃₋₆-cycloalkyl, C₃₋₆-halocycloalkyl, C₁₋₄-alkoxy, and C₁₋₄-haloalkoxy; C₁₋₈-alkyl-S (O) ₀₋₂Rʲ, where Rʲ represents hydrogen, halogen, cyano, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₃ ₋₈-cycloalkyl; C₁₋₆-alkyl- (C = O) -Rⁱ, CRⁱ = NRᵍ, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₁₋₆-haloalkyl, C₂₋₆-haloalkenyl, C₂₋ ₆-haloalkynyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₃₋₈-cycloalkyl, C₄₋₈-cycloalkenyl, C₇₋₁₉-aralkyl, C₅₋₁₂-bicyclic alkyl, C₇₋₁₂-alkenyl, fused or not fused or bicyclic C₃₋₁₈- carbocyclic ring or ring system; in which one or more C atoms of the carbocyclic ring or ring system can be replaced by N, O, S (= O) ₀₋₂, S (= O) ₀₋₁ (= NR¹⁰), C (= O) , C (= S), C (= CR¹⁶R¹⁷) and C = NR¹⁰, R¹² may be optionally substituted with one or more identical or different substituents selected from the group consisting of hydrogen, halogen, cyano, nitro, hydroxy, C₁₋ ₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkylalkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy-C₁₋₄-alkyl, C₁₋₆- hydroxyalkyl, C₂₋₆-haloalkenyl, C₁₋₆-haloalkynyl, C₃₋₈-halocycloalkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-haloalkoxycarbonyl, C₁₋₆-alkylthio, C₁₋₆-haloalkylthio, C₁₋₆-haloalkylsulfinyl, C₁₋₆-haloalkylsulfonyl, C₁₋₆-alkylsulfinyl, C₁₋₆-alkylsulfonyl, C₁₋₆-alkylamino, di-C₁₋₆-alkylamino, C₃₋₈-cycloalkylamino, C₁₋₆-alkyl- C₃₋₈-cycloalkylamino, C₁₋₆-alkylcarbonyl, C₁₋₆-alkoxycarbonyl, C₁₋₆-alkylaminocarbonyl, di-C₁₋₆-alkylaminocarbonyl, C₁₋₆-alkoxycarbonyloxy, C₁₋₆-alkylaminocarbonyloxy, diC₁₋₆-alkylaminocarbonyloxy, a 5 to 11 membered spirocyclic ring, and a 3 to 6 membered carbocyclic or heterocyclic ring; R⁸ and R⁹ are independently selected from the group consisting of hydrogen, halogen, cyano, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃ ₋₈-cycloalkyl, C₁₋₆-alkylthio, C₃₋₈-cycloalkenyl, phenyl-C₁₋₆-alkyl, heteroaryl-C₁₋₆-alkyl, phenyl, naphthyl or a mono or bicyclic carbocyclic ring or a saturated heterocyclic ring, partially 3- to 10-membered unsaturated or aromatic, wherein the members of the heteroaryl-C₁₋₆-alkyl heteroaryl ring and the heterocyclic ring include C, N, O, and S (O) ₀₋₂ and the members of the C ring of the carbocyclic ring or the heterocyclic ring can be replaced by one or more C (= O) and C (= S); and wherein R⁸ and R⁹ are independently unsubstituted or substituted with one or more identical or different R⁸ᵃ and R⁹ᵃ, respectively, wherein R⁸ᵃ and R⁹ᵃ are independently selected from the group consisting of