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公开(公告)号:US5981800A
公开(公告)日:1999-11-09
申请号:US56266
申请日:1998-04-07
申请人: Joseph Schapira , Jean-Claude Cheminaud , Jean-Jacques Gasse , Vincent Schanen , Benoit Rondot , Jean-Claude Lemoine
发明人: Joseph Schapira , Jean-Claude Cheminaud , Jean-Jacques Gasse , Vincent Schanen , Benoit Rondot , Jean-Claude Lemoine
IPC分类号: C07C205/22 , C07C205/23 , C07C205/37 , C07C209/18 , C07C211/52
CPC分类号: C07C209/18 , C07C201/08
摘要: Preparation process for 4-substituted dinitroanilines of formula ##STR1## in which R.sub.1 is chosen from the group containing the tert-butyl, sulphonamido, trifluoromethyl, methyl-sulphonyl and isopropyl radicals,R.sub.2 and R.sub.3, which are identical to or different from one another, represent a hydrogen atom, a linear or branched alkyl, cycloalkyl, haloalkyl or alkenyl radical containing less than 6 carbon atoms, characterized in that that it comprises successively:a dinitration stage of the 4-substituted phenol corresponding to the sought 4-substituted dinitro-aniline, this dinitration stage being carried out in a reaction medium containing a slight excess of nitrating agent, a sufficient quantity of protons and a catalyst chosen from the group containing the soluble salts of the transition metals of columns IV to XII of the Periodic Table, preferably the soluble salts of Fe.sub.III, Fe.sub.II, Zn.sub.II and Cu.sub.II ions,an O-alkylation stage of the dinitrated 4-substituted phenol obtained in the preceding stage, by means of an alkylating agent, andan amination stage of the 4-substituted dinitrated phenoxy-ether obtained in the preceding stage by using a primary or secondary amine.
摘要翻译: 其中R1选自含有叔丁基,磺酰氨基,三氟甲基,甲基 - 磺酰基和异丙基的基团的4-取代二硝基苯胺的制备方法,R 2和R 3彼此相同或不同,表示 氢原子,含有少于6个碳原子的直链或支链烷基,环烷基,卤代烷基或链烯基,其特征在于它包括依次:对应于所寻求的4-取代二硝基苯胺的4-取代苯酚的二硝化阶段, 该二硝化阶段在含有略过量的硝化剂,足够量的质子和选自含有周期表第IV至第Ⅻ族的过渡金属的可溶性盐的基团的反应介质中进行,优选地 FeIII,FeII,ZnII和CuII离子的可溶性盐,前一阶段得到的二硝基四取代苯酚的O-烷基化阶段,m 烷基化试剂的酯,和通过使用伯胺或仲胺在前一阶段获得的4-取代二硝基苯氧基醚的胺化阶段。
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公开(公告)号:US5907062A
公开(公告)日:1999-05-25
申请号:US974104
申请日:1997-11-19
申请人: Alberto Villanti , Giacomo Ravetta
发明人: Alberto Villanti , Giacomo Ravetta
IPC分类号: B01J27/24 , B01J31/02 , C07B61/00 , C07C201/08 , C07C205/23 , C07C209/76 , C07C211/52
CPC分类号: C07C209/76
摘要: A continuous process for the dinitration of alkyl-substituted derivatives of phenol and aniline, using nitric acid substantially free of sulphuric acid, characterized in which the dinitration is conducted in a single step in a tubular reactor in the presence of a catalytically-effective amount of a catalyst capable of reacting with the nitric acid to form nitrous acid in situ.
