ECSP055693A - Proceso para la síntesis de intermediarios útiles para la síntesis de inhibidores de la tubulina - Google Patents

Proceso para la síntesis de intermediarios útiles para la síntesis de inhibidores de la tubulina

Info

Publication number
ECSP055693A
ECSP055693A EC2005005693A ECSP055693A ECSP055693A EC SP055693 A ECSP055693 A EC SP055693A EC 2005005693 A EC2005005693 A EC 2005005693A EC SP055693 A ECSP055693 A EC SP055693A EC SP055693 A ECSP055693 A EC SP055693A
Authority
EC
Ecuador
Prior art keywords
synthesis
tubulin inhibitors
useful
useful intermediaries
intermediaries
Prior art date
Application number
EC2005005693A
Other languages
English (en)
Inventor
Yanzhong Wu
Sreenivasulu Megati
Constatine Gletsos
John Thomas Kendall
Bogdan Kazimierz Wilk
Thurairajah Padmanathan
Panolil Raveendranath
Original Assignee
Wyeth Corp
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 Wyeth Corp filed Critical Wyeth Corp
Publication of ECSP055693A publication Critical patent/ECSP055693A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/02Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
    • C07K5/0205Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)3-C(=0)-, e.g. statine or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C269/00Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/16Preparation of optical isomers
    • C07C231/18Preparation of optical isomers by stereospecific synthesis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/22Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C269/00Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C269/02Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups from isocyanates with formation of carbamate groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C269/00Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C269/08Separation; Purification; Stabilisation; Use of additives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C313/00Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C313/02Sulfinic acids; Derivatives thereof
    • C07C313/06Sulfinamides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/44Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reduction and hydrolysis of nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/56Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds
    • C07C45/57Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom
    • C07C45/58Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom in three-membered rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/02General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length in solution
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

Abstract

La presente invención es un proceso para la preparación de compuestos de la Fórmula (I): donde R1, R2, R3, R4 y R5 son definidos en la especificación, los cuales son intermediarios útiles para la preparación de inhibidores de tubulina útiles en el tratamiento del cáncer.
EC2005005693A 2002-09-20 2005-03-21 Proceso para la síntesis de intermediarios útiles para la síntesis de inhibidores de la tubulina ECSP055693A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US41202402P 2002-09-20 2002-09-20

Publications (1)

Publication Number Publication Date
ECSP055693A true ECSP055693A (es) 2005-05-30

Family

ID=32030783

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2005005693A ECSP055693A (es) 2002-09-20 2005-03-21 Proceso para la síntesis de intermediarios útiles para la síntesis de inhibidores de la tubulina

Country Status (16)

Country Link
US (2) US6951955B2 (es)
EP (1) EP1539682A2 (es)
JP (1) JP2006500407A (es)
KR (1) KR20050054951A (es)
CN (1) CN1705639A (es)
AR (1) AR041321A1 (es)
AU (1) AU2003299042A1 (es)
BR (1) BR0314128A (es)
CA (1) CA2498759A1 (es)
EC (1) ECSP055693A (es)
MX (1) MXPA05002874A (es)
NO (1) NO20051146L (es)
RU (1) RU2005111753A (es)
TW (1) TW200409745A (es)
WO (1) WO2004026814A2 (es)
ZA (1) ZA200502275B (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7297896B2 (en) * 2002-11-21 2007-11-20 Hadco Santa Clara, Inc. Laser trimming of resistors
EP1567302B8 (en) * 2002-11-21 2013-05-15 Hadco Santa Clara, Inc. Laser trimming of resistors
ITRM20050345A1 (it) * 2005-06-30 2007-01-01 Sigma Tau Ind Farmaceuti Sintesi di deossi-biotinil esametilen diammina-dota.
CN102485726B (zh) * 2010-12-02 2015-07-01 天津药明康德新药开发有限公司 一种1-r-1’-螺-(哌啶-4,4’-喹啉)-2’(3’-氢)酮的制备方法
PT2968440T (pt) 2013-03-15 2019-07-31 Zymeworks Inc Compostos citotóxicos e antimitóticos e métodos de utilização dos mesmos
MX2016008448A (es) 2013-12-27 2017-01-09 Zymeworks Inc Conjugados de var2csa-farmaco.
ES2916722T3 (es) 2013-12-27 2022-07-05 Zymeworks Inc Sistemas de enlace que contienen sulfonamida para conjugados de fármacos
IL287645B2 (en) 2014-09-17 2024-04-01 Zymeworks Bc Inc Cytotoxic and anti-mitotic compounds and methods for their use
US10517958B2 (en) 2016-10-04 2019-12-31 Zymeworks Inc. Compositions and methods for the treatment of platinum-drug resistant cancer
TWI758313B (zh) * 2016-10-12 2022-03-21 美商陶氏農業科學公司 一種用於製備(1r,3r)-及(1s,3s)-2,2-二鹵基-3-(經取代之苯基)環丙烷甲酸的方法
CN109580801B (zh) * 2018-06-26 2021-09-07 深圳海王医药科技研究院有限公司 一种检测微管蛋白抑制剂及相关杂质的高效液相色谱法
CN110343056B (zh) * 2019-07-19 2022-01-07 爱斯特(成都)生物制药股份有限公司 一种n-叔丁氧羰基-n-甲基-2-氨基-4,4-二甲基戊酸的制备方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9508195D0 (en) * 1995-04-20 1995-06-07 Univ British Columbia Novel biologically active compounds and compositions,their use and derivation
CA2225325A1 (en) * 1997-12-19 1999-06-19 The University Of British Columbia Hemiasterlin analogs
JP2884081B1 (ja) * 1998-02-13 1999-04-19 名古屋大学長 アリールホウ素化合物触媒を用いたアルデヒド類又はケトン類の製造方法
EP1531846A4 (en) * 2002-02-27 2006-04-19 Us Gov Health & Human Serv CONJUGATES OF LIGAND, LINK AND CYTOTOXIC AGENS, AND RELATED COMPOSITIONS AND USE PROCESSES

