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2. 发明专利

JP2009221124A Polymerizable compound, its polymer, and thin film, charge transfer material and photoconductive material using the same 审中-公开
标题翻译：聚合物，聚合物和薄膜，充电转移材料和使用它的光电材料
公开(公告)号：JP2009221124A
公开(公告)日：2009-10-01
申请号：JP2008065456
申请日：2008-03-14
申请人： Fujifilm Corp , 富士フイルム株式会社
发明人： NISHIO AKIRA
IPC分类号： C07D253/02 , C07D405/12 , C08F20/36 , C08G59/32 , C08G65/18 , C09K11/06
摘要： PROBLEM TO BE SOLVED: To provide a new polymerizable compound, and a polymer, useful for producing the functional films of charge transfer materials. SOLUTION: Provided are the polymerizable compound represented by general formula (1), and the polymer thereof. Therein, X 1 , X 2 and X 3 are each independently a single bond, NR 1 group (R 1 is H or a 1 to 30C alkyl group), O, S, a carbonyl group, a sulfonyl group or a divalent linkage group comprising their combination; Ar 1 , Ar 2 and Ar 3 are each independently an aromatic group or a heterocyclic group; L 1 , L 2 and L 3 are each independently a single bond, NR 2 group (R 2 is H or a 1 to 30C alkyl group), an alkylene group, O, S, a carbonyl group, a sulfonyl group or a divalent linkage group comprising their combination; P 1 , P 2 , and P 3 are each independently a polymerizable group. COPYRIGHT: (C)2010,JPO&INPIT
摘要翻译：要解决的问题：提供可用于制备电荷转移材料的功能膜的新的可聚合化合物和聚合物。解决方案：提供由通式（1）表示的可聚合化合物及其聚合物。其中，X 1 ，X 2 和X 3 各自独立地为单键，NR 1 组 O，S，羰基，磺酰基或包含它们的组合的二价连接基团; Ar 1 ，Ar 2 和Ar 3 各自独立地为芳族基团或杂环基团; L 1 ，L 2 和L 3 各自独立地为单键，NR 2 组（R 2 为H或1〜30C烷基），亚烷基，O，S，羰基，磺酰基或包含它们的组合的二价连接基团; P 1 ，P 2 和P 3 各自独立地为可聚合基团。版权所有（C）2010，JPO＆INPIT

3. 发明专利

JP2000103748A PACKAGE FOR SAFE STORAGE OF ELECTROPHILIC FLUORINATING AGENT AND PACKAGING THEREOF 失效
公开(公告)号：JP2000103748A
公开(公告)日：2000-04-11
申请号：JP27476199
申请日：1999-09-28
申请人： AIR PROD & CHEM
发明人： SYVRET ROBERT GEORGE , JAMES JOSEPH HART , ANDREW JOSEPH WOITECK , FRANK MICHAEL PROSONICK
IPC分类号： C07B39/00 , C07B63/00 , C07D213/89 , C07D253/02 , C07D487/08 , C09B39/00
摘要： PROBLEM TO BE SOLVED: To safely hold an electrophilic fluorinating agent by holding the electrophilic fluorinating agent and a solvent having the compatibility with the above fluorinating agent in a vessel having a sealable orifice and capable of holding the fluorinating agent and the solvent in the liquid phase under ambient conditions and providing the amount of the solvent sufficient to absorb heat of decomposition of the fluorinating agent. SOLUTION: The following requirements (A) to (C) are included in order to safely store, transport and deliver a quaternary electrophilic fluorinating agent e.g. 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)}. (A) a vessel having at least one sealable orifice and capable of holding the above quaternary electrophilic fluorinating agent and a solvent (e.g. water) in a liquid phase under ambient conditions (>=50 deg.C and

