KR840002811A - 테트라히드로프탈이미드 화합물과 그 제조방법 및 사용 - Google Patents
테트라히드로프탈이미드 화합물과 그 제조방법 및 사용 Download PDFInfo
- Publication number
- KR840002811A KR840002811A KR1019820005661A KR820005661A KR840002811A KR 840002811 A KR840002811 A KR 840002811A KR 1019820005661 A KR1019820005661 A KR 1019820005661A KR 820005661 A KR820005661 A KR 820005661A KR 840002811 A KR840002811 A KR 840002811A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- hydrogen
- compound
- bromine
- chlorine
- 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.)
- Ceased
Links
- SPAMRUYRVYMHPV-UHFFFAOYSA-N 3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical class C1=CCCC2C(=O)NC(=O)C21 SPAMRUYRVYMHPV-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 150000001875 compounds Chemical class 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 5
- 229910052794 bromium Chemical group 0.000 claims 5
- 239000000460 chlorine Substances 0.000 claims 5
- 229910052801 chlorine Inorganic materials 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- -1 4-Chloro-2-fluoro-5-methoxy carbonyl methoxyphenyl Chemical group 0.000 claims 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 239000001301 oxygen Substances 0.000 claims 4
- 230000002363 herbicidal effect Effects 0.000 claims 3
- 241000196324 Embryophyta Species 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 244000068988 Glycine max Species 0.000 claims 1
- 235000010469 Glycine max Nutrition 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 240000008042 Zea mays Species 0.000 claims 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 235000005822 corn Nutrition 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 150000003464 sulfur compounds Chemical class 0.000 claims 1
- 238000009333 weeding Methods 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Indole Compounds (AREA)
Abstract
Description
Claims (14)
- 일반식 :의 화합물, 위 식에서 R1은 수소, 알킬, 저급시클로알킬, 저급알킬(저급)시클로알킬, 저급시클로알킬(저급)알킬, 저급알콕시(저급)알킬, 저급알켄일, 저급시클로알켄일, 저급시클로알켄일(저급)알킬, 페닐, 시아노(저급)알킬, 저급알킨일, 저급알킬리덴아미노, 저급알킬티오(저급)알킬, 벤질, 할로(저급)알킬 또는 저급시클로알킬리데아미노산이고, R2는 수소, 저급알킬 또는 저급알콕시이며, X는 염소 또는 브롬이고, Y는 산소 또는 아미노이며, 그리고 Z는 산소 또는 황이다.
- 청구범위 제1항에 있어서, R1이 수소, C1-C6알킬, C3-C7시클로알킬, C1-C6알킬(C3-C7)시클로알킬, C3-C7시클로알킬 (C1-C6)알킬, C1-C6알콕시 (C1-C6)알킬, C2-C6알켄일, C5-C6시클로알켄일, C5-C6시클로알켄일(C1-C|6)알킬, 페닐, 시이노(C1-C6)알킬, C2-C6알킨일, C1-C6알킬리덴아미노, C1-C6알킬티오 (C1-C6)알킬, 벤질, 클로로(C1-C6)알킬, 브로모(C1-C6)알킬 또는 C3-C|7시클로알킬리덴아미노이고, R2는 수소, C1-C6알킬 또는 C1-C6알콕시이며, X는 염소 또는 브롬이고, Y는 산소 또는 이미노이며, 그리고 Z는 산소 또는 황으로된 화합물.
- 청구의 범위 제1항에 있어서, R2가 수소 또는 저급알킬인 화합물.
- 청구범위 제1항에 있어서, R2가 수소 또는 메틸인 화합물.
- 2-(4-클로로-2-플로오로-5-메톡시 카르보닐 메톡시페닐)-4,5,6,7,-테트하드로-2H-인돌-1,3-디온.
- 2-(4-클로로-2-플로오로-5-펜틸톡시 카르보닐 메톡시페닐)-4,5,6,7,-테트하드로-2H-인돌-1,3-디온.
- 2-(4-클로로-2-플로오로-5-시클로펜틸 메틸이미노페닐)-4,5,6,7,-테트라히드로-2H-인돌-1,3-디온.
- 일반식 :의 HY-페닐테트라히드로프탈이미드를 일반식:의 α-할로카르복시산에스테르와 1 내지 240시간동안 0 내지 200℃로 탈할로겐 수소제의 존재 또는 부존하의 용매에서 반응시키는 것으로 된 청구범위 제1항에 의거한 화합물 제조방법.위 식에서 X 및 Y들의 청구범위 제1항에서 정의한 바와 같고, A는 염소 또는 브롬이며, 그리고 R1, R2및 Z들은 각각 청구범위 제1항에서 정의한 바와 같다.
- 유효성분으로 제초에 유효한 량의 청구범위 제1항의 화합물을 함유한 제초 조성물.
- 잡초가 생장 하거나 또는 생장할 수 있는 지역에 제초에 유효한 량의 청구범위 제1항의 화합물을 사용하는 것으로 된 경작지의 잡초를 억제 또는 근절하는 방법.
- 청구범위 제10항에 있어서, 경작지가 옥수수 또는 대두밭인 방법.
- 제초제로서 청구범위 제1항에 의거한 화합물을 사용하는 것.
- X가 염소원자 또는 브롬원자인 일반식의 화합물.
- X가 염소원자 또는 브롬원자인 일반식의 화합물.※참고사항:최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP212396 | 1981-12-25 | ||
| JP56212396A JPS58110566A (ja) | 1981-12-25 | 1981-12-25 | 2−フエニル−4,5,6,7−テトラヒドロ−2h−イソインド−ル誘導体、その製造法およびそれを有効成分とする除草剤 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR840002811A true KR840002811A (ko) | 1984-07-21 |
Family
ID=16621888
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019820005661A Ceased KR840002811A (ko) | 1981-12-25 | 1982-12-17 | 테트라히드로프탈이미드 화합물과 그 제조방법 및 사용 |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JPS58110566A (ko) |
| KR (1) | KR840002811A (ko) |
| ZA (1) | ZA829023B (ko) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55139359A (en) * | 1979-04-13 | 1980-10-31 | Mitsubishi Chem Ind Ltd | Tetrahydrophthalimides, and herbicide containing compound as effective component |
| JPH0245621B2 (ja) * | 1980-10-07 | 1990-10-11 | Mitsubishi Chem Ind | Tetorahidorofutaruimidoruioyobikoreojukoseibuntosurujosozai |
| JPS5813567A (ja) * | 1981-06-29 | 1983-01-26 | ロ−ム・アンド・ハ−ス・コンパニ− | 置換フタルイミド化合物およびその除草性組成物 |
-
1981
- 1981-12-25 JP JP56212396A patent/JPS58110566A/ja active Granted
-
1982
- 1982-12-08 ZA ZA829023A patent/ZA829023B/xx unknown
- 1982-12-17 KR KR1019820005661A patent/KR840002811A/ko not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58110566A (ja) | 1983-07-01 |
| JPH0247467B2 (ko) | 1990-10-19 |
| ZA829023B (en) | 1983-09-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19821217 |
|
| PG1501 | Laying open of application | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 19871014 Comment text: Request for Examination of Application Patent event code: PA02011R01I Patent event date: 19821217 Comment text: Patent Application |
|
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 19881229 Patent event code: PE09021S01D |
|
| PE0601 | Decision on rejection of patent |
Patent event date: 19890429 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 19881229 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |