USRE27347E

USRE27347E - Vii. chs

Info

Publication number: USRE27347E
Authority: US
Priority date: 1962-08-02
Filing date: 1969-01-21
Publication date: 1972-04-25
Also published as: BR6350797D0; GB987381A; US3336186A; CH449320A; BE635767A; DE1169194B; NL296165A

Abstract

THIS INVENTION RELATES TO THE INSECTICIDAL AND ACARICIDAL EFFECTS OF COMPOUNDS OF THE FORMULA

R4,R5,(R1-NH-COO-),(R2-N(-R3)-CH=N-)BENZENE

WHEREIN R1 IS LOWER ALKYL OR CYCLOHEXYL R2 AND R3 ARE LOWER ALKYL AND R2 AND R3 TOGETHER WITH THE NITROGEN ATOM IS A HETEROCYCLIC RING SELECTED FROM THE GROUP CONSISTING OF FIVE-MEMBER AND SIX-MEMBER HETEROCYCLIC RINGS; AND R4 AND R5 ARE HYDROGEN, LOWER ALKYL, LOWER ALKENYL OR HALOGEN.

Description

United States Patent Oflice Re. 27,347 Reissued Apr. 25, 1972 METHOD OF COMBATING INSECTS AND ACARIDS WITH CERTAIN PHENYL-CARBAMATE DE- RIVATIVES Horst Peissker, Wolfenhuttel, Albert Jiiger, Berlin-Hermsdorf, Walter Steinhausen, Grossburgwedel, and Gerhard Boroschewski, Berlin-Charlottenburg, Germany, by Sehering AG, Berlin, Germany, assignee No Drawing. Original No. 3,336,186, dated Aug. 15, 1967, Ser. No. 290,586, June 26, 1963. Application for reissue Jan. 21, 1969, Ser. No. 827,434

Claims priority, application Germany, Aug. 2, 1962, Sch 31,834 Int. Cl. A01n 9/22 US. Cl. 424-248 26 Claims Matter enclosed in heavy brackets II] appears in the original patent but forms no part of this reissue specification; matter printed in italics indicates the additions made by reissue.

ABSTRACT OF THE DISCLOSURE This invention relates to pesticides, and more particularly to novel carbamate derivatives which have insecticidal and acaricidal effects.

We have found that compounds of the formula wherein R is lower alkyl or cyclohexyl, R and R are lower alkyl or jointly constitute a divalent radical which forms a fiveand six-member heterocyclic ring with the associated N atom containing in addition to said N atom only C atoms or an O atom and C atoms; R, and R are hydrogen, lower alkyl, lower alkenyl or halogen; are effective agents for combating insect pests and spider mites which are plant parasites. The compounds of the invention and their salts with any suitable acid are capable of surprisingly long action when incorporated in pesticidal compositions.

Such compositions are highly etfective against a broad spectrum of pest insects. They may be employed to advantage where it is necessary to combat acarids and insects simultaneously, for example, in orchards, vineyards, truck gardens, and hop fields, in cotton crops and in other crops in which insects may occur simultaneously with spider mites.

The compounds of the invention may be employed against pests in their pure form, in mixtures with each other and with other pest control agents such as acaricidal, insecticidal or fungicidal compounds. They may constitute the active agents of compositions of all types commonly employed for the protection of crops against pests. Such compositions, in addition to the active agents, may contain liquid or solid inert carriers. Suitable liquid carriers include water, mineral oil and other solvents. Solid inert carriers include bentonite, fullers earth, gypsum, limestone, diatomaceous earth, pyrophyllite, silicon dioxide in its various natural forms, talcum and powders of vegetable origin such as cotton seed flour or nut shell flour. The composition may contain conventional auxiliary agents such as emulsifiers, wetting agents, binders, stabilizers, propellent gases, perfumes, pest attracting and pest repelling agents. The composition may be applied by dusting or otherwise spreading when they are solid. When liquid, they may be applied by fogging, spraying or atomizing. The liquid compositions may be suspensions, emulsions, or solutions of the active agents, and may also be applied in the form of aerosols or fumigants.

The percentage of active agents in the compositions may be varied within wide limits. The concentration selected will depend on the type of composition, the method of application, the desired pesticidal elfect, and particularly on the type of pest to be controlled. The content of active agents in the compositions of the invention will usually vary between 0.1 and percent by weight. The compositions are generally applied in concentrations between 0.025 and 10 percent. Under exceptional conditions, it may be necessary to apply them in concentrations as high as 20 percent.

