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Extract from the Register of European Patents

EP About this file: EP3045462

EP3045462 - 3-ARYL-2-PHOSPHORYL SUBSTITUTED 1-INDANONES AND THE METHOD FOR THEIR PREPARATION [Right-click to bookmark this link]
StatusNo opposition filed within time limit
Status updated on  12.02.2021
Database last updated on 14.09.2024
FormerThe patent has been granted
Status updated on  21.02.2020
FormerGrant of patent is intended
Status updated on  04.10.2017
FormerExamination is in progress
Status updated on  14.12.2016
Most recent event   Tooltip08.07.2022Lapse of the patent in a contracting state
New state(s): MK		published on 10.08.2022  [2022/32]
Applicant(s)For all designated states
Centrum Badan Molekularnych I Makromolekularnych Pan
Ul. Sienkiewicza 112
90-363 Lodz / PL
[2016/29]
Inventor(s)01 / Balczewski, Piotr
UL. Marzanny 3
91-225 Lodz / PL
02 / Szczesna, Dorota
Wierzchy 28
99-232 Zadzim / PL
 [2016/29]
Representative(s)(deleted)
[2020/13]
Former [2016/29]Brodowska, Iwona
Lex-Pat
Kancelaria Patentowa
ul. Lucka 15/514
00-842 Warszawa / PL
Application number, filing date14460079.831.10.2014
[2016/29]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report 
No.:EP3045462
Date:20.07.2016
Language:EN
[2016/29]
Type: B1 Patent specification 
No.:EP3045462
Date:25.03.2020
Language:EN
[2020/13]
Search report(s)(Supplementary) European search report - dispatched on:EP12.08.2015
ClassificationIPC:C07F9/38, C07F9/40
[2016/29]
CPC:
C07F9/65517 (EP); C07F9/65586 (EP)
Designated contracting statesAL,   AT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HR,   HU,   IE,   IS,   IT,   LI,   LT,   LU,   LV,   MC,   MK,   MT,   NL,   NO,   PL,   PT,   RO,   RS,   SE,   SI,   SK,   SM,   TR [2017/09]
Former [2016/29]AL,  AT,  BE,  BG,  CH,  CY,  CZ,  DE,  DK,  EE,  ES,  FI,  FR,  GB,  GR,  HR,  HU,  IE,  IS,  IT,  LI,  LT,  LU,  LV,  MC,  MK,  MT,  NL,  NO,  PL,  PT,  RO,  RS,  SE,  SI,  SK,  SM,  TR 
TitleGerman:3-ARYL-2-PHOSPHORYLSUBSTITUIERTE 1-INDANONE UND VERFAHREN ZU DEREN HERSTELLUNG[2017/44]
English:3-ARYL-2-PHOSPHORYL SUBSTITUTED 1-INDANONES AND THE METHOD FOR THEIR PREPARATION[2016/29]
French:1-INDANONES 3-ARYL-2-PHOSPHORYL SUBSTITUÉ ET LEUR PROCÉDÉ DE PRÉPARATION[2016/29]
Former [2016/29]3-ARYL-2-PHOSPHORYLSUBSTITUIERTE 1-INDANONE UND VERFAHREN ZUR DEREN HERSTELLUNG
Examination proceduredeletedDeletion: Application deemed to be withdrawn, date of legal effect  [2016/29]
09.12.2014Examination requested  [2016/29]
07.09.2015Despatch of a communication from the examining division (Time limit: M04)
21.12.2015Reply to a communication from the examining division
03.02.2016Despatch of a communication from the examining division (Time limit: M06)
02.06.2016Reply to a communication from the examining division
11.07.2016Despatch of a communication from the examining division (Time limit: M04)
23.08.2016Reply to a communication from the examining division
06.12.2016Despatch of a communication from the examining division (Time limit: M04)
13.12.2016Reply to a communication from the examining division
06.02.2017Despatch of a communication from the examining division (Time limit: M04)
12.06.2017Reply to a communication from the examining division
02.08.2017Despatch of a communication from the examining division (Time limit: M04)
17.08.2017Reply to a communication from the examining division
05.10.2017Communication of intention to grant the patent
05.02.2018Fee for grant paid
05.02.2018Fee for publishing/printing paid
22.05.2018Receipt of the translation of the claim(s)
Opposition(s)12.01.2021No opposition filed within time limit [2021/11]
Request for further processing for:The application is deemed to be withdrawn due to failure to fulfill actions required for granting the patent
26.05.2018Request for further processing filed
26.05.2018Full payment received (date of receipt of payment)
Request granted
11.06.2018Decision despatched
The application is deemed to be withdrawn due to non-payment of the search fee
28.04.2015Request for further processing filed
28.04.2015Full payment received (date of receipt of payment)
Request granted
16.07.2015Decision despatched
The application is deemed to be withdrawn due to non-payment of the filing fee
28.04.2015Request for further processing filed
