7-iodoheptanal - CAS号 72489-61-3

物化性质

沸点：

234.7±23.0 °C(Predicted)
密度：

1.498±0.06 g/cm3(Predicted)

计算性质

辛醇/水分配系数(LogP)：

2.9
重原子数：

9
可旋转键数：

6
环数：

0.0
sp3杂化的碳原子比例：

0.86
拓扑面积：

17.1
氢给体数：

0
氢受体数：

1

反应信息

作为反应物：

描述：

7-iodoheptanal 在咪唑、 bis(triphenylphosphine)nickel(II) chloride 、正丁基锂、碘、三苯基膦作用下，以四氢呋喃、乙醚、正己烷、正庚烷、二氯甲烷、苯为溶剂，反应 32.67h，生成 (E)-13-iodo-2,10-dimethyltrideca-2,10-diene

参考文献：

名称：

非天然，移码的类异戊二烯二磷酸酯类似物的合成

摘要：

开发了一套合成方法，并将其应用于八种移码的类异戊二烯二磷酸酯类似物的合成。设计这些类似物以增加或减少类异戊二烯结构的双键和/或焦磷酸盐部分之间的亚甲基单元。对哺乳动物GGTase-I和FTase的评估表明，小的结构变化可导致底物活性的实质性变化。

DOI：

10.1021/acs.orglett.6b02977
作为产物：

描述：

7-溴庚酸在 4-二甲氨基吡啶、 lithium aluminium tetrahydride 、盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺、三乙胺、 sodium iodide 作用下，以四氢呋喃、二氯甲烷、乙腈为溶剂，反应 33.0h，生成 7-iodoheptanal

参考文献：

名称：

[EN] RAS PROTEIN DEGRADERS, PHARMACEUTICAL COMPOSITIONS THEREOF, AND THEIR THERAPEUTIC APPLICATIONS
[FR] AGENTS DE DÉGRADATION DE LA PROTÉINE RAS, COMPOSITIONS PHARMACEUTIQUES DE CEUX-CI ET LEURS APPLICATIONS THÉRAPEUTIQUES

摘要：

本文提供了RAS蛋白降解剂，例如化合物式（I）的化合物，以及其药物组合物。本文还提供了它们用于治疗、预防或改善RAS介导的疾病、疾病或症状的方法。

公开号：

WO2021051034A1

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文献信息

Method for producing anellated tetrahydro-{1h}-triazoles

申请人：——

公开号：US20040097728A1

公开（公告）日：2004-05-20

The present invention relates to a process for preparing fused tetrahydro-[ 1 H]-triazoles of the formula I 1 where the variables R a , Z, Z 1 , X, W, n and Q are as defined in claim 1, by cyclization of compounds of the formula II 2 where R is C(X)OR 2 or C(X)SR 2 , where X is oxygen or sulfur, and R 2 is as defined in claim 1, in the presence of a base. The invention also relates to compounds of the formula I where W is sulfur if Z is a methylene group optionally substituted by R a , and furthermore to compounds of the formula I where Q is a benzoxazole or benzothiazole radical, and to the use of these compounds as herbicides.

本发明涉及一种制备公式I的熔融四氢咪唑的方法，其中变量Ra、Z、Z1、X、W、n和Q如权利要求1中定义，通过在碱存在下，将公式II的化合物环化得到，其中R为C(X)OR2或C(X)SR2，其中X为氧或硫，R2如权利要求1中定义。该发明还涉及公式I的化合物，其中如果Z是可选地由Ra取代的亚甲基基团，则W为硫，此外还涉及公式I的化合物，其中Q为苯并噁唑或苯并噻唑基团，并将这些化合物用作除草剂。
1 And 2-substituted analogues of certain prostaglandins

申请人：Miles Laboratories, Inc.

