Réaction #1147494

ord-f8d994a250cb4766a4ee77a0a1acb428

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreobtained as a yellow solid in 10% overall yield, MS

Mode opératoire

The title compound was prepared strarting from 4-bromo-1-ethoxy-2-nitro-benzene and piperidine as described for 4-fluoro-N-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-benzamide (Example 275) and obtained as a yellow solid in 10% overall yield, MS: m/e=400 (M+H+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06521754B2uspto-grants-2003_02