DD140143A5 - Verfahren zur herstellung von neuen dithiocarbaminsaeurehydroxyalkylester - Google Patents

Verfahren zur herstellung von neuen dithiocarbaminsaeurehydroxyalkylester Download PDF

Info

Publication number: DD140143A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; compound; group; alk; salt
Prior art date: 1977-01-17

Application number

DD78203244A

Other languages

German (de)

English (en)

Inventor

Ernst Schweizer

Original Assignee

Ciba Geigy Ag

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.)

1977-01-17

Filing date

1978-01-16

Publication date

1980-02-13

1978-01-16 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1980-02-13 Publication of DD140143A5 publication Critical patent/DD140143A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 18
238000002360 preparation method Methods 0.000 title claims abstract description 14
239000002253 acid Substances 0.000 title description 8
-1 phenyloxyphenyl Chemical group 0.000 claims description 53
150000001875 compounds Chemical class 0.000 claims description 22
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 11
150000003839 salts Chemical class 0.000 claims description 10
238000006243 chemical reaction Methods 0.000 claims description 8
239000007858 starting material Substances 0.000 claims description 8
150000002148 esters Chemical class 0.000 claims description 7
229910052736 halogen Inorganic materials 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
239000000460 chlorine Substances 0.000 claims description 5
229910052801 chlorine Inorganic materials 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
125000002947 alkylene group Chemical group 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
125000004423 acyloxy group Chemical group 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
125000004093 cyano group Chemical group *C#N 0.000 claims description 3
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
239000011541 reaction mixture Substances 0.000 claims description 3
239000011734 sodium Substances 0.000 claims description 3
229910052708 sodium Inorganic materials 0.000 claims description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
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 claims description 2
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150000001342 alkaline earth metals Chemical class 0.000 claims description 2
125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 2
DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims description 2
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125000005843 halogen group Chemical group 0.000 claims description 2
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125000001118 alkylidene group Chemical group 0.000 claims 1
150000003863 ammonium salts Chemical class 0.000 claims 1
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FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 3
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108010010803 Gelatin Proteins 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
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230000002378 acidificating effect Effects 0.000 description 3
229910021529 ammonia Inorganic materials 0.000 description 3
DKVNAGXPRSYHLB-UHFFFAOYSA-N amoscanate Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC1=CC=C(N=C=S)C=C1 DKVNAGXPRSYHLB-UHFFFAOYSA-N 0.000 description 3
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GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 2
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229940106681 chloroacetic acid Drugs 0.000 description 1
239000008120 corn starch Substances 0.000 description 1
XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000010685 fatty oil Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
239000007903 gelatin capsule Substances 0.000 description 1
244000000013 helminth Species 0.000 description 1
239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
229920003132 hydroxypropyl methylcellulose phthalate Polymers 0.000 description 1
229940031704 hydroxypropyl methylcellulose phthalate Drugs 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
150000002500 ions Chemical class 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
239000011777 magnesium Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
SVMGVZLUIWGYPH-UHFFFAOYSA-N nitroscanate Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(N=C=S)C=C1 SVMGVZLUIWGYPH-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000003791 organic solvent mixture Substances 0.000 description 1
244000045947 parasite Species 0.000 description 1
230000003071 parasitic effect Effects 0.000 description 1
239000002245 particle Substances 0.000 description 1
229940117953 phenylisothiocyanate Drugs 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
JCBJVAJGLKENNC-UHFFFAOYSA-M potassium ethyl xanthate Chemical compound [K+].CCOC([S-])=S JCBJVAJGLKENNC-UHFFFAOYSA-M 0.000 description 1
229920001592 potato starch Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007901 soft capsule Substances 0.000 description 1
101150035983 str1 gene Proteins 0.000 description 1
239000000126 substance Substances 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
125000004149 thio group Chemical group *S* 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
238000010792 warming Methods 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
- A01N47/20—N-Aryl derivatives thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/14—Dithiocarbamic acids; Derivatives thereof
- C07C333/18—Esters of dithiocarbamic acids
- C07C333/24—Esters of dithiocarbamic acids having nitrogen atoms of dithiocarbamate groups bound to carbon atoms of six-membered aromatic rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