公开号：US04171331A1

公开（公告）日：1979-10-16

Disclosed are trans 1 & 2-di(loweralkyl)phosphono; 1 & 2-chloro, bromo and iodo; 1 & 2-thio and 1 & 2-amino analogues of E.sub.1, A.sub.1, F.sub.1.alpha., F.sub.1.beta., 11 deoxy E.sub.1, 11 deoxy F.sub.1.beta., and 11 deoxy F.sub.1.alpha. prostaglandins. The prostaglandins of this invention are variously useful as antithrombic agents, bronchodilators such as in the treatment of asthma, inhibitors of gastric secretion and as antihypertensive agents. Certain of the prostaglandins disclosed herein are useful as precursors for prostaglandins having one or more of the foregoing utilities.

本发明公开了E.sub.1、A.sub.1、F.sub.1.alpha.、F.sub.1.beta.、11去氧E.sub.1、11去氧F.sub.1.beta.和11去氧F.sub.1.alpha.前列腺素的trans 1和2-二(较低烷基)膦酸酯；1和2-氯、溴和碘；1和2-硫和1和2-氨基类似物。本发明的前列腺素可用作抗凝血剂、支气管扩张剂（如治疗哮喘）、胃酸分泌抑制剂和降压剂。本文所披露的某些前列腺素可用作具有上述一种或多种用途的前列腺素的前体。
N-Haloimide-enabled halogenation via halogen-bond-assisted C–C activation of alkanols

作者：Yan Geng、Yue Ma、Rui Huang、Xingwei Li、Songjie Yu

DOI：10.1039/d2gc03768h

日期：——

halogen-bond-assisted C–C activation of cyclic and acyclic alkanols in the absence of catalysts and oxidants, where the inexpensive N-haloimides act as bifunctional reagents to activate and halogenate alcohols. This redox-neutral protocol is a general method for the halogenation of the C–C bonds of primary, secondary, and tertiary alkanols, thus installing three types of halogen atoms and boronic esters

醇基原料惰性 C-C 键的选择性卤化在合成化学中具有重要意义。以前的卤化反应通常需要金属催化剂和/或氧化剂，并且仅限于裂解叔环烷醇的 C-C 键。在此，我们报告了一种广泛适用的合成碘代烷烃、溴代烷烃和氯代烷烃的策略，在没有催化剂和氧化剂的情况下，通过卤键辅助的环烷醇和无环烷醇的 C-C 活化，其中廉价的N-卤代酰亚胺作为双功能试剂激活和卤化醇。这种氧化还原中性方案是卤化伯、仲和叔烷醇的 C-C 键的通用方法，从而通过一锅脱碘-硼酸酯化在各种原料中安装三种类型的卤素原子和硼酸酯以实用和可持续的方式生产化学品。
[DE] 1-AMINO-3-BENZYLURACILE [EN] 1-AMINO-3-BENZYLURACILS [FR] 1-AMINO-3-BENZYLURACILES

