查询词典 chloro-hydrocarbons

The famciclovir was synthesized from purine by a series of steps by Acylation, Decarboxylation, Reduction ,and so on; Derivatives of these intermediates is described from the 6-chloro- 9H- purin-2-amine as raw materials in different conditions when the iodine and bromide were synthesized with the addition of two intermediate 6-bromo-9H-purin-2-amine and 6-iodo-9H-purin-2-amine; There is elaborated from the main part of a acetophenone, urineaminohydrochloride, phenylhydrazine, ethyl acetoacetate as raw material through a series of reactions to synthetic 3-phenyl-4-formylphenyl pyrazole and 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-aldehyde two pyrazole aldehyde, and then with 2-amino-6-chlorine-9-(2-methicillin-oxo-co-methyl-4-yl) purine reaction of the two new pyrazole purine Schiff bases.

本论文主是采用以鸟嘌呤为原料，经过一系列的酰基化，脱羧，还原等反应作用下最终得到了产物2-氨基-9-(4-乙酰氧基-3-乙酰氧基甲基丁基)嘌呤；其中的中间体衍生物主要是阐述从以2-氨基-6-氯鸟嘌呤为原料通过在不同的条件下进行溴代与碘代分别合成了另外两种中间体2-氨基-6-溴鸟嘌呤及2-氨基-6-碘鸟嘌呤；还有一部分主要是阐述从以苯乙酮，盐酸氨基脲，苯肼，乙酰乙酸乙酯为原料通过一系列的反应先合成3-苯基-4-醛基吡唑及5-氯-3-甲基-1-苯基-1H-吡唑-4-甲醛这两个吡唑醛，然后再与2-氨基-6-氯-9-(2-甲氧羰基丁酸甲酯-4-基)嘌呤反应得到了两个新型的吡唑嘌呤席夫碱

Afterwards, N-(6-chloro-3-pyridinemethyl) phthalimide is prepared by using potassium phthalimide, as nucleophilic reagent, condensation reacting with 2-chloro-5-methylpyridine at a temperature of 70℃.

然后在70℃条件下，以邻苯二甲酸亚胺钾作为亲核试剂，与2-氯－5-氯甲基吡啶发生缩合反应，制备了N-（6-氯－3-吡啶甲基）邻苯二甲酰亚胺。

Then, N-(5-nitro-6-chloro-3-pyridinemethyl) phthalimide is obtained after the nitrating reaction of N-(6-chloro-3-pyridine methyl) phthalimide. The yield of the obtained product is 90.5%, and its melting point is 143.1~143.8℃.

缩合产物再经过硝化，合成N-（5-硝基－6-氯－3-吡啶甲基）邻苯二甲酰亚胺，其熔点为143.1~143.8℃，收率为90.5%。

Their structures were characterized by IR, 1H NMR, of which 4-chloro- 2-methyl-7-(2-bromoethoxy) isoflavone, 2, 4\'-dimethyl-7-(2-bromo-ethoxy)isoflavone and 2-methyl-7-(2-bromoethoxy) isoflavone are rarely reported so far.4\'-chloro-2-methyl-7-(3-bromopropoxy)isoflavone, 2, 4\'-dimethyl-7-(3-bromo- propoxy) isoflavone, 2-methyl-7-(3-bromopropoxy) isoflavone, 4\'-methoxy-2-methyl-7-(3-bromopropoxy) isoflavone and 4\'-hydroxy-2-methyl-7-(3-bromopropoxy) isoflavone were gained by reacting 7-hydroxy-2-methyl isoflavone derivatives with 1, 3-dibromo- propane, respectively.

第三章(来源：73ABC论文网www.abclunwen.com)在丙酮溶液中以K_2CO_3为碱，使溴乙氧基异黄酮和溴丙氧基异黄酮与咪唑偶合，以较高的产率合成出10种目标化合物：2-甲基-4′-氯-7-2-(1-咪唑基乙氧基异黄酮、2，4′-二甲基-7-2-(1-咪唑基乙氧基异黄酮、2-甲基-7-2-(1-咪唑基乙氧基异黄酮、2-甲基-4′-甲氧基-7-2-(1-咪唑基乙氧基异黄酮、2-甲基-4′-羟基-7-2-(1-咪唑基乙氧基异黄酮、2-甲基-4′-氯-7-3-(1-咪唑基丙氧基异黄酮、2，4′-二甲基-7-3-(1-咪唑基丙氧基异黄酮、2-甲基-7-3-(1-咪唑基丙氧基异黄酮、2-甲基-4′-甲氧基-7-3-(1-咪唑基丙氧基异黄酮、2-甲基-4′-羟基-7-3-(1-咪唑基丙氧基异黄酮，经IR、~1H NMR、~(13)C NMR、元素分析等对其结构进行了表征，10种目标产物均未见文(来源：ABC论文cccccc网www.abclunwen.com)献报道。

A series of pyridazino[3,2-c]1,2,4-triazoles were synthesized from hydrazides and 3-aryl-6- chloro pyridazine s (3a～3d), which were obtained from substituted benzene and succinic anhydride by Friedel-Crafts reaction, cyclization with hydrazine hydrate, dehydrogenation and chloro-substitution.