halogen, cyano, nitro, hydroxy, sulfanyl, amino, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-alkylthio, C₁₋₆-haloalkylthio, C₃₋₈-cycloalkyl, amino-C₁₋ ₆-alkyl, di-C₁₋₆-alkylamino, NHSO₂-C₁₋₆-alkyl, -C (= O) -C₁₋₆-alkyl, C (= O) -C₁₋₆-alkoxy, C₁₋₆-alkylsulfonyl , hydroxy-C₁₋₆-alkyl, -C (= O) -NH₂, C (= O) -NH (C₁₋₆-alkyl), C₁₋₆-alkylthio-C₁₋₆-alkyl, C₁₋₆-alkylamino -C₁₋₆-alkyl, di-C₁₋₆-alkylamino-C₁₋₆-alkyl, aminocarbonyl-C₁₋₆-alkyl and C₁₋₆-alkoxy-C₁₋₆-alkyl; or R⁸ and R⁹ together with the atoms to which they are attached form C (= O) or a vinyl group or a monocyclic carbocyclic ring or a saturated or unsaturated 3- to 7-membered heterocyclic ring, in which the ring members heterocyclic include C, N, O, and S (O) ₀₋₂; and wherein the vinyl group, heterocyclic ring, or carbocyclic ring is unsubstituted or substituted with one or more identical or different R⁸ᵇ, wherein R⁸ᵇ is independently selected from the group consisting of halogen, cyano, nitro, hydroxy, sulfanyl, amino, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-alkylthio, C₁₋₆-haloalkylthio, C₃₋₈-cycloalkyl, SO₂- C₁₋₆-alkyl, NHSO₂-C₁₋₆-alkyl, -C (= O) -C₁₋₆-alkyl, C (= O) -C₁₋₆-alkoxy, C₁₋₆-alkylsulfonyl, SO₂-C₆H₄CH₃, and SO₂-aryl; R⁵ is selected from the group consisting of hydrogen, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₁₋₆-haloalkyl, C₂₋₆-haloalkenyl, C₂₋₆-haloalkynyl, C₃₋ ₈-cycloalkyl, C₃₋₈-halocycloalkyl, C₁₋₆-alkyl-C₃₋₈-cycloalkyl, C₃₋₈-cycloalkyl-C₁₋₆-alkyl, C₃₋₈-cycloalkyl-C₃₋₈-cycloalkyl, C₃₋₈- halocycloalkyl-C₁₋₆-alkyl, C₁₋₆-alkyl-C₃₋₈-cycloalkyl-C₁₋₆-alkyl, C₃₋₈-cycloalkenyl, C₃₋₈-halocycloalkenyl, C₁₋₆-alkoxy, C₁₋₆-alkoxy- C₁₋₆; alkyl, C₃₋₈-cycloalkoxy-C₁₋₆-alkyl, C₁₋₆-alkoxy-C₁₋₆-alkoxy-C₁₋₆-alkyl, C₁₋₆-alkyl-C₁₋₆-thioalkyl, C₁₋₆-alkylsulfinyl- C₁₋₆-alkyl, C₁₋₆-alkylsulfonyl-C₁₋₆-alkyl, C₁₋₆-alkylamino, di-C₁₋₆-alkylamino, C₁₋₆-alkylamino-C₁₋₆-alkyl, di-C₁₋₆- alkylamino-C₁₋₆-alkyl, C₁₋₆-haloalkylamino-C₁₋₆-alkyl, C₃₋₈-cycloalkylamino, C₃₋₈-cycloalkylamino-C₁₋₆-alkyl, C₁₋₆-alkylcarbonyl, C₁₋₆-haloalkoxy- C₁₋₆-alkyl, C₁₋₆-hydroxyalkyl, C₂₋₆-hydroxyalkenyl, C₂₋₆-hydroxyalkynyl, C₃₋₈-halocycloalkoxy, C₃₋₈-cycloalkyl-C₁₋₆-alkoxy, C₂₋₆-alkenyloxy, C₂₋ ₆-haloalkenyloxy, C₂₋₆-alkynyloxy, C₂₋₆-haloalkynyloxy, C₁₋₆-alkoxy-C₁₋₆-alkoxy, C₁₋₆-alkylcarbonylalkoxy, C₁₋₆-alkylthio, C₁₋₆-haloalkylthio, C₃₋₈- cycloalkylthio, C₁₋₆-alkylsulfinyl, C₁₋₆-haloalkylsulfinyl, C₁₋₆-alkylsulfonyl, C₁₋₆-haloalkylsulfonyl, C₃₋₈-cycloalkylsulfonyl, C₃₋₈-cycloalkylsulfinyl, tri-C₁₋₆-alkylsilyl, C₁₋₆- alkylsulfonylamino, C₁₋₆-haloalkylsulfonylamino, C₁₋₆-alkylcarbonylthio, C₁₋₆-alkylsulfonyl