JPH039911B2 - - Google Patents
Info
- Publication number
- JPH039911B2 JPH039911B2 JP2659283A JP2659283A JPH039911B2 JP H039911 B2 JPH039911 B2 JP H039911B2 JP 2659283 A JP2659283 A JP 2659283A JP 2659283 A JP2659283 A JP 2659283A JP H039911 B2 JPH039911 B2 JP H039911B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- general formula
- reaction
- formula
- imidazolidin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000004480 active ingredient Substances 0.000 claims description 12
- 230000002363 herbicidal effect Effects 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical class O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000001188 haloalkyl group Chemical group 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 239000004009 herbicide Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 2
- 150000002513 isocyanates Chemical class 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 description 33
- -1 methoxy, ethoxy, n-propyloxy, isopropyloxy Chemical group 0.000 description 18
- 241000196324 Embryophyta Species 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- 239000000203 mixture Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 239000002689 soil Substances 0.000 description 8
- 239000013078 crystal Substances 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003048 aphrodisiac agent Substances 0.000 description 3
- 230000002509 aphrodisiac effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000012279 sodium borohydride Substances 0.000 description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 description 3
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 241000681978 Rhododendron japonicum Species 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- WUDNUHPRLBTKOJ-UHFFFAOYSA-N ethyl isocyanate Chemical compound CCN=C=O WUDNUHPRLBTKOJ-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- NNZVKALEGZPYKL-UHFFFAOYSA-N 1-isocyanato-2-methylpropane Chemical compound CC(C)CN=C=O NNZVKALEGZPYKL-UHFFFAOYSA-N 0.000 description 1
- OQURWGJAWSLGQG-UHFFFAOYSA-N 1-isocyanatopropane Chemical compound CCCN=C=O OQURWGJAWSLGQG-UHFFFAOYSA-N 0.000 description 1
- DUUSMHZSZWMNCB-UHFFFAOYSA-N 2-isocyanatobutane Chemical compound CCC(C)N=C=O DUUSMHZSZWMNCB-UHFFFAOYSA-N 0.000 description 1
- GSLTVFIVJMCNBH-UHFFFAOYSA-N 2-isocyanatopropane Chemical compound CC(C)N=C=O GSLTVFIVJMCNBH-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 244000144706 Aeschynomene indica Species 0.000 description 1
- 235000004051 Aeschynomene indica Nutrition 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 235000003826 Artemisia Nutrition 0.000 description 1
- 235000017519 Artemisia princeps Nutrition 0.000 description 1
- 244000065027 Artemisia princeps Species 0.000 description 1
- 235000003261 Artemisia vulgaris Nutrition 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241001148728 Calamagrostis epigeios Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 244000301850 Cupressus sempervirens Species 0.000 description 1
- 241000234653 Cyperus Species 0.000 description 1
- 240000008620 Fagopyrum esculentum Species 0.000 description 1
