TREA

Thiophenesulfonylurea derivatives

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Information

  • Patent Grant
  • 5461024
  • Patent Number
    5,461,024
  • Date Filed
    Thursday, December 9, 1993
    32 years ago
  • Date Issued
    Tuesday, October 24, 1995
    30 years ago
Information
Abstract
A novel thiophenesulfonylurea derivative having herbicidal activity, having the formula (I): ##STR1## wherein the substituents are herein described.
Description

TECHNICAL FIELD
The present invention relates to novel thiophenesulfonylurea derivatives having agriculturally suitable for herbicidal activity.
BACKGROUND OF THE INVENTION
It is publicly well known that sulfonylurea derivatives have a herbicidal activity. Here are the formulas for the sulfonylureas.
1) U.S. Pat. No. 4,370,480 discloses the compound having the following formula ##STR2## wherein, R is H, alkyl, alkenyl, alkynyl or alkyl substituted with 1.about.4 of F, Cl, Br, OCH.sub.3, CN or CO.sub.2 R.sup.1, alkenyl substituted with 1.about.3 atoms of Cl, cycloalkyl, cycloalkenyl, cycloalkyl substituted with CH.sub.3, CH.sub.2 CH.sub.3, Cl, OCH.sub.3, etc. or CO.sub.2 R.sup.1 ;
X is H, Cl, CH.sub.3, OCH.sub.3, etc.;
Y is H, Cl, C.sub.1 -C.sub.4 of alkyl, halogen, alkoxy or alkyl substituted with CN, etc.;
Z is CH.
2) U.S. Pat. No. 4,786,314 discloses the compound having the following formula ##STR3## wherein, R.sup.1 is alkyl, alkenyl, halogen, NO.sub.2, haloalkenyl, alkynyl, haloalkynyl, alkoxy, haloalkoxy, alkoxyalkyl, ##STR4## etc.; R.sup.2 ##STR5## etc.; R.sup.8 is H, C.sub.1 -C.sub.4 alkyl, alkenyl, alkynyl, CH.sub.2 CH.sub.2 Cl, CH.sub.2 CH.sub.2 F, C.sub.1 -C.sub.2 alkyl substituted with OMe or SMe, or cycloalkyl.
3) U.S. Pat. No. 4,612,035 discloses the compound having the following formula ##STR6## wherein, L is phenyl, naphthyl, pyridine or thiophene having substitutent;
R.sup.1 is ##STR7## R.sup.25 is H or alkyl; R.sup.26 is alkyl.
4) U.S. Pat. No. 4,659,369 discloses the compound having the following formula ##STR8## wherein, Q is Q-1, Q-2, Q-3 or Q-4 as followings. ##STR9## and then, R.sup.1 is ##STR10## R.sup.3 is H, C.sub.1 -C.sub.3 of alkyl or C.sub.1 -C.sub.3 of alkoxy; R.sup.4 and R.sup.5 are respectively C.sub.1 -C.sub.2 of alkyl;
R.sup.6 and R.sup.7 are respectively H or C.sub.1 -C.sub.2 of alkyl;
a is O, S or NCH.sub.3 ;
W.sub.1 is O or s;
A is ##STR11## wherein, X.sup.1 is CH.sub.3, OCH.sub.3, OEt or OCHF.sub.2 ; Y.sup.1 is O or CH.sub.2 ;
Y.sup.2 is H or CH.sub.3.
5) Japanes Patent Laid-Opened So 61-22083 discloses the compound having the following formula ##STR12## wherein, R is H or alkyl group;
X and Y are respectively methyl or methoxy group;
A is N or CH.
As the above patents, many sulfonylurea herbicides have been known until recently.
Even with these herbicides, more and more weeds develop immunity forwards these herbicides and cause undesirable vegetations. Thus, continuous research is in demand to develop more effective and newer for a good harvest.
Therefore, the object of the present invention is to provide new thiophenesulfonylurea derivatives having a very prominent herbicidal activity with a good selectivity for various vegetations and agriculturally suitable herbicides for treatment of pre-emergence and/or post-emergence or plant growth regulants.
SUMMARY OF THE INVENTION
The present invention relates to novel thiophenesulfonylurea derivatives having the following general formula (I) ##STR13## wherein, P is P-1, P-2 or P-3 as followings ##STR14## wherein, R.sup.1 is H, C.sub.1 -C.sub.3 alkyl, C.sub.1 -C.sub.3 haloalkyl, halogen, CN, NO.sub.2, C.sub.1 -C.sub.3 alkoxy, C.sub.1 -C.sub.3 haloalkoxy, SO.sub.2 NR.sup.I R.sup.II, C.sub.1 -C.sub.3 alkylthio, C.sub.1 -C.sub.3 alkylsulfinyl, C.sub.1 -C.sub.3 alkylsulfonyl, SCHF.sub.2, NH.sub.2, NHCH.sub.3, N(Me).sub.2, C.sub.1 -C.sub.2 alkyl substituted with C.sub.1 -C.sub.2 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, SH, SCH.sub.3, CN or OH; or CO.sub.2 R.sup.III ; and then R.sup.1 is H, C.sub.1 -C.sub.4 alkyl, C.sub.2 -C.sub.3 cyanoalkyl, methoxy or ethoxy; R.sup.II is H, C.sub.1 -C.sub.4 alkyl, C.sub.3 -C.sub.4 alkenyl, or when taken together connecting R.sup.I and R.sup.II , --(CH.sub.2).sub.3 --, --(CH.sub.2).sub.4 --, --(CH.sub.2).sub.5 -- or CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub. 2 --, may be formed; R.sup.III is C.sub.1 -C.sub.4 alkyl, C.sub.3 -C.sub.4 alkenyl, C.sub.3 -C.sub.4 alkynyl, C.sub.1 -C.sub.4 alkyl substituted with 1.about.3 halogens or cyano groups, C.sub.5 -C.sub.6 cycloalkyl, C.sub.4 -C.sub.7 cycloalkylalkyl or C.sub.2 -C.sub.4 alkoxyalkyl;
R is ##STR15## wherein, a is O or S; R.sup.2 is C.sub.1 -C.sub.6 alkyl substituted with 1.about.3 halogens; R.sup.4 and R.sup.5 are respectively C.sub.1 -C.sub.4 of alkyl; and R.sup.6 and R.sup.7 are respectively H, C.sub.1 -C.sub.3 alkyl or C.sub.1 -C.sub.3 haloalkyl;
E is CH.sub.2 single bond;
R.sup.3 is H or CH.sub.3 ;
W is O or S;
A is A1, A2, A3, A4, A5, A6 or A7 as followings; ##STR16## wherein, X is H, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkylthio, C.sub.1 -C.sub.4 alkylthio, halogen, C.sub.2 -C.sub.5 alkoxyalkyl, C.sub.2 -C.sub.5 alkoxyalkoxy, amino, C.sub.1 -C.sub.3 alkylamino, di(C.sub.1 -C.sub.3 alkyl) amino or C.sub.3 -C.sub.5 cycloalkyl:
Y is H, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, C.sub.1 -C.sub.4 haloakylthio, C.sub.1 -C.sub.4 alkylthio, C.sub.2 -C.sub.5 alkoxyalkyl, C.sub.2 -C.sub.5 alkoxyalkoxy, amino, C.sub.1 -C.sub.3 alkylamino, di(C.sub.1 -C.sub.3 alkyl)amino, C.sub.3 -C.sub.4 alkenyloxy, C.sub.3 -C.sub.4 alkynyloxy, C.sub.2 -C.sub.5 alkylthioalkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.2 -C.sub.4 alkynyl, azido, cyano, C.sub.2 -C.sub.5 alkylsulfinylalkyl, C.sub.2 -C.sub.5 alkylsulfonylalkyl, CH.sub.2 OH, C.sub.3 -C.sub.5 cycloalkyl, C.sub.3 -C.sub.5 cycloalkoxy, C.sub.2 -C.sub.5 alkylthioalkoxy, ##STR17## m is 2 or 3; L.sup.1 and L.sup.2 are independently O or S;
R.sup.4 and R.sup.5 are independently C.sub.1 -C.sub.4 alkyl;
R.sup.8 is H or CH.sub.3 ;
Z is CH, N, CCH.sub.3 or CC.sub.2 H.sub.5 ;
Y.sup.1 is O or CH.sub.2 ;
X.sup.1 is CH.sub.3, OCH.sub.3, OC.sub.2 H.sub.5 or OCHF.sub.2 ;
Y.sup.2 is CH.sub.3, CH.sub.2 CH.sub.3, OCH.sub.3, OCH.sub.2 CH.sub.3, SCH.sub.3 or SCH.sub.2 CH.sub.3 ;
X.sup.2 is CH.sub.3, CH.sub.2 CH.sub.3, or CH.sub.2 CF.sub.3 ;
Y.sup.3 is H or CH.sub.3 ;
X.sup.3 is CH.sub.3 or OCH.sub.3 ;
Y.sup.4 is CH.sub.3, OCH.sub.3, OC.sub.2 H.sub.5, CH.sub.2 OCH.sub.3 or Cl;
X.sup.4 is CH.sub.3, OCH.sub.3, OC.sub.2 H.sub.5, CH.sub.2 OCH.sub.3 or Cl;
and these may be an agriculturally suitable salt, and then,
(1) if X is Cl, Br, F or I, Z is CH and Y is OCH.sub.3, OC.sub.2 H.sub.5, NCH.sub.3 (OCH.sub.3), NH.sub.2, NHCH.sub.3, N(CH.sub.3).sub.2 or OCHF.sub.2 ;
(2) if X or Y is OCHF.sub.2, Z is CH;
(3) X.sup.4 and Y.sup.4 are not Cl simultaneously;
(4) if W is S, R.sup.3 is H, E is a single bond, A is A.sub.1, Z is CH or N and, Y is CH.sub.3, OCH.sub.3, OCH.sub.2 CH.sub.3, CH.sub.2 OCH.sub.3, C.sub.2 H.sub.5, CF.sub.3, SCH.sub.3, OCH.sub.2 CH.dbd.CH.sub.2, OCH.sub.2 C.tbd.CH, OCH.sub.2 CH.sub.2 OCH.sub.3, CH(OCH.sub.3).sub.2 or ##STR18## (5) if a number of total carbon atoms of X and Y is more than 4, a number of carbon atoms of R.sup.2 is 4 or less than 4.





DETAILED DESCRIPTION OF THE INVENTION
Among the definitions according to the present invention, the following terms have the following meanings:
a) "Alkyl" used ether alone or in compound word such as "alkylthio" or "haloalkyl" etc. denotes straight chain or branched alkyls such as methyl, ethyl, n-propyl, isopropyl or buthyl isomers.
b) "Alkoxy" denotes methoxy, ethoxy, n-propoxy, isopropoxy or butoxy isomers.
c) "Alkenyl" denotes straight chain or branched alkenes, for example, vinyl, 1-propenyl, 2-propenyl or butenyl, pentenyl, hexenyl or heptenyl isomers etc.
d) "Alkynyl" denotes straight chain or branched alkynyl such as ethynyl, 1-propynyl, 2-propynyl, or butynyl, pentynyl or hexynyl isomers.
e) "Halogen" used ether alone or in compound word "halo" denotes chlorine, fluorine, bromine or Iodine.
A preferred group of thiophenesulfonylurea derivatives having the formula(I) shown as the below, in view of easiness of synthesis and herbicidal activity, wherein
(1) R.sup.3 is H; W is O; and E is single bond;
(2) R.sup.1 is H, F, Cl, C.sub.1 -C.sub.2 alkyl, C.sub.1 -C.sub.2 haloalkyl, C.sub.1-C.sub.2 alkoxy, C.sub.1 -C.sub.2 haloalkoxy, C.sub.1 -C.sub.2 alkylthio, CH.sub.2 OCH.sub.3, OR CH.sub.2 SCH.sub.3 ;
(3) X is CH.sub.3, OCH.sub.3, OCH.sub.2 CH.sub.3, Cl, F, Br, OCHF.sub.2, CH.sub.2 F, OCH.sub.2 CH.sub.2 F, OCH.sub.2 CHF.sub.2, OCH.sub.2 CF.sub.3, CF.sub.3, CH.sub.2 Cl or CH.sub.2 Br; Y is H, C.sub.1 -C.sub.3 alkyl, OCH.sub.3, OCH.sub.2 CH.sub.3, CH.sub.2 OCH.sub.3, NHCH.sub.3, NCH.sub.3 (OCH.sub.3), N(CH.sub.3).sub.2, CF.sub.3, SCH.sub.3, OCH.sub.2 CH.dbd.CH.sub.2, OCH.sub.2 C.tbd.CH, CH.sub.2 OC.sub.2 H.sub.5, OCH.sub.2 CH.sub.2 OCH.sub.3, CH.sub.2 SCH.sub.3, OCHF.sub.2, SCHF.sub.2, cyclopropyl, C.tbd.CH, or C .tbd.C--CH.sub.3 ;
(4) R.sup.2 is CH.sub.2 F, CHF.sub.2, CHFCl, CH.sub.2 Cl, CH.sub.2 Br, CHFCH.sub.3, CH.sub.2 CH.sub.2 F, CH.sub.2 CH.sub.2 CH.sub.2 F, CH.sub.2 CH.sub.2 Cl, CHClCH.sub.3, CHCl.sub.2, CHFCH.sub.2 F, CHClCH.sub.2 Cl, CHFCH.sub.2 Cl, CH.sub.2 CF.sub.3 or CF(CH.sub.3).sub.2 ;
(5) A is A.sub.1 ; X is CH.sub.3, OCH.sub.3, OCH.sub.2 CH.sub.3, Cl or OCHF.sub.2 ; Y is CH.sub.3, C.sub.2 H.sub.5, OCH.sub.3, CH.sub.2 OCH.sub.3, CH(OCH.sub.3).sub.2, OCHF.sub.2, NHCH.sub.3, N(Me).sub.2 or cyclopropyl, and R.sup.1 is H, CH.sub.3 or OCH.sub.3.
The novel compounds having the above formula(I) according to the present invention have a very strong herbicide activity and good selectivity for a useful vegetation.
The compounds of the present invention can be prepared by reactions as described in herein below.
The compounds of general formula(I) can be obtained by reacting the compounds having the following formula(II) with an amine compound of the following formula(III). ##STR19## wherein, ##STR20##
The above reaction may be carried out in solvent such as methylene chloride, dichloro ethane or chloroform, and then the solvent can be used with catalytic amount of base such as DABCO(1,4-diazabicyclo[5.4.0]undece-7-ene), DBU(1,8-diazabicyclo[5.4.0]undece-7-ene), etc.
The compounds of general formula(I) can be obtained by reacting the compounds having the following formula(IV) with a carbamate compound of the following formula(V). ##STR21##
The compounds of the above formula(II) can be manufactured by reacting sulfonamide with phosgene. ##STR22##
The thiophenesulfonamide compounds of the above formula(IV) may be prepared by the following reaction process. ##STR23## In the above reaction, L is leaving group such as OEt, NMe.sub.2, or N(CH.sub.3)OCH.sub.3 and R, R.sup.1 and R.sup.2 are as the above defined.
Sulfonamide substituted at 2,3-position of the following formula(IV-b) can be obtained by the method 4 of the above, but 2,3-dibromothiophene is used as the starting material. ##STR24##
Sulfonamide of the following formula(IV-c) can be obtained by the following reaction process, and then 3-bromothiophene is used as the starting material. ##STR25##
The heterocyclic amine compound of formula(III) may be prepared by a skill person in this technical field from a method disclosed in literatures or the simple transformation of it.
For example, European Patent Application No. 84,244 (Pub. Jul. 27, 1983) and J. Am. Chem. Soc., 69,3072(1947) of W. Braker et al. discloses a method for preparing aminopyrimidine and triazine substituted with acetyl group. European patent No. 72,347 and U.S. Pat. Nos. 4,443,243/4,487,915 disclose a method for preparing aminopyrimidine and/or triazine substituted with haloalkyl such as OCHF.sub.2, SCHF.sub.2, OCH.sub.2 CH.sub.2 F anti OCH.sub.2 CF.sub.3 etc. and haloalkylthio as a substitution group.
European Patent No. 108,708, U.S. Pat. Nos. 4,515,626/4,600,428 disclose cyclopropylpyrimidine and/or triazine substituted with alkyl, haloalkyl, alkoxy, haloalkoxy, alkylamino, dialkylamino and alkoxyalkyl group etc.
European Patent No. 15,863 discloses a method for preparing the compound of the above formula(VI), as 5,6-dihydro-puro[2,3-d] pyrimidine-2-amine compounds and cyclopenta[dd]pyrimidine-2-amine compounds which A is A.sub.2 ; and 6,7-dihydro-5H-pyrano-[2,3-d] pyrimidine-2-amine compound which A is A.sub.3.
European Patent No. 46,677 discloses puro[2,3-d]pyridine-2-amine compounds which A is A.sub.4 in the formula(VI), and European Patent No. 73,562 discloses heterocyclic compounds which A is A.sub.5.
The compound of formula(VI) which A is A.sub.6 can be prepared by European Patent No. 94,260. The compound of formula(VI) which A is A.sub.7 can be manufactured by the method of European Patent No. 125,864.
Common methods for preparing aminopyridine and triazine compounds are arranged on the following literatures:
"The chemistry and Heterocyclic compounds", Series, Interscience Publishers, Inc., New York and London; "Pyrimidines", Vol. 16, D. J. Brown Ed.; "S-Triazines and Derivatives", Vol. 13, E. M. Smolin and L. Rapaport. Composition of triazine compounds is disclosed in F. C. Schaefer, U.S. Pat. No. 3,154,547 and K. R. Huffman and F. C. Schaefer, J. Org. Chem., 28, 1812(1963).
On the other hand, salts of the compound of the above formula(I) also are useful as herbicide, and they can be prepared by various methods according to prior art.
For example, metal salts of the compound can be prepared by reacting the above formula(I) compound with strong basic anion, e.g. alkali or alkaline earth metal solution having hydroxyl group, alkoxide or carbonate, and also quaternary amine salt alike.
A salt of the formula(I) compound may also be obtained by cation exchange. The cation exchange can be manufactured by directly reacting solution containing cation for exchange with solution of salt of formula(l), for example, solution of alkali metal or quaternary amine salt.
This method is useful when the desired salt is water insoluble, for example, copper salt is separated by filtering.
This ion exchange may be carried out by passing through a column of cation exchange resin with solution of salt of the formula(I), for example, alkaline metal or quarternary amine salt solution.
This method is useful when the desirable salt is water soluble, especially sodium, potassium or calcium salt.
The above manufacturing methods am summarized briefly, but the methods can be easily carried out by a skill person in this technical field of composition and manufacturing for sulfonyl urea or organic composition.