申请人：BASF AKTIENGESELLSCHAFT

公开号：WO1997001543A1

公开（公告）日：1997-01-16

(DE) 1-Amino-3-benzyluracile (I) und deren Salze (R1 = Halogen; R2, R3 = H, CN, SCN, Halogen, C1-C4-Halogenalkyl, C1-C4-Halogenalkoxy, C1-C4-Halogenalkylthio; R4 = R3 + C1-C4-Alkyl, C1-C4-Alkoxy, C1-C6-Alkyl-NH-CO-; R5 = H, CN, NO2, OH, Halogen, gegebenenfalls substituiertes NH2, gegebenenfalls subst. C1-C6-Halogenalkoxy, C1-C6-Halogenalkylthio, C1-C6-Alkoxy, C1-C6-Alkylthio, C3-C8-Cycloalkoxy, C3-C8-Cycloalkylthio, C3-C6-Alkenyloxy, C3-C6-Alkenylthio, C3-C6-Alkinyloxy, C3-C6-Alkinylthio, C1-C6-Alkyl-COO-, C1-C6-Alkyl-COS-, C3-C6-Alkenyl-COO-, C3-C6-Alkenyl-COS-, C3-C6-Alkinyl-COO-, C3-C6-Alkinyl-COS-, C1-C6-Alkyl-SO2-O- oder C1-C6-Alkyl-SO2-; R6 = 1) H, OH, SH, Halogen, C1-C6-Halogenalkoxy, C1-C6-Halogenalkylthio, C1-C6-Alkylthio-(C1-C6-alkyl)carbonyl, C1-C6-Alkyliminooxy-CO-, 2) gegebenenfalls subst. C1-C6-Alkoxy, C1-C6-Alkylthio, C3-C8-Cycloalkoxy, C3-C8-Cycloalkylthio, C2-C6-Alkenyloxy, C2-C6-Alkenylthio, C2-C6-Alkinyloxy, C2-C6-Alkinylthio, C1-C6-Alkyl-COO-, C2-C6-Alkyl-COS-, C1-C6-Alkoxy-COO-, C2-C6-Alkenyl-COO-, C2-C6-Alkenyl-COS-, C2-C6-Alkinyl-COO-, C2-C6-Alkinyl-COS-, C1-C6-Alkyl-SO2-O-, C1-C6-Alkyl-SO2-, 3) -CY-R11 Y = -O-, -S-, gegebenenfalls subst. -NH-}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$m(0)C-CO-NH-OR20, -C$m(0)C-CO-N(R19)-OR20, -C$m(0)C-CS-NH-OR20, -C$m(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$m(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12) (Z2R13)-SR19, -C(Z1R12) (Z2R13)-N(R23)R24, gegebenenfalls substituiertes Amino oder -CONH2, Azaheterocyclyl, -CO-Azaheterocyclyl, (N + O oder N + O + S) Heterocyclyl enthaltende Kette); als Herbizide, zur Dessikation/Defoliation von Pflanzen.(EN) The invention concerns 1-amino-3-benzyluracils of formula (I) and their salts. In said formula (I), R1 = halogen; R2, R3 = H, CN, SCN, halogen, C1¿-C¿4-alkyl halide, C1-C4-alkoxy halide, C1-C4-alkylthio halide; R4 = R3 + C1-C4-alkyl, C1-C4-alkoxy, C1-C6-alkyl-NH-CO-; R5 = H, CN, NO2, OH, halogen, optionally substituted NH2, optionally substituted C1-C6-alkoxy halide, C1-C6-alkylthio halide, C1-C6-alkoxy, C1-C6-alkylthio, C3-C8-cycloalkoxy, C3-C8-cycloalkylthio, C3-C6-alkenyloxy, C3-C6-alkenylthio, C3-C6-alkinyloxy, C3-C6-alkinylthio, C1-C6-alkyl-COO-, C1-C6-alkyl-COS-, C3-C6-alkenyl-COO-, C3-C6-alkenyl-COS-, C3-C6-alkinyl-COO-, C3-C6-alkinyl-COS-, C1-C6-alkyl-SO2-O- or C1-C6-alkyl-SO2-; R6 = 1) H, OH, SH, halogen, C1-C6-alkoxy halide, C1C6-alkylthio halide, C1-C6-alkylthio-(C1-C6-alkyl)carbonyl, C1-C6-alkyliminooxy-CO-, 2) optionally substituted