噻吩酮

A series of N-bonded donor-acceptor derivatives of phenothiazine containing benzene, anisole, pyridine, naphthalene, acetophenone, and benzonitrile as an electron acceptor was synthesized.

合成了一系列的N-10位取代的吩噻嗪给体受体化合物，这些受体包括苯、苯甲醚、吡啶、萘、苯乙酮和苯乙腈。

Products include: high boiling point products, solvent series, plasticizer series, aromatic hydrocarbon series, Zhong propyl butyl-carbinol, 2- octanone and thiophen.

公司主要产品有：高沸点溶剂系列、增塑剂系列、芳烃系列、仲辛醇、2-辛酮及噻吩等产品。

Four non-ionic europium complexes,〓-phen(11),〓·bipy(12),〓·dia(13) and 〓(14)(TTA=2-thenoyltrifluoroacetone, DBM=dibenzoylmethane, phen=phenanthroline, bipy=2,2'-bipyridine, dia=4,5- diazafluoren-9-one, dmbp=4,4'-dimethyl-2,2,-bipyridine), were synthesised and the triboluminescent phenomena of 12, 13 and 14 were firstly observed. Structure determinations of 11,12 and 14 were carried out. The triboluminescence maxima of 12 and 13 are similar to those of their photoluminescence. X-Ray structure analyses show that Eu atoms all exhibit eight-coordinate tetragonal antiprismatic geometries and complexes 11, 12 and 14 are all centrosymmetric.

二、合成了四个非离子型的铕的配合物：〓、〓、和〓(14)[HTTA=2-噻吩三氟甲酰丙酮，DBM=二苯甲酰基甲烷，phen=邻菲罗啉， bipy=2，2'-联吡啶，dia=4，5-二氮杂芴-9-酮，dmbp=4，4'-二甲基-2，2'-联吡啶]，首次报道了12、13及14的摩擦发光性质，测定了11、12及14的晶体结构，并系统地讨论了晶体结构和摩擦发光活性之间的关系。12及13的摩擦发光光谱的极大值均类似与其相应的光致发光光谱，表明它们有相同的激发态。

Further aza-Wittig reactions of iminophosphorane 3 with aromatic isocyanates gave the carbodiimide s 4, which were reacted with secondary amines to give 2-dialkylamino-thieno[2,3-d]pyrimidin-4(3H)-ones 6 in the presence of catalytic amounts of EtO-Na+ in 58%～82%.

应用膦亚胺3与芳基异氰酸酯的氮杂Wittig反应，生成的碳二亚胺4，再与仲胺作用得到中间体5，而后在醇钠的催化下关环制得2-二烷氨基噻吩并[2，3-d]嘧啶-4(3H)-酮衍生物6，产率为58%～82

Our company supply raw materials and related intermediates as follows: Second dibutyryl cAMP calcium, voriconazole, terbinafine, vecuronium amines, cAMP, thiamphenicol, a chlorophenol hydrochloride esters, card network sodium phosphate tilmicosin, foscarnet, lornoxicam, Tilmicosin, Cephalosporium aspirin acid, ceftiofur hydrochloride, ceftiofur sodium, Ozagrel, ondansetron hydrochloride ketones, hydroxyurea, ticarcillin sodium, telmisartan, esmolol hydrochloride, hydrochloric acid Daguan Nikkomycin, adefovir dipivoxil, buflomedil hydrochloride, granisetron hydrochloride, warfarin sodium,-methyl gabexate acid, nicergoline, pantoprazole sodium,·, tegafur, cefepime hydrochloride, vecuronium bromide, hydrochloric acid meclofenoxate, sertraline hydrochloride, Cefonicid amine salt, aztreonam, ticarcillin, cefdinir, cefodizime sodium, sodium ferulate, colloidal pectin secretion, 2,3 - cyclopentene and pyridine, Piperacillin acid, cefetamet US-acid, hydrochloride Cefmenoxime ,3-TZ, 2 - deoxy-D-glucose, two-amidine urea benzene, sodium Cefonicid, Cefonicid intermediates, ester Cefamandole sodium, Cefalotin acid, intermediates cefpirome, cefepime sulphate, cefepime intermediate nucleus of cefepime, cefpirome nucleus, Cefamandole sodium, ceftriaxone new active ester, oxaliplatin, cyclophosphamide vary gland amines, polyene match him.

