子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 61 | 一种新型脂肪腈蒸馏装置 | CN200920021645.8 | 2009-04-25 | CN201426986Y | 2010-03-24 | 叶建泉; 徐文凯; 杨副国 |
| 本实用新型提供一种新型脂肪腈蒸馏装置，属于一种化工生产用装置，腈蒸馏器下部连接有粗脂肪腈进料管，脂肪腈再沸器的上部出口连接在腈蒸馏器的下部，脂肪腈再沸器的下部进口经蒸馏循环泵与腈蒸馏器的下部出口相连，腈蒸馏器的顶部安装有蒸馏冷凝器，蒸馏冷凝器的顶部出口与辅助冷凝器的进口相连，辅助冷凝器、最终冷凝器的出口与脂肪腈受器的进口相连，腈蒸馏器底部出口经残渣出料泵与残渣蒸馏器的进口相连，残渣蒸馏器的上部出口与残渣蒸馏冷凝器的进口相连，残渣蒸馏冷凝器的出口连接在腈蒸馏器上的填料体的上方。这种脂肪腈蒸馏装置，提高了脂肪腈再沸器的传热效率，提高了蒸馏效率和蒸馏收率，且降低了能耗。 | ||||||
| 62 | Resorcinol derivatives | JP2002528629 | 2001-09-13 | JP3950046B2 | 2007-07-25 | ガレス ウィリアムズ，ジョナサン; トーマス ガトレル，ウィリアム; ビクトリア ゲデン，ジョアンナ; ウィリアム コリントン，エリック; コリン ソア ファイフ，マシュー; エドワード ブラッドリー，スチュアート; ジェイムズ プロクター，マーティン; ジョン マレー，ピーター; ジョン ローリー，ロバート |
| 63 | Compounds useful as an intermediate of 4-amino-quinoline derivative | JP2002585373 | 2002-04-08 | JP3924250B2 | 2007-06-06 | スコット，ロバート・ウィリアム; ダガー，ロバート・ウェイン; デイモン，デイビッド・バーンズ |
| 64 | Acrylonitrile-based compounds, their preparation methods and pest control agents containing them | JP4895598 | 1998-02-12 | JP3671110B2 | 2005-07-13 | 裕治 中村; 宗和 小川; 徹 小柳; 光二 杉本; 雅之 森田; 剛 池田 |
| 65 | Btk inhibitor as well as the identification method and using the same | JP2000544627 | 1999-04-19 | JP2002512216A | 2002-04-23 | ウックン、ファティ、エム．; ゴーシュ、スタパ; ツェン、ヤグー |
| (57)【要約】 本発明はＢＴＫインヒビター、この同定方法、使用方法、およびＢＴＫインヒビターからなる薬学的化合物を提供するものである。 | ||||||
| 66 | Dialkyne compound | JP2001219358 | 2001-07-19 | JP2002105003A | 2002-04-10 | REIFFENRATH VOLKER; LUESSEM GEORG |
| PROBLEM TO BE SOLVED: To provide a dialkyne compound used as a new, stable liquid crystal compound, having such a specific low optical anisotropy (Δn) and a negative or positive dielectric anisotropy (Δε) as to be suitably used as a liquid crystal medium, especially as a component for a TFT(thin film transistor) and STN(super-twisted nematic) display. SOLUTION: This dialkyne compound is expressed by the formula (I) [R1 and R2 are each H, F, a 1-15C substituted or unsubstituted alkyl or the like; X1 to X4 are each H or -C≡C-C≡C-R3 (R3 is H, CF3, a substituted or unsubstituted alkyl or the like); Q is -CH2- or -O-; Y1 and Y2 are each C or Si; A1 and A2 are each a trans-cyclohexylene which may be unsubstituted, or substituted by F or CN, or in which one, two or more nonadjacent CH2 groups are substituted by -O- and/or -S-, or the like; Z1 and Z2 are each a single bond, -CO-O-, -O-, -CF2-O-, -CH2-CH2- or the like; and n and m are each 0-3, provided that (m+n) is 1-3]. | ||||||
| 67 | Pest control agent | JP51830095 | 1994-12-27 | JP3058692B2 | 2000-07-04 | ツィーグラー，フゴ; ツルフリュー，レネ; トラー，ステファン; ファローク，ザレーム |
| 68 | Production method of enantiomers | JP4600899 | 1999-02-24 | JP3038204B2 | 2000-05-08 | イエンス・ペレガールト; クラウス・ペーテル・ボゲゾ |
| 69 | Noxious organism-controlling agent | JP25292499 | 1999-09-07 | JP2000119236A | 2000-04-25 | ZIEGLER HUGO; TRAH STEPHAN; FAROOQ SALEEM; ZURFLUEH RENE |
| PROBLEM TO BE SOLVED: To obtain the subject new compound having bactericidal, acaricidal and insecticidal properties and useful as an active component in agricultural, horticultural and hygienic fields. SOLUTION: This noxious organism-controlling agent is a compound of formula I [X is CH; Y is OR11 (R11 is a 1-4C alkyl); A is oxygen atom or the like; R1 is a 1-4C alkyl, a halo 1-4C alkyl, cyclopropyl or the like; R2 is H, a 1-6C alkyl, or the like; R3 is H, a 1-6C alkyl, a 1-6C haloalkyl having 1-5 halogen atoms or the like], e.g. methyl-3-methoxy-2-[([(3-hydroxyimino-2-butyl) imino]oxy)o-tolyl]acrylate. In the compound of the formula I, a compound in which R3 is not H, is obtained by reacting an oxime of formula III with a benzyl derivative of formula IV (U is a leaving group) in an inert solvent, in the presence of a base and in the presence (absence) of a transition catalyst between phases at 0-50 deg.C. The compound of the formula I is effective e.g. for a plant pathogenic microorganism, especially a mold. | ||||||
| 70 | Production of enantiomer | JP4600899 | 1999-02-24 | JPH11292867A | 1999-10-26 | BOEGESOE KLAUS P; PERREGAARD JENS |
