CY1106370T1 - Επιλεκτικη συνθεση cf3-υποκατεστημενων πυριμιδινων - Google Patents

Επιλεκτικη συνθεση cf3-υποκατεστημενων πυριμιδινων

Info

Publication number
CY1106370T1
CY1106370T1 CY20071100341T CY071100341T CY1106370T1 CY 1106370 T1 CY1106370 T1 CY 1106370T1 CY 20071100341 T CY20071100341 T CY 20071100341T CY 071100341 T CY071100341 T CY 071100341T CY 1106370 T1 CY1106370 T1 CY 1106370T1
Authority
CY
Cyprus
Prior art keywords
formula
substituted pyrimidines
selective synthesis
compound
pyrimidine
Prior art date
Application number
CY20071100341T
Other languages
English (en)
Inventor
John Charles Kath
Daniel Tyler Richter
Michael Joseph Luzzio
Original Assignee
Pfizer Products Incorporated
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Products Incorporated filed Critical Pfizer Products Incorporated
Publication of CY1106370T1 publication Critical patent/CY1106370T1/el

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

Η παρούσα εφεύρεση αναφέρεται σε μια μέθοδο παρασκευής μιας ένωσης του τύπου (I), όπου τα Χ1, Χ2 και R3-R4 είναι όπως ορίστηκε στο παρόν. Η μέθοδος περιλαμβάνει την αντίδραση μιας ένωσης του τύπου (II) με μια αμίνη του τύπου (III) (HNR3R4) παρουσία οξέος του Lewis και μιας μη πυρηνόφιλης βάσης. Η ομάδα 2,4-διαμινο-πυριμιδίνης είναι ένα κοινό συστατικό σε μια ποικιλία βιολογικώς δραστικών μορίων παρόμοιων με φάρμακα και τα παράγωγα πυριμιδίνης βρέθηκαν ότι είναι χρήσιμα στη θεραπεία της μη φυσιολογικής κυτταρικής ανάπτυξης, όπως ο καρκίνος, σε θηλαστικά.
CY20071100341T 2003-09-05 2007-03-12 Επιλεκτικη συνθεση cf3-υποκατεστημενων πυριμιδινων CY1106370T1 (el)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US50073303P 2003-09-05 2003-09-05
PCT/IB2004/002744 WO2005023780A1 (en) 2003-09-05 2004-08-24 Selective synthesis of cf3-substituted pyrimidines

Publications (1)

Publication Number Publication Date
CY1106370T1 true CY1106370T1 (el) 2011-10-12

Family

ID=34272990

Family Applications (1)

Application Number Title Priority Date Filing Date
CY20071100341T CY1106370T1 (el) 2003-09-05 2007-03-12 Επιλεκτικη συνθεση cf3-υποκατεστημενων πυριμιδινων

Country Status (24)

