前苏联专利SU929008A3 Process for producing 1,2,3-triazolecarboxylic acid amides

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专利摘要:
1,2,3-Triazole carboxylic acid amides, of the formula <IMAGE> in which R1, R2, R3, R4 and n have the meaning defined in the specification in connection with formula I. The compounds have a broad biocidal, particularly herbicidal, insecticidal, acaricidal, fungicidal and nematocidal activity. They have a high degree of selectivity towards agriculturally valuable plants.
公开号:SU929008A3
申请号:SU792797788
申请日:1979-08-06
公开日:1982-05-15
发明作者:Крюгер Ханс-Рудольф；Арндт Фридрих；Баумерт Дитрих；Йоппин Хартмут；Альбрехт Пиро Эрнст；Руш Райнхарт
申请人:Шеринг Аг (Фирма)；
IPC主号:

专利说明:

(54) METHOD FOR OBTAINING AMIDES 1,2,3-TRIAZOLKARBONIC ACID
-. one - . The invention relates to a process for the preparation of 1,2,3-triazole amides of 1,2,3-triazolecarboxylic acid having biocidal properties.
The reaction of acylation of amines with carbamoyl halides G1 is known.
The purpose of the invention is a method for producing new 1,2,3-triazolcar amides; an OOH acid having valuable biocidal properties.
This goal is achieved. Since according to the method for producing 1,2,3-triazolecarboxylic acid amides of the general formula
RJ (O) irRi
F
/ N /
where RI is alkyl with 1-6 carbon atoms, allyl, propynyl or benzyl) Rn is hydrogen or alkyl with
carbon atoms Rrf-R. - the same or different
and are hydrogen, unsubstituted alkyl with 1-6 carbon atoms or substituted with halogen; allyl, propynyl, unsubstituted phenyl or substituted alkyl with 13 carbon atoms, or halogeno-, benzyl, cyclohexyl or
RJI R. together form pyrrolidine, piperidine, morpholine, hexamethylenediamine, p-0 or 1, or 2.
1,2,3-triazole of the general formula
H oiff-i.
F
/ N H where Ri, n has the indicated values, with a monovalent or its salt a metal of the general formula% .S (O) J, -RI B K., ClIP have the indicated values; and - a monovalent metal cation, acylated with a carbamoyl halide of the general formula 3 kg-hp: 1T-CO-X R have the indicated values X - halogen, in the presence of a halogen-water acceptor or isocyanate of the general formula R 3 - N - C O where R has the specified values preferably in the presence of an organic base. The reaction is carried out at 0-12.0, usually at room temperature. Reagents are used in equimol p quantities. Organic solvents use nitriles, for example acetonyl, esters, for example tetrahydrofur and dioxane, amides of acids, for example methyl formamide, ketones, for example ac, chlorinated hydrocarbons, for example chloroform and carbon tetrachloride. Such organic bases as triethylamine, S, S-dimethylaniline and pyridine are used as acceptor acids. Excess pyridine can be used as a medium. The compounds of the formula I possess bicidal, insecticidal, acaricinic, fuigicidal and / or nematocidal properties. Amides of 1, 2, 3-triazole-carboxylic lots in comparison with the known means of the same purpose possess not only higher activity with respect to dicotyledonous and monocotyledonous weeds, but also exceptional 8 cultural oppression and lemma, not asthenia. In addition, they possess the properties of specific herbicides and can be used for pre-emergence and post-emergence control of weeds by spraying. These compounds can be bordered with such weeds as Avena fatna, ABopecurus myosuroides, Echinocliloa crus galSi, I igitai-ia Sanguinalis, Gyperus escutentus. Sorghum haEepense, Poa annua, .SteElaria media, Senecio Td1 ag15, Amaranthus retroflexus, Polugonum EapathifoEiim, etc. At the same time, these substances have a selectivity with respect to such crops as maize, cotton, potatoes, legumes, peas, and beans. In addition, the compounds of general formula I possess the properties of plant growth regulators, namely, inhibiting vertical growth, inhibiting the development of roots, intensifying the formation of vegetable dyes and inducing or accelerating foliage falling. These compounds have a broad insecticidal and / or acaricidal effect. A particular advantage is their high initial effect. With the help of new compounds, it is possible to fight against a host of important pests, in particular, from the family of Diptera, Coleoptera, Beakfish, and Coopers. The phytopathogenic nematodes that can be destroyed using the proposed compounds include, for example, the family of nomadic root-headed nematodes, TuEep chorhynchus, PratyEenchus, ParatyEenchus, Heliocotylenchiis, Xiphinema, Trichodorus and Longidorus; root nematodes, such as Meloidogyne hapEa, Meloidogyne incognita, Meloidogyne arenaria, cyst nematodes, such as Globodera rostochiensis and Heterodera schachtii. A. Alkylthio-1,2,3-triazoles. -Methyl-5-methylthio-1,2,3-triazole. To a solution of 13.8 g (0.12 mol) of 5-mercapto-methyl, 2,3-triazole in 60 ml of ethanol, 4.79 g (0.12 mol) of sodium hydroxide are added dropwise at room temperature 20 ml of ethanol. Then at 30 ° C, 19.85 g are added with stirring.
(0.1 mol) of methyl iodide and after aging overnight at room temperature, concentrated in vacuo at.
The precipitate formed is mixed with 150 ml of water and extracted with ether. The organic phase is dried with magnesium sulfate, filtered and concentrated. The precipitated crystals are recrystallized from cyclohexane. Exit lit, 6 g (9.3%), so pl. 71-75.5
In the same way, the following starting products are obtained:
-MethylthioT. Mp 47 ° C
-1,2,3-triazole,
4-Ethylthio1, 2,3-triazole
t-P. propylthio, 2,3-triazole
- Isopropylthio-1, 2 3 triazole
4-butylthio-1, 2,3-triazole
C- (1-Methylpropylthio) -1,2, C-TRIJ 1,5281 azole
A-Allylthio 10 D -1,2, 3 triazole
1.5561
P
- Isobutylthio 10G 1,2,3-triazole 1,
P
, 4- (2-Propinylthio) -1, 2, 3-triazole Semi-crystalline-Benzylthio-1, 2,3-triazole T pl 61.563, 5 ° C
B. Alkylsulfinyl-1,2,3-triazoles-Methylsulfinyl-1,2,3-triazole. A solution of 57.5 g (0.5 mol) -methylthio-1, 2,3-triazole in 200 ml of acetic acid is added dropwise over 10 minutes to 61.1 g (0.6 mol) of 30% hydrogen peroxide is stirred for 30 min at kO-kS C. After aging overnight, it is heated to 80 ° C for another 30 min, cooled to room temperature, and the dark red reaction solution discolor 0.2 g of sodium bisulfite. Then the reaction solution is concentrated at 40 ° C in vacuo. The oily residue is brought to crystallization by repeated mixing with hot diisopropyl ether.
Yield 62.3 g 05%). M.p. 66-b7 S.
C. Alkylsulfonyl-1,2,3-triazoles.
4-propylsulfonyl-1,2,3-triazole.
