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Extract from the Register of European Patents

EP About this file: EP4045494

EP4045494 - SYNTHESIS OF 6-METHYL-N1-(4-(PYRIDIN-3-YL)PYRIMIDIN-2-YL)BENZENE-1,3-DIAMINE [Right-click to bookmark this link]
StatusThe patent has been granted
Status updated on  08.09.2023
Database last updated on 05.07.2024
FormerGrant of patent is intended
Status updated on  07.05.2023
FormerRequest for examination was made
Status updated on  22.07.2022
FormerThe international publication has been made
Status updated on  24.04.2021
Formerunknown
Status updated on  27.10.2020
Most recent event   Tooltip31.05.2024Lapse of the patent in a contracting state
New state(s): ES, HR, NO, PL, RS
published on 03.07.2024  [2024/27]
Applicant(s)For all designated states
Esco Aster Pte. Ltd.
67 Ayer Rajah Crescent, 02-01
Singapore 139950 / SG
[2023/40]
Former [2022/34]For all designated states
Esco Aster Pte. Ltd.
21 Changi South Street 1
Singapore 486777 / SG
Inventor(s)01 / ABRAHAM RAJKUMAR, Gurubatham
c/o Esco Aster Pte. Ltd.
21 Changi South Street 1
Singapore 486777 / SG
02 / LIN, Xiangliang
c/o Esco Aster Pte. Ltd.
21 Changi South Street 1
Singapore 486777 / SG
 [2022/34]
Representative(s)Mewburn Ellis LLP
Aurora Building
Counterslip
Bristol BS1 6BX / GB
[2022/34]
Application number, filing date20792606.413.10.2020
[2022/34]
WO2020EP78761
Priority number, dateSG20191009596R14.10.2019         Original published format: SG10201909596R
[2022/34]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2021074138
Date:22.04.2021
Language:EN
[2021/16]
Type: A1 Application with search report 
No.:EP4045494
Date:24.08.2022
Language:EN
The application published by WIPO in one of the EPO official languages on 22.04.2021 takes the place of the publication of the European patent application.
[2022/34]
Type: B1 Patent specification 
No.:EP4045494
Date:11.10.2023
Language:EN
[2023/41]
Search report(s)International search report - published on:EP22.04.2021
ClassificationIPC:C07D401/14
[2022/34]
CPC:
C07D401/14 (EP,CN,US); C07D401/04 (CN,KR,US); Y02P20/55 (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 [2022/34]  
Extension statesBANot yet paid
MENot yet paid
Validation statesKHNot yet paid
MANot yet paid
MDNot yet paid
TNNot yet paid
TitleGerman:SYNTHESE VON 6-METHYL-N1-(4-(PYRIDIN-3-YL)PYRIMIDIN-2-YL)BENZOL-1,3-DIAMIN[2022/34]
English:SYNTHESIS OF 6-METHYL-N1-(4-(PYRIDIN-3-YL)PYRIMIDIN-2-YL)BENZENE-1,3-DIAMINE[2022/34]
French:SYNTHÈSE DE 6-MÉTHYL-N1-(4-(PYRIDIN-3-YL)PYRIMIDIN-2-YL)BENZÈNE-1,3-DIAMINE[2022/34]
Entry into regional phase05.05.2022National basic fee paid 
05.05.2022Designation fee(s) paid 
05.05.2022Examination fee paid 
Examination procedure23.06.2021Request for preliminary examination filed
International Preliminary Examining Authority: EP
05.05.2022Examination requested  [2022/34]
05.05.2022Date on which the examining division has become responsible
24.11.2022Amendment by applicant (claims and/or description)
08.05.2023Communication of intention to grant the patent
29.08.2023Fee for grant paid
29.08.2023Fee for publishing/printing paid
29.08.2023Receipt of the translation of the claim(s)
Fees paidRenewal fee
02.02.2023Renewal fee patent year 03
Penalty fee
Additional fee for renewal fee
31.10.202203   M06   Fee paid on   02.02.2023
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See the Register of the Unified Patent Court for opt-out data
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  TooltipES11.10.2023
HR11.10.2023
PL11.10.2023
RS11.10.2023
NO11.01.2024
GR12.01.2024
IS11.02.2024
[2024/27]
Former [2024/20]GR12.01.2024
IS11.02.2024
Cited inInternational search[Y]WO2004005281  (NOVARTIS AG [CH], et al) [Y] 12,13* page 24, last paragraph to page 25, line 15; pages 37-38, Example 1b and Example 1c *;
 [A]US2006173182  (KANKAN RAJENDRA N [IN], et al) [A] 1-10 * [0025]; [0027], compound (IV) to compound (II); [0036]-[0037] *;
 [X]CN100537563C  (ZHEJIANG PROV ACADEMY OF MEDIC [CN]) [X] 14-21 * claim 1, wherein R1 is hydrogen, R2 is methyl and R3 is "nitro, amino, dialkyl group substituted-amino, hydroxyl, carboxyl, carboxylic esters, acid amides" *;
 [YA]WO2013035102  (NATCO PHARMA LTD [IN], et al) [Y] 22-24 * page 15, Scheme D, in particular compound (III) to compound (V); see also page 15, Scheme D: compound (V) to compound (VI) in 80% yield and 99.4% HPLC purity * [A] 1-10;
 [Y]WO2015087343  (LAURUS LABS PRIVATE LTD [IN]) [Y] 12,13,22-24 * page 9, steps a) to c); page 10, lines 1-9; examples, in particular Examples 1 to 3 *;
 [XY]CN105801559  (UNIV BEIJING CHEMICAL TECH) [X] 11,14-21 * [0015]; [0038]; [0048]; examples, e.g. Examples 5-8 * [Y] 22-24;
 [Y]US2018334449  (SHI JINPU [CN], et al) [Y] 12,13,22-24 * page 1, compound (4) to compound (5); [0125], Example 1 *;
 [A]  - BAMBOROUGH ET AL, "N-4-Pyrimidinyl-1H-indazol-4-amine inhibitors of Lck: Indazoles as phenol isosteres with improved pharmacokinetics", BIORGANIC & MEDICINAL CHEMISTRY LETTERS, ELSEVIER, AMSTERDAM , NL, (2007), vol. 17, no. 15, doi:10.1016/J.BMCL.2007.04.029, ISSN 0960-894X, pages 4363 - 4368, XP022144705 [A] 1-10 * page 4365, Table 1; page 4368, point 12 *

DOI:   http://dx.doi.org/10.1016/j.bmcl.2007.04.029
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.