US2014031376A1PendingUtilityA1
Iminopropene compound and use thereof
Est. expiryDec 1, 2025(expired)· nominal 20-yr term from priority
C07D 213/70C07D 333/20C07C 323/60C07D 239/38C07D 257/04C07C 2601/02C07D 277/36C07D 233/84A01N 37/36C07C 2601/14C07D 403/04C07D 249/10C07C 317/40C07D 333/28C07D 213/61C07D 277/74C07D 263/58C07D 307/64C07D 213/75C07C 327/58A01N 37/38C07C 255/61C07D 215/58A01N 43/90C07D 271/10A01N 43/653C07D 239/42A01N 43/78C07D 249/02A01N 43/54C07D 277/64C07D 471/04A01N 43/82A01N 43/50C07C 323/45A01N 37/52C07D 263/32A01N 43/76A01N 43/42A01N 43/40
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Claims
Abstract
The compound (I) or a salt thereof has an excellent controlling activity against pests. Then the compound (I) or a salt thereof is useful for an active ingredient of a pesticidal composition.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . An iminopropene compound given by the formula (I) or a salt thereof:
wherein,
X represents OX 1 ,
Y represents SY 4 , or SO 2 Y 5 ,
Z represents a cyano group, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, C(=Q 91 )Z A , C(═O)OZ B , C(=Q 92 )NZ D Z E , SO 2 Z F , NZ G Z H , OZ K or N═C(Z I ) 2 ,
X 1 represents a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted,
C(=Q 11 )X A1 , C(═O)OX B1 , C(=Q 12 )NX D1 X E1 or SO 2 X F1 , NX D1 X H1 or N═C(X I1 ) 2 ,
Y 4 represents a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, C(=Q 81 )Y A4 , C(═O)OY B4 , C(=Q 82 )NY D4 Y E4 or S(O) q Y F4 ,
Y 5 represents a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
X A1 , Y A4 and Z A represent each independently a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
X B1 , Y B4 and Z B represent each independently a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted or an amino group optionally substituted,
X D1 , Y D4 and Z D represent each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, an amino group optionally substituted, a cyano group or OG a1 ,
and
X E1 , Y E4 and Z E represent each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
alternatively, X D1 and X E1 , Y D4 and Y E4 , and Z D and Z E represent a ring structure together with the nitrogen which is bonded with each other,
X F1 and Z F represent each independently a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted or an amino group optionally substituted,
Y F4 represents a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
X G1 and Z G represent each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, C(=Q G1 )G A1 , C(═O)OG B1 , C(=Q G2 )NG D1 G E1 or SO 2 G F1 ,
and
X H1 and Z H represent each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
alternatively, X G1 and X H1 , and Z G and Z H represent a ring structure together with the nitrogen which is bonded with each other,
X I1 and Z I represent each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, OG a2 , SG a3 or NG G1 G H1 ,
alternatively, represent a ring structure together with the carbon which is bonded with each other,
Z K represents lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, C(=Q K1 )G A2 , C(═O)OG B2 , C(=Q K2 )NG D2 G E2 or SO 2 G F2 ,
G a1 , G a2 and G a3 represent each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
G A1 and G A2 represent each independently a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
G B1 and G B2 represent each independently a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted or an amino group optionally substituted,
G D1 and G D2 represent each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, an amino group optionally substituted, a cyano group or OG d1 ,
and
G E1 and G E2 represent each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
alternatively, G D1 and G E1 , and G D2 and G E2 represent a ring structure together with the nitrogen which is bonded with each other,
G F1 and G F2 represent each independently a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted or an amino group optionally substituted,
G G1 represents a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, C(=Q Ga )G A1-1 , C(═O)OG B1-1 , C(=Q Gb )NG D1-1 G E1-1 or SO 2 G F1-1 ,
and
G H1 represents a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
alternatively, G G1 and G H1 represent a ring structure together with the nitrogen which is bonded with each other,
G d1 represents a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
G A1-1 represents a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
G B1-1 represents a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted or an amino group optionally substituted,
G D1-1 represents a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, an amino group optionally substituted, a cyano group or OL,
and
G E1-1 represents a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
alternatively, G D1-1 and G E1-1 represent a ring structure together with the nitrogen which is bonded with each other,
G F1-1 represents a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted or an amino group optionally substituted,
L represents a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
Q 22 , Q 12 , Q 81 , Q 82 , Q 91 , Q 92 , Q G1 , Q K1 , Q Ga and Q Gb represent each independently oxygen or sulfur,
m represents an integer of 1 or 2,
n, p and q represent each independently an integer of 0 or 2;
here, 1) if X is a benzoyloxy group and Y is a methoxy group, then, Z is not a 2-(benzoylamino)vinyl group,
2) if X 2 is a methyl group, then, X 3 is not a methyl group,
3) if X is a methoxy group and Y is a trifluoromethylsulfonyloxy group, then, Z is not a 3-vinyloxypropyl group.
