US2005221990A1PendingUtilityA1
Novel benzohydrazide derivatives as herbicides and desiccant compositions contaning them
Est. expiryJul 17, 2022(expired)· nominal 20-yr term from priority
A01N 43/54C07D 239/56C07D 231/18C07D 239/54C07D 231/20A01N 47/24C07D 249/12C07D 403/12A01N 43/60A01N 43/653C07D 231/14C07D 401/12A01N 43/58A01N 43/56C07D 239/52
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Claims
Abstract
The compound of the formula wherein Y, X, Z, T and Q are defined in the specification.
Claims
exact text as granted — not AI-modified1 . A compound represented by the formula (I) or its salt
wherein
X is hydrogen or halogen;
Y is represented by hydrogen, halogen, nitro, (C 1-4 )alkyl, (C 1-4 )alkoxy, (C 1-4 )haloalkyl or (C 1-4 )haloalkoxy;
T is represented by N or CH;
Z is one of the following groups;
A is oxygen, sulfur or NR 4 ;
R 1 , R 2 , R 3 and R 4 are independent of each other and may be selected from the group consisting of hydrogen, cyano, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkoxy, (C 1-6 )haloalkoxy, (C 1-6 )alkoxyalkyl, (C 2-6 )alkynyl, (C 2-6 )alkenyl, aryl, heteroaryl, aryloxy, heteroaryloxy, (C 3-6 )cycloalkyl, (C 3-6 )cyclocarbonyl, carboxy, (C 1-6 )alkylcarbonyl, arylcarbonyl, (C 1-3 )haloalkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxycarbonyl, (C 1-6 )haloalkoxycarbonyl, (CI I)alkylthiocarbonyl, (C 1-6 )haloalkylthiocarbonyl, (C 1-6 )alkoxythiocarbonyl, (C 1-6 )haloalkoxythiocarbonyl, (C 1-6 )alkylamino, arylsulfonylamino, arylamino, (C 1-6 )alkylthio, arylthio, (C 2-6 )alkenylthio, (C 2-6 )alkynylthio, (C 1-6 )alkylsulfinyl, (C 2-6 )alkenylsulfinyl, (C 2-6 )alkynylsulfinyl, (C 1-6 )alkylsulfonyl, (C 2-6 )alkenylsulfonyl, (C 2-6 )alkynylsulfonyl, arylsulfonyl, where any of these groups may be optionally substituted with one or one more of the following group consisting of halogen, hydroxy, mercapto, cyano, nitro, amino, caboxy, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, haloaryl, alkoxyaryl, aryoxy, arylthio, haloaryloxy, heteroaryl, heteroaryloxy and (C 3-7 )cycloalkyl;
When R 2 and R 3 are taken together with the atoms to which they are attached, they represent a three to seven membered substituted or unsubstituted ring optionally containing oxygen, carbonyl, S(O) n ** or nitrogen with following optional substitutions, one to three halogen, cyano, nitro, hydroxy, amino, carbonyl, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, heteroaryl or (C 3-7 )cycloalkyl;
R 5 and R 6 are independent of each other and may be selected from the group consisting of hydrogen, (C 1-6 )alkyl, (C 2-6 )alkenyl, (C 2-6 )alkynyl, (C 1-6 )alkoxycarbonyl and heteroarylcarbonyl;
where any of these groups may be optionally substituted with one or more of the following groups consisting of halogen, hydroxy, cyano, nitro, amino, caboxyl, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, heteroaryl and (C 3-7 )cycloalkyl;
When R 5 and R& are taken together with the atoms to which they are attached, they represent a three to seven membered substituted or unsubstituted ring optionally containing oxygen, carbonyl, S(O) n ** or nitrogen with following optional substitutions, one to three halogen, cyano, nitro, hydroxy, amino, carbonyl, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, heteroaryl or (C 3-7 )cycloalkyl;
R 7 may be selected from the group consisting of hydrogen, (C 1-6 )alkyl, (C 2-6 )alkenyl or (C 2-6 )alkynyl where any of these groups may be optionally substituted with one or more of the following groups consisting of halogen, hydroxy, cyano, nitro, amino, caboxyl, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, heteroaryl and (C 3-7 )cycloalkyl;
M is halogen, dichloroiodate, tetrachloroiodate, sulfate, nitrate, formate, acetate, propionate or butylate.
