ES2133170T3 - Procedimiento para la obtencion de alcoxitriazolinonas. - Google Patents

Procedimiento para la obtencion de alcoxitriazolinonas.

Info

Publication number
ES2133170T3
ES2133170T3 ES95114212T ES95114212T ES2133170T3 ES 2133170 T3 ES2133170 T3 ES 2133170T3 ES 95114212 T ES95114212 T ES 95114212T ES 95114212 T ES95114212 T ES 95114212T ES 2133170 T3 ES2133170 T3 ES 2133170T3
Authority
ES
Spain
Prior art keywords
sup
alkyl
formula
obtaining
acil
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES95114212T
Other languages
English (en)
Inventor
Heinz-Jurgen Dr Wroblowsky
Klaus Dr Konig
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer AG
Original Assignee
Bayer 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.)
Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Application granted granted Critical
Publication of ES2133170T3 publication Critical patent/ES2133170T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D249/12—Oxygen or sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
    • C07C281/02—Compounds containing any of the groups, e.g. carbazates
    • C07C281/04—Compounds containing any of the groups, e.g. carbazates the other nitrogen atom being further doubly-bound to a carbon atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

ALCOXITRIAZOLINONAS DE LA FORMULA (I) DONDE R 1 Y R{SUP, 2} DE FORMA INDEPENDIENTE UNO DE OTRO SIGNIFICAN SUSTITUIDOS EVENTUALMENTE ALQUILO, ALQUENILO, ALQUINILO, CICLOALQUILO, CICLOALQUILALQUILO, ARILO O ARILALQUILO, (QUE PUEDEN SER UTILIZADOS COMO PRODUCTOS INTERMEDIOS PARA LA ELABORACION DE SUSTANCIAS ACTIVAS HERBICIDAS), OBTENIENDOSE CON UN BUEN RENDIMIENTO Y ALTA PUREZA, DONDE EL DIESTER (II) DE ACIDO IMINOCARBONICO SE TRANSFORMA CON ESTERES (III) DE ACIDO CARBACINICO DONDE R{SUP, 2} Y R{SUP, 3} DE FORMA RESPECTIVA SIGNIFICAN ALQUILO O ARILO, EN TEMPERATURAS DESDE - 20 LOS DERIVADOS DE SEMICARBACIDA FORMADOS BAJO DESDOBLAMIENTO DE R{SUP, 2} - OH (IV) SIENDO CONDENSADOS DE FORMA CICLICA EVENTUALMENTE EN PRESENCIA DE UNA BASE EN TEMPERATURAS DESDE 20 HASTA 150 LMENTE LAS 5 ALCOXITRIAZOLINONAS OBTENIDAS DE LA FORMULA (V) [= FORMULA (I) CON R{SUP, 1} = H] SE TRANSFORMAN CON UN MEDIO DE ALQUILIZACION DE LA FORMULA R{SUP, 1} - X(VI) [X P. EJ. = HALOGENO O - OSO{SUB, 2}OR{SUP, 1}] EVENTUALMENTE EN PRESENCIA DE UNA BASE EN TEMPERATURA DESDE 0 HASTA 150 QUILIZACION ALTAMENTE SELECTIVA).
ES95114212T 1994-09-23 1995-09-11 Procedimiento para la obtencion de alcoxitriazolinonas. Expired - Lifetime ES2133170T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4433967A DE4433967A1 (de) 1994-09-23 1994-09-23 Verfahren zur Herstellung von Alkoxytriazolinonen

Publications (1)

Publication Number Publication Date
ES2133170T3 true ES2133170T3 (es) 1999-09-01

Family

ID=6528978

Family Applications (1)

Application Number Title Priority Date Filing Date
ES95114212T Expired - Lifetime ES2133170T3 (es) 1994-09-23 1995-09-11 Procedimiento para la obtencion de alcoxitriazolinonas.

Country Status (8)

Country Link
US (3) US5599945A (es)
EP (1) EP0708095B1 (es)
JP (1) JP3910652B2 (es)
AT (1) ATE180252T1 (es)
CA (1) CA2158712C (es)
DE (2) DE4433967A1 (es)
DK (1) DK0708095T3 (es)
ES (1) ES2133170T3 (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4433967A1 (de) * 1994-09-23 1996-03-28 Bayer Ag Verfahren zur Herstellung von Alkoxytriazolinonen
ATE245149T1 (de) 1997-10-08 2003-08-15 Lonza Ag Verfahren zur herstellung von alkoxytriazolinonen
US5917050A (en) * 1998-02-11 1999-06-29 Bayer Corporation Process for preparing alkoxytriazolinones
CA2339270A1 (en) 1998-08-03 2000-02-17 Yoshiharu Kinoshita Triazolone derivatives, use thereof, and intermediate therefor
US6197971B1 (en) * 1999-12-27 2001-03-06 Bayer Corporation Process for the manufacture of substituted triazolinones
US6222045B1 (en) 2000-09-20 2001-04-24 Bayer Corporation Process for manufacturing substituted triazolinones
CN105473558B (zh) 2013-06-20 2019-04-19 拜耳作物科学股份公司 作为杀螨剂和杀昆虫剂的芳基硫化物衍生物和芳基硫氧化物衍生物
US10223360B2 (en) * 2014-12-02 2019-03-05 Ricoh Company, Ltd. Print job archives that are optimized for server hardware

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1940367A1 (de) 1969-08-08 1971-02-18 Bayer Ag Neue-Triazolon-Derivate
US5356865A (en) * 1990-09-22 1994-10-18 Bayer Aktiengesellschaft Substituted 5-alkoxy-1,2,4-triazol-3-(thi)ones
DE4110795A1 (de) 1991-04-04 1992-10-08 Bayer Ag Sulfonylaminocarbonyltriazolinone mit ueber sauerstoff gebundenen substituenten
US5241074A (en) * 1988-05-09 1993-08-31 Bayer Aktiengesellschaft Sulphonylaminocarbonyltriazolinones
DE4030063A1 (de) 1990-09-22 1992-03-26 Bayer Ag Substituierte 5-alkoxy-1,2,4,-triazol-3-(thi)one
US5300480A (en) * 1989-04-13 1994-04-05 Bayer Aktiengesellschaft Herbicidal sulphonylaminocarbonyltriazolinones having two substituents bonded via oxygen
US5534486A (en) * 1991-04-04 1996-07-09 Bayer Aktiengesellschaft Herbicidal sulphonylaminocarbonyl triazolinones having substituents bonded via oxygen
DE4123608C1 (es) 1991-07-17 1992-07-02 Skw Trostberg Ag, 8223 Trostberg, De
DE4234801A1 (de) * 1992-10-15 1994-04-21 Bayer Ag Sulfonylaminocarbonyltriazolinone
DE4433967A1 (de) * 1994-09-23 1996-03-28 Bayer Ag Verfahren zur Herstellung von Alkoxytriazolinonen

Also Published As

Publication number Publication date
EP0708095A1 (de) 1996-04-24
CA2158712A1 (en) 1996-03-24
DE59505962D1 (de) 1999-06-24
DE4433967A1 (de) 1996-03-28
JP3910652B2 (ja) 2007-04-25
JPH08325244A (ja) 1996-12-10
US5710303A (en) 1998-01-20
US5892054A (en) 1999-04-06
EP0708095B1 (de) 1999-05-19
CA2158712C (en) 2006-05-30
ATE180252T1 (de) 1999-06-15
DK0708095T3 (da) 1999-11-08
US5599945A (en) 1997-02-04

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