2 . The compound according to claim 1 , wherein
X is OX 1 (wherein, X 1 is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, C(=Q 21 )X A2 (wherein, Q 21 is an oxygen atom, and X A2 is a lower alkyl group optionally substituted), NX G1 X H1 or N═C(X I1 ) 2 ,
Y is SY 4
(wherein, Y 4 is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
Z is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted, C(═O)OZ B (wherein, Z B is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted), SO 2 Z F (wherein, Z F is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted or an amino group optionally substituted), NZ G Z H (wherein, Z G and Z H are each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
alternatively, are formed a ring structure together with the nitrogen which is bonded with each other), OZ K (wherein, Z K is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted), or N═C(Z I ) 2 (wherein, Z I s are each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
alternatively, are formed a ring structure together with the carbon which is bonded with each other).
3 . The compound according to claim 2 , wherein
X is OX 1
(wherein, X 1 is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted a heterocyclic group optionally substituted), NX G1 X H1 , or N═C(X I1 ) 2 ),
Y is SY 4
(wherein Y 4 is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, or a heterocyclic group optionally substituted),
Z is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted,
C(═O)OZ B (wherein, Z B is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted),
SO 2 Z F (wherein, Z F is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted, a heterocyclic group optionally substituted or an amino group optionally substituted),
NZ G Z H (wherein, Z G and Z H are each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
alternatively, are formed a ring structure together with the nitrogen which is bonded with each other),
OZ K (wherein, Z K is a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted), or
N═C(Z I ) 2 (wherein, Z I s are each independently a hydrogen atom, a lower alkyl group optionally substituted, a higher alkyl group, a lower cycloalkyl group optionally substituted, a lower alkenyl group optionally substituted, a higher alkenyl group, a lower cycloalkenyl group optionally substituted, a lower alkynyl group optionally substituted, a higher alkynyl group, an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted,
alternatively, are formed a ring structure together with the carbon which is bonded with each other).
4 . The compound according to claim 3 , wherein
X is OX 1
(wherein, X 1 is a lower alkyl group optionally substituted, an aromatic hydrocarbon group optionally substituted, a lower cycloalkyl group optionally substituted, a di-lower alkyl amino group, a lower alkylidene amino group optionally substituted, or a lower cycloalkylidene amino group optionally substituted),
Y is SY 4
(wherein, Y 4 is a lower alkyl group optionally substituted, or an aromatic hydrocarbon group optionally substituted),
Z is an aromatic hydrocarbon group optionally substituted or a heterocyclic group optionally substituted.
5 . The compound according to claim 4 , wherein
X is OX 1
(wherein, X 1 is a lower alkyl group substituted with at least one aromatic hydrocarbon group optionally substituted with one or more independent substituent(s) selected from the group consisting of (1) a halogen, (2) a lower alkyl group and (3) a lower alkoxy group; lower cycloalkyl group; an aromatic hydrocarbon group optionally substituted with one or more independent substituent(s) selected from the group consisting of (1) a halogen, (2) a lower alkyl group optionally substituted with at least one halogen, (3) a lower alkoxy group, (4) a lower alkoxycarbonyl group, (5) a lower alkanoyl group, (6) a lower alkylthio group, (7) an aromatic hydrocarbon group, (8) a cyano group, (9) a nitro group and (10) an alkylene dioxy group; an alkylidene amino group optionally substituted with at least one aromatic hydrocarbon group; a lower cycloalkylidene amino group; or a di-lower alkyl amino group),
Y is SY 4
(wherein, Y 4 is a lower alkyl group optionally substituted with at least one aromatic hydrocarbon group, or an aromatic hydrocarbon group),
Z is an aromatic hydrocarbon group optionally substituted with one or more independent substituent(s) selected from the group consisting of (1) a halogen, (2) a lower cycloalkylthio group, (3) a hydroxyl group, (4) a lower alkyl group optionally substituted with at least one aromatic hydrocarbon group, (5) a lower alkenyl group, (6) a lower alkoxy group optionally substituted with at least one halogen, (7) a lower alkanoyloxy group, (8) an aromatic hydrocarbon group optionally substituted with at least one lower alkyl group or halogen, (9) a heterocyclic group, (10) a lower alkylthio group, (11) a lower alkyl sulfinyl group, (12) a lower alkyl sulfonyl group, (13) an arylthio group, (14) a lower alkoxy carbonyl group, (15) a lower alkanoyl group, (16) an aromatic hydrocarbon carbonyl group, (17) a lower alkynyl group, (18) a lower alkylene dioxy group and (19) a lower alkylene group; or a heterocyclic group.
6 . A pesticidal composition comprising the compound according to claim 1 or a salt thereof as an active ingredient, and an inert carrier.
7 . A method for controlling a pest which comprises a step of applying an effective amount of the compound according to claim 1 or a salt thereof to a pest or a habitat of pests.Join the waitlist — get patent alerts
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