To a solution of 103.2 g (0.72 mol) of 4-propylthio-1,2,3-triazole in 320 ml of acetic acid and a ml of water is added in portions over 30 minutes at -55 ° C 170.5 g (1 , 08 mole) potassium permanganate. Stir at 10 minutes and add a solution of 159.8 g (0.8 mol) of sodium bisulfite in 500 ml of water until completely discolored. It is then extracted 4 times with 250 ml portions of ethyl acetate. The organic phase is dried with magnesium sulfate, filtered and. concentrated in vacuo to obtain 119 g (9t, 5) of a liquid product, 1.5085.
In the same way, the following starting products are obtained:
A-Methylsulfonyl-1, 2,3T pl.101-103 C
5-triazole
: Isopropylsulfonyl-1, 2,3p 1,5067-triazole
but
{-Benzylsulfonyl-1, 2,3T pl. 1b3-1bb with -triazole "-Ethylsulfonyl-1, 2.35 T pl. triazole
"-Butylsulfonyl-1, 2,3p 1,4948-triazole
0
C- (1-Methylpropylsulfonyl) 1,4858 -1,2,3-triazole
; 4-Isobutylsulfonyl-1, 2.35
M.p. 71-73 ° C
triazole
Example 1. 4-Propylsulfonyl-1, 2,3-tri zrl-1 (2,3) -dipropyl amide of carboxylic acid (compound 1).
8.75 g (0.05 mol) of 4-propylsulfonyl-1, 2,3-triazole in 75 ml of acetonitrile are mixed at room temperature with 5.55 g (0.055 mol) of triethylamine. While stirring for 10 minutes at 70 ° C, 8.18 g (0.05 mol) of dipropylcarbamoyl chloride was added dropwise with Yu. Stir for 2 hours at 70 ° C and incubate overnight. It is then concentrated under vacuum, the precipitate is mixed with 100 ml of ice-water and extracted with ether. The organic phase is then washed with sodium bicarbonate solution, dried over magnesium sulfate, filtered and concentrated to give 12.6 g (83 ° °) of the desired product, 1 ,. An isomeric mixture of N and N carbamoylation products is obtained. An example. -Methyl-5 methylthio-1, 2,3-triazole-1 (2,3) -dimethylamide carboxylic acid (compound 2). 16.4 g (0.127 mol) -methyl-5-methylthio-1, 2,3-triazole in 1bO ml of tetrahydrofuran is mixed at room temperature with 15.35 g (0.152 mol of triethylamine. Then, with stirring at 50 ° C for 5 16.3 g (0.152 mol) of dimethylcarbamoyl chloride are added dropwise to the min. The mixture is then stirred at 50 ° C and kept at room temperature for one day, then concentrated under vacuum, the residue is mixed with 150 ml of water and 75 ml of chloroform are extracted twice. The boundary phase is then washed with 1% sodium bicarbonate solution, dried with sulphate and, filtered and concentrated, 23.5 g (92.5) of center 1, 5370 of the left product are obtained, and.., l One isomer is obtained, probably N- the product of carbamoylylation. Prozem, methylthio-1, 2,3-triazole -1 (2,3) -methyl amide of carboxylic acid (compound 3). 5Methylamide 4 — methylthio-1, 2, -triazol-1 (2,3) -carboxylic acid (isomeric mixture) 6Anylidene-methylthio-1,2, 3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) 7 Ethylamide 4-methylthio-1,2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) 8 Propylamide-methylthio-1,2 -triazol-1 (2,3) -carboxylic acid (isomeric mixture)
4-methylthio-1, 2, 3-triazole-1 (2,3) -carboxylic acid butylamide (isomeric mixture)
1, 8 11.5 g (.0.1 mol) of 4-methylthio-1, 2,3-triazole are dissolved in 100 ml of tetrahydrofuran and mixed with 6.27 g (0.11 mol) of methyl isocyanate at C for 3 min In addition, 0.1 ml of triethylamine is added as a catalyst. Finally, it is stirred for 1 hour at 5 ° C and then for another 1.5 hours at room temperature. It is then concentrated in vacuo at 0 ° C and the resulting residue (isomeric mixture) is recrystallized from 500 ml of water with vigorous stirring. The product yield is 8.7 g (50.5) T PL.107-1090S (decomp.). One isomer is obtained, probably the N product of carbamoylation. Example k. -Methylthio, 2,3-tripiazol-1 (2,3) -methylamino carboxylic acid (compound). 11.5 g (0.1 mol) of 4-methylthio-1, 2, 3, -triazole is dissolved in 126 ml of carbon tetrachloride and mixed with 6.27 g (0.11 mol) of methyl isocyanate at room temperature for 10 min After overnight, the crystals are filtered off with suction and washed with a small amount of carbon tetrachloride. The crystals are recrystallized from benzene / cyclohexane. The yield of the product is 12.2 g (70.91) T pl.109-110 C (decomp.). One isomer is obtained, probably the N product of carbamoylation. Similarly, the following compounds Tpl. 93 ° C (decomp.). T pl. 86,5-89 serazl.) Semicrystalline ,, 5Sh
Cyclohexylamine-methylthio1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture)
4-methylthio-1,2,3-triazol-1 (2,3) -carboxylic acid anilide (N-isomer)
Anilide-methylthio-T, 2,3-triazole-1 (2,3) -carboxylic acid
(N-isomer)
(2-methylanilide) -A-methylthio-1, 2,3-triazole-1 (2,3) -carboxylic acid (N M3OMep)
(2-chloropanilide) -f-methylthio-1, 2,3-triaaol-1 (2,3) -carboxylic acid (N -isomer)
(3-methylanilide) -4-methylthio1, 2,3-triazole-1 (2,3) -carboxylic acid (N-isomer)
(4-methylanilide) - -methylthio-1, 2,3-triazole-1 (2,3) -carboxylic acid (N-isomer)
(3-chloroanilide) -methylthio-1, 2,3-triazole-1 (2,3) -carboxylic acid (N-isomer)
(-chloroanilide) -methylthio-1, 2,3-triazole-1 (2,3) -carboxylic acid (N-isomer)
Allyl amide-methylthio-1,2,3-1 G2,3) -carboxylic acid (N-isomer)
Dimethylamide-methylthio-1, 2,3triazol-1 (2,3) -carboxylic acid (isomeric mixture)
Methylamide A-ethylthio-1,2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture)
Methylamide-propylthio-1,2,3triazol-1 (2,3) -carboxylic acid (isomeric mixture)
T pl. es / t c
t pl. 98-100 s
t pl. 93-95 ° C
Or
T pl. 80-88 ° C
T pl. (different)
T pl. 91-92.5 ° C (decomp)
T pl. 108.5-109.5 ° С (times)
T pl. 10b-107 ° C (decomp.)
T pl. 109-110 ° C (decomp.) T pl. 50-55 С
1.5569
1.5571
T pl. 35-38 0 23 Methylamide-isopropylthio-1,2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture). 2 Methylamide -butylthio-1, 2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) 25Methylamide (1-methylpropylthio) 1, 2.3 triazole-1 (2,3) carboxylic acid (isomeric mixture ) 26 Methylamide-allythio-1,2,3-triazole-1 (2,3) carboxylic acid (isomeric mixture) 27 Methylamide 4-butylthio-1,2,3-triazole-1 G2,3) -carboxylic acid (N isomer ) 28 Methylamide 4- (l-methylpropylthio) -1,2, 3-triazole-1 (2, 3) -carboxylic acid (N-isomer). 29 Methylamide-allythio-1,2,3-triazol-1 (2,3) carboxylic acid (N-isomer) 30 Methylamide-ethylthio-1, 2, 3-triazole-1 (2,3) -carboxylic acid (N-isomer) 31 Methylamide -propylthio-1,2,3-triazole-1 (2,3) -carboxylic acid (N-isomer) 32Methylamide -isopropylthio-1, 2, 3 -triazol-1 (2,3) -carboxylic acid (N -isomer ) 33Methylamide 4-isobutylthio-1,2,3-triazol-1 (2,3) carboxylic acid (isomeric mixture) 34Methylamide - (2-prop 1Ilthio) -1, 2,3-triazol-1 (2,3) - carboxylic acid (isomeric mixture) 35 Methylamide-benzylthio-, 2,3-three acid-1 (2,3) -carboxylic acid (isomeric mixture) nL 1, n 1, nir 1.5390 Semi-crystalline T pl. With T pl. 66-B9 ° C T pl. T pl. 8.5-86 ° C T pl. 75-78 0 T pl 91-92,5С p 1, 5382 Semi-crystalline T pl. WITH
.13929008.ti
Methylamide 4-isobutylthio-1,2,3-triazol-1 (2,3) -carboxylic acid (N-isomer) T pl. 82-83,