摘要翻译: 使用基本上不含硫酸的硝酸对苯酚和苯胺的烷基取代的衍生物进行二硝化的连续方法,其特征在于在催化有效量的条件下,在管式反应器中,在一个步骤中进行二硝化反应 能够与硝酸反应以在原位形成亚硝酸的催化剂。
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公开(公告)号:US5733479A
公开(公告)日:1998-03-31
申请号:US685062
申请日:1996-07-22
申请人: Charles F. Kahle, II , Neil D. McMurdie , Raphael O. Kollah , Daniel E. Rardon , Gregory J. McCollum
发明人: Charles F. Kahle, II , Neil D. McMurdie , Raphael O. Kollah , Daniel E. Rardon , Gregory J. McCollum
IPC分类号: C07C201/08 , A61K9/00 , A61K9/32 , C07C201/12 , C07C205/11 , C07C205/19 , C07C205/23 , C07C205/26 , C07C205/34 , C07C205/42 , C07C215/14 , C07C271/08 , C07C301/00 , C07C309/67 , C07C309/73 , C07C319/14 , C07C323/16 , C07C323/25 , C07C323/29 , C08G18/38 , C08G59/50 , C08G63/685 , C08L101/00 , C09D163/00 , G03F7/00 , G03F7/004 , G03F7/039 , G03F7/16 , C09K15/16
CPC分类号: C07C323/25 , A61K9/0004 , C07C205/11 , C07C205/19 , C07C205/26 , C07C215/14 , C08G18/384 , C08G59/50 , C08G59/504 , C08G63/6856 , C09D163/00 , G03F7/0045 , G03F7/039 , G03F7/164
摘要: Photoreactive compounds are synthesized from 2,5- or 2,6-dinitrobenzyl groups. Also disclosed are methods of synthesizing reactive monomers containing 2,5- or 2,6-dinitrobenzyl groups.
摘要翻译: 光反应性化合物由2,5-或2,6-二硝基苄基合成。 还公开了合成含有2,5-或2,6-二硝基苄基的反应性单体的方法。
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公开(公告)号:US5705703A
公开(公告)日:1998-01-06
申请号:US784554
申请日:1997-01-21
申请人: Karl Bernauer , Janos Borgulya , Hans Bruderer , Mose Da Prada , Gerhard Zurcher
发明人: Karl Bernauer , Janos Borgulya , Hans Bruderer , Mose Da Prada , Gerhard Zurcher
IPC分类号: A61K31/12 , A61K31/195 , A61K31/44 , C07C45/29 , C07C45/30 , C07C45/46 , C07C45/67 , C07C47/565 , C07C47/575 , C07C49/83 , C07C49/84 , C07C69/017 , C07C205/16 , C07C205/23 , C07C205/37 , C07C205/43 , C07C205/44 , C07C205/45 , C07C205/56 , C07C205/59 , C07C255/49 , C07C255/53 , C07D209/12 , C07D213/02 , C07D217/16 , C07D241/44 , C07D253/07 , C07D265/36 , C07D277/24 , C07D277/40 , C07D277/42 , C07D279/16 , C07D285/16 , C07D471/04 , C07D498/02 , C07D513/04 , C07C205/20
CPC分类号: C07D513/04 , C07C205/23 , C07C205/37 , C07C205/43 , C07C205/44 , C07C205/45 , C07C205/56 , C07C205/59 , C07C255/00 , C07C255/53 , C07C45/298 , C07C45/30 , C07C45/305 , C07C45/46 , C07C45/673 , C07C47/565 , C07C47/575 , C07C49/83 , C07C49/84 , C07C69/017 , C07D209/12 , C07D217/16 , C07D241/44 , C07D253/07 , C07D265/36 , C07D277/24 , C07D277/40 , C07D277/42 , C07D279/16 , C07D285/16 , C07D471/04
摘要: Catechol derivatives of the formula ##STR1## wherein Ra, Rb and Rc have the significance given herein. the ester and ether derivatives thereof which are hydrolyzable under physiological conditions and the pharmaceutically acceptable salts thereof are described and possess valuable pharmacological properties. In particular, they inhibit the enzyme catechol-O-methyltransferase (COMT), a soluble, magnesium-dependent enzyme which catalyses the transference of the methyl group of S-adenosylmethionine to a catechol substrate, whereby the corresponding methyl ethers are formed. Suitable substrates which can be O-methylated by COMT and which can thus be deactivated are, for example, extraneuronal catecholamines and exogeneously-administered therapeutically active substances having a catechol structure. Formula Ia above embraces not only compounds which form part of the invention, but also known compounds: the compounds which form part of the invention can be prepared according to known methods.