以取代苯和丁二酸酐为起始原料，经Friedel-Crafts反应，肼合环，Br2/HOAc氧化脱氢后得到一系列1，6-二氢-3-芳基-6-哒嗪酮(2a～2d)。然后将2a～2d与PCl5在POCl3中回流，得到相应的氯代产物3a～3d，将其与酰肼作用，合环后得到一系列未见报道的哒嗪并[3，2-c]1，2，4-三唑类化合物。所有化合物结构均经元素分析，IR，1HNMR和MS谱得以证实，并对其波谱性质进行了讨论

In shallow well water disinfections effective 4～5％ chlorineout of mother liquor of chloro-trisodium phosphate is used,30 minutes later chlorine reach 0.6 to 0.8 mg per liter (0.6～0.8 ppm),this water reach the national sanitary standed of drinking water mother liquor of chloro-trisodium phosphate can be best described as nonpoisonous,no remainer,quick and kill bacterium with wide-range,no corrosion and fine stability,safe,reliable new bactericide.

在浅井水消毒中，用有效氯为4.0—5.0％的氯化磷酸三钠母液投放，有效氯达到0.6—0.8mg/升(0.6ppm—O.8ppm)作用30钟后，该水可完全达到国家饮用水卫生标准。氯化磷酸三钠母液是一种无毒、无残留、速效广谱杀菌，无腐蚀性、稳定性好、安全可靠的新型杀菌剂。

A small cell-permeable compound, BH3I-2 3-iodo-5-chloro-N-[2-chloro-5-((4-chlorophenyl)sulphonyl phenyl]-2-hydroxybenzamide, has been recently reported to have a function similar to Bak BH3 peptide.

最近报道，可通透细胞的小分子化合物，BH3I-2'：3-碘-5-氯-N-{2-氯-5-[(4-氯苯基)磺酰]苯基}-2-水杨酰胺具有与Bak BH3肽相似的作用。

A high performance liquid chromatographic method was studied for the simultaneous determination of pesticide imidacloprid and its two intermediates (2-chloro-5-methyl pyridine and 2-chloro-5-chloromethyl pyridin).

研究了用高效液相色谱法同时分离测定农药吡虫啉原粉和中间体2-氯-5-甲基吡啶及2-氯-5-氯甲基吡啶含量的方法。

Bezaldehyde was used as protective agent in first method.S-Epichloeohydrin was aminated and acidulated to give(2S)-1-Amino-3-chloro-propanol Salts.The acetylation of (2S)-1-Amino-3-chloro-propanol by acetic anhydride produced the intermediate-N-[2--3-chloropropyl]acetamide.And then at 20℃,in the presence of lithium tert-butoxide,benzyl 3-fluoro-4-morpholinophenyl carbamate react with-N-[2--3-chloropropyl]acetamide to give linezolid in total yield of 43.6%.

路线一采用苯甲醛作保护剂，使S-环氧氯丙烷氨解、酸化生成S-1-氨基-3-氯-2-丙醇盐酸盐，然后经乙酰化反应后，生成中间体-N-[2-乙酰氧基-3-氯丙基]乙酰胺，再用N-(3-氟-4-吗啉苯基)氨基甲酸苄酯和中间体在催化剂叔丁醇锂存在下25℃反应生成利奈唑酮，总产率达到43.6%。

For the asymmetric reduction ofα-hydroxyacetophenone and ethyl 4-chloro acetoacetate,-1-phenyl-1,2-ethanediol and-ethyl 4-chloro-3-hydroxybutanoate were produced by the purified enzyme, with the 99% and 94.3% e.e. value respectively.

在纯酶水平验证了近平滑假丝酵母(Candida parapsilosis CCTCCM203011)对外消旋苯基乙二醇的拆分机理，整个去消旋过程是由-苯基乙二醇次级醇脱氢酶和羰基还原酶共同催化完成的。

According to the clear water experiment, aeration performance of the new equipment is good with high total oxygen transfer coefficient and oxygen utilization ratio.

曝气设备的动力效率在叶轮转速为120rpm～150rpm时取得最大值，此时氧利用率和充氧能力也具有较高值。

The environmental stability of that world - including its crushing pressures and icy darkness - means that some of its most famous inhabitants have survived for eons as evolutionary throwbacks, their bodies undergoing little change.

稳定的海底环境─包括能把人压扁的压力和冰冷的黑暗─意谓海底某些最知名的栖居生物已以演化返祖的样态活了万世，形体几无变化。