- 235000009419 Fagopyrum esculentum Nutrition 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WRYCSMQKUKOKBP-UHFFFAOYSA-N Imidazolidine Chemical compound C1CNCN1 WRYCSMQKUKOKBP-UHFFFAOYSA-N 0.000 description 1
- 240000001549 Ipomoea eriocarpa Species 0.000 description 1
- 235000005146 Ipomoea eriocarpa Nutrition 0.000 description 1
- 240000000249 Morus alba Species 0.000 description 1
- 235000008708 Morus alba Nutrition 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 241001076438 Oxya japonica Species 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 240000001341 Reynoutria japonica Species 0.000 description 1
- 235000018167 Reynoutria japonica Nutrition 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 235000003095 Vaccinium corymbosum Nutrition 0.000 description 1
- 235000017537 Vaccinium myrtillus Nutrition 0.000 description 1
- 244000077233 Vaccinium uliginosum Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 244000030166 artemisia Species 0.000 description 1
- 235000009052 artemisia Nutrition 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 244000269888 azena Species 0.000 description 1
- 235000021014 blueberries Nutrition 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 125000006003 dichloroethyl group Chemical group 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000013583 drug formulation Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 230000000887 hydrating effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 125000006606 n-butoxy group Chemical group 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- HNHVTXYLRVGMHD-UHFFFAOYSA-N n-butyl isocyanate Chemical compound CCCCN=C=O HNHVTXYLRVGMHD-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は、新規なイミダゾリジン−2−オン誘
導体、その製造方法及び該誘導体を有効成分とす
る除草剤に関する。
本発明のイミダゾリジン−2−オン誘導体は文
献未載の新規化合物であつて、下記一般式〔〕
で示される。
〔式中Rは低級アルキル基を表わす。Xは水素
原子、ハロゲン原子、低級アルキル基、低級アル
コキシ基、ベンジルオキシ基又は低級ハロアルキ
ル基を表わす。nは1〜3の整数を表わす。〕
本明細書において、低級アルキル基としては例
えばメチル基、エチル基、n−プロピル基、イソ
プロピル基、n−ブチル基、sec−ブチル基、イ
ソブチル基、tert−ブチル基等を挙げることがで
きる。ハロゲン原子としては例えば弗素、塩素、
臭素、沃素原子等を挙げることができる。低級ア
ルコキシ基としては例えばメトキシ基、エトキシ
基、n−プロピルオキシ基、イソプロピルオキシ
基、n−ブトキシ基等を挙げることができる。低
級ハロアルキル基としては例えばモノクロルメチ
ル基、モノクロルエチル基、モノクロルプロピル
基、ジクロルエチル基、モノブロムメチル基、モ
ノブロムエチル基、モノブロムプロピル基、モノ
フルオロメチル基、トリフルオロメチル基、トリ
フルオロエチル基等を挙げることができる。
上記一般式〔〕で表わされる本発明の化合物
は種々の方法により製造されるが、その好ましい
一例を挙げれば下記反応式−1に従い製造され
る。
反応式−1
〔式中R、X及びnは前記に同じ。)
上記反応式−1において、出発原料として用い
られる一般式()で示されるイミダゾリジン−
2−オン誘導体は新規化合物であり、例えば下記
反応式−2に従い公知化合物であるヒダントイン
誘導体()を還元することにより得られる。
反応式−2
〔式中X及びnは前記に同じ。〕
一般式〔〕で示される化合物を還元して一般
式〔〕で示される化合物を得る反応は、適当な
溶媒中で行なうことができる。使用される溶媒と
しては、例えば水、メチルアルコール、エチルア
ルコール、プロピルアルコール、ブチルアルコー
ル等のアルコール類、又はジエチルエーテル、ジ
ブチルエーテル、テトラヒドロフラン、ジオキサ
ン等のエーテル類と前記アルコール類との混合溶
媒を挙げることができる。一般式〔〕で示され
る化合物を還元して一般式〔〕で示される化合
物を得る反応での還元剤としては、例えば水素化
ホウ素ナトリウムが使用される。一般式〔〕で
示される化合物と水素化ホウ素ナトリウムとの使
用割合としては、特に限定がなく広い範囲内から
適宜選択できるが、通常前者に対して後者を0.1
〜5倍モル程度、好ましくは0.25〜等モル程度使
用するのがよい。該反応の反応温度としては特に
制限されないが、通常−50〜100℃程度、好まし
くは0〜50℃程度にて反応が好適に進行し、一般
に1〜5時間程度で反応は終了する。
他の一方の出発原料である一般式〔〕で示さ
れるイソシアネートは公知化合物であり、例えば
メチルイソシアネート、エチルイソシアネート、
n−プロピルイソシアネート、イソプロピルイソ
シアネート、n−ブチルイソシアネート、イソブ
チルイソシアネート、sec−ブチルイソシアネー
ト等を挙げることができる。
一般式〔〕の化合物と一般式〔〕の化合物
との反応は、無溶媒下又は溶媒中で行なわれる。
無溶媒下で行なう場合には、一般式〔〕で示さ
れる化合物の揮散を防ぐため、オートクレーブ中
で加圧反応させるのがよい。溶媒中で行なう場合
の溶媒としては、原料に悪影響を与えない溶媒で
あれば可能であるが、例えばジエチルエーテル、
ジプロピルエーテル、ジブチルエーテル、テトラ