Q is selected from;
wherein
A 1 and A 2 are independently oxygen or sulfur;
R 8 is hydrogen, halogen, cyano, nitro, formyl, (C 1-4 )alkyl, (C 1-4 )haloalkyl, amino, (C 1-4 )alkyl amino, (C 1-4 )haloalkylamino, (C 4-1 )alkoxyamino, (C 1-4 )haloalkoxyamino, (C 1-4 )alkylcarbonyl, (C 1-4 )haloalkylcarbonyl, (C 1-4 )haloalkoxycarbonyl, (C 1-4 )alkylcabonylamino, (C 1-4 )haloalkylcarbonylamino, (C 1-4 )alkoxycarbonylamino, (C 1-4 )haloalkoxycarbonylamino, (C 1-6 )alkoxyalkyl, (C 1-6 )haloalkoxyalkyl, (C 1-6 )alkylthio, (C 1-6 )haloalkylthio, (C 2-6 )alkenyl, (C 2-6 )haloalkenyl, (C 2-6 )alkynyl or (C 2-6 )haloalkynyl;
R 9 and R 10 are independent of each other and may be selected from the group consisting of hydrogen, halogen, cyano, (C 1-4 )alkyl, (C 1-4 )haloalkyl, (C 1-4 )alkoxy, (C 1-4 )haloalkoxy, (C 2-6 )alkenyl, (C 2-6 )haloalkenyl.
R 11 and R 12 are independent of each other and may be selected from the group consisting of hydrogen, halogen, (C 1-3 )alkyl, (C 1-3 )haloalkyl, hydroxy, (C 1-3 )alkoxy, (C 1-3 )haloalkoxy, cyano, nitro, amino or (C 1-6 )alkylamino;
When R 11 and R 12 are taken together with the atoms to which they are attached, they represent a three to seven membered substituted or unsubstituted ring optionally containing oxygen, S(O) n ** or nitrogen with following optional substitutions, one to three halogen, cyano, nitro, hydroxy, amino, carbonyl, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, heteroaryl or (C 3-7 )cycloalkyl;
R 13 may be selected from the group consisting of hydrogen, halogen, cyano, (C 1-4 )alkyl, (C 1-4 )alkoxy, (C 1-4 )haloalkoxy, (C 1-4 )alkylthio, (C 1-4 )haloalkylthio, (C 1-4 )alkylsulfinyl, (C 1-4 )haloalkylsulfinyl, (C 1-4 )alkylsulfonyl, (C 1-4 )haloalkylsulfonyl, (C 2-6 )alkenyl, (C 2-6 )haloalkenyl.
G is nitrogen or CR 15 ;
G′ is carbonyl, NR 14 , oxygen, S(O) n ** or CR 15 R 16 ;
R 14 may be selected from the group consisting of hydrogen, (C 1-6 )alkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )haloalkylcarbonyl, arylcarbonyl and heteroarylcarbonyl;
where any of these groups may be optionally substituted with one or more of the following groups consisting of halogen, hydroxy, cyano, nitro, amino, caboxyl, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, heteroaryl and (C 3-7 )cycloalkyl;
R 15 and R 16 are independent of each other and may be selected from the group consisting of hydrogen, halogen, hydroxy, mercapto, amino, cyano, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkoxy, (C 1-6 )haloalkoxy, (C 1-6 )alkoxyalkyl, (C 2-6 )alkynyl, (C 2-6 )alkenyl, aryl, heteroaryl, aryloxy, heteroaryloxy, (C 3-6 )cycloalkyl, (C 3-6 )cyclocarbonyl, carboxy, (C 1-6 )alkylcarbonyl, arylcarbonyl, (C 1-3 )haloalkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxycarbonyl, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylthiocarbonyl, (C 1-6 )haloalkylthiocarbonyl, (C 1-6 )alkoxythiocarbonyl, (C 1-6 )haloalkoxythiocarbonyl, (C 1-6 )alkylamino, arylsulfonylamino, arylamino, (C 1-3 )alkylthio, arylthio, (C 2-6 )alkenylthio, (C 2-6 )alkynylthio, (C 1-6 )alkylsulfinyl, (C 2-6 )alkenylsulfinyl, (C 2-6 )alkynylsulfinyl, (C 1-6 )alkylsulfonyl, (C 2-6 )alkenylsulfonyl, (C 2-6 )alkynylsulfonyl, arylsulfonyl, where any of these groups may be optionally substituted with one or one more of the following group consisting of halogen, hydroxy, mercapto, cyano, nitro, amino, caboxyl, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, heteroaryl and (C 3-7 )cycloalkyl;
