• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    Novel herbicidal thiadiazoles of the formula: (wherein: R1 represents a group Ra, -S(O)nRa or-SO2NRaRb, where Ra and Rb, which may be the same or different, each represent hydrogen cycloalkyl of 3 to 7 carbon atoms, alkenyl or alkynyl of 2 to 6 carbon atoms, phenyl, phenylalkyl of 7 to 10 carbon atoms, or alkyl of 1 to 10 carbon atoms, any phenyl or alkyl group present being optionally substituted by one or more halogen atoms, cyano groups, alkoxy or alkylthio groups of 1 to 4 carbon atoms, or phenoxy groups, or Ra and Rb together form an alkylene chain of 2 to 6 carbon atoms, and n represents 0, 1 or 2; X represents oxygen or sulphur; Z represents a group -NR°Rd: and Y represents a group -NReRf or a group -N=CReRf; where RC, Rd, Re and Rf, which may be the same or different, each represent a group as defined for Ra, or a carboxy, alkoxy, alkoxycarbonyl, acyl, acyloxy, alkylsulphonyl, cyano, formyl, amido, or heterocyclyl group, any alkyl moiety of which is of 1 to 4 carbon atoms); and the acid addition salts thereof, compositions containing them and processes for their preparation.
    公开号:SU1189343A3
    申请号:SU833550247
    申请日:1983-02-04
    公开日:1985-10-30
    发明作者:Лоли Хью Томас；Питер Джоунз Грэхам
    申请人:Фбс Лимитед.(Фирма)；
    IPC主号:
    专利说明:

    1 The invention relates to a process for the preparation of thiadiazoles having gerbicidal activity of the general formula O II C-NHAlk - S N or where Y is the group NH R - aek, Safk, SOjNCaPk), CgCHNCCCCH3) -, CgEgSO apk - alkyl, N.i. R - may be the same or different and denote hydrogen, C: - C, j-alkyl, phenyl, unsubstituted RviH substituted by one or two halogen atoms, alkoxy containing 1-4 carbon atoms, cyano, or their acid additive salts . Preferred additive acids are salts formed with mineral or organic acids, for example, salts of hydrohalic acids, especially hydrochloric or hydrobromic acids. The invention is illustrated by the following examples. Example 1. Benzaldehyde-4-methyl-2- (5-tert-util-1,3,4-thiadol-2-yl) semicarbazone. 2) 2-Bromo-5-tert-butyl-1,3,4-thiadiazole. 48% aqueous hydrobromic acid (67.5 ml) is added to a solution of 2-amino-5-tert-butyl-1,3, 4-thiadiazole (43 g) in glacial acetic acid (300 ml), the mixture is warmed up and a solution of sodium nitrite (56 g) in water (80 ml) is added dropwise with stirring over 60 minutes at 65-70 ° C. The mixture is cooled to 20 ° C and added to water. The organic layer is extracted into ether (2) (300 ml), and the extract is combined, washed with sodium bicarbonate solution until neutral, and dried over magnesium sulfate. The drying agent is filtered off, and the solvent is evaporated to give a yellow oil, which is distilled under reduced pressure, and 2-bromo-5-tert-buty-1,3,4-thiadiazole (47 g, 78%) as a colorless liquid. bp 134Pb C at 23 mm Hg c) 2-Hydrazino-5-tert-butyl-1, 3,4-thiadiazole. 3 Hydrazine hydrate (12.5 g) was added to a solution of 2-bromo-5-tert-butyl-1, 3,4-thiadiazole (22.1 g) in ethanol (100 ml) and the mixture was heated at reflux. within 2 hours. The solvent is evaporated to give an oily solid, which crystallizes from water, and 2-hydrazino-5-tert-butyl-1, 3,4-thiadiazole (13.7 g, 79%) as white needles , mp 111lU C. c) Benzaldehyde 5-tert-butide-1, 3,4-thiadiazol-2-yl hydrazone. A solution of ben3aldehyde (5.3 g) in methanol (25 ml) was added to a solution of 2-hydrazino-5-tert-butyl-1, 3,4-thiadiazole (8.5 g) in methanol (40 ml). The mixture is stirred for 30 minutes, poured into water (100 ml) and filtered. The solid is crystallized from ethanol to give benzaldehyde 5-tert-butyl-1, 3,4-thiadiazolyl hydrazone (8.2 g, 63%) as a white powder, mp. 195-196 ° C. d) Benzaldehyde 4-methyl-2- (5-tert-butyl-1, 3,4-thiadiazol-2-yl) semicarbazone. Methyl isocyanate (1.88 