ヒドロフラン、ジオキサン等のエーテル類、塩化
メチレン、クロロホルム等のハロゲン化炭化水素
類、ベンゼン、トルエン、キシレン、クロルベン
ゼン等の芳香族系溶媒、ピリジン、アセトニトリ
ル、N,N−ジメチルホルムアミド等を使用する
ことができる。一般式〔〕で示される化合物と
一般式〔〕で示される化合物との使用割合とし
ては、特に限定がなく広い範囲内から適宜選択で
きるが、通常前者に対して後者を等モル〜5倍モ
ル程度、好ましくは等モル〜2倍モル程度使用す
るのがよい。
一般式〔〕で示される化合物と一般式〔〕
で示される化合物との反応を無溶媒下で行なう場
合には、触媒を使用しても使用しなくてもよい
が、溶媒中で行なう場合には、触媒を使用するの
が好ましい。使用される触媒としては、例えば第
3級アミン類、具体的にはトリエチルアミン、ト
リブチルアミン、N,N−ジメチルアニリン、ヘ
キサメチレンテトラミン等を挙げることができ
る。触媒の使用量としては、通常の触媒量でよ
く、例えば一般式〔〕で示される化合物に対し
て通常0.01〜0.5モル程度使用するのがよい。該
反応の反応温度としては特に制限されないが、通
常0〜150℃程度にて反応が進行し、一般に3〜
15時間程度で反応は完結する。
斯くして得られた一般式〔〕の本発明化合物
は、常法の手段、例えば再結晶、溶媒抽出、カラ
ムクロマトグラフイー等で容易に精製される。
上記の方法で得られる本発明の化合物を例示す
ると以下の通りである。
Γ3−メチル−4−メチルカルバモイルオキシイ
ミダゾリジン−2−オン−1−カルボキシアニ
リド
Γ3−メチル−4−エトキシカルバモイルオキシ
イミダゾリジン−2−オン−1−カルボキシア
ニリド
Γ3−メチル−4−イソプロピルカルバモイルオ
キシイミダゾリジン−2−オン−1−カルボキ
シアニリド
Γ2′,3′−ジメチル−4−メチルカルバモイルオ
キシイミダゾリジン−2−オン−1−カルボキ
シアニリド
Γ3,3′−ジメチル−4−メチルカルバモイルオ
キシイミダゾリジン−2−オン−1−カルボキ
シアニリド
Γ2′−クロル−3−メチル−4−メチルカルバモ
イルオキシイミダゾリジン−2−オン−1−カ
ルボキシアニリド
Γ2′−クロル−3−メチル−4−イソプロピルカ
ルバモイルオキシイミダゾリジン−2−オン−
1−カルボキシアニリド
Γ2′,4′−ジクロル−3−メチル−4−メチルカ
ルバモイルオキシイミダゾリジン−2−オン−
1−カルボキシアニリド
Γ3′−クロル−3−メチル−4−メチルカルバモ
イルオキシイミダゾリジン−2−オン−1−カ
ルボキシアニリド
Γ 3−メチル−4′−メトキシ−4−メチルカル
バモイルオキシイミダゾリジン−2−オン−1
−カルボキシアニリド
Γ3−メチル−4′−トリフルオロメチル−4−メ
チルカルバモイルオキシイミダゾリジン−2−
オン−1−カルボキシアニリド
Γ3−メチル−4′−ベンジルオキシ−4−メチル
カルバモイルオキシイミダゾリジン−2−オン
−1−カルボキシアニリド
本発明はまた前記一般式〔〕で示されるイミ
ダゾリジン−2−オン誘導体を有効成分とする除
草剤に関する。
本発明の化合物は、タカサブロウ、アオビユ、
クサネム、スズメノテツポウ、タデ、ヨモギ、オ
オアレチノギク、ギシギシ、アゼナ、キカシグ
サ、ノビエ、メヒシバ、オヒシバ、カヤツリグサ
等の雑草に対して強力な除草効果を示すので、そ
れらの雑草の生育が有害となるミカン、リンゴ、
ダイズ、トウモロコシ、桑、茶、水稲等の農作物
の生産や景観上有害な雑草の防除に有用である。
本発明化合物を除草剤として施用するに当つて
は、本発明化合物をそのまま用いてもよいが、一
般には通常農薬の製剤上使用される補助剤と混合
していずれの剤型としても使用することができ
る。その中でも乳剤、水和剤、粒剤の形態が好適
に用いられる。この際、効果の安定性及び効果の
向上を期するための補助剤としては、例えばケイ
ソウ土、カオリン、クレー、ベントナイト、ホワ
イトカーボン、タルク等の増量剤、ポリオキシエ
チレンアルキルエーテル、ポリオキシエチレンア
ルキルフエニルエーテル、ポリオキシエチレンソ
ルビタン脂肪酸エステル、ポリオキシエチレン脂
肪酸エステル、アルキルベンゼンスルホン酸ナト
リウム、リグニンスルホン酸ナトリウム、アルキ
ル硫酸ナトリウム、ポリオキシエチレンアルキル
硫酸ナトリウム等の非イオン系あるいは陰イオン
系界面活性剤、キシロール、アセトン、メタノー
ル、エタノール、イソプロパノール、ジオキサ
ン、ジメチルホルムアミド、ジメチルスルホキサ
イド、四塩化炭素等の有機溶媒等が使用される。
本発明の除草剤組成物の配合としては、有効成
分が約1〜90重量%、好ましくは約5〜70重量%
になるように補助剤を添加することによつて製剤
される。施用適量は薬剤の製剤形態、施用方法、
施用時期、対象雑草の種類ならびに特に除草効果
に影響を与えやすい気象条件、土壌条件等によつ
てそれぞれ異なるものであり、広い範囲内から適
宜選択されるが、一般的には有効成分量として約
5〜400g/a程度、好ましくは約10〜100g/a
程度が散布される。
以下に参考例、実施例、処方例及び試験例を挙
げて本発明を更に詳しく説明する。尚、試験例に
おける供試化合物番号は実施例の番号に対応す
る。
参考例 1
3,3′−ジメチル−4−ヒドロキシイミダゾリ
ジン−2−オン−1−カルボキシアニリドの製
造
3,3′−ジメチルイミダゾリジン−2,5−ジ
オン−1−カルボキシアニリド7.4g(0.03モル)
をメタノール50mlに懸濁した。10℃に冷却後、攪
拌下で水素化ホウ素ナトリウム1.2g(0.03モル)
を加えた。30分攪拌後、室温に戻し、更に2時間
攪拌した。反応終了後、反応液を濃縮し、残渣に
水を加えて結晶を析出させた。結晶を濾過後エタ
ノールより再結晶し、無色結晶6.7g(収率90%)
を得た。
融点 164〜164.5℃
実施例 1
3,3′−ジメチル−5−メチルカルバモイルオ
キシイミダゾリジン−2−オン−1−カルボキ
シアニリドの製造
3,3′−ジメチル−5−ヒドロキシイミダゾリ
ジン−2−オン−1−カルボキシアニリド5.0g
(0.02モル)をクロロホルム50mlに溶解し、トリ
エチルアミン0.5mlを添加した。5℃に冷却後、
攪拌下でイソシアン酸メチル1.7g(0.03モル)
を滴下した。30分攪拌後、室温に戻し、更に5時
間攪拌した。反応終了後、反応液を減圧濃縮し、
結晶性残渣を得た。これをエタノールより再結晶
し、無色結晶5.2g(収率85%)を得た。
融点 130〜131℃
結晶の重クロロホルム中でのNMRは次のよう
に示した。
δ 2.30ppm(3H)、δ 2.77ppm(3H)
δ 2.80ppm(3H)、δ 3.30ppm(1H)
δ 5.17ppm(1H)、δ 6.75ppm(1H)
δ 6.80〜7.50ppm(4H)
元素分析値(C14H18N4O4=306.32)
分析値% C54.85 H5.93 N18.31
理論値% C54.89 H5.92 N18.29
以上の結果より
を確認した。
実施例 2
4′−クロル−3−メチル−5−エチルカルバモ
イルオキシイミダゾリジン−2−オン−1−カ
ルボキシアニリドの製造
4′−クロル−3−メチル−5−ヒドロキシイミ
ダゾリジン−2−オン−1−カルボキシアニリド