28.04.2015Full payment received (date of receipt of payment)
Request granted
16.07.2015Decision despatched
Fees paidRenewal fee
31.10.2016Renewal fee patent year 03
02.11.2017Renewal fee patent year 04
30.10.2018Renewal fee patent year 05
12.02.2020Renewal fee patent year 06
Penalty fee
Additional fee for renewal fee
31.10.201906   M06   Fee paid on   12.02.2020
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Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Lapses during opposition  TooltipHU31.10.2014
AL25.03.2020
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CZ25.03.2020
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[2022/31]
Former [2022/30]HU31.10.2014
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PL25.03.2020
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BG25.06.2020
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GR26.06.2020
IS25.07.2020
PT18.08.2020
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Former [2021/36]AT25.03.2020
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PL25.03.2020
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SI25.03.2020
SK25.03.2020
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BG25.06.2020
NO25.06.2020
GR26.06.2020
IS25.07.2020
PT18.08.2020
FR31.10.2020
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Former [2021/31]AT25.03.2020
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MC25.03.2020
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SI25.03.2020
SK25.03.2020
SM25.03.2020
BG25.06.2020
NO25.06.2020
GR26.06.2020
IS25.07.2020
PT18.08.2020
LU31.10.2020
Former [2021/24]AT25.03.2020
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FI25.03.2020
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GR26.06.2020
IS25.07.2020
PT18.08.2020
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PL25.03.2020
RO25.03.2020
RS25.03.2020
SE25.03.2020
SK25.03.2020
SM25.03.2020
BG25.06.2020
NO25.06.2020
GR26.06.2020
IS25.07.2020
PT18.08.2020
Former [2021/09]AT25.03.2020
CZ25.03.2020
DK25.03.2020
EE25.03.2020
ES25.03.2020
FI25.03.2020
HR25.03.2020
IT25.03.2020
LT25.03.2020
LV25.03.2020
NL25.03.2020
RO25.03.2020
RS25.03.2020
SE25.03.2020
SK25.03.2020
SM25.03.2020
BG25.06.2020
NO25.06.2020
GR26.06.2020
IS25.07.2020
PT18.08.2020
Former [2021/08]CZ25.03.2020
DK25.03.2020
EE25.03.2020
ES25.03.2020
FI25.03.2020
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BG25.06.2020
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GR26.06.2020
IS25.07.2020
PT18.08.2020
Former [2020/50]CZ25.03.2020
EE25.03.2020
FI25.03.2020
HR25.03.2020
LT25.03.2020
LV25.03.2020
NL25.03.2020
RO25.03.2020
RS25.03.2020
SE25.03.2020
SK25.03.2020
SM25.03.2020
BG25.06.2020
NO25.06.2020
GR26.06.2020
IS25.07.2020
PT18.08.2020
Former [2020/49]CZ25.03.2020
FI25.03.2020
HR25.03.2020
LT25.03.2020
LV25.03.2020
NL25.03.2020
RO25.03.2020
RS25.03.2020
SE25.03.2020
SK25.03.2020
SM25.03.2020
BG25.06.2020
NO25.06.2020
GR26.06.2020
IS25.07.2020
PT18.08.2020
Former [2020/48]FI25.03.2020
HR25.03.2020
LT25.03.2020
LV25.03.2020
NL25.03.2020
RO25.03.2020
RS25.03.2020
SE25.03.2020
SM25.03.2020
BG25.06.2020
NO25.06.2020
GR26.06.2020
IS25.07.2020
PT18.08.2020
Former [2020/47]FI25.03.2020
HR25.03.2020
LT25.03.2020
LV25.03.2020
NL25.03.2020
RS25.03.2020
SE25.03.2020
BG25.06.2020
NO25.06.2020
GR26.06.2020
IS25.07.2020
Former [2020/46]FI25.03.2020
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LV25.03.2020
NL25.03.2020
RS25.03.2020
SE25.03.2020
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GR26.06.2020
IS25.07.2020
Former [2020/45]FI25.03.2020
HR25.03.2020
LV25.03.2020
NL25.03.2020
RS25.03.2020
SE25.03.2020
BG25.06.2020
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GR26.06.2020
Former [2020/39]FI25.03.2020
HR25.03.2020
LV25.03.2020
RS25.03.2020
SE25.03.2020
BG25.06.2020
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Former [2020/38]FI25.03.2020
HR25.03.2020
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Former [2020/35]FI25.03.2020
NO25.06.2020
Documents cited:Search[A]  - VAIDYA, TULAZA ET AL, "A Highly Reactive Dicationic Iridium(III) Catalyst for the Polarized Nazarov Cyclization Reaction", ANGEWANDTE CHEMIE, INTERNATIONAL EDITION, (2010), vol. 49, no. 19, doi:10.1002/ANIE.201000100, ISSN 1433-7851, pages 3363 - 3366, XP002742703 [A] 1-11 * see entry 1 in table 1 on p. 3365 *