C1C6-alkoxy, C1-C6-alkylthio, C3-C8-cycloalkoxy, C3-C8-cycloalkylthio, C2-C6-alkenyloxy, C2-C6-alkenylthio, C2-C6-alkinyloxy, C2-C6-alkinylthio, C1-C6-alkyl-COO-, C2-C6-alkyl-COS-, C1-C6-alkoxy-COO-, C2-C6-alkenyl-COO-, C2-C6-alkenyl-COS-, C2-C6-alkinyl-COO-, C2-C6-alkinyl-COS-, C1-C6-alkyl-SO2-O-, C1-C6-alkyl-SO2-, 3) -CY-R11 Y = -O-, -S-, optionally substituted -NH-}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$m(0)C-CO-NH-OR20, -C$m(0)C-CO-N(R19)-OR20, -C$m(0)C-CS-NH-OR20, -C$m(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20,-C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$m(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, optionally substituted amino or -CONH2, azaheterocyclyl, -CO-azaheterocyclyl, or a chain comprising (N + O or N + O + S) heterocyclyl. These compounds can be used as herbicides for desiccating/defoliating plants.(FR) L'invention concerne des 1-amino-3-benzyluraciles de la formule (I) et leurs sels. Dans ladite formule (I), R1 représente de l'halogène; R2, R3 représentent H, CN, SCN, halogène, halogénure d'alkyle C1-C4, halogénure d'alcoxy C1-C4, halogénure d'alkylthio C1-C4; R4 représente R3 + alkyle C1-C4, alcoxy C1-C4, alkyle C1-C6 -NH-CO-; R5 représente H, CN, NO2, OH, halogène, NH2 éventuellement substitué, halogénure d'alcoxy C1-C6 éventuellement substitué, halogénure d'alkylthio C1-C6, alcoxy C1-C6, alkylthio C1-C6, cycloalcoxy C3-C8, cycloalkylthio C3-C8, alcényloxy C3-C6, alcénylthio C3-C6, alkinyloxy C3-C6, alkinylthio C3-C6, alkyle C1-C6-COO-, alkyle C1-C6-COS-, alcényle C3-C6-COO-, alcényle C3-C6-COS-, alkinyle C3-C6-COO-, alkinyle C3-C6-COS-, alkyle C1-C6-SO2-O- ou alkyle C1-C6-SO2-; R6 représente 1) H, OH, SH, halogène, halogénure d'alcoxy C1-C6, halogénure d'alkylthio C1-C6, alkylthio C1-C6-(alkyle C1-C6) carbonyle, alkyliminooxy C1-C6-CO-, 2) alcoxy C1-C6 éventuellement substitué, alkylthio C1-C6, cycloalcoxy C3-C8, cycloalkylthio C3-C8, alcényloxy C2-C6, alcénylthio C2-C6, alkinyloxy C2-C6, alkinylthio C2-C6, alkyle C1-C6-COO-, alkyle C2-C6-COS, alcoxy C1-C6-COO-, alcényle C2-C6-COO-, alcényle C2-C6 -COS-, alkinyle C2-C6-COO-, alkinyle C2-C6 -COS-, alkyle C1-C6-SO2-O-, alkyle C1-C6-SO2-, 3) -CY-R11 Y = -O-, -S-, -NH- éventuellement substitué}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$m(0)C-CO-NH-OR20, -C$m(0)C-CO-N(R19)-OR20, -C$m(0)C-CS-NH-OR20, -C$m(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$m(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, amino éventuellement substitué ou -CONH2, azahétérocyclyle, -CO-azahétérocyclyle, ou une chaîne comprenant de un hétérocyclyle (N + O ou N + O + S). Ces composés chimiques peuvent être utilisés comme herbicides pour la dessication/défoliation des plantes.

