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4-fluoro-N-piperidin-4-ylbenzenesulfonamide hydrochloride synthesis

4synthesis methods
913634-49-8 Synthesis
4-(4-Fluoro-benzenesulfonylaMino)-piperidine-1-carboxylic acid tert-butyl ester

913634-49-8
16 suppliers
$235.00/250mg

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Yield:913634-50-1 97%

Reaction Conditions:

with hydrogenchloride in ethyl acetate;

Steps:

III.2

Compound ?i-b (10 g, 27.899 mmol) was dissolved in ethyl acetate (120 mL) and saturated with gaseous HCl, and the reaction mixture stirred until all of the starting material was consumed. The mixture was concentrated to give amine hydrochloride salt as a white crystalline solid which was used in next step without further purification (8 g, 97%).[140] 1H-NMR(D2O): δ 7.61-7.68 (m, 2H), 7.10-7.17 (m, 2H), 3.34-3.44 (m, 2H),3.01-3.15 (m, IH), 2.93-3.09 (m, 2H), 2.04-2.15 (m, 2H), 1.63-1.75 (m, 2H).

References:

WO2006/115353,2006,A1 Location in patent:Page/Page column 15