Methylamide (2-propynylthio) 1, 2,3-triazole-1 (2,3) -carboxylic
acid (N-isomer) T pl. 101-102 С
Methylamide 4-benzylthio-1, 2, 3-triazole-1 (2,3) carboxylic acid (N-isomer) T pl. 8t-85 C
4-methylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic dimethylamide
acid (isomeric mixture) T pl. 73-83 С
Methylamide "-methylsulfonyl-1,2, 3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) T pl. 132-13 ° C
Ethylamide-methylsulfonyl-T, 2, 3-triazole-1 (2, 3) -carbonic acid (isomeric mixture) T pl. 110-1PS
4-methylsulfonyl-1,2,3-triazol-1 (2,3) -carboxylic acid propylamide (isomeric mixture) T pl. 66-72 С
Butylamide-methylsulfonyl-1,2,3-triazol-1 (2, 3) -carboxylic acid (isomeric mixture) T pl. 70-72 С
Methylamide 4-methylsulfinyl1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) T pl. 95-97 ° C
Ethylamide-methylsulfinyl-1, 2, 3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) front t, 5370
Propyl amide "-methylsulfinyl-1, 2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture). Ex 1.5288
Anilide-methylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) T pl. 13 -137 ° C
Cyclohexylamide l-methylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) T pl. 9b-103 ° C
("-Chloroanilide) -methylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) T pl. 170-17 s
1592900816
(4-methylanilide) - -methylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) T pl. 156-158 С
Allyl amide-methylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) T pl. 91-92,5 С
Methylamide 1-methyl-5 methylthio-triazole-1 {2,3) carboxylic
- -g gchi gh g f fO. acids (N-isomer)
53 Butylamide "-methylsulfinyl1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) (-methylanilide) - -methylsulfinyl1, 2, 3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) 55 (4-chloroanilide) - -methylsulfinyl1, 2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) 56Arylamide-methylsulfinyl1, 2, 3-triazole-1 (2,3) -carboxylic acid (isomeric mixture)
57 dimethylamide-methylsulfinyl, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) p. 1, 5391
Diethylamide-methylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) p 1, 50b5
Methylamide 4-isopropylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) T pl. Hl-l49C
Dimethylamide-isopropylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (N-isomer) T pl. 112-113 С
Dimethylamide-isopropylsulfonyl, 2,3 triazole-1 (2,3) -carboxylic
acids (N-isomer). 1, 50b1
4-isopropylsulfonyl 1, 2, 3-triazole-1 (2,3) -carboxylic diethylamide
acid (isomeric mixture) p 1, + 909
Methylamide-propylsulfonyl, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) T pl. 99-109С
0
T pl. 102-106 С
10 front 1.5128 T pl. 122-123 С T pl.150 С (decomp.) P 1, 5365
17 929008.8
Dimethylamide- -propylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) nir 1,5131
4-propylsulfonyl 1, 2,3-triazole-1 (2,3) -carboxylic diethylamide
acid (isomeric mixture) p. 1,992
Ethylamide-propylsulfonyl-1,2,3-triazol-1 (2, 3) -carboxylic acid (isomeric mixture) T pl. 48-60 С
(M-ethyl-Y-propyl) amide-propylsulfonyl-1, 2,3 triazole-1 (2,3) carboxylic acid (isomeric.
mixture) p 1.5031
(N-Ethyl-Y-propyl) amide 4-methylsulfonyl-1, 2,3-tripiazol-1 (2,3) - carboxylic acid
(isomeric mixture) p 1.5081
N-ethylanilide i-methylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) nL 1,
N-ethylanilide A-isopropylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) P-1, 538t
N-ethylanilide 4-propylsulfonyl1,2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture). n 1,
(N-Ethyl-N-propyl) 4-isopropylsulfonyl-1, 2,3-triazol-1 (2,3) -carboxylic acid amide
(isomeric mixture) p 1.5028
Dimethylamide + -butylthio-1, 2,3tripiazol-1 (2,3) -carboxylic acid (isomeric mixture) Pr
Dimethylamide | -isobutylthio-1, 2,3-tripiazol-1 (2,3) -carboxylic acid (isomeric mixture) p 1,5321
75 Dimethylamide 4-butylsulfonyl-1, 2,3-triazole-1 () - carboxylic acid (isomeric mixture) p 1,5119
76 i-Butylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic diethylamide
acid (isomeric mixture) p 1,5010
D
ABOUT
B
1992900820
Dimethylamide t-isobutylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) p 1,5107
D-diethylamide C-isobutylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) p 1, EEE
T-ethylsulfonyl-1, 2,3 triazole-1 (2,3) -carboxylic dimethylamide
acid (isomeric mixture) T pl. 79-82 С
Diethylamide 4-ethylsulfonyl-1, 2.3 triazole-1 (2, 3.) Carboxylic
acid (isomeric mixture) p 1.5080
Diethylamide - (1-methylpropylsulfonyl) -1,2,3-triazole-1 (2,3) carboxylic acid
(isomeric mixture) ni. 1.5110
Diethylamide-benzylsulfonyl-1, 2.3 triazole-1 (2,3) carbon
acid (isomeric mixture) T PL, 90-91 C
Diethylamide 1 butylthio-1, 2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) p 1, 52t2
8 Diethylamide + - (1-methylpropylsulfonyl) -1,2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) nL 1, 5019
4-benzylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic dimethylamide
acid (isomeric mixture) p 1, 5538
Dimethylamide 4-ethylthio-1, 2, 3-triazole-1 (2,3) carbon
acid (isomeric mixture) p. 1,
Diethylamide-ethylthio-, 2, 3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) Pr 1, 5351
Diethylamide - isobutylthio-1, 2,3-triazol-1 (2,3) -carboic acid (isomeric mixture) 1,521Q
Dimethylamide i- (1-methylpropylthio)
-1,2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) Pr 1, 5331
/.
D
ao
21929008.22
Diethylamide i - (- methylpropylthio) -1, 2,3-triazol-1 (2,3) caroic
acids (isomeric mixture) nt 1,5235
Dimethylamide-benzylthio-1,2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) front 1.5988
Diethylamide-benzylthio-1, 2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) Ex 1.5760
4-propylsulfonyl-1, 2,3-triazole-1 (2,3) -carboiic propylamide
acid (isomeric mixture) T nos. b7-b9 C
Butylamide-propylsulfonyl, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) T pl. 7b-79 ° C
Isopropylamide-propylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) T pl. 68-72 С
4-propylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic dibutylamide
acid (isomeric mixture) niP 1, 909
4-propylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid pyrrolidide (isomeric mixture) Pt 1.5805
98 Piperidide-propyl sulphenyl, 2,3-triazole-1 (2,3) -carbono-.,
howl acid (isomeric mixture) P | 1.5270
Diallylamide-propylsulfonyl, 2,3-triazole-T (2,3) -carboxylic
acid (isomeric mixture) 1.5176
. Morpholid “-propylsulfonyl-1, 2,3-triazole-1 (2,3) carboxylic acid (isomeric mixture) ni. 1, 5251
(N-ethyl-N-prbpyl) amide of k-butylsulfonyl-1 2, 3-triazole-1 (2,3) -carboxylic acid
(isomeric mixture) h 1,4990
(N-ethyl-N-propyl) amide 4-isobutylsulfonyl-1, 2,3-triazolol (2,3) -carboxylic acid (isomeric mixture) Pr 1,