xi, C₁₋₆-alkylsulfinylooxy, C₆₋₁₀-arylsulfonyloxy, C₆₋₁₀-arylsulfinylooxy, C₆₋₁₀-arylsulfonyl, C₆₋₁₀-arylsulfinyl, C₆₋₁₀-arylthio, C₁₋₆-cyanoalkyl, C₂₋₆-alkenylcarbonyloxy, C₁₋₆-alkoxy-C₁₋₆-alkylthio, C₁₋₆-alkylthio-C₁₋₆-alkoxy, C₂₋₆-haloalkenylcarbonyloxy, C₁₋₆-alkoxycarbonyl-C₁₋₆-alkyl, C₁₋₆-C₂₋-alkoxy ₆-alkynyl, C₂₋₆-alkynylthio, C₃₋₈-halocycloalkylcarbonyloxy, C₂₋₆-alkenylamino, C₂₋₆-alkynylamino, C₁₋₆-haloalkylamino, C₃₋₈-cycloalkyl-C₁₋₆-alkylamino, C₁₋₆- alkoxyamino, C₁₋₆-haloalkoxyamino, C₁₋₆-alkoxycarbonylamino, C₁₋₆-alkylcarbonyl-C₁₋₆-alkylamino, C₁₋₆-haloalkylcarbonyl-C₁₋₆-alkylamino, C₁₋₆-alkoxycarbonyl-C₁₋₆-alkylamino, C₂₋₆-alkenylthio, C₁₋₆-alkoxy-C₁₋₆-alkylcarbonyl, C₁₋₆-haloalkoxycarbonylamino, di (C₁₋₆-haloalkyl) amino-C₁₋₆-alkyl, C₃₋₈-halocycloalkenyloxy-C₁₋₆- alkyl, C₁₋₆-alkoxy (C₁₋₆-alkyl) aminocarbonyl, C₁₋₆-haloalkylsulfonylaminocarbonyl, C₁₋₆-alkylsulfonylaminocarbonyl, C₁₋₆-alkoxycarbonylalkoxy, C₁₋₆-alkylaminothioearbonylamino, C₃₋₈-cyclo alkyl-C₁₋₆-alkylamino-C₁₋₆-alkyl, C₁₋₆-alkylthiocarbonyl, C₃₋₈-cycloalkenyloxy-C₁₋₆-alkyl, C₁₋₆-alkoxy-C₁₋₆-alkoxycarbonyl, di-C₁₋₆- alkylaminothiocarbonylamino, C₁₋₆-haloalkoxy-C₁₋₆-haloalkoxy, C₁₋₆-alkoxy-C₁₋₆-haloalkoxy, C₃₋₈-halocycloalkoxy-C₁₋₆-alkyl, di-C₁₋₆-alkylaminocarbonylamino, C₁₋₆- C₂₋₆-alkoxy-alkenyl, C₁₋₆-alkylthiocarbonyloxy, C₁₋₆-haloalkoxy-C₁₋₆-alkoxy, C₁₋₆-haloalkylsulfonyloxy, C₁₋₆-alkoxy-C₁₋₆-haloalkyl, di (C₁₋₆- haloalkyl) amino, di-C₁₋₆-alkoxy-C₁₋₆-alkyl, C₁₋₆-alkylaminocarbonylamino, C₁₋₆-haloalkoxy-C₁₋₆-haloalkyl, C₁₋₆-alkylaminocarbonyl-C₁₋₆-alkylamino, tri- C₁₋₆-alkylsilyl-C₂₋₆-alkynyloxy, tri-C₁₋₆-alkylsilylooxy, tri-C₁₋₆-alkylsilyl-C₂₋₆-alkynyl, cyano (C₁₋₆-alkoxy) -C₁₋₆-alkyl, di -C₁₋₆-alkylthio-C₁₋₆-alkyl, C₁₋₆-alkoxysulfonyl, C₃₋₈-halocycloalkoxycarbonyl, C₁₋₆-alkyl-C₃₋₈-cycloalkylcarbonyl, C₃₋₈-halocycloalkylcarbonyl, C₂₋₆-alkenyloxycarbonyl, C₂ ₋₆-alkynyloxycarbonyl, C₁₋₆-cyanoalkoxycarbonyl, C₁₋₆-alkylthio-C₁₋₆-alkoxy rbonyl, C₂₋₆-alkynylcarbonyloxy, C₂₋₆-haloalkynylcarbonyloxy, cyanocarbonyloxy, C₁₋₆-cyanoalkylcarbonyloxy, C₃₋₈-cycloalkylsulfonyloxy, C₃₋₈-cycloalkyl-C₁₋₆-alkylsulfonyloxy, C₃₋₈-halocycloalkylsulfonyloxy, C₂₋₆- alkenylsulfonyloxy, C₂₋₆-alkynylsulfonyloxy, C₁₋₆-cyanoalkylsulfonyloxy, C₂₋₆-haloalkenylsulfonyloxy, C₂₋₆-haloalkylsulfonyloxy, C₂₋₆-alkynylcycloalkyloxy, C₂₋₆-cyanoalkenyloxy, C₂₋₆-cyanoalkyloxy, C-alkoxycarbonyloalkynyloxy, C-alkoxycarbonyloxy, C-alkoxy