- 更多网络例句与氨基相关的网络例句 [注：此内容来源于网络，仅供参考]
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In this paper, acetanilide used as start material was chlorosulfonated, then reacted with alkylamines with different length of carbon chain to prepare 4 p-acetylaminophenylsulfonylalkylamine.
本文以乙酰苯胺为起始原料，经氯磺化后分别和不同碳链的正烷基胺反应制得4种不同碳链长度的对乙酰氨基苯磺酰烷基胺，将其水解后制得了对氨基苯磺酰正丁胺、对氨基苯磺酰正辛胺、对氨基苯磺酰正十二胺和对氨基苯磺酰正十八胺。
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Consistent with previous work on 122 GABAA receptors, we found in Xenopus oocytes that 5 MAC cyclopropane enhanced the effect of GABA on 122 GABAA receptors by only 76%, and by a nearly identical enhancement in 132, and 632 receptors.
与先前在α1β2γ2 γ-氨基丁酸 A 受体所得到的相符，我们发现在爪蟾卵上，5倍的环丙烷最低肺泡有效浓度增加了γ-氨基丁酸在α1β2γ2 γ-氨基丁酸 A 受体上的作用仅76％，在α1β3γ2 γ-氨基丁酸 A 受体及α6β3γ2 γ-氨基丁酸 A 受体上的加强作用也几乎一致。
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Amino-5-acety laminobenzenesulfonic acid has been synthesized from 2, 5-diaminobenzene sulfonic acid and Acid Red BG (CI Acid Red 37) has been synthesized by coupling the diazonium salt of 2-amino-5-acetylaminobenzenesulfonic acid with racid.
利用2，5-二氨基苯磺酸为原料合成2-氨基-5-乙酰氨基苯磺酸，并进一步经2-氨基-5-乙酰氨基苯磺酸重氮盐与γ酸的偶合反应合成了酸性红BG（CIAcidRed37），并对影响反应的因素进行了讨论
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Methods Starting from 2-chloro-4-nitrophenol and 2- pyridine hydrochlorid, 3-chloro-4-(pyridin-2-ylmethoxy) aniline was obtained via etherization and reduction. The obtained aniline coupled with N-(4-chloro-3-cyano-7-ethoxyquinolin-6-yl) acetamide to give 4-[3-chloro-4-(2-pyridylmethoxy) phenylamino]-3-cyano-7-ethoxy-6-N-acetylaminoquinoline. And then it was deacetylated, followed by reacting with4- but-2-enoyl chloride to yield the target compound neratinib.
以2-氯－4-硝基苯酚和2-氯甲基吡啶为起始原料，经醚化、硝基还原得到3-氯－4-（吡啶－2-甲氧基）苯胺，3-氯－4-（吡啶－2-甲氧基）苯胺与3-氰基－6-乙酰氨基－7-乙氧基－4-氯喹啉反应得到3-氰基－6-乙酰氨基－4-［3-氯－4-（吡啶－2-甲氧基）苯氨基］－7-乙氧基喹啉，3-氰基－6-乙酰氨基－4-［3-氯－4-（吡啶－2-甲氧基）苯氨基］－7-乙氧基喹啉去乙酰保护基后，与-4-二甲氨基－2-丁烯酰氯经酰化反应得到ner-atinib。
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Odoquinazolin-4(3H)-one,7-methyl-4(3H)-quinazolinone,7-bromoquinazolin-4(3H)-one were synthesized by using anthranilic acid、2-amino-5-nitrobenzoic acid、2-amino-4-nitrobenzoic acid,6-nitro--4(3H)-quinazoline-one、o-amino-terephthalic acid, 2-amino-4-hydroxy benzoic acid、2-amino-5-bromo-benzoic acid、2-amino-5-iodine acid,1、4-butynediol、L-glutamine、isatin anhydride、formamide as starting materials and utilizing microwave-assisted synthetic approach.