ao
392900824
(M-ethyl-M-propyl) amide 4-11-methylpropylsulfonyl) -1,2,3
-triazole.-1 (2,3) -carboxylic
acid (isomeric mixture) Pd 1, EEE
(N-ethyl-N-butyl) amide 4-propylsulfonyl-1, 2,3-triazole-1 (2,3) carboxylic acid (isomeric
mixture) n 1,
Dipentylamide 4-propylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) p 1.4880
(N-ethyl-N-cyclohexyl) amide 4-propylsulfonyl-1,2,3-triazole-1 (2,3) -carboxylic acid
(isomeric mixture) nL 1,5161
4-propylsulfonyl1, 2,3-triazol-1 (2, 3) -carboxylic acid diisopropylamide (isomeric mixture) p 1,5010
(K-ethyl L-propyl) amide 4-ethylsulfonyl-1, 2,3-triazole-1 (2,3) carboxylic acid (isomeric
mixture) Pr 1, 4998
Dipropylamide 4-ethylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) T pl. 60-61 С
4-ethylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic dibutylamide
acid (isomeric mixture) p 1,4931
Dipropylamide 4-butylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) p1 1,4959
4-Butylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid dibutylamide (isomeric mixture) Pr 1, 4900
4- (1-methylpropylsulfonyl) -, 2,3-triazole-1 (2,3) -carboxylic acid dibutylamide
(isomeric mixture) pg 1,4910
4-isobutylsulfonyl-1, 2,3-triazol-1 (2,3) -carboxylic dipropylamide
acid (isomeric mixture) 1, 4920
2592900826
4-Isobutylsulfonyl 1, 2,3-triazole-1 (2,3) -carboxylic dibutylamide
acid (isomeric mixture) p1 1, B87
Dipropylamide - (1-methylpropyl) sulfonyl-1,2,3-triazole-1 (2,3) -carboxylic acid (isomeric p
mixture) PC 1,
Diisopropylamide t- (1-methylpropyl) sulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric
mixture) n 1,
118 (M-ethyl-K-butyl) amide 4-butylsulfonyl-1, 2,3-triazol-1 (2,3) carboxylic acid (isomeric mixture) Ptl 1.951
(N-ethyl-N-butyl) amide-isobutylsulfonyl-1, 2,3-triazole-1 (2,3) carboxylic acid (isomeric
mixture) n 1,
(M-methyl-N-butyl) amide of (1-methylpropyl) -sulfonyl-1,2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) nL 1.9b8
(N-ethyl-N-cyclohexyl) amide-ethylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid
(isomeric mixture) p 1.5160
Dibutylamide-isopropylsulfonyl, 2,3-triazole-1 (2,3) -carboxylic acid ,, ,, acid (isomeric mixture) p, 1,950
Dipropylamide 4-isoprogylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) T pl. 58-60 ° C
(lM-ethyl-N-cyclohexyl) amide of t-butylsulfonyl-1, 2,3-tripiazol-1 (2,3) -carboxylic acid (isomeric mixture) Pd 1.5111
4-1-methylpropylsulfonyl-1 (N-ethyl-Y-cyclohexyl) amide; 1, 2,3-triazol-1 (2,3) -carboxylic acid J. (isomeric mixture); 1,5100
Diisobutylamide-propylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid {isomeric mixture) Ex 1.5011
2792900828
Dihexylamide-propylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) p 1,
(N-ethyl-Y-benzyl) amide of k-propylsulfonyl-1, 2,3-triazol-1 (2,3) -carboxylic acid „(isomeric mixture) ntj 1,
(N-ethyl-Y-isopropyl) amide-propylsulfonyl-1, 2,3-tripiazol-1 (2,3) -carboxylic acid (isomeric mixture) Ptch 1.5055
N-hexamethylene amide 4-propylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic "Q acid (isomeric mixture) p 1, 5272
(2-cyanoethyl) anilide A-propylsulfonyl-1, 2.3, triazole-1 (2,3) -carboxylic
acid (isomeric mixture) T PL 12 C
Methyl anilide-propylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) If i rrno
(N-ethyl-N-butyl) amide-ethylsulfonyl-1, 2,3-triazol-1 (2,3) -car6alic acid.islot (isomeric mixture) pg 1, 3002
(N-ethyl-M-butyl) amide 4-isopropylsulfonyl-1, 2, 3 triazole-1 (2, 3) carboxylic acid (isomeric
mixture) Sprayable
(N-ethyl-M-cyclohexyl) amide-isobutylsulfonyl-T, 2,3-tripiazol-1 (2,3) -carboxylic acid (isomeric mixture) p 1.5078
(M-ethyl-S-isopropyl) amide -butylsulfonyl-1, 2,3-triazolol (2, 3) -carboxylic acid (isomeric mixture) njj 1,
(N-ethyl-N-isopropyl) amide C-isobutylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) p 1,
Diethylamide-propylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric mixture) p 1, 5192
p j-j I, eiu
crystals
29929008.30
t-propylsulfonyl-1, 2,3-triazole-I (2,3) carboxylic acid bis- (2-chloroethyl) amide (isomeric mixture) p 1.5238
(N-ethyl-N-benzyl) amide -butylsulfonyl-1, 2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) 1.5 "29
(N-ethyl-N-benZyl) 4- (1-methylpropyl) sulfonyl-1,2,3-triazole-1 (2,3) -carboxylic acid amide (isomeric mixture) p "1.5392
(N-ethyl-N-benzyl) amide-isobutylsulfonyl-1, 2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) Ptch 1, 5361
(N-ethyl-N-butyl) amide-methylsulfonyl-1, 2,3-triazole-1 (2,3) -carboxylic acid (isomeric
mixture) T pl. 60-62 ° C
4-ethylthio-5-methyl1, 2,3-triazole-1 (2,3) -carboxylic acid dimethylamide (isomeric mixture) Fri, 1,5333
Dnpropylamide "-propylsulfonyl-5-methyl-1, 2,3-triazol-1 (2,3) -carboxylic acid (isomeric mixture) n 1,
(N-Ethyl-Y-isopropyl) amide 4-propylsulfonyl-5-methyl-1, 2,3-triazol-1 (2, 3) -carboxylic acid-Q. lots (isomeric mixture) DD 1, 973
Dimethylamide - (2-propynylthio) -5-methyl-1, 2,3-triazole-1 (2,3) -car-.
bonoic acid (isomeric mixture) Pr 1.55b8
(N-ethyl-N-from-6-propyl) amide C-methylsulfonyl-1, 2,3-triazole 1 (2,3) -carboxylic acid (isomeric mixture), nio ij989
(N-Ethyl-Y-isopropyl) amide 4-ethylsulfonyl-1, 2,3-triazol-1 (2,3) -carboxylic acid (iso.
measured mixture) p 1,500
.ten
ch40
3192900832
(N-ethyl-Y-isopropyl) amide - (1methylpropylsulfonyl) -, 2,3-triazole-1 (2,3) carboxylic acid
(isomeric mixture) Pr 1, 4959
Diisopropylamide-ethylsulfonyl-1, 2, 3-triazole-1 (2, 3) carboxylic q ,. acid (isomeric mixture) Fri 1,
Diisopropylamide-isobutylsulfonyl-1, 2,3-triazole-1 (2,3) carboxylic acid (isomeric mixture) ni, 1, 925
Diisopropylamide -butylsulfonyl1, 2,3-triazole-1 (2,3) -carboxylic
acid (isomeric mixture) ni 1, "935
Diisopropylamide 5 methyl- -propylsulfonyl-1, 2,3-triazole-1 (2,3) carboxylic acid (isomeric mixture) n 1,
Dimethylamide-isopropylthio-5methyl-1, 2. 3Triazole- (2,3) -carbono-j
howl acid (isomeric mixture) P-1, 525t
Dimethylamide-allythio-5-methyl-1, 2,3 triazole-1 (2,3) -carboxylic,. acid (isomeric mixture) PL 1,
T- (2-cyanoethylthio) 5-methyl-1, 2, -3-triazol-1 (2,3) carboxylic acid dimethylamide (isomeric mixture) Pr 1.5 "00