（DE）1-氨基-3-苯并嘧啶尿嘧啶（I）及其衍生物的盐类（R1 = 卤素；R2, R3 = H, CN, SCN, 卤素, C1-C4卤代烷基, C1-C4卤代烷氧基, C1-C4卤代烷硫基; R4 = R3 + C1-C4烷基, C1-C4烷氧基, C1-C6-NH-CO-烷基; R5 = H, CN, NO2, OH, 卤素, 可能是取代的NH2, 可能是取代的C1-C6卤代烷氧基, C1-C6卤代烷硫基, C1-C6烷氧基, C1-C6烷硫基, C3-C8环烷氧基, C3-C8环烷硫基, C3-C6烯基氧基, C3-C6烯基硫基, C3-C6炔基氧基, C3-C6炔基硫基, C1-C6烷基-COO-, C1-C6烷基-COS-, C3-C6烯基-COO-, C3-C6烯基-COS-, C3-C6炔基-COO-, C3-C6炔基-COS-, C1-C6烷基-SO2-O-或C1-C6烷基-SO2-; R6 = 1) H, OH, SH, 卤素, C1-C6卤代烷氧基, C1-C6卤代烷硫基, C1-C6烷硫基-(C1-C6烷基)羰基, C1-C6烷基亚胺氧基-CO-, 2) 可能是取代的C1-C6烷氧基, C1-C6烷硫基, C3-C8环烷氧基, C3-C8环烷硫基, C2-C6烯基氧基, C2-C6烯基硫基, C2-C6炔基氧基, C2-C6炔基硫基, C1-C6烷基-COO-, C2-C6烷基-COS-, C1-C6烷氧基-COO-, C2-C6烯基-COO-, C2-C6烯基-COS-, C2-C6炔基-COO-, C2-C6炔基-COS-, C1-C6烷基-SO2-O-, C1-C6烷基-SO2-, 3) -CY-R11 Y = -O-, -S-, 可能是取代的-NH-}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C(*)(0)C-CO-NH-OR20, -C(*)(0)C-CO-N(R19)-OR20, -C(*)(0)C-CS-NH-OR20, -C(*)(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C(*)(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, 可能是取代的氨基或-CONH2, 含氮杂环基, -CO-含氮杂环基, 或包含（N + O或N + O + S）的杂环基链）。这些化合物可用作除草剂，用于植物的脱水/脱叶。（EN）The invention concerns 1-amino-3-benzyluracils of formula (I) and their salts. In said formula (I), R1 = halogen; R2, R3 = H, CN, SCN, halogen, C1-C4-alkyl halide, C1-C4-alkoxy halide, C1-C4-alkylthio halide; R4 = R3 + C1-C4-alkyl, C1-C4-alkoxy, C1-C6-alkyl-NH-CO-; R5 = H, CN, NO2, OH, halogen, optionally substituted NH2, optionally substituted C1-C6-alkoxy halide, C1-C6-alkylthio halide, C1-C6-alkoxy, C1-C6-alkylthio, C3-C8-cycloalkoxy, C3-C8-cycloalkylthio, C3-C6-alkenyloxy, C3-C6-alkenylthio, C3-C6-alkinyloxy, C3-C6-alkinylthio, C1-C6-alkyl-COO-, C1-C6-alkyl-COS-, C3-C6-alkenyl-COO-, C3-C6-alkenyl-COS-, C3-C6-alkinyl-COO-, C3-C6-alkinyl-COS-, C1-C6-alkyl-SO2-O- or C1-C6-alkyl-SO2-; R6 = 1) H, OH, SH, halogen, C1-C6-alkoxy halide, C1-C6-alkylthio halide, C1-C6-alkylthio-(C1-C6-alkyl)carbonyl, C1-C6-alkyliminooxy-CO-, 2) optionally substituted C1-C6-alkoxy, C1-C6-alkylthio, C3-C8-cycloalkoxy, C3-C8-cycloalkylthio, C2-C6-alkenyloxy, C2-C6-alkenylthio, C2-C6-alkinyloxy, C2-C6-alkinylthio, C1-C6-alkyl-COO-, C2-C6-alkyl-COS-, C1-C6-alkoxy-COO-, C2-C6-alkenyl-COO-, C2-C6-alkenyl-COS-, C2-C6-alkinyl-COO-, C2-C6-alkinyl-COS-, C1-C6-alkyl-SO2-O-, C1-C6-alkyl-SO2-, 3) -CY-R11 Y = -O-, -S-, optionally substituted -NH-}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$(m)(0)C-CO-NH-OR20, -C$(m)(0)C-CO-N(R19)-OR20, -C$(m)(0)C-CS-NH-OR20, -C$(m)(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$(m)(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, optionally