Extract from the Register of European Patents

EP About this file: EP1925610

EP1925610 - Production process of 2-aminooxyethanol [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  26.06.2009
Database last updated on 28.03.2026
Most recent event   Tooltip26.06.2009Application deemed to be withdrawnpublished on 29.07.2009  [2009/31]
Applicant(s)For all designated states
Bayer CropScience AG
Alfred-Nobel-Strasse 50
40789 Monheim am Rhein / DE
[N/P]
Former [2008/22]For all designated states
Bayer CropScience AG
Alfred-Nobel-Strasse 50
40789 Monheim / DE
Inventor(s)01 / Pazenok, Sergiy
Wipperauer Strasse 57
42699 Solingen / DE
02 / Lui, Norbert
Am Geus Garten 2
51519 Odenthal / DE
 [2008/22]
Application number, filing date06024436.524.11.2006
[2008/22]
Filing languageDE
Procedural languageDE
PublicationType: A1 Application with search report 
No.:EP1925610
Date:28.05.2008
Language:DE
[2008/22]
Search report(s)(Supplementary) European search report - dispatched on:EP29.06.2007
ClassificationIPC:C07C239/20, C07C249/12, C07C251/54
[2008/22]
CPC:
C07C239/20 (EP,US); C07C249/12 (EP,US); C07C251/54 (EP,US)
Designated contracting states(deleted) [2009/06]
Former [2008/22]AT,  BE,  BG,  CH,  CY,  CZ,  DE,  DK,  EE,  ES,  FI,  FR,  GB,  GR,  HU,  IE,  IS,  IT,  LI,  LT,  LU,  LV,  MC,  NL,  PL,  PT,  RO,  SE,  SI,  SK,  TR 
TitleGerman:Verfahren zur Herstellung von 2-Aminooxyethanol[2008/22]
English:Production process of 2-aminooxyethanol[2008/22]
French:Procédé de production du 2-aminooxyéthanol[2008/22]
Examination procedure29.11.2008Application deemed to be withdrawn, date of legal effect  [2009/31]
06.02.2009Despatch of communication that the application is deemed to be withdrawn, reason: examination fee not paid in time  [2009/31]
Fees paidPenalty fee
Additional fee for renewal fee
30.11.200803   M06   Not yet paid
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Documents cited:Search[XY] US4086361  (WELLE HENDRICUS BERNARDUS ANTO et al.) [X] 14 * column 4, lines 3-25; example (11)(a) *[Y] 1-13,15-18
 [XY] US3040097  (BACHMAN GUSTAVE B et al.) [X] 14 * column 1, lines 11-47,59-65; examples III,IV; claims 1,4,5,7,9 *[Y] 1-13,15-18
 [XY] US3803235  (VAN DIJK J et al.) [X] 14 * Verbindung (1) aufs Spalte 1; column 3, lines 38-43; examples (1)-(3),(9); claims 1-3 *[Y] 1-13,15-18
 [X] EP0010058  (CIBA GEIGY AG et al.) [X] 14 * Verbindungen Nr 13, 37-39,, 133, 164, 191, 195-196, 198 und 200;; claim 1 *
 [Y]   SCHUMANN E L ET AL: "The synthesis and .gamma.-aminobutyric acid transaminase inhibition of aminooxy acids and related compounds", JOURNAL OF MEDICINAL AND PHARMACEUTICAL CHEMISTRY, AMERICAN CHEMICAL SOCIETY. EASTON, US, vol. 5, 1962, pages 464 - 477, XP009049392 [Y] 1-13,15-18 * Hydrolyse zum H2NOR.HCl auf Seite 466 Tabelle auf Seite 468, Verbindung 15 Herstellungsverfahren von 2-Aminooxyethanol Hydrochloride auf Seiten 474-475 *
 [XDY]   DASHYANT DHANAK ET AL: "A synthesis of pyrrole derivatives from O-(2-hydroxyethyl)-ketoximes", JOURNAL OF THE CHEMICAL SOCIETY, CHEMICAL COMMUNICATIONS, CHEMICAL SOCIETY. LETCHWORTH, GB, 1986, pages 903 - 904, XP002089698, ISSN: 0022-4936 [XD] 14 * Verbindungen (4) und (5), Schema 2 Fussnote auf Seite 903;; table I * [Y] 1-13,15-18
 [Y]   B.J.R. NICOLAUS ET AL.: "o,n-substituierte Hydroxylamine", HELVETICA CHMICA ACTA, vol. 40, 1962, pages 358 - 370, XP009085575 [Y] 1-13,15-18 * Verbindung I Experimenteller Teil (V zur I); pages 358-359; tables 1,2 *

DOI:   http://dx.doi.org/10.1002/hlca.19620450141
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