Dimethylamide-methylthio-5-propyl1, 2,3-triazol-1 (2,3) - carboxylic f, acid "1, 5292
Dimethylamide 5-ethyl- -methylthio-1, 2, 3-triazole-1 (2,3) -carboxylic acid 1, 5370
Dimethylamide 5-isopropyl- -methylthio-1, 2,3-triazole-1 (2,3) -carboxylic acid, 1, 5263
Dimethylamide 5-tert.butyl- -methylthio-1, 2, 3-triazole- 1 (2, 3) -carbono- (,
. Howl acid pn 1, 5271 35 ti with 28 leaves. After a few days, the percentage of fallen leaves was determined. The results of processing are given in table. 6. Example 11. Cotton plants in the 6–7 leaf stage were treated with the following active substances. For each sconing treatment, plants with 25–2 b leaves in total 500 L / ha of composition were consumed. Black for several days set the percentage of fallen leaves. The results of processing cotton plants are summarized in table. 7. Example 12. The proposed dinenei were used in the form of aqueous emulsions or suspensions with the concentration of the active substance O.Ot. Such preparations are applied to the lid of Petri dishes (dosage: 4 mg of formulation per 1 cm). Then, in closed Petri dishes, 2C of 25 pieces of adult fruit of the Mediterranean Myx (Ceratit.is capitata) are kept. The measure of the effectiveness of the action was the mortality of the flies in% after 2k hours. In the table. 8 shows a comparative mortality rate of flies after 2k hours in the treatment of compounds. Example 13. Offered from dineni are used in the form of aqueous emulsions or suspensions with the concentration of the active substance O .. With these preparations they cover the lids and bottoms of Petri dishes (dosage k mg of the composition per 1 cm). Then, in closed petri dishes, they are kept for 8 hours in each of 10 pieces in 1217 day old prusaco (BlatteSIa germanica). The criterion of action was mortality in% in kS h. In Table. 9 shows the comparative mortality of Prusacks after treatment with the proposed compounds. Example l. Offered from dineni used in the form of aqueous emulsions or suspensions at a concentration of the active substance 0 ,. These preparations were actively sprayed with a strong population of black beet aphid and planted beans. After this, the plants were kept (8 hours. The criterion for determining the degree of efficacy was beet aphid mortality in 8 hours. 8 Table 10 shows the aphids mortality data after treatment with the proposed compounds. Example 15. The proposed compounds, as well as comparable means, are used in in the form of aqueous suspensions with an active substance concentration of 0.0012. These preparations were sprayed on the bottoms and covers of Petri dishes (dosage: k kg of the mixture per 1 cm). Then, for kS hours, they are kept in closed Petri dishes (each with 10 pieces of 12-17 day old x Pruskov specimens. The mortality of Prusacs specimens is given in Table 11. Example 16. The proposed compound, as well as the comparative agent, was used in the form of aqueous suspensions with an active substance concentration of 0.00025% .The bottoms and lids of Petri dishes were sprayed with these preparations (dosage k mg of the mixture per 1 cm.) Then, in these closed Petri dishes, for each 48 hours, ten young individuals (in the third stage of molting) of Asian cottonbugs (Dysdercus scingulafus) were kept in each. The criterion for determining the degree of effectiveness was the death rate of bedbugs in% after 48 hours. In the table. 12 shows the mortality of bedbugs. Example 17. The proposed compounds, as well as the compared agents, were used in the form of aqueous emulsions with the desired concentration of the biologically active substance. These preparations were sprayed to the bottom and the lids of Petri dishes (dosage: k mg composition per 1 cm). Then, the Petri dishes sprinkled in this way were kept for 42 hours each with 10 young individuals (in the third stage of the molt) cotton bugs (melons) Asian. The criterion for determining the degree of effectiveness was a knock down after 1.30 and 60 minutes, as well as bedbug mortality after 42 hours. In the table. 13 shows the effectiveness of the effect of the compounds on the young Asian Asian cotton bugs. Example 18. Treatment of seed seeds for protection against Helniinthosporiuni spec. The seeds of barley with a natural degree of damage to Helminthosporiimi graraineum, untreated or processed, with the proposed compounds were planted in pots in the soil and at a temperature below + 16 ° C allowed them to germinate. After the emergence of seedlings, the plants were turned on daily for illumination. After about 5 weeks, the affected plants and all the plants that had sprung were counted. The fungicidal action can be defined as: 100 - 9 2Р§ ЁУУ§ 2§ВЁ 21йУУU. defeat untreated% effect. In table. 14 shows the effectiveness of the proposed compounds on barley seeds. Example 19. Treatment of wheat seeds to protect against Tilbetia caries. Wheat seeds were infected for 1 kg of 3 g spores of the pathogen of Tilletia caries disease. Untreated or processed seeds were pressed into Petri dishes with wet clay and incubated for 3 days at a temperature below. Then the grains were removed and Petri dishes with the remaining spores were incubated further at. After 10 days, the spores were checked for germination. The fungicidal action can be determined as 100 percent germination. QE of the worked percent germination of untreated.% Effect. In Table. 15 shows the effectiveness of the effect of the proposed compounds on wheat seeds. I Example 20. Spraying rice seedlings for protection against Piricularia oryzae. Young rice plants were abundantly sprayed with the active substance concentrations shown in the table. After the coating dried, the treated plants, as well as untreated ones, were inoculated by spraying a suspension from spores (approximately 200,000 per ml) to the Piricularia stain pathogen and incubated in greenhouses moist at 25-27 0. After 5 days, how many percent of the leaf surface was determined amazed. From these data, the fungicidal action is determined. 100 feed of the lesion of untreated% effect. Table. 