(en)A thioacryloyl compound of the formula ##STR1## wherein Z is selected from the group consisting of OR, R and NR 1 R 2 ;
R is selected from the group consisting of hydrogen; (C 1 -C 18 )alkyl; (C 1 -C 8 )alkenyl; (C 1 -C 8 )haloalkynyl; 2-(5-chlorothienyl)methyl; phenyl optionally substituted with one or more substituents selected from the group consisting of halo-, (C 1 -C 3 )alkoxy-, nitro-, and (C 1 -C 3 )alkyl; phenacyl optionally substituted with one or more substituents selected from the group consisting of ring halo-, (C 1 -C 3 )alkoxy-, nitro-, and (C 1 -C 3 )alkyl; arylalkyl optionally substituted with one or more substituents selected from the group consisting of ring halo-, (C 1 -C 3 )alkoxy-, nitro-, and (C 1 -C 3 )alkyl;
R 1 and R 2 are independently selected from (C 1 -C 8 )alkyl and phenyl, or R 1 and R 2 may be joined together with the nitrogen atom to which they are attached to form a ring containing 4 to 5 carbon atoms with or without an oxygen heteroatom;
X is selected from the group consisting of hydrogen, halogen, phenyl, CO 2 CH 3 , and (C 1 -C 3 )alkyl; and
Y is selected from the group consisting of CN, CH(COCH 3 ) 2 , CH 2 COCH 3 , CH 2 CN, CH 2 CO 2 C 2 H 5 -propargyl, SCH═CHCO 2 CH 3 , C(═NH)NH 2 hydrochloride, and 2-(5-chlorothienyl)methyl;
provided that when Z is NR 1 R 2 , Y is CN; and
provided that when Z is R, X is hydrogen, and Y is CN, R is not phenyl.

1.ApplicationNumber: US-16649893-A
1.PublishNumber: US-5464832-A
2.Date Publish: 19951107
3.Inventor: OSEI-GYIMAH; PETER
SHERBA; SAMUEL E.
LANGE; BARRY C.
MEHTA; RAI J.
JOSEPH; RHODA W.

4.Inventor Harmonized: OSEI-GYIMAH PETER(US)
SHERBA SAMUEL E(US)
LANGE BARRY C(US)
MEHTA RAI J(US)
JOSEPH RHODA W(US)

5.Country: US
6.Claims:
(en)A thioacryloyl compound of the formula ##STR1## wherein Z is selected from the group consisting of OR, R and NR 1 R 2 ;
R is selected from the group consisting of hydrogen; (C 1 -C 18 )alkyl; (C 1 -C 8 )alkenyl; (C 1 -C 8 )haloalkynyl; 2-(5-chlorothienyl)methyl; phenyl optionally substituted with one or more substituents selected from the group consisting of halo-, (C 1 -C 3 )alkoxy-, nitro-, and (C 1 -C 3 )alkyl; phenacyl optionally substituted with one or more substituents selected from the group consisting of ring halo-, (C 1 -C 3 )alkoxy-, nitro-, and (C 1 -C 3 )alkyl; arylalkyl optionally substituted with one or more substituents selected from the group consisting of ring halo-, (C 1 -C 3 )alkoxy-, nitro-, and (C 1 -C 3 )alkyl;
R 1 and R 2 are independently selected from (C 1 -C 8 )alkyl and phenyl, or R 1 and R 2 may be joined together with the nitrogen atom to which they are attached to form a ring containing 4 to 5 carbon atoms with or without an oxygen heteroatom;
X is selected from the group consisting of hydrogen, halogen, phenyl, CO 2 CH 3 , and (C 1 -C 3 )alkyl; and
Y is selected from the group consisting of CN, CH(COCH 3 ) 2 , CH 2 COCH 3 , CH 2 CN, CH 2 CO 2 C 2 H 5 -propargyl, SCH═CHCO 2 CH 3 , C(═NH)NH 2 hydrochloride, and 2-(5-chlorothienyl)methyl;
provided that when Z is NR 1 R 2 , Y is CN; and
provided that when Z is R, X is hydrogen, and Y is CN, R is not phenyl.

7.Description:
(en)This application is a divisional of U.S. Ser. No. 08/107,422 filed Aug. 16, 1993, now U.S. Pat. No. 5,302,592, which in turn is a continuation of U.S. Ser. No. 07/880,471 filed May 6, 1992, now abandoned, which in turn is a continuation of U.S. Ser. No. 07/747,157 filed Aug. 15, 1991, now abandoned, which in turn is a continuation-in-part of U.S. Ser. No. 07/568,809 filed Aug. 17, 1990, now abandoned.


BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to the field of antimicrobial agents.
2. Description of the Prior Art
Certain classes of thioacrylates and thioacrylamides have been prepared as antimicrobials but no compound within those classes has achieved commercial success.
U.S. Pat. Nos. 4,115,103; 4,123,254; 4,169,850; and 4,198,304 to Kao Soap Co., disclose alkyl substituted beta-thioacrylamides and beta-thioacrylic adds (and salts thereof) and the corresponding alkyl sulfone and alkyl sulfoxide derivatives as germicidal herbicides, antibiotics, and as antimicrobial agents in non-food or medicinal compositions.
German patent DE 2536252 to Bayer AG discloses beta-thiocyanovinyl aryl ketones as antimicrobial agents. Thioalkyl-and thiocyano-alkyl-alpha-substituted acrylic acids (and esters thereof) are disclosed as plant growth regulators in Japanese Kokai J 50-036622 to Mitsubishi Chemical.
Methyl 3-thiocyanoacrylate and dimethyl alpha-thiocyanofumarate are known compounds (Tetrahedron, 41(4), 801 (1985)), but have not been disclosed as antimicrobial compounds. Cis-3-thiocyanoacrylic acid is a known compound (Justus Liebigs Annalen der Chemie, 8, 1249 (1977)) but has not been disclosed as an antimicrobial compound. Beta-carbomethoxyvinylisothiurium chloride is a known compound (J. Amer. Chem. Soc., 101(21), 6306 (1979)) but has not been disclosed as an antimicrobial compound. Methyl 3-thio(propan-2-on-1-yl)acrylate is a known compound (Berichte, 97(8), 2109-17 (1964)) but has not been disclosed as an antimicrobial compound. N,N-Dimethyl-3-thiocyanoacrylamide is a known compound (J. Org. Chem., 30, 2660-2665 (1965)) but has not been disclosed as an antimicrobial compound.
SUMMARY OF THE INVENTION
Many of the antimicrobials of the prior art have toxicity and/or environmental problems.
It is an object of the present invention to provide novel antimicrobial compounds which have improved toxicity profiles and are not harmful to the environment.
These objects, and others which will become apparent from the following disclosure, are achieved by the present invention which comprises the use as a microbicide of an effective amount of a thioacryloyl compound of the formula ##STR2## wherein Z is selected from the group consisting of OR, R and NR 1 R 2 ;
R is selected from the group consisting of hydrogen;
(C 1 -C 18 )alkyl; (C 1 -C 8 )alkenyl; (C 1 -C 8 )haloalkynyl; 2-(5-chlorothienyl)methyl; phenyl optionally substituted with one or more substituents selected from the group consisting of halo-, (C 1 -C 3 )alkoxy-, nitro-, and (C 1 -C 3 )alkyl; phenacyl optionally substituted with one or more substituents selected from the group consisting of ring halo-, (C 1 -C 3 )alkoxy-, nitro-, and (C 1 -C 3 )alkyl; arylalkyl optionally substituted with one or more substituents selected from the group consisting of ring halo-, (C 1 -C 3 )alkoxy-, nitro-, and (C 1 -C 3 )alkyl;
R 1 and R 2 are independently selected from (C 1 -C 8 )alkyl and phenyl, or R 1 and R 2 may be joined together with the nitrogen atom to which they are attached to form a ring containing 4 to 5 carbon atoms with or without an oxygen heteroatom;
X is selected from the group consisting of hydrogen, halogen, phenyl, CO 2 CH 3 , and (C 1 -C 3 )alkyl; and
Y is selected from the group consisting of CN, CH(COCH 3 ) 2 , CH 2 COCH 3 , CH 2 CN, CH 2 CO 2 C 2 H 5 , propargyl, SCH═CHCO 2 CH 3 , C(═NH)NH 2 hydrochloride, and 2-(5-chlorothienyl)methyl;
provided that when Z is NR 1 R 2 , Y is CN; and
provided that when Z is R, X is hydrogen, and Y is CN, R is not phenyl.
A preferred aspect of the invention comprises the use of methyl cis-3-thiocyanoacrylate, iodopropargyl cis-3-thiocyanoacrylate, methyl trans-3-thiocyanoacrylate, and cis-4-thiocyano-3-buten-2-one at concentrations from about 5 to about 300 ppm in compositions for controlling microorganisms in cooling tower water and paper mill systems.
DETAILED DESCRIPTION OF THE INVENTION AND THE PREFERRED EMBODIMENTS
The compounds of the invention have been discovered to be unexpectedly effective antimicrobials.
Some representative compounds include the following:
1. Methyl cis-3-thiocyanoacrylate
2. Cis-3-thiocyanoacrylic acid
3. Ethyl cis-3-thiocyanoacrylate
4. n-Butyl cis-3-thiocyanoacrylate
5. Phenyl cis-3-thiocyanoacrylate
6. Iodopropargyl cis-3-thiocyanoacrylate
7. Dimethyl alpha-thiocyanofumarate
8. 2,5-Dinitrobenzyl cis-3-thiocyanoacrylate
9. 5-Chloro-thien-2-yl-methyl cis-3-thiocyanoacrylate
10. Benzyl cis-3-thiocyanoacrylate
11. 4-Chlorobenzyl cis-3-thiocyanoacrylate
12. p-Chloroacetophenyl cis-3-thiocyanoacrylate
13. 3-Methoxybenzyl cis-3-thiocyanoacrylate
14. 2,5-Dichlorobenzyl cis-3-thiocyanoacrylate
15. Cis-beta-carbomethoxyvinylisothiouronium chloride
16. Methyl cis-3-thio(1-acetylpropan-2-on-1-yl)acrylate
17. Methyl cis-3-thio(propan-2-on-1-yl)acrylate
18. Bis-cis-(carbomethoxyvinyl)disulfide
19. Methyl trans-3-thiocyanoacrylate
20. Methyl cis-3-propargylthioacrylate
21. Methyl cis-3-(5-chlorothien-2-yl-methyl)acrylate
22. Methyl 3-bromo-3-thiocyanoacrylate
23. N,N-Dimethyl cis-3-thiocyanoacrylamide
24. N-(cis-3-thiocyanoacryloyl)piperidine
25. N-(cis-3-thiocyanoacryloyl)morpholine
26. N-Methyl-N-n-butyl cis-3-thiocyanoacrylamide
27. N-Methyl-N-phenyl cis-3-thiocyanoacrylamide
28. Cis-4-thiocyano-3-buten-2.-one
29. Methyl cis-3-(cyanomethylthio)acrylate
30. Methyl cis-3-(ethylcarboxymethylthio)acrylate
31. Cis-5-thiocyano-4-penten-3-one
32. Cis-8-thiocyano-7-octen-6-one
33. 4-Phenyl-4-thiocyano-3-buten-2-one