2.7g(0.01モル)をクロロホルム40mlに溶解し、
トリエチルアミン0.4mlを添加した。5℃に冷却
後、攪拌下でイソシアン酸エチル1.1g(0.015モ
ル)を滴下した。30分攪拌後、室温に戻し、更に
12時間攪拌した。反応終了後、反応液を減圧濃縮
し結晶性残渣を得た。これをエタノールより再結
晶し、無色結晶2.6g(収率77%)を得た。
融点 156〜157℃
結晶の重クロロホルム中でのNMRは次のよう
に示した。
δ 1.12ppm(3H)、δ 2.82ppm(3H)
δ 3.10〜3.50ppm(3H)
δ 3.70ppm(1H)、δ 5.20ppm(1H)
δ 6.70ppm(1H)、δ 7.28ppm(2H)
7.53ppm(2H)
元素分析値(C14H17N4O4Cl=340.77)
分析値% C49.30 H5.05 N16.45
理論値% C49.35 H5.03 N16.44
以上の結果より
を確認した。
実施例 3〜17
実施例1,2と同様の操作を行ない実施例3〜
17の化合物を得た。融点とNMRデーターを第1
表に示した。
The present invention relates to a novel imidazolidin-2-one derivative, a method for producing the same, and a herbicide containing the derivative as an active ingredient. The imidazolidin-2-one derivative of the present invention is a new compound that has not been described in any literature, and has the following general formula []
It is indicated by. [In the formula, R represents a lower alkyl group. X represents a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a benzyloxy group, or a lower haloalkyl group. n represents an integer from 1 to 3. ] In this specification, examples of lower alkyl groups include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, isobutyl group, and tert-butyl group. Examples of halogen atoms include fluorine, chlorine,
Examples include bromine and iodine atoms. Examples of lower alkoxy groups include methoxy, ethoxy, n-propyloxy, isopropyloxy, and n-butoxy groups. Examples of lower haloalkyl groups include monochloromethyl group, monochloroethyl group, monochloropropyl group, dichloroethyl group, monobromomethyl group, monobromoethyl group, monobromopropyl group, monofluoromethyl group, trifluoromethyl group, and trifluoroethyl group. etc. can be mentioned. The compound of the present invention represented by the above general formula [] can be produced by various methods, but one preferred example thereof is produced according to the following reaction formula-1. Reaction formula-1 [In the formula, R, X and n are the same as above. ) In the above reaction formula-1, the imidazolidine represented by the general formula () used as a starting material -
The 2-one derivative is a new compound, and can be obtained, for example, by reducing a known compound, a hydantoin derivative (), according to Reaction Formula-2 below. Reaction formula-2 [In the formula, X and n are the same as above. ] The reaction of reducing the compound represented by the general formula [] to obtain the compound represented by the general formula [] can be carried out in an appropriate solvent. Examples of the solvent used include water, alcohols such as methyl alcohol, ethyl alcohol, propyl alcohol, and butyl alcohol, or mixed solvents of the above-mentioned alcohols and ethers such as diethyl ether, dibutyl ether, tetrahydrofuran, and dioxane. be able to. For example, sodium borohydride is used as a reducing agent in the reaction of reducing the compound represented by the general formula [] to obtain the compound represented by the general formula []. The ratio of the compound represented by the general formula [] and sodium borohydride is not particularly limited and can be appropriately selected from a wide range, but usually the latter is 0.1% of the former.
