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tert-Butyl 4-[3-(4-fluorophenyl)ureido]piperidine-1-carboxylate synthesis

3synthesis methods
-

Yield:913634-45-4 71%

Reaction Conditions:

in tetrahydrofuran at 20; for 1 - 2 h;

Steps:

II.1

To a solution of compound I-c (5 g, 24.96 mmol) in THF (60 mL) was added compound II-a (R =R =R =R =H, R =F, 4.35 g, 27.43 mmol). The reaction mixture was allowed to stir at room temperature for 1-2 hours. After removing the solvent in vacuo, the residue was purified by column chromatography to give the title compound as a white solid (6 g, 71%).[113] 1H-NMR(CDCl ): δ 7.75-7.81(m, 2H), 7.08-7.27 (m, 2H), 4.09-4.22 (m, 3H),2.85-2.95 (m, 2H), 1.98-2.04 (m, 2H), 1.47 (s, 9H), 1.41-1.45 (m, 2H).

References:

WO2006/115353,2006,A1 Location in patent:Page/Page column 12