Representative carbamate derivatives of the invention which have excellent insecticidal and acaricidal effects are listed in Table 1 together with identifying physical properties. Where the formula of an acid radical appears in conjunction with the name of its salt in Table 1, it will be understood that the compound is characterized by the melting point of its salt.

TABLE 1 1 (CH2);NCH=N o M.P.102-103C.

o ii-NH-c Hi 11 o M.P. s2-a5 c.

(oHmN-oH=N--0-ii-NH-om 1n on, 0 MP. 0.

ll (CHz):N-CH=NOCNHOH:

1v on, o

(Hydrochloride) TABLE 1-00ntinued XX CH: M1. 100-103 C.

.CH.,.N c..=N@0-t NH@ xxr (CH;)gN-CH=N c1 0 M.P. 142.5444" 0.

C1 O-&NH-CH;

XXII O M.P. 105-108 C.

(GHs)1N-OH=NO -NHCaH| xxnr o 011 nu -=1 .5450.

(C a):N-CH=NO- -NH-(CHzh-OH;

xxrv on. 0 n.1 140-141" 0.

(CH|)iN-CH=N- O-HI-NH-C H;

XXV M.P.125 C.

The following examples are illustrative of the biological effects of the compounds of the invention.

Example 1 Bush beans (Phaseolus vulgaris L.) infested with spider mites of the species Tetranychus urticae KOCH in al stages of development were treated in the late two-leaf stage with aqueous suspensions and emulsions or solutions of salts of active agents of the invention in various concentrations. The compositions were applied by spraying from a spray gun having a glass nozzle at a pressure of 0.5 kgJcm." gauge while the potted plants were moving on a rotating table. The amount of liquid applied was 50 milliliters, and ensured wetting of the three plants contained in each pot until excess liquid dripped from them. The mortality of the postembryonal stages of the parasites after seven days was recorded in percent of the parasites present. The results are listed in Table 2.

TABLE 2 Concentra- Mortality tion oi of adults Mortality active and of emerging agent, nymphs larvae, Compound number percent percent percent I 0.1 100 100 0. 100 100 I (Lactate) 0.1 100 100 0.06 100 100 I (Hydrochloride) 0.1 100 100 1 (Dih dr n 11 0 i i3?) i% 0 en es ate".-. y g p p 0.05 100 100 0. 1 100 1006 0.1 100 100 0.05 100 100 0.1 100 100 0. 05 100 100 0.1 100 100 0. 06 100 100 TABLE 2.G0ntlnued Concentra- Mortality tion of of adults Mortality active and of emerging agent, nymphs, larvae, Compound number percent percent percent VL. 0.1 100 100 0.05 100 100 Vrr 0.1 100 100 0.05 100 100 VII (Lactate) 0.1 100 100 0. 05 100 100 VIII 0.1 100 100 0.00 so 00 0.1 so a0 0.1 100 100 0.1 so 00 0.1 100 100 0.1 100 100 0.1 100 100 0.1 100 100 0.05 100 100 XVIII 0.1 100 100 0.05 100 100 XIX 0.1 100 00 0.05 100 XXIII 0.1 00 50 xxv 0.1 0.05 100 100 Example 2 55 The residual effect of representative compounds of the invention was determined by treating bush bean plants in the late two-leaf stage as described in Example 1. Other potted plants were infected for the first time 24 hours after treatment of the first group of plants and again at 00 intervals of two to four days by placing spider mite infected leaves of the first group on leaves of the healthy plants. The mortality of the spider mites on the second group of plants seven days after infection by the applied leaves are tabulated in Table 3.

7 Example 3 The roots (a) or the stalks (b) of cut branches of bush bean plants free from parasites were placed in aqueous emulsions or salt solutions of several representative compounds of the invention when the plants were in the twoleaf stage. They were then infected by contact with leaves carrying spider mites, and a count of surviving parasites 48 hours after infestation gave the results listed in Table 4.

TABLE 4 Mortality of posternbryonal Concentration stages after active seven days, Compound number agent, percent percent (a) I (Hydrochloride) 0.04 0. 02 III 0.01 0.1 0. 033 0.01 VII 0.1 0. 06 D. 025 (b) I (Hydrochloride) 0.1 100 0. 033 1 U0 0.01 95 III 0. 1 100 D. 033 100 0. 01 50 VII. 0.1 100 0. 100 0. 025 100 Example 4 Bush bean seeds were placed in recesses of clay dishes, and the recesses were treated with solid mixtures of two parts of representative active agents of the invention and 98 parts kaolin. No unfavorable effects of the compounds of the invention could be observed in comparison tests between the treated seeds and untreated controls with respect to germination and growth. When the plants had reached the two-leaf stage, they were infected with moving spider mites in all postembryonal stages by application of leaves from infected plants. The mortality of the mites was determined after seven days, and the results obtained are listed in Table 5.