The compounds of the above general formula(I) according to the present invention are specified as the following Tables 1.about.45;
TABLE 1__________________________________________________________________________ ##STR26##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)__________________________________________________________________________H CH.sub.2 F H OCH.sub.3 OCH.sub.3 191-194H CH.sub.2 F H CH.sub.3 OCH.sub.3 185-189H CH.sub.2 F H CH.sub.3 CH.sub.3 179-184H CH.sub.2 F H Cl OCH.sub.3 182-185H CH.sub.2 F H Br OCH.sub.3H CH.sub.2 F H H CH.sub.3H CH.sub.2 F H OCH.sub.3 HH CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 F H OCH.sub. 3 CH(OCH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H C.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H CF.sub.2 OCH.sub.3H CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 F H F OCH.sub.3H CH.sub.2 F H I OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 F H Cl OC.sub.2 H.sub.5H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OC.sub. 2 H.sub.5 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 F H NH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H n-C.sub.3 H.sub.2 OCH.sub.3H CH.sub.2 F H NHCH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 SCH.sub.3H CH.sub.2 F H OCH.sub.3 SCF.sub.2 HH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CCHH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CHCH.sub.2H CH.sub.2 F H OCH.sub.3 CCHH CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 cyclopropylH CH.sub.2 F H OCH.sub.3 NH.sub.2H CH.sub.2 F H OCH.sub.3 CF.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCH.sub.3 CHOH CH.sub.2 F H OCH.sub.3 COCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(SCH.sub.3)OC.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 C(CH.sub.3)(SCH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 C(SC.sub.2 H.sub.5).sub.2H CH.sub.2 F H OCH.sub.3 1,3-dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- oxathiolan-2ylH CH.sub.2 F H OCH.sub.3 1,3-oxathian-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- dithian-2-ylH CH.sub.2 F H OCH.sub.3 4-methyl-1,3- dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-4-dimethyl-1,3- dithiolan-2-ylH CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 CCCH.sub.3H CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 OCF.sub.2 BrH CHFCH.sub.3 H OCH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OCH.sub.3H CHFCH.sub.3 H Br OCH.sub.3H CHFCH.sub.3 H CH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHFCH.sub.3 H OCF.sub.2 H OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 C.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Cl OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Br OCH.sub.3H CHFCH.sub.3 H F OCH.sub.3H CHFCH.sub.3 H I OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CHF.sub.2 CH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OC.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHFCH.sub.3 H OCF.sub.2 H CH.sub.3H CHFCH.sub.3 H Cl OCF.sub.2 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H Br OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub. 2 CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 CH.sub.2 F H F OCH.sub.3H CH.sub.2 CH.sub.2 F H I OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 208-211H CH.sub.2 Cl H CH.sub.3 OCH.sub.3 205-209H CH.sub.2 Cl H CH.sub.3 CH.sub.3 203-206H CH.sub.2 Cl H Cl OCH.sub.3 188-192H CH.sub.2 Cl H Br OCH.sub.3H CH.sub.2 Cl H CH.sub.3 Cl 186-190H CH.sub.2 Cl H OCH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Cl H OCF.sub.2 H OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OC.sub.2 H.sub.5 175-186H CH.sub.2 Cl H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Cl H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Br OCH.sub.3H CH.sub.2 Cl H F OCH.sub.3H CH.sub.2 Cl H I OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Cl H Cl OC.sub.2 H.sub.5 190-193H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Cl H OCF.sub.2 H CH.sub.3H CH.sub.2 Cl H Cl OCF.sub.2 HH CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H CH.sub.3 CH.sub.3H CHClCH.sub.3 H Cl OCH.sub.3H CHClCH.sub.3 H Br OCH.sub.3H CHClCH.sub.3 H CH.sub.3 HH CHClCH.sub.3 H OCH.sub.3 HH CHClCH.sub. 3 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHClCH.sub.3 H OCF.sub.2 H OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OC.sub.2 H.sub.5H CHClCH.sub.3 H CH.sub.3 CH.sub.2 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 C.sub.2 H.sub.5H CHClCH.sub.3 H OC.sub.2 H.sub.5 OCH.sub.3H CHClCH.sub.3 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHClCH.sub.3 H CF.sub.3 OCH.sub.3H CHClCH.sub.3 H CH.sub.2 F OCH.sub.3H CHClCH.sub.3 H CH.sub.2 Cl OCH.sub.3H CHClCH.sub.3 H CH.sub.2 Br OCH.sub.3H CHClCH.sub.3 H F OCH.sub.3H CHClCH.sub.3 H I OCH.sub.3H CHClCH.sub.3 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHClCH.sub.3 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 CHF.sub.2 CH.sub.3H CHClCH.sub.3 H OCH.sub.2 CF.sub.3 CH.sub.3H CHClCH.sub.3 H Cl OC.sub.2 H.sub.5H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHClCH.sub.3 H OCF.sub.2 H CH.sub.3H CHClCH.sub.3 H Cl OCF.sub.2 HH CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 CH.sub.3H CH.sub.2 Br H Cl OCH.sub.3H CH.sub.2 Br H Br OCH.sub.3H CH.sub.2 Br H CH.sub.3 HH CH.sub.2 Br H OCH.sub.3 HH CH.sub.2 Br H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Br H OCF.sub.2 H OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 Br H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Br H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Br H CF.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.2 F OCH.sub.3H CH.sub.2 Br H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Br H CH.sub.2 Br OCH.sub.3H CH.sub.2 Br H F OCH.sub.3H CH.sub.2 Br H I OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Br H Cl OC.sub.2 H.sub.5H CH.sub.2 Br H OCH.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Br H OCF.sub.2 H CH.sub.3H CH.sub.2 Br H Cl CHF.sub.2 HH CF.sub.3 H OCH.sub.3 OCH.sub.3 209-212H CF.sub.3 H CH.sub.3 OCH.sub.3 194-197H CF.sub.3 H CH.sub.3 CH.sub.3 193-196H CF.sub.3 H Cl OCH.sub.3 196-200H CHF.sub.2 H Br OCH.sub.3H CHF.sub.2 H CH.sub.3 HH CHF.sub.2 H OCH.sub.3 HH CHF.sub.2 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHF.sub.2 H OCF.sub.2 H OCH.sub.3H CHF.sub.2 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OC.sub.2 H.sub.5H CHF.sub.2 H CH.sub.3 CH.sub.2 OCH.sub.3H CHF.sub.2 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHF.sub.2 H OCH.sub.3 C.sub.2 H.sub.5H CHF.sub.2 H OC.sub.2 H.sub.5 OCH.sub.3H CHF.sub.2 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHF.sub.2 H CF.sub.3 OCH.sub.3H CHF.sub.2 H CH.sub.2 F OCH.sub.3H CHF.sub.2 H CH.sub.2 Cl OCH.sub.3H CHF.sub.2 H CH.sub.2 Br OCH.sub.3H CHF.sub.2 H F OCH.sub.3H CHF.sub.2 H I OCH.sub.3H CHF.sub.2 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHF.sub.2 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.2 CF.sub.3 CH.sub.3H CHF.sub.2 H OCH.sub.2 CHF.sub.2 CH.sub.3H CHF.sub.2 H Cl OC.sub.2 H.sub.5H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub. 3H CHF.sub.2 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHF.sub.2 H OCF.sub.2 H CH.sub.3H CHF.sub.2 H Cl OCF.sub.2 HH CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H Br OCH.sub.3H CHFCl H CH.sub.3 HH CHFCl H OCH.sub.3 HH CHFCl H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHFCl H OCF.sub.2 H OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H OCH.sub.3 C.sub.2 H.sub.5H CHFCl H OC.sub.2 H.sub.5 OCH.sub.3H CHFCl H OCH.sub.2 CF.sub.3 OCH.sub.3H CHFCl H CF.sub.3 OCH.sub.3H CHFCl H CH.sub.2 F OCH.sub.3H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H CH.sub.2 Br OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H I OCH.sub.3H CHFCl H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHFCl H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHFCl H OCH.sub.2 CHF.sub.2 CH.sub.3H CHFCl H OCH.sub.2 CF.sub.3 CH.sub.3H CHFCl H Cl OC.sub.2 H.sub.5H CHFCl H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 SCH.sub.3H CHFCl H OCF.sub.2 H CH.sub.3H CHFCl H Cl OCF.sub.2 HH CHFCl H n-C.sub.3 H.sub.7 OCH.sub.3H CHFCl H OCH.sub.3 NHCH.sub.3H CHFCl H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 cyclopropylH CHFCl H OCH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.3H CHFCl H OCH.sub.2 H.sub.5 CH.sub.2 SCH.sub.3H CHFCl H OCH.sub.3 CH(SCH.sub.3)OC.sub.2 H.sub.5H CHFCl H OCH.sub.3 CH(SC.sub.2 H.sub.5).sub.2H CHFCl H OCH.sub.3 1,3-dioxolan-2-ylH CHFCl H OCH.sub.3 N(OCH.sub.3)CH.sub.3H CHFCl H OCH.sub.3 C.sub.2 H.sub.5H CHFCl H OCH.sub.3 CF.sub.35-F CH.sub.2 F H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 F H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 Cl H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 CH.sub.35-Cl CH.sub.2 F H Cl OCH.sub.35-Br CH.sub.2 F H OCH.sub.3 OCH.sub.35-CH.sub.2 CN CH.sub.2 F H OCH.sub.3 OCH.sub.35-OCH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-SCH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-OCF.sub.2 H CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.35-Cl CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3__________________________________________________________________________
TABLE 2__________________________________________________________________________ ##STR27##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)__________________________________________________________________________H CH.sub.2 F H OCH.sub.3 OCH.sub.3 134-137H CH.sub.2 F H CH.sub.3 OCH.sub.3 203-207H CH.sub.2 F H CH.sub.3 CH.sub.3 205-210H CH.sub.2 F H Cl OCH.sub.3 180-184H CH.sub.2 F H Br OCH.sub.3H CH.sub.2 F H Cl CH.sub.3H CH.sub.2 F H OCH.sub.3 H 193-198H CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub. 2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5 187-190H CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H C.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 F H F OCH.sub.3H CH.sub.2 F H I OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 F H Cl OC.sub.2 H.sub.5 170-172H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 F H NH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H n-C.sub.3 H.sub.7 OCH.sub.3H CH.sub.2 F H NHCH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 SCH.sub.3H CH.sub.2 F H OCH.sub.3 SCF.sub.2 HH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CCHH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CHCH.sub.2H CH.sub.2 F H OCH.sub.3 CHCHH CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 cyclopropylH CH.sub.2 F H OCH.sub.3 NH.sub.2H CH.sub.2 F H OCH.sub.3 CF.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCH.sub.3 CHOH CH.sub.2 F H OCH.sub.3 COCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(SCH.sub.3)OC.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 C(CH.sub.3)(SCH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 C(SC.sub.2 H.sub.5).sub.2H CH.sub.2 F H OCH.sub.3 1,3-dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- oxathiolan-2ylH CH.sub.2 F H OCH.sub.3 1,3-oxathian-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- dithian-2-ylH CH.sub.2 F H OCH.sub.3 4-methyl-1,3- dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-4-dimethyl-1,3- dithiolan-2-ylH CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 CCCH.sub.3H CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 OCF.sub.2 BrH CHFCH.sub.3 H OCH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OCH.sub.3H CHFCH.sub.3 H Br OCH.sub.3H CHFCH.sub.3 H CH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHFCH.sub.3 H OCF.sub.2 H OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 C.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Cl OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Br OCH.sub.3H CHFCH.sub.3 H F OCH.sub.3H CHFCH.sub.3 H I OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CHF.sub.2 CH.sub.3H CHFCH.sub. 3 H OCH.sub.2 CF.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OC.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHFCH.sub.3 H OCF.sub.2 H CH.sub.3H CHFCH.sub.3 H Cl OCF.sub.2 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H Br OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 CH.sub.2 F H F OCH.sub.3H CH.sub.2 CH.sub.2 F H I OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub. 3 CH.sub.2 SCH.sub.3H CH.sub.2 CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 190-193H CH.sub.2 Cl H CH.sub.3 OCH.sub.3 216-220H CH.sub.2 Cl H CH.sub.3 CH.sub.3 213-217H CH.sub.2 Cl H Cl OCH.sub.3 196-202H CH.sub.2 Cl H Br OCH.sub.3H CH.sub.2 Cl H CH.sub.3 Cl 195-198H CH.sub.2 Cl H OCH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Cl H OCF.sub.2 H OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OC.sub.2 H.sub.5 198-203H CH.sub.2 Cl H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Cl H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Br OCH.sub.3H CH.sub.2 Cl H F OCH.sub.3H CH.sub.2 Cl H I OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Cl H Cl OC.sub.2 H.sub.5 193-196H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Cl H OCF.sub.2 H CH.sub.3H CH.sub.2 Cl H Cl OCF.sub.2 HH CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H CH.sub.3 CH.sub.3H CHClCH.sub.3 H Cl OCH.sub.3H CHClCH.sub.3 H Br OCH.sub.3H CHClCH.sub.3 H CH.sub.3 HH CHClCH.sub.3 H OCH.sub.3 HH CHClCH.sub.3 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHClCH.sub.3 H OCF.sub.2 H OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OC.sub.2 H.sub.5H CHClCH.sub.3 H CH.sub.3 CH.sub.2 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 C.sub.2 H.sub.5H CHClCH.sub.3 H OC.sub.2 H.sub.5 OCH.sub.3H CHClCH.sub.3 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHClCH.sub.3 H CF.sub.3 OCH.sub.3H CHClCH.sub.3 H CH.sub.2 F OCH.sub.3H CHClCH.sub.3 H CH.sub.2 Cl OCH.sub.3H CHClCH.sub.3 H CH.sub.2 Br OCH.sub.3H CHClCH.sub.3 H F OCH.sub.3H CHClCH.sub.3 H I OCH.sub.3H CHClCH.sub.3 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHClCH.sub.3 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.2 CHF.sub.2 CH.sub.3H CHClCH.sub.3 H OCH.sub.2 CF.sub.3 CH.sub.3H CHClCH.sub.3 H Cl OC.sub.2 H.sub.5H CHClCH.sub. 3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHClCH.sub.3 H OCF.sub.2 H CH.sub.3H CHClCH.sub.3 H Cl OCF.sub.2 HH CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 CH.sub.3H CH.sub.2 Br H Cl OCH.sub.3H CH.sub.2 Br H Br OCH.sub.3H CH.sub.2 Br H CH.sub.3 HH CH.sub.2 Br H OCH.sub.3 HH CH.sub.2 Br H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Br H OCF.sub.2 H OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 Br H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H CF.sub. 3 OCH.sub.3H CH.sub.2 Br H CH.sub.2 F OCH.sub.3H CH.sub.2 Br H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Br H CH.sub.2 Br OCH.sub.3H CH.sub.2 Br H F OCH.sub.3H CH.sub.2 Br H I OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Br H Cl OC.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Br H OCF.sub.2 H CH.sub.3H CH.sub.2 Br H Cl OCF.sub.2 HH CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H CH.sub.3 CH.sub.3H CHF.sub.2 H Cl OCH.sub.3H CHF.sub.2 H Br OCH.sub.3H CHF.sub.2 H CH.sub.3 HH CHF.sub.2 H OCH.sub.3 HH CHF.sub.2 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHF.sub.2 H OCF.sub.2 H OCH.sub.3H CHF.sub.2 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OC.sub.2 H.sub.5H CHF.sub.2 H CH.sub.3 CH.sub.2 OCH.sub.3H CHF.sub.2 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHF.sub.2 H OCH.sub.3 C.sub.2 H.sub.5H CHF.sub.2 H OC.sub.2 H.sub.5 OCH.sub.3H CHF.sub.2 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHF.sub.2 H CF.sub.3 OCH.sub.3H CHF.sub.2 H CH.sub.2 F OCH.sub.3H CHF.sub.2 H CH.sub.2 Cl OCH.sub.3H CHF.sub.2 H CH.sub.2 Br OCH.sub.3H CHF.sub.2 H F OCH.sub.3H CHF.sub.2 H I OCH.sub.3H CHF.sub.2 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHF.sub.2 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.2 CF.sub.3 CH.sub.3H CHF.sub.2 H OCH.sub.2 CHF.sub.2 CH.sub.3H CHF.sub.2 H Cl OC.sub.2 H.sub.5H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub. 3H CHF.sub.2 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHF.sub.2 H OCF.sub.2 H CH.sub.3H CHF.sub.2 H Cl OCF.sub.2 HH CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H Br OCH.sub.3H CHFCl H CH.sub.3 HH CHFCl H OCH.sub.3 HH CHFCl H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHFCl H OCF.sub.2 H OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H OCH.sub.3 C.sub.2 H.sub.5H CHFCl H OC.sub.2 H.sub.5 OCH.sub.3H CHFCl H OCH.sub.2 CF.sub.3 OCH.sub.3H CHFCl H CF.sub.3 OCH.sub.3H CHFCl H CH.sub.2 F OCH.sub.3H CHFCl H CH.sub.2 Cl OCH.sub.3H CHF(3 H CH.sub.2 Br OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H I OCH.sub.3H CHFCl H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHFCl H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHFCl H OCH.sub.2 CHF.sub.2 CH.sub.3H CHFCl H OCH.sub.2 CF.sub.3 CH.sub.3H CHFCl H Cl OC.sub.2 H.sub.5H CHFCl H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 SCH.sub.3H CHFCl H OCF.sub.2 H CH.sub.3H CHFCl H Cl OCF.sub.2 HH CHFCl H n-C.sub.3 H.sub.7 OCH.sub.3H CHFCl H OCH.sub.3 NHCH.sub.3H CHFCl H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 cyclopropylH CHFCl H OCH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.3H CHFCl H OC.sub.2 H.sub.5 CH.sub.2 SCH.sub.3H CHFCl H OCH.sub.3 CH(SCH.sub.3)OC.sub.2 H.sub.5H CHFCl H OCH.sub.3 CH(SC.sub.2 H.sub.5).sub.2H CHFCl H OCH.sub.3 1,3-dioxolan-2-ylH CHFCl H OCH.sub.3 N(OCH.sub.3)CH.sub.3H CHFCl H OCH.sub.3 C.sub.2 H.sub.5H CHFCl H OCH.sub.3 CF.sub.35-F CH.sub.2 F H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 F H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 Cl H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 CH.sub.35-Cl CH.sub.2 F H Cl OCH.sub.35-Br CH.sub.2 F H OCH.sub.3 OCH.sub.35-CH.sub.2 CN CH.sub.2 F H OCH.sub.3 OCH.sub.35-OCH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-SCH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-OCF.sub.2 H CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.34-Cl CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3__________________________________________________________________________
TABLE 3______________________________________ ##STR28## mpR.sup.1 R.sup.2 R.sup.3 X Y (.degree.C.)______________________________________H CH.sub.2 F H OCH.sub.3 OCH.sub.3 193- 196H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.3 CH.sub.3 175- 178H CH.sub.2 F H Cl OCH.sub.3 197- 201H CH.sub.2 F H Br OCH.sub.3H CH.sub.2 F H Cl CH.sub.3 195- 199H CH.sub.2 F H OCH.sub.3 HH CH.sub. 2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.3H CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H C.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 F H F OCH.sub.3H CH.sub.2 F H I OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 F H Cl OC.sub.2 H.sub.5 170- 174H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 F H NH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H n-C.sub.3 H.sub.7 OCH.sub.3H CH.sub.2 F H NHCH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 SCH.sub.3H CH.sub.2 F H OCH.sub.3 SCF.sub.2 HH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CCHH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CHCH.sub.2H CH.sub.2 F H OCH.sub.3 CCHH CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 cyclopropylH CH.sub.2 F H OCH.sub.3 NH.sub.2H CH.sub.2 F H OCH.sub.3 CF.sub.3H CH.sub. 2 F H OCH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCH.sub.3 CHOH CH.sub.2 F H OCH.sub.3 COCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(SCH.sub.3)OC.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 C(CH.sub.3)(SCH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 C(SC.sub.2 H.sub.5).sub.2H CH.sub.2 F H OCH.sub.3 1,3-dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- oxathiolan-2ylH CH.sub.2 F H OCH.sub.3 1,3-oxathian-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- dithian-2-ylH CH.sub.2 F H OCH.sub.3 4-methyl-1,3- dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-4-dimethyl-1,3 dithiolan-2-ylH CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 CCCH.sub.3H CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 OCF.sub.2 BrH CHFCH.sub. 3 H OCH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OCH.sub.3H CHFCH.sub.3 H Br OCH.sub.3H CHFCH.sub.3 H CH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHFCH.sub.3 H OCF.sub.2 H OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 C.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Cl OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Br OCH.sub.3H CHFCH.sub.3 H F OCH.sub.3H CHFCH.sub.3 H I OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CHF.sub.2 CH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OC.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHFCH.sub.3 H OCF.sub.2 H CH.sub.3H CHFCH.sub.3 H Cl OCF.sub.2 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H Br OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 CH.sub.2 F H F OCH.sub.3H CH.sub.2 CH.sub.2 F H I OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.3 CH.sub.3H CH.sub.2 Cl H Cl OCH.sub.3H CH.sub.2 Cl H Br OCH.sub.3H CH.sub.2 Cl H CH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Cl H OCF.sub.2 H OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 Cl H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Cl H OC.sub.2 H.sub. 5 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Br OCH.sub.3H CH.sub.2 Cl H F OCH.sub.3H CH.sub.2 Cl H I OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Cl H Cl OC.sub.2 H.sub.5H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Cl H OCF.sub.2 H CH.sub.3H CH.sub.2 Cl H Cl OCF.sub.2 HH CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 CH.sub.3H CH.sub.2 Br H Cl OCH.sub.3H CH.sub.2 Br H Br OCH.sub.3H CH.sub.2 Br H CH.sub.3 HH CH.sub.2 Br H OCH.sub.3 HH CH.sub.2 Br H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Br H OCF.sub.2 H OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 Br H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H CF.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.2 F OCH.sub.3H CH.sub.2 Br H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Br H CH.sub.2 Br OCH.sub.3H CH.sub.2 Br H F OCH.sub.3H CH.sub.2 Br H I OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Br H Cl OC.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Br H OCF.sub.2 H CH.sub.3H CH.sub.2 Br H Cl OCF.sub.2 H______________________________________