TABLE 1__________________________________________________________________________Structures and Physical Data of Representative Compounds of Formula I, Z= ORComp. Melting orNo. R X Y Boiling Point__________________________________________________________________________ 1 CH.sub.3 H CN 69-70° C. 2 H H CN 161-166° C. 3 CH.sub.2 CH.sub.3 H CN 72° C./0.5 mm 4 CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 H CN 85° C./0.3 mm 5 Ph H CN 79-83° C. 6 CH.sub.2 C.tbd.C-I H CN 141-143.2° C. 7 CH.sub.3 COOCH.sub.3 CN 32-35° C. 8 CH.sub.2 Ph(2,5-di-NO.sub.2) H CN 138-140° C. 9 CH.sub.2 (5-Cl-Thien-2-yl) H CN 57-59.5° C.10 CH.sub.2 Ph H CN 48.5-50.5° C.11 CH.sub.2 Ph(4-Cl) H CN 69-70° C.12 CH.sub.2 COPh(4-Cl) H CN 127-129° C.13 CH.sub.2 Ph(3-OCH.sub.3) H CN 64-66° C.14 CH.sub.2 Ph(2,5-di-Cl) H CN 135-138° C.15 CH.sub.3 H C(═NH)NH.sub.2 166-167° C. (hydrochloride salt)16 CH.sub.3 H CH(COCH.sub.3).sub.2 61-64° C.17 CH.sub.3 H CH.sub.2 COCH.sub.3 76-79° C.18 CH.sub.3 H S--CH═CH--COOCH.sub.3 133-136° C.19 CH.sub.3 H CN 70° C./0.3 mm20 CH.sub.3 H CH.sub.2 C═C--H 85° C./0.25 mm21 CH.sub.3 H 5-Cl-Thiophene- 2-methylene 49.5-52° C.22 CH.sub.3 Br CN 139-142.5° C.29 CH.sub.3 H CH.sub.2 CN 63-66° C.30 CH.sub.3 H CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 Oil__________________________________________________________________________


TABLE 2______________________________________Structures and Physical Data of Representative Compounds ofFormula I, Z = NR.sup.1 R.sup.2, X = H, Y = CNComp. Melting PointNo. R.sup.1 R.sup.2 (°C.)______________________________________23 CH.sub.3 CH.sub.3 99-10224 --CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 -- 88-9025 --CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 -- 89-91.526 CH.sub.3 n-Bu Oil27 CH.sub.3 Ph 60-62______________________________________


TABLE 2-A______________________________________Structure and Physical Data of Representative Compounds ofFormula I, Z = R, Y = CNComp. Melting PointNo. R X (°C.)______________________________________28 CH.sub.3 H 44-4631 CH.sub.2 CH.sub.3 H Oil32 CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 H Oil33 CH.sub.3 Ph Oil______________________________________ ##STR3##