substituted amino or -CONH2, azaheterocyclyl, -CO-azaheterocyclyl, or a chain comprising (N + O or N + O + S) heterocyclyl. These compounds can be used as herbicides for desiccating/defoliating plants. （FR）L'invention concerne des 1-amino-3-benzyluraciles de la formule (I) et leurs sels. Dans ladite formule (I), R1 représente de l'halogène; R2, R3 représentent H, CN, SCN, halogène, halogénure d'alkyle C1-C4, halogénure d'alcoxy C1-C4, halogénure d'alkylthio C1-C4; R4 représente R3 + alkyle C1-C4, alcoxy C1-C4, alkyle C1-C6 -NH-CO-; R5 Represents H, CN, NO2, OH, halogène, NH2 éventuellement substitué, halogénure d'alcoxy C1-C6 éventuellement substitué, halogénure d'alkylthio C1-C6, alcoxy C1-C6, alkylthio C1-C6, cycloalcoxy C3-C8, cycloalkylthio C3-C8, alcényloxy C3-C6, alcénylthio C3-C6, alkinyloxy C3-C6, alkinylthio C3-C6, alkyle C1-C6-COO-, alkyle C1-C6-COS-, alcényle C3-C6-COO-, alcényle C3-C6-COS-, alkinyle C3-C6-COO-, alkinyle C3-C6-COS-, alkyle C1-C6-SO2-O- ou alkyle C1-C6-SO2-; R6 représente 1) H, OH, SH, halogène, halogénure d'alcoxy C1-C6, halogénure d'alkylthio C1-C6, alkylthio C1-C6-(alkyle C1-C6) carbonyle, alkyliminooxy C1-C6-CO-, 2) alcoxy C1-C6 éventuellement substitué, alkylthio C1-C6, cycloalcoxy C3-C8, cycloalkylthio C3-C8, alcényloxy C2-C6, alcénylthio C2-C6, alkinyloxy C2-C6, alkinylthio C2-C6, alkyle C1-C6-COO-, alkyle C2-C6-COS, alcoxy C1-C6-COO-, alcényle C2-C6-COO-, alcényle C2-C6-COS-, alkinyle C2-C6-COO-, alkinyle C2-C6-COS-, alkyle C1-C6-SO2-O-, alkyle C1-C6-SO2-, 3) -CY-R11 Y = -O-, -S-, -NH- éventuellement substitué}, -C(R11)(Z1R12)(Z2R13) Z1, Z2 = -O-, -S-}, -C(R11)=C(R14)-CN, -C(R11)=C(R14)-CO-R15, -CH(R11)-CH(R14)-CO-R15, -C(R11)=C(R14)-CH2-CO-R15, -C(R11)=C(R14)-C(R16)=C(R17)-CO-R15, -C(R11)=C(R14)-CH2-CH(R18)-CO-R15, -CO-OR19, -CO-SR19, -CO-N(R19)-OR20, -C$(m)(0)C-CO-NH-OR20, -C$(m)(0)C-CO-N(R19)-OR20, -C$(m)(0)C-CS-NH-OR20, -C$(m)(0)C-CS-N(R19)-OR20, -C(R11)=C(R14)-CO-NH-OR20, -C(R11)=C(R14)-CO-N(R19)-OR20, -C(R11)=C(R14)-CS-NH-OR20, -C(R11)=C(R14)-CS-N(R19)-OR20, -C(R11)=C(R14)-C(R21)=N-OR20, -C(R21)=N-OR20, -C$(m)(0)C-C(R21)=N-OR20, -C(Z1R12)(Z2R13)-OR19, -C(Z1R12)(Z2R13)-SR19, -C(Z1R12)(Z2R13)-N(R23)R24, amino éventuellement substitué ou -CONH2, azahétérocyclyle, -CO-azahétérocyclyle, ou une chaîne comprenant de un hétérocyclyle (N + O ou N + O + S). Ces composés chimiques peuvent être utilisés comme herbicides pour la dessication/défoliation des plantes.
[DE] SUBSTITUIERTE 1-METHYL-3-BENZYLURACILE [EN] SUBSTITUTED 1-METHYL-3-BENZYLURACILS [FR] 1-METHYLE-3-BENZYLURACILES SUBSTITUES