It is preferable to use about 5 to 5 times the mole, preferably about 0.25 to about the same mole. The reaction temperature for this reaction is not particularly limited, but the reaction normally proceeds suitably at about -50 to 100°C, preferably about 0 to 50°C, and is generally completed in about 1 to 5 hours. The other starting material, the isocyanate represented by the general formula [], is a known compound, such as methyl isocyanate, ethyl isocyanate,
Examples include n-propylisocyanate, isopropylisocyanate, n-butyl isocyanate, isobutyl isocyanate, sec-butyl isocyanate, and the like. The reaction between the compound of general formula [] and the compound of general formula [] is carried out without a solvent or in a solvent.
When carrying out the reaction without a solvent, it is preferable to carry out the reaction under pressure in an autoclave in order to prevent the compound represented by the general formula [] from volatilizing. When carrying out the process in a solvent, any solvent that does not adversely affect the raw materials can be used, such as diethyl ether,
Ethers such as dipropyl ether, dibutyl ether, tetrahydrofuran and dioxane, halogenated hydrocarbons such as methylene chloride and chloroform, aromatic solvents such as benzene, toluene, xylene and chlorobenzene, pyridine, acetonitrile, N,N- Dimethylformamide and the like can be used. The usage ratio of the compound represented by the general formula [] and the compound represented by the general formula [] is not particularly limited and can be appropriately selected from a wide range, but the latter is usually equivalent to 5 times the molar amount of the former. It is preferable to use about the same mole to about 2 times the mole. Compounds represented by general formula [] and general formula []
When the reaction with the compound represented by is carried out without a solvent, a catalyst may or may not be used, but when the reaction is carried out in a solvent, it is preferable to use a catalyst. Examples of the catalyst used include tertiary amines, specifically triethylamine, tributylamine, N,N-dimethylaniline, hexamethylenetetramine, and the like. The amount of the catalyst to be used may be a normal catalyst amount, for example, it is usually about 0.01 to 0.5 mole based on the compound represented by the general formula []. The reaction temperature for this reaction is not particularly limited, but the reaction usually proceeds at about 0 to 150°C, and generally at about 3 to 150°C.
The reaction is completed in about 15 hours. The compound of the present invention having the general formula [] thus obtained can be easily purified by conventional methods such as recrystallization, solvent extraction, column chromatography, etc. Examples of the compounds of the present invention obtained by the above method are as follows. Γ3-Methyl-4-methylcarbamoyloxyimidazolidin-2-one-1-carboxyanilide Γ3-methyl-4-ethoxycarbamoyloxyimidazolidin-2-one-1-carboxyanilide Γ3-methyl-4-isopropylcarbamoyloxyimidazo Lysin-2-one-1-carboxyanilide Γ2',3'-dimethyl-4-methylcarbamoyloxyimidazolidin-2-one-1-carboxyanilide Γ3,3'-dimethyl-4-methylcarbamoyloxyimidazolidine-2 -one-1-carboxyanilide Γ2'-chloro-3-methyl-4-methylcarbamoyloxyimidazolidin-2-one-1-carboxyanilide Γ2'-chloro-3-methyl-4-isopropylcarbamoyloxyimidazolidine-2 -on-
1-carboxyanilide Γ2',4'-dichloro-3-methyl-4-methylcarbamoyloxyimidazolidin-2-one-
1-carboxyanilide Γ3'-chloro-3-methyl-4-methylcarbamoyloxyimidazolidin-2-one-1-carboxyanilide Γ 3-methyl-4'-methoxy-4-methylcarbamoyloxyimidazolidin-2-one -1
-carboxyanilide Γ3-methyl-4'-trifluoromethyl-4-methylcarbamoyloxyimidazolidine-2-
imidazolidin-2-one-1-carboxyanilide Γ3-methyl-4'-benzyloxy-4-methylcarbamoyloxyimidazolidin-2-one-1-carboxyanilide The present invention also provides imidazolidin-2-one represented by the general formula [] This invention relates to a herbicide containing a derivative as an active ingredient. The compounds of the present invention include Takasaburou, Aobiyu,
It exhibits a strong herbicidal effect against weeds such as Japanese grasshopper, Japanese knotweed, artemisia, Japanese mugwort, Japanese aphrodisiac, Japanese aphrodisiac, Japanese azalea, Japanese bush grass, Japanese wild grass, Japanese aphrodisiac, Japanese cyperus, and other weeds.
