MX3479E - PROCESS TO PREPARE A 2-SULFINYL OR 2-SULFONYL-PIRIDINE N-OXIDE COMPOUND - Google Patents
PROCESS TO PREPARE A 2-SULFINYL OR 2-SULFONYL-PIRIDINE N-OXIDE COMPOUNDInfo
- Publication number
- MX3479E MX3479E MX7276U MX7276U MX3479E MX 3479 E MX3479 E MX 3479E MX 7276 U MX7276 U MX 7276U MX 7276 U MX7276 U MX 7276U MX 3479 E MX3479 E MX 3479E
- Authority
- MX
- Mexico
- Prior art keywords
- phenyl
- nitro
- halogen
- alkyl
- sulfinyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/89—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
La presente invención se refiere a proceso para preparar un compuesto de n-óxido de 2-sulfinil o 2-sulfonil-piridina de la fórmula (ver gaceta) en que n es 1 o 2; R1 es un hidrógeno o metilo; R2 tiene uno de los siguientes valores cuando R1 es hidrógeno: 2,2-diclorociclopropilo; 2,2-dicloro-1-metilciclopropilo, ciano, naftilo, metilnaftino, fenil monosubstituído en el que el substituyente está en posición orto y se relaciona del alquilo, con 1 a 2 átomos de carbono, halógeno, nitro o fenilo polisubstituído con 2 hasta 5 substituyentes que pueden ser los mismos o distintos y se selecionan del alquilo con 1 a 2 átomos de carbono, halógeno, nitro, metoxi, etoxi, y metilenodioxi; y R2 tiene uno de los siguientes valores: cuando R1 es metilo: fenilo, naftilo, fenilo, substituidos con 1 a 3 substituyentes que pueden ser los mismos o distintos y se seleccionan del alquilo con 1 a 2 átomos de carbono, halógeno y nitro, caracterizados en que el N-óxido de 2-tioperidina se hace reaccionar con un agente oxidante en presencia de un solvente que es agua a una temperatura de desde 0°C, hasta el reflujo, y se emplea un catalizador seleccionado del grupo de sales de tungstaneo vanadio, zirconio y molibdeno.The present invention relates to a process for preparing a 2-sulfinyl or 2-sulfonyl-pyridine n-oxide compound of the formula (see gazette) wherein n is 1 or 2; R1 is a hydrogen or methyl; R2 has one of the following values when R1 is hydrogen: 2,2-dichlorocyclopropyl; 2,2-dichloro-1-methylcyclopropyl, cyano, naphthyl, methylnaphtin, monosubstituted phenyl in which the substituent is in the ortho position and is related to the alkyl, with 1 to 2 carbon atoms, halogen, nitro or polysubstituted phenyl with 2 to 5 substituents which may be the same or different and are selected from C 1 -C 2 -alkyl, halogen, nitro, methoxy, ethoxy, and methylenedioxy; and R2 has one of the following values: when R1 is methyl: phenyl, naphthyl, phenyl, substituted with 1 to 3 substituents which may be the same or different and are selected from alkyl with 1 to 2 carbon atoms, halogen and nitro, characterized in that the 2-thioperidine N-oxide is reacted with an oxidizing agent in the presence of a solvent that is water at a temperature from 0 ° C to reflux, and a catalyst selected from the group of salts of tungstaneo vanadium, zirconium and molybdenum.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US05/559,188 US4019893A (en) | 1975-03-17 | 1975-03-17 | Herbicidal method using 2-sulfinyl or 2-sulfonyl pyridine N-oxide derivatives |
US05/559,196 US3960542A (en) | 1975-03-17 | 1975-03-17 | Herbicidal 2-sulfinyl and 2-sulfonyl pyridine N-oxide derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
MX3479E true MX3479E (en) | 1980-12-15 |
Family
ID=27071993
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX7276U MX3479E (en) | 1975-03-17 | 1976-03-15 | PROCESS TO PREPARE A 2-SULFINYL OR 2-SULFONYL-PIRIDINE N-OXIDE COMPOUND |
Country Status (13)
Country | Link |
---|---|
JP (1) | JPS51115926A (en) |
AR (1) | AR221680A1 (en) |
CH (2) | CH610722A5 (en) |
CS (1) | CS201538B2 (en) |
DD (2) | DD129731A5 (en) |
DE (1) | DE2609204A1 (en) |
FR (1) | FR2304292A1 (en) |
GB (1) | GB1542881A (en) |
HU (1) | HU178363B (en) |
IT (1) | IT1062195B (en) |
MX (1) | MX3479E (en) |
PL (1) | PL99519B1 (en) |
SU (1) | SU583750A3 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4050921A (en) | 1976-04-16 | 1977-09-27 | Uniroyal Inc. | Regulation of the natural growth or development of plants with 2-sulfinyl or 2-sulfonyl pyridine N-oxide compounds |
US4503230A (en) * | 1981-08-20 | 1985-03-05 | Uniroyal, Inc. | Alkylation of substituted sulfonylpyridines |
AT389874B (en) * | 1988-04-29 | 1990-02-12 | Agrolinz Agrarchemikalien | NEW PYRIDYL-THIO-ETHYLAZOLES, METHOD FOR THE PRODUCTION THEREOF AND THEIR FUNGICIDES CONTAINING THEM |
-
1976
- 1976-03-05 DE DE19762609204 patent/DE2609204A1/en not_active Withdrawn
- 1976-03-11 AR AR26252976A patent/AR221680A1/en active
- 1976-03-12 FR FR7607255A patent/FR2304292A1/en active Granted
- 1976-03-15 MX MX7276U patent/MX3479E/en unknown
- 1976-03-15 JP JP2801876A patent/JPS51115926A/en active Pending
- 1976-03-16 CS CS169376A patent/CS201538B2/en unknown
- 1976-03-16 GB GB1047676A patent/GB1542881A/en not_active Expired
- 1976-03-16 IT IT6762876A patent/IT1062195B/en active
- 1976-03-16 DD DD19775076A patent/DD129731A5/en unknown
- 1976-03-16 DD DD19187376A patent/DD124876A5/xx unknown
- 1976-03-16 PL PL18797176A patent/PL99519B1/en unknown
- 1976-03-16 HU HUUI000233 patent/HU178363B/en unknown
- 1976-03-17 CH CH333876A patent/CH610722A5/en not_active IP Right Cessation
- 1976-08-30 SU SU7602391605A patent/SU583750A3/en active
-
1979
- 1979-05-09 CH CH435479A patent/CH615667A5/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE2609204A1 (en) | 1976-10-07 |
IT1062195B (en) | 1983-07-28 |
DD129731A5 (en) | 1978-02-08 |
SU583750A3 (en) | 1977-12-05 |
FR2304292B1 (en) | 1979-01-05 |
AU1181776A (en) | 1977-09-15 |
HU178363B (en) | 1982-04-28 |
DD124876A5 (en) | 1977-03-16 |
CS201538B2 (en) | 1980-11-28 |
PL99519B1 (en) | 1978-07-31 |
GB1542881A (en) | 1979-03-28 |
JPS51115926A (en) | 1976-10-13 |
CH615667A5 (en) | 1980-02-15 |
FR2304292A1 (en) | 1976-10-15 |
AR221680A1 (en) | 1981-03-13 |
CH610722A5 (en) | 1979-05-15 |
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