Fluorine-18 labelled building blocks for PET tracer synthesis

D Van Der Born, A Pees, AJ Poot, RVA Orru… - Chemical Society …, 2017 - pubs.rsc.org
Positron emission tomography (PET) is an important driver for present day healthcare.
Fluorine-18 is the most widely used radioisotope for PET imaging and a thorough overview …

2-[18 F] Fluoroethyl tosylate–a versatile tool for building 18 F-based radiotracers for positron emission tomography

T Kniess, M Laube, P Brust, J Steinbach - MedChemComm, 2015 - pubs.rsc.org
Positron emission tomography (PET) is a modern in vivo imaging technique and an
important diagnostic modality for clinical and pre-clinical research. The incorporation of a …

Discovery and evaluation of clinical candidate AZD3759, a potent, oral active, central nervous system-penetrant, epidermal growth factor receptor tyrosine kinase …

Q Zeng, J Wang, Z Cheng, K Chen… - Journal of medicinal …, 2015 - ACS Publications
Recent reports suggest that an increasing number of patients with lung cancer, especially
those with activating mutations of the epidermal growth factor receptor (EGFR), also present …

Development of [18F] afatinib as new TKI-PET tracer for EGFR positive tumors

P Slobbe, AD Windhorst, M Stigter-van Walsum… - Nuclear medicine and …, 2014 - Elsevier
Introduction Afatinib is an irreversible ErbB family blocker that was approved for the
treatment of EGFR mutated non-small cell lung cancer in 2013. Positron emission …

Synthesis and antitumour activity of 4-aminoquinazoline derivatives

GN Lipunova, EV Nosova, VN Charushin… - Russian Chemical …, 2016 - iopscience.iop.org
Pieces of data on the synthesis and antitumour activity of 4-aminoquinazolines are
summarized and analyzed. Key methods for the synthesis of these compounds are …

Continuous Flow Synthesis of a Key Intermediate Common to Gefitinib and Larotinib

H Zhang, Y Li, X Wu, N Wang, X Chen… - … Process Research & …, 2024 - ACS Publications
Herein, we demonstrate a continuous flow synthesis method for 4-(3-chloro-4-
fluorophenylamino)-6-hydroxy-7-methoxyquinazoline, a key intermediate of Gefitinib and …

The first radiosynthesis of [11C] AZD8931 as a new potential PET agent for imaging of EGFR, HER2 and HER3 signaling

M Wang, M Gao, QH Zheng - Bioorganic & Medicinal Chemistry Letters, 2014 - Elsevier
Abstract The reference standard AZD8931 {2-(4-((4-((3-chloro-2-fluorophenyl) amino)-7-
methoxyquinazolin-6-yl) oxy) piperidin-1-yl)-N-methylacetamide}(11a) was synthesized from …

[PDF][PDF] 18F 标记表皮生长因子受体酪氨酸激酶抑制剂4-苯氨基-喹唑啉类方法进展

孙夕林, 王凯, 赵周社, 李宏利, 孙莹莹… - 现代生物医学 …, 2014 - biomed.cnjournals.com
分子成像可在活体状态下直观判断分子靶向药物靶位点存在状态, 分子靶向药物与靶位点结合率
及精确监测分子靶向药物的治疗疗效, 为临床治疗方案的选择和调整提供依据. EGFR …

An efficient synthesis of quinazoline or pyrrolo[1,2-a]quinazolin-5(1H)-one derivatives in ionic liquids catalyzed by iodine

JQ Liu, F Dong, WT Zhang, XS Wang - Research on Chemical …, 2017 - Springer
The iodine-catalyzed reaction of 2-amino-N′-arylbenzohydrazides and haloketones was
carried out in ionic liquids and was found in good chemoselectivity. 5-Chloropentan-2-one …

Синтез и противоопухолевая активность производных 4-аминохиназолинов

ГН Липунова, ЭВ Носова, ВН Чарушин, ОН Чупахин - Успехи химии, 2016 - elibrary.ru
Обобщены и проанализированы данные по синтезу и противоопухолевой активности 4-
аминохиназолинов. Рассмотрены важнейшие методы синтеза таких соединений, в …