5. 发明专利

JPH0418021A AGENT OF LOWERING SERUM URIC ACID 失效
公开(公告)号：JPH0418021A
公开(公告)日：1992-01-22
申请号：JP30161090
申请日：1990-11-06
申请人： OTSUKA PHARMA FACTORY INC
发明人： SHIBATA HISAO , KUBO HIDEJI , MATSUNO TARO , KAMISAKO TAKUJI
IPC分类号： C07D249/02 , A61K31/38 , A61K31/381 , A61K31/42 , A61K31/421 , A61K31/433 , A61K31/495 , A61K31/496 , A61K31/50 , A61K31/505 , A61P19/06 , C07D233/88 , C07D237/20 , C07D239/42 , C07D241/20 , C07D253/02 , C07D261/14 , C07D263/48 , C07D285/08 , C07D285/12 , C07D285/135 , C07D307/66 , C07D333/36
摘要： PURPOSE:To obtain an excellent agent of lowering serum uric acid useful for treating cardiovascular disorder, gastric disorder, etc., resulting from gout or hyperuricemia as a basic disease, having lowering action on uric acid, containing a p-aminophenol derivative as an active ingredient. CONSTITUTION:An agent of lowering serum uric acid containing at least one selected from a p-aminophenol derivative shown by the formula [R is lower alkyl; R and R are H, lower alkyl or both are bonded to form -(CH2)4- or -CH=CH-CH=CH-; alpha is aromatic heterocyclic 5-membered or 6-membered group containing 1-3 hetero atoms selected from N, O and S, pyrazine-N-oxide ring group, pyridazine-N-oxide ring group, pyrimidine-N-oxide ring group and these groups may contain lower alkyl group, etc., as substituent group] and a slat thereof as an active ingredient. When used, the agent can be used in the dosage form of injection or suppository besides oral administration of tablet, etc.

6. 发明专利

JPS6350354B2 失效
公开(公告)号：JPS6350354B2
公开(公告)日：1988-10-07
申请号：JP13471879
申请日：1979-10-18
申请人： EGYT GYOGYSZERVEGYESZETI GYAR
发明人： IENO KOROSHI , CHIBOORU RANGU , YOZUSEFU SUZEKERII , FUERENKU ANDORASHI , GABOORU ZORUYOMI , YOZUSEFU BORUSHII , KATARIN GORUDOSHUMITSUTO NE HORUBASU , TAMASU HAMORI , GABURIERA SUZABO NE KUJIBURA , ZUSUZUSA MESUZAROSU
IPC分类号： C07D253/02 , A61K31/55 , A61P25/00 , A61P25/20 , C07D243/02 , C07D243/04 , C07D311/76 , C07D405/04 , C07D409/04 , C07D491/056

7. 发明专利

JPS6133823B2 失效
公开(公告)号：JPS6133823B2
公开(公告)日：1986-08-04
申请号：JP9198984
申请日：1984-05-10
申请人： BAYER AG
发明人： HANSU GEORUKU SHUREE , KURAUSU ZATSUSE , RUUTOITSUHI OIE
IPC分类号： C07D251/20 , A01N20060101 , A01N43/64 , A01N43/66 , C07D20060101 , C07D251/00 , C07D251/12 , C07D251/14 , C07D251/16 , C07D251/26 , C07D251/30 , C07D251/38 , C07D251/42 , C07D251/46 , C07D253/00 , C07D253/02 , C07D307/00 , C07D307/52 , C07D405/12 , C07D407/12 , C07D521/00

8. 发明专利

JP2006523210A Method of separating a crystalline form i of 5-azacytidine 有权
公开(公告)号：JP2006523210A
公开(公告)日：2006-10-12
申请号：JP2006507211
申请日：2004-03-16
申请人：アッシュ・スティーヴンス・インコーポレーテッド , ファーミオン・コーポレーション
发明人：イオネスク，ドミトル , シルヴェイ，ゲイリー・エル , ブラムバーグス，ピーター
IPC分类号： C07H19/12 , A61K31/706 , A61K31/7072 , A61P35/02 , B01J20060101 , C07D251/10 , C07D253/02 , C07D405/04
CPC分类号： C07H1/06 , C07H19/12
摘要：本発明は、５−アザシチジン結晶形Ｉを実質的に他の結晶形を含まない形で分離する方法に関し、５−アザシチジンは以下の式にて示される。