16 shows the effectiveness of the effect of the proposed compounds on rice seedlings. Example 21. Spraying tomato seedlings for protection against Botrytiscinerea. Young tomato plants were sprayed abundantly with the active substance concentrations listed in the table. After drying, the treated plants, as well as untreated ones, were inoculated by spraying a suspension from spores (about 1 million per 1 ml of solution) to the gray mold Botrytis cinerea and incubated with a moist .8 greenhouse at about 20 ° C. After untreated plants died (lesion 100), the extent of the lesion of the treated ones was determined, and thereby the fungicidal action was determined by the following formula, 100 lesion of the treated liiLI e..Wi-. Si defeat untreated% effect. The effectiveness of the effect on tomato tops of the proposed compounds is given in Table. 17. Example 22. Test for the maximum effective concentration with respect to nematodes (Meloidogiie Sp.). 20% powdered preparations of the active substance are uniformly mixed with the soil heavily infected with nematodes. Three days later, the cultivated soil was placed in two clay cups, about 0, 5 l, and 10 seeds of cucumber Guntruud were put in each. at 24-27 ° C they were in the greenhouse for 28 days. Then the roots were washed, the water bath was tested for damage by nematodes, and the damage reduction was determined in comparison with untreated in%. The proposed compounds, their amounts consumed and damage reduction are shown in the table below. 39 Calculation of the nematocidal effect: -0 -.- 1 .., „„, where A is the lesion of untreated control roots; B - defeat after treatment. The test for the maximum effective concentration with respect to nematodes is given in Table. 18. I., Example 23. Treatment of grape leaves for protection against Plasmopara viticola. Young grape plants with 5–8 leaves were abundantly sprayed with the indicated concentrations; after sucking the underside of the coating, the underside of the leaves was treated with an aqueous suspension (suspension) of a fungus spore (about 20,000 per 1 ml) and immediately incubated in a greenhouse at an atmosphere of perhaps more saturated with water vapor. From the second day, the air humidity was reduced to 3 days again to a normal level (up to 3070;) and then kept for one day to saturate with water vapor. 8. The conclusion on each sheet indicated the percentage of the area affected by the fungus and the average value was calculated for each treatment to determine the fungicidal effect using the formula. 100 damage to treated treated untreated% effect The effects on young grapes, the plants with the proposed compounds are given in Table. Example 2k, Treatment of pumpkin leaves for protection against Erysiphe cichoracearum. 8 Copiously sprayed with the following concentration of the active substance of the leaves of a young pumpkin after drying, were inoculated with a spray of dry pores of powdery erysipelas Erysiphe cichoracearum, incubated at 2 ° C, and after a week, the affected area was determined in the total leaf area. The fungicidal effect is calculated as follows: inn - l-0 09P§ 5t y 9§P§§2I§t t y5 defeat untreated% effect The effect on pumpkin leaves by the proposed compounds is given in Table. 20. Example 25. Treatment of oat seeds in the field to protect against Ustilago avenae. Oat seeds were immersed in a suspension of spores of the fungus Ustilago avenae and in a vacuum desiccator of the mixture: back under pressure from normal to reduced pressure. After the seeds dried, they were treated with the compounds obtained in the table according to the method of the invention, and the compounds were taken in powder form. 10 weeks after sowing, sick panicles were counted and, thus, the effect was determined by the formula 100 - -52 ° Bv ui§both the defeat of the untreated effect. In Table. 21 shows the effectiveness of the effect of the proposed compounds on oat seeds. Table 1
Oh oh
about
k k k
Ltd
k
929008 42
Continued table. one
3
929008
C Continued table, 1
five
Standard N-these p-propyl-3 - (propylsulfonyl) 1H-1, 2, V -triazole-1 -carboxamide
Unprocessed
: 6
929008 Continued table. one
C O
about
il-cho
vi) vDG
oh oh
about -
about
about
about -
Se -
about
Cv | -
"..§
l t)
about
t; "G
"4 SI
(D
4 11Л -o z a jc
H e- “c; y H o
o
"S: s I t" o
SE 01 c; s with, -s a scoc; fBct
o. bOdsojics:
YU
W Q. with I - 4 I
about
"S - o - -" 0
01
2: 1 I & I 1 o
Connection, no. Dose of active 2 500 58 500 65 500 67 500 Compound, No. Dose of active 2500 Tributyltritiophosphate500 Compound, No. Dose, g / ha
2
67 68
Three-p-butyltrithiophosphate
50
929008 Table 3 2000 2000
15, 61.5 61.5
7.7 substances Leaf dropping,% B, Q 12.0 50.0 13.6, 28.0 Table of substances. Falling leaves,%, 0,, 7 Table 5 Falling leaves,%
51
2
58 73 8i
Table 8
100 100
68
95
100
90
52
90
929008
52
Table 6
Table 7
72 76 88 72 80
Continuation of table.8
55929008
Continued table. Sh
Compare means .1-naphthyl-methylcarbamate.
56 Continued table. ten
0,00025
95
60
0,00025
oh se
w 1L about about with
oh
LTVo
oh oh
r ff
silt
oh oh
SPI oo
1L
. ohhh
oh oh
with;
cI
"Us
2O.
s; x
ai
I
Io.
rf itc
Ho lz
D) S Z
R 0)
ABOUT)
s
Yu.
“D o
il59929008
Table k
60 Continued table. one
f
Continued table. H
20 50 20 50 20 50 20 50 20 50 20 50 20 50
Table15
. 62
Continued table. 15
95,100
63 Continued tabl,
6k
929008
o Continuation of table. 15
65
92900866
T a b l and c a 16
67
92900868
Continued table. sixteen
69929008: 70
Continued tabl, 16
71
0.02 0.00i 0.1 0.02
0.00 0.1
0.02
0, OOA
0.1
0.02
0.00
0.1
0.02
0,
0.1
0.02
0.00
0.1
0.02
0,004
0.1
0.02
0.00
0.1
0.02
0,004
92900872
Pro; sixteen
87 80 96 20
10 80
35
20
87
94 87 62
91
73
31
100
89
54
75
69
94 62 12
73
128
129
132
133
13
135
136
137
138
929008rji
Continued table. sixteen
98 65 30 9B 50 25 99
0.1
0.02
0,004
0.1
0.02
0.00
0.1
0.02
50 57 0.00
0.1
100
0.02
89
0,004
65
0.1
100
0.02
85
0,004
78
0.1
100
0.02
100
0,004
93
0.1
100
0.02
80
0,004
70
,one
100
, 02
80
, 004
thirty
uh
,one
, 02
86 75
, 004
7592900876
. Continuation of the table. sixteen
77
929008
78 Table 17
79
100
97
100
93
100
100
929008
80 Continuation of table 1B
81
Table 19
"one
59
63

