LV10023B - Geometrical isomer of 1-substituted-1-triazolylstyrenes, and their production and use as fungicide, herbicide and/or plant growth regulant - Google Patents
Geometrical isomer of 1-substituted-1-triazolylstyrenes, and their production and use as fungicide, herbicide and/or plant growth regulant Download PDFInfo
- Publication number
- LV10023B LV10023B LVP-92-391A LV920391A LV10023B LV 10023 B LV10023 B LV 10023B LV 920391 A LV920391 A LV 920391A LV 10023 B LV10023 B LV 10023B
- Authority
- LV
- Latvia
- Prior art keywords
- isomer
- compound
- formula
- cont
- triazole
- Prior art date
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- 239000008117 stearic acid Substances 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- RWQNBRDOKXIBIV-UHFFFAOYSA-N thymine Chemical compound CC1=CNC(=O)NC1=O RWQNBRDOKXIBIV-UHFFFAOYSA-N 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- LWHIYPYQKDPFBK-UHFFFAOYSA-L zinc;n,n-dimethylcarbamothioate Chemical compound [Zn+2].CN(C)C([O-])=S.CN(C)C([O-])=S LWHIYPYQKDPFBK-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Claims (6)
- LV 10023 IZGUDROJUMA FORMULA / I. Ģeometriskais izomērs, kura formula irs0RT I 1 CII - R2 kur Rj ir ūdeņraža atoms, Cj-0^ alkil-, C^-C^ alkeuil- vai 2-pro-pinil- grupa, R2 ^i“^6 alkil-, ciklopropil- vai' I-metilciklo-propil- grupa, R^, kura var būt tā pati vai atšķirīga, ir halogēna atoms, alkil-, halogēn- aizvietota Cj-C^ alkil-, Cj- alkoksi-, fenoksi-, fenil-, ciāno- vai nitro- grupa, un n ir vesels skaitlis no 0 līdz 3» un kas iegūts reducējot vienu no diviem triazola savienojuma ģeometriskajiem izomēriem, kura formula ir:R 2 2 kur Rg, Rj un n ir ka definēts augstāk, kuram olefīna protons parādās PMR spektra (deiterohloroformā) stiprākā magnētiskajā laukā, vai ēterif ieejot iegūto reducēšanas produktu, vai tā sāļus. 2. (Ģeometriskais izomērs vai tā sāļi saskaņā ar patenta formulas I.punktu, kur Rj ir ūdeņraža atoms un R^ ir terc-butil-grupa. 3. deometriskais izomērs vai tā sāļi saskaņā ar patenta formulas 2.punktu, kur a ir I un ir hlora atoms 4- stāvoklī. 4. deometriskais izomērs vai tā sāļi saskaņā ar patenta formulas 2.punktu, kur a ir 2 un R^ ir hlora atoms 2- un 4- stāvoklī. 5. deometriskais izomērs saskaņā ar patenta formulas I.punk-tu, kur Rjir ūdeņraža atoms, R2 ir I-metilciklopropil- grupa, Rj ir halogēna atoms un n ir 0, I vai 2.
- 6. Viens no diviem triazola savienojuma ģeometriskajiem izo-mēriem, kura formula ir: R, kur R2, Rj un n ir kā definēts patenta formulas I.punktā, kuram olefīna protons parādās PMR spektra (deiterohloroformā) stiprākā magnētiskajā laukā.
- 7. Viens no diviem triazola savienojuma ģeometriskajiem izo-mēriem, kura formula ir: 0R II c 2 3 LV 10023 kur Rg ir I-metilciklopropil- grupa, in un n ir kā definēts patenta formulas I.punktā, kuram olefīna protons parādās PMR spektra (deiterohloroformā) vājākajā magnētiskajā laukā.
- 8. Iegūšanas paņēmiens, viena no diviem triazola savienojuma ģeometriskajiem izomērīem, kura formula ir 0 jr\ I (Ļ Vch » c - c , r2 <Vn ļļ II kur Rg, Rj un n ir kā definēts patenta formulas I.punktā, kuram olefīna protons parādās PMR spektra (deiterohlorofomā) stiprākajā magnētiskajā laukā, kas atšķiras ar to, ka minēto izomēru iegūst izomerizējot otru ģeometrisko izoz-mē-ru, kuram olefīna protons parādās PMR spektra (deiterohlorofor-mā) vājākajā magnētiskajā laukā, apstarojot ar stariem.
