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    • 2. 发明申请
    • 4-SUBSTITUTED QUINOLINE DERIVATIVES HAVING FUNGICIDAL ACTIVITY
    • 具有杀真菌活性的4-取代的喹啉衍生物
    • WO1998005645A1
    • 1998-02-12
    • PCT/US1997013090
    • 1997-07-31
    • DOW AGROSCIENCES LLC
    • DOW AGROSCIENCES LLCDAEUBLE, JohnDAVIS, L., NavellHELLWIG, KarinKIRBY, NeilPARKER, Marshall, H.PIECZKO, MaryTHOMASON, Lori, K.
    • C07D215/18
    • C07D401/12A01N43/42A01N43/54C07D215/18
    • This invention provides compounds of formula (1) wherein X is CR , where R is H, Cl or CH3; Y is CR where R is H, Cl, or Br; Z is O, S, SO, SO2, NR , where R is H, C1-C4 alkyl, C1-C4 acyl, CR R , where R and R are independently H, C1-C4 alkyl, C1-C4 alkenyl, C2-C4 alkynyl, C1-C4 acyl, CN, or OH, or R and R together combine to form a carbocyclic ring containing four to six carbon atoms; V is CR R where R and R are independently H, C1-C4 alkyl, C1-C4 alkenyl, C2-C4 alkynyl, C1-C4 acyl, CN, optionally substituted phenoxy, halo C1-C4 alkyl, or OH, or R and R together combine to form a carbocyclic ring containing four to six carbon atoms; A is (a) a C1-C18 saturated or unsaturated straight or branched hydrocarbon chain, optionally including a hetero atom selected from O, S, SO, or SO2, and optionally substituted with halo, halo C1-C4 alkoxy, OH, or C1-C4 acyl; (b) C3-C8 cycloalkyl or cycloalkenyl; (c) a possibly substituted phenyl group; (d) a furyl group of formula (3); (e) a thienyl group; (f) a group of formula (5) or (5a); (g) a group selected from pyridyl or substituted pyridyl; (h) a group selected from pyrimidinyl or substituted pyrimidinyl; or (i) a group selected from 1-naphthyl, substituted 1-naphthyl, 4-pyrazolyl, 3-methyl-4-pyrazolyl, 1,3-benzodioxolyl, tricyclo[3.3.1.1(3,7)]dec-2-yl,1-(3-chlorophenyl)-1H-tetrazol-5-yl, pyridyl, substituted pyridyl, or an acid addition salt of a compound of formula (1), or an N-oxide of a compound of formula (1) where Y is CH. The compounds of formula (1) are plant fungicides.
    • 本发明提供式(1)化合物,其中X为CR 5,其中R 5为H,Cl或CH 3; Y是CR 5,其中R 5是H,Cl或Br; Z是O,S,SO,SO 2,NR 6,其中R 6是H,C 1 -C 4烷基,C 1 -C 4酰基,CR 7 R 8,其中R 7和R 7, 8>独立地是H,C 1 -C 4烷基,C 1 -C 4烯基,C 2 -C 4炔基,C 1 -C 4酰基,CN或OH,或R 7和R 8一起组合形成含有四个 至6个碳原子; V是CR 7 R 8,其中R 7和R 8独立地是H,C 1 -C 4烷基,C 1 -C 4烯基,C 2 -C 4炔基,C 1 -C 4酰基,CN,任选取代的苯氧基, 卤代C 1 -C 4烷基或OH,或R 7和R 8一起结合形成含有4-6个碳原子的碳环; A是(a)C1-C18饱和或不饱和的直链或支链烃链,任选地包括选自O,S,SO或SO 2的杂原子,并且任选地被卤素,卤代C 1 -C 4烷氧基,OH或C 1 -C4酰基; (b)C 3 -C 8环烷基或环烯基; (c)可能取代的苯基; (d)式(3)的呋喃基; (e)噻吩基; (f)式(5)或(5a)的基团; (g)选自吡啶基或取代的吡啶基的基团; (h)选自嘧啶基或取代的嘧啶基的基团; 或(i)选自1-萘基,取代的1-萘基,4-吡唑基,3-甲基-4-吡唑基,1,3-苯并二恶唑基,三环[3.3.1.1(3,7) 1-(3-氯苯基)-1H-四唑-5-基,吡啶基,取代的吡啶基或式(1)化合物的酸加成盐或式(1)化合物的N-氧化物, 其中Y是CH。 式(1)的化合物是植物杀真菌剂。