Various esterification methods known in the literature may be used to prepare the compounds. Two useful procedures are described here. A suspension of compound 2 in anhydrous solvents such as acetonitrile, dioxane or toluene is treated with 1,8-diazabicydo-(5.4.0)undec-7-ene, (DBU), at temperatures ranging from 0°-25° C. The resulting solution is allowed to react with commercially available alkyl, arylalkyl, and substituted arylalkyl halides (Aldrich Chemical Company) at temperatures ranging from 0°-25° C. The reaction generally takes place within 1-24 hours. Alternatively, compound 2 may be converted to the mixed anhydride and then treated with alcohols or phenols to give the esters. Thus, compound 2 may be suspended in dry solvents such as toluene, acetonitrile, or dioxane and treated with triethylamine at temperatures ranging from 0°-25° C. The resulting solution is treated with ethyl chloroformate or methane sulfonyl chloride at 0°-25° C. The resulting mixed arthydride is allowed to react with commercially available alcohols or phenols at temperatures ranging from 0°-25° C. The reaction usually takes place within 1 to 24 hours.
Iodopropargyl alcohol is prepared by a published procedure (Bulletin of the Chemical Society of Japan), Ando, T.; Shioi, S.; Nakagawa, M., (1972), 45, 2611).
Cis-3-thiocyanoacrylic acid, compound 2, which serves as the starting material for esterification into many of the compounds of Structure I is known in the literature (G. Simchen and G. Entenmann, Justus Liebigs Annalen der Chemie, No. 8, 1249 (1977). The compound is prepared by treating commercial propiolic add with sodium or ammonium thiocyanate in aqueous sulfuric acid solution at 0° C. and then allowing the mixture to warm to room temperature to precipitate the compound.
The chemistry of the thiocyano group and its addition to triple bonds are discussed in the text: "The Chemistry of Cyanates and their Thio Derivatives", parts 1 and 2, (Ed. S. Patai), Wiley and Sons, (1977).
Methyl cis-3-thiocyanoacrylate, compound 1, is cited in the following literature:
1. M. Giffard, J. Cousseau and L. Gouin, Tetrahedron, 41 (4), 801 (1985).
2. G. F. Dvorko, N.M. Soboleva, and T. F. Karpenko, Dokl, Acad. SSSR, 184(4), 850 (196511; (CA70:96179k).
The compound is readily prepared by treating commercial methyl propiolate with ammonium thiocy, anate in aqueous sulfuric acid solution at 0° C. and then allowing the mixture to warm up to room temperature to precipitate the compound.
A useful procedure for preparing the S-substituted compounds of Formula I, Z═OCH 3 , X═H, and Y═CH(COCH 3 ) 2 , CH 2 CN, CH 2 CO 2 C 2 H 5 , CH 2 COCH 3 , alkynyl, and arylalkyl (Compounds 16, 17, 20, 21, 29 and 30) starts with cis-beta-carbomethoxyvinylisothiouronium chloride, Compound 15, which is prepared and hydrolyzed to the mercaptide according to literature procedure: H.R. Pfaendler, J. Costell, and R. B. Woodward, Journal of the American Chemical Society, 101(21), 6306(1979). The mercaptide, which is not isolated, is treated with commercially available halides of Y at temperatures ranging from -10° to 25° C. in aqueous ethanol solution as shown below. The reaction usually takes place within 1-24 hours. ##STR4##
Methyl trans-3-thiocyanoacrylate, compound 19, is prepared from commercially available trans-3-chloroacrylic add (Aldrich Chemical Company) as follows: An aqueous hydrochloric or sulfuric add solution of ammonium thiocyanate is treated with trans-3-chloroacrylic add methanol at temperatures ranging from 25°-50° C. The mixture is then heated to reflux for a period of 1 to 24 hours. The mixture is extracted with chloroform which is washed with aqueous sodium bicarbonate solution. Compound 19 is obtained upon evaporation of the solvent.
Methyl 3-bromo-3-thiocyanoacrylate, compound 22, is prepared by allowing methyl bromopropioIate to react with ammonium thiocyanate in sulfuric acid solution at temperatures ranging from 0°-25° C. The reaction takes place in 1 to 5 hours. The starting material, methyl bromopropiolate, can be prepared according to a published procedure: W. Chodkiewicz, Ann. Chim. (Paris), 2(13), 819 (1957).
Cis-beta-thiocyanovinyl ketones, e.g., compounds 28, 31, 32 and 33, are prepared by allowing acetylenic ketones to react with ammonium thiocyanate in sulfuric acid solution at temperatures ranging from 0°-25° C. The reaction takes place in 1 to 2 hours.
As stated above, compositions comprising a compound according to formula I and either an agronomically acceptable carrier, a cosmetic agent, a cutting oil, a soap or synthetic detergent, a stabilizer, a film forming material, or the like have a wide range of utility for protecting against or controlling microorganisms from a wide variety of classes including fungus, bacteria, algae, viruses and yeasts. The preferred utilities of the compositions are to protect wood, paint, adhesive, glue, paper, pulp/paper slurries, textile, leather, plastics, cardboard, lubricants, cosmetics, food, caulking, feed and industrial cooling water from microorganisms.
Especially preferred compounds are methyl cis-3-thiocyanoacrylate, iodopropargyl cis-3-thiocyanoacrylate, methyl trans-3-thiocyanoacrylate, and cis-4-thiocyano-3-buten-2-one. Preferred concentrations are about 5 to about 300 ppm based on weight of material being protected. Preferred applications for controlling microorganisms are in industrial cooling water and paper mill systems. For example, especially preferred is using the compounds about at about 5-125 ppm in cooling tower water systems and at about 15-250 ppm in pulp and paper slurries.
The following lists specific industries and applications of the compounds and compositions.