权利要求:
Claims (1)
[1]
Invention Formula
The method of producing 1,2,3-triazolecarboxylic acid amides of the general formula
Rg (
m
/ And
TO(
where K is alkyl with 1-6 carbon atoms, alkyl, propinyl or benzyl-,
929008
82 Continued table. 21
Tab faces 21
20 10 20 10 20
82
70
R (is hydrogen or alkyl with 1 - carbon atoms
I (iCd is the same or different and is hydrogen, unsubstituted alkyl with 1-6 carbon atoms or substituted by halogen; allyl, propinyl, unsubstituted phenyl or substituted alkyl with 1-3 carbon atoms or halogen, benzyl, cyclohexyl or
together form pyrrolidine, piperidine, morpholine, hexamethylenediamine, p O or 1 or 2, characterized in that 1,2,3-tri513ol of the general formula o) where R, n have the indicated value the formulas where R, Rij and p have the indicated meanings are 20 and the b is a monovalent metal cation, 929 are acylated with a carbamoyl halide of the general formula —cox where R a and R have the indicated values, and X is a halogen in the presence of a hydrogen halide acceptor or isocyanate of the formula R N C O where R has the indicated meanings, preferably in the presence of an organic second base. Sources of information taken into account in the examination 1. Weigand-Hilgetag. Experimental methods in organic chemistry. M., Himi, 1968, p. 435.