TABLE 4______________________________________ ##STR29## mpR.sup.1 R.sup.2 R.sup.3 X Y (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 212- 214H CH.sub.2 F H OCH.sub.3 OCH.sub.3 225- 228H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 ClH CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3 180- 185H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 216- 219H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CF.sub.3 H CH.sub.3 OCH.sub.3 205- 209H CF.sub.3 H OCH.sub.3 OCH.sub.3 220- 223H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub. 3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CH.sub.2 Cl H Cl OCH.sub.3 219- 222H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H OCH.sub.3 CH.sub.35-Br CH.sub.2 F H CH.sub.3 OCH.sub.35-CH.sub.2 CN CH.sub.2 F H OCH.sub.3 OCH.sub.35-OCH.sub.3 CH.sub.2 F H CH.sub.3 OCH.sub.35-SCH.sub.3 CH.sub.2 F H CH.sub.3 OCH.sub.35-OCF.sub.2 H CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 Cl H CH.sub.3 OCH.sub.35-Cl CH.sub.2 Br H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.35-Cl CH.sub.2 F H OCH.sub.3 OCH.sub.3______________________________________
TABLE 5______________________________________ ##STR30##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 185-189H CH.sub.2 F H OCH.sub.3 OCH.sub.3 179-182H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3 173-177H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 186-190H CH.sub.2 Cl H OC.sub.2 H.sub.5 Cl 186-188H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.3 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub. 3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 6______________________________________ ##STR31##R.sup.1 R.sup.2 R.sup.3 X Y mp______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 162-167H CH.sub.2 F H OCH.sub.3 OCH.sub.3 195-198H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub. 3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3______________________________________
TABLE 7______________________________________ ##STR32##R.sup.1 R.sup.2 R.sup.3 X.sup.1 Y.sup.1 mp______________________________________H CH.sub.2 F H CH.sub.3 OH CH.sub.2 F H OCH.sub.3 OH CH.sub.2 F H OC.sub.2 H.sub.5 OH CH.sub.2 F H OCF.sub.2 H OH CH.sub.2 F H OCH.sub.3 CH.sub.2H CH.sub.2 Cl H CH.sub.3 OH CH.sub.2 Cl H OCH.sub.3 OH CH.sub.2 Br H CH.sub.3 OH CHFCH.sub.3 H CH.sub.3 OH CHClCH.sub.3 H CH.sub.3 O5-CH.sub.3 CH.sub.2 F H CH.sub.3 O5-Cl CH.sub.2 F H CH.sub.3 O5-CH.sub.3 CH.sub.2 F H CH.sub.3 O5-CH.sub.2 CN CH.sub.2 F H CH.sub.3 OH CH.sub.2 F CH.sub.3 CH.sub.3 OH CHF.sub.2 H OCH.sub.3 O______________________________________
TABLE 8______________________________________ ##STR33##R.sup.1 R.sup.2 R.sup.3 X.sup.1 Y.sub.1 mp______________________________________H CH.sub.2 F H CH.sub.3 OH CH.sub.2 F H OCH.sub.3 OH CH.sub.2 F H OC.sub.2 H.sub.5 OH CH.sub.2 F H OCF.sub.2 H OH CH.sub.2 F H OCH.sub.3 CH.sub.2H CH.sub.2 Cl H CH.sub.3 OH CH.sub.2 Cl H OCH.sub.3 OH CH.sub.2 Br H CH.sub.3 OH CHFCH.sub.3 H CH.sub.3 OH CHClCH.sub.3 H CH.sub.3 O5-CH.sub.3 CH.sub.2 F H CH.sub.3 O5-Cl CH.sub. 2 F H CH.sub.3 O5-CH.sub.3 CH.sub.2 F H CH.sub.3 O5-CH.sub.2 CN CH.sub.2 F H CH.sub.3 OH CH.sub.2 F CH.sub.3 CH.sub.3 OH CHF.sub.2 H OCH.sub.3 O______________________________________
TABLE 9______________________________________ ##STR34##R.sup.1 R.sup.2 R.sup.3 X.sup.1 mp______________________________________H CH.sub.2 F H CH.sub.3H CH.sub.2 F H OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5H CH.sub.2 F H OCF.sub.3 HH CH.sub.2 F H OCH.sub.3H CH.sub.2 F H CH.sub.3H CH.sub.2 Cl H OCH.sub.3H CHFCl H OCH.sub.3H CHFCl H OCH.sub.3H CHFCH.sub.3 H OCH.sub.3H CH.sub.2 F H OCH.sub.35-F CH.sub.2 F H OCH.sub.35-OCH.sub.3 CH.sub.2 F H OCH.sub.35-Cl CH.sub.2 F H OCH.sub.35-CH.sub.3 CH.sub. 2 F H OCH.sub.35-CH.sub.2 CN CH.sub.2 F H OCH.sub.3H CH.sub.2 Cl H OCH.sub.3H CH.sub.2 Br H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3H CHClCH.sub.3 H OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H OCH.sub.3______________________________________
TABLE 10______________________________________ ##STR35##R.sup.1 R.sup.2 R.sup.3 X.sup.1 Y.sup.1 mp______________________________________H CH.sub.2 F H CH.sub.3 OH CH.sub.2 F H OCH.sub.3 OH CH.sub.2 F H OC.sub.2 H.sub.5 OH CH.sub.2 F H OCF.sub.2 H OH CH.sub.2 F H OCH.sub.3 CH.sub.2H CH.sub.2 Cl H C.sub.3 OH CH.sub.2 Cl H OCH.sub.3 OH CH.sub.2 Br H CH.sub.3 OH CHFCH.sub.3 H CH.sub.3 OH CHClCH.sub.3 H CH.sub.3 O5-CH.sub.3 CH.sub.2 F H CH.sub.3 O5-Cl CH.sub.2 F H CH.sub.3 O5-CH.sub.3 CH.sub.2 F H CH.sub.3 O5-CH.sub.2 CN CH.sub.2 F H CH.sub.3 OH CH.sub.2 F H CH.sub.3 OH CHF.sub.2 H OCH.sub.3 O______________________________________
TABLE 11______________________________________ ##STR36##R.sup.1 R.sup.2 R.sup.3 X.sup.1 mp______________________________________H CH.sub.2 F H CH.sub.3H CH.sub.2 F H OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5H CH.sub.2 F H OCF.sub.2 HH CH.sub.2 F H OCH.sub.3H CH.sub.2 F H CH.sub.3H CH.sub.2 Cl H OCH.sub.3H CHFCl H OCH.sub.3H CHFCl H OCH.sub.3H CHFCH.sub.3 H OCH.sub.3H CH.sub.2 F H OCH.sub.35-F CH.sub.2 F H OCH.sub.35-OCH.sub.3 CH.sub.2 F H OCH.sub.35-Cl CH.sub.2 F H OCH.sub.35-CH.sub.3 CH.sub.2 F H OCH.sub.35-CH.sub.2 CN CH.sub.2 F H OCH.sub.3H CH.sub.2 Cl H OCH.sub.3H CH.sub.2 Br H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3H CHClCH.sub.3 H OCH.sub.3H CHF.sub.2 H OCH.sub.34-Cl CH.sub.2 F H OCH.sub.3______________________________________
TABLE 12______________________________________ ##STR37##R.sup.1 R.sup.2 R.sup.3 X.sup.1 mp______________________________________H CH.sub.2 F H CH.sub.3H CH.sub.2 F H OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5H CH.sub.2 F H OCF.sub.2 HH CH.sub.2 Cl H CH.sub.3H CH.sub.2 Cl H OCH.sub.3H CH.sub.2 Br H CH.sub.3H CHF.sub.2 H CH.sub.3H CHF.sub.2 H OCH.sub.3H CHFCH.sub.3 H CH.sub.3H CHFCH.sub.3 H OCH.sub.3H CHFCl H OCH.sub.3H CHFCl H CH.sub.35-Cl CHFCl H CH.sub.35-Cl CHFCl H OCH.sub.35-Cl CH.sub.2 F H CH.sub.35-Cl CH.sub.2 F H OCH.sub.35-CH.sub.3 CH.sub.2 F H CH.sub.35-OCH.sub.3 CH.sub.2 F H CH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3______________________________________
TABLE 13______________________________________ ##STR38##R.sup.1 R.sup.2 R.sup.3 X.sup.1 Y.sup.3 mp______________________________________H CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.3H CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 F H OCH.sub.3 HH CH.sub.2 F H CH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.35-F CH.sub.2 F H OCH.sub.3 OCH.sub.35-OCH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 F H OCH.sub.3 OCH.sub.35-CH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-CH.sub.3 CH.sub.2 F H OCH.sub.3 CH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.3H CHClCH.sub.3 H OCH.sub.3 CH.sub.3H CHF.sub.2 H OCH.sub.3 CH.sub.35-Cl CH.sub.2 F H OCH.sub.3 CH.sub.3______________________________________
TABLE 14______________________________________ ##STR39##R.sup.1 R.sup.2 R.sup.3 X.sup.1 Y.sup.3 mp______________________________________H CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.3H CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 F H OCH.sub.3 HH CH.sub.2 F H CH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CH.sub. 2 F H OCH.sub.3 OCH.sub.35-F CH.sub.2 F H OCH.sub.3 OCH.sub.35-OCH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 F H OCH.sub.3 OCH.sub.35-CH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-CH.sub.2 CN CH.sub.2 F H OCH.sub.3 CH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.3H CHClCH.sub.3 H OCH.sub.3 CH.sub.3H CHF.sub.2 H OCH.sub.3 CH.sub.35-Cl CH.sub.2 F H OCH.sub.3 CH.sub.3______________________________________
TABLE 15______________________________________ ##STR40##R.sup.1 R.sup.2 R.sup.3 X.sup.1 Y.sup.3 mp______________________________________H CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.3H CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 F H OCH.sub.3 HH CH.sub.2 F H CH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.35-F CH.sub.2 F H OCH.sub.3 OCH.sub.35-OCH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-Cl CH.sub.2 F H OCH.sub.3 OCH.sub.35-CH.sub.3 CH.sub.2 F H OCH.sub.3 OCH.sub.35-CH.sub.2 CN CH.sub.2 F H OCH.sub.3 CH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.3H CHClCH.sub.3 H OCH.sub.3 CH.sub.3H CHF.sub.2 H OCH.sub.3 CH.sub.35-Cl CH.sub.2 F H OCH.sub.3 CH.sub.3______________________________________
TABLE 16______________________________________ ##STR41##R.sup.1 R.sup.2 R.sup.3 X.sup.2 Y.sup.2 mp______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 SCH.sub.3H CH.sub.2 F H CH.sub.3 SC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 F H CH.sub.3 C.sub.2 H.sub.5H CH.sub.2 F H C.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHF.sub.2 H CH.sub.3 OCH.sub.35-CH.sub.3 CH.sub.2 F H CH.sub.3 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 OCH.sub.35-OCH.sub.3 CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 CH.sub.35-CH.sub.2 CN CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H CH.sub.3 OCH.sub.3______________________________________
TABLE 17______________________________________ ##STR42##R.sup.1 R.sup.2 R.sup.3 X.sup.2 Y.sup.2 mp______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 SCH.sub.3H CH.sub.2 F H CH.sub.3 SC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 F H CH.sub.3 C.sub.2 H.sub.5H CH.sub.2 F H C.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHF.sub.2 H CH.sub.3 OCH.sub.35-CH.sub.3 CH.sub.2 F H CH.sub.3 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 OCH.sub.35-OCH.sub.3 CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 CH.sub.35-CH.sub.2 CN CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H CH.sub.3 OCH.sub.3______________________________________
TABLE 18______________________________________ ##STR43##R.sup.1 R.sup.2 R.sup.3 X.sup.2 Y.sup.2 mp______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 SCH.sub.3H CH.sub.2 F H CH.sub.3 SC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 F H CH.sub.3 C.sub.2 H.sub.5H CH.sub.2 F H C.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub. 3 OCH.sub.3H CHF.sub.2 H CH.sub.3 OCH.sub.35-CH.sub.3 CH.sub.2 F H CH.sub.3 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 OCH.sub.35-OCH.sub.3 CH.sub.2 F H CH.sub.3 OCH.sub.35-Cl CH.sub.2 F H CH.sub.3 CH.sub.35-CH.sub.2 CN CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H CH.sub.3 OCH.sub.3______________________________________
TABLE 19______________________________________ ##STR44##R.sup.1 R.sup.2 R.sup.3 X.sup.3 mp______________________________________H CH.sub.2 F H CH.sub.3H CH.sub.2 F H OCH.sub.3H CH.sub.2 Cl H CH.sub.3H CH.sub.2 Cl H OCH.sub.3H CHF.sub.2 H OCH.sub.3H CHF.sub.2 H CH.sub.3H CHFCl H CH.sub.3H CHFCl H OCH.sub.3H CHFCH.sub.3 H CH.sub.3H CHFCH.sub.3 H OCH.sub.3H CHClCH.sub.3 H OCH.sub.35-F CH.sub.2 F H OCH.sub.35-Cl CH.sub.2 F H OCH.sub.35-CH.sub.3 CH.sub.2 F H OCH.sub.35-OHC.sub.3 CH.sub.2 F H CH.sub.35-CH.sub.2 CN CH.sub.2 F H CH.sub.35-Cl CH.sub.2 F H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3______________________________________
TABLE 20______________________________________ ##STR45##R.sup.1 R.sup.2 R.sup.3 X.sup.3 mp______________________________________H CH.sub.2 F H CH.sub.3H CH.sub.2 F H OCH.sub.3H CH.sub.2 Cl H CH.sub.3H CH.sub.2 Cl H OCH.sub.3H CHF.sub.2 H OCH.sub.3H CHF.sub.2 H CH.sub.3H CHFCl H CH.sub.3H CHFCl H OCH.sub.3H CHFCH.sub.3 H CH.sub.3H CHFCH.sub.3 H OCH.sub.3H CHClCH.sub.3 H OCH.sub.35-F CH.sub.2 F H OCH.sub.35-Cl CH.sub.2 F H OCH.sub.35-CH.sub.3 CH.sub.2 F H CH.sub.35-OCH.sub.3 CH.sub.2 F H CH.sub.35-CH.sub.2 CN CH.sub.2 F H CH.sub.35-Cl CH.sub.2 F H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3______________________________________
TABLE 21______________________________________ ##STR46##R.sup.1 R.sup.2 R.sup.3 X.sup.3 mp______________________________________H CH.sub.2 F H CH.sub.3H CH.sub.2 F H OCH.sub.3H CH.sub.2 Cl H CH.sub.3H CH.sub.2 Cl H OCH.sub.3H CHF.sub.2 H OCH.sub.3H CHF.sub.2 H CH.sub.3H CHFCl H CH.sub.3H CHFCl H OCH.sub.3H CHFCH.sub.3 H CH.sub.3H CHFCH.sub.3 H OCH.sub.3H CHClCH.sub.3 H OCH.sub.35-F CH.sub.2 F H OCH.sub.35-Cl CH.sub.2 F H OCH.sub.35-CH.sub.3 CH.sub.2 F H CH.sub. 35-OCH.sub.3 CH.sub.2 F H CH.sub.35-CH.sub.2 CN CH.sub.2 F H CH.sub.35-Cl CH.sub.2 F H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3______________________________________
TABLE 22______________________________________ ##STR47##R.sup.1 R.sup.2 R.sup.3 X.sup.4 Y.sup.4 Z.sup.1 mp______________________________________H CH.sub.2 F H CH.sub.3 CH.sub.3 CHH CH.sub.2 F H CH.sub.3 CH.sub.3 NH CH.sub.2 F H OCH.sub.3 CH.sub.3 CHH CH.sub.2 F H OCH.sub.3 CH.sub.3 NH CH.sub.2 F H OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H OCH.sub.3 OCH.sub.3 NH CH.sub.2 F H Cl CH.sub.3 CHH CH.sub.2 F H OCH.sub.3 Cl CHH CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.3 CHH CH.sub.2 F H CH.sub.2 OCH.sub.3 CH.sub.3 NH CH.sub.2 F H CH.sub.2 OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H OC.sub.2 H.sub.5 OC.sub.2 H.sub.5 NH CH.sub.2 Cl H OCH.sub.3 CH.sub.3 CHH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 CHH CH.sub.2 Cl H OCH.sub.3 CH.sub.3 NH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 NH CHF.sub.2 H OCH.sub.3 CH.sub.3 CHH CHFCl H OCH.sub.3 CH.sub.3 CHH CHFCH.sub.3 H OCH.sub.3 CH.sub.3 CHH CHClCH.sub.3 H OCH.sub.3 CH.sub.3 CH5-F CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-CH.sub.3 CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-OCH.sub.3 CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-Cl CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-CH.sub.2 CN CH.sub.2 F H OCH.sub.3 CH.sub.3 CHH CH.sub.2 F CH.sub.3 OCH.sub.3 CH.sub.3 CHH CH.sub.2 CH.sub. 2 F H OCH.sub.3 CH.sub.3 CHH CH.sub.2 CH.sub.2 Cl H OCH.sub.3 CH.sub.3 CHH CHFCl H OCH.sub.3 OCH.sub.3 CH______________________________________
TABLE 23______________________________________ ##STR48##R.sup.1 R.sup.2 R.sup.3 X.sup.4 Y.sup.4 Z.sup.1 mp______________________________________H CH.sub.2 F H CH.sub.3 CH.sub.3 CHH CH.sub.2 F H CH.sub.3 CH.sub.3 NH CH.sub.2 F H OCH.sub.3 CH.sub.3 CHH CH.sub.2 F H OCH.sub.3 CH.sub.3 NH CH.sub.2 F H OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H OCH.sub.3 OCH.sub.3 NH CH.sub.2 F H Cl CH.sub.3 CHH CH.sub.2 F H OCH.sub.3 Cl CHH CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.3 CHH CH.sub.2 F H CH.sub.2 OCH.sub.3 CH.sub.3 NH CH.sub.2 F H CH.sub.2 OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H OC.sub.2 H.sub.5 OC.sub.2 H.sub.5 NH CH.sub.2 Cl H OCH.sub.3 CH.sub.3 CHH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 CHH CH.sub.2 Cl H OCH.sub.3 CH.sub.3 NH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 NH CHF.sub.2 H OCH.sub.3 CH.sub.3 CHH CHFCl H OCH.sub.3 CH.sub.3 CHH CHFCH.sub.3 H OCH.sub.3 CH.sub.3 CHH CHClCH.sub.3 H OCH.sub.3 CH.sub.3 CH5-F CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-CH.sub.3 CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-OCH.sub.3 CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-Cl CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-CH.sub.2 CN CH.sub.2 F H OCH.sub.3 CH.sub.3 CHH CH.sub.2 F CH.sub.3 OCH.sub.3 CH.sub.3 CHH CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.3 CHH CH.sub.2 CH.sub.2 Cl H OCH.sub.3 CH.sub.3 CHH CHFCl H OCH.sub.3 OCH.sub.3 CH______________________________________
TABLE 24______________________________________ ##STR49##R.sup.1 R.sup.2 R.sup.3 X.sup.4 Y.sup.4 Z.sup.1 mp______________________________________H CH.sub.2 F H CH.sub.3 CH.sub.3 CHH CH.sub.2 F H CH.sub.3 CH.sub.3 NH CH.sub.2 F H OCH.sub.3 CH.sub.3 CHH CH.sub.2 F H OCH.sub.3 CH.sub.3 NH CH.sub.2 F H OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H OCH.sub.3 OCH.sub.3 NH CH.sub.2 F H Cl CH.sub.3 CHH CH.sub.2 F H OCH.sub. 3 Cl CHH CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.3 CHH CH.sub.2 F H CH.sub.2 OCH.sub.3 CH.sub.3 NH CH.sub.2 F H CH.sub.2 OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H OC.sub.2 H.sub.5 OC.sub.2 H.sub.5 NH CH.sub.2 Cl H OCH.sub.3 CH.sub.3 CHH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 CHH CH.sub.2 Cl H OCH.sub.3 CH.sub.3 NH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 NH CHF.sub.2 H OCH.sub.3 CH.sub.3 CHH CHFCl H OCH.sub.3 CH.sub.3 CHH CHFCH.sub.3 H OCH.sub.3 CH.sub.3 CHH CHClCH.sub.3 H OCH.sub.3 CH.sub.3 CH5-F CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-CH.sub.3 CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-OCH.sub.3 CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-Cl CH.sub.2 F H OCH.sub.3 CH.sub.3 CH5-CH.sub.2 CN CH.sub.2 F H OCH.sub.3 CH.sub.3 CHH CH.sub.2 F CH.sub.3 OCH.sub.3 CH.sub.3 CHH CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.3 CHH CH.sub.2 CH.sub.2 Cl H OCH.sub.3 CH.sub.3 CHH CHFCl H OCH.sub.3 OCH.sub.3 CH______________________________________
TABLE 25______________________________________ ##STR50##R.sup.1 R.sup.2 R.sup.3 W X Y Z.sup.1 mp______________________________________H CH.sub.2 F H S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H S CH.sub.3 OCH.sub.3 NH CH.sub.2 F H S OCH.sub.3 OCH.sub.3 NH CH.sub.2 Cl H S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 Br H S OCH.sub.3 OCH.sub.3 CHH CHF.sub.2 H S OCH.sub.3 OCH.sub.3 CHH CHFCl H S OCH.sub.3 OCH.sub.3 CHH CHFCH.sub.3 H S OCH.sub.3 OCH.sub.3 CHH CHClCH.sub.3 H S OCH.sub.3 OCH.sub.3 CH5-OCH.sub.3 CH.sub.2 F H S OCH.sub.3 OCH.sub.3 CH5-Cl CH.sub.2 F H S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F CH.sub.3 S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H S OCH.sub.3 CH.sub.3 CH______________________________________
TABLE 26______________________________________ ##STR51##R.sup.1 R.sup.2 R.sup.3 W X Y Z.sup.1 mp______________________________________H CH.sub.2 F H S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H S CH.sub.3 OCH.sub.3 NH CH.sub.2 F H S OCH.sub.3 OCH.sub.3 NH CH.sub.2 Cl H S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 Br H S OCH.sub.3 OCH.sub.3 CHH CHF.sub.2 H S OCH.sub.3 OCH.sub.3 CHH CHFCl H S OCH.sub.3 OCH.sub.3 CHH CHFCH.sub.3 H S OCH.sub.3 OCH.sub.3 CHH CHClCH.sub. 3 H S OCH.sub.3 OCH.sub.3 CH5-OCH.sub.3 CH.sub.2 F H S OCH.sub.3 OCH.sub.3 CH5-Cl CH.sub.2 F H S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F CH.sub.3 S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H S OCH.sub.3 CH.sub.3 CH______________________________________
TABLE 27______________________________________ ##STR52##R.sup.1 R.sup.2 R.sup.3 W X Y Z.sup.1 mp______________________________________H CH.sub.2 F H S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H S CH.sub.3 OCH.sub.3 NH CH.sub.2 F H S OCH.sub.3 OCH.sub.3 NH CH.sub.2 Cl H S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 Br H S OCH.sub.3 OCH.sub.3 CHH CHF.sub.2 H S OCH.sub.3 OCH.sub.3 CHH CHFCl H S OCH.sub.3 OCH.sub.3 CHH CHFCH.sub.3 H S OCH.sub.3 OCH.sub.3 CHH CHClCH.sub. 3 H S OCH.sub.3 OCH.sub.3 CH5-OCH.sub.3 CH.sub.2 F H S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F CH.sub.3 S OCH.sub.3 OCH.sub.3 CHH CH.sub.2 F H S OCH.sub.3 CH.sub.3 CH______________________________________
