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Pyridine, 4-acetyl-2-fluoro

The scheme required to prepare the potent tri-fluoro corticoid cormethasone acetate (292) illustrates the synthetic complexities involved in some of this work. Sequential acetylation of the pregnenolone derivative 278 with first acetic anhydride in pyridine and then acetic anhydride in the presence of tosic acid affords diacetate 279. Reaction of that intermediate with nitrosyl fluoride results initially in addition of the reagent to the 5,6-olefin moiety to afford the fluoro oxime reaction with a second mole of reagent at nitrogen gives the nitroimine derivative 280 passage over alumina serves to hydrolyze the imine function to the corresponding 6-ketone (281). [Pg.194]

AUTONOM 6-Acetyl-3-(2-(3-lttert -butyl-phenyl)-ethylidene)-l-(2-fluoro-2-phenyl-thyl)-5-(8-nethyl-octahydro 2,5-nethano-isoqui olin-3-yl)-7 thioacryloyloxy-2, dihydro-l H pyrrolo[3,2 ltb ]pyridine-2 carboxylic acid vinyl ester... [Pg.62]


See other pages where Pyridine, 4-acetyl-2-fluoro is mentioned: [Pg.201]    [Pg.448]    [Pg.701]    [Pg.110]    [Pg.127]    [Pg.135]    [Pg.239]    [Pg.242]    [Pg.239]    [Pg.220]    [Pg.362]    [Pg.518]    [Pg.4]    [Pg.101]    [Pg.1232]    [Pg.1711]    [Pg.20]    [Pg.101]    [Pg.1320]    [Pg.406]    [Pg.173]    [Pg.448]    [Pg.701]    [Pg.95]    [Pg.193]    [Pg.448]    [Pg.701]    [Pg.406]    [Pg.2042]    [Pg.67]    [Pg.282]    [Pg.109]    [Pg.104]    [Pg.265]   
See also in sourсe #XX -- [ Pg.52 , Pg.222 ]




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Acetylation pyridine

Fluoro pyridines

Pyridine 3- acetyl

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