TABLE 5 Grams active agent per Mortality of 100 g. seed postembryunal material stages, percent Compound number Example 5 Glass plates were treated with aqueous emulsions or solutions of salts of the compounds of the invention in various concentrations. The liquid compositions were applied in amounts of 4 milligrams per square centimeter by means of a spray gun having a glass nozzle at a pressure of 0.5 kilogram per square centimeter. The liquid coatings were permitted to dry, and the plates were placed as top covers on glass cylinders each containing 20 house flies (Musca domestica. L.), four days old. The flies were fed during the experiments which an untreated solution of sugar.

The effects of the compounds on the flies after twenty hours exposure were determined by counting the dead flies, the flies recognizably damaged and lying on their backs, and the flies surviving without visible symptoms. The percentage effect of the various compounds of the invention was calculated according to Abbotts method. The results obtained are listed in Table 6.

TABLE 6 Concentration of active agent, percent Percentage after 20 Compound number hours XXIV Example 6 The bottoms of Petri dishes were treated with various concentrations of compounds of the invention in aqueous emulsions or as solutions of their salts at a dosage of 4 milligrams per square centimeter. After drying of the liquid coatings, the dishes were stocked each with approximately 100 granary weevils (Sitophilus granarius L.).

After 24 hours exposure of the insects in a dark room in the open dishes, a differential count was made of weevils surviving without symptoms, dead weevils, and damaged Weevils lying on their backs. The percentage effect was calculated according to Abbotts method, and the results are listed in Table 7.

Percentage effect after 24 hours exposure IUD I Concentration of active Compound number agent, percent VIII XVIII (p-Toluosultonate) X XV Example 7 The stomach and contact effects of the insecticidal compounds of the invention were determined by treating shoots of tradescantia on a revolving turntable with aqueous emulsions, suspensions, or salt solutions of the compounds of the invention in amounts of 4 mg./cm. After drying of the sprayed coatings, the treated plants were each stocked in a wire gauze cage with 15 fourth-stage larvae of stick insects (Carausius morosus Brunner) which had recently shed their skins. The effects of the compounds on the animals were evaluated daily by separate counts of dead animals, severely damaged animals which reacted to contact only by uncoordinated movement of the extremities, slightly damaged animals and normal animals. The results of the test are listed in Table 8.

Coneentra- Percentage tion of active eflect alter Compound number agent, percent three days I 0. 1 100 0. 06 100 I (Hydrochloride) 0. 1 100 0. 05 100 I (Lactate) 0. 1 1 dr 0. I Dlhy 0 hos hate 0.1

gen p p 0. 05 100 0. l 100 0. 06 100 0. 025 100 0. 2 100 0. I 97 0. 1 100 0. 05 100 0. 025 100 0. 1 100 0 .06 100 0. 025 60 0. 1 100 0. 06 100 0. 1 100 0. 05 100 0. 1 100 0. 05 100 0. 1 97 0. 05 30 0. l 100 0. 05 97 0. 1 67 0. 1 100 0. 05 100 0. 026 93 XIX 0. 2 100 0. 1 83 XX- 0. 2 73 0. l 56 XXI 0. 2 70 0. 1 27 XXII 0. 2 88 0. 1 60 XXIII 0. 2 100 0. 1 50 XXIV 0. l 100 0. 05 100 0. 02 56 Example 8 Tradescantia shoots were treated in the manner of Example 7 with aqueous emulsions or suspensions of active agents of the invention in uniform concentrations of 0.1 percent in amounts of 4 mg. cm). The plants were stocked at various times after treatment with 15 experimental animals as described in Example 7. The results obtained were evaluated in the same manner as in Example 7, and are listed in Table 9.

TABLE 9 Percentage eflect on plants stocked after- 10 the efficiency was evaluated as described in Example 8. The percentage effects achieved after three days with representative compounds of the invention are listed in Table 10.