______________________________________Industry Application______________________________________Adhesives, sealants adhesives caulks sealantsAgriculture/food chain adjuvant preservation agricultural active ingredient agricultural chemical preservative agricultural formulations preservation animal feed preservation dairy chemicals fertilizer preservation food preservation food processing chemicals grain preservation post-harvest produce protection sugar processing tobaccoConstruction products asphalt/concrete cement modifiers construction products roof mastics synthetic stucco wall mastics joint cementCosmetics and toiletries cosmetics raw materials for cosmetics, toiletries toiletriesDisinfectants, antiseptics antiseptic disinfectantEmulsions, dispersions aqueous dispersions dispersed pigments latex photographic emulsions pigment slurries polymer laticesFormulated consumer & indus- air freshenerstrial products fabric softeners hand cleaners polishes, floor, furniture, shoe sponges & towelettes spray starch waxesIndustrial processing, misc dry cleaning fluids preservation electrodeposition paint, baths, rinses electrodeposition pretreatment, post rinses industrial fluids preservation pasteurization baths process aid preservationIndustrial water treatment air washers cooling towers cooling water water coolingLaundry household laundry products laundered goods laundry wash water pre-washers sanitizers-laundry removers, spot & stainLeather, Leather products leather and hide leather and hide productsLubricants, hydraulic aids automotive lubricants and fluids conveyor lubricants greases hydraulic fluids hydraulic oils lubricantsMedical devices diagnostic enzymes diagnostic kits medical devicesMetalworking & related app's cutting fluids metal cleaning metalworking fluidsOdor control (active air conditioningingredient) animal bedding cat litter chemical toilet prep'ns deodorizers humidifiers industrial deodorants sanitary formulations toilet bowlsPaints and coatings coating emulsions paintsPaper and wood pulp, their absorbant materials of paper andproducts wood pulp packaging materials of paper and wood pulp paper paper products paper treatment soap wrap wood pulp wood pulp productsPaper mill paper mill slimicides pulp and paper slurriesPetroleum refining, fuels aviation fuels (jet fuel, aviation gas) burner, diesel and turbine fuel oils coal slurries diesel fuel additives diesel fuels fuels gasoline heating oils hydrocarbons kerosene liquefied petroleum gas petrochemical feedstocks petroleum products, storage, transportation and production recycled petroleum products residual fuel oils turbine oilsPhotographic Chemicals and photographic processing-washprocess water, rinses photoplate processing chemicals (developers, stabilizers etc)Printing fountain solutions (printing) ink components (pigments, resins, solvents, etc) inksSanitizers (active) sanitizers sanitizers-dairy sanitizers-dental sanitizers-fermentation sanitizers-food preparation sanitizers-food processing sanitizers-medical sanitizers-rendering sanitizers-veterinarySoaps, detergents, cleaners cleaners detergents, hand automatic laundry, other household cleaners industrial cleaners liquid soaps, hand, dish, laundry oil and grease remover powdered soaps raw materials for cleaning products. soaps surfactantsTextiles, textile products bonded fabrics burlap canvas canvas goods carpet backing carpets clothing coated fabrics curtains draperies engineering textiles fibers geotextiles goods made of textiles knitted fabrics nets nonwoven fabrics rope rugs textile accessories textile products textiles upholstery woven fabrics yarnTextile processing dye fixatives dyes fiber lubricants hand modifiers sizes textile processing fluidsTherapeutic (active or animal health/veterinarypreservative) aquaculture dental human health pharmaceutical/therapeuticWater purification charcoal beds deionization resins filters membranes reverse osmosis membranes ultrafilters water purification water purification pipes, tubingWood applications lazures (wood stains) wood wood productsMiscellaneous alcohols bedding incorporating water or gels ceramic contact lens cases-leaching electronic circuitry electronics chemicals enzymes-food production enzymes-industrial gel cushions laboratory reagents marine antifoulants mildewcides mining applications natural rubber latex oil field applications pipes plastics polymer systems polymers and resins (synthetic and natural) reagent preservation rubber rubber products skin remover solid protective/decorative films swimming pools waste treatment water beds______________________________________

The amounts of the compound to be used depend on the application. The useful amounts for a particular application are similar to amounts used for other microbicide compounds.
The compound can be used in combination with other microbicides. The term "microbicide" is considered equivalent to "antimicrobial" as used herein.
Suitable methods of application of compounds of formula I to control fungi, bacteria, algae, viruses, yeasts, and the like are in amounts and with carriers, etc., as well known in the art.
The following examples are presented to illustrate a few embodiments of the invention, but are not to be considered as limiting.