申请人：BASF AKTIENGESELLSCHAFT

公开号：WO1997035845A1

公开（公告）日：1997-10-02

(DE) Substituierte 1-Methyl-3-benzyluracile der Formel (I), deren Salze und Enolether als Herbizide oder Desikkantien/Defoliantien, wobei R1 = C1-C4-Halogenalkyl; R2 = H, Halogen; R3 = R2, CN, SCN, C1-C4-Halogenalkyl, C1-C4-Halogenalkoxy, C1-C4-Halogenalkylthio; R4 = R3, C1-C4-Alkyl, C1-C4-Alkoxy, (C1-C6-Alkylamino)-CO-; R5 = R2, CN, NO2, OH, ggf. substituiertes Amino, Alkoxy, Alkylthio, Alkyl-CO2-, Alkyl-COS-, Alkyl-SO2-O-, Alkyl-SO2-, wobei die 6 letztgenannten Reste ggf. funktionalisiert und/oder substituiert sein können; R6 an $g(a), wobei R5 dann an $g(b) steht: OH, SH, Alkyl, Alkoxy, Alkylthio, Alkyl-CO2-, Alkyl-COS-, Alkoxy-CO-, Alkoxy-CO2-, Alkyl-SO2-O-, Alkyl-SO2-, Alkyl-CO-, Alkyl-CS-, Alkyl-(N-alkyl)-imino, Alkyl-(N-alkoxy)-imino, wobei die 13 letztgenannten Reste ggf. funktionalisiert und/oder substituiert sein können; durch ggf. substituiertes Alkoxy, Alkylthio zweifach und ggf. Alkyl einfach substituiertes Methyl; an $g(b), wobei R5 dann an $g(a) steht: die voranstehend für R6 genannten Bedeutungen, sowie Alkylamino-CO-, Alkoxy-CO-, Alkylthio-CO-, Alkyl-CO-, Alkyliminooxycarbonyl, Alkyl-(N-alkoxy)-imino, Alkoxy-(N-alkoxy)-imino, Alkylthio-(N-alkoxy)-imino, wobei die 8 letztgenannten Reste ggf. funktionalisiert und/oder substituiert sein können; durch ggf. substituiertes Alkoxy, Alkylthio, Alkylamino dreifach substituiertes Methyl.(EN) The invention concerns substituted 1-methyl-3-benzyluracils (I) and their salts and enol ethers as herbicides or desiccating/defoliating agents. In formula (I), R1 is C1-C4 alkyl halide; R2 is H or halogen; R3 is R2, CN, SCN, C1-C4 alkyl halide, C1-C4 alkoxy halide or C1-C4 alkylthio halide; R4 is R3, C1-C4 alkyl, C1-C4 alkoxy or (C1-C6 alkylamino)-CO-; R5 is R2, CN, NO2, OH, optionally substituted amino, alkoxy, alkylthio, alkyl-CO2-, alkyl-COS-, alkyl-SO2-O- or alkyl-SO2-, the six last-mentioned groups optionally being functionalized and/or substituted; R6, if it is in the $g(a) position with R5 then being in the $g(b) position, is OH, SH, alkyl, alkoxy, alkylthio, alkyl-CO2-, alkyl-COS-, alkoxy-CO-, alkoxy-CO2-, alkyl-SO2-O-, alkyl-SO2-, alkyl-CO-, alkyl-CS-, alkyl-(N-alkyl)-imino or alkyl-(N-alkoxy)-imino, the thirteen last-mentioned groups optionally being functionalized and/or substituted, or methyl substituted twice by optionally substituted alkoxy and alkylthio and optionally substituted once by alkyl; or R6 in the $g(b) position, with R5 then being in the $g(a) position, has the above meanings, as well as alkyl-amino-CO-, alkoxy-CO-, alkylthio-CO-, alkyl-CO-, alkylimino-oxycarbonyl, alkyl-(N-alkoxy)-imino, alkoxy-(N-alkoxy)-imino or alkylthio-(N-alkoxy)-imino, the eight last-mentioned groups optionally being functionalized and/or substituted, or methyl substituted three times by optionally substituted alkoxy, alkylthio and alkylamino.(FR) L'invention concerne des 1-méthyle-3-benzyluraciles substitués de la formule (I), leurs sels et éthers d'énol utilisés comme herbicides ou dessiccateurs/défoliants. Dans cette formule, R1 = halogénure d'alkyle C1-C4; R2 = H, halogène; R3 = R2, CN, SCN, halogénure d'alkyle C1-C4, halogénure d'alcoxy C1-C4, halogénure d'alkylthio C1-C4; R4 = R3, alkyle C1-C4, alcoxy C1-C4, (alkylamino C1-C6)-CO-; R5 = R3, CN, NO2, OH, amino éventuellement substitué, alcoxy, alkylthio, alkyle-CO2, alkyle-COS, alkyle-SO2-O-, alkyle-SO2-, les 6 derniers restes pouvant être fonctionnalisés et/ou substitués; R6 désigne en $g(a), R5 se trouvant alors en $g(b): OH, SH, alkyle, alcoxy, alkylthio, alkyle-CO2-, alkyle-COS-, alcoxy-CO-, alcoxy-CO2-, alkyle-SO2-O-, alkyle-SO2-, alkyle-CO-, alkyle-CS-, alkyle-(N-alkyle)-imino, alkyle-(N-alcoxy)-imino, les 13 derniers restes étant éventuellement fonctionnalisés et/ou substitués; méthyle substitué deux fois par alcoxy, alkylthio évent. subst. et une fois par alkyle évent. subst.; en $g(b), R5 se trouvant alors en $g(a): les notations mentionnées précédemment pour R6, ainsi que alkyle-amino-CO-, alcoxy-CO-, alkylthio-CO-, alkyle-CO-, alkylimino-oxycarbonyle, alkyle-(N-alcoxy)-imino, alcoxy-(N-alcoxy)-imino, alkylthio-(N-alcoxy)-imino, les 8 derniers restes pouvant être fonctionnalisés et/ou substitués; méthyle substitué trois fois par alcoxy, alkylthio, alkylamino évent. subst.