n and m are independent of each other and represent an integer from 0 to 2; provided that m+n is 2, 3 or 4;
n* is 0 or 1;
n** is represent an integer from 0 to 2;
2 . A compound or its salt according to the claim 1 wherein
X is hydrogen or halogen; Y is represented by hydrogen, halogen, nitro, (C 1-4 )haloalkyl or (C 1-4 )haloalkoxy; T is CH; Z is selected from group (II), (III) or (V); A is oxygen or sulfur; R 1 , R 2 , R 3 and R 4 are independent of each other and may be selected from the group consisting of hydrogen, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkoxy, (C 1-6 )haloalkoxy, (C 1-6 )alkoxyalkyl, (C 2-6 )alkynyl, (C 2-6 )alkenyl, aryl, heteroaryl, aryloxy, heteroaryloxy, (C 3-6 )cycloalkyl, (C 3-6 )cyclocarbonyl, carboxy, (C 1-6 )alkylcarbonyl, arylcarbonyl, (C 1-3 , (C 1-6 )alkoxycarbonyl, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylthiocarbonyl, (C 1-6 )alkoxythiocarbonyl, (C 6 )alkylamino, arylsulfonylamino, arylamino, (C 1-6 )alkylthio, arylthio, (C 2-6 )alkenylthio, (C 1-6 )alkylsulfinyl, (C 2-6 )alkenylsulfinyl, (C 2-6 )alkynylsulfinyl, (C 1-6 )alkylsulfonyl, (C 2-6 )alkenylsulfonyl, arylsulfonyl, where any of these groups may be optionally substituted with one or one more of the following group consisting of halogen, hydroxy, mercapto, cyano, nitro, amino, caboxy, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, haloaryl, alkoxyaryl, aryoxy, arylthio, haloaryloxy, heteroaryl, heteroaryloxy and (C 3-7 )cycloalkyl; R 5 and R 6 are independent of each other and may be selected from the group consisting of (C 1-6 )alkyl, (C 2-6 )alkenyl, (C 2-6 )alkynyl, (C 1-6 )alkoxycarbonyl and heteroarylcarbonyl; where any of these groups may be optionally substituted with one or more of the following groups consisting of halogen, hydroxy, cyano, nitro, amino, caboxyl, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 16)alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, heteroaryl and (C 3-7 )cycloalkyl; R 7 may be selected from the group consisting of hydrogen, (C 1-6 )alkyl, (C 2-6 )alkenyl or (C 2-6 )alkynyl; Q is selected from Q 1 , Q 3 , Q 5 , Q 7 , Q 9 or Q 10 ; wherein A 1 and A 2 are independently oxygen or sulfur; R 8 is hydrogen, (C 1-4 )alkyl, (C 1-4 )haloalkyl, amino; R 9 and R 10 are independent of each other and may be selected from the group consisting of hydrogen, halogen, cyano, (C 1-4 )alkyl, (C 1-4 )haloalkyl, (C 1-4 )alkoxy, (C 1-4 )haloalkoxy, (C 2-6 )alkenyl, (C 2-6 )haloalkenyl. R 13 may be selected from the group consisting of hydrogen, halogen, (C 1-4 )alkyl, (C 1-4 )alkoxy, (C 1-4 )haloalkoxy, (C 1-4 )alkylthio, (C 1-4 )haloalkylthio, (C 1-4 )alkylsulfinyl, (C 1-4 )haloalkylsulfinyl, (C 1-4 )alkylsulfonyl or (C 4-1 )haloalkylsulfonyl G′ is carbonyl, NR 14 , oxygen, S(O) n ** or CR 15 R 16 ; R 14 is hydrogen or (C 1-6 )alkyl; R 15 and R 16 are independent of each other and may be selected from the group consisting of hydrogen, halogen, hydroxy, amino, cyano, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkoxy, (C 1-6 )haloalkoxy, (C 1-6 )alkoxyalkyl, (C 2-6 )alkynyl, (C 2-6 )alkenyl, aryl, heteroaryl, aryloxy, heteroaryloxy, (C 3-6 )cycloalkyl, (C 3-6 )cyclocarbonyl, carboxy, (C 1-6 )alkylcarbonyl, arylcarbonyl, (C 1-3 )haloalkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxycarbonyl, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylthiocarbonyl, (C 