EXAMPLE 1
Phenyl cis-3-Thiocyanoacrylate (Compound 5)
Triethylamine (2.3 g., 0.031 mole) in 5 ml of dry toluene was added dropwise to a stirred, suspension of compound 2 (4.0 g., 0.031 mole) in 30 ml of dry toluene at 0° C. To the resulting solution, methanesulfonyl chloride (3.55 g., 0.031 mole) in 15 ml of dry toluene was added dropwise at 0° C. and stirred for 30 minutes. A solution of phenol (2.9 g., 0.031 mole) and dimethylaminopyridine (DMAP) (3.5 g., 0.028 mole) in 40 ml of dry toluene was added dropwise with stirring at 0° C. The mixture was allowed to warm to room temperature and stirred for an additional 3 hours. The mixture, consisting of yellowish gum in a two-phase mixture with toluene, was diluted with methylene chloride, poured into water and the organic phase was separated. The aqueous phase was extracted with methylene chloride. The combined organic phase was washed with sodium bicarbonate solution, water, dried (MgSO4) and concentrated. The residue was column-chromatographed on silica gel using hexane/ether (4:1) as eluant to give product as white crystals, 2.9 g: mp 79°-83° C.; IR (KBr) 1700, 2175 cm -1 .
EXAMPLE 2
Benzyl cis-3-Thiocyanoacrylate (Compound 10)
To a stirred suspension of compound 2 (3.0 g., 0.023 mole) in dry acetonitrile (40 ml), a solution of DBU (3.54 g., 0.023 mole) in 10 ml of dry acetonitrile was added dropwise, keeping the temperature of the mixture below 25° C. To the resulting solution was added dropwise a solution of benzyl bromide (4.0 g., 0.023 mole) in 15 ml of dry acetonitrile at room temperature. After stirring for 5 hours, the mixture was poured into water, and extracted with ether. The ether extract was washed with water, dried (MgSO4) and concentrated to give an oil which solidified upon standing, 4.3 g. The solid recrystallized from ethanol/hexane mixture as plate-like crystals: mp 48.5°-50.5° C.; IR (KBr) 1695, 2180 cm -1 .
EXAMPLE 3
Methyl cis-3-Thio(1-Acetylpropan-2-on-1-yl) Acrylate (Compound 16)
To a stirred solution of cis-beta-carbomethyoxyvinylisothiouronium chloride (compound 15) (3.92 g., 0.02 mole) in 80 ml of 95% ethanol, a pre-cooled solution of sodium hydroxide (1N, 40 ml, 0.04 mole) was added within 5 minutes at -10° C. To the white precipitate which formed immediately, consisting of sodium cis-beta-carbomethyoxyvinylmercaptide, urea and sodium chloride, was added a solution of 3-chloro-2,4-pentanedione (2.68 g., 0.02 mole) in 30 ml of 95% ethanol at -10° C. After allowing the mixture to warm to room temperature, it was stirred for an additional 5 hours and then poured into water, followed by extraction with chloroform. The chloroform extract was washed with water, dried (MgSO4), and concentrated. The residual oil was purified by column chromatography using hexane/ether (2:3) as eluant. The resulting oil, 2.1 g, solidified on standing and was recrystallized from ethanol/hexane mixture: mp 61°-64° C.; NMR (CDCl 3 ) 17.1 (s, 1H); 6.8 (d, 1H, J=9.3 cps); 5.95 (d, 1H, J=9.3 cps); 3.8 (s, 3H); 2.35 (s, 6H).
EXAMPLE 4
Methyl trans-3-Thiocyanoacrylate (Compound 19)
To a stirred solution of ammonium thiocyanate (7.2 g., 0.095 mole) in 4N sulfuric acid solution (50 ml) at 40° C., a solution of trans-3-chloroacrylic acid (10.0 g., 0.095 mole) in 35 ml of methanol was added dropwise within 5 minutes. The mixture was refluxed for 18 hours, cooled and poured into water which was extracted thoroughly with ether. The ether extract was washed with saturated sodium bicarbonate solution and then with water. After drying (MgSO4), the solution was concentrated to give an oil which distilled at 70° C./0.3 mm; yield, 7.2 g.; NMR (CDCl 3 ) 7.3 (d, 1H, J=14.4 cps); 6.35 (d, 1H, J=14.4 cps); 3.8 (s, 3H); IR(KBr) 2180, 1725 cm -1 .
EXAMPLE 5
Methyl 3-Bromo-3-Thiocyanoacrylate (Compound 22)
To a stirred solution of ammonium thiocyanate (3.06 g., 0.04 mole) in 2M aqueous sulfuric acid (20 ml) at 0° C., methyl 3-bromopropiolate (3.26 g., 0.02 mole) was added dropwise, neat, over 5 minutes. After keeping the temperature at 0° C. for 1 hour, the mixture, consisting of a solid precipitate in the aqueous solution, was extracted with ether which was washed with water, dried (MgSO4), and concentrated. The residual solid was suspended in hexane and removed by filtration, yielding 2.4 g. of product. The solid recrystallized from ethanol as yellowish microcrystals; mp 139°-142.5° C.; IR (KBr) 2170, 1680 cm -1 .
EXAMPLE 6
N-(cis-3-Thiocyanoacryloyl)piperidine (Compound 24)
To a stirred suspension of compound 2 (3.06 g., 0.023 mole) in 60 ml of dry toluene, triethylamine (2.35 g., 0.023 mole) in 10 ml of dry toluene was added dropwise, keeping the temperature of the mixture at 0°-5° C. To the resulting solution was added dropwise, ethyl chloroformate (2.53 g., 0.023 mole) in 15 ml of dry toluene at 0°-5° C. After stirring the mixture for 15 minutes, piperidine (2.0 g., 0.023 mole) in 15 ml of dry toluene was added dropwise at 0°-5° C. The mixture was allowed to warm to room temperature, stirred for an additional 2 hours and filtered. The filtrate was washed with water, dried (MgSO4) and concentrated to give an oil which solidified, 2.6 g. The solid was recrystallized from ethanol: mp 88°-90° C.; IR (KBr) 2175, 1630 cm -1
EXAMPLE 7
Cis-4-Thiocyano-3-buten-2-one (Compound 28)
To a stirred solution of ammonium thiocyanate (7.6 g., 0.1 mole) in 2M sulfuric acid solution (50 ml) at 0° C., 1-butyn-3-one (3.4 g., 0.05 mole) was added neat over 5 minutes. The resulting solid suspension was stirred at 0° C. for 15 minutes and then allowed to warm to room temperature and then stirred for an additional hour. The solid was removed by filtration and washed with water. After drying, the brown solid was purified by column chromatography on silica gel using hexane/ether (1:4) as eluant. The resulting solid, 3.6 g recrystallized from hexane/ethanol mixture as needles upon standing in the refrigerator: mp 44°-46° C.; IR (KBr) 2150, 1665 cm -1 .
EXAMPLE 8
Biological Activity
A. Biocidal Activity:
Biocidal evaluations (bactericidal, algicidal, and fungicidal) were carried out.
A minimum inhibitory concentration (MIC) value is obtained using a broth, two-fold serial dilution test performed as follows: A stock solution or dispersion of the test compound, typically at a concentration of 1%, is made in a 5:3:2 solvent solution of acetone, methanol, and water. A volume of the stock solution is dispensed into culture media to give an initial starting test concentration of 500 ppm compound.
When the test is ready to be done, each vessel in the dilution series, except the first vessel, contains an equal volume of compound free broth. The first vessel contains twice the volume of broth with the starting concentration of test compound. One half of the broth from the first vessel is transferred to the second vessel. After being mixed, one half the resulting volume is removed from the second vessel and transferred to the third vessel. The entire cycle is repeated sufficiently to give a series of concentrations amounting to 500, 250, 125, 63, 31, 16, 8, and 4 ppm (or 100, 50, 25, 12.5, 6.2, 3.1, 1.6, and 0.8), respectively.
Each vessel is then inoculated with a cell suspension of the appropriate test organism. Bacteria are grown in broth, fungi on agar slants for a time and at a temperature appropriate to the spedes being tested, and algae are a mixture of green algae and blue-green bacteria grown in a nutrient media. At the end of the growth period, in the case of bacteria, the broth is vortexed to disperse the cells.
In the case of fungi, the spores are harvested by pipetting water onto the slant and dislodging the spores with a sterile loop. The cell/spore suspension is standardized by controlling incubation time, temperature, and the volume of thee diluent. The suspension is then used to inoculate the vessels containing the broth compound.
The algae culture contains green algae and blue-green bacteria, and is obtained from a cooling tower in Spring House, Penn. The algae culture is grown in Allen's medium on a rotary shaker under flourescent room lighting. This culture is further diluted with Allen's medium and then added to the test vessel.
The vessels are then incubated at the appropriate temperature. After the incubation, the vessels are examined for growth/no growth. The minimum inhibitory concentration (M/C) is defined as the lowest concentration of compound that results in complete inhibition of growth of the test organism.
The organisms tested to demonstrate biocidal activity include:
BACTERIA: Pseudomonas fluorescens (PSFL), gram negative Pseudomonas aerugenosa (PSAE), gram negative Escherichia coli (ECOL), gram negative Staphylococcus aureus (SAUR), gram positive
FUNGI: Aspergillus niger (ANIG) Aureobasidium pullulans (APUL)
The results of the minimum inhibitory concentration (MIC) and SOK tests of compounds of this invention are shown in Table 3 against the microorganisms shown in Table 6.
B. In-Vitro Plant Fungicidal Tests:
h-vitro tests of plant diseases were carried out.
The organisms employed in the test are: PYU Pythium ultimum (Oomycete) PHY Phytophthora capsici (Oomycete) PIR Piricularia oryzae (Ascomycete) HEL Cochliobolus sativus (Ascomycete) BOC Botrytis dnerea (Ascomycete) FUS Fusarium roseurn (Ascomycete) SEP Septoria nodorum (Ascomycete) RHI Rhizoctonia solani (Basidiomycete) XAN Xanthomonas campestris (bacterium)
Methods:
1. Culture maintenance: Transfers in steps 1 and 2 are done in a laminar flow hood. All 8 fungi and the bacterium used in this test are transferred and maintained on potato dextrose agar plates each week (2 plates/organism). Organisms are used when they are the following ages: a. 1 week old: PYU, PHY, RIff; b. 2 weeks old: XAN, FIR, BOC, HEL, FUS, SEP. Pythium ultimum and phytophthora capsici are transferred to aspaxagine-sucrose broth shake cultures (ASB). Rhizoctonia solani, Fusarium roseum, and Zanthomonas campestris are maintained in yeast extract-dextrose broth (YDB) on a shaker. Culture flasks are inoculated with 6 mycelial plugs each (except for Pythium which is inoculated with only 3 plugs) taken from PDA plates. All liquid shaker cultures are used after 2 days growth.
2. Inoculum preparation. Corddia and mycelium from PIR, BOC, HEL, and SEP are lightly scraped off into YDB so that mostly conidia are used as inoculum. The corddial suspension is strained through a double layer of cheesecloth to remove mycelial clumps. One plate produces enough corddia or mycelium to inoculate 100 ml of YDB. XAN broth culture is figured, (1 ml culture/100 ml broth) into YDB. PYU, PHY, RHI and FUS cultures are ground up (2-3 5 second bursts in a blender) and all but Pythium arid Phytophthora are filtered through a double layer of sterile cheesecloth to remove large mycelial clumps. Ten ml of the culture solutions of R. solani and F. roseum are added to 90 ml of YSB and 10 ml of the P. capsici is added to 90 ml ASB. Two md of the culture solution of P. ultimum is added to 98 ml of ASB. Care must be made not to over inoculate (e.g., solutions should appear fairly dear to the eye, yet when held up to light a faint cloudiness should be visible) or standards will not behave properly. The inoculum mixtures are placed in microtiter plates using a 12-tipped pipet. 175 μl (single dose) or 100μl (dose-response test) of inoculum broth is placed in each well of the microtiter plates. The plates with inoculated media are placed in the refrigerator overnight. There are two replications per treatment.
3. Addition of compounds. This operation is carried out in a hood. Six microtiter plates have 245 microliters of sterile water added to their wells ahead of time. 10 Mg a.i. of the compounds are placed in 1 ml 1:1 acetone:methanol. 5 Microliters of this solution is pipetted into the microtiter plates containing the sterile water according to the grid. There are 45 compounds and 3 control treatments per plate. There are 2 replicates per treatment. 25 Microliters of solution is transferred to the inoculated plates with a 96 well replicator. The replicator is flame sterilized with alcohol, rinsed with sterile water, and blotted on sterile paper towels between each transfer.
The results of % control of plant fungi at a certain concentration of some of the compounds of this invention are shown in Table 4.
C. Greenhouse Tests of Plant Disease Control:
Several compounds of this invention were tested for fungicidal activity in vivo against tomato late blight (TLB), wheat powdery mildew (WPM) and wheat leaf rust (WLR) and the results are shown in Table 5. In tests on cereals the plants were trimmed about 24 hours prior to the application of the fungicide compound to provide a uniform plant height and to facilitate uniform application of the compound and inoculation with the fungus. The compounds were dissolved in a 2:1:1 mixture of water, acetone, and methanol, sprayed onto the plants, allowed to dry (four to six hours), and then the plants were inoculated with the fungus. Each test utilized control plants which were sprayed with the water, acetone, and methanol mixture and inoculated with the fungus. The remainder of the technique of each of the tests is given below and the results are reported as percent disease control (percentages of plants treated with the compounds of the present invention lacking disease signs or symptoms compared to the untreated control plants).
Tomato Late Blight (TLB):
Phytophthora infestaris was cultured on four week old Pixie tomato plants in a controlled environment room (65° F. to 70° F. and 100% relative humidity). After storage, the spores were washed from the leaves with water and dispersed by DeVilbiss atomizer over three week old Pixie tomato plants which had been sprayed previously with experimental fungicides. The inoculated plants were placed in a humidity cabinet at 70° F. and constant mist for 24 hours for infection. The plants were then moved to the controlled environment room as above and scored after three more days incubation. Disease control levels were recorded as percent control four days after inoculation and five days after spraying the compounds.
Wheat Powdery Mildew (WPM):
Erysiphe graminis (f. sp. tritici) was cultured on Pennol wheat seedlings in a controlled temperature room at 65° F. to 75° F. Mildew spores were shaken from the culture plants onto Pennol wheat seedlings which had been sprayed previously with the fungicide compound. The inoculated seedlings were kept in a controlled temperature room at 65° F. to 75° F. and subirrigated. The percent disease control was rated 8 to 10 days after the inoculation.
Wheat Leaf Rust (WLR):
Puccinia recondita (f. sp. tritici Races PKB and PLD) was cultured on seven day old wheat (cultivar Fielder) over a 14 day period in the greenhouse. Spores were collected from the leaves with a cyclone vacuum or by settling on aluminum foil. The spores were dearted by sieving through a 250 micron opening screen and stored or used fresh. Storage employed sealed bags in an Ultralow freezer. When stored, spores must be heat shocked for two minutes at 40° F. before use. A spore suspension is prepared from dry ureciia by adding 20 mg (9.5 million) per ml of Soltrol oil. The suspension is dispensed into gelatin capsules (0.7 ml capacity) which attach to the oil atomizers. One capsule is used per flat of twenty of the two inch square pots of seven day old Fielder wheat. After waiting for at least 15 minutes for the oil to evaporate from the wheat leaves, the plants are placed in a dark mist chamber (18°-20° C. and 100% relative humidity) for 24 hours. The plants are then put in the greenhouse for the latent period and scored after 10 days for disease levels. Protective and curative tests were inoculated one day after and two days, respectively, before spraying the plants with the test chemicals.