摘要翻译: 式Ia的儿茶酚衍生物其中R a,R b和R c具有本文给出的含义。 描述了其在生理条件下可水解的酯和醚衍生物及其药学上可接受的盐,并且具有有价值的药理学性质。 特别地,它们抑制了儿茶酚-O-甲基转移酶(COMT),一种可溶性的镁依赖性酶,其催化S-腺苷甲硫氨酸的甲基转移到儿茶酚底物上,由此形成相应的甲基醚。 可以通过COMT进行O-甲基化并因此可以失活的合适的底物是例如外源儿茶酚胺和具有儿茶酚结构的外源性治疗活性物质。 上述式Ia不仅包括形成本发明一部分的化合物,而且包括已知的化合物:形成本发明一部分的化合物可以根据已知方法制备。
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公开(公告)号:US5463129A
公开(公告)日:1995-10-31
申请号:US173451
申请日:1993-12-23
申请人: Zenon Lysenko , Richard G. Pews
发明人: Zenon Lysenko , Richard G. Pews
IPC分类号: C07C39/02 , C07C37/055 , C07C201/12 , C07C205/23 , C07C205/37 , C07C205/38 , C07C213/00 , C07C213/02 , C07C215/80 , C07C211/50
CPC分类号: C07C201/12 , C07C213/02 , C07C213/10
摘要: The present invention relates to a method of cleaving arylethers such as arylethers represented by the formula: ##STR1## wherein R is hydrogen, C.sub.1 -C.sub.6 alkyl, cycloalkyl, phenyl, substituted phenyl or CH.dbd.CH.sub.2 ; each A is independently NO.sub.2, hydroxy, halo, or methoxy; n is an integer from 0 to 5; and x is 1 or 2, comprising contacting the arylether with an amide hydrohalide salt under conditions sufficient to cleave the ether group(s) of the arylether and form a phenol or substituted phenol. The present invention also relates to a method of preparing 4,6-diaminoresorcinol, which is a monomer used for making polybenzoxazoles (PBO).
摘要翻译: 本发明涉及一种裂解芳基醚的方法,例如由下式表示的芳基醚:其中R是氢,C 1 -C 6烷基,环烷基,苯基,取代的苯基或CH = CH 2; 每个A独立地是NO 2,羟基,卤素或甲氧基; n为0〜5的整数, 和x是1或2,包括在足以裂解芳基醚的醚基并形成苯酚或取代的苯酚的条件下使芳基醚与酰胺氢卤酸盐接触。 本发明还涉及一种制备4,6-二氨基间苯二酚的方法,其是用于制备聚苯并恶唑(PBO)的单体。
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公开(公告)号:US5387271A
公开(公告)日:1995-02-07
申请号:US96735
申请日:1993-07-23
IPC分类号: A01N33/22 , A62D3/02 , B09C1/10 , C02F3/00 , C02F3/12 , C02F3/28 , C02F3/30 , C02F3/34 , C05F11/08 , C05G3/00 , C07C205/23 , C09K17/32 , C09K101/00
CPC分类号: C02F3/34 , B09C1/10 , C02F3/1231 , C02F3/2806 , C02F3/286 , C02F3/30 , C02F2101/003 , Y02E50/343 , Y02W10/15 , Y02W30/47 , Y10S71/903
摘要: Novel methods for biodegrading nitroaromatic compounds present as contaminants in soil or water using microorganisms are disclosed. Water is treatable directly; dry soil is first converted into a fluid medium by addition of water. The preferred method comprises two stages, each employing microorganisms: a fermentative stage, followed by an anaerobic stage. The fermentative stage is rapid, wherein an inoculum of aerobic and/or facultative microorganisms ferments a carbohydrate added to the fluid medium, exhausting the oxygen in the fluid medium and thereby inhibiting oxidative polymerization of amino by-products of the nitroaromatics. In the subsequent anaerobic stage an inoculum of a mixed population of anaerobic microorganisms completes the mineralization of the contaminant nitroaromatics, using the remaining carbohydrate as a carbon and energy source. Preferably, the carbohydrate is a starch and the aerobic and/or facultative microorganisms are amylolytic, which cleave the starch at a moderate rate throughout both stages, ensuring a sustained supply of metabolizable carbohydrate. The microorganisms are preferably selected to be resistant to the types and concentrations of nitroaromatics present as contaminants.