g) was added to a stirred suspension of benzaldehyde 5-tert-butsh1-1,3,4-thiadiazlyl-hydrazone (7.8 g) in ethyl acetate (60 ml). Triethylamine (3 drops) is then added and the mixture is stirred for 2 hours. The solvent is evaporated to give a white solid, purified by chromatography. The pure fractions are combined and recrystallized from a mixture of ethyl acetate and hexane to give 4-methyl-2- (5-tert-butyl-1, 3,4-thiadiazol-2-yl) -semicarbazone benzaldehyde (2.1 g, 22 %) in the form of a white powder, so pl. 115-116 C. Examples 2-9. In Example 1, the following compounds of formula 1- are prepared, where X is oxygen and Z-methylamine. Example 10. Acetaldehyde-4-methyl-2- (5-tert-butyl-1,3,4-thiadiazol-2-yl) -semicarbazone. Sodium hydride (0.12 g is added to a stirred solution of acetaldehyde 5-tert-butyl-1,3,4-thiadiazolyl-hydrazone (0.99 g) in dry toluene (25 ml) and the mixture is stirred at room temperature in
    3
    for 15 minutes Then 2-methylaminocarbonyloxyimino-2-phenylacetonitrile (1.01 g) is added, the mixture is stirred for an additional 2 hours and taken into water (20 ml). The organic phase is separated and dried over magnesium sulphate. The drying agent is filtered off, the toluene is evaporated, a yellow oil is obtained, which is purified by chromatography, 4-methyl-2- (5-tert-butyu1-1,3,4-thiadiazol-2-sh1) acetic aldehyde (0 , 6 g, 46%) as a pale yellow oil.
    Found,%: C 46.65, H 7.2, N 27.09
    Calculated,%: C 47.04, H 6.71, N 27.43.
    Examples 11-12. The following compounds are prepared analogously to example 10:
    11) 4-methi -2- (5-trifluoromethyl-1, 3,4-thiadiazol-2-sh1) acetone, semicarbazone, m.p. 89-90 s.
    12) acetaldehyde 4-metsh1-2- (5-trifluorometsh1-1, 3,4-thiadiazol-2-yl) -semicarbazone, so pl. 68-69C.
    . Example 13. 4-Methyl-2- (5-trifluoromethyl-1,3,4-thiadiazol-2-yl) -semicarbazide.
     Concentrated hydrochloric acid (1.0 ml) is added to a stirred suspension of acetaldehyde 4-metsh1-2- (5-: trifluoromesh1-1,3,4-thiadiazole-2-sh1) -semicarbazone in water (200 ml) The mixture is stirred at room temperature for 3 days and filtered. The solid is dried and crystallized from the solid state to give 4-methyl-2 (5-trifluoromethyl 1, 3,4-thiadiazol-2-yl) -semicarbazide (10.0. g) as white solids, mp 181-182 C.
    According to the procedure of Example 13, the following compounds of formula (I) are obtained (see Table 2).
    All of the above compounds have high activity in the tests of examples (A-D).
    Examples 14-15. In Example 14, the following compounds are prepared;
    14) 4-methyl-2- (5-tert-butyl-1, 3,4-thiadiazol-2-yl) -semicarbazide, m.p. 136-138 C,
    893434
    15) 4-H-propyl-2- (5-trifluorome. Tyl-1,3,4-thiadiazol-2-yl) -semicarbazide, mp. 205-206С.
    Get salt additive salt
    5 acids to the compound of example 14, a solution of 1 g of this product in 43.7 ml of 0.1 N. hydrochloric acid solution. The compound obtained has a rating of 5 and correspond to the method
    10 examples of D at a dose
    0.5 kg / ha. The acid addition salts of the compounds of Examples 1 and 19 are prepared in the same manner.
    Example 16. 4-Metnp-2- (5t5-ethylsulfonyl-1,3,4-thiadiazol-2-yl) -semicarbazide.
    2,5-bis (ethanesulfon1) -1,3,4-thiadiazole (67.5 g) is added in portions to the stirred solution
    20 hydrazine hydrate (25.8 g) in methano-. le (1000 ml) at room temperature. The mixture is then stirred for 20 minutes and filtered. The solid is crystallized from
    5 methanol to give 2-hydrazino-5-ethylsulfonyl-1, 3,4-thiadiazole. (16.5 g, mp. 166-167c). The corresponding semicarbazone is prepared from this compound by reaction with acetaldehyde, then with methyl isocyanate by the methods similar to the methods of example 1 and d, and the target compound is obtained by the method of example 13, mp. 151153С.
