MX3364E - PROCEDURE FOR THE PREPARATION OF TETRAHYDRO-2- (NITROMETHYLENE) -2E-1,3-THIAZINE DERIVATIVES - Google Patents
PROCEDURE FOR THE PREPARATION OF TETRAHYDRO-2- (NITROMETHYLENE) -2E-1,3-THIAZINE DERIVATIVESInfo
- Publication number
- MX3364E MX3364E MX001265U MX126575U MX3364E MX 3364 E MX3364 E MX 3364E MX 001265 U MX001265 U MX 001265U MX 126575 U MX126575 U MX 126575U MX 3364 E MX3364 E MX 3364E
- Authority
- MX
- Mexico
- Prior art keywords
- carbon atoms
- nitromethylene
- tetrahydro
- preparation
- thiazine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D279/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D279/04—1,3-Thiazines; Hydrogenated 1,3-thiazines
- C07D279/06—1,3-Thiazines; Hydrogenated 1,3-thiazines not condensed with other rings
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/86—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/06—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings
- C07D265/08—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
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)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
La presente invención se refiere a un procedimiento para la preparación de derivados de tetrahidro-2-(nitrometileno)-2H-1,3 tiazina, de la fórmula general I siguiente; así como tautómeros de los mismos:(ver gaceta) en donde R es hidrógeno o R1 -O-CO en el cual: R1 es alquilo de 1 a 10 átomos de carbono, alquenilo de 2 a 5 átomos de carbono, alquilo de 1 ó 2 átomos de carbono susbtituído con fenilo, clorofenilo, diclorofenilo, metoxifenilo, fenoxifenilo, cianofenilo, furanilo, tetrahidrofuranilo, metoxi, etoxi, metiltio, metoxietoxi, naftalenilo, ciclop[opilo, tienilo, metilsulfinilo, piridinilo, 2,2-dimetil-1,3-diaxalanilo, o flúor, alquenilo de 2 a 5 átomos de carbono substituído con cloro; cicloalquilo de 3 a 5 átomos de carbono; ó un grupo dimetil-octadianilo; caracterizado porque se hace reaccionar 5,6-dihidro-2-metiltio-4H-1,3-tiazina con un alquinitroacetato en la presencia de una cantidad catalítica de iones de zinc a una temperatura de 80° a 130°C.The present invention relates to a process for the preparation of tetrahydro-2- (nitromethylene) -2H-1,3 thiazine derivatives of the following general formula I; as well as tautomers thereof: (see gazette) where R is hydrogen or R1 -O-CO in which: R1 is alkyl of 1 to 10 carbon atoms, alkenyl of 2 to 5 carbon atoms, alkyl of 1 or 2 carbon atoms substituted with phenyl, chlorophenyl, dichlorophenyl, methoxyphenyl, phenoxyphenyl, cyanophenyl, furanyl, tetrahydrofuranyl, methoxy, ethoxy, methylthio, methoxyethoxy, naphthalenyl, cyclop [opyl, thienyl, methylsulfinyl, 2,2 3-diaxalanyl, or fluorine, chloro-substituted C2-C5 alkenyl; cycloalkyl of 3 to 5 carbon atoms; or a dimethyl-octadianyl group; characterized in that 5,6-dihydro-2-methylthio-4H-1,3-thiazine is reacted with an alkynitroacetate in the presence of a catalytic amount of zinc ions at a temperature of 80 ° to 130 ° C.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US46812374A | 1974-05-08 | 1974-05-08 | |
US46812274A | 1974-05-08 | 1974-05-08 | |
US46812574A | 1974-05-08 | 1974-05-08 | |
US46812474A | 1974-05-08 | 1974-05-08 | |
US502115A US3907790A (en) | 1974-08-30 | 1974-08-30 | Tetrahydro-2- (nitromethylene)-2H-1,3-oxazines |
Publications (1)
Publication Number | Publication Date |
---|---|
MX3364E true MX3364E (en) | 1980-10-15 |
Family
ID=27541694
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX001265U MX3364E (en) | 1974-05-08 | 1975-05-07 | PROCEDURE FOR THE PREPARATION OF TETRAHYDRO-2- (NITROMETHYLENE) -2E-1,3-THIAZINE DERIVATIVES |
Country Status (13)
Country | Link |
---|---|
BE (1) | BE828847A (en) |
BR (1) | BR7502770A (en) |
CH (1) | CH620206A5 (en) |
DD (1) | DD119519A5 (en) |
DE (1) | DE2518849C2 (en) |
FR (1) | FR2270251B1 (en) |
GB (1) | GB1513951A (en) |
IL (1) | IL47247A (en) |
IT (1) | IT1037952B (en) |
MX (1) | MX3364E (en) |
NL (1) | NL180717C (en) |
OA (1) | OA04995A (en) |
TR (1) | TR18902A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2118177B (en) * | 1982-03-26 | 1985-11-06 | Shell Int Research | N-substituted-tetrahydrothiazines and their use as pesticides |
GB8324664D0 (en) * | 1983-09-14 | 1983-10-19 | Shell Int Research | N-substituted tetrahydrothiazines |
US4923987A (en) * | 1988-07-25 | 1990-05-08 | E. I. Du Pont De Nemours And Company | Process for the preparation of nitromethylene heterocyclic compounds |
-
1975
- 1975-04-28 DE DE2518849A patent/DE2518849C2/en not_active Expired
- 1975-05-07 TR TR18902A patent/TR18902A/en unknown
- 1975-05-07 BE BE156163A patent/BE828847A/en not_active IP Right Cessation
- 1975-05-07 OA OA55493A patent/OA04995A/en unknown
- 1975-05-07 CH CH590575A patent/CH620206A5/en not_active IP Right Cessation
- 1975-05-07 BR BR3533/75A patent/BR7502770A/en unknown
- 1975-05-07 IT IT23133/75A patent/IT1037952B/en active
- 1975-05-07 FR FR7514405A patent/FR2270251B1/fr not_active Expired
- 1975-05-07 MX MX001265U patent/MX3364E/en unknown
- 1975-05-07 GB GB19181/75A patent/GB1513951A/en not_active Expired
- 1975-05-07 IL IL47247A patent/IL47247A/en unknown
- 1975-05-07 NL NLAANVRAGE7505365,A patent/NL180717C/en not_active IP Right Cessation
- 1975-05-07 DD DD185896A patent/DD119519A5/xx unknown
Also Published As
Publication number | Publication date |
---|---|
TR18902A (en) | 1977-12-09 |
DE2518849A1 (en) | 1975-11-20 |
NL180717B (en) | 1986-11-17 |
FR2270251B1 (en) | 1977-04-15 |
IL47247A0 (en) | 1975-08-31 |
CH620206A5 (en) | 1980-11-14 |
NL180717C (en) | 1987-04-16 |
BE828847A (en) | 1975-11-07 |
IT1037952B (en) | 1979-11-20 |
BR7502770A (en) | 1976-03-16 |
DE2518849C2 (en) | 1986-05-28 |
AU8091975A (en) | 1976-11-11 |
IL47247A (en) | 1979-11-30 |
FR2270251A1 (en) | 1975-12-05 |
GB1513951A (en) | 1978-06-14 |
NL7505365A (en) | 1975-11-11 |
OA04995A (en) | 1980-11-30 |
DD119519A5 (en) | 1976-05-05 |
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