本発明はさらに５−アザシチジン結晶形Ｉを含む薬剤組成物を含む。

9. 发明专利

JPH092906A PROPENOIC ACID DERIVATIVE, ITS PRODUCTION AND BACTERICIDAL COMPOSITION CONTAINING THE SAME 失效
公开(公告)号：JPH092906A
公开(公告)日：1997-01-07
申请号：JP5640395
申请日：1995-02-09
申请人： ZENECA LTD
发明人： JIYON MAACHIN KUROU , KURISUTOFUAA RICHIYAADO AIRESU , POORU JIYON DO FUREINU , BUIBUIENNU MAAGARETSUTO ANTONI , MAIKERU GOODON HATSUCHINGUSU
IPC分类号： A01N20060101 , A01N37/06 , A01N37/10 , A01N37/34 , A01N37/36 , A01N37/38 , A01N37/40 , A01N37/44 , A01N37/46 , A01N37/48 , A01N39/00 , A01N43/02 , A01N43/08 , A01N43/10 , A01N43/12 , A01N43/24 , A01N43/32 , A01N43/40 , A01N43/42 , A01N43/48 , A01N43/54 , A01N43/58 , A01N43/60 , A01N43/64 , A01N43/66 , A01N43/707 , A01N43/713 , A01N47/30 , C07C20060101 , C07C59/64 , C07C65/28 , C07C67/00 , C07C67/31 , C07C69/618 , C07C69/734 , C07C69/736 , C07C201/00 , C07C205/37 , C07C205/38 , C07C205/59 , C07C217/86 , C07C229/34 , C07C231/00 , C07C231/12 , C07C233/18 , C07C233/23 , C07C235/56 , C07C237/40 , C07C239/00 , C07C241/00 , C07C251/24 , C07C253/00 , C07C255/55 , C07C255/57 , C07C275/34 , C07C323/56 , C07C323/60 , C07C323/62 , C07C323/65 , C07D20060101 , C07D213/24 , C07D213/64 , C07D213/65 , C07D213/68 , C07D213/69 , C07D213/70 , C07D213/73 , C07D213/74 , C07D213/75 , C07D213/79 , C07D213/81 , C07D213/84 , C07D213/85 , C07D213/90 , C07D215/12 , C07D215/20 , C07D215/22 , C07D217/02 , C07D237/06 , C07D237/14 , C07D239/26 , C07D239/34 , C07D239/46 , C07D239/52 , C07D241/12 , C07D241/18 , C07D241/36 , C07D241/42 , C07D241/44 , C07D251/14 , C07D251/22 , C07D251/26 , C07D251/30 , C07D253/02 , C07D253/04 , C07D253/06 , C07D253/07 , C07D257/08 , C07D307/00 , C07D307/91 , C07D317/54 , C07D317/64 , C07D319/14 , C07D319/24 , C07D333/02 , C07D333/26 , C07D333/32 , C07D333/52 , C07D333/54 , C07D333/64 , C07D521/00
摘要： PURPOSE: To obtain a new propeonic acid derivative useful as a bactericidal agent to exterminate an infection caused by plant bacteria. CONSTITUTION: This propeonic acid derivative is a compound of formula I [Y is O, S, etc.; R , R are each H, an alkyl, etc.; X is a halogen, an alkyl, an alkenyl, etc.; (n) is 0, 1-4; R is an aryl]) or its derivative, or a compound of formula II [in the case of an (E) isomer, Ab is 2-bromo, 3-iodo, 2-ethyl, 3-amino, 4-phenyl, etc.], e.g. (E)-methyl 2-[2-(3-chlorophenoxymethyl)phenyl]-3- methoxypropenoate. The compound of formula I is obtained by treating a compound of formula III (R is a metal atom) with a compound of the formula: CH3 L (L is a liberative group), removing methanol component from a compound of formula IV, treating a ketoester of formula V with a methoxymethylating reagent, etc.

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