It is useful for the production of agricultural crops such as soybean, corn, mulberry, tea, and paddy rice, and for controlling weeds that are harmful to the landscape. When applying the compound of the present invention as a herbicide, the compound of the present invention may be used as it is, but in general, it may be mixed with an adjuvant commonly used in the formulation of agricultural chemicals and used in any dosage form. Can be done. Among these, emulsion, wettable powder, and granule forms are preferably used. At this time, examples of auxiliary agents to improve stability and effectiveness include fillers such as diatomaceous earth, kaolin, clay, bentonite, white carbon, and talc, polyoxyethylene alkyl ether, and polyoxyethylene alkyl ether. Nonionic or anionic surfactants such as phenyl ether, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene fatty acid ester, sodium alkylbenzene sulfonate, sodium lignin sulfonate, sodium alkyl sulfate, sodium polyoxyethylene alkyl sulfate, Organic solvents such as xylol, acetone, methanol, ethanol, isopropanol, dioxane, dimethylformamide, dimethyl sulfoxide, and carbon tetrachloride are used. The herbicidal composition of the present invention is formulated so that the active ingredient is about 1 to 90% by weight, preferably about 5 to 70% by weight.
It is formulated by adding adjuvants to achieve the desired results. The appropriate amount to be applied depends on the drug formulation form, application method,
The amount of active ingredient varies depending on the time of application, the type of target weed, and the weather conditions and soil conditions that tend to affect the herbicidal effect, and is selected appropriately from a wide range, but in general, the amount of active ingredient is approximately About 5 to 400 g/a, preferably about 10 to 100 g/a
The degree is scattered. The present invention will be explained in more detail by referring to Reference Examples, Examples, Prescription Examples, and Test Examples below. Note that the test compound numbers in the test examples correspond to the numbers in the examples. Reference Example 1 Production of 3,3'-dimethyl-4-hydroxyimidazolidin-2-one-1-carboxyanilide 7.4 g (0.03 mol) of 3,3'-dimethylimidazolidine-2,5-dione-1-carboxyanilide )
was suspended in 50 ml of methanol. After cooling to 10°C, add 1.2 g (0.03 mol) of sodium borohydride under stirring.
added. After stirring for 30 minutes, the mixture was returned to room temperature and further stirred for 2 hours. After the reaction was completed, the reaction solution was concentrated, and water was added to the residue to precipitate crystals. After filtering the crystals, recrystallization from ethanol yielded 6.7 g of colorless crystals (yield 90%).
I got it. Melting point 164-164.5°C Example 1 Production of 3,3'-dimethyl-5-methylcarbamoyloxyimidazolidin-2-one-1-carboxanilide 3,3'-dimethyl-5-hydroxyimidazolidin-2-one- 1-carboxyanilide 5.0g
(0.02 mol) was dissolved in 50 ml of chloroform, and 0.5 ml of triethylamine was added. After cooling to 5℃,
1.7 g (0.03 mol) of methyl isocyanate under stirring
was dripped. After stirring for 30 minutes, the mixture was returned to room temperature and further stirred for 5 hours. After the reaction is completed, the reaction solution is concentrated under reduced pressure.
A crystalline residue was obtained. This was recrystallized from ethanol to obtain 5.2 g of colorless crystals (yield: 85%). Melting point: 130-131°C NMR of the crystal in deuterated chloroform showed the following. δ 2.30ppm (3H), δ 2.77ppm (3H) δ 2.80ppm (3H), δ 3.30ppm (1H) δ 5.17ppm (1H), δ 6.75ppm (1H) δ 6.80-7.50ppm (4H) Elemental analysis value (C 14 H 18 N 4 O 4 = 306.32) Analytical value % C54.85 H5.93 N18.31 Theoretical value % C54.89 H5.92 N18.29 From the above results It was confirmed. Example 2 Preparation of 4'-chloro-3-methyl-5-ethylcarbamoyloxyimidazolidin-2-one-1-carboxyanilide 4'-chloro-3-methyl-5-hydroxyimidazolidin-2-one-1 -carboxyanilide
Dissolve 2.7g (0.01mol) in 40ml of chloroform,
0.4 ml of triethylamine was added. After cooling to 5° C., 1.1 g (0.015 mol) of ethyl isocyanate was added dropwise while stirring. After stirring for 30 minutes, return to room temperature, and then
Stirred for 12 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure to obtain a crystalline residue. This was recrystallized from ethanol to obtain 2.6 g of colorless crystals (yield 77%). Melting point: 156-157°C NMR of the crystal in deuterated chloroform showed the following. δ 1.12ppm (3H), δ 2.82ppm (3H) δ 3.10~3.50ppm (3H) δ 3.70ppm (1H), δ 5.20ppm (1H) δ 6.70ppm (1H), δ 7.28ppm (2H) 7.53ppm ( 2H) Elemental analysis value (C 14 H 17 N 4 O 4 Cl = 340.77) Analysis value % C49.30 H5.05 N16.45 Theoretical value % C49.35 H5.03 N16.44 From the above results It was confirmed. Examples 3 to 17 Performing the same operations as in Examples 1 and 2, Examples 3 to 17
17 compounds were obtained. Melting point and NMR data first
Shown in the table.
