DD258811A5 - Verfahren zur herstellung von (di)alkoxycarbonyl-amino-s-triazine und ihrer schwefelanalogen vertreter - Google Patents

Verfahren zur herstellung von (di)alkoxycarbonyl-amino-s-triazine und ihrer schwefelanalogen vertreter Download PDF

Info

Publication number: DD258811A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; compounds; acid; triazine; amino
Prior art date: 1985-12-02

Application number

DD86296915A

Other languages

German (de)

English (en)

Inventor

Jean-Claude Gehret

Odd Kristiansen

Original Assignee

��@��@��k��

Priority date (The priority date 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 date listed.)

1985-12-02

Filing date

1986-12-01

Publication date

1988-08-03

1986-12-01 Application filed by ��@��@��k�� filed Critical ��@��@��k��

1988-08-03 Publication of DD258811A5 publication Critical patent/DD258811A5/de

Links

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QYWXVBFLPIGNNL-UHFFFAOYSA-L disodium butanedioate 1-octylsulfonyloctane Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O.CCCCCCCCS(=O)(=O)CCCCCCCC QYWXVBFLPIGNNL-UHFFFAOYSA-L 0.000 description 1
YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
OFPKMKYCGJFASS-UHFFFAOYSA-N ethyl n-[4-amino-6-(cyclopropylamino)-1,3,5-triazin-2-yl]carbamate Chemical compound CCOC(=O)NC1=NC(N)=NC(NC2CC2)=N1 OFPKMKYCGJFASS-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000012458 free base Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
125000000262 haloalkenyl group Chemical group 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000002917 insecticide Substances 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
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
230000000366 juvenile effect Effects 0.000 description 1
229930014550 juvenile hormone Natural products 0.000 description 1
239000002949 juvenile hormone Substances 0.000 description 1
150000003633 juvenile hormone derivatives Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 1
230000000974 larvacidal effect Effects 0.000 description 1
230000001418 larval effect Effects 0.000 description 1
239000010871 livestock manure Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-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
LHMUZCNPQGLQPE-UHFFFAOYSA-N n-pyrrolidin-1-ylpyridin-4-amine Chemical compound C1CCCN1NC1=CC=NC=C1 LHMUZCNPQGLQPE-UHFFFAOYSA-N 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000000590 parasiticidal effect Effects 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
238000009304 pastoral farming Methods 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
230000002265 prevention Effects 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
230000035755 proliferation Effects 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
CAEWJEXPFKNBQL-UHFFFAOYSA-N prop-2-enyl carbonochloridate Chemical compound ClC(=O)OCC=C CAEWJEXPFKNBQL-UHFFFAOYSA-N 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 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
239000002002 slurry Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000003206 sterilizing agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 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
229950011008 tetrachloroethylene Drugs 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
230000036325 urinary excretion Effects 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
- C07D251/70—Other substituted melamines

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)

DD86296915A 1985-12-02 1986-12-01 Verfahren zur herstellung von (di)alkoxycarbonyl-amino-s-triazine und ihrer schwefelanalogen vertreter DD258811A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH513085		1985-12-02

Publications (1)

Publication Number	Publication Date
DD258811A5 true DD258811A5 (de)	1988-08-03

Family

ID=4288441

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD86296915A DD258811A5 (de)	1985-12-02	1986-12-01	Verfahren zur herstellung von (di)alkoxycarbonyl-amino-s-triazine und ihrer schwefelanalogen vertreter

Country Status (14)