1-6 )haloalkylthiocarbonyl, (C 1-6 )alkoxythiocarbonyl, (C 1-6 )haloalkoxythiocarbonyl, (C 1-6 )alkylamino, arylsulfonylamino, arylamino, (C 1-3 )alkylthio, arylthio, (C 2-6 )alkenylthio, (C 2-6 )alkynylthio, (C 1-6 )alkylsulfinyl, (C 2-6 )alkenylsulfinyl, (C 2-6 )alkynylsulfinyl, (C 1-6 )alkylsulfonyl, (C 2-6 )alkenylsulfonyl, (C 2-6 )alkynylsulfonyl, arylsulfonyl, where any of these groups may be optionally substituted with one or one more of the following group consisting of halogen, hydroxy, mercapto, cyano, nitro, amino, caboxyl, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkylcarbonyl, (C 1-6 )alkylcarbonyloxy, (C 1-6 )haloalkylcarbonyl, (C 1-6 )haloalkylcarbonyloxy, (C 1-6 )alkoxy, (C 1-6 )alkoxycarbonyl, aminocarbonyl, (C 1-6 )alkylaminocarbonyl, (C 1-6 )haloalkoxy, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylsulfonyl, (C 1-6 )haloalkylsulfonyl, aryl, heteroaryl and (C 3-7 )cycloalkyl; n and m are independent of each other and represent an integer from 0 to 2; provided that m+n is 2, 3 or 4; n** is represent an integer from 0 to 2;
3 . A compound or its salt according to the claim 2 wherein
X and Y are independent of each other represent hydrogen or halogen; T is CH; Z is selected from group (II) or (V); A is oxygen; R 1 , R 2 , R 3 and R 4 are independent of each other and may be selected from the group consisting of hydrogen, (C 1-6 )alkyl, (C 1-6 )haloalkyl, (C 1-6 )alkoxy, (C 1-6 )haloalkoxy, (C 1-6 )alkoxyalkyl, (C 2-6 )alkynyl, (C 2-6 )alkenyl, aryl, heteroaryl, aryloxy, heteroaryloxy, (C 3-6 )cycloalkyl, (C 3-6 )cyclocarbonyl, carboxy, (C 1-6 )alkylcarbonyl, arylcarbonyl, (C 1-3 , (C 1-6 )alkoxycarbonyl, (C 1-6 )haloalkoxycarbonyl, (C 1-6 )alkylthiocarbonyl, (C 1-6 )alkoxythiocarbonyl, (C 1-6 )alkylamino, arylsulfonylamino, arylamino, (C 1-6 )alkylthio, arylthio, (C 2-6 )alkenylthio, (C 1-6 )alkylsulfinyl, (C 2-6 )alkenylsulfinyl, (C 2-6 )alkynylsulfinyl, (C 1-6 )alkylsulfonyl, (C 2-6 )alkenylsulfonyl, arylsulfonyl, R 5 and R 6 are independent of each other and may be selected from the group consisting of (C 1-6 )alkyl, (C 2-6 )alkenyl, (C 2-6 )alkynyl; R 7 may be selected from the group consisting of hydrogen, (Ci)alkyl, (C 2-6 )alkenyl or (C 2-6 )alkynyl; Q is selected from Q 1 , Q 3 or Q 5 ; wherein A 1 and A 2 are oxygen; R 8 is (C 1-4 )alkyl, (C 1-4 )haloalkyl, amino; R 9 and R 10 are independent of each other and may be selected from the group consisting of hydrogen, (C 1-4 )alkyl, (C 1-4 )haloalkyl, (C 1-4 )alkoxy, (C 1-4 )haloalkoxy, (C 2-6 )alkenyl, (C 2-6 )haloalkenyl; R 13 may be selected from the group consisting of hydrogen, halogen, cyano, (C 1-4 )alkoxy, (C 1-4 )haloalkoxy, hydroxy;
4 . A herbicidal composition, characterized in that it contains at least one compound according to claim 1 .
5 . A herbicidal composition which comprises an effctive amount of a compound or its salt of claim 1 and an agricultural adjuvant.
6 . The herbicidal composition according to claim 5 wherein the compounds are formulated into a practical use form such as emulsifiable concentrate (EC), aqueous or oil based suspension concentrate (SC), wettable powder (WP), water dispersible granule (WDG) or microenscapulated (ME) form.
7 . A method for controlling the growth of undesired plant species in plantation crops which comprises applying to the locus of the crop a herbicidally effective amount of a compound or its salt according to claim 1 .