【表】【table】
【表】【table】
【表】
処方例1(30%乳剤)
(重量部)
実施例1の化合物 30
ポリオキシエチレンノニル 10
フエニルエーテルジメチルホルムアミド 20
キシレン 40
処方例2(50%水和剤)
実施例2の化合物 50
リグニンスルホン酸ナトリウム 1
ドデシルベンゼンスルホン酸ナトリウム 4
クレー 45
処方例3(10%粒剤)
実施例3の化合物 10
リグニンスルホン酸ナトリウム 0.5
ドデシルベンゼンスルホン酸ナトリウム 2
ケイソウ土 27.5
ベントナイト 60
尚、乳剤の場合には、各成分を均一に混合溶解
し、水和剤の場合には、各成分を均一に混合粉砕
してそれらを得ることができる。また粒剤の場合
には、各成分を均一に混合し、水を加えて充分混
練したのち造粒し、次いで細かく切断して粒状の
ものとし、乾燥して製造される。
試験例1(茎葉処理テスト)
1/2000aのワグナーポツトに殺菌した沖積土壌
を入れ、第2表に示す供試植物の種子を播種し、
各植物がほぼ一定の大きさ(ほぼ2〜3葉期)に
達したとき、実施例に示す方法で得た化合物を有
効成分とする乳剤を処方例1に準じて製剤し、そ
れぞれ有効成分が100g/aとなるように水で希
釈したものを植物の茎葉全面が充分一様に濡れる
ように散布した。散布後3週間目に各植物に対す
る除草活性を調べた。その結果を第2表に示す。
尚、除草活性は肉眼観察により次の基準に従つて
無処理の場合と対比した指数で評価した。
(指数) (除草活性)
0 変化なし
1 1〜24%阻害
2 25〜49%阻害
3 50〜74%阻害
4 75〜90%阻害
5 完全枯死[Table] Formulation example 1 (30% emulsion) (parts by weight) Compound of Example 1 30 Polyoxyethylene nonyl 10 Phenyl ether dimethylformamide 20 Xylene 40 Formulation example 2 (50% hydrating agent) Compound of Example 2 50 Sodium ligninsulfonate 1 Sodium dodecylbenzenesulfonate 4 Clay 45 Formulation example 3 (10% granules) Compound of Example 3 10 Sodium ligninsulfonate 0.5 Sodium dodecylbenzenesulfonate 2 Diatomaceous earth 27.5 Bentonite 60 In the case of emulsion They can be obtained by uniformly mixing and dissolving each component, and in the case of a wettable powder, by uniformly mixing and pulverizing each component. In the case of granules, the ingredients are uniformly mixed, water is added and thoroughly kneaded, and then granulated, then finely cut into granules and dried. Test Example 1 (Stem and Leaf Treatment Test) Sterilized alluvial soil was placed in a 1/2000a Wagner pot, and seeds of the test plants shown in Table 2 were sown.
When each plant reaches an approximately certain size (approximately 2 to 3 leaf stage), an emulsion containing the compound obtained by the method shown in the example as an active ingredient is formulated according to Formulation Example 1, and each of the active ingredients is A solution diluted with water to a concentration of 100 g/a was sprayed so that the entire surface of the stems and leaves of the plant was thoroughly and uniformly wetted. Three weeks after spraying, the herbicidal activity on each plant was examined. The results are shown in Table 2.
The herbicidal activity was evaluated by visual observation using an index in comparison with that of no treatment according to the following criteria. (Index) (Herbicidal activity) 0 No change 1 1-24% inhibition 2 25-49% inhibition 3 50-74% inhibition 4 75-90% inhibition 5 Complete death
【表】
上表において供試植物A〜Hは次の植物であ
る。
A……アオビユ B……クサネム
C……ノビエ D……ダイコン
E……ソバ F……アサガオ
G……コムギ H……タカサブロウ
試験例2 (土壌処理テスト)
1/2000aのワグナーポツトに殺菌した沖積土壌
を入れ、第3表に示す供試植物の種子を播種し
て、約0.5〜1.0cm覆土した。次いで実施例に示す
方法で得た化合物を有効成分とする水和剤を処方
例2に準じて製剤し、それぞれ有効成分が100
g/aとなるように水で希釈し、これを土壌表面
が均一に濡れるように散布した。散布後3週間目
に各植物に対する除草活性を調べた。その結果を
第3表に示す。評価の基準は試験例1と同じであ
る。[Table] In the above table, test plants A to H are the following plants. A... Blueberry B... Kusanemu C... Wildflower D... Radish E... Buckwheat F... Morning glory G... Wheat H... Takasaburou test example 2 (Soil treatment test) Alluvial soil sterilized in a 1/2000a Wagner pot The seeds of the test plants shown in Table 3 were sown and covered with soil to a depth of about 0.5 to 1.0 cm. Next, wettable powders containing the compound obtained by the method shown in the example as an active ingredient were prepared according to Formulation Example 2, and each powder contained 100% of the active ingredient.
It was diluted with water to give a ratio of g/a, and was sprayed so that the soil surface was evenly wetted. Three weeks after spraying, the herbicidal activity on each plant was examined. The results are shown in Table 3. The evaluation criteria were the same as in Test Example 1.