Country	Link
US (1)	US4732899A (fr)
EP (1)	EP0226536A3 (fr)
JP (1)	JPS62138483A (fr)
AU (1)	AU583685B2 (fr)
CA (1)	CA1262901A (fr)
DD (1)	DD258811A5 (fr)
DK (1)	DK576586A (fr)
GB (1)	GB2183646B (fr)
HU (1)	HUT42688A (fr)
IL (1)	IL80827A0 (fr)
NZ (1)	NZ218457A (fr)
PH (1)	PH23300A (fr)
PT (1)	PT83830B (fr)
ZA (1)	ZA868949B (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2684409B2 (ja) *	1988-03-31	1997-12-03	コニカ株式会社	シアノ基および／またはハロゲン原子で置換されたアニリン類の製造方法およびその製造のために使用される化合物
US5288865A (en) *	1991-11-15	1994-02-22	American Cyanamid Company	Process for preparing amide derivatives from haloaminotriazines and acid halides
EP0541966A3 (en) *	1991-11-15	1994-09-07	American Cyanamid Co	Process for preparing amide derivatives from halomines and acid halides
DE4217864A1 (de) *	1992-05-29	1993-12-02	Bayer Ag	Substituierte Pyrazoline
TW328955B (en) *	1993-05-14	1998-04-01	Cytec Tech Corp	Process for preparing bis- or tris-carbamate functional 1,3,5-triazines, substantially halogen contamination free crosslinker compositions and new bis-or tris-carbamate functional 1,3,5-triazines
US5518757A (en) *	1993-08-31	1996-05-21	The United States Of America As Represented By The Department Of Agriculture	4-allylanisole analog scolytid repellents
US6306913B1 (en)	1993-08-31	2001-10-23	The United States Of America As Represented By The Secretary Of Agriculture	Container for 4-allylanisole and analog scolytid pesticides
US6204382B1 (en) *	1994-08-05	2001-03-20	Cytec Technology Corp.	Carboxylated amino-1,3,5-triazines, derivatives thereof and processes for preparing the same
WO1999001442A1 (fr) *	1997-07-02	1999-01-14	Zeneca Limited	Derives de triazine et leur utilisation comme agents antibacteriens
US20040116558A1 (en) *	2002-11-08	2004-06-17	Akzo Nobel N.V.	New carbamate - melamine formaldehyde cross-linking agents
DE10259672A1 (de) *	2002-12-18	2004-07-01	Basf Ag	Verfahren zur Herstellung von Alkoxycarbonylamino-triazinen
DE102007025451B4 (de) *	2007-05-31	2013-03-28	Ami Agrolinz Melamine International Gmbh	Triazinderivate
WO2008156151A1 (fr) *	2007-06-19	2008-12-24	Kobelco Eco-Solutions Co., Ltd.	Procédé de simulation, appareil de simulation, procédé de traitement biologique et appareil de traitement biologique
DE102008061139A1 (de) *	2008-12-09	2010-06-10	Borealis Agrolinz Melamine Gmbh	Verfahren zur Herstellung von Triazincarbamaten unter Verwendung von Chlorformiaten

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH588213A5 (fr) *	1974-07-25	1977-05-31	Ciba Geigy Ag
CH604517A5 (fr) *	1976-08-19	1978-09-15	Ciba Geigy Ag
US4187305A (en) *	1978-02-17	1980-02-05	Ciba-Geigy Corporation	Procedure for treating mammals to control parasitic diptera larvae
US4187304A (en) *	1978-02-17	1980-02-05	Ciba-Geigy Corporation	Procedure for treating mammals to control parasitic diptera larvae
US4402954A (en) *	1980-11-24	1983-09-06	Ciba-Geigy Corporation	Synergistic pesticidal compositions comprising N-(2-methyl-4-chlorophenyl)-N',N'-dimethylthiourea and 2,4-diamino-6-cyclopropylamino-2-triazine or 2,4-diamino-6-isopropylamino-2-triazine
DE3166207D1 (en) *	1980-11-25	1984-10-25	Ciba Geigy Ag	Pesticide agents
EP0145660B1 (fr) *	1983-12-02	1990-04-18	Ciba-Geigy Ag	Composition insecticide

1986
- 1986-11-24 US US06/934,299 patent/US4732899A/en not_active Expired - Fee Related
- 1986-11-24 PH PH34524A patent/PH23300A/en unknown
- 1986-11-26 EP EP86810545A patent/EP0226536A3/fr not_active Withdrawn
- 1986-11-26 ZA ZA868949A patent/ZA868949B/xx unknown
- 1986-11-28 PT PT83830A patent/PT83830B/pt unknown
- 1986-11-28 CA CA000524057A patent/CA1262901A/fr not_active Expired
- 1986-11-28 GB GB8628459A patent/GB2183646B/en not_active Expired
- 1986-12-01 NZ NZ218457A patent/NZ218457A/xx unknown
- 1986-12-01 HU HU864962A patent/HUT42688A/hu unknown
- 1986-12-01 AU AU65857/86A patent/AU583685B2/en not_active Ceased
- 1986-12-01 IL IL80827A patent/IL80827A0/xx unknown
- 1986-12-01 DK DK576586A patent/DK576586A/da not_active Application Discontinuation
- 1986-12-01 DD DD86296915A patent/DD258811A5/de unknown
- 1986-12-02 JP JP61287575A patent/JPS62138483A/ja active Pending

