AN UNBIASED VIEW OF FLMODAFINIL

To obtain analogs of compound X, the starting acid 2 was reacted having an surplus of dimethyl sulphate and also the received spinoff 3 was subjected to a multidirectional synthesis (Scheme 3). In the initial case, bromine was released into your methyl group to give a compound 3d, by reaction with NBS in CCl4. Within the response from the compound