【表】
対照化合物は第2表と同じである。また供試植
物A〜Gは第2表と同じである。
試験例3(湛水処理テスト)
1/5000aのワグナーポツトに水田土壌を入れ、
さらにその表層にそれぞれノビエ、タマガヤツ
リ、アゼナ及びキカシグサの種子が混入している
土を入れたのち、水深を3cmに保つた。次いで実
施例で示す方法で得た化合物を有効成分とする粒
剤を処方例3に準じて製剤し、それぞれ有効成分
が50g/aとなるように均一に散布し、薬剤施用
後3週間目に各植物に対する除草活性を調べた。
結果を第4表に示す。評価の基準は試験例1と同
じである。[Table] The control compounds are the same as in Table 2. Moreover, the test plants A to G are the same as those in Table 2. Test example 3 (flooding treatment test) Paddy soil was placed in a 1/5000a Wagner pot.
Furthermore, soil mixed with seeds of Japanese wildflower, Japanese cypress, Japanese azalea, and Kikashigusa seeds was added to the surface layer, and the water depth was maintained at 3 cm. Next, granules containing the compound obtained by the method shown in the example as an active ingredient were prepared according to Formulation Example 3, and the active ingredient was uniformly dispersed at 50 g/a. Three weeks after application, Herbicidal activity against each plant was examined.
The results are shown in Table 4. The evaluation criteria were the same as in Test Example 1.
【表】【table】
【表】
対照化合物は第2表と同じである。また供試植
物C,I〜Kは次の通りである。
C……ノビエ I……タマガヤツリ
J……アゼナ K……キカシグサ[Table] The control compounds are the same as in Table 2. The test plants C, I to K are as follows. C...Novie I...Tamagayatsuri J...Azena K...Kikashigusa
Claims (1)
原子、ハロゲン原子、低級アルキル基、低級アル
コキシ基、ベンジルオキシ基又は低級ハロアルキ
ル基を表わす。nは1〜3の整数を表わす。〕 で示されるイミダゾリジン−2−オン誘導体。 2 一般式 〔式中Xは水素原子、ハロゲン原子、低級アル
キル基、低級アルコキシ基、ベンジルオキシ基又
は低級ハロアルキル基を表わす。nは1〜3の整
数を表わす。〕 で示されるイミダゾリジン−2−オン誘導体と一
般式 RNCO 〔式中Rは低級アルキル基を表わす。〕 で示されるイソシアネートを反応させて一般式 〔式中R、X及びnは前記に同じ。〕 で示されるイミダゾリジン−2−オン誘導体を得
ることを特徴とするイミダゾリジン−2−オン誘
導体の製造方法。 3 一般式 〔式中Rは低級アルキル基を表わす。Xは水素
原子、ハロゲン原子、低級アルキル基、低級アル
コキシ基、ベンジルオキシ基又は低級ハロアルキ
ル基を表わす。nは1〜3の整数を表わす。〕 で示されるイミダゾリジン−2−オン誘導体を有
効成分とする除草剤。[Claims] 1. General formula [In the formula, R represents a lower alkyl group. X represents a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a benzyloxy group, or a lower haloalkyl group. n represents an integer from 1 to 3. ] An imidazolidin-2-one derivative represented by: 2 General formula [In the formula, X represents a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a benzyloxy group, or a lower haloalkyl group. n represents an integer from 1 to 3. ] An imidazolidin-2-one derivative represented by the general formula RNCO [wherein R represents a lower alkyl group]. ] The isocyanate represented by is reacted to form the general formula [In the formula, R, X and n are the same as above. ] A method for producing an imidazolidin-2-one derivative, which comprises obtaining an imidazolidin-2-one derivative represented by the following. 3 General formula [In the formula, R represents a lower alkyl group. X represents a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a benzyloxy group, or a lower haloalkyl group. n represents an integer from 1 to 3. ] A herbicide containing an imidazolidin-2-one derivative as an active ingredient.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2659283A JPS59152375A (en) | 1983-02-18 | 1983-02-18 | Imidazolidin-2-one derivative |
US06/619,149 US4578107A (en) | 1982-09-27 | 1983-09-27 | Herbicidal imidazolidine-2-one derivatives |
PCT/JP1983/000318 WO1984001383A1 (en) | 1982-09-27 | 1983-09-27 | Imidazolidin-2-one derivatives, process for their preparation, and herbicides containing them |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2659283A JPS59152375A (en) | 1983-02-18 | 1983-02-18 | Imidazolidin-2-one derivative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59152375A JPS59152375A (en) | 1984-08-31 |
JPH039911B2 true JPH039911B2 (en) | 1991-02-12 |
Family
ID=12197802
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2659283A Granted JPS59152375A (en) | 1982-09-27 | 1983-02-18 | Imidazolidin-2-one derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59152375A (en) |
-
1983
- 1983-02-18 JP JP2659283A patent/JPS59152375A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59152375A (en) | 1984-08-31 |
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