- 9. Iegūšanas paņēmiens, viena no diviem triazola savienojuma ģeometriskajiem izomēriera, kura formula ir:C - R, N -ļļ I!—n kur Rg, Rj un n ir kā definēts patenta formulas I.punktā, kuram olefīna protons parādās PMR spektra (deiterohloroformā) stiprākajā magnētiskajā laukā, kas a t š ķ i r a s ar to, ka minēto izomēru iegūst izomerizējot aku ģeometrisko izomēru maisījumu, to apstarojot ar stariem. 10. deometriskā izomēra iegūšanas paņēmiens, kura formula.- 4 kur Rj un n ir kā definēts patenta formulas I. punktā, kas atšķiras ar to, ka minēto izomēru iegūst reducējot vienu no dieviem triazola savienojuma ģeometriskajiem izomēriem, kura for™ mula irj - 4R 2 kur R^, Rj un n ir kā definēts patenta formulas I.punktā, kuram olefīna protons parādās PMR spektra (deiterohloroformā) stiprākajā magnētiskajā laukā. •II. Ģeometriskā izomēra iegūšanas paņēmiens, kura formula ir: ORjkur Rj ir Cj-C^ alkil-, C^-O^ alkenil- vai 2-propinil- grupa, un R^, R^ un n ir kā definēts patenta formulas I.punktā, kas atšķirasarto, ka minēto izomēru iegūst pakļaujot ķīmiskai iedarbībai ģeometrisko izomēru, kura formula ir: OE! VCH * C - CH - R, (H 5>n N HI!-1 kur un n ir kā definēts patenta formulas I.punktā, un kas iegūts reducējot vienu no diviem triazola savienojuma ģeometriskajiem izomāriem, kura formula ir: 5 LV 10023 Οkur Ej un n ir ka definēts patenta formulas I. punktā, kuram olefīna protons parādās PMR spektra (deiterohloroformā) stiprākajā magnētiskajā laukā, vai tā alkoholātu ar reagēt-spējigu Cj-G^ alkil-, C^-O^ alkenil- vai 2-propinil atvasinājumu bāzes klātienē, vai arī sāļus.
- 12. Fungicīdi, herbicīdi un/vai lauksaimniecības un dārzkopības augu augšanas regulatori, kas raksturīgi ar to, ka satur kā aktīvo komponenti ģeometrisko izomēru ar formulu, n-GH <Vn 0RT I 1 = C-CH - R I Ņ II -N kur Rj, Rp, Rj un n ir kā definēts patenta formulas I.punktā, karš iegūts reducējot vienu no triazola savienojuma ģeometriskajiem izomēriem, kura formula iri 0^TVgH = G - C - R, I /IK » 1 u_N kur R£» Rj un n ir ka definēts patenta formulas I.punktā, kuram olefīna protons parādās FM8 spektra (deiterohloroformā) stiprākajā magnētiskajā laukā, vai sekojoši ēterificējot iegūto reducēšanas produktu, vai sāļus.
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3287679A JPS55124771A (en) | 1979-03-20 | 1979-03-20 | Triazole-based geometrical isomerism compound or its salt, its preparation, and fungicide for agriculture and gardening comprising it as active ingredient |
JP4165979A JPS55147265A (en) | 1979-04-05 | 1979-04-05 | Triazole geometrical isomer compound and its preparation |
JP10054779A JPS5625105A (en) | 1979-08-06 | 1979-08-06 | Plant growth regulator and herbicide containing geometrical isomer of triazole compound or its salt as effective component |
JP11657679A JPS5640671A (en) | 1979-09-10 | 1979-09-10 | Triazole compound or its salt, its preparation and agricultural and horticultural germicide, herbicide and plant growth regulator containing the same as active constituent |
JP12236679A JPS5645462A (en) | 1979-09-21 | 1979-09-21 | Triazole compound and its preparation |
JP12348579A JPS5646869A (en) | 1979-09-25 | 1979-09-25 | Geometrical isomer of triazole compound or its salt, its preparation, and agricultural and horticultural fungicide, plant growth regulating agent, and herbicide containing the same as effective component |
JP12457179A JPS5646870A (en) | 1979-09-26 | 1979-09-26 | Geometrical isomer of triazole compound and its preparation |
JP1056880A JPS56108773A (en) | 1980-01-30 | 1980-01-30 | Triazole compound and its salt, their preparation, and fungicide, herbicide, and plant growth regulating agent containing said compound as effective component |
Publications (2)
Publication Number | Publication Date |
---|---|
LV10023A LV10023A (lv) | 1994-05-10 |
LV10023B true LV10023B (en) | 1995-02-20 |
Family
ID=27571676
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
LVP-92-391A LV10023B (en) | 1979-03-20 | 1992-12-22 | Geometrical isomer of 1-substituted-1-triazolylstyrenes, and their production and use as fungicide, herbicide and/or plant growth regulant |
Country Status (19)
Country | Link |
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US (2) | US4554007A (lv) |
