苄胺

Tebufenpyrad, a new high effective pyrazoleamide acaricide , was synthesized from 1-methyl-3-ethyl-4-chloro-5-pyrazolecarbon acid and 4-t-butylbenzylamine, the raw material are propionyl pyruvic ethyl ester and 4-t-butyl benzylchloride.

吡螨胺是一种新型、高效的吡唑酰胺类杀螨剂，本文以中间体1-甲基-3-乙基-4-氯-5-吡唑甲酸和4-叔丁基苄胺合成，起始原料丙酰丙酮酸乙酯和4-叔丁基苄氯，总收率为61.23%。

The new aproach of which can be achieved via the oxidation of 2-naphthylamine (39) by CuCl〓benzylamine or ethanolamine (2: 1) in methanol under mild condition with isolated yield up to 74％.

本文开发出利用2-萘胺（39）为原料，以氯化铜—苄胺或乙醇胺（2：1）作为氧化偶合试剂，在温和的条件下和甲醇溶剂中，以高达74％的产率合成40的新方法。

Factories strong technical force, advanced production equipment, production of meglumine, Portugal TOA, benzylamine and its family of products, sesame phenol, quetiapine fumarate major intermediate, 4 - hydroxy droperidol, and other products sold at home and abroad.

工厂技术力量雄厚，生产设备先进，生产的葡甲胺、葡辛胺、苄胺及其系列产品、芝麻酚、富马酸喹硫平主要中间体、4-羟基哌啶等产品远销海内外。

Five Butenafine's analogues were designed and synthesized according to the structure-activity relationship and operating mechanism of benzylamine antimycotics.

根据苄胺类抗真菌化合物的构效关系、作用机理，设计合成了 5个布替萘芬类似物，N (2 氯 5 吡啶甲基) N 甲基 1 萘甲胺，N ，N 二(4 叔丁基苄基) 1 萘甲胺，N (4 叔丁基苄基) N (2 氯 5 吡啶甲基) 1 萘甲胺，N ，N 二苄基 4 叔丁基苯甲胺，N (2 氯 5 吡啶甲基) N 苄基 4 叔丁基苯甲胺。

Based on broad information collection, author compared and studied on the old synthesis process, and proposed the better process that started from benzyl chloride, then according to the sequence of " synthesis of benzylamine, synthesis of N-benzyl-N--acetamine, synthesis of 2-chloro-5-methylpridine ,2-chloro-5-trichloromethylpyridine,2-chloro-5-trifluropyridine " five steps to get the final product, CTFP.

本文在查阅大量文献资料和对2-氯-5-三氟甲基吡啶合成路线进行分析比较的基础上，提出了较佳合成路线，即以氯化苄为原料，合成的反应步骤为&苄胺&合成、&N-苄基-N--乙酰胺&合成、&2-氯-5-甲基吡啶&合成、&2-氯-5-三氯甲基吡啶&合成、&2-氯-5-三氟甲基吡啶&合成五步。

The results of bioassay suggest that 2-methylthio-6-methyl-4-substituted pyrimidine and 4, 6-dimethoxy-2-substituted pyrimidine derivatives show herbicidal activity. In these target compounds, 4, 6-dimethoxy-2-substituted pyrimidine benzylamine and 4, 6-dimethoxy-2-Substituted pyrimidine benzylidene amine exhibit good herbicidal activity, and the herbicidal will be affected by the substituents in the benzene ring.

对分子库中的目标分子进行了生物活性筛选研究，发现其中的2-甲硫基-6-甲基-4-取代嘧啶衍生物和4，6-二甲氧基-2-取代嘧啶类化合物显示出除草活性，其中4，6-二甲氧基-2-取代嘧啶苄胺类化合物和4，6-二甲氧基-2-取代嘧啶亚苄胺类化合物具有较好的除草活性，而且其活性和苯环上的取代基有关。

Three kinds of small molecular copper and zinc superoxide dismutase mimics were synthesized with N, N-bis (benzimidazol-2-ylmethyl) amine (N3), N, N-bis (benzimidazol-2-ylmethyl) methylamine(MN3) and N,N-bis (benzimidazol-2-ylmethyl) benzylamine(BN3) as ligands. The com-plexes were characterized by UV, IR and element analysis and the structures were proposed.