    Examples 17-19. In Example 1-6, the following compounds of formula (I) are prepared (see Table 3).
    0 Example 20. 4-methyl-2- (5-tert-butyl-1, 3,4-thiadiazol-2-yl) -semicarbazide.
    Methyl isocyanate (g) is added dropwise over 5 minutes.
    5 to a stirred suspension of acetapedehyde 5-tert-butyl-1,3,4-thiadiazolip hydrazone (49.5 g) plus potassium carbonate (8.0 g) in acetonitrile (300 ml) at room temperature.
    0 The mixture is stirred for 20 minutes and filtered, the filtrate is evaporated, obtaining an orange oil (64 g), which contained 80% acetaldehyde 4-methyl-2- (5-tert-butsh1-1,3,4-tia5 diaz ol-2 -il) semicarbazone.
    The crude product is stirred. by heating under reflux in ethanol (300 ml) with hydrazine hydrate (12.5 g) for 2 hours. The solvent is evaporated to give an oily solid, which is treated with water (150 ttn) and. filtered. The solid is washed with water and dried. Crystallization from a mixture of ethyl acetate and hexane gives 4-methyl-2- (5-tert-butyl-1,3,4-thiadiazole-2-sh1) -semicarbazide (32 g, T.Sh1. 141-142 ° C).
    The compounds of formula (1) and their acid addition salts are active in a herbicidal manner, in particular they are active against oat (Avena fatua), foxtail (A opecurus myosuroides) and broadleaf weeds and are relatively inactive against some Cultivated species, namely wheat , Barley, corn and cotton. Thus, the compounds can be used as selective herbicides in crops of cultivated plants, as well as dp destroying weeds in places contaminated with them or iodine contamination by them. The proposed method involves the use with respect to the location of the herbicidally effective amount of one or more compounds. By mixing the ingredients, concentrates are obtained, for example, containing 0.5-99%, especially 0.5-85% of compounds that are diluted with water or hydrocarbons to a concentration of 0.05-5%. Percentages and parts are given by weight.
    The compositions contain a surfactant and / or carrier.
    The carrier may be water used to dilute the concentrate or an organic solvent immiscible with water, for example a hydrocarbon boiling in the temperature range of 130-270 ° C, in which the compound is dissolved or suspended. A concentrate containing a water-immiscible solvent {also contains a surface-active agent that acts as a self-emulsified oil when mixed with water} and a solvent used as a carrier can be a water-miscible solvent, for example 2-methoxy- ethanol, methanol
    propileglycol, dystilenglycol, diethylene glycol monostillamine zfir, formamide or methylformamide.
    The carrier may be finely divided solid, for example, lime, clay, sand, mica, chalk, attapulgite, diatomite, perlite, sepiolite, silicas, silicates, lignosulfonates and solid fertilizers. The carrier may be of natural or synthetic origin, or may be modified with a natural substance.
    Wettable powders, soluble or dispersible in water, can be prepared by mixing the compound in the form of particles with a carrier in the form of particles or by spraying the molten compound on the carrier in the form of particles, mixing the wetting agent and dispersing agent and finely grinding the whole powder mixture.
    The aerosol composition can be obtained by mixing the compound with propellant, for example a polyhalogenated alkane, such as dichlorofluoromethane, as well as with a suitable solvent.
     A flowable suspension concentrate can be formed by diluting the compound with water, a wetting agent and a suspending agent.
    Thus, the inventive composition may be solid, for example in the form of dust or granules, and contain a solid or liquid carrier, for example, in the form of a emulsifiable concentrate, and contain a liquid carrier, which is a hydrocarbon boiling in the range of 130-270 ° C.
    Flouring, dispersing and wetting agents are used as surfactants.
    Used surface-active agents may include anionic surface-active agents, for example mono - and di-complex esters. phosphoric acid with an ethoxylated fatty alcohol product or salts of such esters; fatty alcohol sulfates, such as sodium dodecyl sulfate, ethoxylated fatty alcohol sulfates, ethoxylated alkylphenol sulfates, ligninsulfates, and petroleum sulfonates.
    alkylaryl sulfoates, such as alkyl benzenesulfonates or lower alkyl naphthylene sulfonates, salts of sulfonated naphthalene formaldehyde condensates, salts of sulfonated phenol formaldehyde condensates, or more complex sulfonates, such as amide sulfonates, for example, a sulfonated condensation unit, I don't need to give a set. α-sulfosuccinates, for example, sodium dioctylsuccinate sulfonate.