TABLE 10 Concentration Percentage active effect after Compound number agent, percent three days I 0. 2 100 0. l 100 0. 04 80 II 0. 2 100 0. l 90 III 0. 2 100 0. l 100 0. 05 100 0. 0| 100 IV 0. 2 100 0. l 100 0. 04 V 0. 2 100 0. 1 100 0. 05 100 0. 02 100 VII 0. 2 100 0. 1 100 0. 05 100 0. 025 100 0. 01 100 VIII 0. 2 100 0r 1 100 0. 05 100 0. 02 60 XI 0. 2 100 0. l 87 XIII 0.2 100 0. l 85 0. 2 I00 0. l 100 XVI 0. 2 100 0. 1 100 0. 05 100 XVII 0. 2 100 0. 1 100 The pesticidal compounds of the invention which had not been known before were prepared in the following manner:

0.05 mole of a formamidinophenol was dissolved in a solvent such as tetrahydrofuran or in a mixture of 0.5 to 5 parts by weight of tetrahydrofuran and one part of dimethylformamide. The solution was mixed by shaking at room temperature with 0.05 mole of an alkyl or cycloalkylisocyanate. The reaction mixture was left to stand 48 hours at room temperature. Crystallization started during this time. The mixture was then heated to a boil Compound number 8 days 6 days 9 days 14 days 21 days 28 days 28 days I III-.. 100 100 100 100 100 100 100 VII. 100 100 98 96 82 79 72 1 The treated plants were showered prior to the test with an amount of 15 liters per square meter within 45 minutes, and were stocked with test animals after sir drying.

Example 9 Young oak shoots having approximately equal amounts of leaves were treated with 4 milligrams of a sprayed aqueous coating of emulsions or suspension of compounds of the invention per square centimeter. The spraying was performed on a turntable in the manner described above. After drying, the shoots were stocked with 10 caterpillars (L IV stage, immediately after shedding of skins) of the gypsy moth (Porthetria dispar L). The animals were retained in wire gauze cages. The eifects of the pesticidal compounds were determined daily, and ionate, or the chloracetate.

The following examples will illustrate the method of preparing the carbamate derivatives of the invention.

Example 32.8.4 grams (0.2 mole) of 3-(N,N-dimethylaminomethylenimino)-phenol were dissolved in a mixture of 120 milliliters tetrahydrofuran and 120 milliliters dimethylformamide, and the solution was left to stand 48 hours at room temperature. It was subsequently heated to a boil for 30 minutes, and the solvent mixture was evaporated in a vacuum. The oily residue was dissolved in chloroform, and filtered over aluminum oxide (neutral). After evaporation of the chloroform in a vacuum, the residue was crystallized in the presence of a small amount of ether, and was recrystallized from ethyl acetate. The yield was 26.6 grams (60%), the melting point 102- 103 C.

The elementary analysis corresponded to that of the compound C11H15N302.

Calculated: C, 59.70; H, 6.83; N, 18.99. Found: C, 59.88; H, 7.14; N, 19.06, which is N-methyl-3-(NN'-dimcthylaminomethylenimino -phenylcarbamate.

The phenols which were employed as starting materials for preparing the pesticidal agents of the invention were prepared as follows:

0.1 mole of a suitably substituted aminophenol was dissolved either in milliliters dimethylformamide or in another suitable solvent, such as acetonitrile, in the presence of 0.1 mole dimethylformamide; 9.15 milliliters phosphorus oxychloride were added drop by drop with agitation while the temperature was held at or below 60/ C., by means of external cooling. After completion of the phosphorus oxychloride addition, the mixture was agitated for additional minutes at 60 C. When ethanol was added and the mixture was cooled to room temperature, crystallization of the desired hydrochloride usually occurred very rapidly. If necessary, crystallization was made more complete by addition of ethyl ether.

If the hydrochloride obtained was not satisfactorily pure, it was recrystallized from ethanol or from a mixture of ethanol and ether. It was then dissolved or suspended in water, and an equivalent amount of a strong base such as triethylamine, NaOH or Na CO was added whereupon the free phenol crystallized. If necessary, the aminophenol was recrystallized from a mixture of tetrahydrofuran and a light petroleum fraction.

The pesticidal compounds of the invention may also be prepared by reacting a corresponding phenol with a mono-substituted carbamic acid chloride in a manner well known in itself.

While the invention has been described with particular reference to specific embodiments, it is to be understood that it is not limited thereto, but is to be construed broadly, and restricted solely by the scope of the appended claims.

We claim:

1. A method of combating insects and acarids which comprises contacting said insects and acarids with a pesticidal amount of a compound of the formula wherein R is selected from the group consisting of lower alkyl and cyclohexyl', R and R are lower alkyls and R and R together with the nitrogen atom is a helerocyclic ring selected from the group consisting of five member and six-member heterocyclic rings containing in addition to said nitrogen atom only carbon atoms, and of sixmember heterocyclic rings containing in addition to said nitrogen atom an oxygen atom and carbon atoms; and R and R are members of the group consisting of hydrogen, lower alkyl, lower alkenyl and halogen.