| PROBLEM TO BE SOLVED: To obtain (+)-citalopram useful as an antidepressant by dissolving the enantiomer mixture of a specific compound and ring-closing the obtained (-)-enantiomer by treating with a base in the presence or absence of an acid derivative capable of producing a reactive ester residue and isolating the objective compound. SOLUTION: This production of an enantiomer is to dissolve two enantiomers of a compound expressed by the formula (R is H or the like) to obtain the (-)-enantiomer of the formula generating (+)-citalopram and ring-close the enantiomer by treating with a base, or when R in the formula is H, ring-close the enantiomer with a base in the presence of an acid derivative capable of generating a reactive ester residue, then, isolate (+)-citalopram as it is or as a nontoxic acid-added salt and obtain the objective compound. When R in the formula is H, it is preferable to react the enantiomer with a pure acid derivative [preferably (+)-α-methoxy-α-trifluoromethylphenylacetyl chloride], separate the diastereomer and treat with a strong base. COPYRIGHT: (C)1999,JPO | ||||||
| 71 | JPH0428302B2 - | JP19206984 | 1984-09-12 | JPH0428302B2 | 1992-05-14 | HIROSE HISAHIRO; SAWADA KYOSHI; KINOSHITA AKIRA; KAWAKAMI SOTA |
| 72 | Cyclo(d-phenylalanyl-d-histidyl) dipeptide catalyst | JP16432990 | 1990-06-25 | JPH03238053A | 1991-10-23 | DONARUDO DABURIYUU SUTAUTOMAIA; CHIYAARUZU EICHI TAIMAN; UORUTAA DONGU |
| PURPOSE: To prepare optically-active S-α-cyano-3-phnoxy-benzyl alcohol by reacting 3-phenoxybenzaldehyde with hydrogen cyanide in the presence of a specified catalyst. CONSTITUTION: Cyclo(D-phenylalanyl-D-histidine)dipeptide catalysts such as di- and poly-peptides having alanine (including portion thereof) are obtained from alanine, β-aminoalanine, β-phenylalanine, 3,4-dihydroxyphenylalanine, etc. Optionally substd. 3-phenoxybenzaldehyde is reacted with a hydrogen cyanide donor in the presence of the cyclo(D-phenylalanyl-D-histidine)dipeptide catalyst, to prepare optically active, optionally substd. S-α-cyano-3-phnoxybenzyl alcohol. COPYRIGHT: (C)1991,JPO | ||||||
| 73 | JPH034891B2 - | JP10470982 | 1982-06-19 | JPH034891B2 | 1991-01-24 | DEIUIDO JII REPADO |
| 74 | JPH027565B2 - | JP50073386 | 1986-01-16 | JPH027565B2 | 1990-02-19 | HIDASHI GYORUGII; SUZEKERII ISUTOBAN; BERUTOTSUKU BERA; ZORUTAN SANDOORU; NAGII RAYOSU; GAYARI ANTARU; SOMUFUEI EBA; HEGEJUUSU AGUNESU; PATSUPU RASUZURO; SOOSU RUDORUFU; RADOBANII ERUZUSEBETSUTO; BOTARU SANDOORU |
| 75 | JPH0149701B2 - | JP25171188 | 1988-10-04 | JPH0149701B2 | 1989-10-25 | EDOWAADO AARU RABAGUNIINO; ANDORYUU JEI PAIKU; JATSUKU BII KYANBERU |
| 76 | JPH0135809B2 - | JP17306380 | 1980-12-08 | JPH0135809B2 | 1989-07-27 | MISHERU BUTSUSE; MISHURU SHINIAKU; KUROODO GURAN; SHARURU PIJUROORU |
| 77 | Production of fluorene derivative | JP25171188 | 1988-10-04 | JPH01125363A | 1989-05-17 | EDOWAADO AARU RABAGUNIINO; ANDORIYUU JIEI PAIKU; JIYATSUKU BII KIYANBERU |
| NEW MATERIAL: A compd. of the formula I (R and R 1 are each H, 1-4C alkyl, F or Cl; R 4 and R 5 are each H or 1-6C alkyl). EXAMPLE: 9-Carbamoyl-9-(2-cyanoethyl)fluorene. USE: An intermediate for synthesis of an antiarrhythmic agent. PROCESS: A compd. of the formula I is obtd. by bringing the 9-carbamoylfluorene of formula II and acrylonitrile into reaction at 35 to 75°C in an inert org. solvent in the presence of a base (preferably benzyltrimethyl ammonium hydroxide). COPYRIGHT: (C)1989,JPO | ||||||
| 78 | Manufacture of 5,6-substituted-2,4- quinazolinediamines | JP17609287 | 1987-07-16 | JPS6330474A | 1988-02-09 | EREN MAIRA BAAMAN; MAAKU JIEIMUZU SUUTO |
| 79 | Manufacture of basic substituted phenylacetonitrile | JP13868681 | 1981-09-04 | JPS5780358A | 1982-05-19 | GERUHARUTO KASUTONAA; HARUDOO JIIGERU; KAARUUHAINTSU GAISU |
| 80 | Crystalline and insecticidal pyrethroid antipode and its manufacture | JP7498980 | 1980-06-05 | JPS55164608A | 1980-12-22 | RERANDO AASAA SUMERUTSU |
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