DD78203244A 1977-01-17 1978-01-16 Verfahren zur herstellung von neuen dithiocarbaminsaeurehydroxyalkylester DD140143A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH52877		1977-01-17

Publications (1)

Publication Number	Publication Date
DD140143A5 true DD140143A5 (de)	1980-02-13

Family

ID=4189065

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD78203244A DD140143A5 (de)	1977-01-17	1978-01-16	Verfahren zur herstellung von neuen dithiocarbaminsaeurehydroxyalkylester

Country Status (19)

Country	Link
US (1)	US4161534A (fr)
JP (1)	JPS5390239A (fr)
AR (1)	AR220697A1 (fr)
AT (1)	AT356673B (fr)
AU (1)	AU517806B2 (fr)
BE (1)	BE862922A (fr)
DD (1)	DD140143A5 (fr)
DE (1)	DE2801194A1 (fr)
DK (1)	DK20478A (fr)
EG (1)	EG13018A (fr)
ES (1)	ES466026A1 (fr)
FR (1)	FR2377380A1 (fr)
GB (1)	GB1582931A (fr)
HU (1)	HU177973B (fr)
IL (1)	IL53812A0 (fr)
NL (1)	NL7800449A (fr)
OA (1)	OA05871A (fr)
SE (1)	SE7800479L (fr)
ZA (1)	ZA78306B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4758362A (en) *	1986-03-18	1988-07-19	The Lubrizol Corporation	Carbamate additives for low phosphorus or phosphorus free lubricating compositions
US5698498A (en) *	1993-06-28	1997-12-16	The Lubrizol Corporation	Hydroxyalkyl dithiocarbamates, their borated esters and lubricants, functional fluids, greases and aqueous compositions containing the same

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3342835A (en) *	1964-01-22	1967-09-19	American Cyanamid Co	Novel preparation of 2-imino-1, 3-dithiolanes and 2-imino-1, 3-dithianes
AU502396B2 (en) *	1975-07-03	1979-07-26	Cl BAGET. CY AG	Dithiocapbamic acid esters

1978
- 1978-01-06 US US05/867,649 patent/US4161534A/en not_active Expired - Lifetime
- 1978-01-11 EG EG18/78A patent/EG13018A/xx active
- 1978-01-12 DE DE19782801194 patent/DE2801194A1/de not_active Withdrawn
- 1978-01-13 NL NL7800449A patent/NL7800449A/xx not_active Application Discontinuation
- 1978-01-13 FR FR7800918A patent/FR2377380A1/fr active Pending
- 1978-01-13 GB GB1399/78A patent/GB1582931A/en not_active Expired
- 1978-01-16 DD DD78203244A patent/DD140143A5/de unknown
- 1978-01-16 HU HU78CI1802A patent/HU177973B/hu unknown
- 1978-01-16 ES ES466026A patent/ES466026A1/es not_active Expired
- 1978-01-16 IL IL53812A patent/IL53812A0/xx unknown
- 1978-01-16 AT AT28278A patent/AT356673B/de not_active IP Right Cessation
- 1978-01-16 AU AU32457/78A patent/AU517806B2/en not_active Expired
- 1978-01-16 BE BE184332A patent/BE862922A/fr unknown
- 1978-01-16 DK DK20478A patent/DK20478A/da unknown
- 1978-01-16 SE SE7800479A patent/SE7800479L/xx unknown
- 1978-01-16 AR AR270723A patent/AR220697A1/es active
- 1978-01-17 JP JP286678A patent/JPS5390239A/ja active Pending
- 1978-01-17 ZA ZA00780306A patent/ZA78306B/xx unknown
- 1978-02-03 OA OA56392A patent/OA05871A/fr unknown

