摘要:
The present invention relates to hydrates of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)amino]-sulfonyl]benzamide. The invention also relates to a process for the preparation of these hydrates and to plant protection formulations which comprise hydrates of the phenyluracil I.
摘要:
The present invention relates to a crystalline form of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)-amino]sulfonyl]benzamide. The invention also relates to a process for the preparation of this crystalline form and to plant protection formulations which comprise this crystalline form of the phenyluracil.
摘要翻译:本发明涉及2-氯-5- [3,6-二氢-3-甲基-2,6-二氧代-4-(三氟甲基)-1-(2H)嘧啶基] -4-氟 - N - [[甲基(1-甲基乙基) - 氨基]磺酰基]苯甲酰胺。 本发明还涉及制备该结晶形式的方法以及包含该苯基尿嘧啶的该结晶形式的植物保护制剂。
摘要:
The present invention relates to hydrates of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)amino]-sulfonyl]benzamide. The invention also relates to a process for the preparation of these hydrates and to plant protection formulations which comprise hydrates of the phenyluracil I.
摘要:
The present invention relates to a crystalline form of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)-amino]sulfonyl]benzamide. The invention also relates to a process for the preparation of this crystalline form and to plant protection formulations which comprise this crystalline form of the phenyluracil.
摘要翻译:本发明涉及2-氯-5- [3,6-二氢-3-甲基-2,6-二氧代-4-(三氟甲基)-1-(2H)嘧啶基] -4-氟 - N - [[甲基(1-甲基乙基) - 氨基]磺酰基]苯甲酰胺。 本发明还涉及制备该结晶形式的方法以及包含该苯基尿嘧啶的该结晶形式的植物保护制剂。
摘要:
The present invention relates to a process for preparing 3-phenyl(thio)uracils and -dithiouracils of the formula I where the variables are each as defined in the description, and also intermediates for their preparation.
摘要:
The present invention relates to a process for preparing 3-phenyl(thio)uracils and -dithiouracils of the formula I where the variables are each as defined in the description, and also intermediates for their preparation.
摘要:
A process is described for preparing 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I, by reacting a phenyl iso(thio)cyanate of the formula II with an enamine of the formula III and, if appropriate, in a further step, the resulting 3-phenyl(thio)uracil or 3-phenyldithiouracil of the formula I where R1=R1a, when R1=hydrogen, is reacted with an aminating agent of the formula IV to give 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I where R1=amino where the variables R1, R1a, R2, R3, R4, X1, X2, X3, Ar, A and L1 are each as defined in claim 1.
摘要翻译:描述了制备式I的3-苯基(硫代)尿嘧啶或3-苯基二硫尿嘧啶的方法,通过使式II的苯基异(硫代)氰酸酯与式III的烯胺反应,如果合适, 所得到的式I的3-苯基(硫代)尿嘧啶或3-苯基二硫尿嘧啶,其中R 1 = R 1a,当R1 =氢时,与式Ⅳ的胺化剂反应得到3-苯基(硫代)尿嘧啶或3 其中R1 =氨基,其中变量R1,R1a,R2,R3,R4,X1,X2,X3,Ar,A和L1各自如权利要求1所定义。
摘要:
A process for preparing phenyl iso(thio)cyanates of the formula I in which a compound of the formula II or its HCl adduct is reacted with a phosgenating agent where W is oxygen or sulfur and Ar and A are as defined in claim 1 is described. Moreover, the invention relates to the use of the phenyl iso(thio)cyanates for preparing crop protection agents.
摘要:
A process for preparing phenyl iso(thio)cyanates of the formula I in which a compound of the formula II or its HCl adduct is reacted with a phosgenating agent where W is oxygen or sulfur and Ar and A are as defined in claim 1 is described. Moreover, the invention relates to the use of the phenyl iso(thio)cyanates for preparing crop protection agents.
摘要:
A process is described for preparing 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I, by reacting a phenyl iso(thio)cyanate of the formula II with an enamine of the formula III and, if appropriate, in a further step, the resulting 3-phenyl(thio)uracil or 3-phenyldithiouracil of the formula I where R1=R1a, when R1=hydrogen, is reacted with an aminating agent of the formula IV to give 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I where R1=amino where the variables R1, R1a, R2, R3, R4, X1, X2, X3, Ar, A and L1 are each as defined in claim 1.
摘要翻译:描述了制备式I的3-苯基(硫代)尿嘧啶或3-苯基二硫尿嘧啶的方法,通过使式II的苯基异(硫代)氰酸酯与式III的烯胺反应,如果合适, 步骤,得到的式I的3-苯基(硫代)尿嘧啶或3-苯基二硫尿嘧啶,其中R 1 = R 1a,R 1, =氢,与式IV的胺化剂反应,得到式I的3-苯基(硫代)尿嘧啶或3-苯基二硫尿嘧啶,其中R 1 =氨基,其中变量R 1 R 1,R 2,R 2,R 3,R 4,X 1, X 2,X 3,X 3,Ar,A和L 1各自如权利要求1所定义。