本文利用微波辅助合成的方法，以邻氨基苯甲酸、2-氨基-5-硝基苯甲酸、2-氨基-4-硝基苯甲酸、邻氨基对苯二甲酸、2-氨基-4-羟基苯甲酸、2-氨基-5-溴苯甲酸、2-氨基-5-碘苯甲酸、5-甲基-2-氨基苯甲酸等为原料与甲酰胺反应，以及以1，4-丁炔二醇、L-谷氨酰胺与靛红酸酐反应，共合成了13个喹唑啉酮衍生。。。
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Therelationship of the amount of catalyst and the ee% of product was seen to be negative nonlin-ear. Catalyst 3 was used in the enantioselective addition of diethylzinc to aromatic aldehydesand gave good results. The configuration of products was determined by the configuration ofthe catalysts' chiral carbon linked with hydroxy group. Using β- amino alcohols bearing only one chiral center as catalysts for the enantiose-lective addition were studied. D-N, N-dialkyl-2-amino butanol gave poor catalytic effect be-cause of their structure. The configuration of the product is the same as the catalyst. Anotherkind of β- amino alcohols - phenylglycine derivatives and valine derivatives have chiralcenter on the carbon linked with amino group. Catalyzed by-phenylglycine derivatives 6,7, 9, 10, the reactions gave satisfied results. The optical yields exceeded 80%.
在探讨了含有两个手性中心的β-氨基醇之后，选择了只有一个手性中心的β-氨基醇，一是手性中心为连羟基的手性碳原子：D-N，N-二烷基-2-氨基丁醇；二是手性中心为连氨基的手性碳原子：D-苯基甘氨酸衍生物和L-缬氨酸衍生物。D-2-氨基丁醇的催化效果不太好，这与其结构的空间位阻较小有关系，反应产物与连羟基手性碳构型一致；由苯基甘氨酸和缬氨酸出发合成五种β-氨基醇6-10，研究了不同ee％的-6作用下的二乙基锌-苯甲醛加成反应，发现该催化剂具有不对称放大效应；-7，9，lO的催化效果也比较令人满意，光学产率80％以上，所得产物构型与催化剂构型一致。
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The new synthetic technology of some important anthraquinone intermediates derived from 1-amino- anthraquinone, l-amino-4-hydroxy-anthraquinone, l-amino-4-bromo- anthraquinone-2-sulfonic acid, 1,5- and 1,8 dinitro- anthraquinone, have been studied.
本文研究了几种重要的由1-氨基蒽醌衍生的蒽醌型中间体：1-氨基-4-羟基蒽醌、1-氨基-4-溴蒽醌-2-磺酸和1，5-及1，8-二硝基蒽醌的合成化学，在此基础上开发了上述中间体的合成新技术。现行1-氨基-4-羟基蒽醌的生产技术是从1-氨基蒽醌出发，经二溴化再水解制得，溴的耗量在1.5mol以上。
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For the test of such mechanism,we have measured the solubilities of n-valeric acid at 25℃in the aqueous solutions of following five cobalt ammines:(1) luteo,(2) purpuro,(3) xantho,(4) croceo and (5) flavo.
根据这样的机构，我们在25°下测了在下面五种钴络盐水溶液中正戊酸的溶度：(1)氯化六氨基钴；(2)氯化一氯五氨基钴；(3)氯化一硝基五氨基钴；(4)氯化反二硝基四氨基钴；(5)氯化顺二硝基四氨基钴。
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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
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In the first part, five new 4-acyl pyrazolone 4-ethyl-thiosemicarbazones compounds: 1-Phenyl-3-methyl-4-(4-bromo)benzal-pyrazol-5-one N(4)-ethyl-thiosemicarbazone (PM4Br BP-ETSC), 1-Phenyl-3-methyl-4-(4-methyl)benzal-pyrazol-5-one N(4)-ethyl-thiosemicarbaz -one (PM4MBP-ETSC), 1-Phenyl-3-methyl-4-benzal-pyrazol-5-one N(4)-ethyl-thiosemicarba -zone, 1,3-diphenyl-4-benzal-pyrazol-5-one N(4)-ethyl-thiosemicarbazone and 1-Phenyl-3-methyl-4-phenylacetyl-pyrazol-5-one N(4)-ethyl-thiosemi -carbazone have been synthesized and characterized by elemental analyses, IR, 1H NMR spectra and single-crystal XRD.