摘要翻译: 公开了使用微生物在土壤或水中作为污染物存在的硝基芳族化合物生物降解的新方法。 水可直接对待; 干土首先通过加水转化成流体介质。 优选的方法包括两个阶段,每个阶段使用微生物:发酵阶段,然后是厌氧阶段。 发酵阶段是快速的,其中有氧和/或兼性微生物的接种物将加入到流体介质中的碳水化合物发酵,排出流体介质中的氧,从而抑制硝基芳族化合物的氨基副产物的氧化聚合。 在随后的厌氧阶段,厌氧微生物的混合群体的接种物完成了污染物硝基芳族化合物的矿化,使用剩余的碳水化合物作为碳和能源。 优选地,碳水化合物是淀粉,并且需氧和/或兼性微生物是淀粉分解的,其在两个阶段以适中的速度切割淀粉,确保可代谢的碳水化合物的持续供应。 优选选择微生物以对作为污染物存在的硝基芳族化合物的类型和浓度具有抗性。
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公开(公告)号:US5236952A
公开(公告)日:1993-08-17
申请号:US686210
申请日:1991-04-16
申请人: Karl Bernauer , Janos Borgulya , Hans Bruderer , Mose DaPrada , Gerhard Zurcher
发明人: Karl Bernauer , Janos Borgulya , Hans Bruderer , Mose DaPrada , Gerhard Zurcher
IPC分类号: A61K31/12 , A61K31/195 , A61K31/44 , C07C45/29 , C07C45/30 , C07C45/46 , C07C45/67 , C07C47/565 , C07C47/575 , C07C49/83 , C07C49/84 , C07C69/017 , C07C205/16 , C07C205/23 , C07C205/37 , C07C205/43 , C07C205/44 , C07C205/45 , C07C205/56 , C07C205/59 , C07C255/49 , C07C255/53 , C07D209/12 , C07D213/02 , C07D217/16 , C07D241/44 , C07D253/07 , C07D265/36 , C07D277/24 , C07D277/40 , C07D277/42 , C07D279/16 , C07D285/16 , C07D471/04 , C07D498/02 , C07D513/04
CPC分类号: C07D513/04 , C07C205/23 , C07C205/37 , C07C205/43 , C07C205/44 , C07C205/45 , C07C205/56 , C07C205/59 , C07C255/00 , C07C255/53 , C07C45/298 , C07C45/30 , C07C45/305 , C07C45/46 , C07C45/673 , C07C47/565 , C07C47/575 , C07C49/83 , C07C49/84 , C07C69/017 , C07D209/12 , C07D217/16 , C07D241/44 , C07D253/07 , C07D265/36 , C07D277/24 , C07D277/40 , C07D277/42 , C07D279/16 , C07D285/16 , C07D471/04
摘要: Catechol derivatives of the formula ##STR1## wherein Ra, Rb and Rc have the significance given herein, the ester and ether derivatives thereof which are hydrolyzable under physiological conditions and the pharmaceutically acceptable salts thereof are described and possess valuable pharmacological properties. In particular, they inhibit the enzyme catechol-O-methyltransferase (COMT), a soluble, magnesium-dependent enzyme which catalyses the transference of the methyl group of S-adensoylmethionine to a catechol substrate, whereby the corresponding methyl ethers are formed. Suitable substrates which can be O-methylated by COMT and which can thus be deactivated are, for example, extraneuornal catecholamines and exogeneously-administered therapeutically active substances having a catechol structure.Formula Ia above embraces not only compounds which form part of the invention, but also known compounds; the compounds which form part of the invention can be prepared according to known methods.
