61594-81-8Relevant articles and documents
Chemical development of ZD9331: Synthesis of a bromomethylquinazolinone avoiding a nonselective radical bromination
Bentley, Dagmar,Godfrey, Andrew A.,Warren, Kenneth E. H.
, p. 553 - 555 (2006)
An efficient regiospecific synthesis of ZD9331 Pivaloyloxymethyl (POM) Bromide (4) has been accomplished via ZD9331 Quinacetate HCl (15) avoiding a nonselective bromination. The original route used a radical bromination on a substrate with three methyl groups, which generated a range of bromomethyl derived compounds that carried through to the final active pharmaceutical ingredient (API). A strategy, based on the Zinin reaction, was developed to synthesize the required bromomethyl compound in a regioselective manner. This approach was successfully scaled to manufacture a tonne of material.
N-desmethyl analogues of (+)-4-dimethylamino-2,α-dimethylphenethylamine. Synthesis and configurational relationships
Florvall,Persson
, p. 141 - 146 (2007/10/02)
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