2. A method as set forth in claim 1 in which the compound is N-methyl 3 (N'N-dimethyIaminomethyleneimino)-phenyl carbamate.

3. A method as set forth in claim 1 in which the compound is N methyl-4-(N',N-dimethylaminomethyleneimino)-phenyl carbamate.

4. A method as set forth in claim I in which the compound is N-methyl 4-(N',N'-dimethylaminomethylenimino)-3-methylphenyl carbamate.

5. A method as set forth in claim 1 in which the compound is N-methyl 4 (N',N' diethylaminomethylenimino)-3-methyl-phenyl carbamate.

6. A method as set forth in claim I in which the compound is N-ethyl 4 (N', '-dimethylamin0methylenim ino)-3-methyl-phenyl carbamate.

7. A method as set forth in claim I in which the compound is N-methyl 4 (N',N'-dimethylaminomethylenimino)-2-allyl-phenyl carbamate.

8. A method as set forth in claim I in which the compound is N-methyl 4 (N',N'-dimethylaminomethylenimino)-3,5-dimethyl-phenyl carbamate.

9. A method as set forth in claim 1 in which the compound is N-methyl 4 (N',N-diethylaminomethylenimino)-3,5-dimethyl-phenyl carbamate.

10. A method as set forth in claim I in which the compound is N-methyl 4 (N',N'-dimethylaminomethylenimino)-3-methyl-6-isopropylphenyl carbamate.

1]. A method as set forth in claim 1 in which the com pound is N methyl 4 (N',N'-diethylaminomethylenimino)-3-methyl-6-isopropylphenyl carbamate.

12. A method as set forth in claim I in which the compound is N-methyl 4 (N,N-diethylaminomethylenimino)-2-methyl-5-isopropyl phenyl carbamate.

13. A method as set forth in claim 1 in which the compound is N-methyl 4 (N',N'-dimethylaminomethylenimino)-3-methyl-5-isopropyl-phenyl carbamate.

14. A method as set forth in claim 1 in which the compound is N-methyl 4 (N,N'-diethylaminomethylenimino)-3-methyI-S-isopropyl-phenyl carbamate.

15. A method as set forth in claim I in which the compound is N-methyl 4 (N,N'-tetmmethylenaminomethylenimino)-3,5-dimethyl phenyl carbamate.

16. A method as set forth in claim 1 in which the compound is N-methyl-4-(N,N'-pentamethylenaminomethylenimino)3,5-dimethylphenyl carbamate.

17. A method as set forth in claim I in which the compound is N methyl-4-morpholinomethylenimino-3,5-dimethyl-phenyl carbamate.

18. A method as set forth in claim I in which the compound is N (methyl-3-(N,N-dimethylaminomlethylenimino)-4-methyl-phenyl carbamate.

19. A method as set forth in claim I in which the compound is N butyl 3 (N,N' dimethylaminomethylenimino) -phenyl carbamate.

20. A method as set forth in claim I in which the compound is N methyl-2-chlor-4-(N',N'-dimethylaminomethylenimino)-phenyl carbamate.

2]. A method as set forth in claim 1 in which the compound is N cyclohexyl-4-(N',N'-dimethylaminomethylenimino)-3-methyl-phenyl carbamate.

22. A method as set forth in claim 1 in which the compound t's N methyl-2,4-dichlor-3-(N',N'-dimethylaminomethylenimino)-phenyl carbamate.

23. A method as set forth in claim I in which the compound is N-ethyl-4-(N,N-dimethylaminomethylenimino)- phenyl carbamate.

24. A method as set forth in claim I in which the cornpound is N propyl 4 (N',N-dimetltylaminomethylenimino)-phenyl carbamate.

25. A method as set forth in claim: I in which the com- UNTTED STATES PATENTS pound is N-elhyl-4(N,Ndimethylaminomethylenimino)- 2 9 4 2 5 19 1 Kacding 2 0 479 3,5-dlmethylphe'lyl 3,012,068 12/1961 Shulgin 260-482 26. A method as set forth an claim I m which the COM- 3 071 506 X 19 3 Gruenhagen 42 27 pound is N-methyl 2 (N ',N'-dimethylaminomethylen- 5 3,072,643 1/1963 Bonvicino 260 240 iminawhenyl carbamare- 3,072,649 1/1963 Semb et al 26o 240 3,080,279 3/1963 Constantin et a1 424-266 References Cited The following references, cited by the Examiner, are m of record in the patented file of this patent or the original patent. 424-267, 274, 300

JEROME D. GOLDBERG, Primary Examiner US. Cl. X.R.