    Surface-active agents may also include non-ionic agents, for example, condensation products of fatty acid esters, fatty alcohols, fatty acid amides or alkyl-substituted phenols with ethylene oxide, esters of polyhydric alcohol ethers, such as sorbitan fatty acid esters, condensation products of such ethylene oxide esters, for example polyoxyethylene sorbitan fatty acid esters, block copolymers of ethylene oxide and propylene oxide, acetylene glycols, such as 2,4,7,9-tetramethyl-5- etsin-4, 7-diol, or ethoxylated acetylenic glycols.
    Surface-active agents may also include cationic agents, for example, alkyl and / or aryl-substituted quaternary ammonium compounds, such as cetyltrimethylammonium bromide, or ethoxylated tertiary fatty amine.
    Preferred surface active agents include ethoxylated fatty alcohol sulfates, lignin sulfonates, apkilarilsulfonaty, salts of sulfonated naphthalene formaldehyde condensates, salts of sulphonated fenolformal, degidnyh condensates, sodium oleoyl N-methyltauride, dialkyl sulphosuccinates, alkyl phenol ethoxylates, and fatty alkyl ethoxylates.
    The proposed active compounds can be mixed with other pesticides, for example, a herbicide, an insecticide, or a fungicide or with a plant growth regulator, or with a fertilizer.
    Effectively alternate mixing of the proposed compounds with one
    herbicides by dami before planting or before the emergence of crop sprouts, and the second - after the appearance of seedlings.
    The herbicide used in the post-emergence period may be, for example, a substituted benzofuranic herbicide, phenoxy aliphatic acid, substituted urea, tri-
    azine, phenol, nitrile, bipyridylium compound, substituted benzoic acid, halogenated aliphatic. Chescic acid, carbamate, thiocarbamate, chloroacetamide, diazine, arsenic or other herbicidal compound, preferably substituted phenoxy aliphatic acid. In the pre-emergence period, a second benzofuran, substituted urea, or triazine is preferred as a second herbicide.
    The substituted benzofuranium herbicide is a compound of formula
    where is hydrogen or alkoxy (especially ethoxy, propoxy or isopropoxy),
    R is alkyl (especially methyl or ethyl.).
    The preferred substituted benzofuraNyl compound for mixing with the compounds of the invention is 2-ETOXY-2, 3-dipadro-3, 3-dimethylbenzofuran-5-yl methanesulfonate (etofumezate).
    Phenoxy aliphatic acid typically includes alkyl and / or halogen substituted phenoxy aliphatic acids and their salts, for example alkali metal salts, amine and alkanol amine salts, and functional derivatives, for example, esters and amides. These compounds have strong or weak herbicidal activity.
    Substituted urea usually includes a tri- or tetra-substituted urea.
     The triazine herbicide typically comprises a compound of the formula
    2
    N-- -N
    20
    (i i - ,, R,
    N -R2I
    where X is a halogen, an OA group, or an SV group, where Y is an alkyl group, and R, R2o jj are hydrogen or alkyl.
    Specific preferred mixtures are mixtures of compounds with one or more components, including atrazine, ametrine, alachlor, borban, benzoylprop-ethyl, chlorotoluron, chlorosulfuron, cyanesine, 2,4-D, dicamba, difenzoquat, famprop-methyl, dichloro- methyl, isoproturon, linuron, metolachlor, methoxuron, simazine, triallat or tribune.
    JipejyiaraeMbie compounds are placed in a container container in which one or more compounds are in the first container and one or more additional pesticides plant growth regulator or fertilizer in the second container. The toolkit, either separately attached, or by mixing the contents of the container or for individual use, is embedded in one of the containers.
    The ratio of the present compounds to the second pesticide can vary widely, depending on the particular compounds that are used and on the purpose of use. Typically, the ratio of the proposed compound to the second pesticide is in the range from 1:99 to 99: 1, or from 1: 0.1 to 1:15, or 1: 0.2 to 5: 1 or from 1; 0.3 to 3: 1.
    Infusion can be mixed with non-phytotoxic oils.
