氨基化合物

The influence of the position of amino associated with pyrimidine on the reaction yields was discussed.

以取代的氨基嘧啶为共试剂，与多种芳香族硝基化合物进行了硒催化的羰基化反应，产率最高可达90％左右。

The five quinazoline compounds were prepared by using 2 amino 4,5 dimethoxy benzoic acid as original material, which underwent ring closing, halogenation and substitution.

以2 氨基 4，5 二甲氧基苯甲酸为原料，分别经过环化、氯代、取代等反应，合成了五种目标化合物。

Special attention was directed toward finding inhibitors selective against KDR tyrosine kinase in order to ensure that the in vivo profile of a specific Src inhibitor could be determined. The 4-aminobenzodioxole quinazoline series gave compounds with excellent potency and selectivity.

一直以来，人们为了确保能够在体内测定Src酶专属性抑制剂的特性，把研究焦点放在对KDR酪氨酸激酶选择性的抑制剂的寻找上。4-氨基苯并间二氧五环喹唑啉系列化合物具有极好的效力和选择性。

After investigation of a series of synthetic routes of Cefepime, we determined the best route and researched each step of the synthetic process for the goal of cost-cut, simplifying operation procedure and improving yield.

以7-ACA为起始原料，经硅烷化保护氨基和羧基、碘代、置换、脱保护、成盐、缩合、成盐等六步反应，合成了目标化合物，总收率为21％（以7-ACA计）。产品结构经1H-NMR、MS确证。

The p-aminobenzene sulfpnamide group was connected to stilbene skeleton of stilbenes, and many twin drugs were prepared.

由拼合法将对氨基苯磺酰胺基团接到芪类化合物母体二苯乙烯骨架上，可得到多种孪生药物。

Treatment of 3-amino-4-chlorobenzoic acid with trimethoxymethane generated methyl 3-amino-4-chlorobenzoate in 80.0% yield.2-ethyl pivalate was oxidized by sulfuryl chloride,an...

所得中间体2-乙基特戊酸酯低温下经磺酰氯氧化，与中间体3-氨基-4-氯苯甲酸甲酯反应，所得产物经重排、水解和酰化反应得到目标化合物，总产率25.8%。

A novel compound——N-naphthalene acylN′-substituted p-chlorobenzamido thiocarbamide was synthesized by reaction of p-chlorobenzamido hydrazine and α-naphthalene acyl mustard oil,which was obtained by potassium thiocyanate combined with α-naphthalene acyl chloride formed from α-naphthylacetic acid and SOCl2 in anhydrous benzene.

通过α-萘乙酸和SOCl2在无水苯中反应制得α-萘乙酰氯，然后与硫氰酸钾反应生成α-萘乙酰基异硫氰酸酯，再与对氯苯甲酰肼进行加成反应，合成了新型化合物N-萘乙酰基-N′-对氯苯甲酰氨基硫脲，用薄层色谱法跟踪最后一步反应，确定了反应时间。

Naphthalene acetyl chloride was prepared firstly by the reaction between α-naphthylacetic acid and SOCl2 in anhydrous benzene,then reacted with potassium thiocyanate to obtain α-naphthalene acetyl isosulfocyanate,as taking an addition reaction with p-chloro benzoyl hydrazine the novel compound N-naphthalene acetyl-N'-p-chloro benzoylamino thiocarbamide was finally synthesized.

通过α-萘乙酸和SOC l2在无水苯中反应制得α-萘乙酰氯，然后与硫氰酸钾反应生成α-萘乙酰基异硫氰酸酯，再与对氯苯甲酰肼进行加成反应，生成新型化合物N-萘乙酰基-N'-对氯苯甲酰氨基硫脲。

Naphthalene acetyl chloride was prepared firstly by the reaction betweenα-naphthylacetic acid and SOCl2 in anhydrous benzene, then reacted with potassium thiocyanate to obtainα-naphthalene acetyl isosulfocyanate, as taking an addition reaction with p-chloro benzoyl hydrazine the novel compound N-naphthalene acetyl-N'-p-chloro benzoylamino thiocarbamide was finally synthesized.

通过α-萘乙酸和SOCl2在无水苯中反应制得α-萘乙酰氯，然后与硫氰酸钾反应生成α-萘乙酸基异硫氰酸酯，再与对氯苯甲酰肼进行加成反应，生成新型化合物N-萘乙酰基－N'-对氯苯甲酰氨基硫脲。

Reactions of 2,6-pyridinedicarboxylic acid or 2,6-dibromomethyl pyridine with 5-(4-hydroxyphenyl)-10,15,20-triphenyl porphyrin, 5-(4-aminophenyl)-10,15,20 triphenyl porphyrin gave three novel bridged diporphyrins 3-5, respectively.

通过将2，6-吡啶二羧酸或2，6-二溴甲基吡啶分别与5-(4-羟基苯基)-10，15，20-三苯基卟啉(1)和5-(4-氨基苯基)-10，15，20-三苯基卟啉(2)反应，合成了3种新型的双卟啉化合物3~5。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。