Dow Agrosciences LLC

Adama Makhteshim, Ltd.

Other

Dow Argosciences LLC

Corteva Agriscience LLC

Beth Lorsbach

Qiang Yang

W John Owen

Chenglin Yao

Carl Vincent DeAmicis

Gary A Roth

Yu Zhang

Kaitlyn C Gray

Joseck M Muhuhi

Xiaoyong Li

Ronald Ross, Jr

Gregory T Whiteker

Jeffery Dale Webster

Timothy A Boebel

Timothy P Martin

David E Podhorez

Greg Whiteker

Kristy Bryan

Thomas P Clark

Michael Thomas Sullenberger

Mark Andrew Pobanz

Ann Marie Buysse

Scott Thornburgh

Elisabeth J Kane

Belgin Canturk

Jeffrey S Nissen

Noormohamed Mohamed Niyaz

Lindsay Stelzer

Thomas Clarence Sparks

Daniel Knueppel

James M Ruiz

Jeffery D Webster

Kevin Gerald Meyer

Paul Renee LePlae, Jr

Irene Mae Morrison

George E Davis

Carla J R Klittich

Lindsey Stelzer

Chris V Galliford

Ronald Ross

Carl Deamicis

John W Owen

Gary D Crouse

David Hamilton Young

Michael R Loso

Peter Lee Johnson

William C Lo

Jeffrey Brian Epp

Natalie Christine Giampietro

Gerald Bryan Watson

Akshay Patny

Bassam S Nader

Zoltan Laszlo Benko

Erich W Baum

Lindsey Gayle Fischer

Gary David Gustafson

James Edward Hunter

Pravin S Iyer

Francis Eugene Tisdell

Debra L Camper

Jeff Petkus

Paul Richard Graupner

William Kirkland Brewster

Nneka Tuere Breaux

Dan Pernich

Hemant Joshi

Gary Roth

Yan Hao

Carl DeAMICIS

Frisby Davis Smith

Christopher Galliford

Adiraj Mandaleswaran

Ramadevi Sanam

Rambabu Gundla

Alice Meitl

Andrew L Ward

Paul Leplae

Kaitlyn Gray

Timothy Martin

Timothy Boebel

Michael Sullenberger

Jeffery Webster

Michael T Sullenberger

Jr Ronald Ross

Nneka Breaux

James Ruiz

David Young

John Owen W

W J Owen

Mark A Pobanz

A fungicidal composition containing a fungicidally effective amount of the compound of Formula I: 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one, and at least one fungicide to provide synergistic control of selected fungi wherein the at least one fungicide is a fungicidal sterol biosynthesis-inhibitor.

Synergistic fungicidal mixtures and compositions comprising 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one for fungal control (SBI)

A fungicidal composition containing a fungicidally effective amount of the compound of Formula I: 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one, and at least one fungicide to provide synergistic control of selected fungi wherein the at least one fungicide is a multi-site inhibitor or a strobilurin inhibitor.

Synergistic fungicidal mixtures and compositions comprising 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one for fungal control (MSI)

A fungicidal composition containing a fungicidally effective amount of the compound of Formula I: 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one, and at least one fungicide to provide synergistic control of selected fungi, wherein the at least one fungicide is a succinate dehydrogenase-inhibitor.

Synergistic fungicidal mixtures and compositions comprising 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one for fungal control (SDHI)

Synergistic fungicidal mixtures and compositions comprising 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one for fungal control

The present application provides processes for making pesticidal compounds and compounds useful both as pesticides and in the making of pesticidal compounds.

Processes for the preparation of pesticidal compounds

This present disclosure is related to the field of 3-alkyl-5-fluoro-4-substituted-imino-3,4-5 dihydropyrimidin-2(1H)-ones and their derivatives and to the use of these compounds as fungicides. Also provided are methods of controlling a fungal disease such as, comprising administering an effective amount of the fungicide compound to at lease one surface associated with the plant, seed or soil.

[object Object]

3-(3-Chloro-1H-pyrazol-1-yl)pyridine is prepared by cyclizing 3-hydrazinopyridine.dihydrochloride with commercially available 3-ethoxyacrylonitrile to provide 3-(3-amino-1H-pyrazol-1-yl)pyridine, and by converting the amino group to a chloro group by a Sandmeyer reaction.

Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine

3-(3-chloro-1H-pyrazol-1-yl)pyridine is prepared by cyclizing 3-hydrazinopyridine-.dihydrochloride with a dialkyl maleate to provide an alkyl 5-oxo-2-(pyridin-3-yl)pyrazolidine-3-carboxylate, by chlorinating to provide an alkyl 3-chloro-1-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylate, by oxidizing to provide an alkyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate, by converting the ester to the carboxylic acid by hydrolysis to provide 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acid hydrochloride, and by removing the carboxylic acid by a decarboxylation reaction.

Process for the preparation of 3-(3-chloro-1H-pyrazol-1-yl)pyridine

This present disclosure is related to the field of N-(substituted)-5-fluoro-4-imino-3-methyl-2-oxo-3,4-di-hydropyrimidine-1(2H)-carboxylates and their derivatives and to the use of these compounds as fungicides. Also provided are methods of controlling a fungal disease such as, comprising administering an effective amount of the fungicide compound to at lease one surface associated with the plant, seed or soil. 

N-(substituted)-5-fluoro-4-imino-3-methyl-2-oxo-3,4-dihydropyrimidine-1(2H)-carboxylate derivatives

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Indianapolis, IN, United States of America

Beth Lorsbach