    The present compounds are typically used in an amount of from 0.5 to 8 kg hectare, for example 1-4 kg per hectare.
    Example A. Compounds listed below and transformed into a finished product of the preparation in the form of dusts with a mixture of attaglins and sand, introduced into a John Jnnes 1 potty compost in an amount equivalent to 26 mg of active ingredient per 1 liter of compost, and placed in anodized aluminum cuvettes 19 cm “9.5 cm long x5.0 wide with depth. This dose is equivalent to the application of 11.2 kg of active ingredient per hectare on the soil surface when cultivated to a depth of 5 cm. The seeds of the plant species listed below were sown into treated compost, watered and
    placed in a room with adjustable environmental conditions (, 65-86% relative humidity, artificial light 14 hours a day with an intensity of 13,000 lux) for 21 days.
    0 The plants were then evaluated visually for the herbicidal effect or for the effect of growth control. All differences from untreated control plants were classified or 5 were evaluated according to the following scale: from indicator O - no effect, up to 100 - complete destruction. The results are shown in table 4.
    0. Example V. Seeds of Species
    The plants listed below were sown in anodized aluminum cuvettes 19 cm long, 5 cm wide f 5 cm deep, containing
    5 John Junes compost 1. Then it was watered and placed in a room with controlled environmental conditions (, 65–85% relative humidity, 14 hours a day artificial light at 13,000 lux). 14 days after sowing, the saplings were treated by spraying the foliage with the compounds listed below, converted into formulations in the form of a solution in 1: 1 by volume of aqueous acetone.
    The concentration of the compounds tested and the volume applied were adjusted to achieve 0
    equivalence rate
    2.8 kg of compound per 450 l per hectare. After 14 days of cultivation in a room with controlled environmental conditions, the plants were evaluated for the effect of herbicidal or growth control. All differences from the control experiments without treatment were evaluated on a scale of indices, in which O is the absence of effect and 100 is complete destruction. The results are shown in table 5. .
    Example C. The seeds of the weed species listed below were sown in anodized aluminum cuvettes 19 cm long x 9.5 cm wide “5 cm deep, containing sterilized sandy-loamy
    The soil was then moistened and sprayed with the compounds listed below, converted into aqueous suspension formulations together with 2 g of polyoxyethylene (20 mol) monolaurate wetting agent per liter.
    The concentration of each test compound and the volume to be used to obtain the desired degree of application of the compound in 450 liters per hectare were calculated. After four weeks of growth in a room with controlled environmental conditions (22 ° C, 65-85% relative humidity, 14 hours a day of artificial illumination with an intensity of 13000 lux), the plants were evaluated visually for the herbicidal effect.
    All the differences from the untreated control were classified according to the scale according to which the index O is the lack of effect, 1 is very weak, 2 is weak, 3 is moderate, 4 is strong, and 5 is complete destruction. The following results were obtained (see table 6).
    Example D. The seeds of the plant species listed below were sown in anodized aluminum cuvettes of size: 19 cm long x 9.5 with a width of containing sterilized sandy loam. Then they were moistened and placed in a room with controlled environmental conditions (22s, 65–85% relative humidity 14 hours a day, artificial lighting at 13,000 lux). Fourteen or twenty-one days after sowing (depending on the species, but at the time when most plants had a stage, two or three true leaves), they sprayed the leaves with the compounds listed below as an aqueous suspension. with 2 g of polyoxyethylene (20 mol) monolaurate wetting agent per liter
    The concentration of each test compound was calculated so as to obtain the desired degree of application of the compound in 450 liters per hectare.
    After 14 days of plant growth in a room with controlled environmental conditions, the plants were evaluated visually for the herbicidal action.
    All differences from the untreated control were graded on a scale, according to which the indicator O is the absence of action, 1 is a very weak effect, 2 is a weak action, 3 is a moderate action, 4 is a strong action and 5 is complete destruction.
    Example E. A 50% wettable powder was prepared by grinding the following ingredients,%:
    Connection example 13 50
    Reax 45 L (sodium lignosulfonate) 5
    Chinese clay 45
    Similar formulations were prepared for each of the compounds of Examples 1 and 12-19, containing 0.5, 1.5, 10, 25, 40, 75 and. 85% by weight of the active ingredient.
    Example G. A preparative form in the form of a 20% emulsifiable concentrate was prepared by dissolving the following ingredients in Solvesso 200 solvent (a mixture of aromatic hydrocarbons) to obtain 1 liter, g:
    Connection example 12 200 Toksimul D15
    Toximul H. 85
    Toximul D and Toximul H are anionic (non-ionic mixed surfactants).