DOI:   http://dx.doi.org/10.1002/anie.201000100
 [A]  - LAWRENCE, N. J. ET AL., TETRAHEDRON LETTERS, (2006), vol. 47, pages 1637 - 1640, XP025003671 [A] 1-11 * see scheme 2 and synthesis of compounds 4a to 4s in table 2 *

DOI:   http://dx.doi.org/10.1016/j.tetlet.2005.12.110
 [A]  - HAMASHIMA, YOSHITAKA ET AL, "Highly enantioselective fluorination reactions of .beta.-ketoesters and .beta.-ketophosphonates catalyzed by chiral palladium complexes", TETRAHEDRON, (2006), vol. 62, no. 30, doi:10.1016/J.TET.2005.12.070, ISSN 0040-4020, pages 7168 - 7179, XP002742789 [A] 1-11 * see fluorination of compound 11c in table 5 on p. 7171 *

DOI:   http://dx.doi.org/10.1016/J.TET.2005.12.070
by applicant   - V. GEVORGYAN; L. G. QUAN; Y. YAMAMOTO, TETRAHEDRON LETT., (1999), pages 4089 - 4092
    - A. SAITO; M. UMAKOSHI; N. YAGYU; Y. HANZAWA, ORG. LETT., (2008), vol. 10, pages 1783 - 1785
    - N. AHMED; B. V. BABU; H. KUMAR, SYNTHESIS, (2011), vol. 15, pages 2471 - 2477
    - Y. SHAO; C. YANG; W. GUI; Y. LIU; W. XIA, CHEM. COMMUN., (2012), vol. 48, pages 3560 - 3562
    - J. NIE; H.-W. ZHU; H.-F. CUI; M.-Q. HUA; J.-A. MA, ORG. LETT., (2007), vol. 9, pages 3053 - 305
    - N. J. LAWRENCE; E. S. M. ARMITAGE; B. GREEDY; D. COOK; S. DUCKI; A. T. MCGOWN, TETRAHEDRON LETT., (2006), vol. 47, pages 1637 - 1640
    - T. VAIDYA; A. C. ATESIN; R. HERRICK; A. J. FRONTIER; R. EISENBERG, ANGEW. CHEM., (2010), vol. 122, pages 3435 - 3438
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.