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Dive into the research topics where Frank Robert Busch is active.

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Featured researches published by Frank Robert Busch.


Synthetic Communications | 2008

Synthesis of (1‐(Aminomethyl)‐2,3‐dihydro‐1H‐inden‐3‐yl)methanol: Structural Confirmation of the Main Band Impurity Found in Varenicline® Starting Material

Frank Robert Busch; Paul E. Concannon; Robert Eugene Handfield; Jason D. McKinley; Megan E. McMahon; Robert A. Singer; Timothy J. N. Watson; Gregory J. Withbroe; Mariano Stivanello; Lucia Leoni; Chiara Bezze

Abstract Described here is the synthesis of (1‐(aminomethyl)‐2,3‐dihydro‐1H‐inden‐3‐yl)methanol 1, the previously unidentified impurity found in the synthesis of 2,1 providing a confirmation of the structure. Fabbrica Italiano Sintetici (FIS), working in conjunction with Pfizer Groton, reported an unidentified impurity, referred to as the “main band impurity”, in 2 at levels of 0.4 to 0.8%. The structure was postulated to be 1, the open‐ring product of the lithium aluminum hydride (LAH) reduction of 3 to 2. Although the cis isomer of 1 was previously reported in the literature,2 a much shorter racemic synthesis was developed using intermediates employed for the production of Varenicline®. Several reducing agents were screened for the synthesis of 1, with LiAlH4 followed by basic workup conditions giving optimal results. High performance liquid chromatography (HPLC) analysis ultimately confirmed the structure of 1 as the main band impurity generated during the synthesis of 2.


Archive | 1992

Monohydrate of 5-(2-(4-(1,2 benzisothiazol-3-yl)-1- piperazinyl)-ethyl)-6-chloro-1,3-dihydro-2h-indol-2-one hydrochloride

Douglas John Meldrum Allen; Frank Robert Busch; Sabeto A Diroma; Dennis M Godek


Archive | 1993

Process for Preparing Aryl Piperazinyl-Heterocyclic Compounds

Frank Robert Busch; Douglas John Meldrum Allen; Paul Bowles; Sabeto A Diroma; Dennis M Godek


Archive | 1997

Mesylate dihydrate salts of 5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)-ethyl)-6-chloro-1,3-dihydro-2(1H)-indol-2-one (=ziprasidone), its preparation and its use as dopamine D2 antagonist

Frank Robert Busch; Carol A. Rose; Russell James Shine


Archive | 2003

Controlled synthesis of ziprasidone and compositions thereof

Frank Robert Busch; Adam Worth Grobin; Harry Ralph Howard; Kyle R. Leeman


Archive | 1993

Process for preparing aryl piperazinyl-heterocyclic compounds with a piperazine salt

Frank Robert Busch; Paul Bowles; Douglas John; Meldrum Allen; Sabeto A Diroma; Dennis M Godek


Organic Process Research & Development | 2002

Practical Large-Scale Synthesis of 3,4-Isopropylidenedioxypyrrolidine Hydrotosylate: Atom Economical Self-Hydrogenolysis of a Crystalline Borane−Benzylamine Adduct

Michel Couturier; Brian M. Andresen; Jeffrey B. Jorgensen; John L. Tucker; Frank Robert Busch; Steven J. Brenek; Pascal Dubé; David J. am Ende; Joanna Teresa Negri


Archive | 2003

Ziprasidone composition and synthetic controls

Frank Robert Busch; Adam Worth Grobin; Kyle R. Leeman; Harry Ralph Howard


Organic Process Research & Development | 2004

Use of DOE for Rapid Development of a Red-Al Reduction Process for the Synthesis of 3,4-Isopropylidenedioxypyrrolidine Hydrotosylate

Asaf Alimardanov; Mark T. Barrila; Frank Robert Busch; James J. Carey; Michel Couturier; Curtis Cui


Archive | 1992

Method for making steroidal peracyl glycosides

Douglas J. M. Allan; Frank Robert Busch; John Francis Lambert; Russell James Shine; Stanley Walter Walinsky

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