TABLE 28______________________________________ ##STR53## mpR.sup.1 R.sup.2 R.sup.3 X Y (.degree.C.)______________________________________H CH.sub.2 F H OCH.sub.3 OCH.sub.3 115- 117H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.3 CH.sub.3 125- 130H CH.sub.2 F H Cl OCH.sub.3H CH.sub.2 F H Br OCH.sub.3H CH.sub.2 F H H CH.sub.3H CH.sub.2 F H OCH.sub.3 HH CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H C.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 F H F OCH.sub.3H CH.sub.2 F H I OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 F H Cl OC.sub.2 H.sub.5H CH.sub.2 F H OC.sub.2 H.sub. 5 NHCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 F H NH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H n-C.sub.3 H.sub.7 OCH.sub.3H CH.sub.2 F H NHCH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 SCH.sub.3H CH.sub.2 F H OCH.sub.3 SCF.sub.2 HH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CCHH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CHCH.sub.2H CH.sub.2 F H OCH.sub.3 CCHH CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 cyclopropylH CH.sub.2 F H OCH.sub.3 NH.sub.2H CH.sub.2 F H OCH.sub.3 CF.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCH.sub.3 CHOH CH.sub.2 F H OCH.sub.3 COCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(SCH.sub.3)OC.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 C(CH.sub.2)(SCH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 C(SC.sub.2 H.sub.5).sub.2H CH.sub.2 F H OCH.sub.3 1,3-dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- oxathiolan-2ylH CH.sub.2 F H OCH.sub.3 1,3-oxathian-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- dithian-2-ylH CH.sub.2 F H OCH.sub.3 4-methyl-1,3- dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-4-dimethyl-1,3- dithiolan-2-ylH CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 CCCH.sub.3H CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 OCF.sub.2 BrH CHFCH.sub.3 H OCH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CF.sub.3 H CH.sub.3 CH.sub.3 196- 199H CHFCH.sub.3 H Cl OCH.sub.3H CHFCH.sub.3 H Br OCH.sub.3H CHFCH.sub.3 H CH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHFCH.sub.3 H OCF.sub.2 H OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 C.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Cl OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Br OCH.sub.3H CHFCH.sub.3 H F OCH.sub.3H CHFCH.sub.3 H I OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CHF.sub.2 CH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OC.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHFCH.sub.3 H OCF.sub.2 H CH.sub.3H CHFCH.sub.3 H Cl OCF.sub.2 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H Br OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 CH.sub.2 F H F OCH.sub.3H CH.sub.2 CH.sub.2 F H I OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CF.sub.3 H Cl OC.sub.2 H.sub.5 165- 167H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCF.sub.2 HH CF.sub.3 H OCH.sub.3 OCH.sub.3 180- 182H CF.sub.3 H CH.sub.3 OCH.sub.3 188- 191H CH.sub.2 Cl H CH.sub.3 CH.sub.3 166- 169H CF.sub.3 H Cl OCH.sub.3 173- 174H CH.sub.2 Cl H Br OCH.sub.3H CH.sub.2 Cl H CH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Cl H OCF.sub.2 H OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 Cl H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Cl H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Br OCH.sub.3H CH.sub.2 Cl H F OCH.sub.3H CH.sub.2 Cl H I OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Cl H Cl OC.sub.2 H.sub.5H CH.sub.2 Cl H OCH.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Cl H OCF.sub.2 H CH.sub.3H CH.sub.2 Cl H Cl OCF.sub.2 HH CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 OCH.sub. 3H CH.sub.2 Br H CH.sub.3 CH.sub.3H CH.sub.2 Br H Cl OCH.sub.3H CH.sub.2 Br H Br OCH.sub.3H CH.sub.2 Br H CH.sub.3 HH CH.sub.2 Br H OCH.sub.3 HH CH.sub.2 Br H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Br H OCF.sub.2 H OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 Br H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H CF.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.2 F OCH.sub.3H CH.sub.2 Br H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Br H CH.sub.2 Br OCH.sub.3H CH.sub.2 Br H F OCH.sub.3H CH.sub.2 Br H I OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Br H Cl OC.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Br H OCF.sub.2 H CH.sub.3H CH.sub.2 Br H Cl OCF.sub.2 H______________________________________
TABLE 29______________________________________ ##STR54## mpR.sup.1 R.sup.2 R.sup.3 X Y (.degree.C.)______________________________________H CH.sub.2 F H OCH.sub.3 OCH.sub.3 172- 175H CH.sub.2 F H CH.sub.3 OCH.sub.3 186- 187H CH.sub.2 F H CH.sub.3 CH.sub.3 190- 194H CH.sub.2 F H Cl OCH.sub.3 148- 151H CH.sub.2 F H Br OCH.sub.3H CH.sub.2 F H Cl CH.sub.3 172- 176H CH.sub.2 F H OCH.sub.3 HH CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5 160- 163H CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H C.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 F H F OCH.sub.3H CH.sub.2 F H I OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CHF.sub. 2 CH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 F H Cl OC.sub.2 H.sub.5 140- 145H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 F H NH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H n-C.sub.3 H.sub.7 OCH.sub.3H CH.sub.2 F H NHCH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 SCH.sub.3H CH.sub.2 F H OCH.sub.3 SCF.sub.2 HH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CCHH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CHCH.sub.2H CH.sub.2 F H OCH.sub.3 CCHH CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 cyclopropylH CH.sub.2 F H OCH.sub. 3 NH.sub.2H CH.sub.2 F H OCH.sub.3 CF.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCH.sub.3 CHOH CH.sub.2 F H OCH.sub.3 COCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(SCH.sub.3)OC.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 C(CH.sub.3)(SCH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 C(SC.sub.2 H.sub.5).sub.2H CH.sub.2 F H OCH.sub.3 1,3-dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- oxathiolan-2ylH CH.sub.2 F H OCH.sub.3 1,3-oxathian-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- dithian-2-ylH CH.sub.2 F H OCH.sub.3 4-methyl-1,3- dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2,4-dimethyl-1,3- dithiolan-2-ylH CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 CCCH.sub.3H CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 OCF.sub.2 BrH CHFCH.sub.3 H OCH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OCH.sub.3H CHFCH.sub.3 H Br OCH.sub.3H CHFCH.sub.3 H CH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHFCH.sub.3 H OCF.sub.2 H OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 C.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Cl OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Br OCH.sub.3H CHFCH.sub.3 H F OCH.sub.3H CHFCH.sub.3 H I OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CHF.sub.2 CH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OC.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHFCH.sub.3 H OCF.sub.2 H CH.sub.3H CHFCH.sub.3 H Cl OCF.sub.2 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H Br OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 ClH CH.sub.2 CH.sub.2 F H OCH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 CH.sub.2 F H F OCH.sub.3H CH.sub.2 CH.sub.2 F H I OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OCH.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.3 OCH.sub.3 157- 160H CH.sub.2 Cl H Cl OCH.sub.3 156- 159H CH.sub.2 Cl H Br OCH.sub.3H CH.sub.2 Cl H CH.sub.3 Cl 149- 153H CH.sub.2 Cl H OCH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Cl H OCF.sub.2 H OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OC.sub.2 H.sub.5 178- 180H CH.sub.2 Cl H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Cl H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Br OCH.sub.3H CH.sub.2 Cl H F OCH.sub.3H CH.sub.2 Cl H I OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Cl H Cl OC.sub.2 H.sub.5 147- 149H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Cl H OCF.sub.2 H CH.sub.3H CH.sub.2 Cl H Cl OCF.sub.2 HH CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 CH.sub.3H CH.sub.2 Br H Cl OCH.sub.3H CH.sub.2 Br H Br OCH.sub.3H CH.sub.2 Br H CH.sub.3 HH CH.sub.2 Br H OCH.sub.3 HH CH.sub.2 Br H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Br H OCF.sub.2 H OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 Br H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H CF.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.2 F OCH.sub.3H CH.sub.2 Br H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Br H CH.sub.2 Br OCH.sub.3H CH.sub.2 Br H F OCH.sub.3H CH.sub.2 Br H I OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Br H Cl OC.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Br H OCF.sub.2 H CH.sub.3H CH.sub.2 Br H Cl OCF.sub.2 H______________________________________
TABLE 30______________________________________ ##STR55##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 172-177H CH.sub.2 F H OCH.sub.3 OCH.sub.3 183-187H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 31______________________________________ ##STR56##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 129-133H CH.sub.2 F H OCH.sub.3 OCH.sub.3 139-142H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3 138-141H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 133-136H CH.sub.2 Cl H OC.sub.2 H.sub. 5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub. 3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.3 H OCH.sub.3 OCH.sub.3 165-166H CHF.sub.3 H CH.sub.3 OCH.sub. 3 174-176H CHF.sub.3 H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 32______________________________________ ##STR57##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 153-157H CH.sub.2 F H OCH.sub.3 OCH.sub.3 135-139H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3 138-140H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3 127-129H CH.sub.2 Cl H OC.sub. 2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub. 3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 33______________________________________ ##STR58##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 168-171H CH.sub.2 F H OCH.sub.3 OCH.sub.3 145-148H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub. 3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 34__________________________________________________________________________ ##STR59##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)__________________________________________________________________________H CH.sub.2 F H OCH.sub.3 OCH.sub.3 146-148H CH.sub.2 F H CH.sub.3 OCH.sub.3 145-148H CH.sub.2 F H CH.sub.3 CH.sub.3 177-178H CH.sub.2 F H Cl OCH.sub.3 149-150H CH.sub.2 F H Br OCH.sub.3H CH.sub.2 F H H CH.sub.3H CH.sub.2 F H OCH.sub.3 HH CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 F H C.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 F H F OCH.sub.3H CH.sub.2 F H I OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 F H Cl OC.sub.2 H.sub.5H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 F H NH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 F H n-C.sub.3 H.sub.7 OCH.sub.3H CH.sub.2 F H NHCH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 SCH.sub.3H CH.sub.2 F H OCH.sub.3 SCF.sub.2 HH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CCHH CH.sub.2 F H OCH.sub.3 OCH.sub.2 CHCH.sub.2H CH.sub.2 F H OCH.sub.3 CCHH CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 cyclopropylH CH.sub.2 F H OCH.sub.3 NH.sub.2H CH.sub.2 F H OCH.sub.3 CF.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.3H CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 F H OCH.sub.3 CHOH CH.sub.2 F H OCH.sub.3 COCH.sub.3H CH.sub.2 F H OCH.sub.3 CH(SCH.sub.3)OC.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 C(CH.sub.3)(SCH.sub.3).sub.2H CH.sub.2 F H OCH.sub.3 C(SC.sub.2 H.sub.5).sub.2H CH.sub.2 F H OCH.sub.3 1,3-dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- oxathiolan-2ylH CH.sub.2 F H OCH.sub.3 1,3-oxathian-2-ylH CH.sub.2 F H OCH.sub.3 2-methyl-1,3- dithian-2-ylH CH.sub.2 F H OCH.sub.3 4-methyl-1,3- dioxolan-2-ylH CH.sub.2 F H OCH.sub.3 2-4-dimethyl-1,3- dithiolan-2-ylH CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 CCCH.sub.3H CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 F H OCH.sub.3 OCF.sub.2 BrH CHFCH.sub.3 H OCH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OCH.sub.3H CHFCH.sub. 3 H Br OCH.sub.3H CHFCH.sub.3 H CH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 HH CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CHFCH.sub.3 H OCO.sub.2 H OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OC.sub.2 H.sub.5H CHFCH.sub.3 H CH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 C.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CF.sub.3 OCH.sub.3H CHFCH.sub.3 H CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Cl OCH.sub.3H CHFCH.sub.3 H CH.sub.2 Br OCH.sub.3H CHFCH.sub.3 H F OCH.sub.3H CHFCH.sub.3 H I OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 F OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.2 CHF.sub.2 CH.sub.3H CHFCH.sub.3 H OCH.sub.2 CF.sub.3 CH.sub.3H CHFCH.sub.3 H Cl OC.sub.2 H.sub.5H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 CH.sub.2 SCH.sub.3H CHFCH.sub.3 H OCF.sub.2 H CH.sub.3H CHFCH.sub.3 H Cl OCF.sub.2 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H Br OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 HH CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OCF.sub.2 H OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Cl OCH.sub.3H CH.sub.2 CH.sub.2 F H CH.sub.2 Br OCH.sub.3H CH.sub.2 CH.sub.2 F H F OCH.sub.3H CH.sub.2 CH.sub.2 F H I OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OC.sub.2 H.sub.5H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 CH.sub.2 F H OCF.sub.2 H CH.sub.3H CH.sub.2 CH.sub.2 F H Cl OCF.sub.2 HH CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.3 CH.sub.3H CH.sub.2 Cl H Cl OCH.sub.3H CH.sub.2 Cl H Br OCH.sub.3H CH.sub.2 Cl H CH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 HH CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Cl H OCF.sub.2 H OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 Cl H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Cl H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CF.sub.3 OCH.sub.3H CH.sub.2 Cl H CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Cl H CH.sub.2 Br OCH.sub.3H CH.sub.2 Cl H F OCH.sub.3H CH.sub.2 Cl H I OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.2 CHF.sub.2 CH.sub.3H CH.sub.2 Cl H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Cl H Cl OC.sub.2 H.sub.5H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Cl H OCF.sub.2 H CH.sub.3H CH.sub.2 Br H Cl OCF.sub.2 H.sub.5H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.3 CH.sub.3H CH.sub.2 Br H Cl OCH.sub.3H CH.sub.2 Br H Br OCH.sub.3H CH.sub.2 Br H CH.sub.3 HH CH.sub.2 Br H OCH.sub.3 HH CH.sub.2 Br H OCH.sub. 3 CH.sub.2 OC.sub.2 H.sub.5H CH.sub.2 Br H OCF.sub.2 H OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH(OCH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OC.sub.2 H.sub.5H CH.sub.2 Br H CH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 C.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H CF.sub.3 OCH.sub.3H CH.sub.2 Br H CH.sub.2 F OCH.sub.3H CH.sub.2 Br H CH.sub.2 Cl OCH.sub.3H CH.sub.2 Br H CH.sub.2 Br OCH.sub.3H CH.sub.2 Br H F OCH.sub.3H CH.sub.2 Br H I OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 F OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CH.sub.2 CF.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.2 CHF.sub.3 CH.sub.3H CH.sub.2 Br H OCH.sub.2 CF.sub.3 CH.sub.3H CH.sub.2 Br H Cl OC.sub.2 H.sub.5H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 CH.sub.2 SCH.sub.3H CH.sub.2 Br H OCF.sub.2 H CH.sub.3H CH.sub.2 Br H Cl OCF.sub.2 H__________________________________________________________________________
TABLE 35______________________________________ ##STR60##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 36______________________________________ ##STR61##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub. 2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 37______________________________________ ##STR62##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 148-150H CH.sub.2 F H OCH.sub.3 OHC.sub.3 157-158H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3 )H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub. 3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub. 3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 38______________________________________ ##STR63##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OHC.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 39______________________________________ ##STR64##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 40______________________________________ ##STR65##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.3 169-172H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 Cl 174-178H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 Cl 142-148H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub. 3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 CH.sub.3 162-165H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub. 2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 41______________________________________ ##STR66##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 131-133H CH.sub.2 F H OCH.sub.3 OCH.sub.3 145-148H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub. 3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 42______________________________________ ##STR67##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 F H OCH.sub.3 OCH.sub.3 168-171H CH.sub.2 F H OC.sub.2 H.sub.5 Cl 153-156H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 CH.sub.3 94-96H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub. 3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 43______________________________________ ##STR68##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 164-167H CH.sub.2 F H OCH.sub.3 OCH.sub.3 145-149H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub. 2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub.3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 44______________________________________ ##STR69##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 167-172H CH.sub.2 F H OCH.sub.3 OCH.sub.3 150-158H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F H CH.sub.3 CH.sub.3 182-184H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub.3 N(OCH.sub.3)(CH.sub.3 )H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub. 3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CH.sub.2 F H Cl OCH.sub.3 181-183H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.3 OCH.sub.3______________________________________
TABLE 45______________________________________ ##STR70##R.sup.1 R.sup.2 R.sup.3 X Y mp (.degree.C.)______________________________________H CH.sub.2 F H CH.sub.3 OCH.sub.3 88-90H CH.sub.2 F H OCH.sub.3 OCH.sub.3 93-95H CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Cl H CH.sub.3 OCH.sub.3H CH.sub.2 Cl H OCH.sub.3 OCH.sub.3H CH.sub.2 Cl H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Cl H OCH.sub. 3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Cl H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 Br H CH.sub.3 OCH.sub.3H CH.sub.2 Br H OCH.sub.3 OCH.sub.3H CH.sub.2 Br H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 Br H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 Br H OCH.sub.3 N(CH.sub.3).sub.2H CHF.sub.2 H CH.sub.3 OCH.sub.3H CHF.sub.2 H OCH.sub.3 OCH.sub.3H CHF.sub.2 H OC.sub.2 H.sub.5 NHCH.sub.3H CHF.sub.2 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHF.sub.2 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 F CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 OCH.sub.3 OCH.sub.3H CH.sub.2 Cl CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 Br CH.sub.3 CH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 OCH.sub.3 OCH.sub.3H CHF.sub.2 CH.sub.3 CH.sub.3 OCH.sub.3H CH.sub.2 F CH.sub.3 OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 F CH.sub.3 OCH.sub.3 N(CH.sub.3).sub.2H CHFCH.sub.3 H CH.sub.3 OCH.sub.3H CHFCH.sub.3 H OCH.sub.3 OCH.sub.3H CHFCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHFCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHFCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CHClCH.sub.3 H CH.sub.3 OCH.sub.3H CHClCH.sub.3 H OCH.sub.3 OCH.sub.3H CHClCH.sub.3 H OC.sub.2 H.sub.5 NHCH.sub.3H CHClCH.sub.3 H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CHClCH.sub.3 H OCH.sub.3 N(CH.sub.3).sub.2H CH.sub.2 CH.sub.2 F H CH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 OCH.sub.3H CH.sub.2 CH.sub.2 F H OC.sub.2 H.sub.5 NHCH.sub.3H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(OCH.sub.3)(CH.sub.3)H CH.sub.2 CH.sub.2 F H OCH.sub.3 N(CH.sub.3).sub.2H CHFCl H OCH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 OCH.sub.3H CHFCl H CH.sub.3 CH.sub.3H CHFCl H Cl OCH.sub. 3H CHFCl H OCH.sub.3 CH.sub.2 OCH.sub.3H CHFCl H CH.sub.3 OC.sub.2 H.sub.5H CHFCl H CH.sub.2 Cl OCH.sub.3H CHFCl H F OCH.sub.3H CHFCl H OCH.sub.3 CH(OCH.sub.3).sub.2H CHFCl H OCHF.sub.2 OCH.sub.3H CHFCl H C.sub.2 H.sub.5 OCH.sub.35-F CH.sub.2 F H CH.sub.2 OCH.sub.3______________________________________
Test results indicate that the compounds of the present invention are highly active pre-emergent or post-emergent herbicides or plant growth regulants. Many of them have utility for broad-spectrum pre- and/or post-emergency weed control in areas where complete control of all vegetation is desired, such as around fuel storage tanks, ammunition depots, industrial storage areas, parking lots, drive-in theaters, around billboards, highway and railroad structures. Some of the compounds have utility for selective weed control in crops such as wheat and barley. Alternatively, the subject compounds are useful to modify plant growth.