Also Published As

Publication number Publication date
US20050288486A1 (en) 2005-12-29
AU2003299042A1 (en) 2004-04-08
EP1539682A2 (en) 2005-06-15
CA2498759A1 (en) 2004-04-01
RU2005111753A (ru) 2005-11-20
WO2004026814A2 (en) 2004-04-01
CN1705639A (zh) 2005-12-07
AR041321A1 (es) 2005-05-11
BR0314128A (pt) 2005-06-28
MXPA05002874A (es) 2005-05-27
NO20051146L (no) 2005-04-18
US20040063904A1 (en) 2004-04-01
US6951955B2 (en) 2005-10-04
ZA200502275B (en) 2007-10-31
KR20050054951A (ko) 2005-06-10
TW200409745A (en) 2004-06-16
WO2004026814A3 (en) 2004-08-12
US7078572B2 (en) 2006-07-18
JP2006500407A (ja) 2006-01-05

Similar Documents

Publication Publication Date Title
ECSP055693A (es) Proceso para la síntesis de intermediarios útiles para la síntesis de inhibidores de la tubulina
UY28333A1 (es) Inhibidores de caspasa y sus usos.
HN2002000067A (es) Inhibidores de la rho - quinasa.
CR10072A (es) Derivados de pirimidinil-aril-urea que son inhibidores de fgf
BRPI0510177B8 (pt) composto, composição farmacêutica e uso do mesmo
GT200600215A (es) Metodos para sintetizar derivados de 6-alquilaminoquinolina
UY27225A1 (es) Inhibidores de la rho-quinasa
ATE398125T1 (de) Chinazolin-derivate als tgf-beta-inhibitoren
GT200300292A (es) Derivados de pirimidina para el tratamiento de crecimiento celular anormal
DOP2006000169A (es) Inhibidores espiropiperidina de beta-secretasa para el tratamiento de la enfermedad de alzheimer
UY27427A1 (es) Nuevas dihidro-pteridinonas, procedimientos para su preparación y su utilización como medicamentos
GT200500296A (es) Sintesis asimetrica de derivados del dehidrobenzofurano
UY29360A1 (es) Nuevos derivados de pirazol, composiciones farmacéuticas que los contienen, procedimientos de preparación y aplicaciones.
PE20060504A1 (es) Derivados de pirimidina en el tratamiento de cancer
UY28144A1 (es) Agentes terapéuticos
SV2010003598A (es) Derivados de tiazol usados como inhibidores de pi 3-cinasa
UY28695A1 (es) Derivados de difenilazetidona
CR8350A (es) 4-anilino-3-quinolincarbonitrilos para el tratamiento de leucemia mielogenica cronica
CY1109569T1 (el) Υποκατεστημενα παραγωγα κυκλοεξανο-1,4-διαμινης
TNSN06260A1 (en) Process for the preparation of tryptase inhibitors
UY28754A1 (es) Proceso quimico
ECSP045396A (es) Proceso para preparar derivados de 6-alquiliden penem
HK1096548A1 (en) Imidazopyridine-derivatives as inductible no-synthase inhibitors
SE0403085D0 (sv) Novel componds
SI1606288T1 (sl) Derivati benzensulfonamida, postopek za njihovo pripravo in njihova uporaba za zdravljenje bolečine