C₂₋₆-alkenyloxycarbonyloxy, C₂₋₆-alkynyloxycarbonyloxy, C₁₋₆-alkoxy-C₁₋₆-alkylcarbonyloxy, sulfilimines, sulfoximines, SF₅, -NR¹⁴R¹⁵ and Z¹Q¹; R⁵ may be optionally substituted with one or more selected from R⁶ and / or Q², R¹⁴ and R¹⁵ are independently selected from the group consisting of hydrogen, halogen, cyano, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₂₋₆-alkenyl, C₂₋₆-alkynyl, C₃₋₈-cycloalkyl, C₁₋₆-alkylthio, C₃₋₈-cycloalkenyl, phenyl-C₁₋₆-alkyl, benzyl, heteroaryl-C₁₋ ₆-alkyl, phenyl, naphthyl or a mono or bicyclic carbocyclic ring or a 3- to 10-membered saturated, partially unsaturated or aromatic heterocyclic ring, wherein the heteroaryl-C₁₋₆-alkyl heteroaryl ring members and the ring heterocyclic include C, N, O and S (O) ₀₋₂ and the C ring members of the carbocyclic ring or the heterocyclic ring can be replaced by one or more C (= O) and C (= S); and wherein R¹⁴ and R¹⁵ may be optionally substituted with one or more identical or different R¹⁴ᵃ and R¹⁵ᵃ groups; R¹⁴ᵃ and R¹⁵ᵃ are independently selected from the group consisting of halogen, cyano, nitro, hydroxy, sulfanyl, amino, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁ ₋₆-alkylthio, C₁₋₆-haloalkylthio, C₃₋₈-cycloalkyl, amino-C₁₋₆-alkyl, di-C₁₋₆-alkylamino, NHSO₂-C₁₋₆-alkyl, -C (= O) -C₁₋ ₆-alkyl, C (= O) -C₁₋₆-alkoxy, C₁₋₆-alkylsulfonyl, hydroxy-C₁₋₆-alkyl, -C (= O) -NH₂, C (= O) -NH (C₁₋₆ -alkyl), C₁₋₆-alkylthio-C₁₋₆-alkyl, C₁₋₆-alkylamino-C₁₋₆-alkyl, di-C₁₋₆-alkylamino-C₁₋₆-alkyl, aminocarbonyl-C₁₋₆-alkyl and C₁₋₆-alkoxy-C₁₋₆-alkyl; or R¹⁴ and R¹⁵ together with the atoms to which they are attached form C (= O) or a vinyl group or a 3 to 10 membered saturated or unsaturated monocyclic or bicyclic heterocyclic ring or carbocyclic ring, in which the members of the heterocyclic ring include C, N, O, S (O) ₀₋₂ and -S (= O) ₀₋₂, (= NR⁴ᶜ) -, and wherein the C atom of the carbocyclic ring or heterocyclic ring can be replaced with C (= O) or C (= S); and wherein the vinyl group, carbocyclic ring, or heterocyclic ring is optionally further substituted with an identical or different R¹⁴ᵇ, wherein R¹⁴ᵇ is selected from the group consisting of halogen, cyano, nitro, hydroxy, sulfanyl, amino , C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-alkylthio, C₁₋₆-haloalkylthio, C₃₋₈-cycloalkyl, SO₂-C₁₋₆-alkyl , NHSO₂-C₁₋₆-alkyl, -C (= O) -C₁₋₆-alkyl, C (= O) -C₁₋₆-alkoxy, C₁₋₆-alkylsulfonyl, SO₂-C₆H₄CH₃ and SO₂-aryl; Z¹ is selected from a direct bond, CR²ᵃR³ᵃ, NR⁴ᵃ, O, C (O), C (S), |
| priorityDate | 2019-04-08-04:00^^<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: 41.