The rates of application for the compounds of the present invention are determined by a number of factors, including their use as plant growth modifiers or as herbicides, the crop species involved, the types of weeds to be controlled, weather and climate, formulations selected, mode of application, amount of foliage present, etc.
In general tens, the subject compounds should be applied at levels of around 0.05 to 10 kg/ha, the lower rates being suggested for use on lighter soils and/or those having a low organic matter content, for plant growth modifications or for situations where only short-term persistence is required.
Formulations
Useful formulations of the compounds of formula(I) can be prepared in conventional ways. They include dusts, granules, pellets, solutions, suspensions, emulsions, wettable powders, emulsifiable concentrates and the like. Many of these may be applied directly.
Sprayable formulations can be extented in suitable media and used at spray volumes of from a few liters to several hundred liters per hectare. High strength compositions are primarily used as intermediates for further formulation. The formulations, broadly, contain about 0.1% to 99% by weight of active ingredient(s) and at least one of (1) about 0.1% to 20% surfactant(s) and (2) about 1% to 99.9% solid or liquid inert diluent(s). More specially, they will contain these ingredients in the following approximate proportions:
______________________________________ Weight Percent* ActiveFormulations Ingredient Diluent(s) Surfactant(s)______________________________________Wettable Powders 20-90 0-74 1-10Oil Suspensions, 3-50 40-95 0-15Emulsions, Solutions(including Emulsifiableconcentrates)Aqueous Suspension 10-50 40-84 1-20Dusts 1-25 70-99 0-5Granules and Pellets 0.1-95 5-99.9 0-15High Strength 90-99 0-10 0-2Compositions______________________________________ *Active ingredient plus at least one of a surfactant or a diluent equals 100 weight percent.
Lower or higher levels of active ingredient can, of course, be present depending on the intended use and the physical properties of the compound. Higher ratios of surfactants to activate ingredient are sometimes desirable, and are achieved by incorporation into the formation or by tank mixing.
Typical solid diluents are described in Watkins, et al., "Handbook of Insecticide Dust Diluents and Carriers", 2nd Ed., Dorland Books, Caldwell, N.J., but other solids, either mined or manufactured, may be used. The more absorptive diluents are preferred for wettable powders and the denser ones for dusts.
Typical liquid diluents and solvents are described in Marsden, "Solvent Guide", 2nd Ed., Interscience, New York, 1950. Solubility under 0.1% is preferred for suspension concentrates; Solution concentrates are preferably stable against phase separation at 0.degree. C. "McCutcheon's Detergents and Emulsifiers Annual", MC Publishing Corp., Ridgewood, N.J., as well as Sisely and Wood, "Encyclopedia of Surface Active Agents", Chemical Publishing Co., Inc., New York, 1964, list surfactants and recommended uses.
All formulations can contain minor amounts of additives to reduce foaming, caking, corrosion, microbiological growth, etc.
The methods of making such compositions are well known. Solutions are prepared by simply mixing the ingredients. Fine solid compositions are made by blending and, usually, grinding as in a hammer or fluid energy mill. Suspensions are prepared by wet milling (see, for example, Littler, U.S. Patent No. 3,060,084). Granules and pellets may be made by spraying the active material upon preformed granular carriers or by agglomeration techniques.
See J. E. Browning, "Agglomeration", Chemical Engineering, Dec. 4, 1967, pp, 147ff. and "Perry's chemical Engineer's Handbook", 5th Ed., McGraw-Hill, New York, 1973, pp. 8-57ff.
For further information regarding the an of formulation, see for example:
H. M. Loux, U.S. Pat. No. 3,235,361, Feb. 15, 1966, Col. 6, line 16 through Col. 7, line 19 and Examples 10 through 41; R. W. Luckenbaugh, U.S. Pat. No. 3,309,192, Mar. 14, 1967, Col. 5, line 43 through Col. 7, line 62 and Examples 8, 12, 15, 39, 41, 52, 53, 58, 132, 138-140, 162-164, 166, 167 and 169-182; H. Gysin and E. Knusli, U.S. Pat. No. 2,891,855, June 23, 1959, Col. 3, line 66 through Col. 5, line 17 and Examples 1-4; G. C. Klingman, "Weed Control as a Science", John Wiley and S. A. Evans, "Weed control Handbook", 5th Ed., Blackwell Scientific Publications, Oxford, 1968, pp. 101-103.
The compounds of the present invention can be used independently and may be used in combination with any other commercial herbicide. A summary of the possible combination herbicides is given below
______________________________________Common Name______________________________________acetochlor acifluorfen AC 252,214AC 263,499 acrolein alachlorametryn amitrole AMSasulam assure atrazineBAS-514 barban benefinbensulfuron methyl bensulide bentazonbenzofluor benzoylprop bifenoxbromacil bromoxynil butachlorbuthidazole butralin butylatecacodylic acid CDAA CDECCGA 82725 CH-83 chlorambenchlorbromuron chlorimuron ethyl chloroxuronchlorpropham chlorsulfuron chlortoluroncinmethylin clethodim clomazonecloproxydim clopyralid CMAcyanzine cycloate cycluroncyperquat cyprazine cyprazolecypromid dalapon dazometDCPA desmediphan desmetryndiallate dicamba dichlorbenildichlorprop dichlofop diethatyldifenzoquat dinitramine dinosebdiphenamid dipropetryn diquatdiuron DNOC DOWCO453MEDPX-M6316 DSMA endothallEPTC ethalfluralin ethoxfumesateExpress fenac fenoxaprop ethylfenuron fenuron TCA flampropfluazifop fluazifop-butyl fluazifop-Pfluchloralin fluometuron fluorochloridonefluorodifen fluoroglycofen fluridonefomesafen fosamine glyphosatehaloxyfop harmoney hexafluratehexazinone HW-52 imazamethabenzimazapyr imazaquin imazethapyrioxynil isopropalin isoproturonisouron isoxaben karbutilatelactofen lenacil linuronMAA MAMA MCPAMCPB mecoprop mefluididemethalpropalin methabenzthiazuron methammethazole methoxuron metolachlormetribuzin metsulfuron methyl MHmolinate monolinuron monuronmonuron TCA MSMA My-93napropamide naproanilide naptalamneburon nitralin nitrofennitrofluorfen norea norfluazonNTN-801 oryzalin oxadiazonoxyfluorfen paraquat pebulatependimethalin perfluidone phenmediphampicloram PPG-1013 pretilachlorprocyazine profluralin prometonprometryn pronamide propachlorpropanil propazine prophamprosulfalin prynachlor pyrazonpyrazolate quizalofop ethyl quizalofopSC-2957 secbumeton sethoxydimsiduron simazine SL-49sulfometuron methyl TCA tebuthiuronterbacil terbuchlor terbuthylazineterbutol terbutryn thiameturon methylthiobencarb triallate triclopyrtridiphane trifluralin trimeturon2,4-D 2,4-DB vernolateX-52 xylachlor______________________________________
EXAMPLE 1
3-Bromo-4-fluoroacetylthiophene
3,4-Dibromothiophene(10 g, 0.041 mol)was dissolved in anhydrous ether and the solution was cooled to -78.degree. C. under nitrogen atmosphere, and herein 17 ml of 2.5N n-butyl lithium was added dropwise.
The solution stirred for 10 min at -78.degree. C. was cooled to -100.degree. C., and herein ethyl fluoroacetate(4.8 ml, 0.05 mol) was added dropwise.
After stirring for 40 min, an excess of saturated solution of ammonium chloride was added and stirred.
The temperature of the reaction mixture was raised to room temperature, and herein an excess of ether was added to separate organic layer.
The organic layer was dried with magnesium sulfate, filtered and concentrated, and then the obtained residue was chromatographed through silica gel using 2:1 solution of methylene chloride/hexane to afford 6 g of the desired product. (white solid, yield:65%)
m.p.: 76.degree..about.77.degree. C.
.sup.1 H NMR (CDCl.sub.3) .delta. 5.40(d, 2H, J.dbd.48 Hz), 7.42(d, 1H, J.dbd.4 Hz), 8.37(d, 1H, J.dbd.4 Hz)
EXAMPLE 2
3-Bromo-4-(2-fluoromethyl- 1,3-dioxalan-2-yl)thiophene
3-Bromo-4-fluoracetylthiolphene(10 g, 0.045 mol) was added in ethylene glycol, and herein trimethyl silyl chloride (22.7 ml, 0.18 mol) was added under stirring.
After stirring for 12 hr, the solution was poured in an excess of saturated solution of sodium bicarbonate and stirred, and then an excess of ether was added and shaked to separate ether layer.
The ether layer was dried with magnesium sulfate, filtered and concentrated to afford 10.4 g of the desired product. (light brown liquid, yield: 87%)
.sup.1 H NMR (CDCl.sub.3) .delta.4.1 (m, 4H), 4.7 (d, 2H, J=48Hz), 7.4 (d, 1H, J.dbd.4 Hz), 7.6(d, 1H, J.dbd.4 Hz)
EXAMPLE 3
3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-4-thiophenesulfonamide
3-Bromo-4-(2-fluoromethyl- 1,3-dioxalan-2-yl)thiophene (19 g, 0.07 mol) was dissolved in anhydrous ether and the solution was cooled to -78.degree. C. under nitrogen atmosphere, and herein n-butyl lithium (31 ml, 0.08 mol) was added dropwise.
After stirring for 10 min at -78.degree. C., an excess of sulfur dioxide gas was added, and then the solution was stirred for 30 min at -78.degree. C. The temperature of the reaction mixture was raised to room temperature, and the solution was filtered.
The obtained white solid was washed with ether, dried and dissolved in solution mixed 40 ml of water with 40 ml of isopropyl alcohol, and then the solution was cooled to 0.degree. C.
After adding portion wise N-chlorosuccinimide (11.4 g, 0.085 mol), the solution was stirred for 2 hr at room temperature, and filtered to obtain a white solid.
The white solid was washed with water and dissolved in ethylacetate solution, and herein an excess of aqueous ammonia was added.
After stirring for 1 hr, the reacting solution was concentrated, and then the obtained solid was washed with a small quantity of ether to afford 13 g of the desired product (light yellow solid, yield: 68%).
m.p.: 126.degree..about.30.degree. C.
.sup.1 H NMR (CDCl.sub.3 +DMSO-d.sub.6) .delta. 4.2(m, 4H), 4.86(d, 2H, J.dbd.48Hz), 6.6(brs, 2H), 7.85(d, 2H, J.dbd.4 Hz), 8.3(d, 2H, J.dbd.4 Hz)
IR(KBr): .nu. 3350, 3250 cm.sup.-1
EXAMPLE 4
3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6-methyltriazin-2- yl)aminocarbonyl]-4-thiophenesulfonamide
3-(2-fluoromethyl- 1,3-dioxalan-2-yl)-4-thiophenesulfonamide (1 g, 0.0037 mol) was dissolved in 20 ml of acetonitrile and phenyl (4-methoxy-6-methyltriazin-2-yl) carbamate (0.86 g, 0.0037 mol) was added at room temperature, and herein 0.8 ml of DBU was added dropwise.
After stirring for 1 hr, the reacting solution was diluted with 100 ml of methylene chloride, and was washed with hydrochloric acid solution.
The organic layer was dried with magnesium sulfate, filtered and concentrated. The obtained solid was washed with a small quantity of ether to afford 1.3 g of the desired product (yield: 84%).
m.p. :212.degree..about.214.degree. C.
.sup.1 H NMR (DMSO-d.sub.6) .delta. 2.51(s, 3H), 3.7-4.1(m, 4H), 4.05(s, 3H), 4.7(d, 2H, J.dbd.48Hz), 7.8(d, 2H, J.dbd.4 Hz), 8.5(d, 2H, J.dbd.4 Hz), 11.1(brs, 1H), 12.5(brs, 1H)
IR(KBr): .nu. (C=O) 1720 cm.sup.-1
EXAMPLE 5
3-Bromo-2-fluoroacetylthiophene
2,3-dibromothiophene (10 g, 0.041 mol) was dissolved in anhydrous ether and cooled to -78.degree. C. under nitrogen atmosphere, and herein 17 ml of 2.5N n-butyl lithium was added dropwise.
After stirring for 10 min at -78.degree. C., the temperature of the reacting solution was cooled to -100.degree. C., and herein ethylfluoro acetate(4.8 ml, 0.5 mol) was added dropwise.
After stirring for 40 min, an excess of saturated solution of ammonium chloride was added and stirred, and after raising the temperature to room temperature, an excess of ether was added to separate organic layer.
The obtained organic layer was dried with magnesium sulfate, filtered and concentrated. The residue was chromatographed through silica gel using 2:1 solution of methylene chloride and hexane to afford 6 g of the desired product (white solid, yield: 65%).
.sup.1 H NMR (CDCl.sub.3) .delta. 5.6(d, 2H, J.dbd.48 Hz), 7.25(d, 1H, J.dbd.5Hz), 7.75(d, 1H, J.dbd.5 Hz)
EXAMPLE 6
3-Bromo-2-(2-fluoromethyl- 1,3-dioxalan-2-yl)thiophene
3-Bromo-2-fluoroacetylthiophene (10 g, 0.045 mol) was dissolved in ethylene glycol, anti trimethylsilyl chloride (22.7 ml, 0.18 mol) was added under stirring.
After stirring for 12 hr, the solution was poured in an excess of saturated solution of sodium bicarbonate and stirred, and herein an excess of ether was added and stirred to separate ether layer.
The obtained ether layer was dried with magnesium sulfate, filtered and concentrated to afford 11 g of the desired product (light brown liquid, yield: 92%).
.sup.1 H NMR (CDCl.sub.3) .delta.4.1(m, 4H), 4.7(d, 2H, J.dbd.48 Hz), 6.95(d, 1H, J.dbd.5 Hz), 7.2(d, 1H, J.dbd.5 Hz)
EXAMPLE 7
2-(2-Fluoromethyl-1,3-dioxalan-2-yl)-3-thiophenesulfonamide
3-Bromo-2-(2-fluoromethyl-1,3-dioxalan-2-yl)thiophene (19 g, 0.07 mol) was dissolved in anhydrous ether anti the solution was cooled to -78.degree. C., and herein n-butyl lithium (31 ml, 0.08 mol) was added dropwise under nitrogen atmosphere.
After stirring for 10 min at -78.degree. C., an excess of sulfur dioxide gas was added, and after stirring 30 min at -78.degree. C., the temperature of the reacting solution to filter the solid material.
The solid was dried and dissolved in solution mixed 40 ml of water with 40 ml of isopropyl alcohol, and after cooling to 0.degree. C., herein N-chlorosuccinimide (11.4 g, 0.085 mol) was added portionwise.
After stirring for 2 hr at room temperature and filtering, the obtained solid was washed with water and dissolved in ethyl acetate solution, and herein an excess of aqueous ammonia was added while stirring for 1 hr at room temperature.
The reacted solution was concentrated, and then the obtained solid was washed with a small quantity of ether to afford 14 g of the desired product (yield: 74%).
m.p.: 120.degree..about.121.degree. C.
.sup.1 H NMR (CDCl.sub.3 +DMSO-d.sub.6) .delta. 4.1(m, 4H), 4.75(d, 2H, J.dbd.48 Hz), 6.7(brs, 2H), 7.4(s, 2H)
IR(KBr): .nu. (NH.sub.2) 3380, 3270 cm.sup.-1
EXAMPLE 8
2-(2-Fluoro-methyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6-methyltriazin-2-yl) aminocarbonyl]-3-thiophenesulfonamide
2-(2-fluoromethyl-1,3-dioxalan-2-yl)-3-thiophenesulfonamide (1 g, 0.0037 mol) was dissolved in 20 ml of acetonitrile and phenyl(4-methoxy-6-methyltriazin-2-yl) carbamate (0.86 g, 0.0037 mol) was added at room temperature, and herein 0.80 ml of DBU was added dropwise.
After stirring for 1hr, the solution was diluted with 100 ml of methylene chloride, and was washed with 5% hydrochloric acid solution.
The separated organic layer was dried with magnesium sulfate, filtered and concentrated, and then the obtained solid was washed with hexane or a small quantity of ether to afford 1.34 g of the desired product (yield: 87%).
m.p.: 186.degree..about.189.degree. C.
.sup.1 H NMR (DMSO-d.sub.6) .delta. 2.55(s, 3H), 4.0(m, 4H), 4.85(d, 2H, J.dbd.48 Hz), 7.6(q, 2H), 10.9(brs, 1H)
IR(KBr): .nu. (C=O) 1700 cm.sup.-1
EXAMPLE 9
3-Fluoroacetylthiophene
3-Bromothiophene(10 g, 0.061 mol) was dissolved in anhydrous ether and the solution was cooled to -78.degree. C. under nitrogen atmosphere, and herein 27 ml of 2.5N n-butyl lithium was added dropwise.
After stirring for 10 min at -78.degree. C., the temperature of the solution was cooled to 100.degree. C., and herein ethylfluoroacetate (7.1 ml, 0.074 mol) was added dropwise.
The solution was stirred for 40 min, and an excess of saturated solution of ammonium chloride was added.
After raising to room temperature, the reaction mixture was extracted with an excess of ether.
The obtained residue was dried with magnesium sulfate, filtered and concentrated, and then chromatographed through silica gel using 2:1 solution of methylenechloride/hexane to afford 6.4 g of the desired product (yield: 72%).
.sup.1 H NMR (CDCl.sub.3) .delta. 5.48(d, 2H, J.dbd.48 Hz), 7.35.about.8.4 (m, 3H)
EXAMPLE 10
3-(2-Fluoromethyl- 1,3-dioxalan-2-yl)thiophene
3-Fluoroacetylthiophene (10 g, 0.069 mol) was dissolved in ethylene glycol, and herein trimethylsilyl chloride (35 ml, 0.275 mol) was added under stirring.
After stirring for 12 hr, the solution is poured in saturated solution of sodium bicarbonate and stirred.
The reaction mixture was extracted with an excess of ether, and then the obtained residue was dried with magnesium sulfate, filtered and concentrated to afford 11 g of the desired product(yield: 85%).
.sup.1 H NMR (CDCl.sub.3) .delta. 4.0(m, 4H), 4.44(d, 2H, J.dbd.48 Hz), 7.0-7.5(m, 3H)
EXAMPLE 11
3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-2-thiophenesulfonamide
3-(2-Fluoromethyl-1,3-dioxalan-2-yl)thiophene(5 g, 0.026 mol) was dissolved in anhydrous ether, and herein 12 ml of n-butyl lithium was added dropwise under nitrogen atmosphere.
After stirring for 1 hr at room temperature, the temperature of the solution was raised in order to reflux for 30 min, and the solution was cooled to -78.degree. C. and sulfur dioxide gas was added.
