844694-85-5Relevant academic research and scientific papers
Donepezil hydrochloride impurities and preparation method thereof
-
Paragraph 0019, (2022/03/02)
The present invention relates to a new impurity of donepezil hydrochloride as shown below and a method for preparing it, said method comprising reacting donepezil and benzyl chloride or bromide to form a quaternary ammonium salt, and then reactivated by rearrangement to obtain a target compound. Impurities obtained by the present invention are very useful for studying the source of impurities and the development of new analytical methods.
CRYSTALLINE FORM OF DONEPEZIL HYDROCHLORIDE
-
Page/Page column 9, (2008/06/13)
A process for preparing crystalline form I of donepezil hydrochloride comprises: a) condensing 5,6-dimethoxy-2-piperidin-4-yl-methyl-indan-1-one with benzyl bromide and reacting a condensation product with hydrobromic acid to form donepezil hydrobromide; and b) hydrolyzing donepezil hydrobromide, followed by reacting with aqueous hydrochloric acid.
New synthesis of donepezil through palladium-catalyzed hydrogenation approach
Elati, Chandrashekar R.,Kolla, Naveenkumar,Chalamala, Subrahmanyeswara Rao,Vankawala, Pravinchandra J.,Sundaram, Venkataraman,Vurimidi, Himabindu,Mathad, Vijayavitthal T.
, p. 169 - 174 (2007/10/03)
A new, economical, and efficient process has been developed for large-scale synthesis of donepezil 1, an anti-Alzheimer's drug. The process involves palladium-catalyzed hydrogenation of (2E)-5,6-dimethoxy-2-(pyridin-4- ylmethylene)indan-1-one 6 to provide 5,6-dimethoxy-2-(piperidin-4-ylmethyl) indan-1-one 8 as a key step. Copyright Taylor & Francis LLC.