第一部分合成了五个4-酰基吡唑啉酮缩4-乙基-氨基硫脲化合物：1-苯基-3-甲基-4-（4-溴）苯甲酰基-5-吡唑啉酮缩4-乙基-氨基硫脲(PM4BrBP-ETSC)，1-苯基-3-甲基-4-(4-甲基)苯甲酰基-5-吡唑啉酮缩4-乙基-氨基硫脲(PM4MBP-ETSC)，1-苯基-3-甲基-4-苯甲酰基-5-吡唑啉酮缩4-乙基-氨基硫脲，1，3-二苯基-4-苯甲酰基-5-吡唑啉酮缩4-乙基-氨基硫脲和1-苯基-3-甲基-4-苯乙酰基-5-吡唑啉酮缩4-乙基-氨基硫脲，其中前四个具有光致变色性质。
- 更多网络解释与氨基相关的网络解释 [注：此内容来源于网络，仅供参考]
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Amino resin：氨基树脂
氨基树脂(amino resin)是由氨基化合物和甲醛缩聚而成的热固性树脂,它通常作为涂料生产的原料.涂料工业所用的氨基树脂必须用醇类醚化改性,使之可溶于有机溶剂中,它在热固性涂料中起交联作用.氨基树脂漆中,氨基树脂与醇酸树脂,聚酯树脂,
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Amino resin：氨基树脂氨基塑料
amino plastic 氨基塑料 | amino resin 氨基树脂;氨基塑料 | amino resin 氨基树脂氨基塑料
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PABA：对氨基苯甲酸
伍兹发现酵母提取物所含的对氨基苯(甲)酸(PABA)与具有对抗作用的对氨基苯磺酰胺极为相似. 这种对抗作用发生在生物体需要对氨基苯(甲)酸的生物新陈代谢过程中. 几年后,在对叶酸的研究中发现,对氨基苯(甲)酸是叶酸分子的一个组成部分.
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aminoanthraquinone dyes：氨基蒽醌類染料 氨基蒽醌类染料
amino sugar 胺基糖 氨基糖 | aminoanthraquinone dyes 氨基蒽醌類染料 氨基蒽醌类染料 | aminocyclitols 胺基環醇類 氨基环醇类
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aminobenzaldehyde：氨基苯醛
aminoazonaphthalene氨基偶氮萘 | aminobenzaldehyde氨基苯醛 | aminobenzaldoxime氨基苯甲醛肟 氨基苯醛肟
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ANTHRANILIC ACID：邻氨基苯甲酸
c acid)单抗鼠抗人邻氨基苯甲酸(Anthranilic acid)单抗规格: 0.2ml鼠抗人邻氨基苯甲酸(Anthranilic acid)单抗价格: 询价鼠抗人邻氨基苯甲酸(Anthranilic acid)单抗说明书:简单说明: 鼠抗人邻氨基苯甲酸(Anthranilic acid)单抗英文名:Mou
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ANTHRANILIC ACID：氨基苯甲酸
鼠抗人邻氨基苯甲酸(Anthranilic acid)单抗品名: 鼠抗人邻氨基苯甲酸(Anthranilic acid)单抗鼠抗人邻氨基苯甲酸(Anthranilic acid)单抗规格: 0.2ml鼠抗人邻氨基苯甲酸(Anthranilic acid)单抗价格: 询价鼠抗人邻氨基苯甲酸(Anthranilic a
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carbamic：氨基甲酸的, 由氨基甲酸获得的
carbamic chloride | 氨基甲酰氯 | carbamic | 氨基甲酸的, 由氨基甲酸获得的 | carbamide resin | 脲树脂 碳酰胺树脂
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sulfamic acid：氨基苯磺酸 氨基磺酸
suicide substrate of enzyme 自殺型酶受質 自杀型酶底物 | sulfamic acid 氨基苯磺酸 氨基磺酸 | sulfanilic acid 對氨基苯磺酸 对氨基苯磺酸
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Sulfamic acidSulfamic acidSulfamic acidSulfamic acid：不含氨基磺酸不含氨基磺酸不含氨基磺酸不含氨基磺酸
不含硫酸不含硫酸不含硫酸不含硫酸SulfuS... | 不含氨基磺酸不含氨基磺酸不含氨基磺酸不含氨基磺酸Sulfamic acidSulfamic acidSulfamic acidSulfamic acid | 不含石油醚不含石油醚不含石油醚不含石油醚PetPetPetPetrr...