The reacting solution was stirred for 30 min at -78.degree. C., and the temperature was raised to room temperature. The obtained solid was filtered, dried and dissolved ill solution mixed 20 ml of water with 20 ml of isopropyl alcohol, and after cooling to 0.degree. C., N-chlorosuccinimide (3.9 g, 0.029 mol) was added portionwise.
After stirring for 2 hr at room temperature, the obtained solid was filtered, washed with water and was dissolved in ethyl acetate, and herein an excess of aqueous ammonia was added.
After stirring for 1hr at room temperature, the reaction mixture was concentrated, and then the obtained solid was washed with a small quantity of ether to afford 2 g of the desired product (yield: 92%).
.sup.1 H NMR (CDCl.sub.3 +DMSO-d.sub.6).delta. 4.1(m, 4H), 4.65(d, 2H, J.dbd.48 Hz), 6.7(brs, 2H), 7.1 (d, 1H, J.dbd.5 Hz), 7.4(d, 1H, J.dbd.5 Hz)
EXAMPLE 12
3-(2-Fluoromethyl- 1,3-dioxalan-2-yl)-N-[(4-methoxy-6-methyltriazin-2- yl)aminocarbonyl]-2-thiophenesulfonamide
3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-2-thiophenesulfonamide (1 g, 0.0037 mol) was dissolved in 20 ml of acetonitrile and phenyl(4-methoxy-6-methyltriazin-2-yl)-carbamate (0.86 g, 0.0037 mol) was added at room temperature, and herein 0.8 ml of DBU was added dropwise.
After stirring for 1 hr, the solution was diluted with methylene chloride, and was washed with 5% hydrochloric acid solution. The separated organic layer was dried with magnesium sulfate filtered and concentrated, and then the obtained solid was washed with hexane and ether to afford 1.3 g of the desired product (yield: 84%).
mp.: 167.degree..about.170.degree. C.
.sup.1 H NMR (DMSO-d.sub.6) .delta. 2.55(s, 3H), 4.0(m, 4H), 4.7(d, 2H, J.dbd.48 Hz), 7.3(d, 1H, J.dbd.5 Hz), 7.8(d, 1H, J.dbd.5 Hz), 10.9(brs, 1H)
IR(KBr): .nu. (C=O) 1700 cm.sup.-1
EXAMPLE 13
4-(1,1-Diethoxy-2-fluoroethyl)-N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl-3-thiophenesulfonamide
4-(1,1-Diethoxy-2-fluoroethyl)-3-thiophenesulfonamide (1 g, 0.0034 mol) was dissolved in 20 ml of acetonitrile, and phenyl(4-methoxy-6-methylpyrimidin-2-yl) carbamate(0.87 g, 0.0034 mol) was added at room temperature, and herein 0.8 ml of DBU was added dropwise.
After stirring for 1 hr, the solution was diluted with 100 ml of methylene chloride, and washed with 5% hydrochloric acid solution. The residue was dried with magnesium sulfate, filtered and concentrated, and then the obtained solid was washed with hexane and ether to afford 1.2 g of the desired product.
m.p.: 145.degree..about.148.degree. C.
IR(KBr): .nu. (C=O) 1710cm.sup.-1
EXAMPLE 14
3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl)-4-thiophenesulfonamide
3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-4-thiophenesulfonamide (1 g, 0.0037 mol) was dissolved in 20 ml of acetonitrile and phenyl (4-methoxy-6- methylpyrimidin-2-yl)carbamate (0.86 g, 0.0037 mol) was added at room temperature, and herein 0.8 ml of DBU was added dropwise.
After stirring for 1 hr, the solution was diluted with 100 ml of methylene chloride, and was washed with 5% hydrochloric acid solution. The separated organic layer was dried with magnesium sulfite, filtered and concentrated, and then the obtained solid was washed with hexane and ether to afford 1.3 g of the desired product (yield: 84%).
m.p.: 185.degree..about.189.degree. C.
IR(KBr): .nu. (C=O) 1709 cm.sup.-1
EXAMPLE 15
Wettable Powder
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 80%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidesodium alkylnaphthalenesulfonate 2%sodium ligninsulfonate 2%synthetic amorphous silica 3%kaolinite 13%______________________________________
The ingredients are blended, hammer-milled until all the solids are essentially under 50 microns, reblended, and packaged.
EXAMPLE 16
Wettable Powder
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 50%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidesodium alkylnaphthalenesulfonate 2%low viscosity methyl cellulose 2%diatomaceous earth 46%______________________________________
The ingredients are blended, coarsely hammer-milled and then air-milled to produce particles essentially all below 10 microns in diameter. The product is reblended before packaging.
EXAMPLE 17
Granule
______________________________________wettable powder of Example 16 5%attapulgite granules (U.S.S. 20-40 mesh; 0.84.about.0.42 95%______________________________________
A slurry of wettable powder containing 25% solids is sprayed on the surface of attapulgite granules in a double-cone blender.
The granules are dried and packaged.
EXAMPLE 18
Extruded Pellet
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 25%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamide 10%anhydrous sodium sulfatecrude calcium lignisulfonate 5%sodium alkylnaphthalenesulfonate 1%calcium/magnesium bentonite 59%______________________________________
The ingredients are blended, hammer-milled and then moistened with about 12% water. The mixture is extruded as cylinders about 3 mm diameter which are cut to produce pellets about 3 mm long. They may be used directly after drying, or the dried pellets may be crushed to pass a U.S.S. No. 20 sieve(0.84 mm openings). The granules held on a U.S.S. No. 40 sieve(0.42 mm openings) may be packaged for use and the fines recycled.
EXAMPLE 19
Oil Suspension
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 25%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidepolyoxyethylene sorbitol hexaoleate 5%highly aliphatic hydrocarbon oil 70%______________________________________
The ingredients are ground together in sand mill until the solid particles have been reduced to under about 5 microns. The resulting thick suspension may be applied directly, but preferably after being extended with oils or emulsified in water.
EXAMPLE 20
Wetting Powder
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 20%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidesodium alkylnaphthalenesulfonate 4%sodium ligninsulfonate 4%low viscosity methyl cellulose 3%attapulgite 69%______________________________________
The ingredients are thoroughly blended. After grinding in a hammer-mill to produce particles essentially all below 100 microns, the material is reblended and sifted through a U.S.S. No. 50 sieve(0.3 mm openings) and packaged.
EXAMPLE 21
Low Strength Granule
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 1%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamideN,N-dimethylformamide 9%attapulgite granule (U.S.S. 20-40 sieve) 90%______________________________________
The active ingredient is dissolved in the solvent and the solution is sprayed upon dedusted granules in a double cone blender.
After spraying of the solution has been completed, the blender is allowed to run for a short period and then the granules are packaged.
EXAMPLE 22
Aqueous Suspension
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 40%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidepolyacrylic acid thickener 0.3%dodecylphenol polyethylen glycol ether 0.5%disodium phosphate 1%monosodium phosphate 0.5%polyvinyl alcohol 1%water 56.7%______________________________________
The ingredients are blended and ground together in a sand mill to produce particles essentially all under 5 microns in size.
EXAMPLE 23
Solution
______________________________________ammonium salt of N-[(4,6-dimethoxytriazin-2-yl)amino- 5%carbonyl]-3-(2-fluoromethyl-1,3-dioxalan-2-yl)-4-thiophensulfonamidewater 95%______________________________________
The salt is added directly to the water with stirring to produce the solution, which may then be packaged for use.
EXAMPLE 24
Low Strength Granule
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 0.1%methyltriazin-2-yl)aminocarbonyl]-4-thiophene-sulfonamideattapulgite granules (U.S.S. No. 20-40 mesh) 99.9%______________________________________
The active ingredient is dissolved in a solvent and the solution is sprayed upon dedusted granules in a double-cone blender. After spraying of the solution has been completed, the material is warmed to evaporate the solvent. The material is allowed to cool and packaged.
EXAMPLE 25
Wettable Powder
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 40%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidedioctyl sodium sulfosuccinate 1.5%sodium ligninsulfonate 3%low viscosity methyl cellulose 1.5%attapulgite 54%______________________________________
The ingredient are throughly blended, passed through an air mill, to produce an average particle size under 15 microns, reblended, and sifted through a U.S.S. No. 50 sieve(0.3 mm opening) before packaging. All compounds of the invention may be formulated in the same manner.
EXAMPLE 26
Granule
______________________________________wettable powder of Example 25 15%gypsum 69%potassium sulfate 16%______________________________________
The ingredients are blended in rotating mixer and water sprayed on to accomplish granulation. When most of the material has reached the desired range of 1.0 to 0.42 cm (U.S.S. #18 to 40 sieves), the granules are removed, dried, and screened. Oversized material is crushed additional material in the desired range. These granules contain % active ingredient.
EXAMPLE 27
High Strength Concentrate
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 99%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidesilica aerogel 0.5%synthetic amorphous silica 0.5%______________________________________
The ingredient are blended and ground in a hammer-mill to produce a material essentially all passing a U.S.S. No. 50 screen (0.3 mm opening). The concentrate may be formulated further if necessary.
EXAMPLE 28
Wettable Powder
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 90%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidedioctyl sodium sulfosuccinate 0.1%synthetic fine silica 9.9%______________________________________
The ingredient are blended and ground in a hammer-mill to produce particles essentially all below 100 microns. The material is sifted through a U.S.S. No. 50 screen and the packaged.
EXAMPLE 29
Wettable Powder
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 40%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidesodium ligninsulfonate 20%montmorillonite clay 40%______________________________________
The ingredients are throughly blended, coarsely hammer-milled and then air-milled to produce particles essentially all below 10 microns in size. The material is reblended and the packaged.
EXAMPLE 30
Oil Suspension
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 35%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamideblended of polyalcohol carboxylic ester and oil soluble 6%petroleum sulfonatexylene 59%______________________________________
The ingredients are combined and ground together in a sand mill to produce particle essentially all below 5 microns. The product can be used directly, extended with oil, or emulsified in water.
EXAMPLE 31
Dust
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 10%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamideattapulgite 10%pyrophyllite 80%______________________________________
The active ingredient is blended with attapulgite and then passed through a hammer-mill to produce particles substantially all below 200 microns. The ground concentrate is then blended with powdered pyrophyllite until homogeneous.
EXAMPLE 32
Emulsifiable Concentrate
______________________________________3-(2-Fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6- 10%methyltriazin-2-yl)aminocarbonyl]-4-thiophenesulfonamidechlorobenzene 84%sorbitan monostearate and polyoxyethylene condensates 6%thereof______________________________________
The ingredients are combined and stirred to produce a solution which can be emulsified in water for application.
EXAMPLE 33
Pre-emergence test
To produce a suitable preparation of active compound, 1 pan by weight of active compound is mixed with 5 parts by weight of acetone, 1 pan by weight of alkylaryl polyglycol ether of emulsifier is added and the concentrate is diluted with water to the desired concentration
Seeds of the test plants are shown in normal soil and, after 24 hours, watered with the preparation of the active compound.
It is expedient to keep constant the amount of water per unit area. The concentration of the active compound in the preparation is of no importance, only the amount of active compound applied per unit area being desicive.
After three weeks, the degree of damage to the plants is rated in % damage in comparison to the development of the untreated control.
The figures denote:
0%=no action (like untreated control)
20% =slight effect
70% =herbicidal effect
100% =total destruction.
In this test, the active compounds(I) according to the preparation Examples exhibit a better herbicidal activity against nomo- and dicotyledon weeds.
EXAMPLE 34
Post-emergence test
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with 5 parts by weight of acetone, 1 part by weight of alkylaryl polyglycol ether of emulsifier is added and the concentrate is diluted with water to the desired concentration.
Test plants which have a height of 5.about.15 cm are sprayed with the preparation of the active compound in such a way as to apply the particular amounts of active compound desired per unit area. The concentration of the spray liquor is so chosen that the particular amounts of active compound desired are applied in 2,000 l of water/ha. After three weeks, the degree of damage to the plants is rated in % damage in comparasion to the development of the untreated control.
The figures denote:
0%=no action (like untreated control)
20%=slight effect
70%=herbicidal effect
100% =total destruction.
In this test, the active compounds(I) according to the preparation Examples exhibit a better herbicidal activity against mono- and dicotyledon weeds.
It is understood that the specification and examples are illustrative but not limitative of the present invention and that other embodiments within the spirit and scope of the invention will suggest themselves to those skilled in the art.
The herbicidal proficiency of the active ingredients of the present invention is evident from the test results which are recorded in following Tables.
The following Tables are represented pre- and post-emergence herbicidal evaluation of following "test compounds".