8 . A method for controlling undesired vegetation in a crop field such as corn, peanut, cotton, wheat, sorghum, sunflower, soybean or rice by applying to the locus of the crop to be protect a herbicidally effective amount of a compound or its salt of claim 1 .
9 . A method for controlling weeds, which comprises applying to the locus to be protected a herbicidally effective amount of a compound or its salt of claim 1 in combination with one or more other herbicides for providing an additive or synergistic herbicidal effect.
10 . A method for controlling weeds of claim 7 wherein the compound or its salt of claim 1 is applied to the soil as a pre-plant incorporated, pre-emergent or delayed pre-emergent herbicide.
11 . A method for controlling weeds of claim 9 wherein the compound or its salt of claim 1 is applied to the soil as a pre-plant incorporated, pre-emergent or delayed pre-emergent herbicide.
12 . A method for controlling weeds of claim 7 wherein the compound or its salt of claim 1 is applied as a post-emergent herbicide to plant foliage.
13 . A method for controlling weeds of claim 9 wherein the compound or its salt of claim 1 is applied as a post-emergent herbicide to plant foliage.
14 . A method for controlling weeds of claim 9 wherein the other herbicide is an acetanilide, oxyacetamide, sulfonylurea, triazine, triketone, urea, amide, glyphosate or any referenced in the text.
15 . A method to defoliate potato and cotton using a compound or its salt of claim 1 .
16 . A process for the preparation of the compound or its salt represented by the formula (XI) in said claim 1 , which comprises reacting a compound according to formula (IX) with a compound of the formula (X).
wherein
X, Y, A 1 , A 2 , T, R 1 , R 2 , R 3 , R 8 and R 9 are as previously.
17 . A process for the preparation of the compound or its salt represented by the formula (XVI) in said claim 1 , which comprises reacting a compound of formula (IX) with a compound of the formula (X′).
wherein
X, Y, A 1 , A 2 , T, R 1 , R 5 , R 6 , R 8 and R 9 are as previously.
18 . A process for the preparation of the compound or its salt represented by the formula (XVII) in said claim 1 , which comprises reacting a compound according to formula (XXII) with aldehyde or ketone.
wherein
X, Y, A, A 1 , A 2 , T, R 2 , R 3 , R 8 and R 9 are previously defined.
19 . A process for the preparation of the compound or its salt represented by the formula (XXVII) in said claim 1 , which comprises transformation of a compound according to formula (XXIV) by Lawesson's reagent and reacting it with R 4 -M and R 7 -M.
wherein
X, Y, T, R 1 , R 2 , R 3 , R 4 , R 7 , R 8 , R 10 and R 13 are previously defined.
20 . A process of the preparation of the compound or its salt represented by the formula (XV) in said claim 1 , which comprises reacting a compound according to formula (XIV) with R 7 -M.
wherein
X, Y, A, A 1 , A 2 , T, R 2 , R 3 , R 4 , R 7 , R 8 , R 9 and M are previously defined.
21 . A process of the preparation of the compound or its salt represented by the formula (XIII) in said claim 1 , which comprises reacting a compound according to formula (XII) with R 7 -M.
wherein
X, Y, A, A 1 , A 2 , T, R 1 , R 2 , R 3 , R 7 , R 8 and R 9 are previously defined.
22 . A process of the preparation of the compound or its salt represented by the formula (XIV) and (XII) in said claim 1 , which comprises reacting a compound according to formula (IV) with R 4 -M and R 1 -M respetively.
wherein
X, Y, A, A 1 , A 2 , T, R 1 , R 2 , R 3 , R 4 , R 8 and R 9 are previously defined.
23 . A process of the preparation of the compound or its salt represented by the formula (XVI) and (XVIII) in said claim 1 , which comprises reacting a compound according to formula (XVII) with R 1 -M and R 4 -M reapectively.
wherein
X, Y, A, A 1 , A 2 , T, R 1 , R 4 , R 5 , R 6 , R 8 and R 9 are previously defined.
24 . A process of the preparation of the intermediate represented by the formula (XXX), which comprises reducing a compound according to formula (XXIX).
wherein
X, Y, T and Z are previously defined.
25 . A process for the preparation of the intermediate represented by the formula (XXIX) in said claim 24 , which comprises nitrating a compound according to formula (XXVIII)
wherein
X, Y, T and Z are previously defined.Join the waitlist — get patent alerts
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