TABLE 3__________________________________________________________________________Biocides Secondary MIC/SOK Test Data (in PPM)for Compounds of Formula ICpd #SOK PSFL PSAE ECOL SAUR ANIG APUL__________________________________________________________________________ 1 >500 63 125 250 125 16 8 2 >250 >250 >250 250 >250 >250 >250 3 250 125 250 250 125 32 250 4 250 250 >250 >250 >250 63 32 5 >250 16 250 125 16 2 4 6 125 16 250 250 16 <.13 1 7 250 >250 >250 >250 >250 >250 125 8 250 32 >250 >250 >250 63 >250 9 32 8 >250 >250 125 8 1610 32 16 >250 >250 125 8 3211 32 16 >250 >250 125 8 3212 250 >250 >250 >250 >250 8 6313 125 32 >250 >250 63 32 1614 125 >250 >250 >250 >250 >250 >25015 >250 >250 >250 >250 >250 >250 12516 >250 >250 >250 >250 >250 >250 0.6317 >1000 >250 >1000 >1000 >1000 >1000 >100018 >250 >250 >250 >250 >250 >250 6319 >250 16 63 63 63 4 220 >1000 >250 >1000 >1000 1000 1000 100021 >250 >250 250 >250 >250 250 25022 >250 32 >125 250 250 63 1623 >250 >250 >250 >250 >250 250 6324 >250 >250 >250 >250 >250 250 12525 >250 >250 >250 >250 >250 250 12526 >250 >250 >250 >250 >250 125 6327 >250 >250 >250 >250 >250 32 6328 125 32 32 63 16 16 429 >250 250 >250 >250 >250 >250 >25030 >250 250 >250 >250 > 250 >250 >25031 63 -- 63 63 >250 2 132 >250 -- 32 >250 >250 63 6333 >250 -- >250 >250 16 16 8__________________________________________________________________________