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同族专利:

公开号 | 公开日

ES483115A1|1980-04-16|

SE7906602L|1980-02-08|

YU149179A|1983-01-21|

IE48787B1|1985-05-15|

TR20593A|1982-02-19|

RO77561A|1981-11-04|

BE878127A|1980-02-07|

RO81505A|1983-04-29|

DE2834879A1|1980-02-21|

IL57927D0|1979-11-30|

CS205149B2|1981-04-30|

IT7924631D0|1979-07-25|

CH640518A5|1984-01-13|

FR2433018A1|1980-03-07|

FR2433018B1|1983-04-15|

IE791488L|1980-02-07|

NO792575L|1980-02-08|

BR7905011A|1980-05-13|

MX5623E|1983-11-09|

NZ191185A|1981-05-29|

EG14370A|1984-03-31|

IL57927A|1983-05-15|

IN152609B|1984-02-18|

ATA536579A|1981-07-15|

DD145364A5|1980-12-10|

LU81578A1|1979-12-07|

AT365892B|1982-02-25|

MA18557A1|1980-04-01|

AU4959479A|1980-02-14|

PH16769A|1984-02-22|

PT69999A|1979-08-01|

PL118237B1|1981-09-30|

CA1129425A|1982-08-10|

DK301879A|1980-02-08|

US4233059A|1980-11-11|

AU523909B2|1982-08-19|

IT1122324B|1986-04-23|

PL217595A1|1980-05-19|

NL7904611A|1980-02-11|

GB2028319A|1980-03-05|

GB2028319B|1983-04-27|

ZA794084B|1980-08-27|

AR222039A1|1981-04-15|

GR72718B|1983-12-01|

JPS5524179A|1980-02-21|

FI792423A|1980-02-08|

RO81505B|1983-04-30|

引用文献:

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

US3952001A|1970-07-01|1976-04-20|The Boots Company Limited|1-Carbamoyl-1,2,4-triazoles|US4280831A|1980-08-04|1981-07-28|Gulf Oil Corporation|Benzylsulfonyl diethylcarbamyl triazole and use as a selective herbicide|

US4596597A|1985-06-21|1986-06-24|Stauffer Chemical Company|Esters of 1,2 and 3-N,N-dialkylcarbamyl-5-substituted-1H-1,2,3-triazole-4-carboxylic acid|

US4596596A|1985-06-21|1986-06-24|Stauffer Chemical Company|1-,2-,and 3-N,N-dialkylcarbamyl-1-H-1,2,3-triazoles|

RU2005108046A|2002-08-22|2006-02-27|Зингента Партисипейшнс Аг |1, 2, 3-TRIAZOLE DERIVATIVES HAVING BACTERICIDALACTIVITY|

BR122013027950A2|2008-12-24|2019-12-10|BIAL PORTELA & Cª S A|pharmaceutical compounds|

WO2012138877A1|2011-04-06|2012-10-11|The Scripps Research Institute|N1- and n2-carbamoyl-1,2,3-triazole serine hydrolase inhibitors and methods|

CN102775361B|2012-07-27|2014-11-12|浙江工业大学|1, 2, 4-trizole derivative and preparation method and applications thereof|

US11085342B2|2018-06-20|2021-08-10|Ngk Insulators, Ltd.|Honeycomb filter|

法律状态:

优先权:

申请号 | 申请日 | 专利标题

DE19782834879|DE2834879A1|1978-08-07|1978-08-07|1,2,3-TRIAZOLE CARBONIC ACID AMIDES, METHOD FOR PRODUCING THESE COMPOUNDS AND BIOCIDES CONTAINING THEM|

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