__________________________________________________________________________Structure X Y Z Comp. No.__________________________________________________________________________ ##STR71## ##STR72## ##STR73## ##STR74## ##STR75## ##STR76## ##STR77## ##STR78## ##STR79## ##STR80## ##STR81## ##STR82## ##STR83## ##STR84## ##STR85## ##STR86## ##STR87## ##STR88## ##STR89## ##STR90## ##STR91## ##STR92## ##STR93## ##STR94## ##STR95## ##STR96## ##STR97## ##STR98## ##STR99## ##STR100## ##STR101## ##STR102## ##STR103## ##STR104## ##STR105## ##STR106## ##STR107## ##STR108## ##STR109## ##STR110## ##STR111## ##STR112## ##STR113## ##STR114## ##STR115## ##STR116## ##STR117## ##STR118## ##STR119## ##STR120## ##STR121## ##STR122## ##STR123## ##STR124## ##STR125## ##STR126## ##STR127## ##STR128## ##STR129## ##STR130## ##STR131## ##STR132## ##STR133## ##STR134## ##STR135## ##STR136## ##STR137## ##STR138## ##STR139## ##STR140## ##STR141## ##STR142## ##STR143## ##STR144## ##STR145##__________________________________________________________________________
__________________________________________________________________________PLANT RESPONSE SCREENING (Herbicide) BROJAComp. (SETVI)No. TYPE kg/ha SORBI ECHOR [AGRSM] DIGSA PANDI SOLNI AESIN ABUTH XANSI CAGHE__________________________________________________________________________ 1 PRE .05 90 90 90 70 90 20 40 65 80 100 POST .05 70 90 100 20 0 0 60 25 70 100 2 PRE .05 100 100 100 90 100 20 40 50 90 100 POST .05 90 100 100 40 10 90 100 60 60 3 PRE .05 65 30 40 15 10 20 0 50 25 POST .05 10 20 30 20 0 0 0 0 0 020 PRE .1 100 100 100 60 65 90 40 90 90 100 POST .1 80 100 90 50 30 75 90 100 100 9021 PRE .05 40 60 0 10 0 0 0 10 0 POST .05 50 60 30 0 0 0 0 0 0 022 PRE .05 15 0 0 30 0 20 10 10 60 0 POST .05 20 20 0 20 0 0 0 0 0 025 PRE .05 100 100 100 100 100 80 90 90 90 100 POST .05 100 100 100 100 90 80 90 100 100 10026 PRE .05 100 100 100 100 100 60 100 90 100 100 POST .05 100 100 100 100 90 50 90 100 100 10027 PRE .05 100 100 100 100 100 60 80 90 90 60 POST .05 90 100 80 100 100 50 100 100 100 10028 PRE .05 90 100 80 90 100 90 60 40 80 30 POST .05 30 100 100 70 80 90 70 100 10029 PRE .05 100 100 90 100 90 60 100 100 90 100 POST .05 100 100 100 100 90 60 100 100 100 10030 PRE .05 90 100 80 100 90 50 100 100 95 100 POST .05 100 100 100 100 60 70 100 100 100 10040 PRE .05 60 40 60 50 70 0 0 0 0 20 POST .05 50 30 80 10 40 0 0 40 041 PRE .05 30 80 80 30 20 0 0 60 80 POST .05 30 60 50 0 30 20 0 70 042 PRE .05 40 10 60 0 40 0 0 0 0 35 POST .05 20 0 20 0 60 0 0 100 2043 PRE .05 50 60 20 70 20 0 20 0 20 POST .05 70 60 0 0 30 0 0 30 6044 PRE .05 0 0 0 0 0 20 0 0 30 30 POST .05 60 0 80 0 0 20 0 90 5045 PRE .05 100 100 100 100 100 30 90 90 75 100 POST .05 100 100 100 100 100 60 100 100 100 10046 PRE .05 100 90 100 60 100 20 50 65 100 100 POST .05 90 100 100 50 100 0 80 50 100 3047 PRE .05 20 70 0 0 0 70 0 0 0 0 POST .05 40 35 0 0 0 70 15 0 30 048 PRE .05 100 60 0 40 0 20 20 0 20 POST .05 100 90 80 0 0 0 40 0 65 4049 PRE .05 70 70 40 50 0 20 20 0 0 POST .05 100 70 100 20 0 0 50 0 70 3050 PRE .06 100 100 90 100 100 50 70 20 80 100 POST .05 100 100 90 80 90 50 90 70 10051 PRE .06 100 100 85 90 100 20 70 65 80 100 POST .05 100 100 100 100 100 30 100 90 10052 PRE .06 90 90 60 70 85 25 60 70 70 60 POST .05 90 100 90 60 70 50 90 60 7053 PRE .06 20 30 0 20 20 0 0 0 0 60 POST .05 60 25 20 20 40 20 30 0 054 PRE .06 90 90 40 90 50 20 90 80 90 100 POST .05 100 90 90 90 40 40 100 90 9055 PRE .06 90 80 60 80 90 20 80 80 90 100 POST .05 100 90 80 70 65 40 100 90 9056 PRE .05 90 30 25 65 0 0 0 0 30 POST .05 70 60 90 35 90 0 50 15 100 8557 PRE .05 90 90 70 90 85 20 0 20 70 80 POST .05 70 100 60 25 100 30 65 10 100 2058 PRE .05 25 60 20 35 65 50 0 0 0 0 POST .05 70 70 50 30 65 25 30 0 25 3059 PRE .05 80 25 30 35 50 0 35 20 75 90 POST .05 100 80 30 50 90 25 100 60 70 6560 PRE .05 35 0 0 0 0 0 20 0 60 60 POST .05 80 60 25 20 30 20 65 50 30 6561 PRE .1 65 20 70 0 70 0 0 0 80 POST .1 70 55 80 0 0 20 0 0 0 8062 PRE .1 100 100 100 100 100 50 90 90 90 100 POST .1 100 100 100 70 100 25 70 25 100 10063 PRE .05 50 20 0 0 20 0 0 0 50 90 POST .05 60 50 20 40 40 20 0 0 10 10064 PRE .1 100 80 100 70 70 60 50 90 95 POST .1 90 80 90 40 20 0 80 90 100 10065 PRE .1 100 90 90 65 65 60 80 80 90 100 POST .1 100 90 70 30 10 0 80 50 20 8066 PRE .1 100 80 60 40 30 20 40 70 60 60 POST .1 90 80 60 10 20 20 70 30 85 7068 PRE .1 100 100 100 90 100 20 15 40 100 POST .1 80 90 90 80 95 30 20 30 90 10076 PRE .05 100 100 100 100 100 60 0 0 10 20 POST .05 90 65 95 65 100 40 0 0 0 5077 PRE .05 100 100 100 100 100 20 0 30 90 60 POST .05 80 100 100 100 100 30 100 30 100 10078 PRE .05 100 80 10 60 20 0 0 0 50 POST .05 90 80 50 20 100 0 50 0 55 5079 PRE .05 60 70 10 50 100 0 0 0 0 0 POST .05 70 70 0 20 20 60 0 40 6080 PRE .05 100 100 100 90 100 90 10 50 50 100 POST .05 90 100 100 80 100 50 60 50 100 10081 PRE .05 100 100 100 100 100 90 90 90 90 100 POST .05 100 100 100 100 100 90 100 60 100 10082 PRE .05 100 100 70 100 100 30 60 60 80 100 POST .05 90 100 90 90 100 0 100 60 100 10083 PRE .05 60 100 100 20 80 60 0 0 0 90 POST .05 60 90 0 0 100 40 30 0 40 6084 PRE .05 40 100 70 60 100 20 0 0 50 65 POST .05 80 100 70 30 100 30 60 20 70 9085 PRE .05 10 100 20 30 80 70 0 0 0 60 POST .05 30 70 0 20 0 40 40 0 20 4086 PRE .05 100 100 100 100 100 80 90 90 100 100 POST .05 100 100 100 100 100 100 100 100 100 10087 PRE .05 90 70 70 40 30 0 20 20 100 POST .05 30 45 80 20 20 20 0 60 2088 PRE .05 65 100 60 90 100 0 0 0 20 55 POST .05 50 70 100 20 100 20 0 0 60 5089 PRE .05 30 40 30 30 0 0 0 20 0 POST .05 0 0 20 0 30 0 0 0 50__________________________________________________________________________
PLANT RESPONSE SCREENING (Herbicide) UPLAND WEED SPECIES SETVI POLHY PADDY WEED SPECIES Comp. No. TYPE kg/ha LYPES TRZAW GLXMX ZEAMX DACGL AMAVI (SETVI) RUMJA (COMCO) AESIN CAGHE ORYSA ECHOR CYPDI ANEKE 4 PRE .1 90 100 100 100 90 100 (100) 85 100 100 100 100 100 100 60 POST .1 60 80 100 90 100 100 (100) 100 100 100 100 100 100 100 65 5 PRE .1 100 60 90 100 90 100 (80) 90 100 100 90 100 95 100 50 POST .1 90 35 85 90 100 100 (60) 90 85 100 100 90 90 100 10 6 PRE .1 90 100 90 100 100 100 (100) 90 100 90 100 100 90 100 20 POST .1 90 70 100 90 100 100 (70) 90 80 100 100 90 100 90 10 7 PRE .1 90 50 100 100 100 100 (100) 90 100 100 100 100 100 100 90 POST .1 70 45 100 100 100 100 (100) 100 100 100 100 100 100 100 70 8 PRE .1 90 60 100 100 90 100 (100) 90 100 100 100 100 100 100 80 POST .1 100 25 100 100 100 100 (100) 100 100 100 100 90 100 100 70 9 PRE .1 15 0 0 0 20 20 (25) 10 0 0 60 90 60 0 POST .1 30 10 15 0 60 60 (25) 30 90 0 25 60 10 30 0 10 PRE .1 30 65 15 90 70 90 (90) 70 95 100 90 90 90 100 20 POST .1 40 70 90 60 90 100 (90) 100 100 40 100 65 70 100 0 11 PRE .1 60 40 10 30 70 90 (90) 80 95 15 95 70 60 0 POST .1 10 10 80 30 90 100 (40) 65 80 10 100 60 60 80 0 12 PRE .1 70 10 65 20 65 100 (95) 40 95 65 95 100 80 100 80 POST .1 80 20 100 35 75 100 (60) 70 100 100 100 65 75 100 10 13 PRE .1 60 0 0 0 30 (0) 10 20 50 90 80 100 90 POST .1 20 10 45 0 50 70 (10) 20 90 20 35 25 60 0 14 PRE .1 50 0 0 0 0 0 (0) 0 20 15 0 0 0 0 POST .1 15 0 0 0 0 15 (0) 15 50 0 0 10 10 0 15 PRE .1 50 0 0 0 40 (25) 0 60 20 0 70 0 0 POST .1 20 0 0 0 15 40 (20) 0 0 0 0 10 0 70 0 16 PRE .1 90 15 100 100 70 90 (70) 85 95 80 80 90 80 90 50 POST .1 65 10 90 90 70 90 (60) 90 100 100 100 60 100 60 0 17 PRE .1 70 0 70 70 90 100 (60) 80 95 65 60 40 50 100 10 POST .1 50 10 90 30 20 80 (20) 70 100 90 85 35 30 60 0 18 PRE .1 95 10 100 90 65 90 (90) 95 100 65 60 80 40 0 POST .1 70 10 90 65 35 100 (40) 70 80 100 100 20 65 100 10 19 PRE .1 90 90 100 100 80 90 (100) 70 100 90 95 100 100 100 70 POST .1 70 40 100 90 100 100 (80) 80 100 90 100 100 100 95 0 23 PRE .1 100 10 100 100 80 90 (100) 75 100 100 90 100 100 90 90 POST .1 30 0 100 100 100 100 (70) 100 100 100 100 70 100 65 30 24 PRE .1 100 0 100 100 80 90 (100) 75 100 100 100 100 95 100 70 POST .1 85 0 100 100 70 100 (60) 90 100 100 100 80 90 100 30 31 PRE .1 90 90 70 100 80 90 (100) 80 100 70 90 100 90 100 60 POST .1 70 80 90 100 100 100 (100) 100 100 90 100 70 100 100 40 32 PRE .1 70 25 20 100 70 100 (100) 60 100 25 40 60 60 100 0 POST .1 70 35 70 90 75 80 (70) 60 90 65 30 65 70 100 0 33 PRE .1 30 20 30 90 70 90 (100) 70 90 25 90 100 100 100 60 POST .1 100 60 100 100 100 100 (100) 100 100 100 100 90 100 100 0 34 PRE .1 70 40 10 20 70 100 (100) 50 90 10 60 100 100 100 60 POST .1 100 40 70 90 100 100 (100) 100 90 90 30 100 100 100 30 35 PRE .1 70 10 20 10 20 90 (90) 40 80 0 10 90 70 100 0 POST .1 100 10 60 60 80 70 (60) 40 60 10 20 85 80 100 0 36 PRE .1 30 0 10 0 0 0 (0) 0 60 0 0 60 0 100 15 POST .1 65 0 55 0 15 50 (55) 60 50 30 0 60 0 100 0 37 PRE .1 100 10 100 100 70 90 (100) 70 100 100 100 80 90 70 90 POST .1 100 25 100 100 100 100 (100) 90 100 100 100 90 100 100 30 38 PRE .1 100 10 100 65 60 90 (100) 70 90 90 60 90 25 100 60 POST .1 100 10 100 100 100 100 (100) 100 100 100 100 30 70 100 0 39 PRE .1 100 20 90 90 10 90 (100) 70 90 70 60 90 60 0 0 POST .1 100 20 100 100 70 100 (100) 90 100 100 100 35 80 100 0 67 PRE .1 30 0 0 0 60 70 (65) 0 20 0 40 80 60 70 0 POST .1 40 35 30 0 70 100 (40) 20 10 80 70 65 80 0 69 PRE .1 10 20 20 85 70 90 (65) 10 80 0 80 100 90 100 0 POST .1 40 15 80 65 80 70 (40) 70 90 50 100 60 80 70 0 70 PRE .1 55 0 0 0 20 40 (60) 0 0 0 0 20 20 100 0 POST .1 65 10 0 55 60 (0) 10 50 40 20 0 0 0 71 PRE .1 90 0 70 90 80 90 (80) 20 90 30 80 100 40 100 10 POST .1 70 20 85 100 100 100 (60) 70 70 70 70 70 80 0 72 PRE .1 70 10 60 40 30 90 (65) 25 90 20 55 25 0 0 0 POST .1 70 10 90 20 60 70 (60) 60 65 65 55 0 50 40 73 PRE .1 80 90 30 100 70 90 (100) 65 90 20 90 100 90 100 0 POST .1 100 70 60 100 100 100 (100) 70 90 65 100 90 100 100 15 74 PRE .1 100 10 25 100 70 100 (100) 70 90 20 90 100 65 100 40 POST .1 100 20 90 100 100 100 (100) 90 100 90 100 100 100 100 20 75 PRE .1 90 10 15 70 50 90 (100) 70 90 20 65 90 70 90 0 POST .1 100 10 85 100 65 100 (100) 90 100 65 65 60 90 100 10
PRIMARY SCREENING (Herbicide) BROJA (SETVI) Comp. No. TYPE kg/ha ZEAMX GLXMX GOSHI TRZAW ORYSA SORBI ECHOR [AGRSM] DIGSA PANDI SOLNI AESIN ABUTH XANSI CAGHE 2 PRE .1 80 70 60 50 100 70 80 70 90 100 60 70 90 80 100 .05 70 65 50 30 100 80 90 90 80 90 50 70 80 80 100 .025 50 50 20 10 80 70 60 90 65 80 40 30 65 70 90 .012 10 40 10 0 60 45 50 65 10 65 40 20 50 40 100 .006 0 20 0 0 20 10 0 50 0 30 20 10 10 10 70 POST .1 70 100 50 60 100 90 90 80 30 100 20 100 100 100 100 .05 70 100 30 30 80 80 65 70 20 100 20 100 90 100 100 .025 20 100 20 20 50 70 50 65 10 20 20 100 40 100 100 .012 10 100 20 10 30 70 40 50 10 20 10 80 30 40 .006 0 100 0 0 30 30 10 40 0 0 0 65 20 70 0 20 PRE 1 70 60 100 30 100 100 100 70 80 90 90 40 90 90 100 .05 40 50 60 0 100 90 100 60 70 90 90 30 70 90 100 .025 20 45 0 70 70 70 30 40 30 70 10 60 70 50 .012 0 20 40 0 50 30 50 0 20 0 50 0 0 60 0 .006 0 0 40 0 40 20 30 0 0 0 30 0 0 0 0 POST .1 60 80 50 10 65 100 95 100 50 100 75 100 100 100 100 .05 20 80 30 10 60 100 90 100 40 100 70 100 100 100 100 .025 10 60 20 10 50 100 90 90 40 100 65 80 65 95 100 .012 0 50 10 0 50 90 65 80 10 90 50 60 20 65 100 .006 0 40 0 0 10 70 40 50 0 60 50 40 20 30 30 25 PRE .1 100 80 90 60 100 100 90 90 100 100 90 65 90 90 100 .05 100 70 90 50 100 100 90 70 100 100 90 60 90 90 100 .025 90 50 70 35 100 90 70 70 100 100 70 40 80 70 50 .012 50 30 50 0 70 90 60 70 70 100 60 30 60 50 .006 50 0 40 0 50 60 30 70 40 80 50 0 20 20 20 POST .1 100 100 60 95 100 100 80 100 100 100 85 100 100 100 100 .05 95 100 50 90 100 100 85 100 100 100 80 100 100 100 100 .025 90 70 40 65 100 100 65 100 90 100 70 100 85 90 100 .012 65 65 30 30 95 90 60 100 60 100 50 90 70 65 60 .006 10 50 10 20 95 80 60 95 30 100 50 65 50 40 50 26 PRE 1 100 100 100 100 100 100 100 100 100 100 90 100 100 100 100 .05 100 100 100 100 100 100 100 100 100 100 70 80 100 100 100 .025 100 80 100 90 100 100 100 100 100 100 60 70 100 100 100 .012 100 70 100 80 100 100 100 100 100 100 50 40 90 80 100 .006 90 60 60 60 100 80 90 90 90 90 20 0 80 80 100 POST .1 100 100 65 100 100 100 100 100 100 100 70 100 100 100 100 .05 100 100 65 100 100 100 100 100 100 100 60 100 90 100 100 .025 100 100 60 100 100 100 100 100 90 100 50 100 90 100 100 .012 100 80 50 65 100 100 100 70 90 100 50 90 70 100 100 .006 100 50 50 50 100 100 95 70 60 100 30 80 40 65 60 27 PRE .1 100 100 100 90 100 100 90 (100) 100 100 70 60 100 100 100 .025 100 70 40 20 100 50 50 (65) 100 100 30 40 65 40 40 .00625 60 30 0 0 90 30 30 (30) 80 100 0 0 0 0 0 .00156 0 0 0 0 30 0 0 (0) 40 90 0 0 0 0 0 POST .1 100 100 100 70 100 100 100 (100) 100 100 50 100 100 100 100 .025 70 100 50 50 100 100 65 (100) 100 100 50 100 100 100 100 .00625 40 100 0 0 90 80 40 (20) 20 100 0 70 50 40 0 .00156 0 40 0 0 40 30 0 (0) 0 60 0 40 0 0 0 28 PRE 1 100 80 90 40 100 90 100 (30) 100 100 100 60 80 100 100 .025 50 30 20 0 100 30 60 (0) 40 100 60 0 40 40 100 .00625 0 0 0 0 80 0 0 (0) 0 100 0 0 0 0 0 .00156 0 0 0 0 40 0 0 (0) 0 40 0 0 0 0 0 POST .1 80 100 50 40 90 100 100 (65) 40 100 100 100 100 100 65 .025 70 50 0 0 90 100 100 (20) 0 50 90 65 100 80 30 .00625 20 30 0 0 70 30 30 (0) 0 10 0 20 70 60 0 .00156 0 0 0 0 20 0 0 (0) 0 0 0 0 65 0 0 29 PRE .1 100 100 100 50 100 100 100 100 100 100 90 100 100 100 100 .05 100 100 100 10 100 100 100 100 100 90 80 90 100 100 100 .025 100 100 90 0 100 100 100 100 100 80 60 90 100 100 100 .012 100 100 90 0 100 100 100 80 100 70 50 90 90 100 100 .006 100 90 80 0 90 100 80 65 90 50 0 50 70 90 100 POST .1 100 100 100 90 100 100 100 100 100 100 70 100 100 100 100 .05 100 100 60 50 100 100 100 100 100 100 65 100 100 100 100 .025 100 100 50 60 100 100 100 100 90 100 60 100 100 100 100 .012 100 100 30 25 100 100 100 100 90 90 50 100 90 100 100 .006 100 100 0 0 100 100 80 65 20 65 30 100 70 100 65 30 PRE 1 100 90 90 0 100 100 90 70 100 90 70 80 80 90 70 .05 100 90 90 0 100 90 80 60 100 90 70 70 80 90 60 .025 100 90 90 0 100 90 70 60 100 90 70 70 70 90 50 .012 90 90 90 0 100 80 50 30 90 90 60 50 50 90 40 .006 40 70 90 0 60 60 30 20 40 50 60 30 30 70 40 POST .1 100 100 50 40 100 100 100 100 100 100 60 100 100 100 100 .05 100 100 40 40 100 100 80 100 100 100 60 100 100 100 100 .025 100 100 10 10 100 100 60 100 100 100 50 100 100 10 100 .012 90 100 0 10 50 100 60 100 90 100 50 100 90 100 100 .006 80 90 0 0 30 90 50 70 70 95 40 100 65 85 60 40 PRE .1 10 0 0 30 100 100 60 (40) 100 100 50 0 0 40 40 .05 0 0 0 0 90 80 20 (0) 60 60 40 0 0 20 10 .025 0 0 0 0 60 10 0 (0) 40 40 0 0 0 0 0 .0125 0 0 0 0 30 0 0 (0) 30 30 0 0 0 0 0 .006 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 POST .1 0 0 0 50 50 60 30 (40) 30 40 0 0 0 50 40 .05 0 0 0 30 40 50 0 (20) 10 20 0 0 0 0 0 .025 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 .0125 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 .006 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 41 PRE 1 100 20 40 50 100 90 60 (50) 50 70 70 20 0 80 100 .05 50 0 0 20 70 40 40 (40) 20 40 40 0 0 70 60 .025 20 0 0 0 50 20 20 (0) 0 40 30 0 0 0 0 .0125 0 0 0 0 20 0 0 (0) 0 20 0 0 0 0 0 .006 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 POST .1 70 40 20 20 60 40 40 (20) 0 30 0 20 0 80 100 .05 40 10 0 0 40 30 20 (0) 0 20 0 0 0 50 100 .0125 20 0 0 0 0 20 0 (0) 0 0 0 0 0 0 70 .012 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 40 .006 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 40 45 PRE .1 0 0 0 0 40 40 30 (0) 20 40 50 0 0 20 40 .05 0 0 0 0 40 0 0 (0) 0 0 0 0 0 0 20 .025 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 .0125 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 .006 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 POST .1 0 20 0 20 30 10 0 (0) 0 20 0 20 20 60 20 .05 0 0 0 0 0 0 0 (0) 0 0 0 0 0 40 0 .025 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 .0125 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 .006 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 50 PRE 1 100 50 40 60 100 100 100 100 100 100 90 30 60 90 100 .05 100 40 20 40 100 100 60 100 100 100 80 10 20 90 90 .025 50 20 0 30 90 100 30 90 80 60 80 0 0 50 60 .0125 30 0 0 0 50 70 0 65 80 40 60 0 0 20 30 .006 20 0 0 0 20 20 0 30 50 20 10 0 0 0 20 POST .1 100 90 40 100 100 100 100 100 100 100 70 60 40 80 100 .05 100 65 30 80 90 100 100 100 90 100 60 50 30 80 100 .025 90 50 20 40 90 90 55 90 40 100 50 20 20 70 60 .012 20 20 0 20 70 90 30 60 0 100 40 0 0 40 60 .006 10 0 0 0 40 65 0 50 0 60 30 0 0 30 40 51 PRE .1 100 100 70 100 100 100 100 100 100 100 70 60 80 100 100 .05 100 90 60 90 100 90 100 80 100 90 40 40 20 90 100 .025 50 70 30 60 90 90 100 80 100 90 30 20 20 90 70 .012 30 50 0 40 90 90 40 50 90 70 30 0 0 70 50 .006 0 30 0 30 50 80 20 40 70 50 0 0 0 70 20 POST .1 100 100 60 100 100 100 100 100 100 100 60 70 100 100 100 .05 80 100 40 100 100 100 100 100 100 100 50 80 70 100 100 .025 60 100 40 65 80 100 100 90 65 100 50 60 60 100 60 .012 40 90 30 50 70 70 100 90 40 100 40 65 20 60 50 .006 0 90 0 0 60 70 70 50 0 100 40 40 0 50 30 54 PRE 1 100 100 90 30 100 100 100 70 100 100 65 70 80 90 100 .05 100 90 70 20 100 90 100 50 100 100 60 65 65 90 100 .025 100 70 60 0 70 90 70 30 100 90 50 50 50 90 90 .012 40 40 0 0 50 70 50 0 70 20 50 0 0 80 50 .006 0 0 0 0 30 60 20 0 40 0 40 0 0 20 POST .1 100 100 70 50 100 100 100 100 100 100 60 90 80 100 100 .05 100 100 60 20 100 100 90 90 85 100 40 90 70 100 90 .025 100 75 50 0 90 90 80 70 60 80 30 90 50 70 60 .012 90 65 40 0 65 90 70 50 60 80 30 50 40 30 60 .006 60 40 20 0 30 90 50 30 10 50 30 50 20 30 50 55 PRE .1 100 100 100 40 100 100 100 65 100 100 70 70 70 100 100 .05 100 90 80 30 100 90 100 30 100 90 60 65 70 100 80 .025 60 80 0 100 80 70 30 90 50 60 50 60 90 90 .012 50 50 0 0 60 50 30 0 30 30 20 20 0 90 60 .006 30 40 0 0 20 20 0 0 0 10 0 0 0 90 0 POST .1 100 100 50 10 100 90 100 80 100 100 50 100 100 100 100 .05 90 90 40 0 100 90 100 70 30 100 40 90 70 100 100 .025 90 80 20 0 90 70 50 30 0 80 30 65 60 100 100 .012 40 70 20 0 50 70 50 0 0 80 30 40 20 60 20 .006 30 65 20 0 30 60 40 0 0 80 20 20 0 50 0 62 PRE 1 50 65 90 50 100 100 80 80 80 100 60 40 80 80 100 .05 40 50 60 40 100 90 70 70 60 100 40 30 70 80 100 .025 0 30 50 0 80 80 40 50 40 100 20 30 30 70 100 .012 0 20 20 0 60 50 20 40 30 100 20 10 20 65 80 .006 0 0 0 0 50 0 0 30 10 80 0 0 0 30 60 POST .1 40 80 70 60 95 70 90 70 90 100 40 100 30 75 100 .05 30 75 40 40 80 65 60 70 40 100 30 60 20 80 .025 10 70 30 20 60 60 40 40 40 100 20 40 10 0 65 .012 10 60 10 10 50 45 20 30 20 100 10 20 0 60 .006 0 40 0 10 40 20 0 10 0 100 0 0 0 20 64 PRE .1 10 40 50 0 65 60 40 60 50 80 40 65 40 90 90 .05 0 20 0 0 60 60 30 30 40 20 30 20 20 65 90 .025 0 0 0 0 30 30 10 0 0 0 20 0 0 0 80 .012 0 0 0 0 0 0 0 0 0 0 20 0 0 0 60 .006 0 0 0 0 0 0 0 0 0 0 10 0 0 0 40 POST .1 10 80 10 0 50 70 60 70 30 100 40 100 30 80 90 .05 0 80 10 0 40 70 40 65 30 100 40 90 20 100 100 .025 0 70 0 0 30 60 10 40 10 100 30 40 0 100 .012 0 70 0 0 20 40 0 30 0 100 20 10 0 30 40 .006 0 65 0 0 10 30 0 10 0 80 10 0 0 20 68 PRE 1 70 50 50 30 100 80 70 65 80 100 50 40 50 80 100 .05 50 40 50 0 70 50 60 50 65 100 50 0 30 50 100 POST .1 80 70 40 40 70 70 90 75 90 100 50 30 30 100 .05 50 50 20 10 60 60 65 65 80 100 30 0 10 60 100 76 PRE 1 100 0 30 30 100 100 100 (90) 100 100 60 0 0 20 100 .05 10 0 10 0 90 100 70 (90) 100 100 40 0 0 0 40 .025 50 0 0 0 40 80 50 (50) 100 100 30 0 0 0 10 .0125 0 0 0 0 0 50 30 (20) 40 90 0 0 0 0 0 .006 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 POST .1 100 40 0 30 70 100 100 (100) 100 100 60 20 0 20 100 .05 100 30 0 0 40 60 100 (80) 100 80 60 0 0 0 50 .025 80 0 0 0 0 40 40 (40) 80 20 60 0 0 0 40 .0125 0 0 0 0 0 0 0 (0) 20 0 30 0 0 0 10 .006 0 0 0 0 0 0 0 (0) 0 0 0 0 0 0 0 77 PRE .1 100 70 70 30 100 100 100 (100) 100 100 40 40 65 80 100 .05 100 50 60 10 100 80 100 (100) 100 100 30 10 0 40 70 .025 20 20 30 0 80 80 100 (65) 100 100 0 0 0 0 60 POST .1 100 100 40 0 60 100 100 (100) 100 100 60 100 60 100 100 .05 100 100 30 0 50 100 100 (100) 100 100 50 80 40 100 100 .025 40 100 20 0 50 40 100 (100) 50 100 30 65 0 0 100 80 PRE .1 100 40 50 70 100 100 100 (100) 100 100 50 0 40 100 100 .05 60 30 30 40 100 100 70 (50) 100 100 30 0 0 50 100 .025 40 0 0 40 90 90 70 (40) 60 100 0 0 0 30 100 POST .1 100 40 0 70 100 100 100 (70) 100 100 0 65 20 40 100 .05 100 20 0 40 90 100 100 (60) 60 100 0 40 0 10 100 .025 40 0 0 0 60 40 60 (50) 50 60 0 20 0 0 60 81 PRE .1 100 100 100 100 100 100 100 (100) 100 100 60 90 100 80 100 .05 100 100 100 100 100 100 100 (100) 100 100 50 80 100 80 100 .025 100 90 90 70 100 100 100 (100) 100 100 50 50 90 70 100 .0125 100 70 65 40 100 100 100 (100) 100 100 0 40 50 50 100 .006 90 60 50 0 100 90 100 (70) 100 100 0 0 30 30 100 POST .1 100 100 70 100 100 100 100 (100) 100 100 0 100 60 100 100 .05 100 90 70 60 100 100 100 (100) 100 100 0 100 40 60 100 .025 100 70 50 50 100 50 100 (70) 100 100 0 90 30 30 100 .0125 100 50 20 40 90 40 100 (60) 100 80 0 70 0 0 100 .006 100 40 0 0 80 30 70 (60) 60 80 0 50 0 0 60 82 PRE 1 100 100 100 50 100 100 100 (100) 100 100 70 90 90 100 .05 100 100 90 10 100 100 100 (100) 100 100 40 50 80 100 .025 70 80 70 0 100 70 100 (90) 100 100 20 20 80 100 .0125 60 70 50 0 100 50 60 (60) 100 100 0 0 60 80 .006 30 50 40 0 50 30 40 (60) 100 100 0 0 40 40 POST .1 60 100 70 20 70 100 100 (100) 100 100 0 100 80 80 100 .05 50 100 50 0 60 100 100 (80) 100 100 0 100 70 30 100 .025 40 100 40 0 50 50 100 (50) 50 100 0 80 0 20 30 .0125 30 70 20 0 40 40 100 (50) 50 90 0 70 0 0 0 .006 0 50 0 0 40 40 70 (40) 40 80 0 60 0 0 0 86 PRE 1 0 0 0 0 40 100 70 (0) 80 65 50 0 40 30 0 .05 0 0 0 0 0 50 30 (0) 0 40 30 0 0 0 0 87 PRE 1 40 30 20 0 50 60 65 (40) 50 70 40 0 0 80 40 .05 10 0 0 0 20 30 40 (20) 20 60 0 0 0 60 20 POST .1 50 20 10 20 50 30 70 (40) 10 40 50 40 0 70 50 .05 20 10 0 0 20 20 0 (0) 0 0 0 0 0 40 0
__________________________________________________________________________PRIMARY SCREENING (PADDY SUBMERGED)- Herbicide ORYSA ORYSAComp. No. DAT kg/ha (3 Leaf) (seed) ECHOR SCPJU MOOVA CYPSE SAGPY__________________________________________________________________________ 1 2 .05 60 60 50 80 70 100 80 2 2 .05 60 70 60 100 90 90 90 3 3 .05 40 70 40 40 70 70 7020 2 .1 90 80 80 100 90 100 80 .1 100 90 100 100 100 100 100 .05 90 90 80 100 100 100 100 .025 80 90 80 100 100 100 90 .012 70 60 70 90 100 100 80 .006 50 40 50 80 90 80 6021 2 .05 30 50 50 70 70 90 8022 2 .05 60 60 50 80 70 70 7025 2 .05 50 70 60 100 90 80 90 3 .1 80 100 100 100 100 100 100 .05 80 100 90 100 100 100 10 .025 80 100 70 100 90 100 100 .012 80 100 60 100 90 90 90 .006 80 100 50 90 90 70 9026 2 .05 60 90 100 100 90 70 70 3 .1 80 100 100 100 100 100 100 .05 80 100 100 100 100 100 90 .025 80 100 90 100 100 100 90 .012 80 100 80 100 100 90 90 .006 80 100 70 100 100 90 9027 2 .05 90 100 100 100 100 100 100 .1 100 100 100 100 100 100 .025 100 100 100 100 100 90 .006 100 80 70 100 100 90 .0015 50 50 0 40 100 50 .0004 30 20 0 0 0 028 2 .05 90 100 100 100 100 100 100 .1 100 100 100 100 100 90 .025 100 90 100 100 100 70 .006 70 80 50 60 80 40 .0015 60 40 0 30 40 2029 2 .05 60 80 70 100 90 40 90 3 .1 80 100 100 100 100 70 100 .05 80 100 80 100 100 60 100 .025 80 100 50 100 70 30 100 .012 50 30 0 50 50 0 80 .006 30 0 0 30 30 0 6030 2 .05 60 80 70 90 90 40 90 3 .1 80 100 100 100 100 90 100 .05 80 100 100 100 100 80 100 .025 70 100 90 100 100 50 100 .012 60 100 10 100 100 40 90 .006 50 100 0 90 90 20 7040 2 .05 50 40 0 20 0 30 042 2 .05 30 0 10 60 30 90 5043 2 .05 0 0 0 0 30 0 044 2 .05 40 30 0 0 60 40 045 2 .05 60 60 40 50 60 80 6046 2 .05 60 60 60 90 90 90 70 3 .1 90 100 100 100 100 100 90 .025 90 90 60 100 90 100 80 .006 40 70 50 60 50 100 6047 2 .05 60 50 0 10 50 70 048 2 .05 60 50 20 50 60 40 049 2 .05 50 60 100 70 60 0 3 .1 80 90 80 80 70 80 70 .025 30 40 50 30 20 0 0 .006 0 0 10 0 0 0 050 1 .05 80 70 40 90 90 70 6051 1 .05 70 80 100 100 100 100 90 2 .1 100 100 100 100 100 100 100 .025 100 100 90 100 100 100 90 .006 80 70 60 100 80 90 90 .0015 40 20 60 70 30 40 4052 1 .05 70 80 70 100 100 90 70 3 .1 90 100 100 100 100 100 90 .025 80 90 80 100 80 100 80 .006 60 30 10 30 20 90 5053 1 .05 60 70 50 90 100 100 40 2 .1 80 90 90 100 90 100 60 .025 50 30 40 60 70 80 20 .006 10 0 20 10 0 0 054 1 .05 80 90 60 100 100 50 90 2 .1 90 100 80 100 100 70 90 .025 80 70 50 100 100 50 80 .006 50 10 0 0 90 0 2055 1 .05 70 70 50 100 100 60 6056 2 .05 0 0 0 0 0 40 057 2 .05 60 60 80 100 80 100 9058 2 .05 0 30 50 70 50 70 40 3 .5 100 100 100 100 100 100 .25 60 90 100 100 100 100 .125 40 65 100 90 100 85 .0625 30 30 100 90 90 80 .0312 0 0 90 90 90 7559 2 .05 20 50 30 70 70 0 4060 2 .05 0 0 40 20 40 0 061 2 .1 60 50 20 30 0 40 4062 2 .1 70 60 70 90 80 100 80 .1 70 70 80 100 100 100 100 .05 70 60 50 100 20 70 100 .025 70 50 30 80 0 60 80 .012 40 30 0 60 0 30 60 .006 0 20 0 20 0 20 2063 1 .05 70 70 20 70 40 40 8064 2 .1 50 60 60 90 90 90 80 .1 70 80 70 100 100 100 100 .05 70 80 50 100 100 100 100 .025 70 70 10 90 60 60 90 .012 60 30 0 80 40 20 30 .006 30 20 0 80 0 0 3065 2 .1 60 90 40 40 60 30 5066 2 .1 50 60 30 40 50 30 5068 2 .1 60 60 80 90 60 70 9076 2 .05 60 50 20 40 40 50 077 2 .05 60 70 70 90 90 90 60 3 .1 90 100 100 100 100 100 90 .025 90 90 50 100 100 100 90 .006 60 80 20 80 60 100 9078 2 .05 50 50 40 50 70 0 079 2 .05 40 50 10 30 40 30 080 2 .05 70 20 0 10 30 0 4081 2 .05 60 50 100 100 100 60 100 .1 90 100 100 100 90 .025 90 70 90 100 90 .006 20 10 0 0 2082 2 .05 80 90 90 100 100 100 100 .1 100 100 100 100 100 .025 100 90 100 100 80 .006 90 50 30 0 4083 2 .05 60 50 60 30 40 70 5084 2 .05 30 20 0 0 0 0 2085 2 .05 10 10 20 40 70 0 086 2 .05 0 0 20 20 30 0 087 2 .05 0 0 0 0 0 0 088 2 .05 0 0 0 0 0 0 089 2 .05 0 0 0 0 0 0 0__________________________________________________________________________
__________________________________________________________________________PRIMARY SCREENING (PADDY SUBMERGED)- HerbicideComp. No. DAT kg/ha ORYSA ECHOR SCPJU BR.s CYPSE SAGPY__________________________________________________________________________ 4 2 .125 80 90 90 90 100 90 .05 90 100 100 100 100 100 .01 80 90 100 80 100 100 .005 70 90 100 50 100 100 5 2 .125 70 80 100 100 100 90 6 2 .125 70 80 90 80 70 80 7 2 .125 80 90 100 90 50 70 8 2 .125 70 80 100 90 70 100 9 2 .125 40 40 40 50 20 4010 2 .1 60 60 100 60 60 5011 2 .1 40 40 0 70 60 6012 2 .1 50 60 20 80 100 7013 2 .125 40 50 30 30 70 5014 2 .1 10 0 30 60 60 4015 2 .1 30 0 20 60 40 3016 2 .125 60 50 80 80 30 7017 2 .125 0 30 70 50 40 6018 2 .1 10 20 0 70 50 7019 2 .1 90 90 90 90 100 10023 2 .1 60 90 100 100 100 10024 2 .1 50 100 100 100 100 10031 2 .125 60 80 90 90 80 6032 2 .125 10 60 70 70 40 5033 2 .125 70 100 100 100 100 9034 2 .125 90 100 100 100 100 8035 2 .125 60 60 60 50 60 3036 2 .125 40 30 50 60 60 3037 2 .125 60 100 100 100 30 8038 2 .125 50 60 90 80 60 7039 2 .125 50 60 100 90 60 10067 2 .1 40 50 40 40 70 6068 2 .1 30 60 60 30 60 6069 2 .1 70 60 50 50 60 7071 2 .1 60 30 0 10 30 4072 2 .1 50 20 50 40 40 4073 2 .125 70 100 80 40 90 5074 2 .125 70 90 60 50 0 8075 2 .125 60 60 60 70 0 50__________________________________________________________________________
Claims
  • 1. A compound of formula (I): ##STR146## wherein Q is Q-1, Q-2 or Q-3 are: ##STR147## wherein R.sup.1 is H, C.sub.1 -C.sub.3 alkyl, C.sub.1 -C.sub.3 haloalkyl, halogen, CN, NO.sub.2, C.sub.1 -C.sub.3 alkoxy, C.sub.1 -C.sub.3 haloalkoxy, SO.sub.2 NR.sup.I R.sup.II, C.sub.1 -C.sub.3 alkylthio, C.sub.1 -C.sub.3 alkysulfinyl, C.sub.1 -C.sub.3 alkylsulfonyl, SCHF.sub.2, NH.sub.2, NHCH.sub.3, N(Me).sub.2, C.sub.1 -C.sub.2 alkyl substituted with C.sub.1 -C.sub.2 alkoxy, C.sub.1 -C.sub.2 haloalkoxy, SH, SCH.sub.3, CN or OH; or CO.sub.2 R.sup.III ; wherein R.sup.I is H, C.sub.1 -C.sub.4 alkyl, C.sub.2 -C.sub.3 cyanoalkyl, methoxy or ethoxy; R.sup.II is H, C.sub.1 -C.sub.4 alkyl, C.sub.3 -C.sub.4 alkenyl, or when taken together connecting R.sup.I and R.sup.II, --(CH.sub.2).sub.3 --, (CH.sub.2).sub.4 --, --(CH.sub.2).sub.5 -- or CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 --, may be formed; R.sub.III is C.sub.1 -C.sub.4 alkyl, C.sub.3 -C.sub.4 alkenyl, C.sub.3 -C.sub.4 alkynyl, C.sub.1 -C.sub.4 alkyl substituted with 1.about.3 halogens or cyano groups, C.sub.5 -C.sub.6 cycloalkyl, C.sub.4 -C.sub.7 cycloalkylalkyl or C.sub.2 -C.sub.4 alkoxyalkyl;
  • R is ##STR148## wherein, a is O or S; R.sup.2 is C.sub.1 -C.sub.6 alkyl substituted with 1.about.3 halogens; R.sup.4 and R.sup.5 are respectively C.sub.1 -C.sub.4 alkyl; and R.sub.6 and R.sub.7 are respectively H, C.sub.1 -C.sub.3 alkyl or C.sub.1 -C.sub.3 haloalkyl;
  • E is CH.sub.2 or single bond;
  • R.sup.3 is H or CH.sub.3 ;
  • W is O or S;
  • A is ##STR149## wherein, X is H, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkylthio, C.sub.1 -C.sub.4 alkylthio, halogen, C.sub.2 -C.sub.5 alkoxyalkyl, C.sub.2 -C.sub.5 alkoxylalkoxy, amino, C.sub.1 -C.sub.3 alkylamino, di(C.sub.1 -C.sub.3 alkyl ) amino or C.sub.3 -C.sub.5 cycloalkyl;
  • Y is H, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, C.sub.1 -C.sub.4 haloalkylthio, C.sub.1 -C.sub.4 alkylthio, C.sub.2 -C.sub.5 alkoxyalkyl, C.sub.1 -C.sub.5 alkoxyalkoxy, amino, C.sub.1 -C.sub.3 alkylamino, di(C.sub.1 -C.sub.3 alkyl ) amino, C.sub.3 -C.sub.4 alkenyloxy, C.sub.3 -C.sub.4 alkynyloxy, C.sub.2 -C.sub.5 alkylthioalkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.2 -C.sub.4 alkynyl, azido, cyano, C.sub.2 -C.sub.5 alkylsulfinylalkyl, C.sub.2 -C.sub.5 alkylsulfonylalkyl CH.sub.2 OH, C.sub.3 -C.sub.5 cycloalkyl, C.sub.3 -C.sub.5, cycloalkoxy, C.sub.2 -C.sub.5 alkylthioalkoxy, ##STR150## m is 2 or 3; L.sup.1 and L.sup.2 are independently O or S;
  • R.sup.4 and R.sup.5 are independently C.sub.1 -C.sub.2 alkyl;
  • R.sup.6 is H or CH.sub.3 ;
  • Z is N;
  • X.sup.3 is CH.sub.3 or OCH.sub.3 ;
  • or agriculturally suitable salts thereof.
  • 2. A compound as defined in claim 1, wherein W is O; E is single bond; and R.sup.3 is H.
  • 3. A compound as defined in claim 1, wherein R.sup.1 is selected from the group consisting of H, halogen, C.sub.1 -C.sub.2 alkyl, C.sub.1 -C.sub.2 alkoxy, C.sub.1 -C.sub.2 haloalkyl, C.sub.1 -C.sub.2 alkylthio, haloalkoxy and CH.sub.2 CN; X is selected from the group consisting of C.sub.1 -C.sub.2 alkyl, C.sub.1 -C.sub.2 alkoxy, Cl, F, Br, I, OCHF.sub.2, CH.sub.2 F, CF.sub.3, OCH.sub.2 CH.sub.2 F, OCH.sub.2 CHF.sub.2, OCH.sub.2 CF.sub.3, CH.sub.2 Cl and CH.sub.2 Br; and Y is H, C.sub.1 -C.sub.2 alkyl, C.sub.1 -C.sub.2 alkoxy, CH.sub.2 OCH.sub.3, CH.sub.2 OCH.sub.2 CH.sub.3, NHCH.sub.3, N(OCH.sub.3)CH.sub.3, N(CH.sub.3).sub.2, CF.sub.3, SCH.sub.3, OCH.sub.2 CH.dbd.CH.sub.2, OCH.sub.2 .tbd.CH, OCH.sub.2 CH.sub.2 OCH.sub.3, CH.sub.2 SCH.sub.3, ##STR151## OCHF.sub.2, OCF.sub.2 Br, SCHF.sub.2, cyclopropyl, C.tbd.CH or C.tbd.C--CH.sub.3, and then R.sup.4 and R.sup.5 and C.sub.1 -C.sub.2 alkyl, R.sup.8 is H or CH.sub.3, L.sup.1 and L.sup.2 are O or S, and m is 2 or 3.
  • 4. A compound as defined in claim 1, wherein A is A.sub.1 ; X is CH.sub.3, C.sub.2 H.sub.5, OCH.sub.3, OCH.sub.2CH.sub.3, Cl or OCHF.sub.2 ; and Y is CH.sub.3, OCH.sub.3, OC.sub.2 H.sub.5, C.sub.2 H.sub.5, CH.sub.2 OCH.sub.3, NHCH.sub.3, CH(OCH.sub.3).sub.2 or cyclopropyl.
  • 5. A compound as defined in claim 1, wherein R.sup.2 is CH.sub.2 F, CH.sub.2 CH.sub.2 F, CHFCH.sub.3, CH.sub.2 Cl, CH.sub.2 Br, CHCl.sub.2, CHFCl, CH.sub.2 CHCl, CHClCH.sub.3, CHF.sub.2, CHClCH.sub.2 Cl, CHFCH.sub.2 Cl, CHFCH.sub.2 F or CH.sub.2 CHF.sub.2.
  • 6. A compound as defined in claim 1, wherein said general formula(I) is 3-(2-fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6-methyltriazin-2-yl)aminocarbonyl]4-thiophenesulfonamide.
  • 7. A compound as defined in claim 1, wherein said general formula(I) is N-[(4,6-dimethoxytriazin-2-yl)aminocarbonyl]-3-(2-fluoromethyl-1,3-dioxalan-2-yl)-4-thiophenesulfonamide.
  • 8. A compound as defined in claim 1, wherein said general formula (I) is 2-(2-fluoromethyl-1,3-dioxalan-2-yl)-N-[(4-methoxy-6-methyltriazin-2-yl)aminocarbonyl]-3-thiophenesulfonamide.
  • 9. A compound as defined in claim 1, wherein said general formula(I) is N-[(4,6-dimethoxytriazin-2-yl)aminocarbonyl]-2-(2-fluoromethyl-1,3-oxalan-2-yl)-3-thiophenesulfonamide.
  • 10. An herbicidal composition comprising one or more compounds of formula (I) of claim 1 in combination with an inert carrier.
  • 11. A method of controlling weeds comprising applying an effective amount of one or more compounds of formula (I) of claim 1 to a weedy area.
Priority Claims (1)
Number Date Country Kind
91-4063 Mar 1991 KRX
PCT Information
Filing Document Filing Date Country Kind 102e Date 371c Date
PCT/KR92/00009 3/14/1992 12/9/1993 12/9/1993
Publishing Document Publishing Date Country Kind
WO92/16525 10/1/1992
Non-Patent Literature Citations (1)
Entry
Kimura et al, Chemical Abstracts, vol. 104, entry 186457 (1986).