| 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 | Ionic liquid | JP2001158540 | 2001-05-28 | JP2002187893A | 2002-07-05 | HILARIUS VOLKER; HEIDER UDO; SCHMIDT MICHAEL |
| PROBLEM TO BE SOLVED: To provide an ionic liquid having broad liquid range, high temperature stability and low corrosiveness and useful as a solvent for organic syntheses and an electrolyte liquid of an electrochemical battery. SOLUTION: The ionic liquid is expressed by general formula K+A- (K+ is selected from a group composed of specific cations; and A- is selected from a group composed of specific anions). Concrete example of the ionic liquid is shown by the following formula. COPYRIGHT: (C)2002,JPO | ||||||
| 62 | Bis-o-amino(thio)phenol and its production | JP27039398 | 1998-09-24 | JPH11189573A | 1999-07-13 | SEZI RECAI; KEITMANN MICHAEL; WEBER ANDREAS |
| PROBLEM TO BE SOLVED: To obtain a new compound useful for the production of a polymer precursor excellent in solubility and capable of producing, on a substrate, after cyclized, polybenzoxazole or polybenzothiazole having low hygroscopicity, high temperature stability and high planar formation degree. SOLUTION: This compound is expressed by formula I A<1> to A<3> are each H, CH3 or the like; T is O or S; Z is expressed by formula II to IV [Q is N or C-A (A is H, F or the like); up to 3 N atoms can exist and 2 N atoms thereof can be adjacent to each other on a separated aromatic ring, while up to 2 N atoms can exist per ring on a polycyclic system; M is a single bond, CH(CH3 ) or the like] or the like}, for example, 4,4'-bis(4-amino-3-hydroxy- phenoxy)-octafluorobiphenyl. The compound of formula I is obtained, e.g. by reacting a halogen compound of the formula X-Z-X (X is a halogen) with a compound of formula V (R is a residue, such as <=6C alkyl) in the presence of a base at 20-100 deg.C, and reducing the resultant dinitro compound to the corresponding diamino compound and eliminating the group R. | ||||||
| 63 | 3-aminocrotonic acid ester | JP23609589 | 1989-09-12 | JPH0399064A | 1991-04-24 | NISHIZAWA SUSUMU; FUKADA FUMIO; KAKEYA SENJI |
| NEW MATERIAL:A compound of formula I (A is alkylene having two carbon atoms bonded to alkyl groups and having a total carbon number of ≥5; R 2 is acyl, alkoxycarbonyl, acylalkyl, N-alkyl-substituted carbamoylalkyl, alkenyl, etc.; (m) is 1-3). EXAMPLE: 3-Aminocrotonic acid 3-(4-allyl-1-piperidinyl)-2.2-dimethylpropyl ester. USE: Useful as an intermediate for synthesizing 1,4-dihydropyridine derivatives having vasodepressor activity, vasodilation activity, etc. PREPARATION: A compound of formula II is reacted with diketene (ketene dimer) of formula III in the presence of a base (e.g. pyridine) in a solvent such as methylene chloride or in the absence of the solvent at -10 to 130°C to prepare a compound of formula IV, which is reacted with ammonia gas or with a solution of solvent such as methanol saturated with ammonia to provide the compound of formula I. COPYRIGHT: (C)1991,JPO&Japio | ||||||
| 64 | JPH03501772A - | JP50138589 | 1988-12-30 | JPH03501772A | 1991-04-18 | |
| 65 | JPH0219110B2 - | JP3600182 | 1982-03-09 | JPH0219110B2 | 1990-04-27 | TOBIASU OREGON IERIN; DEUITSUTO JON GIRUMAN |
| 66 | Pharmacologically active substituted benzamide | JP11674488 | 1988-05-13 | JPS63313757A | 1988-12-21 | IBUO MONKOBUITSUKU; DEIBUITSUDO UIRUNAA |
| 67 | Antitumoral compound | JP11342988 | 1988-05-10 | JPS63297364A | 1988-12-05 | RICHIYAADO WARUTSU HAAPAA; JIEIMUZU JIEFURII HAUBAATO; JIERARUDO OOSUTON PUUA; BURENTO JIEFURII RIIDAA; EDEI BII-PINGU TAO |
| 68 | Aryl-azolylmethyl-benzocycloalkene derivative, its production and its use | JP5430587 | 1987-03-11 | JPS62230771A | 1987-10-09 | UORUFUGANGU SHIYAPERU; ANDOREASU FUUSU; UORUFUGANGU REETERU; UARUTERU DEITOMAARU; HAINTSU HENEERU; HERUMAN YOOZEFU GERUHARUTSU; BURUKUHARUTO ZATSUHAZE |
| 69 | Antibiotic substance, production and use thereof | JP28013985 | 1985-12-12 | JPS62201887A | 1987-09-05 | YOSHIOKA KOICHI; HARADA SETSUO; OCHIAI MICHIHIKO |