该发明涉及取代的译码1-甲基-3-苯基尿嘧啶(I)，其盐及其κ-β-烯醇作为除草剂或去水剂/防止扩展剂。在公式(I)中，R1为甲基 C1-C4卤化物；R2为 H 或卤素；R3为 R2, CN, SCN, 甲基 C1-C4卤化物, 甲基 C1-C4卤氧化物或甲基 C1-C4硫化物；R4为 R3, 甲基 C1-C4烷基, 甲基 C1-C4卤氧或(C1-C6烷基氨基)-CO-；R5为 R2, CN, NO2, OH, 氵l可选氨基、卤氧、烷基硫化、烷基-COO-或烷基-COS-，六个最后提到的基团可被功能化和/或替代；R6在 $g(a)位置时，当 R5位于 $g(b)位置时，则为 OH, SH,烷基、卤氧、烷基硫化、烷基-COO-、烷基-COS-、卤氧-COO-、卤氧-COO-、烷基-SO2-O-、烷基-SO2-、烷基-CO-、烷基-CS-、烷基-(N-烷基)二胺或烷基-(N-卤氧)二胺，这些十三个最后提到的基团可被功能化和/或替代，或通过可能带有卤氧和烷基硫回味二次的甲基，而且再通过取代可能带有烷基的第二个替换基团；或者、当 R6在 $g(b)位置时，当 R5位于 $g(a)位置时，前面提到对于 R6的基团，再加上烷基-氨基-CO-、卤氧-CO-、烷基硫化-CO-、烷基-CO-、烷基二酰氨基-oxycarbonyl、烷基-(N-卤氧)二胺、卤氧-(N-卤氧)二胺、烷基硫化-(N-卤氧)二胺，这些八个最后提到的基团可被功能化和/或替代，或通过可能带有卤氧、烷基硫化和烷基氨基三次取代的甲基。

7-iodoheptanal | 72489-61-3

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