Also Published As

Publication number	Publication date
DK20478A (da)	1978-07-18
IL53812A0 (en)	1978-04-30
AU3245778A (en)	1979-07-26
OA05871A (fr)	1981-05-31
FR2377380A1 (fr)	1978-08-11
NL7800449A (nl)	1978-07-19
ATA28278A (de)	1979-10-15
DE2801194A1 (de)	1978-07-20
AT356673B (de)	1980-05-12
ES466026A1 (es)	1978-10-01
AR220697A1 (es)	1980-11-28
AU517806B2 (en)	1981-08-27
HU177973B (en)	1982-02-28
GB1582931A (en)	1981-01-14
BE862922A (fr)	1978-07-17
EG13018A (en)	1980-07-31
SE7800479L (sv)	1978-07-18
JPS5390239A (en)	1978-08-08
US4161534A (en)	1979-07-17
ZA78306B (en)	1978-12-27

Publication	Publication Date	Title
DE69129333T2 (de)	1998-08-20	Diphenylpiperazinderivat und dieses enthaltendes arzneimittel für kreislauforgane
DE2926472A1 (de)	1981-01-15	Neue benzoylderivate, deren herstellung und deren verwendung als arzneimittel
DE2820375A1 (de)	1978-11-23	Schwefelhaltige benzimidazol-derivate, ihre herstellung, bei ihrer herstellung anwendbare zwischenprodukte sowie pharmazeutische mittel
DE2632400C2 (fr)	1988-06-09
EP0093252B1 (fr)	1988-03-09	Dérivés de thiométhylpyridine, procédé pour leur préparation et médicaments les contenant
AT371460B (de)	1983-06-27	Verfahren zur herstellung neuer benzopyranderivate und ihrer salze
DD140143A5 (de)	1980-02-13	Verfahren zur herstellung von neuen dithiocarbaminsaeurehydroxyalkylester
DE1593728C3 (de)	1980-02-14	Substituierte Amidine und Verfahren zu ihrer Herstellung
CH637120A5 (de)	1983-07-15	Verfahren zur herstellung von acylierten benzimidazol-2-derivaten.
DE2334355A1 (de)	1975-01-16	Diphenylharnstoffderivate und ihre herstellung
EP0035972B1 (fr)	1983-10-19	Cyanoalkyl-phényl urées possédant des propriétés herbicides sélectives, leur préparation et leurs compositions
EP0124630B1 (fr)	1987-01-28	Dérivés de pyrimidinothioalkyle pyridine, procédé pour leur préparation et médicaments contenant ces composés
EP0042354B1 (fr)	1985-12-11	Imidazobenzothiadiazépines, procédé pour leur préparation et compositions pharmaceutiques les contenant
DE2629262A1 (de)	1977-01-27	Dithiocarbaminsaeureester und verfahren zu ihrer herstellung
CH630341A5 (en)	1982-06-15	Process for the preparation of novel cyanoacetic anilide derivatives.
CH426780A (de)	1966-12-31	Verfahren zur Herstellung von Trifluormethylphenylsulfonsäuretrifluormethylphenylamiden
DE1241816B (de)	1967-06-08	Verfahren zur Herstellung neuer Sulfonylharnstoffe
DE2009387C2 (de)	1983-11-17	Anilin-acetamidine und ihre nichttoxischen Säureadditionssalze, Verfahren zu ihrer Herstellung und pharmazeutische Zubereitungen, welche diese Verbindungen enthalten
LU85231A1 (de)	1985-09-12	Benzamid-derivate
DE2656227A1 (de)	1978-06-15	Basisch alkylierte dithiosalicylsaeureamide, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
DE3426634A1 (de)	1985-02-07	Neue phenoxyalkylphosphinate und -phosphonate
DD207376A5 (de)	1984-02-29	Verfahren zur herstellung von thiazolderivaten
DE1003716B (de)	1957-03-07	Verfahren zur Herstellung von neuen Benzolsulfonylharnstoffen
AT355044B (de)	1980-02-11	Verfahren zur herstellung von neuen dithiocarbanilsaeurehydroxyalkylestern
CH602623A5 (en)	1978-07-31	Carboxyalkyl N-aryl dithiocarbamates