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2010-12-08T20:43:42+01:00
2010-10-30T17:23:42+01:00
2010-12-08T20:43:42+01:00
Jouve S.A., EPO - Publication - KB, TaggedPDF v1.27
EP-0264020-A3-19890712
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EP-0264020-A3-19890712
Man erhält die herbizid wirksmen 0-Aryl-N'-pyrimidin-2-yl-harnstoffe der allgemeinen Formel (I)(worin die Reste R1, R2, R3, R4 und R5 die in der Beschreibung angegebenen Bedeutungen haben) in guten Ausbeuten, indem man Iminokohlensäureester der Formel (II)mit Aminen der Formel (III)in Gegenwart von Säureakzeptoren und gegebenenfalls in Gegenwart von Verdünnungsmitteln bei Temperaturen zwischen 0 °C und 150 °C umsetzt.
Man erhält die herbizid wirksmen 0-Aryl-N'-pyrimidin-2-yl-harnstoffe der allgemeinen Formel (I)(worin die Reste R1, R2, R3, R4 und R5 die in der Beschreibung angegebenen Bedeutungen haben) in guten Ausbeuten, indem man Iminokohlensäureester der Formel (II)mit Aminen der Formel (III)in Gegenwart von Säureakzeptoren und gegebenenfalls in Gegenwart von Verdünnungsmitteln bei Temperaturen zwischen 0 °C und 150 °C umsetzt.
de
European Patent Office
EP0264020
EP 0264020
C07D 239/42
A01N 47/36
C07C143/72
Process for the preparation of 0-aryl-N'-pyrimidin-2-yl-isourea
Verfahren zur Herstellung von 0-Aryl-N'-pyrimidin-2-yl-isoharnstoffen - European Patent Office - EP 0264020 A3
Verfahren zur Herstellung von 0-Aryl-N'-pyrimidin-2-yl-isoharnstoffen - European Patent Office - EP 0264020 A3
Adobe PDF Library 8.0
"EP0264020"; "EP 0264020"; "C07D 239/42"; "A01N 47/36"; "C07C143/72"; "Process for the preparation of 0-aryl-N'-pyrimidin-2-yl-isourea"
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EP
0264020
A3
1989-07-12
87114213
1987-09-29
DE
3634926
1986-10-14
C07D 239/42
A01N 47/36
C07C143/72
BAYER AG
Fest, Christa, Dr.
Verfahren zur Herstellung von 0-Aryl-N'-pyrimidin-2-yl-isoharnstoffen
Verfahren zur Herstellung von 0-Aryl-N'-pyrimidin-2-yl-isoharnstoffen
Process for the preparation of 0-aryl-N'-pyrimidin-2-yl-isourea
Procédé de préparation de 0-aryle-N'-pyrimidine-2-yl-isourée
Man erhält die herbizid wirksmen 0-Aryl-N'-pyrimidin-2-yl-harnstoffe der allgemeinen Formel (I)(worin die Reste R1, R2, R3, R4 und R5 die in der Beschreibung angegebenen Bedeutungen haben) in guten Ausbeuten, indem man Iminokohlensäureester der Formel (II)mit Aminen der Formel (III)in Gegenwart von Säureakzeptoren und gegebenenfalls in Gegenwart von Verdünnungsmitteln bei Temperaturen zwischen 0 °C und 150 °C umsetzt.
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