AR (1) | AR226305A1 (lv) |
AU (1) | AU536825B2 (lv) |
BR (1) | BR8001617A (lv) |
CA (1) | CA1154449A (lv) |
CH (1) | CH644851A5 (lv) |
DE (1) | DE3010560A1 (lv) |
DK (1) | DK157811C (lv) |
FR (1) | FR2460939B1 (lv) |
GB (1) | GB2046260B (lv) |
HU (1) | HU186281B (lv) |
IL (1) | IL59671A (lv) |
IT (1) | IT1143014B (lv) |
LV (1) | LV10023B (lv) |
MY (1) | MY8700898A (lv) |
NL (1) | NL192791C (lv) |
NZ (1) | NZ193168A (lv) |
PL (1) | PL123010B1 (lv) |
YU (1) | YU42969B (lv) |
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DE2738847A1 (de) * | 1977-08-29 | 1979-03-15 | Albrecht W Gaspard | Geraet zur besseren nutzung der in beheizten raeumen nach oben steigenden waerme |
JPS6053018B2 (ja) * | 1977-09-07 | 1985-11-22 | 住友化学工業株式会社 | アゾ−ル系化合物、その製造法および該化合物からなる殺菌剤 |
DE2743767A1 (de) * | 1977-09-29 | 1979-04-12 | Bayer Ag | Diastereomere triazolyl-0,n-acetale, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
US4182862A (en) * | 1978-10-18 | 1980-01-08 | Rohm And Haas Company | Process for the preparation of 1,3-disubstituted-2-azoyl-2-propen-1-ones |
EP0015387B1 (de) * | 1979-02-16 | 1983-01-12 | Bayer Ag | 1-Vinyltriazol-Derivate, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Wachstumsregulatoren und Fungizide |
DE2920437A1 (de) * | 1979-05-19 | 1980-11-27 | Bayer Ag | Geometrische isomere von 4,4- dimethyl-1-phenyl-2-(1,2,4-triazol-1-yl)- 1-penten-3-olen, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
DE2929602A1 (de) * | 1979-07-21 | 1981-02-12 | Bayer Ag | Triazolyl-alken-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
DE2944223A1 (de) * | 1979-11-02 | 1981-05-27 | Basf Ag, 6700 Ludwigshafen | Fungizide entriazole, ihre herstellung und verwendung |
DE3000643A1 (de) * | 1980-01-10 | 1981-07-16 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von azolyl-vinyl-ketonen |
-
1980
- 1980-03-13 US US06/130,108 patent/US4554007A/en not_active Expired - Lifetime
- 1980-03-18 CA CA000347897A patent/CA1154449A/en not_active Expired
- 1980-03-18 NZ NZ193168A patent/NZ193168A/xx unknown
- 1980-03-18 IT IT48189/80A patent/IT1143014B/it active
- 1980-03-18 BR BR8001617A patent/BR8001617A/pt not_active IP Right Cessation
- 1980-03-19 PL PL1980222822A patent/PL123010B1/pl unknown
- 1980-03-19 CH CH217080A patent/CH644851A5/de not_active IP Right Cessation
- 1980-03-19 DK DK118580A patent/DK157811C/da not_active IP Right Cessation
- 1980-03-19 DE DE19803010560 patent/DE3010560A1/de active Granted
- 1980-03-19 HU HU80652A patent/HU186281B/hu unknown
- 1980-03-19 AU AU56571/80A patent/AU536825B2/en not_active Expired
- 1980-03-19 YU YU766/80A patent/YU42969B/xx unknown
- 1980-03-19 FR FR8006155A patent/FR2460939B1/fr not_active Expired
- 1980-03-19 AR AR280359A patent/AR226305A1/es active
- 1980-03-19 GB GB8009190A patent/GB2046260B/en not_active Expired
- 1980-03-19 IL IL59671A patent/IL59671A/xx unknown
- 1980-03-20 NL NL8001658A patent/NL192791C/nl not_active IP Right Cessation
-
1985
- 1985-09-04 US US06/772,429 patent/US4749716A/en not_active Expired - Lifetime
-
1987
- 1987-12-30 MY MY898/87A patent/MY8700898A/xx unknown
-
1992
- 1992-12-22 LV LVP-92-391A patent/LV10023B/en unknown
Also Published As
Publication number | Publication date |
---|---|
YU42969B (en) | 1989-02-28 |
DE3010560C2 (lv) | 1990-09-20 |
FR2460939B1 (fr) | 1985-06-28 |
NL8001658A (nl) | 1980-09-23 |
US4554007A (en) | 1985-11-19 |
PL222822A1 (lv) | 1981-02-13 |
GB2046260A (en) | 1980-11-12 |
NL192791C (nl) | 1998-02-03 |
BR8001617A (pt) | 1980-11-18 |
NZ193168A (en) | 1983-04-12 |
IL59671A (en) | 1984-02-29 |
YU76680A (en) | 1983-10-31 |
FR2460939A1 (fr) | 1981-01-30 |
AR226305A1 (es) | 1982-06-30 |
NL192791B (nl) | 1997-10-01 |
MY8700898A (en) | 1987-12-31 |
DK118580A (da) | 1980-09-21 |
PL123010B1 (en) | 1982-09-30 |
DK157811B (da) | 1990-02-19 |
IT1143014B (it) | 1986-10-22 |
AU5657180A (en) | 1980-09-25 |
DK157811C (da) | 1990-08-13 |
IT8048189A0 (it) | 1980-03-18 |
US4749716A (en) | 1988-06-07 |
CH644851A5 (de) | 1984-08-31 |
IL59671A0 (en) | 1980-06-30 |
CA1154449A (en) | 1983-09-27 |
AU536825B2 (en) | 1984-05-24 |
LV10023A (lv) | 1994-05-10 |
HU186281B (en) | 1985-07-29 |
DE3010560A1 (de) | 1980-10-02 |
GB2046260B (en) | 1983-12-21 |
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