模拟铜一锌超氧化物歧化酶的活性中心，以二(2-苯并咪唑)丙烷为桥、二(2-苯并咪唑亚甲基)胺(N3)、二(2-苯并咪唑亚甲基)甲胺(MN3)及二(2-苯并咪唑亚甲基)苄胺(BN3)为配体合成了3种异双核的小分子模型化合物，并进行了紫外、红外表征及元素分析，推测了可能的结构。

The pyrimidine lead compound is obtained via herbicidal activity screen. The optimization of lead compound leads to find the good pyrimidine benzylamine candidates with highly effective herbicidal activity. The novel herbicidal mechanism of pyrimidine benzylamine is put forward. N-(2-bromophenyl)-2-(4, 6-dimethoxypyrimidin-2-yloxy)benzylamine (103-1) has potential as a new selective post-emergent herbicide in oilseed rape.

通过系统的研究工作，发现了具有除草活性的嘧啶先导结构，经结构优化，筛选出具有高除草活性的嘧啶苄胺类优选结构，发现并提出了此类化合物的除草作用新机理，最终经田间试验证实了N-(2-溴苯基)-2-(4，6-二甲氧基-2-嘧啶氧基)苄胺(103-1)可作为超高效油菜田除草剂进行工业性的研究与开发。

Temperature-sensitive hydrogels P(NIPA-co-DiAB) with aromatic group as hydrophobe was were prepared by free radical micellar crosslinking copolymerization with N-isopropyl acrylamide, N,N-dially benzylamine as comonomers, N,N-methylene-bis-acrylamide as crosslinker, sodium dodecyl sulfate as surfactant and ammonium persulfatetetramethylethylenediamine as initiator system.

以N-异丙基丙烯酰胺、N，N-双烯丙基苄胺为共聚单体、N，N-亚甲基双丙烯酰胺为交联剂、十二烷基硫酸钠为表面活性剂、过硫酸铵-四甲基乙二胺为氧化还原引发体系，采用自由胶束交联共聚法合成了疏水基团为芳香基的疏水改性温敏性智能水凝胶P(NIPA-co-DiAB)。

Seven Schiff bases of N-(4-hydroxyphenylmethylene)-1-naphthylamine, N-(4-hydroxyphenylmethylene)-p-methoxyaniline, N-(4-hydroxyphenylmethylene)-benzylamine, N-(4-hydroxy-3-methoxyphenylmethylene) furfurylamine, N-(4-hydroxy-3-methoxyphenyl methylene)-p-methylaniline, N-(4-hydroxy-3-methoxyphenylmethylene)-p-methoxyaniline and N-salicylidene-4-aminoantipyrine were first synthesized by the one step solid phase reactions between aromatic aldehydes with phenolic hydroxyl and amines at room temperature without solvent.

分别以带酚羟基的芳醛与胺类反应，首次通过室温固相反应一步合成了N-（4-羟基苯基亚甲基）-1-萘胺、N-（4-羟基苯基亚甲基）-对甲氧基苯胺、N-（4-羟基苯基亚甲基）-苄胺、N-（4-羟基-3-甲氧基苯基亚甲基）糠胺、N-（4-羟基-3-甲氧基苯基亚甲基）-对甲苯胺、N-（4-羟基-3-甲氧基苯基亚甲基）-对甲氧基苯胺和N-亚水杨基-4-氨基安替比林7种Schiff碱，反应15min完成，产率均超过90％。

Now, however, all children continue in "comprehensive" schools, and the eleven-plus determines which courses of study the child will follow.

然而现在，所有的孩子都要在综合学校继续学习，所以这次考试只是决定他们将要学习哪些课程。

Cultivatable land , and led to a general recognition that development must not be carried at the cost of agriculture .

城区的迅速扩大在很多情况下侵占了宝贵的可耕地，使人们普遍认识到发展不能以牺牲农业为代价。