    Similar formulations were prepared containing 50, 100, 200, 300 and 400 g per liter of the compounds of examples 1 and 12-19. In repeated field experiments with flat barley, the following results were obtained (expressed as a percentage of the destruction of the plant) and 19 days after the treatment.
    200 liters per hectare when the plants had 2-3 leaves each.
    Isoproturon is a urea herbicide used in agriculture.
    Cleavers
    (Gaf ium aparine)
    Veronika arable
    (Veronica spp)
    Buckwheat (Polygonumavicu
    tare).
    Pansies
    (Viola arvensis). The results show that the abrasions obtained according to the proposed
    99
    100
    ten
    60
    100
    60
    100 methods are significantly more active than the known compound. Table.
    table 2
    Table 4
    Continued table. five
    Avena fatua5 5 5
    Echinochfoa crus-gaEPi 55 5
    Continued table. 7
    5 55 555
    权利要求:
    Claims (2)
    [1]
    The method of obtaining thiadiazoles of General formula I
    , 11 II II
    · Ν — С-ННА1К
    I
    at
    1 2 £ where Υ is a group ΝΗ 2 or —Y = CE. К К 1 - а К, ЗО 2 а8к, Zayek, 30 2 I (а К) 2 ,
    sesn 2 s (fn 3 ) 2 -, Sun 9 9 2 ,
    and to - Cd-C 1o- alkyl,
    and k / - may be the same
    or different and mean hydrogen,
    C 1 -C 1 () -alkyl, phenyl, unsubstituted or substituted by one or two halogen atoms, alkoxy containing 1-4 carbon atoms, cyano, or their acid additive salts, characterized in that the hydrazone of general formula II
    In 1
    mnm = l e in £
    1 e £
    where K, K. and K have the above values, is subjected to interaction with the isocyanate or with the compound of the formula III
    C 6 H 5 C (CU = ^ O-C-L1CHN 3
    about
    in the presence of a strong base, followed by either isolating the resulting product in free form or as a salt, or in the case of preparing compound (I), where Υ-ΝΗ 2 group, by reacting with concentrated hydrochloric acid or hydrazine and isolating the target product in free form or in the form of salt.
    »8 and 1189343
    >
    one
    1189343
    [2]
    2
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    同族专利:
    公开号 | 公开日
    JPS58140084A|1983-08-19|
    ES8500251A1|1984-10-01|
    ZW2683A1|1983-08-24|
    IL67827D0|1983-06-15|
    US4501605A|1985-02-26|
    HU189221B|1986-06-30|
    DK37483D0|1983-01-31|
    PL240436A1|1985-01-16|
    ES519489A0|1984-10-01|
    DK37483A|1983-08-05|
    BR8300513A|1983-11-08|
    FI830336L|1983-08-05|
    ZA83730B|1983-11-30|
    AU1089483A|1983-08-25|
    CS236871B2|1985-05-15|
    NZ203188A|1985-03-20|
    EP0088484A1|1983-09-14|
    TR21722A|1985-04-19|
    KR840003380A|1984-09-08|
    NO830367L|1983-08-05|
    FI830336A0|1983-02-01|
    AU533703B2|1983-12-08|
    DD206730A5|1984-02-08|
    CA1189513A|1985-06-25|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    GB1195672A|1968-02-01|1970-06-17|Mobil Oil Corp|Novel Urea Derivatives and Herbicides containing the same|
    US3849567A|1970-04-27|1974-11-19|Mobil Oil Corp|Use of thiadiazole hydrazones as bactericides|
    US4239524A|1979-03-05|1980-12-16|Schering Aktiengesellschaft|Thiadiazolyl ureas with herbicidal effect|AU596819B2|1985-12-16|1990-05-17|Eli Lilly And Company|Thiadiazole antiviral agents|
    JP2690742B2|1987-03-30|1997-12-17|第一製薬株式会社|Heterocyclic amine derivative|
    TW280760B|1992-04-28|1996-07-11|Du Pont|
    US8314119B2|2006-11-06|2012-11-20|Abbvie Inc.|Azaadamantane derivatives and methods of use|
    PE20131394A1|2010-09-23|2014-01-11|Abbvie Inc|MONOHYDRATE OF AZA-ADAMANTAN DERIVATIVES|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    GB8203223|1982-02-04|
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