Atropisomers of pyridazinone derivatives as herbicides
The present disclosure provides atropisomers of pyridazinone derivatives of a compound of Formula 1a and Formula 1b, N-oxides or salts thereof, wherein R 1 , R 2 , R 3 , R 4 and R 5 are defined in the disclosure. Also disclosed is a composition containing a compound of Formula 1a or 1b, and methods for controlling undesired vegetation comprising contacting the undesired vegetation or its environment with an effective amount of a compound of Formula 1a or 1b or a composition thereof. Also disclosed are methods for preparing a compound of Formula I.
1 . An optically active compound selected from atropisomers of Formula 1a and Formula 1b:
wherein
R 1 is Cl or CH 3 ,
R 2 is CH 3 or difluoromethoxy;
R 3 is CH 3 or H;
R 4 is H; and
R 5 is H or —(C═O)CH 2 CH 3 ; and
wherein
the atropisomer of Formula 1a or 1b, has a plus (+) optical rotation value and is present in excess of its corresponding enantiomer.
2 . The compound of claim 1 wherein
R 1 is Cl;
R 2 is CH 3 ;
R 3 is CH 3 or H;
R 4 is H; and
R 5 is H or —(C═O)CH 2 CH 3 .
3 . The compound of claim 2 wherein
R 1 is Cl;
R 2 is CH 3 ;
R 3 is CH 3 ;
R 4 is H; and
R 5 is H.
4 . A herbicidal composition comprising the compound of claim 1 and at least one component selected from the group consisting of surfactants, solid diluents, and liquid diluents.
5 . A herbicidal composition comprising a compound of claim 1 , at least one additional active ingredient selected from the group consisting of other herbicides and herbicide safeners, and at least one component selected from the group consisting of surfactants, solid diluents and liquid diluents.
6 . A herbicidal mixture comprising (a) a compound of claim 1 , and (b) at least one additional active ingredient.
7 . A method for controlling the growth of undesired vegetation comprising contacting the vegetation or its environment with a herbicidally effective amount of a compound of claim 1 .
8 . A process for preparing a compound of Formula 1a or 1b
wherein
R 1 is Cl or CH 3 ;
R 2 is CH 3 or difluoromethoxy;
R 3 is CH 3 or H;
R 4 is H; and
R 5 is H or —(C═O)CH 2 CH 3 ;
the process comprising:
1) loading a racemic mixture of a compound of Formula 1 comprising the atropisomers of Formulae 1a and 1b onto a chiral supported supercritical fluid chromatography column and eluting with a mobile phase which comprises carbon dioxide;
2) isolating two separate fractions with different retention times; one containing an atropisomer with a positive optical rotation value [α] 1 (+); and one atropisomer with a negative optical rotation value [α] 1 (−).
9 . The process of claim 8 wherein
R 1 is Cl;
R 2 is CH 3 ;
R 3 is CH 3 or H;
R 4 is ; and
R 5 is H or —(C═O)CH 2 CH 3 .
10 . The process of claim 9 wherein
R 1 is Cl;
R 2 is CH 3 ;
R 3 is CH 3 ;
R 4 is H; and
R 5 is H.