| NEW MATERIAL:A 2-(4-substituted amino-3-oxo-2-isoxazolidinyl)-5-oxo-2- tetrahydrofurancarbox-ylic acid derivative expressed by formula I (R<1> is amino or organic residue through N; R<2> is COOH or a group derived therefrom; X is H, methoxy or formylamino, provided that R<2> is not p-nitrobenzyloxycarbonyl or benzhydryloxycarbonyl when R<1> is acetylamino or amino and X is H). EXAMPLE:Sodium 2-{(4S)-4-[2-(2-amino-4-thiazolyl)-(Z)-2-(methoxyimino)acet- amido]-3-oxo-2-isoxazolidinyl}-5-oxo-2-tetrahydrofurancarbo-xylate. USE:A low toxic antimicrobial agent against Gram-positive and Gram-negative bacteria. PREPARATION:A compound expressed by formula II is reacted with a compound capable of introducing a group forming an organic residue through N. | ||||||
| 70 | Nitrogen-containing heterocyclic compound, its preparation, and noxious life controlling agent containing said compound as active component | JP7246984 | 1984-04-10 | JPS60215671A | 1985-10-29 | NISHIDA SUMIO; KISHIDA HIROSHI; MATSUO NORITADA; HATAGOSHI MAKOTO |
| NEW MATERIAL:The nitrogen-containing heterocyclic compound of formula I [R 1 is group of formula II or formula III (R 7, R 8, R 9 and R 10 are H, halogen, 1W4C alkyl, 1W4C alkoxy, etc.); R 2 and R 3 are H, halogen or methyl; R 4 is halogen or methyl; R 5 and R 6 are H, halogen, 1W4C alkyl or 1W4C alkoxy; X, Y and Z are O, S or methylene; m is 0W4; n is 0W2]. EXAMPLE: 2-[2-(4-Phenoxyphenoxy)ethoxy]pyrimidine. USE: It has juvenile hormone activity, and is useful as a noxious life controlling agent having extremely excellent controlling effect to insects of coleopterous, lepidopterous or hemipterous order, etc. and mites such as spider mite, at a low concentration. PREPARATION: The compound of formula I can be prepared by reacting the compound of formula IV (R 2' and R 3' are H or methyl; A 1 is halogen or mesyloxy) with the compound of formula V or its alkali metal salt. COPYRIGHT: (C)1985,JPO&Japio | ||||||
| 71 | JPS6014036B2 - | JP11678276 | 1976-09-29 | JPS6014036B2 | 1985-04-11 | ISHIKAWA FUMYOSHI; OZASAYAMA AKIRA; ABIKO KAZUFUMI |
| 72 | Guanidine derivative, manufacture and pharmaceutical composition containing same and having gastric acid secretion control | JP4367382 | 1982-03-18 | JPS57167969A | 1982-10-16 | DERIKU FUREETO JIYONZU; KEITO OORUDOHAMU |
| 73 | 4-nitro-2-trichloromethylbenzole sulfenic acid derivative and bactericide containing it | JP7238481 | 1981-05-15 | JPS5718661A | 1982-01-30 | HERUMUUTO HAAGEN; HANSU TSUIIGURAA; JIERIA YOOAN MATSUPESU; ERUNSUTOOHAINRIHI POMAA |
| 74 | Condensed quinazoline derivatives | JP11678276 | 1976-09-29 | JPS5344592A | 1978-04-21 | ISHIKAWA FUMIYOSHI; KOSAYAMA AKIRA; ASOGO KAZUFUMI |
| PURPOSE: Condensed quinazoline derivative I [X is O, S, CH 2, = N-, -NR 1-(R 1 is H, lower alkyl, etc.); n is 2-4; when X is = N-, R is lower alkyl; excluding n is 2 and R 1 is H or ethyl] and its acid addition salt; e.g. 6phenyl-1,2,3,4-tetrahydro-6H-pyrimido [2,1-b] quinazoline. COPYRIGHT: (C)1978,JPO&Japio | ||||||
| 75 | Process for preparing acylcyanide | JP3624677 | 1977-04-01 | JPS52122304A | 1977-10-14 | KURUTO FUINDAIZEN; HERUBERUTO SHIYUBUARUTSU |
| 76 | Process for preparing acylcyanide | JP3624577 | 1977-04-01 | JPS52122303A | 1977-10-14 | KURUTO FUINDAIZEN |
| 77 | Tetrazolee55carboxyamide derivative | JP11791176 | 1976-09-28 | JPS52116470A | 1977-09-29 | JIYON EICHI SERUSUTETSUDO; CHIYAARUSU JIEI GUUINOTSUSO; ARUBAATO JIEI BEGANII; DAIETAA EICHI KURAUBAATO |
| 78 | Heterocyclic compounds | JP128676 | 1976-01-01 | JPS5283892A | 1977-07-13 | KUWATA YUTAKA; MEGURO KANJI; NATSUKARI HIDEAKI |
| PURPOSE: Heterocyclic compounds of formula I (R 1, R 2 are H, alkyl which may be substituted by alkylamino, OH, or alkoxy, or in combination may form a heterocyclic ring together with the adjacent N atom; R 3 is H, lower alkyl; Y is O,S,NH; B is lower alkylene; ring A may be substituted by halogen, nitro, etc.); for example, 1-2-(2-pyridinecarbonyl)phenyl-5-chloromethyl-1H-1,2,4-triazole3-carboxamide. COPYRIGHT: (C)1977,JPO&Japio | ||||||
| 79 | JPS50111021A - | JP10103673 | 1973-09-07 | JPS50111021A | 1975-09-01 | |
| 80 | JPS5037790A - | JP7835874 | 1974-07-10 | JPS5037790A | 1975-04-08 | |
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