196603-96-0Relevant articles and documents
A where the shall he loni intermediate and its preparation method
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, (2019/04/04)
The present invention provides a where the shall he loni intermediate and its preparation method, the where the shall he loni intermediate by compound 8 in the sodium methoxide or metal lithium, sodium, potassium and the like under the action 9 acidifying the resulting: Wherein X fluorine, chlorine, bromine, move in the halogen, R3 is lithium, sodium, potassium and the like metal. The invention conducive to product quality control, the reaction condition is more simple, moderate, environmental protection, high requirements on equipment, each step the reaction yield is higher.
Tyrosine kinase inhibitors implant he loni and its key intermediate for the preparation of
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, (2018/10/19)
The invention discloses tyrosine kinase inhibitor implant he loni and its key intermediate of the preparation method, which belongs to the medicine, in the field of fine chemicals. The invention of the preparation method of gefitinib, is a brand-new preparation scheme, from whatever a intermediate starting, can be obtained in accordance with the requirements of the target compound. The method of the invention has short steps, the reaction operation is simple, safe and reliable, high yield, low cost, high purity, pollution little and simple operation and the like.
Synthesis and in vitro evaluation of [18F](R)-FEPAQ: A potential PET ligand for VEGFR2
Prabhakaran, Jaya,Arango, Victoria,Majo, Vattoly J.,Simpson, Norman R.,Kassir, Suham A.,Underwood, Mark D.,Polavarapu, Hanish,Bruce, Jeffrey N.,Canoll, Peter,John Mann,Dileep Kumar
scheme or table, p. 5104 - 5107 (2012/09/07)
Synthesis and in vitro evaluation of [18F](R)-N-(4-bromo-2- fluorophenyl)-7-((1-(2-fluoroethyl)piperidin-3-yl)methoxy)-6-methoxyquinazolin- 4-amine ((R)-[18F]FEPAQ or [18F]1), a potential imaging agent for the VEGFR2, usin