IP Library Granted Patent US 7,569,519
Granted Patent B2
US 7,569,519 · App. 11/807,820 · Granted Aug 4, 2009

Substituted benzoyl derivatives as herbicides

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,569,519
App. No.
11/807,820
Granted
Aug 4, 2009
Kind
B2
Abstract

What is described are derivatives of benzoyl derivatives of the formula (I) and their use as herbicides. In this formula (I), R 1 , R 2 and R 3 are different radicals, X is a bridge atom selected from the group consisting of oxygen and sulfur and Het is a saturated heterocyclic group which comprises oxygen and carbon atoms.

Claims (49)

1. A compound of the formula (I) or a salt thereof

in which the radicals and indices are as defined below:

R 1 , R 2 independently of one another are hydrogen, mercapto, nitro, halogen, cyano, thiocyanato, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -haloalkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -haloalkynyl, C 3 -C 6 -cycloalkyl, —OR 4 , OCOR 4 , OSO 2 R 4 , S(O) n R 4 , SO 2 OR 4 , SO 2 N(R 4 ) 2 , NR 4 SO 2 R 4 , NR 4 COR 4 , C 1 -C 6 -alkyl-S(O) n R 4 , C 1 -C 6 -alkyl-OR 4 , C 1 -C 6 -alkyl-OCOR 4 , C 1 -C 6 -alkyl-OSO 2 R 4 , C 1 -C 6 -alkyl-SO 2 OR 4 , C 1 -C 6 -alkyl-SO 2 N(R 4 ) 2 or C 1 -C 6 -alkyl-NR 4 COR 4 ;

R 3 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl or C 2 -C 6 -alkynyl;

R 4 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, phenyl or phenyl-C 1 -C 6 -alkyl, where the six last-mentioned radicals are substituted by s radicals selected from the group consisting of hydroxy, mercapto, amino, cyano, nitro, thiocyanato, OR 3 , SR 3 , N(R 3 ) 2 , ═NOR 3 , OCOR 3 , SCOR 3 , NR 3 COR 3 , CO 2 R 3 , COSR 3 , CON(R 3 ) 2 , C 1 -C 4 -alkyliminooxy, C 1 -C 4 -alkoxyamino, C 1 -C 4 -alkylcarbonyl, C 1 -C 4 -alkoxy-C 2 -C 6 -alkoxycarbonyl and C 1 -C 4 -alkylsulfonyl;

Het is 3-tetrahydrofuranyl, 3-tetrahydropyranyl, 4-tetrahydropyranyl, 1,3-dioxan-5-yl or γ-butyrolacton-2-yl, which may be substituted by n radicals R 5 ;

n is 0, 1 or 2;

s is 0, 1, 2 or 3;

X is O or S(O) n ;

R 5 is hydroxy, mercapto, amino, cyano, nitro, halogen, formyl, C 1 -C 6 -alkylamino, C 1 -C 6 -dialkylamino, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 4 -alkylcarbonyloxy, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkylthio, C 1 -C 6 -haloalkylthio, C 1 -C 6 -alkoxy, or C 1 -C 6 -haloalkoxy or R 5 together with the carbon atom to which it is attached forms a carbonyl group;

Q is a radical of group Q1 or Q2;

R 6 , R 7 independently of one another are hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl or C 3 -C 6 -cyclopropyl;

R 8 is hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -haloalkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -alkylsulfonyl, C 1 -C 6 -haloalkylsulfonyl, phenylcarbonyl, phenylcarbonylmethyl, phenyloxycarbonyl or phenylsulfonyl, where the phenyl ring of the four last-mentioned radicals is substituted by s radicals selected from the group consisting of halogen, nitro, cyano, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy and C 1 -C 6 -haloalkoxy.

2. A compound as claimed in claim 1 , in which

R 1 , R 2 independently of one another are hydrogen, nitro, halogen, C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -haloalkenyl, C 2 -C 6 -alkynyl, C 2 -C 6 -haloalkynyl, C 3 -C 6 -cycloalkyl, —OR 4 , S(O) n R 4 , SO 2 OR 4 , SO 2 N(R 4 ) 2 , NR 4 SO 2 R 4 or C 1 -C 6 -alkyl-S(O) n R 4 ;

R 4 is hydrogen, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, phenyl or phenyl-C 1 -C 4 -alkyl, where the six last-mentioned radicals are substituted by s radicals selected from the group consisting of cyano, nitro, R 3 , OR 3 , SR 3 and N(R 3 ) 2 .

3. A compound as claimed in claim 1 , in which

R 3 is hydrogen;

R 5 is cyano, nitro, halogen, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkylcarbonyl, C 1 -C 4 -alkylcarbonyloxy, C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkylthio, C 1 -C 6 -alkoxy, or C 1 -C 6 -haloalkoxy, or R 5 together with the carbon atom to which it is attached forms a carbonyl group.