我公司供应的原料药及相关中间体为：二丁酰环磷腺苷钙、伏立康唑、盐酸特比萘芬、维库溴胺、环磷腺苷、甲砜霉素、盐酸甲氯酚酯、卡络磺钠、磷酸替米考星、膦甲酸钠、氯诺昔康、替米考星、头孢匹胺酸、头孢噻呋盐酸盐、头孢噻呋钠、奥扎格雷、盐酸恩丹西酮、羟基脲、替卡西林钠、替米沙坦、盐酸艾司洛尔、盐酸大观霉素、阿德福韦酯、盐酸丁咯地尔、盐酸格拉司琼、华法林钠、甲磺酸加贝酯、尼麦角林、泮托拉唑钠、普拉洛芬、替加氟、盐酸头孢吡肟、维库溴铵、盐酸甲氯芬酯、盐酸舍曲林、头孢尼西胺盐、氨曲南、替卡西林、头孢地尼、头孢地嗪钠、阿魏酸钠、胶体果胶泌、2，3-环戊烯并吡啶、哌拉西林酸、头孢他美酸、头孢甲肟盐酸盐、3-TZ、2-脱氧-D-葡萄糖、双脒苯脲、头孢尼西钠、头孢尼西中间体、头孢孟多酯钠、头孢噻吩酸、头孢匹罗中间体、头孢吡肟硫酸盐、头孢吡肟中间体、头孢吡肟母核、头孢匹罗母核、头孢孟多钠、头孢曲松新型活性酯、奥沙利铂、异环磷腺胺，多烯他赛。

Diamines are performed. An new and effective atom economy, domino reaction is developed, and 5, 6dihydro-4H-thieno [2, 3-b] thiopyran are synthesized by 4-(4-methyl-1, 3-dithiol-2-ylidene)-1, 7-diaryl-1, 6-diene-3, 5-dione

然后以4-[（4-甲基-1，3-二噻烷-2-亚甲基）-1，7-二芳基]-1，6-二烯-3，5-二酮类化合物为合成子探索稠杂环合成方法，并发现一个高效的，具有原子经济性的多米诺效应合成方法，并成功的利用其合成了一系列噻喃并噻吩衍生物。

RESULTS Specific inhibitors of respiratory chain complexes Ⅰ,Ⅱ,Ⅲ, and Ⅳ of rotenone, thenoyltrifluoroacetone, antimycin A and potassium cyanide, and the mitochondrial uncoupler carbonyl cyanide mchlorophenylhydrazone resulted in obvious changes of intracellular ROS production.

结果 呼吸链复合物Ⅰ，Ⅱ，Ⅲ，和Ⅳ抑制剂鱼藤酮、噻吩甲酰三氟丙酮、抗霉素A、氰化钾及氧化磷酸化解偶联剂羰氰苯腙能够明显改变But所致细胞内活性氧的产生。

A general novel synthetic method to Symmetrically or unsymmetrically 2,3,6,7- substituted thieno[2,3-d:5,4-d\']dipyrimidine-4,5(3H,6H)-diones and 2-substituted benzothieno[3,2-d] pyrimidin-4(3H)-dione by utilizing aza-Wittig reaction was proposed firstly. This synthetic method has the advantage of easily accessible starting material, mild condition and good yields.

具体研究内容如下：1、首次研究了应用aza-Wittig反应方法合成2，3，6，7-对称与不对称四取代噻吩并[2，3-d；5，4-d\']双嘧啶-4，5(3H，6H)-二酮以及2-取代苯并噻吩并[3，2-d]嘧啶-4(3H)-酮衍生物的通用新方法，该方法原料易得，条件温和，收率较高。

The best of them were 4c and 8d which exhibited 87% and 89% inhibition of Penicilium digitatum . And benzothieno[3,2-d]imidazol[1,2-a]pyrimidin-2,5(1H, 3H)-diones or benzothieno[3,2-d][1,2,4]triazol[1,5-a]pyrimidin-10(3H)-one only exhibited moderate inhibition.

而苯并噻吩并[3，2-d]嘧啶-4(3H)-酮和苯并噻吩并[3，2-d]咪唑并[1，2-a]嘧啶-2，5(1H，3H)-二酮以及苯并噻吩并[3，2-d][1，2，4]三唑[1，5-a]嘧啶-10(3H)-酮衍生物以及三唑醇衍生物均只表现出中等的抑制率。

And benzothieno[3,2-d]imidazol[1,2-a]pyrimidin-2,5(1H, 3H)-diones or benzothieno[3,2-d][1,2,4]triazol[1,5-a]pyrimidin-10(3H)-one only exhibited moderate inhibition.

而苯并噻吩并[3，2-d]嘧啶-4(3H)-酮和苯并噻吩并[3，2-d]咪唑并[1，2-a]嘧啶-2，5(1H，3H)-二酮以及苯并噻吩并[3，2-d][1，2，4]三唑[1，5-a]嘧啶-10(3H)-酮衍生物以及三唑醇衍生物均只表现出中等的抑制率。

But we don't care about Battlegrounds.

但我们并不在乎沙场中的显露。

Ah! don't mention it, the butcher's shop is a horror.

啊！不用提了。提到肉，真是糟透了。