Also Published As

Publication number	Publication date
ZA868949B (en)	1987-08-26
HUT42688A (en)	1987-08-28
EP0226536A2 (fr)	1987-06-24
US4732899A (en)	1988-03-22
AU583685B2 (en)	1989-05-04
JPS62138483A (ja)	1987-06-22
PH23300A (en)	1989-06-30
CA1262901A (fr)	1989-11-14
PT83830B (en)	1988-12-09
GB2183646B (en)	1989-11-01
EP0226536A3 (fr)	1988-06-15
AU6585786A (en)	1987-06-04
NZ218457A (en)	1989-10-27
GB8628459D0 (en)	1987-01-07
GB2183646A (en)	1987-06-10
DK576586D0 (da)	1986-12-01
PT83830A (en)	1986-12-01
DK576586A (da)	1987-06-03
IL80827A0 (en)	1987-03-31

Publication	Publication Date	Title
DE2820696C2 (fr)	1988-04-14
EP0077759B1 (fr)	1987-12-09	Phénylurées
EP0244360B1 (fr)	1992-08-19	Pyrimidines substituées
EP0306696A1 (fr)	1989-03-15	Guanidines substituées
EP0303570A2 (fr)	1989-02-15	Isothiourées substituées
CH673557A5 (fr)	1990-03-30
CH644371A5 (de)	1984-07-31	In 2- und 4-stellung disubstituierte 5-thiazolcarbonsaeuren und deren funktionelle derivate.
DE2227012C2 (de)	1982-12-23	3-(2,4-Dichlor-5-propargyloxyphenyl)-5-tert.-butyl-1,3,4-oxadiazolon-(2), seine Herstellung und die Zusammensetzungen, die es enthält
EP0226536A2 (fr)	1987-06-24	Dérivés de la (di)alcoxycarbonylamino-s-triazine avec activité contre les insectes parasites des animaux et des plantes
EP0016729B1 (fr)	1984-07-25	N-(p-aminophényl)-N'-benzoylurées substituées, procédé pour leur préparation, compositions contenant ces dérivés et leur utilisation en tant que pesticides; dérivés substitués par un groupement alcényle de la p-amino-aniline
EP0145660B1 (fr)	1990-04-18	Composition insecticide
CH638223A5 (de)	1983-09-15	N-((phosphinyl)amino)thio-methylcarbamate bzw. n-((phosphinothioyl)amino)thio-methylcarbamate, verfahren zu ihrer herstellung sowie ihre verwendung in pestiziden.
DE3003112C2 (fr)	1990-11-08
EP0288432A1 (fr)	1988-10-26	Biocides
DE1443933C2 (de)	1972-07-13	Thiocyano-phenyl-isothiocyanate und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0118392B1 (fr)	1987-08-12	Composés de N-benzoylurée utilisés comme pesticides
EP0174274A1 (fr)	1986-03-12	Dérivés de phénylbenzoylurée
US4423065A (en)	1983-12-27	Naphthalenamine insecticides
EP0084758B1 (fr)	1986-02-12	Dérivés de pyrimidine actifs comme parasiticides
DE3033358C2 (de)	1983-12-29	Isovaleriansäure-Derivate, Verfahren zu deren Herstellung und diese enthaltende insektizide und acarizide Mittel
EP0065487B1 (fr)	1985-08-28	Dérivé de phénylurée
DD234266A5 (de)	1986-03-26	Verfahren zur herstellung von neuen substituierten acylomino-s-triazin-verbindungen
EP0375613A2 (fr)	1990-06-27	Nitroènamine
CH636866A5 (de)	1983-06-30	Thiadiazolylbenzamide und sie enthaltende insektizide mittel.
DE2230076A1 (de)	1972-12-28	Verfahren zur Herstellung neuer heterocyclischer Stoffe