TABLE 4______________________________________In-Vitro Plant Fungicide Test Results for Compounds ofFormula ICpd. % control at 25 ppm# PYU PIR PHY BOC HEL RHI FUS SEP XAN______________________________________ 1 100 100 100 100 100 100 100 100 0 5 100 100 100 100 100 100 100 100 0 6 100 100 100 100 100 100 100 100 0 8 100 100 100 100 100 100 100 100 0 9 0 100 100 100 0 100 0 100 010 100 100 100 100 100 100 100 100 011 100 100 100 100 100 100 100 100 012 0 100 100 0 100 0 0 0 013 100 100 100 100 100 100 100 100 025 100 100 100 100 100 100 100 100 0______________________________________


TABLE 5______________________________________Green House Test Results of Plant Disease Controlfor Compounds of Formula I % ControlComp. # Rate (ppm) TLB WLR WPM______________________________________ 8 600 90 75 010 600 75 90 011 600 0 50 012 600 50 90 018 600 75 75 0______________________________________


TABLE 6______________________________________Microorganisms Used in the Biocides Tests GRAM AbbreviationName ATCC No. used______________________________________BACTERIA1. Pseudomonas aeruginosa (-) 15442 PSAE2. Staphylococcus aureus (+) 6538 SAUR3. Escherichia coli (-) 11229 ECOL4. Pseudomonas fluorescens (-) 948 PSFLFUNGI1. Aspergillus niger 6275 ANIG2. Aureobasidium pullulans 9348 APUL______________________________________