4. A compound as claimed in claim 1 , in which

R 6 , R 7 independently of one another are hydrogen or C 1 -C 4 -alkyl;

R 8 is hydrogen, C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkylcarbonyl, C 1 -C 4 -haloalkylcarbonyl, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkylsulfonyl, C 1 -C 4 -haloalkylsulfonyl, phenylcarbonyl, phenylcarbonylmethyl, phenyloxycarbonyl or phenylsulfonyl, where the phenyl ring of the four last-mentioned radicals is substituted by s radicals selected from the group consisting of halogen, nitro, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy and C 1 -C 4 -haloalkoxy.

5. A compound as claimed in claim 1 , in which

R 1 is chlorine, bromine, iodine, nitro, methyl, thiomethyl, thioethyl, methylsulfonyl, ethylsulfonyl or methoxy;

R 2 is bromine, chlorine, methylsulfonyl or ethylsulfonyl;

R 2 is located in the 4-position of the phenyl ring; and

R 8 is hydrogen.

6. A herbicidal composition which comprises a herbicidally effective amount of at least one compound of the formula (I) as claimed in claim 1 .

7. A herbicidal composition as claimed in claim 6 in a mixture with at least one formulation auxiliary selected from the group consisting of stickers, wetters, dispersants, emulsifiers, penetrants, preservatives, antifreeze agents, solvents, fillers, carriers, colorants, antifoams, evaporation inhibitors, pH regulators and viscosity regulators.

8. A compound of the formula (I) or a salt thereof

in which the radicals and indices are as defined below:

R 1 , R 2 independently of one another are hydrogen, mercapto, nitro, halogen, cyano, thiocyanato, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -haloalkenyl, C 2 -C 6 -alkynyl, C 3 - C 6 -haloalkynyl, C 3 -C 6 -cycloalkyl, —OR 4 , OCOR 4 , OSO 2 R 4 , S(O) n R 4 , SO 2 OR 4 , SO 2 N(R 4 ) 2 , NR 4 SO 2 R 4 , NR 4 COR 4 , C 1 -C 6 -alkyl-S(O) n R 4 , C 1 -C 6 -alkyl-OR 4 , C 1 -C 6 -alkyl-OCOR 4 , C 1 -C 6 -alkyl-OSO 2 R 4 , C 1 -C 6 -alkyl-SO 2 OR 4 , C 1 -C 6 -alkyl-SO 2 N(R 4 ) 2 or C 1 -C 6 -alkyl-NR 4 COR 4 ;

R 3 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl or C 2 -C 6 -alkynyl;

R 4 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, phenyl or phenyl-C 1 -C 6 -alkyl, where the six last-mentioned radicals are substituted by s radicals selected from the group consisting of hydroxy, mercapto, amino, cyano, nitro, thiocyanato, OR 3 , SR 3 , N(R 3 ) 2 , ═NOR 3 , OCOR 3 , SCOR 3 , NR 3 COR 3 , CO 2 R 3 , COSR 3 , CON(R 3 ) 2 , C 1 -C 4 -alkyliminooxy, C 1 -C 4 -alkoxyamino, C 1 -C 4 -alkylcarbonyl, C 1 -C 4 -alkoxy-C 2 -C 6 -alkoxycarbonyl and C 1 -C 4 -alkylsulfonyl;

Het is 3 -tetrahydrofuranyl, 3-tetrahydropyranyl, 4-tetrahydropyranyl, 1 ,3-dioxan-5-yl or γ-butyrolacton-2-yl;

n is 0, 1 or 2;

s is 0, 1, 2 or 3;

X is O or S(O) n ;

Q is a radical of group Q1 or Q2;

R 6 , R 7 independently of one another are hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl or C 3 -C 6 -cyclopropyl;

R 8 is hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -haloalkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -alkylsulfonyl, C 1 -C 6 -haloalkylsulfonyl, phenylcarbonyl, phenylcarbonylmethyl, phenyloxycarbonyl or phenylsulfonyl, where the phenyl ring of the four last-mentioned radicals is substituted by s radicals selected from the group consisting of halogen, nitro, cyano, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy and C 1 -C 6 -haloalkoxy.

9. A compound as claimed in claim 1 , in which:

Q is Q1;

n is 0;

R 1 is Cl;

R 2 is SO 2 Me;

R 3 is H;

X is O; and

Het is 3-tetrahydrofuranyl.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 15, 2015
From: BAYER CROPSCIENCE AG
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 036801/0914 →
MERGER AND CHANGE OF NAME Recorded Aug 3, 2015
From: BAYER CROPSCIENCE GMBH; BAYER CROPSCIENCE AG
To: BAYER CROPSCIENCE AG
Reel/Frame 036235/0989 →