摘要翻译: 式Ia的儿茶酚衍生物其中Ra,Rb和Rc具有本文给出的含义,其在生理条件下可水解的酯和醚衍生物及其药学上可接受的盐被描述并且具有有价值的药理学性质。 特别地,它们抑制了儿茶酚-O-甲基转移酶(COMT),一种可溶性的镁依赖性酶,其催化S-邻苯二甲酰甲硫氨酸的甲基转移到儿茶酚底物上,由此形成相应的甲基醚。 可以通过COMT进行O-甲基化并因此可以失活的合适的底物是例如外来儿茶酚胺和具有儿茶酚结构的非常给予的治疗活性物质。 上述式Ia不仅包括形成本发明一部分的化合物,而且包括已知的化合物; 构成本发明一部分的化合物可以根据已知方法制备。
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公开(公告)号:US4912246A
公开(公告)日:1990-03-27
申请号:US110754
申请日:1987-10-19
申请人: Zenon Lysenko , Cynthia L. Rand
发明人: Zenon Lysenko , Cynthia L. Rand
IPC分类号: B01J27/02 , C07B61/00 , C07C201/08 , C07C201/12 , C07C205/21 , C07C205/23 , C07C205/43 , C07C213/02 , C07C215/78
CPC分类号: C07C205/43 , C07C205/23
摘要: High purity amino-1,3-benzenediols are prepared by (a) contacting a 1,3-bis(alkylcarbonato)benzene with a nitrating agent under rection conditions such that a 1,3-bis(alkylcarbonato)nitrobenzene is formed, (b) contacting the 1,3-bis(alkylcarbonato)nitrobenzene with a hydrolyzing agent under conditions such that a nitro-1,3-benzenediol is produced, and (c) contacting the nitro-1,3-benzenediol with a reducing agent under conditions such that an amino-1,3-benzenediol is produced. Of the amino-1,3-benzenediols, 4,6-diamino-1,3-benzenediol is particularly useful in the preparation of high molecular weight polybenzoxazoles.
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公开(公告)号:US4863587A
公开(公告)日:1989-09-05
申请号:US171372
申请日:1988-03-21
申请人: Takashi Tonari , Yasuhiko Ikeda
发明人: Takashi Tonari , Yasuhiko Ikeda
IPC分类号: C07C7/04 , C07C1/00 , C07C7/20 , C07C15/46 , C07C67/00 , C07C201/00 , C07C201/16 , C07C205/23 , C07C251/46
CPC分类号: C07C201/16 , C07C7/20
摘要: A phenolic polymerization inhibitor is recovered from a styrene distillation residue containing the phenolic polymerization inhibitor by a method which comprises extracting the inhibitor from the styrene distillation residue with an oxygen-containing organic solvent having not more than 6 carbon atoms, adding an aromatic hydrocarbon solvent to the oxygen-containing organic solvent phase consequently obtained, and subjecting the resultant mixture to distillation thereby separating the mixture into a solution of the phenolic polymerization inhibitor in the aromatic hydrocarbon solvent and the oxygen-containing organic solvent. The recovered solution is put to use as a polymerization inhibitor either in the unmodified form or in a form separated from the aromatic hydrocarbon solvent.
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公开(公告)号:US4621157A
公开(公告)日:1986-11-04
申请号:US607794
申请日:1984-05-07
申请人: Larry A. McDaniel
发明人: Larry A. McDaniel
IPC分类号: C07C205/22 , C07C205/23 , C07C85/24 , C07C79/10
CPC分类号: C07C209/76 , C07C201/08
摘要: The present invention relates to improvements in processes of preparing dinitrated aromatic compounds, particularly dinitrated aniline and dinitrated substituted aniline compounds, employing relatively dilute and then more concentrated nitric acid as the nitrating agent.
摘要翻译: 本发明涉及使用相对稀的然后更浓缩的硝酸作为硝化剂来制备二硝基化芳族化合物,特别是二硝基苯胺和二硝基取代的苯胺化合物的方法的改进。
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