Country Link
US (1) US7122670B2 (el)
EP (1) EP1663991B1 (el)
JP (1) JP4842816B2 (el)
KR (1) KR100694732B1 (el)
CN (1) CN100465164C (el)
AR (1) AR045557A1 (el)
BR (1) BRPI0414059B8 (el)
CA (1) CA2537373C (el)
CO (1) CO5650237A2 (el)
CY (1) CY1106370T1 (el)
DE (1) DE602004004287T2 (el)
DK (1) DK1663991T3 (el)
ES (1) ES2276344T3 (el)
HK (1) HK1091824A1 (el)
IL (1) IL173363A (el)
MX (1) MXPA06002552A (el)
NO (1) NO334383B1 (el)
NZ (1) NZ544969A (el)
PL (1) PL1663991T3 (el)
PT (1) PT1663991E (el)
RU (1) RU2315759C2 (el)
TW (1) TWI283667B (el)
WO (1) WO2005023780A1 (el)
ZA (1) ZA200600747B (el)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GEP20084357B (en) * 2002-12-20 2008-04-29 Pfizer Prod Inc Pyrimidine derivatives for the treatment of abnormal cell growth
US20060205945A1 (en) * 2004-05-14 2006-09-14 Pfizer Inc Pyrimidine derivatives for the treatment of abnormal cell growth
JP4778717B2 (ja) * 2005-03-25 2011-09-21 富士フイルム株式会社 複素環式化合物の製造方法
DE102007010801A1 (de) 2007-03-02 2008-09-04 Bayer Cropscience Ag Diaminopyrimidine als Fungizide
CN101678215B (zh) * 2007-04-18 2014-10-01 辉瑞产品公司 用于治疗异常细胞生长的磺酰胺衍生物
KR101294731B1 (ko) * 2007-06-04 2013-08-16 삼성디스플레이 주식회사 어레이 기판, 이를 갖는 표시패널 및 이의 제조방법
UY31714A (es) * 2008-03-20 2009-11-10 Boehringer Ingelheim Int Preparación selectiva de pirimidinas sustituidas
WO2009115583A1 (en) * 2008-03-20 2009-09-24 Boehringer Ingelheim International Gmbh Regioselective preparation of substituted pyrimidines
DE102009006643A1 (de) 2009-01-29 2010-08-05 Saltigo Gmbh Herstellung von halogenierten N-heteroaromatischen Polyhalogenderivaten
TW201100441A (en) 2009-06-01 2011-01-01 Osi Pharm Inc Amino pyrimidine anticancer compounds
US8933227B2 (en) 2009-08-14 2015-01-13 Boehringer Ingelheim International Gmbh Selective synthesis of functionalized pyrimidines
WO2011018517A1 (en) 2009-08-14 2011-02-17 Boehringer Ingelheim International Gmbh Regioselective preparation of 2-amino-5-trifluoromethylpyrimidine derivatives
JP6000273B2 (ja) 2010-11-29 2016-09-28 オーエスアイ・ファーマシューティカルズ,エルエルシー 大環状キナーゼ阻害剤
UY33817A (es) 2010-12-21 2012-07-31 Boehringer Ingelheim Int ?nuevas oxindolpirimidinas bencílicas?.
EP2675793B1 (en) 2011-02-17 2018-08-08 Cancer Therapeutics Crc Pty Limited Fak inhibitors
CN103534240B (zh) 2011-02-17 2015-12-09 癌症疗法Crc私人有限公司 选择性fak抑制剂
WO2014126954A1 (en) 2013-02-13 2014-08-21 OSI Pharmaceuticals, LLC Regioselective synthesis of substituted pyrimidines
US9656970B2 (en) 2014-05-08 2017-05-23 Tosoh F-Tech, Inc. 5-(trifluoromethyl)pyrimidine derivatives and method for producing same
JP6391985B2 (ja) * 2014-05-16 2018-09-19 東ソー・ファインケム株式会社 2−置換−4−(2,2,2−トリフルオロエトキシ)−5−(トリフルオロメチル)ピリミジン誘導体及びその製造方法
JP6391988B2 (ja) * 2014-05-21 2018-09-19 東ソー・ファインケム株式会社 5−(トリフルオロメチル)ピリミジン誘導体の製造方法及び新規5−(トリフルオロメチル)ピリミジン誘導体
CN108440499A (zh) * 2018-03-22 2018-08-24 盐城师范学院 一种色瑞替尼及其关键中间体的制备方法
CN114213339B (zh) * 2021-12-20 2023-10-31 苏州康纯医药科技有限公司 一种表皮细胞生长因子受体突变抑制剂的制备方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003030909A1 (en) * 2001-09-25 2003-04-17 Bayer Pharmaceuticals Corporation 2- and 4-aminopyrimidines n-substtituded by a bicyclic ring for use as kinase inhibitors in the treatment of cancer
ATE407678T1 (de) * 2001-10-17 2008-09-15 Boehringer Ingelheim Pharma Pyrimidinderivate, arzneimittel enthaltend diese verbindungen, deren verwendung und verfahren zu ihrer herstellung

Also Published As

Publication number Publication date
KR100694732B1 (ko) 2007-03-14
PL1663991T3 (pl) 2007-04-30
CN1845906A (zh) 2006-10-11
TWI283667B (en) 2007-07-11
CN100465164C (zh) 2009-03-04
BRPI0414059B8 (pt) 2021-05-25
CA2537373A1 (en) 2005-03-17
KR20060030918A (ko) 2006-04-11
BRPI0414059B1 (pt) 2018-11-06
DE602004004287T2 (de) 2007-06-21
ES2276344T3 (es) 2007-06-16
CA2537373C (en) 2009-10-20
NZ544969A (en) 2008-07-31
IL173363A (en) 2010-05-31
JP2007504211A (ja) 2007-03-01
AR045557A1 (es) 2005-11-02
BRPI0414059A (pt) 2006-10-24
TW200514773A (en) 2005-05-01
ZA200600747B (en) 2007-03-28
CO5650237A2 (es) 2006-06-30
DK1663991T3 (da) 2007-04-10
AU2004270480A1 (en) 2005-03-17
JP4842816B2 (ja) 2011-12-21
US20050101620A1 (en) 2005-05-12
MXPA06002552A (es) 2006-06-20
EP1663991B1 (en) 2007-01-10
RU2315759C2 (ru) 2008-01-27
WO2005023780A1 (en) 2005-03-17
NO20061509L (no) 2006-04-03
IL173363A0 (en) 2006-06-11
NO334383B1 (no) 2014-02-24
DE602004004287D1 (de) 2007-02-22
US7122670B2 (en) 2006-10-17
HK1091824A1 (en) 2007-01-26
RU2006106727A (ru) 2006-06-27
PT1663991E (pt) 2007-02-28
EP1663991A1 (en) 2006-06-07

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