HCID 22494716, Verbindung → HCID 58107469, Verbindung

A solution of 0.227 g of 1-(4-bromo-phenyl)-4-phenyl-piperidine in tetrahydrofuran (5 mL) is cooled to −78° C. and treated with 2 portions of 0.29 mL each of tert-butyllithium (1.5 M in pentane). After 20 min at −78° C. the reaction mixture is treated with 0.1 g of 4-chloro-N-methoxy-N-methyl-3-sulfamoyl-benzamide in tetrahydrofuran (5 mL) and stirred for another 1.5 h. The temperature is then increased slowly to 0° C. and after completion the reaction is quenched by addition of 2 mL of saturated aqueous ammonium chloride and extracted with diethyl ether. The organics are washed with water, dried over magnesium sulfate, concentrated to 0.27 g of crude product which is purified by silica gel chromatography (1:1 hexanes/ethyl acetate) to give 2-chloro-5-[4-(4-phenyl-piperidin-1-yl)-benzoyl]-benzenesulfonamide as a powder. MS (m/z): (M−1) 453; Rf 0.65 (1:1 hexanes/ethyl acetate)

1. customafter completion the reaction is quenched by addition of 2 mL of saturated aqueous ammonium chloride
2. extractionextracted with diethyl ether
3. washThe organics are washed with water
4. dry with materialdried over magnesium sulfate
5. concentrationconcentrated to 0.27 g of crude product which
6. customis purified by silica gel chromatography (1:1 hexanes/ethyl acetate)

ORD-Eintrag

ord-56d3da5f88ad40d08a5c971e437a6e4c

Quelldatensatz

uspto-grants-2015_03

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08975439B2